nursing through the lifespan i exam 3(1)

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Nursing Through the Lifespan I Exam 3 1 The Human Eye: The 3 Layers of the Eye: 1.) Sclera & Cornea (outer layer) 2.) Uveal Tract (iris, choroid, ciliary body) (middle layer) 3.) Retina (inner layer) Structures & Functions of the Eye: Sclera o White of the eye o Helps protect the intraocular structures Cornea o Transparent & avascular o Allows light to enter the eye o Refracts (bends) incoming light rays to help focus them on the retina o Has no vascular system

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Study Guide, Nursing 201, Shelton State

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Nursing Through the Lifespan I Exam 3  

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The  Human  Eye:    

The  3  Layers  of  the  Eye:  1.)  Sclera  &  Cornea  (outer  layer)  2.)  Uveal  Tract  (iris,  choroid,  ciliary  body)  (middle  layer)  3.)  Retina  (inner  layer)      Structures  &  Functions  of  the  Eye:  

-­‐ Sclera  o White  of  the  eye  o Helps  protect  the  intraocular  structures  

-­‐ Cornea  o Transparent  &  avascular  o Allows  light  to  enter  the  eye  o Refracts  (bends)  incoming  light  rays  to  help  focus  them  on  the  retina  o Has  no  vascular  system  

     

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-­‐ Ciliary  Body  o Changes  the  shape  of  the  lens  and  secretes  aqueous  humor    o The  aqueous  humor  bathes  and  nourishes  the  lens  &  cornea  o Excess  production  or  decreased  outflow  of  aqueous  humor  can  elevate  intraocular  

pressure  above  the  normal  10-­‐21  mm  Hg.  -­‐ Lens  

o Bends  light  rays  to  fall  on  the  retina    -­‐ Choroid  

o Highly  vascular  structure  that  nourishes  the  ciliary  body,  the  iris,  &  the  outermost  portion  of  the  retina  

-­‐ Retina  o Forms  the  optic  nerve  o Cannot  regenerate  as  it  is  composed  primarily  of  neurons  o Converts  images  the  brain  can  understand  as  vision    o Photoreceptor  cells:  rods  and  cones    o Rods  stimulated  in  dim  light  o Cones  receptive  to  color  in  bright  light    o Fovea  centralis  provides  sharpest  vision    o Macula  surrounds  the  fovea  

-­‐  External  Structures:  (Eyebrows, Eyelids, Eyelashes)  o Serve  as  a  physical  barrier  primarily  for  protection  of  the  eyeball  or  globe    

-­‐ Conjunctiva:  o Secrete  mucus  and  tears  

 Assessment  of  Visual  System:  

-­‐ Subjective  Data  o Past  health  history  o Ocular  information  such  as  visual  tests,  family  history,  and  head  or  eye  trauma  o Nonocular  health  problems  such  as  systemic,  cardiac,  or  pulmonary  diseases    o Medications  including  OTC,  eye  drops,  herbal  therapies,  or  dietary  supplements o Surgery  or  other  procedures,  including  brain  surgery  or  laser  treatments o Patient’s  perception  of  the  problem    o Safety  o Allergies    o Hereditary  diseases  and  visual  problems    o Nutritional-­‐metabolic  pattern (Vitamins A, D, E & Beta-carotene) o Elimination pattern

-­‐ Objective  Data  o Physical  Examination  (May  be  as  brief  as  measuring  visual  acuity  or  in-­‐depth  and  

require  special  training.  Always  based  on  what  is  appropriate  and  necessary  for  the  specific  patient)  

o Snellen  Eye  Chart  (chart  with  the  big  E  at  top)  o Jaegar  Eye  Chart  (hand-­‐held  vision  screener  with  varying  print  sizes)  o Ishihara  Color  Test  (color  vision)  

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o Stereoscopic  Vision  (depth  perception)    Six  Cardinal  Positions  of  Gaze:  

   Visual  Problems:  

-­‐ Refractive  Errors:  o Myopia:  nearsightedness  (can’t  see  far  away)  o Hyperopia:  farsightedness  (can’t  see  close  up)  o Presbyopia:  farsightedness  due  to  aging  o Astigmatism:  irregular  corneal  curvature  o Aphakia:  no  lens  

