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    Management of Hyperglycemiain Hospitalized Patientsin Non-Critical Care Setting:

    An Endocrine Society Clinical Practice Guideline

    T h e E n d o c r i n e S o c i e t y s

    CC Gs

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    Authors: Guillermo . mpierrez, Richard Hellman, Mary T. Korytkowki, Mikhail Koiborod, Gregory .

    Maynard,VictorM.Montori,JaneJ.seley,andGreetVandenBerghe

    Afliations:moryniverityschoolofMedicine(G...),tlanta,Georgia30322;HeartofmericaiabeteReearch Foundation and niverity of Miouri-Kana Cityschool of Medicine (R.H.), orth Kana City,

    Miouri64112;niverity ofPittburgh school ofMedicine(M.T.K.),Pittburgh,Pennylvania15213;saint

    ukeMid-mericaHeartntituteandniverityofMiouri-KanaCity(M.K.),KanaCity,Miouri64111;

    niverityofCaliforniasaniegoMedicalCenter(G..M.),saniego,California92037;MayoClinicRocheter

    (V.M.M.),Rocheter,Minneota55905;ewYork-PrebyterianHopital/WeillCornellMedicalCenter(J.J.s.),

    ewYork,ewYork10065;andCatholicniverityofeuven(G.V.d.B.),3000euven,Belgium

    Co-Sponsoring Associations: merican iabete ociation, merican Heart ociation, merican

    ociationofiabeteducator,uropeansocietyofndocrinology,societyofHopitalMedicine.

    Disclaimer: ClinicalPracticeGuidelinearedevelopedto beofaitanceto endocrinologitandotherhealth

    careprofeionalbyprovidingguidanceandrecommendationforparticularareaofpractice.TheGuideline

    houldnotbe conideredincluiveofallproperapproacheormethod,orexcluiveof other.TheGuideline

    cannotguaranteeanypecicoutcome,nordotheyetablihatandardofcare.TheGuidelinearenotintended

    to dictate thetreatmentof a particular patient.Treatment deciionmut be madebaed on theindependent

    judgmentofhealthcareproviderandeachpatientindividualcircumtance.

    The ndocrine society make no warranty, expre or implied, regarding the Guideline and pecically

    excludeanywarrantieofmerchantabilityandtneforaparticularueorpurpoe.Thesocietyhallnotbeliable

    for direct, indirect, pecial, incidental, or conequential damage related to the ue of the information

    containedherein.

    FirtpublihedinJournal of Clinical Endocrinology & Metabolism, January 2012, 97 (1):1638.

    Thendocrinesociety,2012

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    Management of Hyperglycemiain Hospitalized Patientsin Non-Critical Care Setting:

    An Endocrine Society Clinical Practice Guideline

    T h e E n d o c r i n e S o c i e t y s

    CC Gs

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    Table of Contents

    btract. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3

    summaryofRecommendation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4

    Methodofevelopmentofvidence-BaedClinicalPracticeGuideline. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7

    iagnoiandRecognitionofHyperglycemiaandiabeteintheHopitalsetting. . . . . . . . . . . . . . . . . . . . . . . .8

    MonitoringGlycemiaintheon-CriticalCaresetting. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10

    GlycemicTargetintheon-CriticalCaresetting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11

    ManagementofHyperglycemiaintheon-CriticalCaresetting. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .11

    specialsituation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .17

    RecognitionandManagementofHypoglycemiaintheHopitalsetting. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .22

    mplementationofaGlycemicControlProgramintheHopital. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .24

    PatientandProfeionalducation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25

    Reference. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .27

    OrderForm. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .35

    Reprintnformation,Quetion&Correpondence . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . nideBackCover

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    3

    M

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    caresetting

    Abstract

    Objective: The aim wa to formulate practiceguideline on the management of hyperglycemia in

    hopitalizedpatientinthenon-criticalcareetting.

    Participants:TheTakForcewacompoedofachair,elected by the Clinical Guideline subcommittee

    ofThendocrinesociety,ixadditionalexpert,and

    amethodologit.

    Evidence: Thievidence-baedguidelinewa devel-opeduingtheGradingofRecommendation,e-

    ment, evelopment, and valuation (GR)

    ytemtodecribeboththetrengthofrecommenda-

    tionandthequalityofevidence.

    Consensus Process: One group meeting, everalconferencecall,ande-mailcommunicationenabled

    conenu. ndocrine society member, mericaniabete ociation, merican Heart ociation,

    merican ociation of iabete ducator, uro-

    pean society of ndocrinology, and the society of

    Hopital Medicine reviewed and commented on

    preliminarydraftofthiguideline.

    Conclusions: Hyperglycemiaiacommon,eriou,and cotly health care problem in hopitalized

    patient. Obervational and randomized controlled

    tudie indicate that improvement in glycemic

    control reult in lower rate of hopital complica-

    tioningeneralmedicineandurgerypatient.mple-

    mentingatandardizedcinulinorderetpromoting

    the ue of cheduled baal and nutritional inulin

    therapyiakeyinterventionintheinpatientmanage-

    mentofdiabete.Weproviderecommendationfor

    practical, achievable,and afe glycemic targetand

    decribeprotocol,procedure,andytemimprove-

    ment required to facilitate the achievement of

    glycemic goal in patient with hyperglycemia and

    diabeteadmittedinnon-criticalcareetting.

    J Clin Endocrinol Metab, January 2012, 97

    (1):1638.

    Abbreviations: BG, Blood glucose; CII, continuous insulin infusion; EN, enteral nutrition; HbA1C, hemoglobin A1C; ICU, intensive care unit; MNT,medical nutrition therapy; NPH, neutral protamine Hagedorn; NPO, nil per os (nothing by mouth); PN, parenteral nutrition; POC, point of care; SSI,sliding scale insulin; TZD, thiazolidinedione.

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    SMMA O

    ECOMMENATONS

    1.0. iagnosis and recognition of hyperglycemiaand diabetes in the hospital setting

    1.1. Werecommendthatclinicianaeallpatient

    admitted to the hopital for a hitory of diabete.

    Whenpreent,thidiagnoihouldbeclearlyidenti-

    edinthemedicalrecord.(1| )

    1.2. Weuggetthatallpatient,independentofa

    prior diagnoi of diabete, have laboratory blood

    glucoe(BG)tetingonadmiion.(2| )

    1.3. Werecommendthatpatientwithoutahitoryof diabete with BG greater than 7.8 mmol/liter

    (140mg/dl)bemonitoredwithbedidepointofcare

    (POC)tetingforatleat24to48h.ThoewithBG

    greater than 7.8 mmol/liter require ongoing POC

    teting with appropriate therapeutic intervention.

    (1| )

    1.4. We recommend that in previouly normogly-

    cemic patient receiving therapie aociated with

    hyperglycemia,uchacorticoteroidoroctreotide,

    enteralnutrition()andparenteralnutrition(P)bemonitored withbedide POCtetingforat leat

    24to48hafterinitiationoftheetherapie.Thoe

    with BG meaure greater than 7.8 mmol/liter

    (140mg/dl)requireongoingPOCtetingwithappro-

    priatetherapeuticintervention.(1| )

    1.5. Werecommendthatallinpatientwithknown

    diabete or with hyperglycemia (> 7.8 mmol/liter)

    beaeedwithahemoglobin1C(Hb1C)level

    if thi ha not been performed in the preceding

    23month.(1| )

    2.0. Monitoring glycemia in the non-criticalcare setting

    2.1. We recommend bedide capillary POC

    tetingathepreferredmethodforguidingongoing

    glycemic management of individual patient.

    (1| )

    2.2. We recommend the ue of BG monitoring

    device that have demontrated accuracy of ue in

    acutelyillpatient.(1| )

    2.3. Werecommendthattimingofglucoemeaure

    match the patient nutritional intakeand medica-

    tionregimen.(1| )

    2.4. We ugget the following chedule for POC

    teting:beforemealandatbedtimeinpatientwho

    areeating,orevery46hinpatientwhoarePO

    [receivingnothingbymouth(nilpero)]orreceiving

    continuouenteralfeeding.(2| )

    3.0. Glycemic targets in the non-criticalcare setting

    3.1. We recommend a premeal glucoe target oflethan140mg/dl(7.8mmol/liter)andarandom

    BGoflethan180mg/dl(10.0mmol/liter)forthe

    majority of hopitalized patient with non-critical

    illne.(1| )

    3.2. We ugget that glycemic target be modied

    accordingtoclinicaltatu.Forpatientwhoareable

    to achieve and maintain glycemic control without

    hypoglycemia, a lower target range may be reaon-

    able. For patient with terminal illne and/orwith

    limited life expectancyor at high rik for hypogly-

    cemia,ahighertargetrange(BG

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    4.1.2. Weuggetthatprovidingmealwithaconi-

    tent amount of carbohydrate at each meal can be

    uefulincoordinatingdoeofrapid-actinginulinto

    carbohydrateingetion.(2| )

    4.2. Transition from home to hospital

    4.2.1. We recommend inulin therapy a the

    preferredmethodforachievingglycemiccontrolin

    hopitalizedpatientwithhyperglycemia.(1| )

    4.2.2. Weuggetthedicontinuationoforalhypo-

    glycemic agent and initiation of inulin therapy

    forthemajorityofpatientwithtype2diabeteat

    thetime ofhopital admiion for an acute illne.

    (2| )

    4.2.3. Weuggetthatpatienttreatedwithinulinbefore admiion have their inulin doe modied

    accordingtoclinicaltatuaawayofreducingthe

    rikforhypoglycemiaandhyperglycemia.(2| )

    4.3. Pharmacological therapy

    4.3.1. Werecommendthatallpatientwithdiabete

    treatedwithinulinathomebetreatedwithached-

    uledcinulinregimeninthehopital.(1| )

    4.3.2. Weuggetthatprolongedueoflidingcaleinulin(ss)therapybeavoidedatheolemethod

    forglycemiccontrolinhyperglycemicpatientwith

    hitoryofdiabeteduringhopitalization.(2| )

    4.3.3. We recommend that cheduled c inulin

    therapyconitofbaalorintermediate-actinginulin

    givenonceortwiceadayincombinationwithrapid-

    orhort-actinginulinadminiteredbeforemealin

    patientwhoareeating.(1| )

    4.3.4. Weuggetthatcorrectioninulinbeincludeda a component of a cheduled inulin regimen

    fortreatmentofBGvalueabovethedeiredtarget.

