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INFECTION CONTROL & PREVENTION A PEDIATRICIAN’S GUIDE PEER-REVIEWED FEATURE Deciphering bacterial meningitis “When can my child return to school?” HOSPITAL ZONE Children’s Hospital Los Angeles’ novel facial cleft care ContemporaryPediatrics.com Expert Clinical Advice for Today’s Pediatrician JULY 2016 VOL. 33 | NO. 07 Contemporary PEDIATRICS CONTEMPORARY PEDIATRICS JULY 2016 VOL. 33 NO. 07 INFECTION CONTROL & PREVENTION DECIPHERING BACTERIAL MENINGITIS CHILDREN'S HOSPITAL LOS ANGELES' NOVEL FACIAL CLEFT CARE EYE ON WASHINGTON FDA Seeks to Define “Healthy”

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INFECTION CONTROL

&PREVENTION

A PEDIATRICIAN’S GUIDE

PEER-REVIEWED FEATURE

Deciphering bacterialmeningitis

“When can my childreturn to school?”

HOSPITAL ZONE

Children’s HospitalLos Angeles’ novel facial cleft care

ContemporaryPediatrics.comExpert Clinical Advice for Today’s Pediatrician ContemporaryPediatrics.comExpert Clinical Advice for Today’s Pediatrician

JULY 2016VOL. 33 | NO. 07Contemporary

PEDIATRICS

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' NO

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L CLEFT C

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EYE ON

WASHINGTON

FDA Seeks to

Defi ne “Healthy”

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 64

editorial advisory boardContemporaryPEDIATRICS

physician contributing editors

founding editor

Frank A Oski, MD

OUR MISSION Office- and hospital-based pediatricians and nurse practitioners use Contemporary Pediatrics’ timely, trusted, and

practical information to enhance their day-to-day care of children. We advance pediatric providers’ professional development through

in-depth, peer-reviewed clinical and practice management articles, case studies, and news and trends coverage.

contentSARA MICHAELVP, Content & Strategy

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CUSTOMER SERVICE888.527.7008

Scott A Shipman, MD, MPH Director of Primary Care Initiatives

and Workforce Analysis,

Association of American Medical

Colleges, Washington, DC, and

Assistant Professor of Pediatrics,

Dartmouth Institute for Health

Policy and Clinical Practice, Geisel

School of Medicine at Dartmouth,

Lebanon, New Hampshire

Michael G Burke, MDSection Editor for Journal

Club, Chairman, Department of

Pediatrics, Saint Agnes Hospital,

Baltimore, Maryland

Bernard A Cohen, MDSection Editor for Dermcase,

Professor of Pediatrics and

Dermatology, Johns Hopkins

University School of Medicine,

Baltimore, Maryland

Michael S Jellinek, MD Professor of Psychiatry and of

Pediatrics, Harvard Medical School,

Boston, and Chief Executive

Officer, Community Network,

Lahey Health System, Burlington,

Massachusetts

Jane A Oski, MD, MPH Department of Pediatrics, Tuba City

Regional Health Care Corporation,

Tuba City, Arizona

W Christopher Golden, MDAssistant Professor of Pediatrics

(Neonatology), Johns Hopkins

University School of Medicine, and

Medical Director, Full Term Nursery,

Johns Hopkins Hospital, Baltimore,

Maryland

Steven M Selbst, MD Professor of Pediatrics, Vice Chair

for Education, Director, Pediatric

Residency Program, Sidney Kimmel

Medical College at Thomas

Jefferson University, Philadelphia,

Pennsylvania, and Attending

Physician, Pediatric Emergency

Medicine, Nemours/Alfred I duPont

Hospital for Children, Wilmington,

Delaware

Harlan R Gephart, MD Clinical Professor of Pediatrics,

University of Washington School of

Medicine, Seattle, Washington

Andrew J Schuman, MDSection Editor for Peds v2.0,

Clinical Assistant Professor

of Pediatrics, Geisel School of

Medicine at Dartmouth, Lebanon,

New Hampshire

Gary L Freed, MD, MPH Director, Division of General

Pediatrics, Professor of Pediatrics

and Health Management and

Policy, and Director, Child Health

Evaluation and Research (CHEAR)

Unit, University of Michigan Health

Systems, Ann Arbor, Michigan

Donna Hallas, PhD, CPNP, PNP-BC, PMHS, FAANPClinical Professor, New York

University (NYU) College of

Nursing, and Coordinator, Pediatric

Nurse Practitioner Program, New

York, New York

Trust Eucerin. Over 100 years committed

to skin science.Reference: 1. Weber TM, Samarin F, Babcock MJ, Filbry A, Rippke F. Steroid-free over-the-counter eczema skin care formulations reduce risk of flare, prolong time to flare, and reduce eczema symptoms in pediatric subjects with atopic dermatitis. J Drugs Dermatol. 2015;14(5):478-485.

Eucerin Eczema Relief Body Creme relieves dry,

itchy skin and provides hydration for patients

with eczema-prone skin1—in a light, fast-absorbing

daily formula

FLARE FREE AND LOVING ITEUCERIN® ECZEMA RELIEF BODY CREME HELPED

4 OUT OF 5 CHILDREN STAY FLARE FREE FOR 6 MONTHS1*

*Subjects applying daily Eucerin® Eczema Relief Body Creme demonstrated a statistically significant difference (P =0.006) in the prevention of eczema flares compared with control group subjects.1

©2016 Beiersdorf Inc.

SKIN PROTECTANT

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 66

ContemporaryPEDIATRICS

13 puzzlerBOY WITH FEVER, COUGH, AND ORAL LESIONS

J David Sterns, MD; Riva Kamat, MD, FAAP

44 dermcaseHYPERPIGMENTATION AROUND A TEEN’S EYE

Jessica A Gangaram, MD

July 2016

VOL. 33 NO. 7

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Contemporary Pediatrics (Print ISSN: 8750-0507, Digital ISSN: 2150-6345) is published monthly by UBM Medica, 131 W. 1st Street, Duluth, MN 55802. Subscription rates: one year $89, two years $150 in the United States & Possessions, $105 for one year, $189 for two years in Canada and Mexico; all other countries $105 for one year, $189 for two years. Single copies (prepaid only) $18 in the United States; $22 in Canada and Mexico, and $24 in all other countries. Include $6.50 per order plus $2.00 per additional copy for U.S. postage and handling. Periodicals postage paid at Duluth, MN 55806 and additional mailing offices. POSTMASTER: Please send address changes to Contemporary Pediatrics, PO Box 6083, Duluth, MN 55806-6083. Canadian GST number: R-124213133RT001. Publications Mail Agreement Number 40612608. Return Undeliverable Canadian Addresses to: IMEX Global Solutions, P. O. Box 25542, London, ON N6C 6B2, CANADA . Printed in the U.S.A.© 2016 UBM. All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical including by photocopy, recording, or information storage and retrieval without permission

in writing from the publisher. Authorization to photocopy items for internal/educational or personal use, or the internal/educational or personal use of specific clients is granted by UBM for libraries and other users registered with the Copyright Clearance Center, 222 Rosewood Dr. Danvers, MA 01923, 978-750-8400 fax 978-646-8700 or visit http://www.copyright.com online. For uses beyond those listed above, please direct your written request to Permission Dept. fax 440-756-5255 or email: [email protected] Medica provides certain customer contact data (such as customers’ names, addresses, phone numbers, and e-mail addresses) to third parties who wish to promote relevant products, services, and other opportunities that may be of interest to you. If you do not want UBM Medica to make your contact information available to third parties for marketing purposes, simply call toll-free 866-529-2922 between the hours of 7:30 a.m. and 5 p.m. CST and a customer service representative will assist you in removing your name from UBM Medica’s lists. Outside the U.S., please phone 218-740-6477.Contemporary Pediatrics does not verify any claims or other information

appearing in any of the advertisements contained in the publication, and cannot take responsibility for any losses or other damages incurred by readers in reliance of such content.Contemporary Pediatrics welcomes unsolicited manuscripts for consideration. To assist the Editor in the safekeeping and return of submitted materials, authors must transmit manuscripts and their accessory parts (photographs, computer diskettes, permissions, etc.) to Contemporary Pediatrics by reputable overnight courier, certified or registered US Postal Service mail (including “return receipt requested” service), or messenger. Library Access Libraries offer online access to current and back issues of Contemporary Pediatrics through the EBSCO host databases. To subscribe, call toll-free 888-527-7008. Outside the U.S. call 218-740-6477.

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NEW VIDEOS AT CONTEMPORARYPEDIATRICS.COM

NEW to Contemporary Pediatrics! Check out our latest evidence-based Medical Minute videos from Bobby Lazzara, MD. This month? A nationally representative survey asks parents what they want to know about vaccines. PLUS! Dr. Lazzara explains the latest recommendations for pediatric dermatology conditions.

peer-reviewed feature14 Deciphering bacterial meningitisPediatricians need to understand not only how bacterial meningitis can be prevented in

children through vaccination, but also its risks, symptoms, workup, and treatment.

Pat F Bass III, MD, MS, MPH

clinical feature21 Infection control and prevention:

“When can my child return to school?”Teaching parents and educators about infection control practices can improve

prevention and decrease risk of disease transmission to help keep kids in school.

Pat F Bass III, MD, MS, MPH

the hospital zone32 CLEFT LIP AND

PALATE: TEAM APPROACH

TO TREATMENTA multidisciplinary center for children

with facial clefts ensures that patients

treated by its team of specialty

providers emerge with little or no

evidence of their cleft deformities.

Lisette Hilton

peer-reviewed feature25 SOARS model: Risk assessment of nonsuicidal self injury A new asssessment tool helps physicians screen adolescents for self-harming

behaviors, then develop a treatment plan or referral to therapy for these patients.

Nicholas J Westers, PSYD; Jennifer J Muehlenkamp, PHD, May Lau, MD, MPH

departments9 INTER@CTIVE

Readers react.

10 EYE ON WASHINGTON

FDA revamps nutrition facts labels.

11 JOURNAL CLUB

in addition4 EDITORIAL ADVISORY BOARD

45 ADVERTISING INDEX

© 2016 Impax Laboratories, Inc.

All rights reserved. Printed in USA 04/2016 PP-ADP-MEB-US-0005

NOW AVAILABLEReferences: 1. EMVERM [prescribing information]. Horsham, PA: Amedra Pharmaceuticals LLC; 2015. 2. Committee on Infectious Diseases, American

Academy of Pediatrics. Red Book: 2012 Report of the Committee on Infectious Diseases. 29th ed. Elk Grove Village, IL: American Academy of Pediatrics;

2012:566-567,851. 3. Friedman AJ, Ali SM, Albonico M. [published online December 24, 2012]. J Trop Med. 2012;2012:590463. doi:10.1155/2012/590463.

4. Treatment. Centers for Disease Control and Prevention website. http://www.cdc.gov/parasites/pinworm/treatment.html. Updated July 19, 2013.

Accessed January 22, 2016.

INDICATION

EMVERM (mebendazole) 100 mg chewable tablet is indicated in adults and children over 2 years of age for the treatment of Enterobius vermicularis (pinworm), Trichuris trichiura (whipworm), Ascaris lumbricoides (common roundworm), Ancylostoma duodenale (common hookworm), and Necator americanus (American hookworm) in single or mixed infections.

IMPORTANT SAFETY INFORMATION

Mebendazole is contraindicated in persons who have shown hypersensitivity to the drug.

Warnings: There is no evidence that mebendazole, even at high doses, is effective for hydatid disease. There have been rare reports of neutropenia and agranulocytosis when mebendazole was taken for prolonged periods and at dosages substantially above those recommended.

Precautions: Periodic assessment of organ system functions, including hematopoietic and hepatic, is advisable during prolonged therapy.

Adverse reactions include: Transient symptoms of abdominal pain and diarrhea with expulsion of worms in cases of massive infection; liver function test elevations [AST (SGOT), ALT (SGPT), and GGT]; and on rare occasions hypersensitivity (rash, urticaria and angioedema); rare reports of neutropenia, agranulocytosis (see WARNINGS) and hepatitis when mebendazole was taken for prolonged periods and at dosages substantially above those recommended; and very rare cases of convulsions.

Drug Interactions: Preliminary evidence suggests that cimetidine inhibits mebendazole metabolism and may result in an increase in plasma concentrations of mebendazole.

Pregnancy Category C: Mebendazole has shown embryotoxic and teratogenic activity in pregnant rats at single oral doses as low as 10 mg/kg (approximately equal to the human dose, based on mg/m2). In view of these fi ndings the use of mebendazole is not recommended in pregnant women.

Nursing Mothers: It is not known whether mebendazole is excreted in human milk. Because many drugs are excreted in human milk, caution should be exercised when mebendazole is administered to a nursing woman.

Pediatric Use: The drug has not been extensively studied in children under two years; therefore, in the treatment of children under two years the relative benefi t/risk should be considered.

Overdosage: In the event of accidental overdosage, gastrointestinal complaints lasting up to a few hours may occur. Vomiting and purging should be induced. Activated charcoal may be given.

Information for Patients:

% Patients should be informed of the potential risk to the fetus in women taking mebendazole during pregnancy, especially during the fi rst trimester (See Pregnancy Category C).

% Patients should also be informed that cleanliness is important to prevent reinfection and transmission of the infection.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088. To report SUSPECTED ADVERSE REACTIONS contact Impax Laboratories, Inc. at 1-877-994-6729.

See full Prescribing Information at www.EMVERMHCP.com and Brief Summary on following page.

AAP, American Academy of Pediatrics; CDC, Centers for Disease Control and Prevention; FDA, US Food and Drug Administration.