-­‐ Conjunctivitis:  o Extraocular  disorder  o Infection  or  inflammation  o Bacterial  (pink  eye)  or  viral  (contaminated  swimming  pools)  o Can  be  caused  by  a  chlamydial  infection  (adult  inclusion  conjunctivitis)  o Allergic  conjunctivitis  (defining  symptom  is  itching)  

-­‐ Keratitis  o Corneal  inflammation  or  infection  o Bacterial  or  viral  o Keratoconjunctivitis  involves  the  conjunctiva  &  cornea  o Herpes  simplex  virus  (most  common  infectious  cause  of  corneal  blindness)  o Herpes  zoster  opthamicus  (caused  by  varicella-­‐zoster  virus  o Causes:  Ocular  trauma,  homemade  or  purchased  lens  care  solutions  or  cases,  

exophthalmos  or  masses  behind  eye  

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-­‐ Corneal  Ulcer  o Tissue  loss  caused  by  infection  of  the  cornea  o Aggressive  treatment  necessary  to  avoid  permanent  vision  loss  

-­‐ Dry  Eye  Disorders  o Keratoconjunctivitis  sicca  (dry  eyes)  

-­‐ Strabismus  o The  PT  cannot  consistently  focus  2  eyes  simultaneously  on  the  same  object  (crosseyed)  o Esotropia  (eye  deviates  in)  o Exotropia  (eye  deviates  out)  o Hypertropia  (eye  deviates  up)  o Hypotropia  (eye  deviates  down)  o Primary  complaint  is  double  vision  

-­‐ Retinopathy  o Slow  or  rapid  process  of  microvascular  damage  to  the  retina  o Common  complication  in  uncontrolled,  long-­‐standing  diabetes  (diabetic  retinopathy)  o Hypertension  can  create  vascular  blockages  in  retinal  blood  vessels  (hypertensive  

retinopathy)  o Retinopathy  is  irreversible    

-­‐ Retinal  Detachment  o Almost  all  patients  become  blind  in  effected  eye  if  untreated  o Symptoms:  light  flashes,  floaters,  or  rings  in  vision  are  painless  o Surgical  intervention  is  indicated  

-­‐ Age-­‐Related  Macular  Degeneration  o Is  most  common  cause  of  central  vision  loss  in  older  adults  o Nonexudative  is  slower  to  progress  &  more  common  (dry)  o Exudative  is  more  severe  &  rapid  (wet)  

-­‐ Cataract  o An  opacity  (cloudiness)  within  the  lens  o Leading  cause  of  blindness  o Most  common  surgical  procedure  for  those  aged  over  65  o Factors:  Age,  blunt  trauma,  congenital,  UV  light  exposure,  long-­‐term  corticosteroid  

use,  ocular  inflammation  o Senile  cataract  (most  common  type;  age  related)  o S/S:  decrease  in  vision,  abnormal  color  perception  (color  not  as  bright  or  sharp),  

glaring  of  vision  o No  nonsurgical  cure  o Surgical  therapy:  antianxiety  medication  before  local  anesthesia;  cataract  extracted  &  

sutured;  corticosteroid  &  ABT  ointment  applied  with  protective  shield  o Visual  acuity  improves  immediately  after  surgery  o There  should  be  no  pain  after  surgery  (notify  MD  immediately  if  PT  reports  pain)  

-­‐ Glaucoma  o A  group  of  disorders  characterized  by:  increased  IOP  &  consequences  of  elevated  

pressure,  optic  nerve  atrophy,  peripheral  visual  field  loss  o 2nd  leading  cause  of  blindness  

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o leading  cause  of  blindness  in  African  Americans  o Primary  open-­‐angle  glaucoma  (POAG):  most  common,  outflow  of  aqueous  humor  is  

decreased  in  trabecular  meshwork;  develops  slowly,  no  symptoms,  IOP  is  22-­‐32  mm  Hg  

o Primary  angle-­‐closure  glaucoma  (PACG):  angle  closure  decreases  the  flow  of  aqueous  humor,  caused  by  age  &  pupil  dilation,  possibly  drug  induced  

o Acute  angle-­‐closure  glaucoma:  sudden  onset,  excruciating  pain  in  or  around  eyes,  N/V,  seeing  colored  halos  around  lights,  blurred  vision,  ocular  redness,  IOP  is  >50  mm  Hg  

o Peripheral  vision  does  not  come  back  -­‐ Intraocular  Pressure  (IOP):  

o Elevated  in  glaucoma  o Normal  IOP  10-­‐21  mm  Hg  

-­‐ Legally  Blind:  20/200      The  Human  Ear:    