    (2| )

    4.4. Transition from hospital to home

    4.4.1. We ugget reintitution of preadmiion

    inulin regimen or oral and non-inulin injectable

    antidiabetic drug at dicharge for patient with

    acceptable preadmiion glycemic control and

    without a contraindication to their continued ue.

    (2| )

    4.4.2. Weuggetthatinitiationofinulinadmini-

    trationbeintitutedatleatonedaybeforedicharge

    toallowaementoftheefcacyandafetyofthitranition.(2| )

    4.4.3. Werecommendthatpatientandtheirfamily

    orcaregiverreceive both written andoralintruc-

    tionregardingtheirglycemicmanagementregimen

    atthetimeofhopitaldicharge.Theeintruction

    needtobeclearlywritteninamannerthatiunder-

    tandable to the peron who will adminiter thee

    medication.(1| )

    5.0. Special situations

    5.1. Transition from iv continuous insulininfusion (C) to sc insulin therapy

    5.1.1. Werecommendthatallpatientwithtype1

    andtype2 diabete betranitionedto cheduledc

    inulintherapyatleat12hbeforedicontinuation

    ofC.(1| )

    5.1.2. We recommend that c inulin be admini-

    tered before dicontinuation of C for patientwithoutahitoryofdiabetewhohavehyperglycemia

    requiringmorethan2/h.(1| )

    5.1.3. We recommend POC teting with daily

    adjutmentoftheinulinregimenafterdicontinua-

    tionofC.(1| )

    5.2. Patients receiving EN or PN

    5.2.1. WerecommendthatPOCtetingbeinitiated

    for patient with or without a hitory of diabetereceivingandP.(1| )

    5.2.2. WeuggetthatPOCtetingcanbedicon-

    tinuedinpatientwithoutapriorhitoryofdiabete

    ifBGvaluearelethan7.8mmol/liter(140mg/dl)

    without inulin therapy for 2448 h after achieve-

    mentofdeiredcaloricintake.(2| )

    5.2.3. Weuggetthatcheduledinulintherapybe

    initiatedinpatientwithandwithoutknowndiabete

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    6.0. ecognition and management ofhypoglycemia in the hospital setting

    6.1. We recommend that glucoe management

    protocol with pecic direction for hypoglycemia

    avoidanceandhypoglycemiamanagementbeimple-

    mentedinthehopital.(1| )

    6.2. Werecommendimplementationofatandarized

    hopital-wide, nure-initiated hypoglycemia treat-

    ment protocol to prompt immediate therapy of

    anyrecognizedhypoglycemia,denedaaBGbelow

    3.9mmol/liter(70mg/dl).(1| )

    6.3. Werecommendimplementationofaytemfor

    trackingfrequencyofhypoglycemiceventwithroot

    caueanalyiofeventaociatedwithpotentialfor

    patientharm.(1| )

    7.0. mplementation of a glycemic controlprogram in the hospital

    7.1. Werecommendthathopitalprovideadmini-

    trative upport for an interdiciplinary teering

    committeetargetingaytemapproachtoimprove

    careofinpatientwithhyperglycemiaanddiabete.

    (1| )

    7.2. Werecommendthateachintitutionetablihauniform method of collecting andevaluating POC

    tetingdataandinulinueinformationaawayof

    monitoring the afety and efcacy of the glycemic

    controlprogram.(1| )

    7.3. We recommend that intitution provide

    accurate device for glucoe meaurement at the

    bedidewithongoingtaffcompetencyaement.

    (1| )

    8.0. Patient and professional education

    8.1. We recommend diabete elf-management

    education targeting hort-term goal that focu on

    urvival kill: baic meal planning, medication

    adminitration, BG monitoring, and hypoglycemia

    andhyperglycemiadetection,treatment,andpreven-

    tion.(1| )

    8.2. We recommend identifying reource in the

    community to which patient can be referred for

    whohavehyperglycemia,denedaBGgreaterthan

    7.8mmol/liter(140mg/dl),andwhodemontratea

    peritentrequirement(i.e.>12to24h)forcorrec-

    tioninulin.(2| )

    5.3. Perioperative BG control

    5.3.1. Werecommendthatallpatientwithtype1

    diabete who undergo minor or major urgical

    procedurereceiveeitherCorcbaalinulinwith

    bolu inulin a required to prevent hyperglycemia

    duringtheperioperativeperiod.(1| )

    5.3.2. Werecommenddicontinuationoforaland

    noninulin injectable antidiabetic agent before

    urgery with initiation of inulin therapy in thoe

    whodevelophyperglycemiaduringtheperioperativeperiodforpatientwithdiabete.(1| )

    5.3.3. When intituting c inulin therapy in the

    poturgical etting, we recommend that baal (for

    patientwhoarePO)orbaalbolu(forpatient

    whoareeating)inulintherapybeintitutedathe

    preferredapproach.(1| )

    5.4. Glucocorticoid-induced diabetes

    5.4.1. WerecommendthatbedidePOCtetingbeinitiated for patient with or without a hitory of

    diabetereceivingglucocorticoidtherapy.(1| )

    5.4.2. WeuggetthatPOCtetingcanbedicon-

    tinued innondiabetic patient ifall BG reult are

    below 7.8 mmol/liter (140 mg/dl) without inulin

    therapyforaperiodofatleat2448h.(2| )

    5.4.3. Werecommendthatinulintherapybeiniti-

    atedforpatientwithperitenthyperglycemiawhile

    receivingglucocorticoidtherapy.(1| )

    5.4.4. WeuggetCaanalternativetocinulin

    therapyforpatientwithevereandperitenteleva-

    tioninBGdepiteueofcheduledbaalboluc

    inulin.(2| )

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    panelitconideredinmakingtherecommendation;

    in ome intance, there are remark, a ection in

    whichpanelitoffertechnicaluggetionforteting

    condition,doing,andmonitoring.Theetechnical

    commentreectthebetavailableevidenceapplied

    toatypicalperonbeingtreated.Oftenthievidence

    come from the unytematic obervation of the

    panelitandtheirvalueandpreference;therefore,

    theeremarkhouldbeconidereduggetion.

    The prevalence of diabete ha reached epidemic

    proportion in the nited state. The Center for

    ieae Control and Prevention recently reported

    that25.8millionpeople,or8.3%ofthepopulation,

    have diabete (3). iabete repreent the eventh

    leadingcaueofdeath(4)andithefourthleading

    comorbidconditionamonghopitaldichargeinthenitedstate(5).pproximatelyoneinfourpatient

    admitted to the hopital ha a known diagnoi of

    diabete (6, 7), and about 30% of patient with

    diabeterequiretwoormorehopitalizationinany

    givenyear(7).Theprevalenceofdiabeteihigher

    in elderly patient and reident of long-term-care

    facilitie,inwhomdiabeteireportedinuptoone

    thirdofadultaged6575yrandin40%ofthoe

    olderthan80yr(8,9).

    The aociation between hyperglycemia in hopi-

    talized patient (with or without diabete) and

    increaed rik for complication and mortality i

    well etablihed (6, 1014). Thi aociation i

    oberved for both admiion glucoe andmean BG

    level during the hopital tay. lthough mot

    randomizedcontrolledtrialinvetigatingtheimpact

    of treating hyperglycemia on clinical outcome

    havebeenperformedincriticallyillpatient,there

    are extenive obervational data upporting the

    importance of hyperglycemia management amongnon-critically ill patient admitted to general

    medicine and urgery ervice. n uch patient,

    hyperglycemiaiaociatedwithprolongedhopital

    tay, increaed incidence of infection, and more

    diability after hopital dicharge and death

    (6,1519).Thimanucriptcontaintheconenu

    recommendation for the management of hyper-

    glycemia in hopitalized patient in non-critical

    care etting by The ndocrine society and other

    continuingdiabeteelf-managementeducationafter

    dicharge.(1| )

    8.3. We recommend ongoing taff education to

    updatediabeteknowledge, awella targeted taff

    education whenever an advere event related to

    diabetemanagementoccur.(1| )

    METHO O EEOPMENT

    O EENCE-BASE CNCA

    PACTCE GENES

    The Clinical Guideline subcommittee of The

    ndocrinesocietydeemedthemanagementofhyper-

    glycemia in hopitalized patient in a non-critical

    care etting a priority area in need of practice

    guidelineandappointedaTakForcetoformulate

    evidence-baed recommendation. The Tak Force

    followedtheapproachrecommendedbytheGrading

    of Recommendation, ement, evelopment,

    and valuation (GR) group, an international

    groupwithexpertieindevelopmentandimplemen-

    tation of evidence-baed guideline(1). detailed

    decriptionofthegradingchemehabeenpublihedelewhere(2).TheTakForceuedthebetavailable

    reearchevidencetodevelopomeoftherecommen-

    dation.TheTakForcealouedconitentlanguage

    and graphical decription of both the trength of

    a recommendation and the quality of evidence. n

    termofthetrengthoftherecommendation,trong

    recommendation ue the phrae we recommend

    and the number 1, and weak recommendation

    uethephraeweuggetandthenumber2. Cross-

    filled circles indicatethequalityoftheevidence,uch

    that denote very low quality evidence;

    , lowquality; ,moderatequality;and

    ,highquality.TheTakForcehacondence

    thatperonwhoreceivecareaccordingtothetrong

    recommendationwillderive,onaverage,moregood

    than harm. Weak recommendation require more

    careful coniderationof the peron circumtance,

    value,andpreferencetodeterminethebetcoure

    of action. inked to each recommendation i a

    decription of the evidence and the value that

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    therapie. Thoe with BG meaure greater than

    7.8 mmol/liter (140 mg/dl) require ongoing POC

    teting with appropriate therapeutic intervention.

    (1| )

    1.1.1.4. Evidence

    n-hopital hyperglycemia i deneda anyglucoe

    value greaterthan 7.8 mmol/liter(140 mg/dl)(20,

    21).Hyperglycemiaoccurnotonlyinpatientwith

    known diabete but alo in thoe with previouly

    undiagnoeddiabeteandotherwithtrehyper-

    glycemiathatmayoccurduringanacuteillneand

    thatreolvebythetimeofdicharge(20,22,23).

    Obervational tudie report that hyperglycemia i

    preent in 32 to 38% of patient in community

    hopital(6, 24), 41% ofcritically ill patient withacute coronary yndrome (13), 44% of patient

    with heart failure (13), and 80% of patient after

    cardiac urgery (25, 26). n thee report, approxi-

    mately onethirdof non-intenive care unit (C)

    patient and approximately 80% of C patient

    hadnohitoryofdiabetebeforeadmiion(6,13,

    2730).