THE EMVERM SAVINGS CARD IS AVAILABLE ONLINE AT

WWW.EMVERMHCP.COM/SAVINGS

>��The ONLY FDA-APPROVED prescription treatment indicated for pinworm2

>� Mebendazole—prescribed by physicians for MORE THAN 40 YEARS3

>��The AAP Red Book recommends mebendazole as a DRUG OF CHOICE for highly contagious pinworm infections2

>��The AAP Red Book and CDC recommend TREATING THE ENTIRE HOUSEHOLD since family members are frequently infected2,4

>� ONE 100-MG CHEWABLE TABLET, for ONE DAY is the same dosage schedule for children and adults1

WITH ITS 95% CURE RATE1

IS BACKMEBENDAZOLE

NOW AVAILABLE FOR PINWORM

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9J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

inter ctive JOIN US AND JOIN IN WITH YOUR PEDIATRIC PEERS AT CONTEMPORARYPEDIATRICS.COM

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 6

40

ANDREW J SCHUMAN, MD SECTION EDITOR

peds v2.0

Every few years I like to speculate about the future of medical technol-ogy as well as the future of pediat-ric practice. Both, you see, are very much intertwined, and in my view the future of pediatric practice looks very good indeed.One needs to consider that we practice medicine at a time when innovation is progressing at an amazing pace. In the tech sector, experts speak frequently of “dis-ruptive technologies” that create entirely new ways of doing things, or shake up an industry entirely. For example, personal computers replaced the typewriter decades ago, and downloadable media is replac-ing compact disc media, just as compact discs replaced videocas-sette tapes and vinyl records. Let’s take a look at some current medical technologies that are “begging” for disruption, and other technologies that may prove to be “game chang-ers” over the next few years.

To help improve pediatric prac-tice, physicians must remain nim-ble, optimistic, and ever willing to try new things. We also must be innovators ourselves, to challenge the status quo and to aggressively confront government or insurance reforms when they are not in our patients’ best interest or ours. It is important to remember that inno-vation is not limited to keeping an open mind toward new office tech-nologies. It also involves being cre-ative when it means implementing new models of care or new work-flows, and utilizing improved meth-ods of educating parents to keep our patients healthy.

Curing MDSDYep, I have just identified a new medical condition—one that is not yet listed in the Diagnostic and Statistical Manual of Mental Dis-orders, Fifth Edition! Medical docu-mentation stress disorder (MDSD)

unfortunately affects many physi-cians who have been forced by the government to prematurely adopt expensive and inefficient electronic health record (EHR) systems. I dis-cussed improving medical docu-mentation (ie, avoiding “note bloat”) in the January 2016 issue of Contem-porary Pediatrics.If you are unfamiliar with this condition, let me enlighten you. Medical documentation stress dis-order is a “click”-related disorder, caused by the inability of provid-ers to expedite completion of office notes, therefore requiring taking an hour or more of one’s personal time to complete notes at home. Symptoms include staring into space or yelling at one’s computer screen, as well as a compulsion to frequently check one’s retirement funds, and chronic pain in one’s dominant hand.

Fortunately, MDSD is a treatable condition. Management modali-ties include scribes, virtual scribes (see Contemporary Pediatrics , November 2015), and my favor-ite, voice recognition software (see Contemporary Pediatrics, June

Disruptive technology and pediatric practiceHere is a closer look at several innovative medical technologies that are poised to become “game changers” in pediatric practice.

Part of the

Contemporary Pediatrics is part of the ModernMedicine Network, a Web-based portal for health professionals offering best-in-class content and tools in a rewarding and easy-to-use environment for knowledge sharing among members of our community.

Hearing You on Deafness

our digital guru, Dr. Andrew

Schuman, considers game-changing tech for your

pediatric practice. Don’t miss his latest Peds v2.0 article at

ContemporaryPediatrics.com/Schuman-0716

We heard from you about Dr. Andrew

Schuman’s latest article “MOC reform:

One year later,” June 2016, and

also regarding Dr. Rachel St. John’s

commentary “Pathologizing deafness,”

May 2016. Here are just a few of your

thoughts on these articles.

Thank you for the excellent article

regarding the update on MOC. Here

is a very brief summary of my opinion

regarding MOC. I did research before

going to medical school and became a

doctor because I did not want to continue

doing research. The very small amount

of knowledge gleaned from the large

amount of time utilized to complete MOC

part 4 is not acceptable to me. I hardly

have enough time in the day just to see

my patients. I have no problem with

examinations to assess my competency,

but the rest of MOC is a huge waste of

time designed by and for academicians.

—Ron Beckel, MD

****

I just fi nished reading the Contemporary

Pediatrics article about MOC reform.

I love what the ABA has done with

weekly/monthly questions. I’m in for

piloting that with ABP!

— Thomas D. Miller, MD

I enjoyed your recent article on the

latest in MOC. There are at least 2 other

things wrong with MOC, besides what

you point out:

1. There is no distinction between

academics and those in private practice.

If one is actively engaged in teaching

and research, there should be some

sort of a waiver for the educational

part —eg, if I publish articles and give

talks, that should be proof enough that

I am keeping up (at least in my area of

specialization).

2. The fee schedule borders on extortion.

After passing my last exam in 2012 and

completing all of my MOC requirements,

the ABP would not list me as board

certifi ed until I paid for the next 10 years!

And the fee is nonrefundable, so if I died

the next day, my widow would be out

$1200.

—Ben Z. Katz, MD

****

This is very useful. I am planning to

approach [my] state legislature about

MOC reform to implement a similar law

as Oklahoma.

—Paul G. Mathew, MD, FAAN, FAHS

MORE TALK ON MOCI respect your opinion, and

I know that there [are] loud

advocates from the “disabilities

movement” that are getting

a lot of media attention. Yet, I

disagree. Would you say the

same about blindness? Would

you say the same about spasticity

with cerebral palsy? Yes, there

are hundreds of individuals that

live meaningful lives despite or

because of the above conditions.

But these are still conditions

that require prevention and

accommodation.

— Francisco Enriquez, MD, FAAP

Dr. St. John’s letter was the

epitomy of political correctness,

unless I am totally naive after forty

years of practice. Is being blind a

pathological situation? We can

teach Braille and getting around

with a cane. Who would not want

their eyesight restored? Lacking 1

of the 5 senses is a defi ciency. It

is fi ne to try to accommodate for

the absence of a sense, but even

better to restore it.

— Irwin H. Berkowitz, MD, FAAP

Congratulations to

our Editorial Advisory

Board Member,

Dr. Donna Hallas,

recipient of the

2016 American

Association of Nurse

Practitioners (AANP) Nurse

Practitioner State Award

for Excellence (New York),

which recognizes outstanding

achievements by NPs and NP

advocates. Brava!

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 610

washingtonBY KATHRYN FOXHALL

washingtonEYE ON

FOR MORE NEWS @CONTEMPEDSCONTEMPORARYPEDIATRICS.COM/EOW

In May 2016, the US Food and

Drug Administration (FDA) an-

nounced the revamping of the

rules for the “nutrition facts” la-

bel box on packaged foods, the

fi rst major such overall in 20 years.

With the obesity epidemic con-

tinuing, much of the emphasis in

the announcement was on things

such as the FDA’s new requirement

that manufacturers list “added sug-

ars” and that they use a new for-

mat which, among other things,

will display the calories much more

prominently.

Less talked about was the fact

that in the 2 years since the FDA

proposed the changes, there has

been a massive discussion, via the

agency’s regulatory process, on the

many aspects of nutrition science

and policy.

As 1 example, in a comment to

the FDA last fall, the American

Academy of Pediatrics (AAP) said it

was comfortable with the proposal

of a Daily Reference Value (DRV)

of 25 g “for added sugars based on

a 1000-calorie reference amount for

children 1 through 3 years of age.”

However, the AAP said, it’s a

problem that the rules would, in

effect, extend the added sugar rec-

ommendations for an adult to chil-

dren as young as age 4 years, which

would indicate it would be okay for

them to eat up to 14% of their calo-

ries in added sugar.

The FDA declined to make

a change based on the AAP’s

comment, saying that a separate

DRV for different child age groups

“could clutter the label, cause con-

fusion, and draw attention to the

added sugars declaration because

more space would be required for

2 separate percent DV declarations

on the label.”

In another instance, the AAP,

the March of Dimes, and about

22 other groups said the change in

the way the FDA will require that

folic acid be listed could lead to

public confusion, limit the ability

to monitor intake and safety, and

negatively impact birth outcomes.

The new rule would mandate the

expression of the Recommended

Dietary Allowance (RDA) for folate

in “Dietary Folate Equivalents

(DFEs).” The groups’ comments

said, “Because of the difference

between measuring folate/folic acid

in DFEs versus micrograms, this

means the RDA is lower than the

[US Public Health Service] rec-

ommendation for intake among

women of childbearing age.”

The FDA, however, noted that

the DFE, developed by the Institute

of Medicine, “accounts for the

dif ferences in bioavai labi l ity

between food folate (natural folate)

and folic acid, which is more bio-

available (about 1.7 times more

bioavailable).”

The AAP also urged the FDA

to require that foods be labeled for

caffeine because of its numerous

adverse effects. It noted findings

from the American Association of

Poison Control Centers that “more

than 40% of 5156 calls about energy

drinks to US poison control centers

involved children younger than

6, with some suffering serious car-

diac and neurological symptoms.”

In other rules related to obesity,

the FDA says that because pack-

age size affects what people eat,

packages that are between 1 and

2 servings must be labeled as 1 serv-

ing in terms of calories and other

nutrients because people typically

consume those packages in 1 sitting.

Examples are a 20-ounce soda or a

15-ounce can of soup.

Large food manufacturers have

2 years to comply with all the new

requirements, by July 26, 2018, and

those with less than $10 million in

sales have another year after that.

FDA revamps nutrition facts label box

CME VIDEO FOR PHYSICIANS

The FDA and the American Medical Association have announced a

new continuing medical education (CME) video for physicians about

discussing the nutrition facts labels with patients. For this CME, go to

https://cme.ama-assn.org/Activity/4252182/Detail.aspx

11J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

journal clubBY MARIAN FREEDMAN COMMENTARY BY MICHAEL G BURKE, MD

journal club CONTEMPORARYPEDIATRICS

A new clinical decision sup-

port tool prompts clini-

cians to ask parents about

secondhand smoke ex-

posure, provides an elec-

tronic nicotine replacement therapy

(NRT) prescription, and makes

referrals for follow-up and further

guidance. A study found that the

tool is easy to use and has a clinical

impact.

Investigators conducted the study

within the Children’s Hospital of

Philadelphia Pediatric Research

Consortium, which includes 31 prac-

tices in 2 states. The tool, which

interfaces with the electronic health

record (EHR), first prompts the

clinician to ask the parent about

smoking status and whether he or

she wants to quit. An affirmative

response triggers a link to an elec-

tronic NRT prescription (nicotine

patch or gum) with dosing guid-

ance. Finally, the tool prompts cli-

nicians to refer parents to an adult

tobacco treatment program and

additional resources and to update

the EHR.

During a 3-month period, clini-

cians used the tool at about three-

quarters of more than 3000 visits at

which 165 parents expressed inter-

est in quitting smoking and were

offered treatment. Although clini-

cian use of the tool varied substan-

tially, more than 75% of clinicians

used the tool at more than 60% of

visits. Of 24 clinicians (18 pediatri-

cians and 6 nurse practitioners) who

used the tool, 17 completed a follow-

up survey. Of these, 94% reported

that they were satisfied with the tool

and found it helpful.

Among the tool’s advantages,

ease of use, a reminder to screen all

parents about smoking, and access

to an electronic NRT prescription

were cited by respondents. Nearly

90% of parents interested in quitting

who were surveyed reported being

satisfied or very satisfied with their

treatment (64% received an NRT

prescription and 25% had filled a

prescription and were using it), and

28% noted that they were moti-

vated to be treated because quitting

was framed around helping their

child (Jenssen BP, et al. Pediatrics.

2016;137[5]:e20154185).

This smoking cessation intervention works!

An analysis of data on the inci-

dence of pertussis shows that

although acellular pertussis (Tdap)

vaccine had a posit ive impact

among adolescents in the 4 years

after it was introduced in 2005,

in 2010 pertussis incidence in this

age group began to increase more

rapidly than it did in all other age

groups. This abrupt shift in inci-

dence occurred in the same year

that 11-year-olds represented the

f irst group of children to have

received acellular vaccines for all

doses of the childhood series, fol-

lowing the 1997 transition from

Tdap booster in teens less effective after initial acellular vaccine series

We know that we should screen for smoke exposure in the home, offer

counseling and referral to smoking cessation resources, and arrange for NRT,

but, as several studies have shown, we don’t. During a short offi ce encounter,

we face obstacles all along the way. The tool described here is an example of

how the EHR makes it easier to get done what we know needs to be done. It

prompts the physician to screen for smoke exposure, presents information on

smoking cessation, allows arrangements for a recruitment call from a smoking

cessation counselor, and provides a prescription for nicotine replacement with

dosing information included. By removing obstacles, this EHR application could

improve health for both parents and children. —Michael G Burke, MD

commentary

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 612

journal club

whole pertussis to acellular vac-

cines. These findings indicate that

a Tdap booster vaccine in ado-

lescence has a diminished effect

among those who were primed

with acellular pertussis vaccine in

early childhood.

The extended analysis of reported

pertussis cases between 1990 and

2014 shows that pertussis incidence

was highest among infants aged

younger than 1 year throughout the

period. Pertussis rates were com-

parable among all other age groups

until the late 2000s when the per-

tussis burden increased among chil-

dren aged 1 to 10 years; between

2007 and 2011, the incidence of

pertussis in children in this age

group was 1 to 2 times higher than

in adolescents aged 11 to 18 years.

However, when trends reversed

in 2010, rates of pertussis among

11- to 18-year-olds increased at a

faster rate than it did in all other

age groups combined, and by 2014

adolescents had overtaken all but

young infants in pertussis incidence

(Skoff TH, et al. JAMA Pediatr.

2016;170[5]:453-458).

This means that pertussis is not going away and, despite Tdap boosters, incidence will continue to rise as more children

initially vaccinated with acellular pertussis vaccine move through adolescence. In the words of the researchers, “[S]usceptible

individuals will continue to accumulate in the population.” Until a new solution is devised, it is up to us to continue to think

about pertussis, recognize it early, and initiate treatment to decrease spread. —Michael G Burke, MD

Among children with mild gastroen-

teritis and minimal dehydration, ini-

tial oral hydration with dilute apple

juice followed by preferred f luids is

more beneficial than electrolyte main-

tenance solution, a large study in a

pediatric emergency department (ED)

found.

The 647 study participants, aged 6 to

60 months, were divided into an inter-

vention group that received half-strength

apple juice and a control group that

was given an apple-flavored electrolyte

maintenance solution. After discharge,

the apple juice group was instructed to

drink whatever fluids they wished, while

the electrolyte maintenance solution

group replaced f luids with electrolyte

maintenance solution.

At fol low-up, fewer ch i ld ren

in the apple juice/preferred f lu-

ids group received intravenous rehy-

dration (Freedman SB, et al. JAMA.