   

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External  Ear:  -­‐ Auricle  (pinna),  external  auditory  canal,  tympanic  membrane  (TM)    -­‐ Collect  &  transmit  sound  waves  to  the  tympanic  membrane  (eardrum)  

 Middle  Ear:  

-­‐ Eustachian  (auditory)  tube,  malleus,  incus,  stapes  (ossicles)  -­‐ Transmits  sound  waves  from  the  TM  to  the  liquid  medium  of  the  inner  ear  

 Inner  Ear:  

-­‐ Contains  the  functional  organs  for  hearing  &  balance  -­‐ Cochlea,  semicircular  canals,  vestibule  -­‐ Cochlea  is  the  main  organ  for  translating  

 Transmission  of  Sound:  

-­‐ Air  Conduction:  Conduction  and  amplification  of  sound  waves  from  the  environment  -­‐ Bone  Conduction:  the  bones  of  the  skull  transmit  sound  directly  to  the  inner  ear  (tuning  fork)  

 Subjective  Data:  

-­‐ Past  medical  history  (measles  &  mumps  can  affect  hearing)  -­‐ Medications  (ototoxic  meds:  PCN,  ASA,  Lasix)  -­‐ Surgery  or  other  treatments  -­‐ Auditory  &  vestibular  problems  may  be  hard  to  differentiate:  

o Vertigo:  a  sense  that  the  person  or  objects  around  the  person  are  moving  or  spinning  &  is  usually  stimulated  by  movement  of  the  head  

o Dizziness:  a  sensation  of  being  off  balance  that  occurs  when  standing  or  walking  o Nystagmus:  an  abnormal  eye  movement  that  may  e  observed  as  a  twitching  of  the  

eyeball  or  described  by  the  patient  as  a  blurring  of  vision  with  head  or  eye  movement    Objective  Data:  

-­‐ Physical  examination    o Ears  symmetric  in  location  &  shape  o Auricles  &  tragus  nontender,  without  lesions  o Canal  clear,  tympanic  membrane  intact,  landmarks  &  light  reflex  intact  o Able  to  hear  low  whisper  at  30  cm.  Weber  test  results,  no  lateralization.  Rinne  test  

results  AC>BC.    -­‐ Tuning  Fork  Test  

o Aid  in  differentiating  between  conductive  &  sensorineural  hearing  loss  o Weber  Test  The  examiner  places  an  activated  tuning  fork  on  the  midline  of  the  skull  or  

the  forehead.  Ask  the  patient  to  indicate  where  the  sound  is  heard  best.  In  normal  auditory  function,  the  patient  perceives  a  midline  tone  and  the  sound  is  heard  equally  in  both  ears.  If  a  patient  has  conductive  hearing  loss  in  one  ear,  the  sound  will  be  heard  louder  (lateralizes)  in  that  ear.  If  sensorineural  loss  is  present,  the  sound  is  louder  (lateralizes)  in  the  unaffected  ear.  Normal  results:  no  lateralization  

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o Rinne  Test  The  examiner  holds  the  base  of  a  tuning  fork  against  the  mastoid  bone  (BC—bone  conduction  of  sound)  and  notes  the  time.  When  the  sound  is  no  longer  perceived  behind  the  ear  (BC),  the  time  is  noted  once  again  and  the  still  vibrating  fork  is  moved  0.5  to  2  inches  in  front  of  the  ear  canal  (AC—air  conduction  of  sound).  Have  the  patient  report  when  the  sound  next  to  the  ear  canal  (AC)  is  no  longer  heard  and  note  the  time.  Normally,  the  sound  is  heard  twice  as  long  in  front  of  the  ear  as  it  is  on  the  bone.  The  Rinne  test  is  positive  when  the  patient  reports  that  air  conduction  (AC)  is  heard  longer  than  bone  conduction  (BC).  This  can  indicate  a  sensorineural  hearing  loss.  If  the  patient  hears  the  tuning  fork  better  by  bone  conduction,  the  Rinne  test  is  negative,  which  suggests  a  conductive  hearing  loss.    