    The Clinical Practice Recommendation

    endoretheinitiationofglucoemonitoringforboth

    thoe with diabete and thoe without a knownhitory of diabete who are receiving therapie

    aociatedwithhyperglycemia(31).Weagreewith

    theerecommendationbutalouggetthatinitial

    glucoe meaurement on admiion by the hopital

    laboratoryiappropriateforallhopitalizedpatient,

    irrepective of the preence of preexiting diabete

    hitory or expoure to obviou hyperglycemia

    inducer. The high prevalence of inpatient hyper-

    glycemia with aociated poor outcome and the

    opportunity todiagnoe newdiabete warrant thi

    approach(6,24,32,33).Becauethedurationofcare

    i frequently brief in the inpatient etting, the

    aementofglycemiccontrolneedtobeperformed

    earlyinthehopitalcoure.BedidePOCtetingha

    advantage over laboratory venou glucoe teting.

    POC teting at the point of care allow identi-

    cationof patient who require initiation ormodi-

    cationofaglycemicmanagementregimen(20,21).

    POC monitoring ha been demontrated to be

    eential in guiding inulin adminitration toward

    organization of health care profeional involved

    in inpatientdiabete care, includingthe merican

    iabete ociation (), merican Heart

    ociation, merican ociation of iabete

    ducator (), uropean society of ndocri-

    nology, and thesociety ofHopitalMedicine.The

    central goal wa to provide practical, achievable,

    and afe glycemic goal and to decribe protocol,

    procedure, and ytem improvement needed to

    facilitate their implementation. Thi document i

    addreed to health care profeional, upporting

    taff,hopitaladminitrator,andothertakeholder

    focuedonimprovedmanagementofhyperglycemia

    ininpatientetting.

    1.0. AGNOSS AN

    ECOGNTON O HPE-

    GCEMA AN ABETES N

    THE HOSPTA SETTNG

    Recommendations

    1.1. Werecommendthatclinicianaeallpatientadmitted to the hopital for a hitory of diabete.

    Whenpreent,thidiagnoihouldbeclearlyidenti-

    edinthemedicalrecord.(1| )

    1.2. Weuggetthatallpatient,independentofa

    priordiagnoiofdiabete,havelaboratoryBGteting

    onadmiion.(2| )

    1.3. We recommend that patient without a

    hitoryofdiabetewithBGgreaterthan7.8mmol/

    liter (140 mg/dl) be monitored with bedide POCteting for at leat 24 to 48 h. Thoe with BG

    greater than 7.8 mmol/liter require ongoing POC

    teting with appropriate therapeutic intervention.

    (1| )

    1.4. We recommend that in previouly normo-

    glycemicpatientreceivingtherapieaociatedwith

    hyperglycemia,uchacorticoteroidoroctreotide,

    andPbemonitoredwithbedidePOCteting

    for at leat 24 to 48 h after initiation of thee

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    diabete. Our recommendation reect conenu

    opinionandthepracticalutilityofthitrategy.

    Clinician mut keep in mind that an Hb1C

    cutoffof6.5%identiefewercaeofundiagnoed

    diabetethandoeahighfatingglucoe(38).several

    epidemiological tudie have reported a low eni-

    tivity(44to66%)butahighpecicity(76to99%)

    for Hb1C greater than 6.5% in an outpatient

    population (39, 40). mong hopitalized hypergly-

    cemic patient, an Hb1C level above 6.0% wa

    reported to be 100% pecic and 57% enitive

    for the diagnoi of diabete, where a an Hb1C

    below 5.2% effectively excluded a diagnoi of

    diabete(41).

    Glucoe and Hb1C value, together with themedical hitory, can be ued to tailor therapy and

    ait in dicharge planning (42, 43). icharge

    planning, education, and care tranition are

    dicued in more detail in Section 4.4. Briey, the

    dicharge plan optimally include the diagnoi of

    diabete(ifpreent),recommendationforhort-and

    long-term glucoe control, follow-up care, a lit of

    educationalneed,andconiderationofappropriate

    creening and treatment of diabete comorbiditie

    (30,42,44).

    There are limitationto the ue of anHb1C for

    diagnoi of diabete in an inpatient population.

    Thee include the relatively low diagnotic eni-

    tivityandpotentialalteredvalueinthepreenceof

    hemoglobinopathie(hemoglobinCorsCdieae),

    high-doe alicylate, hemodialyi, blood tranfu-

    ion, and iron deciency anemia (45). When

    Hb1Ciuedforetablihingadiagnoiofdiabete,

    analyihouldbeperformeduingamethodcertied

    by the ational Glycohemoglobin standardization

    Program (31), becauePOC Hb1C tetingi not

    ufcientlyaccurateatthitimetobediagnotic.

    achievingandmaintainingdeiredglycemicgoala

    wellaforrecognizinghypoglycemicevent(16,21,

    34,35).Motcurrentlyuedbedideglucoemeter,

    althoughdeignedforcapillarywholebloodteting,

    arecalibratedtoreportreultcompatibletoplama,

    whichallowforreliablecompariontothelaboratory

    glucoetet(16,22,36,37).

    1.1.1.4. Values and preferences

    Ourrecommendationreectconiderationoftheface

    validityofolicitingandcommunicatingthediagnoi

    ofdiabeteorhyperglycemiatomemberofthecare

    team.Therik-to-benetofglucoetetinganddocu-

    menting a hitory of diabete favor thi approach

    depitethelackofrandomizedcontrolledtrial.

    Recommendation

    1.5. Werecommendthatallinpatientwithknown

    diabeteorwithhyperglycemia(>7.8mmol/liter)be

    aeedwithanHb1Clevelifthihanotbeen

    performedinthepreceding23month.(1| )

    1.5. Evidence

    We upport the recommendation of uing a

    laboratorymeaureofHb1Cbothforthediagnoi

    ofdiabete andfor theidentication ofpatient at

    rik for diabete (31). The recommendation

    indicate that patient with an Hb1C of 6.5% or

    higher can be identied a having diabete, and

    patientwithanHb1Cbetween5.7and6.4%can

    beconideredabeingatrikforthedevelopmentof

    diabete(31).

    MeaurementofanHb1Cduringperiodofhopi-

    talization provide the opportunity to identify

    patientwithknowndiabetewhowouldbenetfrom

    intenication of their glycemic management

    regimen.npatientwithnewlyrecognizedhypergly-

    cemia, an Hb1C may help differentiate patient

    with previouly undiagnoed diabete from thoe

    with tre-induced hyperglycemia (32, 38). t i

    importanttonotethattherearenorandomizedtrial

    demontrating improved outcome uing Hb1C

    leveltoaitinthediagnoiofdiabeteininpatient

    withnewhyperglycemiaortoaitintailoringthe

    glycemic management of inpatient with known

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    Conitent ampling ite and method of

    meaurementhouldbeuedbecaueglucoereult

    can vary ignicantly when alternating between

    nger-tickandalternativeite,orbetweenample

    runinthelaboratoryvs.aPOCtetingdevice(53).

    intheoutpatientetting,erroneoureultcanbe

    obtainedfromnger-tickamplewhenevertheBG

    irapidlyriingorfalling(53).

    QualitycontrolprogramareeentialtomeetFood

    andrugdminitration(F)requirementandto

    maintaintheafety,accuracy,andreliabilityofBG

    teting(21).TheFrequirethattheaccuracyof

    glucoeanalyzerinthecentrallabbewithin10%of

    the real value,whereaPOC meterare conidered

    acceptable within 20% (21, 37); however, recent

    reporthaveadvocatedimprovementortighteningofPOC meter accuracy tandard (37). ing meter

    withbarcodingcapabilityhabeenhowntoreduce

    data entry error inmedicalrecord (37).Capillary

    BGvaluecanvarybetweenPOCmeter,epecially

    athighorlowhemoglobinlevel,lowtiueperfuion,

    and with ome extraneou ubtance (36, 53).

    lthoughpatientcanbringtheirownglucoemeter

    devicetothehopital,peronalmeterhouldnotbe

    uedfordocumentationorfortreatmentofhypergly-

    cemia.Hopitalmeterhouldfollowregulatoryand

    licening quality control procedure to enure

    accuracy and reliability of reult. Hopital ytem

    withdatamanagementprogramcantranferreult

    into electronic record to allow evaluation of

    hopital-widepatternofglycemiccontrol(54).

    Healthcareworkerhouldkeepinmindthatthe

    accuracy of mot hand-held glucoe meter i far

    fromoptimal(53).Therearepotentialinaccuracie

    of POC teting including intrinic iue with the

    technologyandvariabilitybetweendifferentlotoftet trip, inadequate ampling ite, varying

    hemoglobin concentration, and other interfering

    hematological factor in acutely ill patient (37,

    55, 56). One tudy from the Center for ieae

    Control (CC) of ve commonly ued glucoe

    meter howed mean difference from a central

    laboratorymethodtobeahigha32%andacoef-

    cientofvariationof6to11%withaingletrained

    medicaltechnologit(37).

    2.0. MONTONG GCEMA N

    THE NON-CTCA CAE SETTNG

    Recommendations

    2.1. WerecommendbedidecapillaryPOCteting

    athepreferredmethodforguidingongoingglycemic

    managementofindividualpatient.(1| )

    2.2. We recommend the ue of BG monitoring

    device that have demontrated accuracy of ue in

    acutelyillpatient.(1| )

    2.3. Werecommendthattimingofglucoemeaure

    matchthepatientnutritionalintakeandmedicationregimen.(1| )

    2.4. We ugget the following chedule for POC

    teting: before meal and at bedtime in patient

    who are eating, or every 46 h in patient who

    are PO or receiving continuou enteral feeding.

    (2| )

    2.1.2.4. Evidence

    MatchingthetimingofPOCtetingwithnutritional

    intakeandthediabetemedicationregimeninthe

    hopitalettingiconitentwithrecommendation

    for the outpatient etting. POC teting i uually

    performed four time daily: before meal and at

    bedtimeforpatientwhoareeating(16,21).Premeal

    POCtetinghouldbeobtainedacloetothetime

    ofthemealtraydeliveryapoibleandnolonger

    than1hbeforemeal(4648).Forpatientwhoare

    PO or receiving continuou , POC teting i

    recommended every 46 h. More frequent glucoe

    monitoring i indicated in patient treated withcontinuou iv inulin infuion (49, 50) or after a

    medicationchangethatcouldalterglycemiccontrol,

    e.g. corticoteroid ue or abrupt dicontinuation of

    orP(48,51,52),orinpatientwithfrequent

    epiodeofhypoglycemia(16,28).