2016;315[18]:1966-1974).

Mild gastroenteritis? Try dilute apple juice!

Dilute apple juice or other liquids were not only as good as electrolyte solution in this

study, they were better. Perhaps IV hydration and admission were more common in

the electrolyte solution group because parents had to purchase the solution after ED

discharge, while those in the dilute apple juice arm of the study could be given any fluid

available at home. It is important to note that this study included only patients aged at

least 6 months and only those with mild dehydration; 81% of the enrolled patients had

dehydration scores of 0 or 1 on an 8-point scale. Diarrhea leading to life-threatening

dehydration and electrolyte disturbances is a real and scary thing, even in developed

countries. Dilute apple juice may be fine for mildly dehydrated children, but in moderate to

severe diarrhea I will stick with electrolyte solution. —Michael G Burke, MD

commentary

commentary

Marijuana use can trigger

recurrent cyclic vomiting

in teenagers. A new report

points out that 1 known

cause of cyclic vomiting

syndrome (CVS) is chronic

use of cannabis. Cyclic

vomiting syndrome is a

constellation of recurrent

vomiting, nausea,

and abdominal pain.

When linked to chronic

marijuana use, CVS has

the unique characteristic

of being temporarily

relieved by frequent hot

showers. The researchers

recommend screening for

marijuana use by history

and a urine drug screen

in adolescents with CVS

who take hot showers for

symptomatic relief (Sawni

A, et al. Clin Pediatr.

2016;55[6]:560-563). 

also of note

13J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

puzzlerIM

AG

E C

RE

DIT

/AU

TH

OR

SU

PP

LIE

D

Boy with fever, cough, and oral lesions

A previously healthy, 16-year-old Hispanic boy initially presents to the clinic

with a 5-day history of tactile fevers, achy malaise, congestion, and a dry

cough. He was afebrile with negative rapid strep and monospot tests, but was

prescribed fluticasone, benzonatate, and ibuprofen for a presumed upper

respiratory infection. He was encouraged to return if symptoms did not

improve. FOR MORE ON THIS CASE, TURN TO PAGE 38.

THE CASE

J DAVID STERNS, MD; RIVA KAMAT, MD, FAAP

S FIGURE 1 Patient’s CXR AP with subtle yet inconclusive

findings for atypical pneumonia. Taken in the emergency

department on day 9 of illness prior to the start of an empiric

course of azithromycin.

S FIGURE 2 Patient’s CXR AP with marginally

progressed pulmonary findings from previous imaging.

Taken prior to transfer to pediatric tertiary care center

on day 14 of illness.

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 614

PEER-REVIEWED FEATURE

Dr Bass is chief medical

information officer and

associate professor of

medicine and of pediatrics,

Louisiana State University

Health Sciences Center–

Shreveport. The author

has nothing to disclose in

regard to affiliations with

or financial interests in

any organizations that may

have an interest in any part

of this article.

The introduction of conjugated vaccines

has decreased the incidence of bacte-

rial meningitis in children, amounting to

one of the biggest public health successes

in the practicing pediatrician’s career. In

fact, the median age of patients success-

fully treated for bacterial meningitis has

increased from younger than age 5 years

to age 42 years and older. Improvements

have been seen in every age group, except

in those aged younger than 2 months.

Cases of meningitis from strains of bac-

teria not covered by vaccination and

drug-resistant strains, however, remain a

concern for pediatric patients.

Etiology, epidemiology, and risk factorsThe most common causes of bacterial

meningitis are Streptococcus pneumoniae,

Neisseria meningitidis, Haemophilus

influenzae type b (Hib; rarely a cause since

the development of a vaccine), group B

Streptococcus (GBS), and Listeria monocy-

togenes.1-3 Etiology depends on the age of

the patient (Table 1).3,4 Introduction of the

conjugate Hib vaccine in the 1990s almost

eliminated Hib in countries in which it was

introduced and decreased the overall inci-

dence of meningitis by nearly 55%.3 This

was followed by the introduction of the

heptavalent pneumococcal vaccine (PCV7)

in 2000, which reduced pneumococcal

meningitis by nearly 60% in children aged

younger than 2 years.3-5

In the years between 1998 and 2007,

herd immunity continued to drop the rate

of meningitis by more than 30%, from a

rate of 2 cases per 100,000 to 1.38 cases

per 100,000.3,6 Despite these advances,

Deciphering bacterial meningitisPAT F BASS III, MD, MS, MPH

Pediatricians need to understand not only how bacterial meningitis can be prevented through vaccination, but also its risks, symptoms, workup, and treatment.

Bacterial Meningitis

15J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

peer-reviewed

however, case fatality rates did not

change and rates of pneumococcal

disease from strains not covered by

the PCV7 strain began to emerge.

In 2010, the 13-valent pneumo-

coccal conjugate vaccine (PCV13)

was introduced, but S pneumoniae

remains the most common cause

of bacterial meningitis for children

aged older than 1 month.3

More recently, introduction of

a vaccine targeting N meningitidis

serogroup C disease significantly

reduced invasive meningococcal

disease. In Canada, the serogroup C

vaccination led to a decrease in inci-

dence from 0.07 to 0.25 per 100,000

(depending on the province) to

fewer than 0.05 per 100,000 per

year, a reduction of 14% per year.

It is estimated that this annually

decreases the burden of N meningit-

idis serogroup C by 75 to 85 invasive

meningococcal disease cases and

10 to 12 deaths.7

For the United States, the

Immunization Action Coalition

reports that the incidence dur-

ing 2005 to 2011 was 0.3 cases per

100,000 population and decreased

to an incidence of 0.18 cases per

100,000 populat ion in 2013.8

Serogroups B, C, and Y were equally

responsible for reported cases. Two

quadrivalent conjugated meningo-

coccal vaccines (MenACWY-DT

a nd Men ACW Y-CR M197

) a re

licensed in the United States, and

another is licensed in Europe

(MenACWY-TT).9 In the United

States, there are programs for both

infant and child, as well as adoles-

cent immunization.

Despite the shifting incidence of

meningitis, patients aged younger

than 2 months still have the highest

incidence of bacterial meningitis

CAUSES OF BACTERIAL MENINGITIS BY AGEBirth to 1-3 mo } Group B Streptococcus

} Gram-negative enteric bacilli

} Listeria monocytogenes

} Streptococcus pneumoniae

3 mo-2 y } S pneumoniae

} Neisseria meningitidis

} Haemophilus influenzae type b

2-18 y } N meningitidis

} S pneumoniae

From: Swanson D3; Whitney CG, et al.4

1

2 RISK FACTORS FOR MENINGITIS

NEONATE OLDER CHILDREN

Low birth weight (<2500 g) Absent or underimmunization

Prematurity (<37 wk gestation) Daycare exposure (increased 1st 2 mo;

declines after 6 mo)

Premature rupture of membranes Age <2 y

Fetal hypoxia Functional or surgical absence of spleen

Traumatic delivery Immunosuppressed (eg, HIV, malignancy,

complement deficiency, chronic steroid

use)

Urinary tract abnormalities Chronic kidney disease

Maternal GBS infection Chronic liver disease

Diabetes mellitus

Galactosemia Cochlear implant

CSF leak

Head trauma

Travel to areas with endemic meningitis

Live with large group in confined space

(dorms, military recruits)

Abbreviations: CSF, cerebrospinal fluid; GBS, group B Streptococcus; HIV, human immunodeficiency virus.From: Brouwer MC, et al10; Hjuler T, et al11; Revest M, et al.12

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 616

peer-reviewed

primarily associated with the differ-

ent etiologies (Table 1).3,4 In this age

group, GBS and Escherichia coli are

responsible for 70% to 80% of cases.

Although routine maternal GBS and

intrapartum antibiotic treatment

have decreased early-onset GBS dis-

ease by 86%, the incidence of late-

onset disease has not changed.3

Risk factors for pediatric men-

ingitis, which also vary by age, are

presented in Table 2.10-12

Differential diagnosisA number of different diseases can

mimic meningitis, and not all chil-

dren presenting with signs and

symptoms of meningitis have the

disease. In a review of 650 children

undergoing a lumbar puncture,

there were many diseases found to

mimic meningitis symptoms such

as pneumonia, otitis media, phar-

yngitis, and gastroenteritis. In this

review study, neck stiffness was

twice as likely (50% vs 25%) and a

positive Brudzinski test was 3 times

as likely in patients diagnosed with

meningitis.13,14 Viral illness, sinus-

itis, and migraine were common

causes of headache, with no cases

of bacterial meningitis in 2 stud-

ies of patients presenting to an

emergency department with head-

ache.15,16 Although 30% of patients

presenting to an emergency depart-

ment with signs of meningismus

had meningitis, 8% had pneumonia

and 46% were diagnosed with upper

respiratory tract infection or other

self-limiting illnesses.17

Other causes of meningitis also

can mimic bacterial meningitis

such as viruses, fungi, mycobacte-

ria, and parasites. Retropharyngeal

abscess is a relatively common infec-

tious disease process that mimics

meningitis. Other infectious mim-

ickers include brain abscess, sub-

dural or epidural abscess, and

encephalitis.3

PresentationThe clinical features of bacterial

meningitis are often nonspecific

and can vary by age. The younger

the child, the less likely he or she

will present with classic symptoms

of fever, headache, and meningeal

signs. A neonate or young infant

may only present with apnea, bulg-

ing fontanel, diarrhea, fever, irri-

tability, lethargy, poor feeding,

temperature instability, or vomit-

ing.18 Symptoms are variable, how-

ever, and the patient may have fever,

hypothermia, or euthermia. Parents

may describe their infant as fussy,

jittery, or inconsolable.3 Seizure may

be a presenting sign in 20% to 50%

of cases of Hib meningitis (less in

other etiologies), but neck stiffness

is uncommon.

In older children, changes in

mentation, fever, headaches, nausea,

photophobia, and vomiting may be

present. Symptoms may evolve over

several days or a period of hours.3

Seizure may be the sole presenting

sign in patients with pneumococ-

cal meningitis. A positive Kernig

or Brudzinski sign has low sensi-

tivity for meningitis, and their

absence does not rule out meningi-

tis.18 Rash and petechiae are present

3 SIGNS AND SYMPTOMS OF MENINGITIS BASED ON AGE

SIGNS AND SYMPTOMS OF NEONATAL

MENINGITIS

SIGNS AND SYMPTOMS OF MENINGITIS IN

INFANTS AND CHILDREN

} Apathy

} Apnea

} Bulging fontanel

} Fever

} Grunting

} Hypoglycemia

} Hypothermia

} Hypotonia

} Inconsolable

} Irritability

} Jaundice

} Lethargy

} Listlessness

} Metabolic acidosis

} Nasal flaring

} Nuchal rigidity uncommon

} Pallor and poor capillary refill

} Poor feeding

} Seizures

} Shock

} Shrill cry

} Tachypnea

} Alterations of the sensorium

} Anorexia

} Brudzinski sign

} Bulging fontanel

} Coma

} Convulsions

} Cushing triad: hypertension, bradycardia,

and respiratory depression indicating

increased intracranial pressure

} Fever (generally present, but some

severely ill children present with

hypothermia)

} Headache

} Irritability

} Kernig sign

} Lethargy

} Nausea

} Nuchal rigidity

} Opisthotonos

} Photophobia

} Vomiting

From: Swanson D3; Tunkel AR, et al.18

17J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

peer-reviewed

in about 50% of cases of invasive

disease attributed to N meningiti-

dis. Symptoms of bacterial men-

ingitis presenting in neonates and

older children are listed in Table

3.3,18 Table 4 shows how different

signs may display in different age

groups.14,19

DiagnosisBlood cultures, a complete blood

count, and electrolytes should be

obtained. White blood cell (WBC)

counts can be normal, high, and

may be low in neonates. More than

80% of patients (the percentage is

higher for Hib and lower for other

causes) not pretreated with antibiot-

ics will have positive blood cultures

with bacterial meningitis. Procalci-

tonin levels will be elevated in bac-

terial meningitis, but these cannot

distinguish between bacterial and

viral meningitis. If petechiae or low

platelet counts are present, dissem-

inated intravascular coagulation

should be considered and worked

up. Syndrome of inappropriate

antidiuretic hormone (SIADH) is

suggested by a low sodium level and

other testing.3

A lumbar puncture (LP) should

be obtained unless contraindicated

in patients because of:

} Hemodynamic instability,

} Increased intracranial pressure,

} Coagulopathy, or

} Neurologic findings indicating a

mass lesion.

Computed tomography (CT)

is not routinely needed prior to

LP. The CT findings not appar-

ent on physical exam are unlikely

to change clinical management.20

Patients with coma, papilledema,

and focal neurologic f indings

should have a CT prior to LP. The

need for CT, however, should not

delay obtaining blood cultures or

antibiotic administration. Patients

without these findings do not need a

CT prior to LP.21,22 If CT is obtained,

LP should be performed after CT if

there are no contraindications.

Spinal fluid should be sent for:

} WBC count and differential;

} Glucose;

} Total protein; and

} Gram stain and bacterial culture.

In the bacterial meningitis patient

not treated with antibiotics before

presentation, elevated WBCs, low

glucose, and elevated protein in the

spinal fluid are suggestive of bacte-

rial meningitis. Spinal f luid nor-

mals are based on the patient’s age.

Occasionally, cerebrospinal (CSF)

fluid may appear normal when the

spinal tap is performed very early in

a child’s illness.