-­‐ Whisper  Test:  o Stand  12-­‐24  in  to  the  side  of  the  patient  &  after  exhaling,  speak  in  a  low  whisper  o Test  each  ear  separately  o The  ear  not  being  tested  is  covered  by  the  patient  

-­‐ Audiometry  o The  audiometer  produces  pure  tones  at  varying  intensities  to  which  the  patient  can  

respond.  o Hertz  (Hz)  is  the  unit  of  measurement  used  to  classify  the  frequency  of  a  tone  o Decibels  (dB)  measures  the  intensity  or  strength  of  a  sound  wave  

 Auditory  Problems:  

-­‐ Presbycupsis:  o Hearing  loss  as  a  result  of  aging  o Factors:  noise  exposure,  systemic  diseases,  poor  nutrition,  ototoxic  drugs,  pollution  

exposure  over  the  lifespan  o Is  greater  for  high  pitched  sounds  

-­‐ Tinnitus:  o Ringing  in  the  ears  o Prevalence  expected  to  rise  as  life  span  increases  

-­‐ Trauma  o Blows  to  the  ear  can  cause  conductive  hearing  loss  o Head  trauma  that  injures  the  temporal  lobe  of  the  cerebral  cortex  can  impair  the  

ability  to  understand  the  meaning  of  sounds  -­‐ External  Otitis  

o Involves  inflammation  or  infection  of  the  epithelium  of  the  auricle  &  ear  canal  o Swimmer’s  Ear  o Ear  pain  (otalgia)  is  one  of  the  first  signs  of  external  otitis  o Muffled  hearing,  drainage  &  fever  (occurs  when  the  infection  spreads  to  surrounding  

tissues)  o Moist  heat,  mild  analgesics  &  topical  anesthetic  drops  usually  control  the  pain  

-­‐ Otitis  Media  o Infection  of  the  middle  ear  o S/S:  pain,  fever,  malaise  &  reduced  hearing  o Acute  Otitis  Media:  common  in  children  

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o Otitis  media  with  effusion:  is  an  inflammation  of  the  middle  ear  with  a  collection  of  fluid  in  the  middle  ear  space  

-­‐ Otosclerosis  o Is  a  hereditary  autosomal  dominant  disease  o Results  in  conductive  hearing  loss  o Examination  may  reveal  a  reddish  blush  of  the  tympanum  (Schwartz’s  Sign)  

-­‐ Ménière’s  Disease  o Is  characterized  by  symptoms  caused  by  inner  ear  disease,  including  episodic  vertigo,  

tinnitus,  fluctuating  sensorineural  hearing  loss,  &  aural  fullness.  o Symptoms  usually  begin  between  30-­‐60  years  of  age  o The  cause  is  unknown  o Attacks  may  last  hours  or  days  &  may  occur  several  times  a  year  

-­‐ Benign  Paroxysmal  Positional  Vertigo  o BPPV  is  a  common  cause  of  vertigo  o Free  floating  debris  in  the  semicircular  canal  causes  vertigo  with  specific  head  

movements  o Treatment:  Epley  maneuver  (ear  debris  is  moved  from  one  area  to  another)  

-­‐ Acoustic  Neuroma  o Is  a  unilateral  benign  tumor  that  occurs  where  the  vestibulocochlear  nerve  enters  the  

internal  auditory  canal.  o Symptoms  begin  between  40-­‐60  years  of  age  o Removal  of  small  tumors  preserve  hearing  o Removal  of  large  tumors  can  cause  permanent  hearing  loss  

-­‐ Conductive  Hearing  Loss  o Occurs  when  conditions  in  the  outer  or  middle  ear  impair  the  transmission  of  sound  

through  air  to  the  inner  ear  o Causes:  Otitis  media  with  effusion,  impacted  cerumen,  perforation  of  the  TM  

-­‐ Sensorineural  Hearing  Loss  o Is  caused  by  impairment  of  function  of  the  inner  ear  or  the  vestibulocochlear  nerve.  o Causes:  congenital,  hereditary,  noise  trauma  over  time,  aging,  Ménière’s  Disease,  

ototoxicity,  Paget’s  disease,  DM,  bacterial  meningitis  o The  main  problems  are  the  ability  to  hear  sound  but  not  to  understand  speech  

-­‐ Central  Hearing  Loss  o Involves  an  inability  to  interpret  sound,  including  speech,  because  of  a  problem  in  the  

brain  (CNS).  -­‐ Functional  hearing  Loss  

o May  be  caused  by  an  emotional  or  psychologic  factor  -­‐ Classification  of  Hearing  Loss  

o Normal  hearing:  0-­‐15  dB  o Profound  Deafness:  >90  (congenitally  deaf)  