    Capillary BG data facilitate the ability to adjut

    inulintherapybaedinpartoncalculationoftotal

    correction inulin doe over the preceding 24 h.

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    RecenttudieuggetthatcontinuouBGmonitoring

    device may be helpful in reducing incidence of

    evere hypoglycemia in acute care (57, 58). More

    tudie, however, are needed to determine the

    accuracyandreliabilityofcontinuouBGmonitoring

    deviceinhopitalizedpatient.lthoughpromiing,

    continuouBGmonitoringhanotbeenadequately

    tetedinacutecareandthereforecannotberecom-

    mendedforhopitalizedpatientatthitime.

    3.0. GCEMC TAGETS N THE

    NON-CTCA CAE SETTNG

    Recommendations

    3.1. We recommend a premeal glucoe target of

    lethan140mg/dl(7.8mmol/liter)andarandom

    BGoflethan180mg/dl(10.0mmol/liter)forthe

    majority of hopitalized patient with non-critical

    illne.(1| )

    3.2. We ugget that glycemic target be modied

    accordingtoclinicaltatu.Forpatientwhoareable

    to achieve and maintain glycemic control without

    hypoglycemia,alowertargetrangemaybereaonable.

    Forpatientwithterminalillneand/orwithlimited

    life expectancy or at high rik for hypoglycemia, a

    highertargetrange(BG

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    ithe ability toreinforceeducation regarding meal

    planningformanyperonwithdiabete.lthough

    therearenorandomizedcontrolledtudiecomparing

    different inpatient nutritional trategie, one tudy

    conducted during a tranition from conitent

    carbohydratetopatient-controlledmealplanfound

    imilar glycemic meaure, with a trend toward le

    hypoglycemia with a conitent carbohydrate plan

    (16,61,68).

    4.2. Transition from home to hospital

    Recommendations

    4.2.1. Werecommendinulintherapyathepreferred

    methodforachievingglycemiccontrolinhopitalized

    patientwithhyperglycemia.(1| )

    4.2.2. We ugget the dicontinuation of oral

    hypoglycemicagentandinitiationofinulintherapy

    forthemajorityofpatientwithtype2diabeteat

    thetime of hopital admiion for an acute illne.

    (2| )

    4.2.3. We uggetthatpatient treatedwithinulin

    before admiion have their inulin doe modied

    accordingtoclinicaltatuaawayofreducingthe

    rikforhypoglycemiaandhyperglycemia.(2| )

    4.2.1.4.2.3. Evidence

    Patient with type 1 diabete have an abolute

    requirement for inulin therapy and require treat-

    ment with baal bolu inulin regimen to avoid

    evere hyperglycemia and diabetic ketoacidoi.

    Manypatientwithtype2diabetereceivinginulin

    therapy a baal bolu or multiple daily injection

    beforeadmiionareatrikforeverehyperglycemia

    in the hopital if inulin therapy i dicontinued.ementoftheneedformodicationofthehome

    inulin regimen i important becaue requirement

    varyaccordingtoclinicaltreor,reaonforadmi-

    ion,alteredcaloricintakeorphyicalactivity,and

    changeinmedicalregimenthatcanaffectglycemic

    level.Therearepatientwhorequirereductionin

    inulindoetoavoidhypoglycemia,whereaother

    requirehigherinulindoetoavoidortreatuncon-

    trolledhyperglycemia(69).

    beuefulincoordinatingdoeofrapid-actinginulin

    tocarbohydrateingetion.(2| )

    4.1.1.4.1.2. Evidence

    MTianeentialcomponentofinpatientglycemic

    managementprogram.MTidenedaaproceof nutritional aement and individualized meal

    planning in conultation with a nutrition profe-

    ional(31, 60). Thegoalof inpatientMTareto

    optimizeglycemiccontrol,toprovideadequatecalo-

    rie to meet metabolic demand, and to create a

    dicharge plan for follow-up care (16, 6064).

    lthoughthemajorityofnon-criticallyillhopital-

    ized patient receive nutrition upport a three

    dicretemealwithorwithoutchedulednackeach

    day,omerequireorPupport(eesection5).

    ackofattentiontoMTinthehopitalcontribute

    tounfavorablechangeinBG(28,46,65).utrition

    requirementoftendifferinthehomev.thehopital

    etting.Thetypeoffoodmaychangeortherouteof

    adminitration may differ, e.g. enteralor parenteral

    feeding may be ued intead of olid food. utri-

    tionalmanagementinthehopitalifurthercompli-

    cated by hopital routine characterized by abrupt

    dicontinuationofmealinpreparationfordiagnotic

    tudie orprocedure, variability in appetite duetotheunderlyingillne,limitationinfoodelection,

    and poor coordination between inulin admini-

    tration and meal delivery that create difcultie

    in predicting the efcacy of glycemic management

    trategie(46).

    conitent carbohydrate meal-planning ytem

    mayhelptofacilitateglycemiccontrolinthehopital

    etting (16, 46). The ytem i baed on the total

    amount of carbohydrate offered rather than on

    peciccaloriecontentateachmeal.Motpatient

    receiveatotalof1,5002,000calorieperday,witha

    rangeof1215carbohydrateerving.Themajority

    ofcarbohydratefoodhouldbewholegrain,fruit,

    vegetable,andlow-fatmilk,withretrictedamount

    ofucroe-containingfood(66,67).nadvantage

    totheueofconitentcarbohydratemealplani

    that they facilitate matching the prandial inulin

    doetotheamountofcarbohydrateconumed(16).

    notheradvantageofaconitentcarbohydratediet

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    Converiontobaalboluinulintherapybaedon

    POC BG reult i both afe andefcaciou inthe

    managementof hyperglycemic patient with type 2

    diabete (33, 35, 69, 74). Patient with BG level

    above 140 mg/dl (7.8 mmol/liter) who are eating

    uual meal can have baal bolu inulin therapy

    initiatedata totaldailydoebaedonbodyweight

    (33,35,75).PatientwhoarePOcanreceivebaal

    inulin alone with correction doe with a rapid-

    actinganalogevery4horwithregularinulinevery

    6 h (16, 33, 76, 77). n example of baal bolu

    protocolandcorrectionaldoeprotocoliprovidedin

    Table 1 (33, 35); however, many ucceful inulin

    regimenhavebeenreportedintheliterature(16,28,

    78,79).

    The practice of dicontinuing diabete medicationand writing order for ss at the time of hopital

    admiion reult in undeirable level of hypogly-

    cemiaandhyperglycemia(8082).nonetudy(81),

    therikforhyperglycemia(BG>11.1mmol/literor

    200 mg/dl) increaed 3-fold in patient placed on

    aggreiveliding-caleregimen.

    4.2.1.4.2.3. Values and preferences

    The recommendation to dicontinue agent other

    thaninulinatthetimeofhopitalizationibaedinpartonthefactthatcontraindicationtotheueof

    thee agent are preent in a high percentage of

    patient on admiion or during hopitalization

    (71,73).naddition,theueoforalagenttotreat

    newlyrecognizedhyperglycemiacanreultindelay

    inachievingdeiredglycemictarget,withthepoten-

    tialtoadverelyaffectpatientoutcome.

    4.2.1.4.2.3. Remarks

    Hopitalareencouragedto:

    Provide prompt to alert care provider that a

    patient i receiving an oral antidiabetic agent

    that may be contraindicated for ue in the

    inpatientetting(e.g.ulfonylureaormetformin

    in patient with renal inufciency or TZ in

    patientwithheartfailure).

    mplement educational order et that guide

    appropriateueofcheduledinulintherapyin

    thehopital(16,46,77,78,83).

    Preadmiiondiabetetherapyinpatientwithtype2

    diabete can include diet, oral agent, non-inulin

    injectable medication, inulin, or combination of

    theetherapie.Carefulaementoftheappropri-

    atene of preadmiion diabete medication i

    requiredatthetimeofhopitaladmiion.Theueof

    oralandothernon-inulintherapiepreentunique

    challengein thehopital ettingbecauethereare

    frequent contraindication to their ue in many

    inpatientituation(epi,POtatu,ivcontrat

    dye, pancreatic diorder, renal failure, etc.) (21).

    selectedpatientmaybecandidateforcontinuation

    ofprevioulyprecribedoralhypoglycemictherapyin

    thehopital.Patientcriteriaguidingthecontinued

    ueoftheeagentincludethoewhoareclinically

    table and eating regular meal and who have no

    contraindicationtotheueoftheeagent.achofthe available clae of oral antidiabetic agent

    poee characteritic that limittheir deirability

    for inpatient ue. sulfonylurea are long-acting

    inulin ecretagogue that can caue evere and

    prolongedhypoglycemia,particularlyintheelderly,

    inpatientwithimpairedrenalfunction,andinthoe

    withpoornutritionalintake(70).Therearenodata

    on hopital ue of the hort-acting inulin ecreta-

    goguerepaglinideandnateglinide;however,therik

    ofhypoglycemiaiimilartothatwithulfonylurea,uggeting the need for caution in the inpatient

    etting.Metforminmutbedicontinuedinpatient

    with decompenated congetive heart failure, renal

    inufciency, hypoperfuion, or chronic pulmonary

    dieae(71, 72) and in patient who are atrik of

    developingrenalfailureandlacticacidoi,ucha

    mayoccurwiththeadminitrationofivcontratdye

    orurgery(73).Thiazolidinedione(TZ)cantake

    everal week for thefullhypoglycemiceffect, thu

    limitingtheuefulneoftheeagentforachieving

    glycemic control in the hopital. Thee agent are

    contraindicated in patient with congetive heart

    failure, hemodynamic intability, or evidence of

    hepaticdyfunction.ipeptidylpeptidaeVinhib-

    itor delay the enzymatic inactivation of endoge-

    nouly ecreted glucagon-like peptide-1, acting

    primarilytoreducepotprandialglycemicexcurion.

    Theeagentareleuefulinpatientwhoarenot

    eatingorhavereducedoralintake.

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    4.3.2.Weuggetthatprolongedueofsstherapy

    beavoidedatheolemethodforglycemiccontrolin

    hyperglycemic patient with hitory of diabete

    duringhopitalization.(2| )

    4.3.3. We recommend that cheduled c inulin

    therapyconitofbaalorintermediate-actinginulin

    4.3. Pharmacological therapy

    Recommendations

    4.3.1.Werecommendthatallpatientwithdiabete

    treatedwithinulinathomebetreatedwithached-

    uledcinulinregimeninthehopital.(1| )

    TABLE 1. Example of a basal bolus insulin regimen for the management of non-critically ill patients with type 2 diabetes

    A. Basalinsulinorders

    Discontinueoraldiabetesdrugsandnon-insulininjectablediabetesmedicationsuponhospitaladmission.