The spinal tap results can be

altered following a traumatic tap,

making it difficult to diagnose bac-

terial meningitis. Following a trau-

matic tap, cell counts are difficult to

4 SYMPTOMS PRESENT IN MENINGITIS BASED ON AGE

SIGN 0-2 MO (%) 2-24 MO (%) 2-5 Y (%) 5-12 Y (%)

ROTHROCK

≤24 MO (%)

Fever 80 96 82 100 >95

Lethargy 40 57 36 17 87-95

Irritability 40 18 18

Altered mentation

53-78

Seizure 4 22-23

Vomiting 20 57 73 100 54-71

Focal neuro exam

5-6

Bulging fontanel

40 18

Nuchal rigidity

29 55 67 54-59

Kernig sign 7 27 33 9-11

Brudzinski sign

64 69 83 10-13

From: Levy M, et al14 (columns 2-5); Rothrock SG, et al.19

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 618

peer-reviewed

interpret. The easiest formula is to

subtract 1 to 2 CSF WBCs for every

1000 CSF red blood cells (RBCs)/

mm3. This formula and the formula

comparing the ratio of CSF WBCs

to CSF RBCs to blood WBCs to

blood RBCs, however, should be

interpreted with caution and likely

empiric antibiotics should be started

pending culture results.3

Pretreatment with antibiotics

decreases likelihood of a positive

CSF culture. Reports demonstrate

a positive culture result in bacte-

rial meningitis with oral and par-

enteral antibiotics of only 71% and

66%, respectively. Parenteral anti-

biotics sterilize the CSF within a

couple of hours, but antimicrobial

pretreatment does not impact the

ability to diagnose bacterial menin-

gitis using cell counts, protein, and

glucose.3,23-25

Although latex agglutination

tests are available to assist in mak-

ing a diagnosis, these rarely alter

the treatment plan and the tests are

not needed in most instances.10 In

fact, such testing is no longer rou-

tinely recommended for antibiotic-

pretreated patients.3

Empiric antibioticsThe goal is to administer anti-

biotics as early as possible once the

diagnosis of bacterial meningitis

is considered. Although adverse

outcomes are not associated with

duration of symptoms prior to

treatment, delay of antibiotic

administration is associated with

poor outcomes.26,27 Empiric anti-

biotic therapy should target likely

pathogens based on the patient’s

age, underlying health conditions,

and local efficacy and susceptibility

patterns. Antibiotic choices should

have good penetration into CSF and

have bactericidal properties.3,28

Empiric antibiotics for bacterial

meningitis in the neonatal period

are primarily ampicillin plus genta-

micin or ampicillin plus cefotaxime.

The latter regimen is more com-

mon when clinicians are concerned

about increasing resistance of E coli

to ampicillin. Once an organism is

identified, the antibiotic coverage

can be tailored for the infant.3,28

Empiric antibiotics for bacte-

rial meningitis outside the neo-

natal period include vancomycin

(because of cephalosporin-resistant

pneumococci) plus either cefotax-

ime or ceftriaxone. Vancomycin

can be discontinued if the etiology

of bacterial meningitis is suscep-

tible to penicillin or cephalosporins.

Rifampin may be added in certain

situations for pneumococcal men-

ingitis, and the pediatrician should

consider consultation with an infec-

tious diseases specialist.3,28

In children with signif icant

allergic reactions to penicillins

and cephalosporins, vancomycin

plus rifampin or vancomycin plus

meropenem are options for initial

therapy.3,28

Antibiotics may be discontinued

when blood and CSF cultures are

negative in patients with an unre-

markable CSF in which bacterial

meningitis is ruled out. Children

with positive blood cultures and an

abnormal CSF, but a negative CSF

culture, are often treated as if the

CSF culture were positive. If both

CSF and blood cultures are nega-

tive but the child had an abnormal

CSF evaluation, consultation with a

pediatric infectious diseases expert

is recommended.3,28

Total duration of antibiotic ther-

apy will depend on the patient’s

age and bacterial etiology. For

uncomplicated neonatal meningi-

tis with GBS or S pneumoniae, a

14- to 21-day course of treatment is

usually sufficient. Outside the neo-

natal period, the usual course of

treatment for uncomplicated bac-

terial meningitis is 10 to 14 days

for S pneumoniae and 7 days for

N meningitidis.3,28

Dexamethasone therapySteroids are believed to decrease

neurologic complications in bac-

terial meningitis by decreasing

inflammatory response and mod-

ulating mediators that are released

when initial antibiotics result in the

lysis of cell walls.29 However, dexa-

methasone therapy outside of treat-

ment for H influenzae (for which it

is clearly indicated) remains con-

troversial. There is also a potential

concern that steroids may decrease

the effectiveness of vancomycin by

decreasing inflammation and fur-

ther reduce its already suboptimal

Empiric antibiotic therapy should target likely pathogens based on the patient’s age, underlying health conditions, and

local efficacy and susceptibility patterns.

GERMS. VOMIT. OVER ANXIOUS

PARENTS.

REMEMBER WHEN THAT WAS ALL YOU HAD TO WORRY ABOUT?

LET DOCTORSBE DOCTORS™

NETWORK-ENABLED EHR, PRACTICE MANAGEMENT, CARE COORDINATION, AND PATIENT ENGAGEMENT SERVICES

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 620

peer-reviewed

CSF penetration.3,28

The American Academy of

Pediatrics (AAP) Committee on

Infectious Diseases recognizes the

benefit of dexamethasone therapy

in H influenzae type b meningitis.

The AAP says clinicians can con-

sider its use in bacterial meningitis

in patients aged older than 6 weeks

after considering the risks and ben-

efits. If used, dexamethasone should

be administered with the first dose

of antibiotics because it has no bene-

fit if administered more than 1 hour

after the antibiotic.3,28

ComplicationsAmong survivors of bacterial men-

ingitis, 50% are reported to have

at least 1 complication at 5 years.

The most commonly cited bacte-

rial cause associated with complica-

tions is H influenzae. Complications

may be categorized as intellectual/

behavioral deficits (78%), neurologic

(14%), hearing loss (7%), and vision

loss (3%).30,31

Examples of intellectual and

behavioral deficits include:

} Cognitive impairment,

} Academic limitations, and

} Attention-deficit/hyperactivity

disorder.

Intellectual disability (intelli-

gence quotient [IQ]<70) is noted in

4% of survivors of bacterial menin-

gitis, and studies have found lower

IQ scores in survivors of bacterial

meningitis compared with their

siblings.30,31 In a report of 130 sur-

vivors evaluated at a single center

(average age, 8 and 6 years following

meningitis episode), children expe-

riencing meningitis did worse than

age-matched controls on assess-

ments of fine motor function, IQ

scores, and tests of school behavior,

neuropsychologic function, and

auditory figure-ground differen-

tiation, even though the children

with meningitis performed in the

average range.32-34 Onset of menin-

gitis before age 12 months is associ-

ated with poor performance on tests

requiring language and executive

skills 12 years after disease onset.33

The complications can extend

well into adulthood. In a British

cohort, survivors of meningitis at

age 16 years were more likely to

have attended special education (at

a rate of 4 times the national aver-

age); more than 3 times as likely to

not pass a General Certificate of

Secondary Education (GCSE; an

internationally recognized certifi-

cate in a particular subject); and

twice as likely to not pass core sub-

jects (eg, basic English, math, foreign

language) on a GCSE.35 Similarly,

a Danish cohort reported lifelong

impairment, with meningitis cases

less likely than controls to complete

high school, attain higher educa-

tion, or achieve economic self-suf-

ficiency.36 Finally, mood problems,

behavioral problems, socialization

problems, thought problems, and

attention problems are reported in

multiple studies years after the ini-

tial treatment of meningitis.30,37

The pediatrician needs to be

aware of the educational issues that

may be facing survivors of bacte-

rial meningitis so that parents

and teachers can be on the look-

out for problems and intervene

as necessary and as early as pos-

sible.38 Commonly reported neu-

rologic complications include

spasticity, motor def icits, and

seizure disorder.

Generalized seizures are more

likely to occur at disease onset,

while partial seizures are more

likely to occur at several days of hos-

pital admission. Seizures occurring

early in the course that are easily

controlled are not likely to lead to

neurologic sequelae. Seizures occur-

ring later in the course of treatment

or that are more difficult to control

are more likely to be associated with

permanent neurologic sequelae.38

Hemiparesis or quadriparesis is

generally associated with some sort

of intracranial pathology (eg, cere-

bral edema), which can generally

resolve over time.39

Hearing loss can be either tran-

sient or permanent. It is important

to screen for hearing loss after men-

ingitis. Risk factors for hearing loss

at presentation include:40

} S pneumoniae infection, 2 to

3 times greater compared with

other etiologies;

} Ataxia;

} Symptoms for several days prior

to admittance; and

} Absence of petechiae.

Interestingly, hemiparesis and

subdural empyema seem to have

increased in frequency after the

introduction of PCV13.41

ConclusionMeningitis remains a significant

burden in the pediatric age

group, and complications may

lead to lifelong impairment. It is

important for the pediatrician not

only to understand how bacterial

meningitis can be prevented

through vaccinations but also to

understand its risks, workup, and

treatment.

For references, go to

ContemporaryPediatrics.com/

bacterial-meningitis

21J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

CLINICAL FEATURE

Dr Bass is chief medical

information officer and

associate professor of

medicine and of pediatrics,

Louisiana State University

Health Sciences Center–

Shreveport. The author

has nothing to disclose in

regard to affiliations with

or financial interests in

any organizations that may

have an interest in any part

of this article.

Two common questions asked of pediatri-

cians by parents of children with infections

are “When can my child return to school?”

and “How long will I be staying home with

my child?” Understanding when, how

long, and under what conditions a pediat-

ric patient with an infection is contagious

to others is an important part of disease

prevention and treatment. Similarly, the

pediatrician needs to educate parents and

educators about infection control practices

that improve prevention and decrease risk

of disease transmission.

These practices are particularly impor-

tant in regard to school-aged children

because inappropriate exclusion can lead to

a significant number of school days missed.

At times, the pediatrician may need to con-

tact a school if a child is inappropriately

excluded and provide sound reasoning as

to why exclusion is not appropriate.

This article is not a complete review

of communicable diseases or preven-

tion control measures. Rather, the article

reviews a number of diseases that do not

require exclusion; common diseases and

problems that may require some aspect

of exclusion; and a number of prevention

control measures.

Infections spread via respiratory routesWhen children cough or sneeze, aerosol-

ized droplets can be inhaled by individu-

als who are nearby, placing them at risk for

an infection. A person is more commonly

infected, however, when the droplet comes

to rest on a surface that he or she touches,

and then touches that hand to face, nose,

or mouth. As a result, if a child covers a

cough or sneezes into his/her hands, this

may increase the risk of transmission by

Infection control and prevention“When can my child return to school?”

PAT F BASS III, MD, MS, MPH

Teaching parents and educators about infection control practices can improve prevention and decrease risk of disease transmission to help keep kids in school.

Infection control And prevention

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 622

clinical feature

contaminating surfaces with mucus

from his/her nose, eyes, or throat.1

Children should be taught to

sneeze or cough into a tissue or

paper towel. If this is not avail-

able, they should be instructed to

sneeze into the crook of the elbow.

Children should then perform good

hand-washing hygiene.

Preventing infections via direct contactChildren touch everything and

often touch their nose, face, and

mouth. Good hand hygiene pre-

vents the risk of transmission of dis-

eases through direct contact.

The Centers for Disease Control

and Prevention (CDC) recommends

a 5-step hand-washing process to

avoid getting sick and spreading

germs to others:2

Wet. Wet hands first with clean,

running water and apply soap.

Lather. Rub hands together to

lather up, focusing on the backs of

the hands, between the fingers, and

under finger nails.

Scrub. Scrub hands for at least

20 seconds. Asking children to

sing “Happy Birthday” to them-

selves twice will be about the right

amount of time.

R inse. Hold ha nds u nder

running water and not standing

water. Standing water potentially

increases risk of reinfection with

the germ or virus. Tell the child to

think of the germ/virus as circling

the drain away from him.

Dry. Dry hands with a clean

towel or let them air dry.

If access to hand-washing is

not available, hand sanitizer is an

option.

Infections not requiring exclusionIn general, school-aged children

with the conditions presented in the

Table1 do not need to be excluded

from school if they feel well enough

to participate in their regular activ-

ities, and if they do not have fever,

rash, or severe illness symptoms

requiring temporary exclusion.

Specific conditions that may require exclusionBoils, abscesses, cellulitus. Signs

and symptoms include furuncles

and carbuncles (boils) that occur in

hairy areas and contain pus. Skin

abscesses are collections of pus and

may be tender, painful, and fluctu-

ant. With cellulitis, skin is red and

tender. Fever may be present with

boils, abscesses, or cellulitus.

Incubation period depends on the

causative agent. It is spread through

person-to-person contact, with a

smaller risk of indirect spread via a

contaminated surface or object.

Staph and strep are the most

common bacteria causing boils,

abscesses, or cellulitus. These infec-

tions are contagious if the infected

area is open and draining. The child

does not need to be excluded unless

there are other symptoms (eg, fever);

if the draining lesion cannot be

INFECTIONS THAT DO NOT REQUIRE EXCLUSION FROM SCHOOL

} Canker sores, cold sores, or aphthous ulcers as long as there is not

excessive drooling

} Chronic hepatitis B or C

} Croup

} Cytomegalovirus, although sports and physical education may be

limited if there is liver or spleen enlargement

} Diseases spread by mosquitoes such as West Nile virus

} Diseases spread by ticks such as ehrlichiosis, Rocky Mountain spotted

fever, and tularemia

} Ear infections

} Fifth disease (ie, erythema infectiosum)

} HIV infection

} Molluscum contagiosum

} Mononucleosis, although sports and physical education may be limited

if there is liver or spleen enlargement

} Rash without fever or behavioral changes

} Roseola after fever is gone

} Thrush

} Urinary tract infections

} Warts

Abbreviation: HIV, human immunodeficiency virus.

From Silfverdal S-A.1

TABLE

23J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

clinical feature

covered; or if drainage is significant

and seeping through the bandage,

contaminating other surfaces.1

Good hand-washing is an impor-

tant way to avoid the spread of infec-

tions from child to child. Infected

children should be instructed not

to share personal items such as tow-

els. Having a methicillin-resistant

Staphylococcus aureus (MRSA)

infection or being a MRSA carrier

is not a reason for exclusion in and

of itself.

C h i c k e n p o x (v a r i c e l l a ) .

Regarding signs and symptoms of

chickenpox, after a prodrome that

may include fever, malaise, phar-

yngitis, or loss of appetite, a mac-

ular rash appears that progresses

to pruritic vesicles and then scabs.

Eruptions occur in crops, so that

a person may have findings in all

3 stages.

The incubation period is usually

from 14 to 16 days. As to how it is

spread, the disease is communicable

from 48 hours before the appear-

ance of the rash until the vesicles

have dried and no new vesicles are

forming. It is spread through aero-

solized droplets or direct contact

with fluid from a skin vesicle.

Although immunization has

made these infections much less

common in the pediatrician’s office

(vaccine is ~70% to 90% effective in

preventing chickenpox), infections

may still be seen in unimmunized

patients, or atypical presentations

seen in immunized or underimmu-

nized populations. School exclusion

is appropriate for active cases, and

school systems also may exclude

at-risk, unimmunized children.