       

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Endocrine  System:  Pituitary  Gland                                                    

Anterior  Pituitary:  Growth  Hormone:  -­‐ Target  tissue:  long  bones  &  soft  tissue  -­‐ Overproduction  of  GH  in  adulthood:  Acromegaly  -­‐ Overproduction  of  GH  in  childhood:  Gigantism  -­‐ Often  occurs  as  a  result  of  a  benign  pituitary  tumor  (adenoma)  -­‐ S/S:  enlargement  of  hands,  feet  &  face  -­‐ Diagnostic  Studies:  

o Oral  glucose  tolerance  test  -­‐ Surgical  therapy:  

o Hypophysectomy:  removal  of  pituitary  gland  o Treatment  of  choice  o Permanent  loss  of  all  pituitary  hormones  o Hormone  therapy  continues  throughout  life  

-­‐ Post-­‐op  Care:  o Elevate  head  of  bed  30°  o Perform  mouth  care  every  4  hrs  o Avoid  tooth  brushing  for  10  days  o Avoid  vigorous  coughing,  sneezing,  straining  at  stool  to  prevent  CSF  leakage  

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-­‐ Drug  therapy:  o Sandostatin  (reduces  GH  levels)  o Given  SQ  3  times  a  week  o GH  levels  are  measured  every  2  weeks  to  guide  dosing  

 

   

-­‐ Posterior  Pituitary:  Syndrome  of  Inappropriate  Antidiuretic  Hormone  (SIADH):  -­‐ Abnormlly  high  production  or  sustained  secretion  of  ADH  -­‐ Characterized  by  fluid  retention  -­‐ S/S  are  same  as  hyponatremia:  

o Muscle  cramping,  pain,  weakness  o Thirst  o Dyspnea  on  exertion  o Fatigue  o Low  urine  output  &  increased  body  weight  o Lethargy  o Confusion  o Seizures  

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-­‐ Diagnostic:  o Simultaneous  measurements  of  urine  &  serum  osmolarity  o Dilutional  hyponatremia:  serum  sodium  less  than  134  mEq/L  o Normal  sodium  levels:  135-­‐145  

-­‐ Treatment:  o Fluid  restriction  o Position  head  of  bed  flat  or  elevated  no  more  than  10°  to  enhance  venous  return  o IV  hypertonic  saline  solution  (3-­‐5%)  may  be  slowly  administered  (monitor  B/P)  o Loop  Diuretic  (Lasix)  o Declomycin:  blocks  the  effect  of  ADH  

 Posterior  Pituitary:  Diabetes  Insipidus:  

-­‐ Deficiency  of  production  or  secretion  of  ADH  -­‐ The  decrease  in  ADH  results  in  fluid  &  electrolyte  imbalances  -­‐ Causes  increased  urine  output  &  increased  plasma  osmolality  -­‐ Characterized  by  polydipsia  (excessive  thirst)  &  polyuria  (excessive  urination)  

o Urine  output  of  2-­‐20  liters/day  o Very  low  specific  gravity  <1.005  o Hypernatremia  caused  by  pure  water  loss  (irritability  &  mental  dullness)  o Fatigued  from  nocturia  (excessive  urination  during  the  night)  o Generalized  weakness  

-­‐ If  oral  fluid  intake  cannot  keep  up  with  urinary  losses,  severe  dehydration  results  o Poor  skin  turgor  o Hypotension  o Tachycardia  o Hypovolemic  shock  

-­‐ Diagnostic  Studies:  Water  Deprivation  Test  o Before  the  test,  body  weight,  urine  osmolarity,  volume  &  specific  gravity  are  measured  o Patient  is  deprived  of  water  for  8-­‐12  hours  o Patient  is  given  desmopressin  (increases  ADH)  SQ  or  nasally  o Patients  with  DI  exhibit  a  drastic  increase  in  urine  osmolarity  &  significant  decrease  in  

urine  volume  o Nurse  will  want  to  stop  test  immediately  if  dehydration  symptoms  occur    