    Startinginsulin:calculatethetotaldailydoseasfollows:

    0.2to0.3U/kgofbodyweightinpatients:aged70yrand/orglomerularltrationratelessthan60ml/min.

    0.4U/kgofbodyweightperdayforpatientsnotmeetingthecriteriaabovewhohaveBGconcentrationsof7.811.1mmol/liter(140200mg/dl).

    0.5U/kgofbodyweightperdayforpatientsnotmeetingthecriteriaabovewhenBGconcentrationis11.222.2mmol/liter(201400mg/dl).

    Distributetotalcalculateddoseasapproximately50%basalinsulinand50%nutritionalinsulin.

    Givebasalinsulinonce(glargine/detemir)ortwice(detemir/NPH)daily,atthesametimeeachday.

    Giverapid-acting(prandial)insulininthreeequallydivideddosesbeforeeachmeal.Holdprandialinsulinifpatientisnotabletoeat.

    Adjustinsulindose(s)accordingtotheresultsofbedsideBGmeasurements.

    B. Supplemental(correction)rapid-actinginsulinanalogorregularinsulin

    Supplementalinsulinorders.

    Ifapatientisableandexpectedtoeatallormostofhis/hermeals,giveregularorrapid-actinginsulinbeforeeachmealandatbedtimefollowingtheusualcolumn (Section C below).

    Ifapatientisnotabletoeat,giveregularinsulinevery6h(612612)orrapid-actinginsulinevery4to6hfollowingthesensitivecolumn (Section C below).

    Supplementalinsulinadjustment.

    Iffastingandpremealplasmaglucosearepersistentlyabove7.8mmol/liter(140mg/dl)intheabsenceofhypoglycemia,increaseinsulinscaleofinsulinfromtheinsulin-sensitivetotheusualorfromtheusualtotheinsulin-resistantcolumn.

    Ifapatientdevelopshypoglycemia[BG141180 2 4 6 181220 4 6 8

    221260 6 8 10

    261300 8 10 12

    301350 10 12 14

    351400 12 14 16

    >400 14 16 18

    The numbers in each column of Section C indicate the number of units of regular or rapid-acting insulin analogs per dose. Supplemental dose is to beadded to the scheduled insulin dose. Give half of supplemental insulin dose at bedtime. If a patient is able and expected to eat all or most of his/her meals,supplemental insulin will be administered before each meal following the usual column dose. Start at insulin-sensitive column in patients who are not eating,elderly patients, and those with impaired renal function. Start at insulin-resistant column in patients receiving corticosteroids and those treated with more than80 U/d before admission. To convert mg/dl to mmol/liter, divide by 18. Adapted from Refs. 16, 35, and 69.

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    10mmol/liter(180mg/dl)wererandomizedtoreceive

    baalboluinulinwithglargineandgluliineinulin

    orssalone.Thoeinthebaalbolugroupachieved

    mean glucoe level of le than 10 mmol/liter

    (180mg/dl)byday2andoflethan8.8mmol/liter

    (160 mg/dl)by day4 with no increae in hypogly-

    cemia (35). mong patient randomized to ss

    alone,14%requiredrecuetherapywithbaalbolu

    inulin dueto peritent BGabove13.3mmol/liter

    (240mg/dl).econdmulticentertudycompared

    two differentbaal bolu inulin regimen (detemir

    pluapartv.PHpluregular)in130nonurgical

    patient with type 2 diabete, of whom 56% were

    receivinginulintherapybeforehopitalization(69).

    There were no group difference in the level of

    glycemic control achieved or in the frequency of

    hypoglycemia,whichoccurredinapproximately30%of patient in each group. The majority of the

    hypoglycemic event occurred in patient treated

    withinulinbeforeadmiionwhowerecontinuedon

    theameinulindoeatthetimeofrandomization,a

    ndingthatemphaizetheimportanceoftherecom-

    mendationtoevaluatethehomeinulinregimenat

    thetimeofhopitalization.

    4.3.1.4.3.4. Remarks

    cheduled regimen of c baal bolu inulin i

    recommended for mot patient with diabete in

    non-Chopitaletting.uggetedmethodfor

    determining tarting doe of cheduled inulin

    therapyininulin-naivepatientinthehopitalcan

    bebaedonapatientbodyweightandadminitered

    aarangeof0.2to0.5/kgathetotaldailydoe

    (Table1).Thetotaldailydoecanbedividedintoa

    baal inulin component given once (glargine,

    detemir)ortwice(PH,detemir)dailyandanutri-

    tional or bolu component given before meal inpatientwhoareeatingorevery4to6hinpatient

    oncontinuouorP.npatientwhoarePO

    or unable to eat, bolu inulin mut be held until

    nutrition i reumed; however, doe of correction

    inulin can be continued to treat BG above the

    deired range. djutment of cheduled baal and

    boluinulincanbebaedontotaldoeofcorrection

    inulin adminitered inthe previou 24h (35, 74).

    When correction inulin i required before mot

    givenonceortwiceadayincombinationwithrapid-

    orhort-actinginulinadminiteredbeforemealin

    patientwhoareeating.(1| )

    4.3.4. Weuggetthatcorrectioninulinbeincluded

    a a component of a cheduled inulin regimen

    fortreatmentofBGvalueabovethedeiredtarget.

    (2| )

    4.3.1.4.3.4. Evidence

    The preferred c inulin regimen for inpatient

    glycemicmanagementincludetwodifferentinulin

    preparation adminitered a baal bolu inulin

    therapy,frequentlyincombinationwithacorrection

    inulincale.Thebaalcomponentrequireadmini-

    tration of an intermediate- or long-acting inulin

    preparationonceortwiceaday.Theboluorpran-

    dialcomponentrequiretheadminitrationofhort-

    orrapid-actinginulinadminiteredincoordination

    withmealornutrientdelivery(Table1).Correction

    inulinrefertotheadminitrationofupplemental

    doeofhort-orrapid-actinginulintogetherwith

    theuualdoeofboluinulinforBGabovethetarget

    range.Forpatientwhoarenoteating,baalinulini

    continuedoncedaily(glargineordetemir)ortwice

    daily[detemir/neutral protamine Hagedorn (PH)]

    plucorrectiondoeofarapidinulinanalog(apart,lipro, gluliine) or regular inulin every 4- to 6-h

    interval a needed. Correction-doe inulin hould

    notbe confued with liding cale inulin,which

    uuallyrefertoaetamountofinulinadminitered

    forhyperglycemiawithoutregardtothetimingofthe

    food,thepreenceorabenceofpreexitinginulin

    adminitration, or even individualization of the

    patientenitivitytoinulin.Correctioninulini

    cutomizedtomatchtheinulinenitivityforeach

    patient. Mot tandardized order et for c inulin

    provide everal different correction-doe cale to

    chooe from, depending on the patient weight or

    totaldailyinulinrequirement.

    Theafetyofcheduledbaalboluinulininpatient

    witheithernewlyrecognizedhyperglycemiaortype2

    diabete ha been demontrated in everal tudie

    ofnoncriticallyillhopitalizedpatient(33,35,69,

    74). n one tudy (35), 130 inulin-naive patient

    with type 2 diabete who hadglucoe level above

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    4.4. Transition from hospital to home

    Recommendations

    4.4.1. We ugget reintitution of preadmiion

    inulin regimen or oral and non-inulin injectable

    antidiabetic drug at dicharge for patient with

    acceptable preadmiion glycemic control and

    without a contraindication to their continued ue.

    (2| )

    4.4.2. Weuggetthatinitiationofinulinadmini-

    trationbeintitutedatleatonedaybeforedicharge

    toallowaementoftheefcacyandafetyofthi

    tranition.(2| )

    4.4.3. Werecommendthatpatientandtheirfamily

    orcaregiver receive both written andoralintruc-tionregardingtheirglycemicmanagementregimen

    atthetimeofhopitaldicharge.Theeintruction

    needtobeclearlywritteninamannerthatiunder-

    tandable to the peron who will adminiter thee

    medication.(1| )

    4.4.1.4.4.3. Evidence

    Hopital dicharge repreent a critical time for

    enuring a afe tranition to the outpatient etting

    and reducing the need for emergency departmentviit and rehopitalization. Poor coordination of

    patientcareatthetimeofpatienttranferbetween

    ervice, tranfer to rehabilitation facilitie, or

    dichargetohomeiaociatedwithmedicalerror

    andreadmiion(88).

    For patient dichargedhomeon inulin therapy a

    a new medication, it i important that patient

    education and written information be provided for

    themethodandtimingofadminitrationofprecribed

    doeandrecognitionandtreatmentofhypoglycemia(44).ngeneral,initiationofinulintherapyhould

    be intituted at leat one day before dicharge to

    allowaementoftheefcacyandafetyoftherapy.

    nulinregimenareoftencomplex,uuallyentailing

    the adminitration oftwodifferent inulin prepara-

    tion that may require adjutment according to

    home glucoe reading. Becaue hopital dicharge

    can be treful to patient and their family,

    orally communicated intruction alone are often

    meal,itioftenthebaalinulinthatcanbetitrated

    upward.WhenBGremainconitentlyelevatedat

    onetimepoint,the doe ofboluinulinpreceding

    that meaurement can be adjuted (78, 79). Many

    patientrequiredailyinulinadjutmenttoachieve

    glycemic control and to avoid hypoglycemia. The

    hometotalbaalandprandialinulindoehouldbe

    reducedonadmiioninpatientwithpoornutrition

    intake,impairedkidneyfunction,orwithadmiion

    BGlevellethan5.6mmol/liter(100mg/dl).

    Thee recommendation apply for patient with

    type1andtype2diabete;however,type1diabete

    patient completely lack endogenou inulin

    production. Type 1 diabete patient need to be

    providedcontinuou,exogenoubaalinulin,even

    whenfating,touppregluconeogeneiandketoneproduction.Failuretoprovidebaalinulintoatype

    1diabetepatientcanleadtotherapiddevelopment

    of evere hyperglycemia and diabetic ketoacidoi

    (84,85).ngeneral,type1diabetepatienttypically

    exhibit le inulin reitance and require lower

    daily inulin doage than type 2 diabete patient,

    epeciallyiftheyarenotobee.