Children with uncomplicated vari-

cella infections may return to school

when the rash has crusted or no new

lesions are present in 24 hours in

an appropriately immunized child

without crusts.3 This often occurs

about 6 days after the start of the

rash.

Conjunctivitis (bacterial and

viral [pinkeye]). Signs and symp-

toms include redness of the eye

and discharge. Discharge may be

mucopurulent or clear. Eyes are

often matted shut in the morning.

Patients also may report itching,

pain, burning, sandy, or gritty feel-

ing in the eye.

The incubation period for bacte-

rial conjunctivitis is 24 to 72 hours,

whereas for adenovirus (the most

common cause of viral conjunctivi-

tis) it is 5 days. As to how it is spread,

both bacterial and viral pathogens

are highly contagious. Spread is via

direct contact with discharge from

the eye or indirect contact from a

contaminated surface or object.

Although the safest preven-

tive measure would be to exclude

children until the discharge has

resolved, this is not feasible. Hand

hygiene is important, especially

when touching the eyes, nose, or

mouth. Infected individuals should

not share towels, cosmetics, or

other personal items. Many schools

require 24 hours of antibiotics for a

child with an eye discharge before

the child can return to school.

This is appropriate to decrease risk

of infecting others with bacterial

conjunctivitis, but it will not impact

risk of spread of viral conjunctivi-

tis. If concerned about school sys-

tems requiring antibiotic treatment,

explaining that pinkeye is like the

common cold and that exclusion

is not appropriate for the common

cold may get the child back in school

without an unneeded treatment.1

D i a r r h e a l i l l n e s s . S i g n s

and symptoms of diarrheal ill-

ness include 3 or more large,

loose (increased water content or

decreased form) stools per day.

Patients often have other symptoms

such as nausea or vomiting.

Incubation period depends on

the causative agent. It is spread by

person-to-person contact via fecal-

oral route.

Good hand-washing and per-

sonal hygiene are paramount in the

prevention and control of diarrheal

illnesses. If good hand-washing

and personal hygiene are not prac-

ticed, there is an increased chance of

spread of illness between children,

particularly if food is contaminated

and shared among students.

Most cases of diarrhea are viral,

and a pathogen is never identified.

An etiology for bloody diarrhea is

more commonly sought and may

identify a pathogen.  Younger chil-

dren who are not able to reliably

toilet and practice good personal

hygiene should stay home until

diarrhea has resolved for 24 hours.

Staph and strep are the most common bacteria causing boils, abscesses, or

cellulitus. These infections are contagious if the infected area is open and draining.

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 624

clinical feature

Older children who are able to

reliably toilet and practice good

personal hygiene, and who do not

have other symptoms requiring

exclusion (eg, fever), do not need

to stay home unless the diarrhea is

uncontrollable.

Children who have experienced

2 or more episodes of vomiting in

a 24-hour period related to acute

gastroenterit is should remain

excluded from school. Children may

return to school when the child has

no accidents using the toilet and

stool frequency is no more than

2 stools per day more than the

child’s normal stooling frequency.4

The National Institute for Health

and Care Excellence   has a more

conservative recommendation and

advises exclusion until 48 hours

after the last episode of diarrhea.5

If an enteric pathogen is identi-

fied as the cause of diarrhea, these

additional exclusions will apply:1

} Shigella: the child should be

excluded until diarrhea resolves

and 1 or more stool cultures are

negative. The requirements will

vary by state.

} S h i g a t o x i n - p r o d u c i n g

Escherichia coli: the child should

be excluded until there are 2 neg-

ative cultures 24 hours apart.

Additionally, state and local

jurisdictions may have differ-

ent laws governing exclusion and

return to school.

Strep throat. Signs and symp-

toms of strep throat include fever;

sore throat; variable throat exam

that may or may not reveal visible

pus spots; or tender and swollen

lymph nodes.

Incubation period is 1 to 3 days.

Strep throat is spread by large

respiratory droplets from a child

with an infection (or a carrier), or

direct contact with nasal/throat

secretions. Indirect transmission is

uncommon.

Strep throat can cause real havoc

in the lives of families with dual

working parents. One parent needs

to leave work early and bring a child

to the pediatrician’s office, and then

current guidelines and many school

systems advise exclusion until the

completion of 24 hours of antibiot-

ics and avoidance of close contact

with other students.4

A 2015 article published in the

Pediatric Infectious Disease Journal,

however, found that a single dose

(50 mg/kg) of amoxicillin led to

91% of children having undetectable

testing the next morning. This led

the investigators to conclude that

children with strep throat treated by

5 pm may return to school the next

day if afebrile and improved.6

Infections are a common reason

for school exclusion. Pediatricians

need to be comfortable discussing

appropriate exclusion and willing

to intervene if children are being

inappropriately excluded from

school or daycare.

R E F E R E N C E S

1. Silfverdal S-A. Book review. Managing Infectious

Diseases in Child Care and Schools: A Quick

Reference Guide. 3rd ed. Aronson SS, Shope TR, eds. Elk Grove Village, IL: American Academy of Pediatrics; 2013. Acta Paediatr. 2015;104(5):535.

2. Centers for Disease Control and Prevention. When and how to wash your hands. Available at: http://www.cdc.gov/handwashing/when-how-handwash-ing.html. Updated September 4, 2015. Accessed June 23, 2016.

3. American Academy of Pediatrics. Summaries of infectious diseases: varicella-zoster virus infections. In: Kimberlin DW, Brady MT, Jackson MA, Long SS, eds. Red Book: 2015 Report of the Committee on

Infectious Diseases. 30th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2015:846-860.

4. American Academy of Pediatrics. Recommendations for care of children in special circumstances. Children in out-of-home child care: recommendations for inclusion or exclusion. In: Kimberlin DW, Brady MT, Jackson MA, Long SS, eds. Red Book: 2015 Report

of the Committee on Infectious Diseases. 30th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2015:132-151.

5. National Institute for Health and Care Excellence. Diarrhoea and vomiting caused by gastroenteritis in under 5s: diagnosis and management. https://www.nice.org.uk/guidance/cg84. Published: April 22, 2009. Accessed June 1, 2016.

6. Schwartz RH, Kim D, Martin M, Pichichero ME. A reappraisal of the minimum duration of antibiotic treatment before approval of return to school for chil-dren with streptococcal pharyngitis. Pediatr Infect Dis

J. 2015;34(12):1302–1304.

7. Clark RC. ‘No-nit’ policy adopted to battle lice in schools. Star News. February 4, 2014. Available at: http://www.starnewsonline.com/article/20140204/articles/140209863?tc=ar. Accessed June 23, 2016.

8. American Academy of Pediatrics. Recommendations for care of children in special circumstances. School health: infections spread by direct contact. In: Kimberlin DW, Brady MT, Jackson MA, Long SS, eds. Red Book: 2015 Report of the Committee on

Infectious Diseases. 30th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2015:156-157.

9. American Academy of Pediatrics. Summaries of infectious diseases: pediculosis capitis. In: Kimberlin DW, Brady MT, Jackson MA, Long SS, eds. Red

Book: 2015 Report of the Committee on Infectious

Diseases. 30th ed. Elk Grove Village, IL: American Academy of Pediatrics; 2015:597-600.

Investigators conclude that children with strep throat treated by 5 pm may return

to school the next day if afebrile and improved.6

For additional resources, go to

ContemporaryPediatrics.com/

infection-control-prevention

25J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

PEER-REVIEWED FEATURE

Dr Westers is clinical

psychologist and assistant

professor, Children’s

Health Children’s Medical

Center Dallas, Texas,

and University of Texas

Southwestern Medical

Center, Dallas.

Dr Muehlenkamp is

associate professor of

psychology, University of

Wisconsin–Eau Claire.

Dr Lau is assistant

professor, Children’s

Health Children’s Medical

Center Dallas, Texas,

and University of Texas

Southwestern Medical

Center, Dallas. Drs Westers

and Muehlenkamp have

nothing to disclose in

regard to affiliations with

or financial interests in

any organizations that

may have an interest in

any part of this article.

Dr Lau reports that she

has ownership interest

in Gilead, which does not

affect her ability to be

unbiased in this article.

Medical providers, particularly pediatri-

cians, are often the first to learn that their

patients have been intentionally harming

themselves.1,2 Nonsuicidal self-injury

(NSSI) is defined as directly and

intentionally inflicting damage

to one’s own body tissue with-

out intention of suicide and

not consistent with cultural

expectations or norms.3 Epide-

miologic studies of community

samples indicate an approximately

5.9% lifetime prevalence of NSSI among

adults and 18% among adolescents, with

rates even higher among psychiatric treat-

ment-seeking youth.4-6 Nevertheless, only

1 in 4 clinicians routinely inquires about

and addresses NSSI with his or her adoles-

cent patients.7

Several authors have provided sugges-

tions for how healthcare providers can

respond to patients who self-injure.1,2,8,9 We

developed the SOARS model for medical

providers to use as a brief screening and

assessment of NSSI. Each letter of SOARS

represents an area to assess: Suicidal ide-

ation; Onset, frequency, and methods;

Aftercare; Reasons; and Stage of

change (Figure 1). Using theory,

research, and consideration of

real-world practice, we high-

light the most important ques-

tions to ask, the reasoning for

these questions, and recommen-

dations for how to ask them. Before

screening and assessing NSSI, however,

an important step for medical providers

is to first evaluate their own values and

beliefs about NSSI.8

Being empathic toward individuals who

engage in a behavior typically considered

contrary to protecting one’s health can be

difficult at times. Any negative biases, mis-

conceptions, or judgments about NSSI (eg,

manipulative or done primarily for atten-

tion) may result in a poor response and lack

SOARS modelRisk assessment of nonsuicidal self-injuryNICHOLAS J WESTERS, PSYD; JENNIFER J MUEHLENKAMP, PHD; MAY LAU, MD, MPH

A new assessment tool helps physicians screen adolescents for self-harming behaviors, then develop a treatment plan or referral to therapy for these patients.

SOARS Model

FAST FACT

Approximate lifetime prevalence

of NSSI among adolescents is

18%.7

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 626

peer-reviewed

of empathy for patients struggling

with this behavior. Providers who

are aware of their own emotions and

perspectives are better able to moni-

tor them and can help their patients

more effectively.8

Screening for NSSIProviders who use the HEEADSSS

assessment [Home environment,

Education and employment, Eating,

peer-related Activities, Drugs, Sex-

uality, Suicide/depression, Safety

from injury and violence] to obtain

a psychosocial history from ado-

lescents would likely find the most

opportune time to screen for NSSI

prior to screening for suicide.10 It

may seem easiest to simply ask if

they have ever hurt themselves on

purpose without intending suicide.

Asking about NSSI using a broad

question like this, however, typically

results in lower prevalence rates of

the behavior than does asking about

NSSI in a checklist format.5 We rec-

ommend normalizing the behav-

ior (eg, “I know that some people

who experience stressors similar to

yours think about hurting them-

selves on purpose without intend-

ing suicide.”), asking them directly

about it (“Have you ever hurt your-

self on purpose without intending to

end your life or attempt suicide?”),

and finishing the question by list-

ing common forms of NSSI similar

to checklist format (“like cutting,

biting, burning, or hitting?”). If

patients disclose engaging in NSSI,

providers can do a brief assessment

using SOARS. Similar to asking

about suicide, no iatrogenic effects

have been shown from asking about

NSSI.11

Assessing NSSI using the SOARS modelSUICIDAL IDEATION

Because NSSI, by nature, is not sui-

cidal, it should not be confused

with or misinterpreted as a suicide

attempt. Some adolescents fear that

disclosing their NSSI will unneces-

sarily lead to an inpatient psychi-

atric hospitalization. Nevertheless,

immediately after screening for

NSSI, and as part of the HEEADSSS

assessment, it is important to assess

any suicidal ideation concurrent or

in tandem with NSSI.

This is important for at least 2

reasons: For those who engage in

the behavior, using NSSI as a cop-

ing strategy to avoid suicide has

been shown to be among the stron-

gest risk factors for attempting sui-

cide, and a history of NSSI has

been shown to be among the stron-

gest risk factors for future suicide

attempt, and for depressed youth,

even more so than a history of a past

suicide attempt.12-15

How to ask. To obtain the most

honest response from adolescents

who engage in NSSI and to decrease

any anxiety that they may be alone,

it is best to normalize that some

young persons who self-injure think

about suicide when they engage in

NSSI. So, the question can be posed

as: “I know self-injury isn’t usually

about suicide, but some people may

think about suicide when they self-

injure. Do you ever think about pur-

posely ending your life when you

self-injure?

SOARS ASSESSMENT POCKET CARD

Responding to nonsuicidal self-injury (NSSI) using SOARS assessment

Have you ever hurt yourself on purpose without intending to end your life or

attempt suicide, like cutting, biting, burning, hitting?

Suicidal ideation

} I know self-injury isn’t usually about suicide, but some people may think

about suicide when they self-injure. Do you ever think about purposely

ending your life when you self-injure?

Onset, frequency, and methods

} When was the first/most recent time?

} How many times a week/month do you self-injure?

} What do you typically do or use?

Aftercare

} How do you take care of the wounds afterward?

} Have you ever hurt yourself so badly that you needed medical attention,

even if you never got it?

Reasons

} It sounds like this has been helpful for you. What does it do for you?

(In what ways does it help?)

Stage of change

} Is this something you would like to stop?

} Have you ever considered stopping?

1

27J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

peer-reviewed

ONSET, FREQUENCY, AND

METHODS

It is important to ask about onset of

NSSI (to determine duration); how

many episodes of NSSI in which

adolescents have engaged (to deter-

mine frequency); and what they typ-

ically use to self-injure (to determine

number of methods). Each of these

characteristics has been shown to

be positively associated with an

increased risk for suicide.

According to the interpersonal-

psychological theory of suicidal

behavior (IPTS), individuals die

by suicide because they have both

the desire to die (based on feelings

of perceived burdensomeness and

perceptions of not belonging or fit-

ting in with anyone, which are often

symptoms of depression) and the

capability to act on that desire.16 The

capability for suicide is acquired

over time, theoretically, as a result

of exposure to painful and provoca-

tive experiences (eg, childhood mal-

treatment, combat exposure, past

suicide attempt, and NSSI) that

cause a decreased fear of death and

an increased tolerance of physical

pain.