-­‐ Treatment:  o Increase  fluids  o Hypotonic  IV  solutions  (D5W)  o Monitor  blood  sugar,  B/P,  heart  rate,  urine  output,  S/S  of  dehydration  o Monitor  intake  &  output  o Monitor  daily  weights  to  determine  fluid  volume  status  o Low-­‐Sodium  diet  (3g/day)  o Desmopressin  (DDAVP):  ADH  hormone  replacement  (SQ  or  nasal  spray)  

 Anterior  Pituitary:  Hyperthyroidism:  

-­‐ A  sustained  increase  in  synthesis  &  release  of  thyroid  hormones  by  thyroid  gland  

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-­‐ Most  common  form  is  Graves’  Disease  o Autoimmune  disease  of  unknown  etiology  o Characterized  by  thyroid  enlargement  &  excessive  thyroid  hormone  secretion  o Remissions  &  exacerbations  o Hyperthyroidism  &  thyrotoxicosis  occur  together  

                                             

-­‐ Thyrotoxicosis  (Thyrotoxic  Crisis  or  Thyroid  Storm)  o Physiologic  effect/clinical  syndrome  of  hypermetabolism  o Is  the  result  of  increased  circulating  levels  of  T3  &  T4  o All  the  symptoms  of  hyperthyroidism  are  prominent  &  severe  o Severe  tachycardia,  heart  failure,  shock,  hyperthermia  (up  to  105.3°F)  o Avoid  palpation  of  thyroid  (causes  more  T3  &  T4  to  be  released)  

-­‐ Diagnostic  Studies:  o Decreased  TSH  levels  &  elevated  free  T4    o Total  T3  &  T4  levels  may  be  assessed,  but  they  are  not  as  definitive  

-­‐ Drug  Therapy:  o Pylthiouracil  (PTU)  &  Mehimazole  (Tapazole)  o Inhibit  the  synthesis  of  thyroid  hormones  o Improvement  begins  1-­‐2  weeks  after  start  of  therapy  o Abrupt  discontinuation  can  result  in  a  return  of  hyperthyroidism  

-­‐ Radioactive  Iodine  Therapy:  (RAI)  o Treatment  in  nonpregnant  adults  o Damages  or  destroys  thyroid  tissue  

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o Has  a  delayed  response,  maximum  effect  may  not  be  seen  for  up  to  3  months  o Administered  on  an  outpatient  basis  o Pregnancy  test  is  done  before  initiation  of  therapy  o May  cause  dryness  &  irritation  of  the  mouth  &  throat  o Iodine  is  mixed  with  water  or  juice,  sipped  through  a  straw  &  administered  after  meals  

-­‐ Home  precautions  for  RAI:  o Flush  2-­‐3  times  after  toilet  use  o Separately  laundering  towels,  bed  linens,  &  clothes  daily  o Do  not  prepare  food  for  others  that  require  prolonged  handling  with  bare  hands  o Avoid  being  close  to  pregnant  women  or  children  for  7  days  after  therapy  

-­‐ Nutritional  Therapy:  o A  high  caloric  diet  (4,000-­‐5,000/day)  o Six  full  meals  a  day  &  snacks  high  in  protein  &  carbs  o Avoid  highly  seasoned  &  high-­‐fiber  foods  (stimulate  the  GI  tract)  o Avoid  caffeine  containing  liquids  (increase  restlessness  &  sleep  disturbances)  

-­‐ Thyroidectomy:  o Removal  of  the  thyroid  gland  o Patient  is  given  antithyroid  drugs,  iodine  &  beta  blockers  to  achieve  a  euthyroid  state  o Oxygen,  suction  equipment,  &  a  tracheostomy  tray  should  be  readily  available  in  the  

patient’s  room  o Pre-­‐op  Teaching:  

! Importance  of  performing  leg  exercises  ! How  to  support  the  head  while  turning  in  bed  ! Range  of  motion  exercises  of  the  neck  ! Talking  is  likely  to  be  difficult  a  short  time  after  the  surgery  ! Routine  post  op  care  such  as  IV  infusions  

o Post-­‐op  Complications:  ! Hypothyroidism  ! Damage  or  accidental  removal  of  parathyroid  glands  ! Hemorrhage  ! Injury  to  laryngeal  nerve  (vocal  cord  paralysis)  (both  cords=spastic  airway  

obstruction)  ! Laryngeal  Stridor  (harsh,  vibatory  sound  during  inspiration  &  expieration)  ! Thyrotoxic  crisis  ! Infection  

o Post-­‐op  Care:  ! Assess  Q2hrs  for  signs  of  hemorrhage  or  tracheal  compression  (irregular  

breathing,  neck  swelling,  frequent  swallowing,  sensations  of  fullness  at  the  incision  site,  choking,  blood  on  the  anterior  or  posterior  dressings)  