    Withincreaingutilizationofinulinpumptherapy,

    manyintitutionallowpatientoninulinpumpto

    continueuingtheedeviceinthehopital;other

    expreconcernregardingueofadeviceunfamiliar

    totaff,particularlyinpatientwhoarenotableto

    managetheirownpumptherapy(86).Patientwho

    uecontinuoucinulininfuionpumptherapyin

    theoutpatientettingcanbecandidatefordiabete

    elf-managementinthehopital,providedthatthey

    havethementalandphyicalcapacitytodoo(20,

    86,87).Theavailabilityofhopitalperonnelwith

    expertieincontinuoucinulininfuiontherapyi

    eential (16, 86, 87). t i important that nuringperonneldocumentbaalrateandboludoeona

    regularbai(atleatdaily).Clearpolicieandproce-

    durehouldbeetablihedattheintitutionallevel

    toguidecontinuedueofthetechnologyintheacute

    careetting.

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    Hopital are encouraged to tandardize dicharge

    intruction heet that provide information on

    principaldiagnoi,keytetreultfromthehopital

    tay, timing and adjuting of inulin doe, home

    glucoe monitoring, and ign and ymptom of

    hypoglycemiaandhyperglycemia.

    5.0. SPECA STATONS

    5.1. Transition from iv C to sc insulin therapy

    Recommendations

    5.1.1. Werecommendthatallpatientwithtype1andtype2 diabete betranitionedto cheduledc

    inulintherapyatleat12hbeforedicontinuation

    ofC.(1| )

    5.1.2. We recommend that c inulin be admini-

    tered before dicontinuation of C for patient

    withoutahitoryofdiabetewhohavehyperglycemia

    requiringmorethan2/h.(1| )

    5.1.3. We recommend POC teting with daily

    adjutmentoftheinulinregimenafterdicontinu-ationofC.(1| )

    5.1.1.5.1.3. Evidence

    patientrecoveringfromcriticalillnebeginto

    eatregularmealoraretranferredtogeneralnuring

    unit,theyrequiretranitionfromivtocinulinto

    maintainreaonablelevelofglycemiccontrol(25,

    51,90,91).Programthatincludetranitionproto-

    colapartoftheirglycemicmanagementtrategyin

    patientundergoingurgicalprocedurehavedemon-trated ignicant reduction in morbidity and

    mortality,withlowercotandleneedfornuring

    time(25,90).

    several different protocol have been propoed to

    guidethetranitionfromCtocinulin(43,88).

    Themajority ofpatient without a prior hitory of

    diabetereceivingCatarateof1/horleatthe

    time of tranition may not require a cheduled c

    inulin regimen (78, 83, 92,93). Many of thee

    inadequate.Toaddrethiproblem,everalintitu-

    tionhave etablihed formalized dicharge intruc-

    tionforpatientwithdiabeteaawayofimproving

    the clarity of intruction for inulin therapy and

    glucoemonitoring(44,79,89).naddition,patient

    a well a the provider adminitering pothopital

    care hould be aware of the need for potential

    adjutmentininulintherapythatmayaccompany

    adjutment of other medication precribed at the

    timeofhopitaldicharge(e.g.corticoteroidtherapy,

    octreotide)(51).

    Meaurement of Hb1C concentration during the

    hopital tay can ait in tailoring the glycemic

    management of diabetic patient at dicharge.

    Patient with Hb1C below 7% can uually be

    dicharged on their ame outpatient regimen (oralagentand/orinulintherapy)iftherearenocontra-

    indication to therapy (i.e. TZ and heart failure;

    metforminandrenalfailure).Patientwithelevated

    Hb1C require intenication of the outpatient

    antidiabeticregimen(oralagent,inulin,orcombi-

    nationtherapy).Patientwithevereandymptomatic

    hyperglycemia may benet from ongoing inulin

    therapy(baalorbaalboluregimen).

    4.4.1.4.4.3. Remarks

    We ugget that the following component of

    glycemic management be included a part of the

    tranitionandhopitaldichargerecord:

    principaldiagnoiorproblemlit;

    Thereconciledmedicationlit,includinginulin

    therapy;

    Recommendationfortimingand frequency of

    homeglucoemonitoring;

    nformation regarding ign and ymptom of

    hypoglycemia and hyperglycemia with intruc-

    tionaboutwhattodoineachoftheecae;

    formorlogbookforrecordingPOCmeaure

    andlaboratoryBGreult;

    lit of pending laboratory reult upon

    dicharge;and

    denticationofthehealthcareproviderwhoi

    reponible for the ongoing diabete care and

    glycemicmanagement.

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    5.2. Patients receiving EN or PN

    Recommendations

    5.2.1.WerecommendthatPOCtetingbeinitiated

    for patient with or without a hitory of diabete

    receivingandP.(1| )

    5.2.2. WeuggetthatPOCtetingcanbedicon-

    tinuedinpatientwithoutapriorhitoryofdiabete

    ifBGvaluearelethan7.8mmol/liter(140mg/dl)

    withoutinulintherapyfor2448hafterachievement

    ofdeiredcaloricintake.(2| )

    5.2.3. We ugget that cheduled inulin therapy

    be initiated in patient with and without known

    diabete who have hyperglycemia, dened a BG

    greater than 7.8 mmol/liter (140 mg/dl), and whodemontrateaperitentrequirement( i.e.>12to24

    h)forcorrectioninulin.(2| )

    5.2.1.5.2.3. Evidence

    Malnutritionireportedinupto40%ofcriticallyill

    patient(65)andiaociatedwithincreaedrikof

    hopitalcomplication,highermortalityrate,longer

    hopital tay, and higherhopitalization cot(95).

    mprovingthenutritionaltatemayretoreimmuno-

    logical competence and reduce the frequency andeverity of infectiou complication in hopitalized

    patient(9699).

    There are everal retropective and propective

    tudiedemontratingthattheueofandPi

    an independent rik factor for the onet or aggra-

    vation of hyperglycemia independent of a prior

    hitoryofdiabete(65,100,101).Hyperglycemiain

    thigroupofpatientiaociatedwithhigherrikof

    cardiaccomplication,infection,epi,acuterenal

    failure,anddeath(102104).nonetudy,atrong

    correlationwareportedbetweenP-inducedhyper-

    glycemiaandpoorclinicaloutcome.BGmeaureof

    morethan150mg/dlbeforeandwithin24hofiniti-

    ationofPwerepredictorofbothinpatientcompli-

    cationandhopitalmortality(105).Together,thee

    reultuggetthatearlyinterventiontopreventand

    correcthyperglycemiamayimproveclinicaloutcome

    inpatientreceivingandP.

    patient can be treated with correction inulin to

    determine whether they will require cheduled c

    inulin.ncontrat,allpatientwithtype1diabete

    andmotpatientwithtype2diabetetreatedwith

    oral anti-diabetic agent or with inulin therapy

    before admiion require tranition to c long- and

    hort-actinginulinwithdicontinuationofC.

    To preventrecurrence of hyperglycemia duringthe

    tranitionperiodtocinulin,itiimportanttoallow

    an overlap of 12 h between dicontinuation of iv

    inulin and the adminitration of c inulin. Baal

    inulinigivenbeforetranitionandcontinuedonce

    (glargine/detemir) or twice (detemir/PH) daily.

    Rapid-actinginulinanalogorregularinulinigiven

    beforemealoracorrectiondoeinthepreenceof

    hyperglycemia.

    5.1.1.5.1.3. Remarks

    n general, the initial doe and ditribution of c

    inulin atthe time oftranition canbe determined

    by extrapolating the iv inulin requirement over

    thepreceding6to8htoa24-hperiod.dmini-

    tering60to80%ofthetotaldailycalculateddoea

    baalinulinhabeendemontratedtobebothafe

    andefcaciouinurgicalpatient(16,90).ividing

    the total daily doe a a combinationof baal andbolu inulin ha been demontrated to be afe in

    medicallyillpatient(90,92,94).

    t i important that conideration be given to a

    patient nutritional tatu and medication, with

    continuationofglucoemonitoringtoguideongoing

    adjutment inthe inulin doe becauechange in

    inulin enitivity can occur during acute illne.

    Correction doe of rapid-acting analog or regular

    inulincanbeadminiteredforBGvalueoutidethe

    deired range. Hopital are encouraged to include

    protocol that guide the tranition from C to c

    inulin a a way of avoiding glycemic excurion

    outidethetargetrange.Theueofprotocolhelp

    reducerandompracticethatreultinhyperglycemia

    orunwarrantedhypoglycemia.

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    overtherapid-actinganaloginthigroupofpatient

    becaue of the longer duration of action, requiring

    fewerinjection(Table2).

    For patient receiving P, regular inulin admini-

    teredapartofthePformulationcanbebothafeand effective. subcutaneoucorrection-doe inulin

    ioftenued,inadditiontotheinulinthatimixed

    withthenutrition.WhentartingP,theinitialue

    ofaeparateinulininfuioncanhelpinetimating

    thetotaldailydoeofinulinthatwillberequired.

    separateivinulininfuionmaybeneededtotreat

    markedhyperglycemiaduringP.