According to the IPTS and NSSI

research, individuals may first

engage in NSSI without ever before

having considered suicide. Over

time, individuals who repetitively

engage in NSSI have a greater risk

of suicide because of pain habitua-

tion and decreased fear of death.3,17

Research suggests that risk for a

suicide attempt among those who

self-injure peaks between 20 and

50 lifetime episodes of NSSI and

then declines afterward, likely

because the NSSI has become an

effective coping strategy for those

individuals.12

Using a greater number of meth-

ods for NSSI (eg, cutting, carving,

burning, hitting) is also related to

suicide attempts, especially when

frequency of NSSI is high.3,18,19 Each

type of method may elicit a different

kind of pain (eg, tearing, burning,

bruising) and may independently be

classified as a painful and provoca-

tive experience, thereby increasing

acquired capability for suicide via

both habituation to various forms of

pain and decreased fear of death.19

How to ask. To obtain an idea of

how long an adolescent has engaged

in NSSI, simply ask “When was

the first time you [cut] yourself?”

followed by “When was the most

recent time?” Similar to assessing

other high-risk behaviors using

the HEEADSSS format, providers

should be specific when assessing

frequency and lifetime number of

episodes of NSSI. Rather than ask-

ing vaguely (eg, “How often . . .”),

we recommend that providers be

specific and first ask “How many

times a week do you self-injure?”

or “How many times a month do

you self-injure?” Asking about

increased severity is also impor-

tant, particularly because this may

indicate growing tolerance for pain

and acquired capability for a suicide

attempt: “Have you found that you

have begun to self-injure more often

or more deeply than a year ago (or

when you first started)?” At least

1 study found that an absence of

pain during NSSI is linked to an

elevated risk for suicide attempts.3

To determine the number of dif-

ferent types of methods, providers

can ask “What do you typically do

or use?” If an adolescent responds

that he or she cuts using a blade

from a small pencil sharpener, the

razor from the shower, or a piece

of glass, these are all considered

1 method (ie, cutting), and provid-

ers can then ask about other meth-

ods such as those assessed during

the initial screening question.

AFTERCARE

Medical providers are often in the

best position to screen for NSSI and

to determine severity of injury. Poor

wound care can increase risk for

infection and even scarring. Some

individuals might hurt themselves

more severely than intended and

require medical attention, although

some may not seek it out.

How to ask. As with all assess-

ment questions about NSSI, it is best

to use a low-key and nonjudgmen-

tal demeanor that shows a respect-

ful curiosity.20 Providers can ask

“How do you typically take care of

the wounds afterward?” and “Have

you ever hurt yourself so badly that

you needed medical attention, like

stitches, even if you never got it?”

Over time, individuals who repetitively engage in NSSI have a greater risk of

suicide because of pain habituation and decreased fear of death.3,17

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 628

peer-reviewed

Some providers have suggested that

if an injury is discovered on assess-

ment, they should ask “Do you have

any other wounds?” and then state

matter-of-factly “I need to assess

your wounds so we can be sure to

provide the proper care and avoid

infection.”9

REASONS

Individuals who engage in NSSI

typically do so because it is helpful

as a short-term solution or relief, or

serves some particular function(s),

such as to deal with stress or over-

whelming emotions, in response

to feeling emotional numbness, to

punish themselves, or to commu-

nicate their feelings to someone

(Table 1). Determining the reasons

the adolescent engages in NSSI will

likely be the primary focus of the

assessment, particularly because

this will guide providers in their

brief intervention and help deter-

mine the treatment plan.

For medical providers who have

limited time to spend with their

patients, a brief intervention may

simply mean assessing severity

of NSSI and safety, followed by a

referral for therapy. A follow-up

telephone call or an in-person acute

care follow-up visit within 2 to

3 weeks may be indicated to deter-

mine if the patient or parent has

identified a therapist. For medical

providers who have an additional

few minutes to provide medical

counsel, a brief intervention may

include specific targeted advice

regarding alternative coping strat-

egies based on function of the

behavior.

For example, if the adolescent’s

purpose for the behavior is to cope

with overwhelming emotional

distress, an important element of

the brief intervention is exploring

additional helpful strategies that he

or she can utilize before or instead

of engaging in NSSI. Focus should

be on bolstering healthy coping

skills rather than simply removing

unhealthy ones; addition is better

(and easier) than subtraction.20 If

the purpose of self-injuring is to

communicate the adolescent’s feel-

ings to parents or friends, a brief

intervention may include exploring

alternative strategies for effectively

communicating his or her emo-

tional needs. Essential elements in

all brief medical counsel include

validating that the adolescent’s NSSI

seems helpful, sensitively expressing

1 STRATEGIES FOR BRIEF MEDICAL INTERVENTION

REASON FOR NSSI BRIEF INTERVENTION EXAMPLE RESPONSE

To reduce emotional tension and stress

Identifying alternative strategies to reduce

emotional distress (eg, talking to a friend/

parent, journaling, drawing, exercising,

using relaxation techniques).

“What are some other ways you can manage

when you’re feeling overwhelmed, even if they

don’t work as quickly as self-injury?”

To feel something due to feeling numb or empty

Identifying alternative strategies for

generating feelings (eg, taking a cold

shower, eating a hot pepper) or discussing

how patients might tolerate numbness for

the time being (eg, accepting temporary

emotional numbness).

“What are some other ways you can feel

something when you’re feeling numb or empty,

even if they don’t work as quickly as self-

injury?”

To communicate with others Identifying alternative strategies for

communicating emotional needs

(eg, asking for encouragement, advice,

a hug, to sit in silence together, to do

something together).

“How might you ask your mom/dad/friend for

emotional support and help without hurting

yourself or telling them that you’re going to?”

To self-punish Introducing concept of self-forgiveness

and acceptance of imperfections.

“Sounds like you’re experiencing enough of

life’s punishments right now. Instead of adding

more punishment to yourself, what would it be

like to allow yourself some room for mistakes

or self-forgiveness?”

Abbreviation: NSSI, nonsuicidal self-injury.

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CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 630

peer-reviewed

concern about the behavior, kindly

advising against it for health rea-

sons, exploring alternative strate-

gies, and offering to make a referral

for therapy.

Unfortunately, many adolescents

who resort to NSSI cannot readily

integrate information on alterna-

tive, healthier coping strategies. In

these situations, listening to them

without judgment, empathizing

with their emotional distress, and

exploring openness to therapy may

be therapeutic and the best way to

respond if an adolescent is over-

whelmed in the moment. Simply

telling an adolescent to stop self-

injuring or reacting negatively may

inadvertently communicate to him

or her that it is not safe to talk about

the behavior, and the adolescent

may choose to continue to engage in

NSSI but no longer talk about it with

his/her provider.

The more reasons behind engag-

ing in NSSI, the greater the risk

for suicide.12 Reasons for NSSI that

are most strongly related to suicide

attempts include: to avoid suicide,

to cope with self-hatred, and to end

dissociation or feel something other

than emptiness or profound anxi-

ety. Many physicians who see ado-

lescents take confidentiality very

seriously and discuss confidentiality

and its limits at the beginning of

the appointment. Each adolescent is

unique, so breaking confidentiality

about NSSI behavior is often based

on the clinical judgment of the med-

ical provider.1 At this point in the

SOARS interview, clinicians will

likely have a good idea of how safe

or at risk an adolescent who self-

injures is for suicidal behavior. If

the purpose of an adolescent’s NSSI

is to avoid suicide, we recommend

that providers break confidentiality

and involve parents. This is impor-

tant because no one may know if

or when the NSSI becomes ineffec-

tive as a strategy to avoid suicide,

and then the adolescent decides to

attempt suicide.

How to ask. It is important to

first acknowledge how NSSI is not

the true problem for those who

engage in the behavior but instead

a solution to feelings coming from a

deeper problem. Validating that it is

a helpful way to cope is not the same

as agreeing with the behavior or

condoning it. Thus, we recommend

that providers ask about the reasons

for engaging in NSSI by stating “It

sounds like this has been helpful

for you. What does it do for you (in

what ways does it help you)?”

However, NSSI does not help all

adolescents. These young persons

typically respond that they heard

about NSSI as an effective coping

2 COMMON APPROACHES FOR ADDRESSING NSSISTRATEGY GENERAL FOCUS SNAPSHOT IN PRACTICE

Motivational interviewing (MI)

Respectfully guiding individuals to engage

in healthy behavioral change by resolving

ambivalence and eliciting motivation for change

Exploring the pros and cons of continuing to

engage in NSSI and the pros and cons of ceasing

NSSI

Cognitive behavioral therapy (CBT)

Modifying thoughts and behaviors to improve

mood and emotions

Differentiating between feelings (eg, anxiety) and

behaviors (eg, NSSI) and modifying the thought

that one must self-injure to improve mood

Dialectical behavior therapy (DBT)

Mindfulness and balancing dialectical (ie,

philosophy of opposing ideas) tension between

acceptance and change by teaching distress

tolerance, emotion regulation, and interpersonal

effectiveness skills

Identifying reason(s) for engaging in NSSI,

nonjudgmentally accepting associated

distressing emotions, and engaging in alternative,

healthier behavior

Emotion-regulation group therapy (ERGT)

Addressing NSSI by learning to regulate

emotions through understanding and acceptance

of emotions, control of behavior, and value-

directed living (ie, identifying meaningful things

in life and making choices consistent with those

values)

Identifying and pursuing meaningful activities in

life and inhibiting impulsive behavior (eg, NSSI),

even if it means experiencing negative emotions

along the way

Abbreviation: NSSI, nonsuicidal self-injury.From: Rollnick S, et al22; Beck AT, et al23; Linehan MM24; Gratz KL, et al.25

31J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

peer-reviewed

strategy, tried it once or twice, found

that it was unhelpful, and stopped

engaging in it. Among those who

have already ceased the behavior,

affirming their choice of healthier

coping strategies is sometimes all

that is necessary to prevent future

episodes.

STATE OF CHANGE

Although many adolescents who

self-injure are not ready to stop

or cannot stop their NSSI, some

desire to stop their self-injury but

are unsure how. Some see no need

to change at all. The transtheoreti-

cal model of behavior change may

be a helpful way of conceptualizing

whether adolescent patients want to

change or are ready to change.21 For

those who are not yet ready to give

up their NSSI, using motivational

interviewing can be a helpful way

of collaborating with these adoles-

cents, guiding them toward moti-

vation for change and exploring the

pros and cons of life without NSSI

(Table 2).22-25 Medical providers do

not need to go into great depth dur-

ing this conversation, but posing a

question about readiness for change

is a good first step for the adoles-

cent to consider how he or she might

stop self-injuring and to determine

if there is a desire to do so.

How to ask. After an adolescent

has disclosed the reasons for his

or her NSSI and the functions it

serves, a provider can ask, “Is this

something you would like to stop?”

or, “Have you ever considered stop-

ping?” If the adolescent responds

that he or she would like to stop

and needs help, then referral to a

mental health professional who has

experience treating adolescents who

self-injure is appropriate. If the ado-

lescent responds that he or she sees

no need to change, then brief medi-

cal counsel could focus on exploring

the pros and cons of the behavior

(eg, perhaps it is harming his/her

relationship with someone impor-

tant, such as parents). The adoles-

cent’s response may also provide a

sense of the likelihood that he or

she will follow up with a referral to a

mental health professional.

SummaryClinicians can choose to spend

much more time discussing and

assessing NSSI, but the purpose

behind the SOARS model for assess-

ing NSSI is to be able to conduct a

brief screening and assessment of

NSSI by recommending what ques-

tions are most important to ask, why

they are important to ask (based on

empirical research and theory), and

how to ask them. Primary focus

should be on the reasons behind

the behavior, which will inform the

brief intervention or counsel medi-

cal providers may give to their ado-

lescent patients. All brief medical

counsel should validate the utility

of NSSI for each patient, sensitively

express concern about the behavior,

kindly advise use of healthier strat-

egies for coping (addition is better

than subtraction), and offer a refer-

ral to therapy.

If using the full SOARS assess-

ment model is not realistic in

a given scenario because of time

constraints, an even shorter ver-

sion (Suicidality, Aftercare, Reasons

[SAR]) can be used that addresses

the 3 most important assessment

questions: Suicidality: “Are you

thinking about suicide when you

self-injure?”; Aftercare: “How do

you take care of your injuries?”;

Reasons: “In what ways is this help-

ing you?” (Figure 2).

Although no empirically sup-

ported treatment targeted spe-

ci f ica l ly for NSSI yet ex ists

(psychotherapeutic or pharmaco-

logic), most treatments that help

patients with NSSI have a tendency

to address the context in which the

behavior occurs (eg, depression,

anxiety, emotion dysregulation).2

As a result, referrals to experts

with a broad background including

empirically supported treatments

such as cognitive behavioral therapy

(CBT), dialectical behavior therapy

(DBT), or emotion-regulation group

therapy (ERGT) will likely be most

helpful (Table 2).23-25

For references, go to

ContemporaryPediatrics.com/

SOARS-for-NSSI

SAR: 3 KEY QUESTIONS

Suicidality Aftercare Reasons

Are you thinking

about suicide when

you self-injure?

How do you

take care of

your injuries?

In what ways

is this helping

you?

2

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 632

HOSPITAL ZONE

Ms Hilton is a medical

writer who has covered

health and medicine for

25 years. She resides in

Boca Raton, Florida. She

has nothing to disclose in

regard to affiliations with

or financial interests in

any organizations that may

have an interest in any part

of this article.

The misconception that children born

with cleft lip, cleft palate, or both need

only a single surgery to address their cleft

can leave patients with a lifetime of phys-

ical and emotional challenges. Pedi-

atricians who encounter children

with these facial differences should

encourage parents and caregiv-

ers to pursue a focused, long-

term, multidisciplinary approach

to treating and managing cleft lip

and/or palate because all affected

children benefit.1

Cleft lip and palate is more than a plas-

tic surgery issue, according to Karla A.

Haynes, RN, MPH, MS, CPNP, pediatric

nurse practitioner, at Children’s Hospital

Los Angeles Craniofacial and Cleft Center,

California, one of the country’s largest

multidisciplinary centers for children born

with congenital facial differences, such as

cleft lip, cleft palate, and other craniofacial

conditions.