! Place  the  pt  in  semi-­‐Fowler’s  position  &  support  head  with  pillows.    ! Avoid  flexion  of  the  neck  &  any  tension  on  the  suture  line  ! Monitor  vital  signs  &  calcium  levels  ! Check  for  tetany  (Trousseau’s  &  Chvostek  Signs)  ! Control  post-­‐op  pain  by  giving  medications  

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! Patient  ambulates  within  hours  after  surgery  ! Eats  a  soft  diet  the  day  after  surgery  ! Permitted  to  take  fluid  as  soon  as  tolerated  

 Anterior  Pituitary:  Hypothyroidism:  

-­‐ A  deficiency  of  thyroid  hormone  that  causes  a  general  slowing  of  the  metabolic  rate  -­‐ Iodine  deficiency  is  the  most  common  cause    -­‐ Cretinism  (hypothyroid  in  infants)  

                                     

-­‐ Diagnostic  Studies:  o Serum  TSH  levels  help  determine  the  cause  of  hypothyroidism  o ↑TSH  the  defect  is  in  the  thyroid  o ↓TSH  the  defect  is  in  the  pituitary  or  hypothalamus  o ↑Cholesterol  &  triglycerides  o Anemia  o ↑Creatine  kinase  

-­‐ Complications:  o Myxedema  Coma  

! Medical  emergency  ! Unresponsiveness  or  lethargy  

o Treatment  of  myxedema  coma:  ! Vital  functions  must  be  supported  ! IV  thyroid  hormone  replacement  administered  

-­‐ Treatment:  

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o Hormone  replacement  therapy  o Levothyroxine  (synthroid)  

! The  drug  of  choice  ! Initial  doses  are  low  

o Carefully  monitor  patients  with  cardiovascular  disease  o Monitor  heart  rate  &  report  pulse  >100  beats/min  or  an  irregular  heartbeat  o Promptly  report  chest  pain,  weight  loss,  nervousness,  tremors  &/or  insomnia  

-­‐ Patient  Teaching:  o Discuss  the  importance  of  thyroid  hormone  therapy  o Caution  patient  not  to  switch  brands  of  the  hormone  o Emphasize  the  need  for  a  comfortable  warm  environment  o Teach  measures  to  prevent  skin  breakdown  o Caution  the  patient  to  avoid  sedatives  o Discuss  with  the  patient  measures  to  minimize  constipation  o Tell  patient  to  avoid  using  enemas  because  they  produce  vagal  stimulation  

 Anterior  Pituitary:  Hyperparathyroidism:  

-­‐ An  increased  secretion  of  parathyroid  hormone  (PTH)  -­‐ PTH  helps  regulate  serum  calcium  -­‐ ↑serum  calcium  levels  -­‐ Excessive  levels  of  PTH  usually  lead  to  hypercalcemia  &  hypophosphatemia  -­‐ Clinical  Manifestations:  

o Muscle  weakness  o Loss  of  appetite  o Constipation  o Fatigue  o Osteoporosis  o Fractures  o Kidney  stones  

-­‐ Complications:  o Renal  Failure  o Pancreatitis  o Cardiac  changes  o Long  bone,  rib  &  vertebral  fractures  

-­‐ Diagnostic  Studies:  o ↑PTH  levels  o ↑Serum  calcium  levels  >10mg/dL  

-­‐ Surgical  Therapy  o Criteria  for  surgery:  

! ↑Serum  calcium  levels  ! Hypercalciuria  ! Markedly  reduced  bone  mineral  density  ! Those  under  age  50  

o Autotransplantation:  

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! Normal  parathyroid  tissue  is  placed  in  the  forearm  -­‐ Nonsurgical  Therapy:  

o High  fluid  &  moderate  calcium  intake  o Several  drugs  help  lower  calcium  levels  but  do  not  treat  the  underlying  cause  

 Anterior  Pituitary:  Hypoparathyroidism:  