    5.3. Perioperative BG control

    Recommendations

    5.3.1.Werecommendthatallpatientwithtype1

    diabetewhoundergominorormajorurgicalproce-

    durereceiveeitherCorcbaalinulinwithbolu

    inulinarequiredtopreventhyperglycemiaduring

    theperioperativeperiod.(1| )

    5.3.2. Werecommenddicontinuationoforaland

    noninulin injectable antidiabetic agent before

    Toaddrethiquetion,everalclinicaltrialhave

    invetigatedtheueofdiabete-pecicformulaa

    a way of ameliorating the rik for hyperglycemia

    with . Thee diabete pecic formula differ

    from tandard formulation by upplying a lower

    percentage of total calorie a carbohydrate and

    ubtitutingmonounaturatedfattyacidforamajor

    component of adminitered fat calorie (106).n a

    meta-analyi of tudie comparing thee with

    tandard formulation, the potprandial rie in BG

    wareducedby1.031.59mmol/liter(1829mg/dl)

    (106). Thee reult ugget that the majority of

    hyperglycemic patient will till require inulin

    therapyforcontrolofhyperglycemiawhilereceiving

    thitypeofnutritionalupport.

    chieving deired glycemic goal in patientreceiving poe unique challenge (65, 74).

    nanticipated dilodgement of feeding tube,

    temporarydicontinuationofnutritionduetonauea,

    formedicationadminitration(e.g. T4,phenytoin),or

    for diagnotic teting, and cycling of with oral

    intakein patient with an inconitent appetite all

    poe clinical challenge to the precribing of

    cheduled inulin therapy. n one tudy, patient

    with peritent elevation in BG above 7.2 mmol/

    liter (above 130 mg/dl) during therapy were

    randomizedtoreceiveglargineoncedailyatatarting

    doeof10,incombinationwithsswithregular

    inulinadminiteredevery6h,orssalone.pprox-

    imately50%ofpatientrandomizedtossrequired

    recue therapy with PH to achieve a mean BG

    below 10 mmol/liter (180 mg/dl) (74). The doe

    of glargine inulin wa adjuted on a daily bai

    accordingtoreultofPOCteting.fmorethanone

    BGwaabove10mmol/literintheprior24h,the

    doeofglarginewaincreaedbyapercentageofthe

    totaldoeofcorrectioninulinadminiteredonthepreceding day. With ue of thi approach, a mean

    glucoeofapproximately8.8mmol/liter(160mg/dl)

    waachievedwithlowrikforhypoglycemia.

    suggeted approache uing c inulin therapy in

    patientreceivingcontinuou,cycled,orintermittent

    therapyappearinTable2.Manymemberofthi

    writingtakforcepreferfrequentinjectionofhort-

    actingregularinulinorintermediate-actinginulin

    Table 2. Approaches to insulin therapy during EN

    ContinuousEN

    Administerbasalinsulinonce(glargine,detemir)ortwice(detemir/NPH)adayincombinationwithashort-orrapid-actinginsulinanalogindivideddoses

    every4h(lispro,aspart,glulisine)to6h(regularinsulin).Cycledfeeding

    Administerbasalinsulin(glargine,detemir,orNPH)incombinationwithshort-orrapid-actinginsulinanalogatthetimeofinitiationofEN.

    Repeatthedoseofrapid-actinginsulin(lispro,aspart,glulisine)at4-hintervalsorshort-acting(regular)insulinat6-hintervalsforthedurationoftheEN.Itispreferabletogivethelastdoseofrapid-actinginsulinapproximately4hbeforeandregularinsulin6hbeforediscontinuationoftheEN.

    Bolusfeeding

    Administershort-actingregularorrapid-actinginsulinanalog(lispro,aspart,glulisine)beforeeachbolusadministrationofEN.

    Adapted from Refs. 16, 74, and 101.

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    adminitering50%ofthebaalinulindoepreopera-

    tively wa demontrated in one nonrandomized

    qualityimprovementinitiative(114).dmiionBG

    levelin584patientwithdiabetetreatedaccording

    tothee recommendation rangedbetween 3.9 and

    11.1mmol/liter(70200mg/dl)in77%ofpatient.

    Hypoglycemia,denedaaBGoflethan3.9mmol/

    liter,occurredinonly1.7%ofpatient.

    Patient with type 2 diabete well-controlled by a

    regimenofdietandphyicalactivitymayrequireno

    pecial preoperative interventionfor diabete (111,

    115). Glucoe level in thi group of patient can

    oftenbecontrolledwithmalldoeofupplemental

    hort-actinginulin.nulintreatedpatientorthoe

    with poor metabolic control while onoral antidia-

    beticagentwillrequireivinulininfuionorabaalbolucinulinregimentoachievethedeiredlevel

    ofglycemiccontrol.

    Patient with type 1 diabete undergoing minor or

    majorurgicalprocedurerequireCorcbaalbolu

    inulin adminitration adjuted according to the

    reultofBGtetingtopreventthedevelopmentof

    diabetic ketoacidoi (85, 116118). n one tudy,

    BGvalueinagroupofubjectwithtype1diabete

    whoreceivedtheirfulldoeofglargineinulinona

    fatingdaywerecomparedwiththoeobtainedona

    controldaywhentheparticipantwereeatingtheir

    uualmeal(119).Therewerenoignicantdiffer-

    ence in mean BG level between thee two day,

    uggetingthatitiafetoadminiterthefulldoeof

    baal inulin when a patient i made PO. For

    patient with type 1 diabete whoe BG i well

    controlled,mildreduction(between10and20%)in

    thedoing ofbaal inulin areuggeted. For thoe

    whoeBGiuncontrolled[i.e. BG>10mmol/liter

    (200 mg/dl)], full doe of baal inulin can beadminitered.

    Becaue the pharmacokinetic propertie of PH

    inulindifferfromthoeofglargineanddetemir,doe

    reduction of 2550% are uggeted, together with

    theadminitration of hort-or rapid-acting inulin

    forBG>8.3mmol/liter(150mg/dl)(Table3).

    Prolongedueofssregimeninotrecommendedfor

    glycemiccontrolduringthepotoperativeperiodin

    urgery with initiation of inulin therapy in thoe

    whodevelophyperglycemiaduringtheperioperative

    periodforpatientwithdiabete.(1| )

    5.3.3. When intituting c inulin therapy in the

    poturgical etting, we recommend that baal (for

    patientwhoarePO)orbaalbolu(forpatient

    whoareeating)inulintherapybeintitutedathe

    preferredapproach.(1| )

    5.3.1.5.3.3. Evidence

    There are everal cae-control tudie that demon-

    trate an increaed rik for advere outcome in

    patientundergoingelectivenoncardiacurgerywho

    have either preoperative or potoperative hyper-

    glycemia (19, 107110). Potoperative BG valuegreater than 11.1 mmol/liter (200 mg/dl) are

    aociatedwithprolongedhopitallengthoftayand

    an increaed rik of potoperative complication,

    includingwoundinfectionandcardiacarrhythmia

    (107110).nonetudy,theincidenceofpotoper-

    ative infection in patient with glucoe level

    above 12.2 mmol/liter (220 mg/dl) wa 2.7 time

    higher than in thoe with glucoe level below

    12.2 mmol/liter (109). n a recent report of 3,184

    noncardiacgeneralurgerypatient,aperioperative

    glucoevalueabove8.3mmol/liter(150mg/dl)wa

    aociated with increaed length of tay, hopital

    complication,andpotoperativemortality(107).

    Perioperative treatment recommendation are

    generallybaedonthetypeofdiabete,natureand

    extentoftheurgicalprocedure,antecedentpharma-

    cological therapy, and tate of metabolic control

    beforeurgery(110,111).keyfactorfortheucce

    of any regimen i frequent glucoe monitoring to

    allowearlydetectionofanyalterationinmetabolic

    control.

    ll patient receiving inulin before admiion

    requireinulinduringtheperioperativeperiod(112,

    113). For mot patient, thi requirement include

    adminitration of a percentage of the uual baal

    inulin (PH, detemir, glargine) in combination

    with correction doe of regular inulin or rapid-

    actinginulinanalogforglucoelevelfrom8.3to

    11.1 mmol/liter (150 to 200 mg/dl). The afety of

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    5.4. Glucocorticoid-induced diabetes

    Recommendations

    5.4.1. We recommend that bedide POC teting

    be initiated for patient with or without a hitory

    of diabete receiving glucocorticoid therapy.

    (1| )

    5.4.2. WeuggetthatPOCtetingcanbedicon-

    tinuedin nondiabetic patient ifall BG reult are

    below 7.8 mmol/liter (140 mg/dl) without inulin

    therapyforaperiodofatleat2448h.(2| )

    5.4.3. We recommend that inulin therapy be

    initiated for patient with peritent hyperglycemia

    whilereceivingglucocorticoidtherapy.(1| )

    5.4.4. WeuggetCaanalternativetocinulin

    therapy for patient with evere and peritent

    elevationinBGdepiteueofcheduledbaalbolu

    cinulin.(2| )

    5.4.1.5.4.4. Evidence

    Hyperglycemiaiacommoncomplicationofgluco-

    corticoid therapy with a prevalence between 20

    and50%amongpatientwithoutapreviouhitory

    of diabete (51, 120, 121). Corticoteroid therapyincreaehepaticglucoeproduction,impairglucoe

    uptakein peripheral tiue, and timulate protein

    catabolimwithreultingincreaedconcentrationof

    circulatingaminoacid,thuprovidingprecurorfor

    gluconeogenei (122124). The oberved decreae

    inglucoeuptakewithglucocorticoidtherapyeem

    tobeamajorearlydefect,contributingtoincreaein

    potprandial hyperglycemia. epite it frequency,

    the impactof corticoteroid-induced hyperglycemia

    onclinicaloutcomeuchamorbidityandmortality

    inotknown.Fewtudiehaveexaminedhowbetto

    treat glucocorticoid-induced hyperglycemia. n

    general, dicontinuation of oral antidiabetic agent

    with initiation of c baal bolu inulin therapy i

    recommended for patient with glucocorticoid-

    induced hyper-glycemia. The tarting inulin doe

    and timing of inulin adminitration hould be

    individualized depending on everity of hypergly-

    cemia and duration and doage of teroid therapy.

    For patient receiving high-doe glucocorticoid

    hyperglycemicpatientwithdiabete.nonetudyof

    211 general urgery patient with type 2 diabete

    randomly aigned toreceive baal bolu inulin or

    ss, glycemic control and patient outcome were

    ignicantly better with the former (33). Patientwho were treated with ss hadhigher mean POC

    glucoevalueandmorepotoperativecomplication

    including wound infection, pneumonia, repiratory

    failure, acute renal failure, and bacteremia. The

    reult of that tudy indicate that treatment with

    glargine once daily plu rapid-acting inulin before

    mealimproveglycemiccontrolandreducehopital

    complicationingeneralurgerypatientwithtype2

    diabete(33).

    5.3.1.5.3.3. Values and preferences

    We place a high value on maintaining glycemic

    controlevenforbriefperiodoftime,aoccurduring

    period of fating for urgical or other procedure.

    lthough avoidance of hypoglycemia i deired,

    adminiteringapercentageoftheuualdoeoflong-

    orintermediate-actinginulinappeartobeafeand

    well tolerated,even for patient who arriveon the

    morningoftheprocedure.

    5.3.1.5.3.3. Remarks

    Hopitalareencouragedto:

    mplement protocol that guide afe glycemic

    management of patient with hyperglycemia

    duringandafterurgicalprocedure,and;

    bandon practice that allow for random and

    inconitent glycemic management in urgical

    patient.

    Table 3. Pharmacokinetics of sc insulin preparationsa

    nsulin Onset Peak uration

    Rapid-actinganalogs

    515min 12h 46h

    Regular 3060min 23h 610h

    NPH 24h 410h 1218hGlargine 2h Nopeak 2024h

    Detemir 2h Nopeak 1224h

    a Renal failure leads to prolonged insulin action and alteredpharmacokinetics (162).