“The best practice is a multidisciplinary

evaluation, which can be an issue because,

sometimes, people who aren’t very famil-

iar with this patient population might

see craniofacial abnormalities as a plastic

surgery problem. They may not under-

stand that this is a chronic condition, and

that there is a need for ongoing monitor-

ing and care throughout childhood,”

Haynes says.

Cleft lip and palate facts and figuresOccurring in about 1 in 600 live

births in the United States, clefts

involving the lip and/or palate are

among the most common congen-

ital anomalies affecting the craniofacial

region.1,2

Oral facial clefts vary in incidence

according to gender and ethnic back-

ground. Clefting is known to occur more in

males, and Asians and Native Americans

have the highest birth prevalence, with 1

in 500 births. The lowest prevalence is in

people of African descent.2

Cleft palate and cleft lip often occur

together. About two-thirds of those

affected have clefts of the lip and palate.2

Cleft lip alone is more likely to occur

than cleft palate alone, but when it does

Cleft lip and palateTeam approach to treatmentLISETTE HILTON

A multidisciplinary center for children born with cleft lip, cleft palate, or other craniofacial conditions ensures that patients emerge with little evidence of deformity.

Facial Clefts

Karla A. Haynes,

RN, MPH, MS,

CPNP

33J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

hospital zone

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occur, cleft palate is more common

among females.

Because many of the syndromes

associated with clefting are inher-

ited in an autosomal dominant pat-

tern, each offspring of an affected

person has up to a 50% chance

of inherit ing the syndrome. 2

Recurrence of isolated cleft is low,

however—around 2% to 6%. The

risk increases as the number of

affected persons in a family grows.

What’s meant to happen in utero, doesn’tThe lip normally fuses by 35 days

in utero.3 The lip’s failure to fuse

can impair subsequent closure of

the palatal shelves, which typically

close in the 8th to 9th week.

Although the cause of cleft

l ip sequence typical ly is

a myster y, clef ts occur

in syndromic or isolated

categories.2 Skeletal, cra-

niofacial, eye, and other

anomalies generally occur

with syndromic clef ts .

Cleft-associated syndromes

can originate from intrauterine

exposures to alcohol, isotretinoin,

cigarette smoke, and more, as well

as result from genetic disorders.

Children with clefting are at

higher risk for abnormal tooth

development, as well as mild ocular

hypertelorism, hypernasal speech,

speech delay, recurrent otit is

media, and hearing loss.3

Often detected in utero

Typically, community obstetrics

providers will see a fetal cleft

lip on ultrasound (the cleft

palate generally is not so vis-

ible), according to Haynes.

Cleft lip not detected

before birth should be seen

in the immediate postnatal

period. Cleft palate might

be diagnosed later, during a rou-

tine newborn intraoral examina-

tion, especially if the newborn has a

milder variant, such as bifid uvula or

submucosal clefting. Pediatricians

and others who diagnose cleft palate

should conduct a systemic examina-

tion because every sixth newborn

that has cleft palate is at higher risk

for other malformations, including

S FIGURE 1 Patient with an

unrepaired right unilateral

complete cleft lip and palate. She is

aged 19 days in this photo.

S FIGURE 2 Patient is 5 months

postoperative following cleft lip

repair. She is aged 8 months.

S FIGURE 3 Patient is 3 years postoperative from her palate repair surgery and

2 years postoperative from lip revision surgery.

Alessia Johns,

PhD

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 634

hospital zone

congenital heart disease or urinary

tract anomalies.1

To differentiate between an

isolated or syndromic cleft, the

pediatrician should consult with

a craniofacial team and geneticist,

and take a careful family history of

clefts and features of clefting syn-

dromes, including skin disorders

and speech abnormalities.2 The

pediatrician should also ask about

prenatal exposures. In addition,

assessments for vision and hearing

should be done as early as possible.

Immediate concernsBecause cleft palate prevents an

infant from effectively sucking,

these babies have trouble with

breastfeeding. Pediatricians can

recommend that mothers pump

their breast milk and give it to

their babies using a special nip-

ple designed to facilitate feeding

infants with clefting.

The good news is breastfeeding

can be successful in babies with iso-

lated cleft lip only.2 However, par-

ents should know that these babies

tend to take in more air while feed-

ing and might require more frequent

burping. With palatal openings or

dysfunction, nasal regurgitation

also can occur.

Pediatricians should diligently

monitor these children’s growth and

more because children with palatal

clefts are at significantly greater risk

for eustachian tube dysfunction,

recurrent otitis media, and conduc-

tive hearing loss.2

According to Haynes, feeding

and growth can be significantly

impaired and babies can really

struggle to gain weight, with a small

percentage requiring admission for

failure to thrive until families mas-

ter the feeding techniques. This can

be challenging, she says.

Takes a villageChildren’s Hospital Los Angeles

Craniofacial and Cleft Center fea-

tures 13 subspecialty disciplines on

its craniofacial team. The full list

of specialty providers is plastic sur-

gery, nurse practitioners, ears/nose/

throat, audiology, speech pathol-

ogy, genetics, dentistry, ortho-

dontics, psychology, social work,

pediatrics, pulmonology, and a reg-

istered dietician. PH

OT

OS

PR

OV

IDE

D B

Y K

AR

LA

HA

YN

ES

, R

N,

MP

H,

MS

, C

PN

P, C

HIL

DR

EN

’S H

OS

PIT

AL

LOS

AN

GE

LES

.

S FIGURE 5 Patient is 6 weeks postoperative following a sphincter

pharyngoplasty (not visible) to address hypernasal speech. She is aged 7

years 9 months in this photo.

S FIGURE 4 Patient is now 5 years postoperative following cleft lip revision.

She is aged 7 years 3 months in this photo.

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CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 636

hospital zone

PH

OT

OS

PR

OV

IDE

D B

Y K

AR

LA

HA

YN

ES

, R

N,

MP

H,

MS

, C

PN

P, C

HIL

DR

EN

’S H

OS

PIT

AL

LOS

AN

GE

LES

.

Nurse practitioners coordinate

care at the center, and the surgical

care is directed by a plastic surgeon

who relies heavily on the input of

the team members, Haynes says.

“Our patients all have their own

community pediatricians that

do their usual well-child health

surveillance and sick visits,” Haynes

said. “The pediatricians on our cra-

niofacial team monitor patients . . .

looking at signs of obstructive sleep

apnea or gastroesophageal reflux or

some of the things that kids with

cleft lip and cleft palate or other cra-

niofacial diagnoses are more likely

to have.”

The care of these patients often

begins in utero, according to Haynes.

“My nurse practitioner colleagues

and I also do prenatal counseling

in conjunction with a program at

our hospital called the Institute for

Maternal-Fetal Health,” she says.

A nurse practitioner and the

institute’s perinatologist will meet

with pregnant mothers who are

referred to the institute because of

a possible cleft on ultrasound. “[We]

will do another anatomy scan with,

in our case, the craniofacial nurse

practitioner standing right beside

the perinatologist, so we’re looking

at the images together. And based

on what the 2 providers see, the par-

ents are counseled on the diagno-

sis,” Haynes says. “About half, if not

more, of our babies are identified

before birth.”

There are other centers of excel-

lence focused on children with

craniofacial conditions, includ-

ing Seattle Children’s Hospital in

Washington state, Brigham and

Women’s Hospita l /Chi ldren’s

Hospital in Boston, Massachusetts,

a nd Ch i ld ren’s Hospit a l of

Philadelphia, Pensylvania, accord-

ing to Haynes.

At the very least, teams charged

with the care of children with

cleft lip and palate should include

speech-language pathology, surgery,

and orthodontics specialists. The

core team should have ready access

S FIGURE 6 Patient is 12 days postoperative following repair of left

alveolar cleft to stabilize her dental arch and maxilla. She is aged 10 years

3 months in this photo.

S FIGURE 7 Patient is 6 weeks postoperative following repair of left

alveolar cleft (as in Figure 6). She is aged 10 years 4 months in this photo.

37J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

hospital zone

to psychology, social work, audiol-

ogy, genetics, general and pediatric

dentistry, otolaryngology, and pedi-

atrics/primary care professionals.

The team should also be able to refer

to a neurosurgeon, an ophthalmolo-

gist, a radiologist, and a geneticist,

according to the American Cleft

Palate-Craniofacial Association.4

Best practicesPediatric patients with cleft lip and

palate require numerous surger-

ies throughout their childhood

and into early adulthood to correct

the aesthetic and functional issues

associated with their diagnoses. In

1 sample of patients, the aver-

age number of surgical procedures

required was 8.6.5

“For all of the facial structures

and sociologic processes that are

affected by craniofacial [condi-

tions], we use different providers

on our team that are looking out for

all of these areas that are at risk,”

Haynes says. “Sometimes, a lack

of continuity of care is a problem.

But definitely pediatricians should

know that if there is a child who is

born with a cleft, they need to be

with ongoing team care.”

There are different stages in the

surgery. When they’re done depends

a lot on the phase of dentition,

according to Haynes. She describes

a potential timeline of treatment for

children with cleft lip and palate:

“The very first surgery that’s done

is usually an initial cleft lip repair,

in which the lip is repaired and the

external nose, as well. That’s usu-

ally done anywhere between 1 and

3 months of age. Sometimes it can

be a little later,” she says. “The sec-

ond surgery is to repair the palate,

which of course is the roof of the

mouth, but it’s also the floor of the

nose. So, it does address that second

nasal component, and that’s usually

done sometime around 1 year of

age, ideally.”

The next surgery that many of

these children need is an alveolar

bone graft, which is done to repair

the dental arch of the maxilla where

the cleft has gone through the gums.

“That can be done in several ways,”

says Haynes, “but the children gen-

erally need to be in mixed dentition

before they can do the orthodontics

that allow them to have that surgery.

That surgery literally can’t be done

before they’re 7, 8, or 9 years of age.”

There are some optional surger-

ies, including scar revisions. “For

many of our kids, once they reach

skeletal maturity, they may need

an orthognathic jaw procedure

because one of the things that hap-

pens with kids with cleft lip and

cleft palate is they often end up

with a pretty significant under-

bite,” Haynes says. “Some of this is

correctable through orthodontics,

but for many kids the only way is

to do a surgery that involves mov-

ing the bones in the face. And that

can’t be done until kids are in their

later teenaged years.”

Care outcomesChildren with cleft lip and palate

have a poor quality of life.6 In addi-

tion, fragmented or uncoordinated

care of these children leads to poor

outcomes in speech and hearing.7

Haynes says the children that get

their care at Children’s Hospital Los

Angeles emerge with little if any

evidence of their cleft deformities.

“When the proper stepwise

approach is taken, children have

surgeries that address each ana-

tomic issue to ultimately result in a

child with good intelligible speech,

normal hearing, a stable maxilla,

proper occlusion of the jaws, and

symmetric facial features,” Haynes

says. “For families and providers

both, one of the biggest, most com-

pelling questions that remains is

‘Why does clefting happen?’ We

may be getting closer to having a

better understanding of the origin

of the ‘isolated’ clefts because of

the relative availability of exome

sequencing. We would also like to

know more about the role environ-

mental factors, such as maternal

diabetes, play.”

Haynes says Children’s Hospital

Los Angeles is conducting research

on the incidence of postpartum

depression in mothers of infants

born with cleft, and investigating

safe infant sleep for infants born

with Pierre Robin sequence.

For additional information to

help pediatricians discuss

facial clefts with families, as well

as references for this article, go to

ContemporaryPediatrics.com/

Hospital-Zone-facial-clefts

Facial clefts involving the lip and/or palate occur in about 1 in 600 live births

in the United States.1,2

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 638

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At home, the patient’s cough per-

sisted with the addition of several

episodes of nonbloody, nonbilious

posttussive emesis. On day 9 of ill-

ness, he developed oral vesicular

lesions associated with discom-

fort when swallowing solid foods,

prompting a visit to the local emer-

gency department (ED). There,

his temperature was 102.92°F, but

physical exam and chest imaging

performed at that time were reas-

suring for a safe discharge home

with close follow-up after being

given a 5-day course of azithromy-

cin for bronchitis (Figure 1).

By day 12 of his il lness, the

patient’s course was worsening.

The vesicular oral lesions were fri-

able and beginning to bleed. His

coughing episodes were increas-

ingly f requent and produced

blood-streaked sputum. Severe

odynophagia prevented him from

consuming both solids and liquids.

A complete physical exam by his

pediatrician at follow-up revealed

red, round, ulcerative lesions of the

ventral penile shaft along with skin

peeling and scant mucus discharge

at the urethral opening. Because

of his poor f luid intake and pro-

gressing symptomatology, he was

quickly referred back to the ED and

admitted for continued evaluation

and management (Figure 2).

HistoryThe patient endorsed a history of

acne vulgaris for which he took

minocycline daily. There was, how-

ever, no prior history of surgeries,

abnormal development, or varia-

tions from a regular healthy diet.

Family history was signif icant

only for maternal allergic reac-

tion of unknown severity to Perco-

cet (oxycodone hydrochloride with

acetaminophen) and Motrin (ibu-

profen). The patient had no known

drug allergy prior to presenta-

tion, and his immunizations were

up-to-date.

Upon HEA DDSSS (Home,

Education, Activities, Drug use

and abuse, Death, Sexual behavior,

Suicidality and depression, Safety)

assessment, the boy stated that

he lives at home with his mother,

father, and 2 younger sisters, the

oldest of which was recently diag-

nosed with pneumonia and suc-

cessfully treated with azithromycin.

He denied having pets in the home.

He was in the 11th grade and doing

well academically. Daily physical

activity was limited because he was

not interested in sports but rather

enthusiastically committed to play-

ing video games. He denied illicit

substance use, depressive symp-

toms, safety concerns, sexual activ-

ity of any kind, or suicidal ideation.

Physical examUpon physical examination, the

patient was afebrile with normal

vital signs. He appeared uncom-

fortable, tired, and in mild distress.

His eyes were without discharge or

conjunctival injection. External ear

canals were normal. Nares revealed

hemorrhagic crusts (Figure 3). Fri-

able, ulcerative lesions and dried

blood were found on his lips (Fig-

ure 4). The superf icia l buccal

mucosa was sloughing and actively

bleeding (Figure 5). The surface of

his tongue was covered by white

ulcerations posteriorly; the pal-

ate and posterior oropharynx were

BOY WITH FEVER, COUGH, AND ORAL LESIONSpuzzlerCONTINUED FROM PAGE 13

S FIGURE 3 Nares with hemorrhagic crusts. Day 16 of illness.