-­‐ Inadequate  circulating  PTH  -­‐ Characterized  by  hypocalcemia  -­‐ Clinical  Manifestations:  

o Painful  tonic  spasms  of  smooth  &  skeletal  muscles  can  cause  dysphagia  &  laryngospasms,  which  compromise  breathing  

o Lethargy    o Anxiety  o Personality  changes  o Tetany    

                           

-­‐ Treatment:  o Goal:   treat  acute  

complications,  maintain  normal  calcium  levels,  prevent  long-­‐term  complications  o Give  IV  calcium  chloride,  calcium  gluconate  slowly  o Use  ECG  monitoring  during  IV  therapy  o Rebreathing  may  partially  alleviate  acute  neuromuscular  symptoms  o Oral  calcium  supplements  are  usually  prescribed  o Vitamin  D  is  used  to  enhance  intestinal  calcium  absorption    o Tell  the  PT  to  avoid  foods  containing  oxalic  acid  (spinach,  rhubarb)  o ↑Calcium  meal  plan  (dark  green  vegetables,  soybeans,  tofu)  

 Anterior  Pituitary:  Cushing  Syndrome:  

-­‐ A  clinical  condition  that  results  from  chronic  exposure  to  excess  corticosteroids,  particularly  glucocorticoids  

-­‐ Manifestations:  

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o Related  to  excess  levels  of  corticosteroids                                              

-­‐ Diagnostic  Studies:  o Plasma  cortisol  levels  may  be  elevated  o A  24-­‐hr  urine  collection  for  free  cortisol  is  done  o Normal  urine  cortisol  levels  (80-­‐120mcg/24hr)  o If  results  are  borderline  a  low-­‐dose  dexamethasone  suppression  test  is  done  

-­‐ Treatment:  o Goal:  to  normalize  hormone  secretion  o Surgical  removal  is  the  standard  treatment  o Mitotane  (Lysodren)  suppresses  cortisol  production  when  surgery  is  contraindicated  

 Anterior  Pituitary:  Adrenocortical  Insufficiency:  

-­‐ Hypofunction  of  the  adrenal  cortex  (Addison’s  Disease)  -­‐ Lack  of  pituitary  ACTH  secretion  -­‐ Clinical  Manifestations:  

o Do  not  become  evident  until  90%  of  the  adrenal  cortex  is  destroyed  o Manifestations  have  a  slow  onset  

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 -­‐ Complications:  Addisonian  Crisis  (acute  adrenal  insufficiency)  

o Life-­‐threatening  emergency  o Insufficient  adrenocortical  hormones  o Triggered  by:    

! Stress  ! Sudden  withdrawal  of  corticosteroid  hormone  therapy  ! Adrenal  surgery  ! Sudden  pituitary  gland  destruction  

o Symptoms:  ! Postural  hypotension  ! Tachycardia  ! Dehydration  ! Hyponatremia  ! Hyperkalemia  ! Hypoglycemia  ! Fever  ! Weakness  ! Confusion  ! Severe  vomiting    ! Diarrhea  ! Abdominal  Pain  

-­‐ Diagnostic  Studies:  o Depressed  serum  &  urinary  cortisol  levels  

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-­‐ Treatment:  o Hormone  therapy  o Hydrocortisone  (mineralcorticoid  &  glucocorticoid  properties)  o Fludrocortisone  (Florinef)  mineralcorticoid  o Increase  salt  intake  in  diet  

-­‐ Patient  Teaching:  o The  PT  should  carry  an  emergency  kit  at  all  times  

! 100mg  IM  hydrocortisone  ! Syringes  ! Instructions  for  use  

 Pheochromocytoma:  

-­‐ Tumor  in  the  adrenal  medulla  -­‐ Excess  production  of  catecholamines  (epinephrine  &  norepinephrine)  -­‐ Manifestations:  

o Severe  hypetension  o Severe  pounding  headache  o Tachycardia  with  palpitations  o Profuse  sweating  o Unexplained  abdominal  or  chest  pain  o Attacks  may  last  from  a  few  minutes  to  several  hours  

-­‐ Diagnostic  Studies:  o Measurement  of  urinary  fractionated  metanephrines  (catecholamine  metabolites)  o Usually  done  as  a  24-­‐hr  urine  collection  

-­‐ Treatment:  o Surgical  removal  of  tumor  o Beta  blockers  are  required  pre-­‐op  to  control  B/P  &  to  prevent  an  intraoperative  

hypertensive  crisis