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    6.1.6.3. Evidence

    Hypoglycemia i dened a any glucoe level

    below 3.9 mmol/liter (70 mg/dl) (127, 128). Thi

    i thetandarddenition in outpatient andcorre-

    late with the initial threhold for the releae of

    counter-regulatory hormone (128, 129). severe

    hypoglycemia ha been dened by many a le

    than2.2mmol/liter(40mg/dl)(128),althoughthi

    i lower than the approximately 2.8 mmol/liter

    (50 mg/dl) level at which cognitive impairment

    begininnormalindividual(129).

    Thefearofhypoglycemiaiakeybarriertotheimple-

    mentation of targeted glucoe control. lthough

    notacommonahyperglycemia,hypoglycemiaia

    well-recognized and feared complication in hopi-talizedpatientwithorwithoutetabliheddiabete

    (130). The rik for hypoglycemia i higher during

    periodofhopitalizationduetovariabilityininulin

    enitivityrelatedtotheunderlyingillne,change

    in counter-regulatory hormonal repone to proce-

    dureorillne,andinterruptioninuualnutritional

    intake(131,132).

    Theprevalenceofhypoglycemiceventvarieacro

    tudiedependingon thedenitionofhypoglycemia

    and the pecic patient population evaluated. n a3-month propective review of conecutive medical

    recordin2174hopitalizedpatientreceivingantidi-

    abeticagent,206patient(9.5%)experiencedatotal

    of484hypoglycemicepiode(133).largeglycemic

    urveyexaminingreultofPOCbedideglucoetet

    from126hopitalreportedaprevalenceofhypogly-

    cemia(

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    pecically at reducing hypoglycemia are lacking,

    everal trategie appear reaonable. Thee include

    ueofevidence-baedglucoecontrolprotocolwith

    a demontrated afety record, etablihment of

    hopital-wide policie that provide guidance on

    identication of high-rik patient, and tandard-

    izationofprocedurefordetectionandtreatmentof

    hypoglycemia acro nuring unit (74, 143, 144).

    Many patient require daily inulin adjutment to

    avoidhypoglycemia(BG

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    7.0. MPEMENTATON O A

    GCEMC CONTO POGAM

    N THE HOSPTA

    Recommendations

    7.1. Werecommendthathopitalprovideadmini-

    trative upport for an interdiciplinary teering

    committeetargetingaytemapproachtoimprove

    careofinpatientwithhyperglycemiaanddiabete.

    (1| )

    7.2. Werecommendthateachintitutionetablih

    a uniform method of collecting and evaluating

    POC teting data and inulin ueinformation a a

    way of monitoring the afety and efcacy of the

    glycemiccontrolprogram.(1| )

    7.3. We recommend that intitution provide

    accurate device for glucoe meaurement at the

    bedidewithongoingtaffcompetencyaement.

    (1| )

    7.1.7.3. Evidence

    tiimportantformedicalcentertotargetimproved

    careofinpatientwithhyperglycemiaand/ordiabete

    by creating and upporting an interdiciplinary

    teering committee with repreentation from key

    group involved in thecare of thee patient (51).

    Theteeringcommitteeideallywouldincluderepre-

    entativefromphyiciangroup,nure,pharmacit,

    cae manager, nutrition, information upport, and

    qualityimprovementperonnelempoweredto:

    eafetyandefcacyofproceeforglycemic

    managementwithafocuonimprovingcareatthe identied area of deciency, within a

    frameworkofqualityimprovement.

    mplement trategie that guide taff and

    phyician education with written policie,

    protocol,andorderetwithintegrateddeciion

    upportuingcomputerorderentry.

    Conider ue of checklit, algorithm, and

    tandardizedcommunicationforpatienttranfer

    andhandoff.

    appropriatetreatmentwithoutdelay,andretetBGat

    precribedtimeintervalaftertreatment(148).For

    theereaon,educationalinitiativeatthetimeof

    protocolimplementationwithperiodicreinforcement

    areeential(149).

    Table 5. Suggested nurse-initiated strategies fortreating hypoglycemia

    FortreatmentofBGbelow3.9mmol/liter(70mg/dl)inapatientwhoisalertandabletoeatanddrink,administer1520gofrapid-actingcarbohydratesuchas:a

    one1530gtubeglucosegelor4(4g)glucosetabs(preferredforpatientswithendstagerenaldisease).

    46ouncesorangeorapplejuice.

    6ouncesregularsugarsweetenedsoda.

    8ouncesskimmilk.

    FortreatmentofBGbelow3.9mmol/liter(70mg/dl)inanalertandawakepatientwhoisNPOorunabletoswallow,administer20mldextrose50%solutioniv

    andstartivdextrose5%inwaterat100ml/h.FortreatmentofBGbelow3.9mmol/literinapatientwithanalteredlevelofconsciousness,administer25mldextrose50%(1/2amp)andstartivdextrose5%inwaterat100ml/h.

    Inapatientwithanalteredlevelofconsciousnessandnoavailableivaccess,giveglucagon1mgim.Limit,twotimes.

    RecheckBGandrepeattreatmentevery15minuntilglucoselevelisatleast4.4mmol/liter(80mg/dl).

    a Dose depends on severity of the hypoglycemic event.

    Table 4. Key components of hypoglycemia preventionand management protocol

    Hospital-widedenitionsforhypoglycemiaandseverehypoglycemia.

    Guidanceondiscontinuationofsulfonylureatherapyandotheroralhypoglycemicmedicationsatthetimeofhospitaladmission.

    Directionsforadjustmentsininsulindoseand/oradministrationofdextrose-containingivuidsforbothplannedandsuddenchangesinnutritionalintake.

    Specicinstructionsforrecognitionofhypoglycemiasymptoms,treatment,andtimingforretestingdependingonglucoselevelsanddegreeofthepatientsneurologicalimpairmentandforretestingofglucoselevels.

    Standardizedformfordocumentationandreportingofhypoglycemicevents,includingseverity,potentialcause(s),treatmentprovided,physiciannotication,andpatientoutcome.

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    8.0. PATENT AN POESSONA

    ECATON

    Recommendations

    8.1. We recommend diabete elf-management

    education targeting hort-term goal that focu on

    urvival kill: baic meal planning, medication

    adminitration, BG monitoring, and hypoglycemia

    andhyperglycemiadetection,treatment,andpreven-

    tion.(1| )

    8.2. We recommend identifying reource in the

    community to which patient can be referred for

    continuingdiabeteelf-managementeducationafterdicharge.(1| )

    8.3. We recommend ongoing taff education to

    updatediabeteknowledge, awella targeted taff

    education whenever an advere event related to

    diabetemanagementoccur.(1| )

    8.1.8.3. Evidence

    iabeteelf-managementeducationhatheability

    to reduce length of hopital tay and improveoutcome after dicharge (16). n a meta-analyi

    of 47 tudie on the effect of diabete education

    on knowledge, elf-care, and metabolic control,

    educational intervention were hown to increae

    patientknowledgeandabilitytoperformelf-care

    (156). The inpatient poition tatement

    recommendinitiationofdiabeteelf-management

    education early during the hopitalization to

    allow time to addre potential decit in patient

    knowledge(48).Withearlyintervention,thepatient

    willhavemoreopportunitietopracticeandmater

    urvival kill. Family member hould be included

    whenever poible to upport and reinforce elf-

    managementeducation(157,158).

    n patient diabete educational goal hould focu

    onthefollowingurvivalkill:baicmealplanning,

    medication adminitration, POC teting, and

    hypoglycemia detection, treatment, and prevention

    (21,48).iabeteeducationimorecomplexinthe

    Monitor the ue of order et and protocol,

    intervening to reinforce protocol ue, and

    reviing protocol a needed to improve

    integration,clarity,andeaeofue.

    ntitute continuing education program for

    medical, nuring, and dietary taff to enhanceadherencetoprotocol.

    The inpatient care of individual with diabete

    and hyperglycemia i complex, involving multiple

    providerwithvaryingdegreeofexpertiewhoare

    diperedacromanydifferentareaofthehopital.

    multidiciplinaryytemapproachcanhelpguide

    meaningful progre away from clinical inertia and

    toward afe glycemic control, hypoglycemia

    prevention,andpatientpreparationforcaretrani-

    tion(20,54,143,144,147).

    The tranfer of patient between nuring unit of

    clinicalcareteamiamajorcaueoferrorinthe

    careofpatientwithhyperglycemiainthehopital.

    Poor coordination of glucoe monitoring, meal

    delivery, and inulin adminitration i a common

    barriertooptimalcare(43,150,151).

    vidence for the advantage of uing a ytem

    approach come from everal ource: indutry and

    highreliabilityorganization;endorementbymajor

    profeional organization, baed on conenu

    opinionandexperience(21,152);extrapolationof

    experience applied to other dieae entitie (152);

    and ucceful intitutionalglycemic control effort

    viathiapproach(78,153155).

    Reource outliningthe multidiciplinary approach,

    protocol, and order et deign, implementation

    trategie,andmethodformonitoringandcontinu-

    ouly improving the proce are available in print

    andinternetmedia(88).

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    hyper-glycemia protocol, tracking of hypoglycemia

    frequency and everity, providing diabete elf-

    management education, and identication of a

    program champion or team to pearhead glycemic

    controlinitiative(160).

    Theprincipleofdiabeteeducationandmanagement

    inthehopitalapplyforpatientwithtype1andtype

    2 diabete. ue to the lack endogenou inulin

    production, patient with type 1 diabete require

    exogenouinulintobeprovidedatalltimetoavoid

    evere hyperglycemia and diabetic ketoacidoi (84,

    85).naddition,patientwithtype1diabetearele

    inulinreitantandaremorevulnerabletohypogly-

    cemic event than thoe with type 2 diabete.

    ttention to type of diabete, a well a to family

    dynamicandpychologicalandemotionalmaturity,i eential in developing and implementing an

    optimaldiabeteregimen.

    hopitalettingbecauepatientareacutelyill,may

    beexperiencingpain,andareundertre.Keeping

    eionhortandfocuedwithminimalditraction

    andinterruption contribute to a more productive

    learningenvironment(48).

    ocumentation ofteaching eion by health care

    profeional promote communication of progre

    to the next health care provider and ait in

    dicharge planning. n ituation where failure to

    performdiabeteelfcarepracticecontributedtothe

    needforthehopitalization,educationcanbefocued

    on the area of deciency a a way of preventing

    readmiion(e.g.diabeticketoacidoi)(16,48,88).

    Writtendichargeintructionondiabeteelf-care,

    offered in the patient primary language wheneve