39J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

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erythematous and edematous; and

tonsillar exudates were appreci-

ated bilaterally. Lung exam was

somewhat limited by dry cough-

ing upon deep inspiration, but rales

were appreciated bilaterally in the

lower lung fields. Mild erythema of

the urethral opening along with a

single ulcerative lesion of the ven-

tral penile shaft was found. The

remainder of his physical exam,

including a thorough skin exami-

nation, was normal.

Differential diagnosisTaking into account the patient’s

presenting history and physical

exam findings, the team proposed

a fairly wide differential (Table).

Included in the list were an atypi-

cal presentation of the autoimmune

mechanisms underlying Crohn dis-

ease, absent of any associated gas-

trointestinal manifestations, and

Behçet disease, without its char-

acteristic ulcerative and erythem-

atous nodules or anterior uveitis.

Ingestion of a corrosive agent that

might precipitate the mucocuta-

neous oral findings also was con-

sidered, although the patient’s age

and absence of any intention for

self-harm made this possibility less

likely.

Infectious etiologies were pos-

tulated as well, including herpan-

gina of an enterovirus infection

or herpes simplex mucositis, most

commonly seen as a reactivation

event of a prior primary infection

in immunocompromised patients.

Even a severe drug reaction to ibu-

profen, such as Stevens-Johnson

syndrome (SJS), was introduced as

a possibility, although the limited

involvement of his pathology to the

nasal-oral and genital areas lessened

the team’s concern (Figure 6).

In narrowing the differential,

patient demographics such as age

and gender, benign past medical

history, absence of high-risk sexual

or self-harm behavior, and context

S FIGURE 4 Friable, ulcerative lesions and dried blood on patient’s lips and

tongue surface. Day 16 of illness.

S FIGURE 5 Sloughing superficial buccal mucosa with mildly active bleeding.

Day 16 of illness.

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 640

puzzler

of presentation with corresponding

respiratory symptoms, fever, and

limited cutaneous findings led the

team to favor an infectious etiol-

ogy. What remained to be deter-

mined was the causative organism

and the extent of the pathology it

would instigate in the patient.

Further testingOvernight, ibuprofen was dis-

continued for concerns of SJS and

empiric acyclovir was started for

suspected primary herpes simplex

virus (HSV) infection. A complete

blood count with manual differen-

tial and complete metabolic panel

were normal. A urinalysis showed

scant leukocyte esterase and 5 to

DIFFERENTIAL DIAGNOSIS FOR PEDIATRIC MUCOSITIS

INFECTIOUS ALLERGIC DRUGS POISONING AUTOIMMUNE

Herpangina SJS Chemotherapy Corrosive

agent ingestion

Aphthous

stomatitis

Herpetic mucositis

Erythema

multiforme

NSAIDs and

ASA

Behçet

disease

HIV Crohn

disease

Primary syphilis

SLE

Celiac sprue

Abbreviations: ASA, acetylsalicylic acid; HIV, human immunodeficiency virus; NSAIDs, nonsteroidal anti-inflammatory drugs; SJS, Stevens-Johnson syndrome; SLE, systemic lupus erythematosus.

We’ve made yours “to go”

ContemporaryPediatrics.com/PedsApp

puzzler

41J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

1. Corrosive ingestion} Identify specific

agent and time of ingestion

} Assess and protect airway

} CBC, CMP, ABG for baseline; repeat if suspicious for systemic toxicity

} Consult Poison Control, GI, or Surgery if unstable

} Psych eval if suicidal intent

} Supportive care

2. Aphthous stomatitis } HIV status and CBC

for assessment of neutropenia

} Ulcer Severity Score} Vitamin deficiency

assessment and correction

} Negative transglutaminase assay and Tzanck smear (rule out celiac and HSV)

} Supportive care

1. Mycoplasma-induced rash and mucositis} Respiratory infection-

like prodrome and fever} CXR with pneumonia} Findings limited to

oral, nasal, and genital mucosa +/- localized rash

} Mycoplasma PCR for diagnosis confirmation

} Antibiotic (azithromycin)

} Supportive measures with Magic Mouthwash and fluids

} Steroids +/- IVIG if severe

2. Herpangina} Febrile illness with

vesicular and/or ulcerative lesions

} Usually summer months} Constitutional

symptoms such as HA, backache, nausea, or stomach pain

} PCR of nasopharyngeal swab for enterovirus RNA

} Supportive care

1.Herpetic mucositis} Most commonly in the

immunocompromised patient

} Flu-like prodrome} Ulcerative and necrotic

lesions often localized to oral mucosa but can become systemic

} Anti-HSV titers} Acyclovir PO vs IV

along with antibiotics if superimposed bacterial superinfection

2. Erythema multiforme} Infectious vs type IV

hypersensitivity reaction} Flu-like prodrome} Spectrum of presentation

from local cutaneous involvement (target lesions) to widespread pathology of the oral, genital, orbital, and respiratory mucosa

} Clinical diagnosis, although HSV PCR can help confirm diagnosis and CMP can reveal electrolyte abnormalities and renal/hepatic involvement

} Supportive care, wound dressings, and steroids if severe

1. Stevens-Johnson syndrome} Respiratory infection-

like prodrome} Acute development of

targetoid lesions} Minimal to extensive

sloughing of the skin} Commonly idiopathic

but sometimes associated with drugs/infections

} Skin biopsy with full-thickness necrosis diagnostic

} BCx/UCx for superimposed bacterial infection

} Treated like burn patients in ICU

2. Behçet disease} Recurrent aphthous

ulcers, genital ulcers, and uveitis; sometimes with skin involvement and arthritis

} Most commonly affects mid-20s to mid-30s age range

} Extensive workup to rule out disease mimics (SLE, reactive arthritis, HIV)

} Treatment tailored to specific organ involved; multiple consultations may be necessary

Extensive skin findings?

Noninfectious? Infectious? Noninfectious?

Limited skin findings?

DIAGNOSTIC APPROACH

MUCOSITIS?

Abbreviations: ABG, arterial blood gas; BCx, blood culture; CBC, complete blood count; CMP, comprehensive metabolic panel; CXR, chest x-ray; GI, gastrointestinal; HA, headache; HIV, human immunodeficiency virus; HSV, herpes simplex virus; ICU, intensive care unit; IV, intravenous; IVIG, intravenous immunoglobulin; PCR, polymerase chain reaction; PO, per os; RNA, ribonucleic acid; SLE, systemic lupus erythematosus; UCx, urine culture.

6

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 642

puzzler

10 white blood cell counts, but no

red blood cells. Serum cultures,

bacterial genital cultures, HSV-1

and HSV-2 polymerase chain reac-

tion tests, culture swabs of the oral

and genital lesions, and Neisseria

gonorrhoeae and Chlamydia tra-

chomatis RNA urine tests all were

sent, none of which returned posi-

tive. Chest x-ray was repeated and

was significant for subtle right

lower lobe infiltrates.

Because initial workup in the

community hospital failed to pro-

vide an identifiable etiology for

the patient’s clinical course, he was

transferred to the nearest pediatric

tertiary care center where he was

found to have Mycoplasma-induced

rash and mucositis, also known as

MIRM.

Treatment and outcomeWith suspicion for MIRM second-

ary to inadequately treated M pneu-

moniae pneumonia, the patient was

started on a second 5-day course of

azithromycin along with intrave-

nous (IV) maintenance f luids and

supportive care for the oral lesions.

Famotidine was begun for prophy-

lactic treatment of presumed gastro-

intestinal mucositis. A telemedicine

dermatology consult was utilized to

help confirm the suspected diag-

nosis, and a 5-day course of pred-

nisone was initiated. Mycoplasma

immunoglobulin (Ig)G and IgM

serology were ordered and returned

positive after hospital discharge on

his 16th day of illness. During a fol-

low-up phone call with the mother,

she noted significant improvement

in his symptoms with normal oral

intake and a successful return to

school 3 days after leaving the hos-

pital (Figure 7).

Dr Sterns is a pediatric intern at Naval

Medical Center, San Diego, California.

Dr Kamat is a pediatric hospitalist, Inova

Children’s Hospital, Falls Church, Virginia.

The authors have nothing to disclose in

regard to affiliations with or financial

interests in any organizations that may have

an interest in any part of this article.

For an in-depth discussion of

MIRM with references, go to

ContemporaryPediatrics.com/puzzler-0716

Symptom onset

} Tactile

fevers

} Malaise

Initial PCP

evaluation

URI diagnosis

} Friable oral

lesions

} Poor oral intake

} PCP follow-up;

genital lesions

found

} Return to ED

and hospital

admission

} Azithromycin

discontinued

} Workup started

} Mucositis stable

} Oral intake much

improved

} Day of discharge

} Congestion

} Dry cough

} Oral lesions

} Productive cough

and posttussive

emesis

} ED visit with

negative CXR

} Azithromycin

started

} Transfer to children’s

hospital

} 2nd course of

azithromycin begun

} Mycoplasma IgM/IgG

serologies drawn

} Dermatology consult

and start of oral

steroid course

} Resolution

of symptoms

and return to

school

Day 2 Day 5 Day 9 Day 12 Day 14 Day 16 Day 19

PATIENT’S DISEASE COURSE

Abbreviations: CXR, chest x-ray; ED, emergency department; IgG, immunoglobulin G, IgM, immunoglobulin M; PCP, primary care physician; URI, upper respiratory infection.

7

dermcase

43J U LY 2 01 6 | CON T EMPORARYP ED I AT R I C S . C O M

CONTINUED FROM PAGE 44

Nevus of Ota (also known as “con-

genital melanosis bulbi,” “nevus fus-

coceruleus ophthalmomaxillaris,”

or “oculodermal melanocytosis”)

is a variant of Mongolian spot that

presents with bluish-green to grey-

brown pigmentation on the face.

Approximately half of the cases are

congenital, and the others typically

are acquired in the teenaged years.    

Nevus of Ota occurs most fre-

quently in Asians, with an estimated

prevalence of 0.014% to 0.034%, and

it is uncommon among Caucasians.1

It also develops frequently in East

Indians and African Americans,

and is 5 times more common in

females than males.2

Nevus of Ota is caused by the

entrapment of melanocytes in the

upper third of the dermis, involv-

ing the first and/or second (oph-

thalmic and maxillary) branches

of the trigeminal nerve. Although

unconfirmed, investigators suggest

that nevus of Ota may occur when

melanocytes arising from the neural

crest do not migrate to their normal

position in the basal cell layer of

the epidermis during early embryo-

logic development.3 Whereas biopsy

usually is not necessary to establish

the diagnosis, histology shows uni-

formly distributed melanocytes in

the dermis. Differential diagnoses

include blue nevi, café au lait spots,

melasma, and cutaneous melanoma.

Nevus of Ota is usually unilat-

eral (90%), generally involving only

1 side of the face over the cheek,

nose, forehead, temple, and around

the eye; however, it also can be

bilateral, although rarely.4 There

have been a few case reports of

oral mucosal involvement, which is

extremely rare.2 Given the involve-

ment of the trigeminal nerve, it can

cause discoloration of the eyelid,

sclera, cornea, and/or retina. The

sclera is involved in two-thirds of

patients, and scleral involvement is

associated with an increased risk

for glaucoma, which occurs in 10%

of patients.5 For this reason, all

patients with a nevus of Ota that

involves any structure of the eye or

eyelid should be referred to ophthal-

mology for routine screening.

Risk of melanomaThe lesion remains unchanged

throughout life but it may darken

with sun exposure. Because of its

location and high visibility, nevus

of Ota may be associated with

major psychosocial issues for both

children and adults. As a conse-

quence, all patients should be evalu-

ated for possible treatment with the

Q-switched lasers that offer a good

clinical response with little or no

risk of scarring.1

Essentially, nevus of Ota is similar

in pathophysiology and appearance

to the Mongolian spot, but differs

in location. It is a benign condi-

tion that may be managed by the

primary care physician. However,

monitoring should continue given

its rare potential to transform into a

malignant melanoma.

Dr Gangaram is a third-year pediatric

resident, Herman and Walter Samuelson

Children’s Hospital at Sinai, Baltimore,

Maryland. Dr Cohen, section editor for

Dermcase, is professor of pediatrics and

dermatology, Johns Hopkins University

School of Medicine, Baltimore, Maryland.

The author and section editor have nothing

to disclose in regard to affiliations with

or financial interests in any organizations

that may have an interest in any part of this

article. Vignettes are based on real cases

that have been modified to allow the author

and section editor to focus on key teaching

points. Images also may be edited or

substituted for teaching purposes.

R E F E R E N C E S

1. Chan HH, Kono T. Nevus of Ota: clinical aspects and management. Skinmed. 2003;2(2):89-96.

2. Shetty SR, Subhas BG, Rao KA, Castellino R. Nevus of ota with buccal mucosal pigmentation: a rare case. Dent Res J (Isfahan). 2011;8(1):52-55.

3. Hori Y, Takayama O. Circumscribed dermal melano-ses. Classification and histologic features. Dermatol

Clin. 1988;6(2):315-326.

4. Magarasevic L, Abazi Z. Unilateral open-angle glau-coma associated with the ipsilateral nevus of Ota.

Case Rep Ophthalmol Med. 2013; 2013: 924937.

5. Khawly JA, Imami N, Shields MB. Glaucoma associated with the nevus of Ota. Arch Ophthalmol. 1995;113(9):1208-1209.

NEVUS OF OTA

All patients with a nevus of Ota that involves any structure of the eye or eyelid should be referred to ophthalmology for

routine screening.

To read previous

Dermcase articles, go to

ContemporaryPediatrics.com/tag/

Contemporary-Pediatrics-Dermcase

BERNARD A COHEN, MD SECTION EDITORdermcase

CON T EMPORARYP ED I AT R I C S . C O M | J U LY 2 01 644

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Hyperpigmentation around a teen’s eyeAn adolescent girl is referred by her pediatrician to dermatology for evaluation

of a birthmark on her face. FOR MORE ON THIS CASE, TURN TO PAGE 43.

W FIGURE Congenital

hyperpigmented patch involving

the right side of the face and

bulbar conjunctiva.

THE CASE

NEVUS OF OTAdiagnosisDERMCASE

JESSICA A GANGARAM, MD

45j u ly 2 01 6 | CON T EMPORARYP ED I AT R I C S . c o m

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