vasopressor & inotropes

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    Basic

    LifeSupport

    VASOPRESSOR & INOTROPES

    IN SHOCK IMBIBE IT & APPLY

    IT

    VASOPRESSOR & INOTROPES

    IN SHOCK IMBIBE IT & APPLY

    IT

    DR.S.ARUNKUMAR M.D(EM), PG.DIP.(USG),FELL!S"IP IN

    IN#ENSI$E %ARE MEDI%INE & E%"%ARDIGRAP"'

    EMERGEN%' & %RI#I%AL %ARE P"'SI%IANAS"!INI SPE%IALI#' "SPI#AL,SLAPUR

    DR.S.ARUNKUMAR M.D(EM), PG.DIP.(USG),FELL!S"IP IN

    IN#ENSI$E %ARE MEDI%INE & E%"%ARDIGRAP"'

    EMERGEN%' & %RI#I%AL %ARE P"'SI%IANAS"!INI SPE%IALI#' "SPI#AL,SLAPUR

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    Structure of ta*+Structure of ta*+

    What is in your hand ?

    Various receptors & its effect

    Drugs Heroic & villain character

    Clinical approach to cardiogenic & septic shock

    Studies quoting what you should use & what you shouldnot

    eco!!endations

    "rou#leshooting during ad!inistration

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    $asoacti-e ae/ts$asoacti-e ae/ts

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    So,what are theadrenergic

    receptors & how

    does it efect on?

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    #"ER SPE%IFI% RE%EP#RS#"ER SPE%IFI% RE%EP#RS

    DPAMINE RE%EP#RS

    Present in the renal,

    splanchnic, coronary,

    cerebral & vascular beds. Sti!ulation of these

    receptors leads to

    vasodilation$

    Second su#type of

    dopa!ine receptors causesvasoconstriction #y inducing

    norepinephrine release at

    doses %'!cg(kg(!t

    $ASPRESSIN RE%EP#RS

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    Pri/cip*es f Use f

    $asopressors a/0 I/otropes

    Pri/cip*es f Use f

    $asopressors a/0 I/otropes

    Hypotension !ay result fro!) "po-o*eia

    Pup fai*ure

    Pat1o*oic a*0istri2utio/ of 2*oo0 f*o3

    Vasopressors are indicated for) Decrease of 456 "7869 fro 2ase*i/e

    SBP or

    MAP :;6 " a/0 E-i0e/ce of e/0ora/ 0sfu/ctio/ 0ue to

    1poperfusio/

    Hypovole!ia !ust #e corrected first

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    Epi/ep1ri/eEpi/ep1ri/e

    Dose &0i*utio/

    Dose ) *+'!cg(!t

    ,'$-!cg(kg(!t #eta

    effects

    %'$-!cg(kg(!t+ alpha

    effects

    .C/S 0+-1!cg(!t

    2ntratracheal dose *+*$1ti!es 2V dose

    Dilution ) 3!g(*1'!l

    Dose of '$*!g(kg CC4

    or 44 overdose

    %op*icatio/s

    "achyarrhyth!ia

    /eucocytosis

    .ngina & 2ncreases!yocardial o5ygen

    de!and

    /actic acidosis

    Dec renal & splanchnic#lood flow

    Hypertension &

    pul!onary ede!a

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    Nor epi/ep1ri/eNor epi/ep1ri/e

    Dose & Di*utio/

    Dose ) *+'!cg(!t

    .C/S 0+-1!cg(!t

    Dilution 3!g(*1'!l Nora0re/a*i/e 2itartrate 8

    (/ora0re/a*i/e 2ase

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    Dopai/eDopai/e

    Dose & Di*utio/

    Dose )

    '$1+1!cg(kg(!t+

    vasodilation 1+'!cg(kg(!t cardiac

    sti!ulation7.C/S9

    %'!cg(kg(!t+

    vasoconstriction

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    Do2utai/eDo2utai/e

    Dose & Di*utio/

    :redo!inantly #eta

    effects 7#eta%#eta*9

    :otent2notropic(chronotropic

    Dose ) *+*' !cg(kg(!in

    =a5) 3'!cg(kg(!t

    Dilution )*1'!g(*1'!l =a@or use) Systolic

    dysfunction

    %op*icatio/s

    "achyarrhyth!ia &

    ventricular ectopy

    2ncreases !yocard >*de!and

    Aever & headache

    Dyspnoea

    Can decrease =.: involu!e depleted patients

    >ccasional B2 stress

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    $asopressi/$asopressi/

    Dose & 0i*utio/

    Dose :0.01-0.04

    units/minute

    Dilution :1unit/ml Doses >0.04 units/mt

    causes !" & !ardiac

    ischemia

    pressor e##ects preserved

    durin$ hypo%ic and acidotic

    conditions

    =ay restore C:: after cardiac

    arrest without producing

    tachycardia

    %op*icatio/s

    .#d cra!ping8 nausea8

    vo!iting

    4ronchoconstriction

    2ncr liver eny!es

    =esentric ische!ia

    Venous thro!#osis

    Chest pain & =2

    Decrease platelets

    lactic acidosis

    Water into5ication

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    I/0icatio/ of -asopresssi/I/0icatio/ of -asopresssi/

    Hyper+dyna!ic catechola!ine+resistant

    vaso+plegic state

    6ot as late rescue therapy in severe

    refractory shock

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    R"'#"M F DRUGS N

    ALP"A & BE#A A%#I$I#'

    R"'#"M F DRUGS N

    ALP"A & BE#A A%#I$I#'

    stro/est

    NR

    EPINEP"RINE =EPI

    NEP"RINE 4DPAMINE4 P"EN'LEP"RINE!EAKES#

    EPI

    NEP"RINEDPAMINE

    NR

    EPINEP"RINE4 4

    BE#A A%#I$I#'

    ALP"A

    A%#I$I#'

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    #ac1p1*a>is#ac1p1*a>is

    esponsiveness to these drugs can decreaseover ti!e due to tachyphyla5is

    Doses !ust #e constantly titrated to ad@ust for

    this pheno!enon & for changes in patient clinical

    condition

    How to counteract addition of second line drug

    earlier

    ioavailability o# subcutaneous heparin or insulin can

    be reduced durin$ treatment 'ith vasopressors due

    to cutaneous vasoconstriction$

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    %*i/ica* Approac1 to s1oc+e0 patie/t%*i/ica* Approac1 to s1oc+e0 patie/t

    !1at is s1oc+ ?De#ined by circulatory insu##iciency that creates an imbalance

    bet'een the tissue o%y$en supply(delivery) & o%y$en demand

    (consumption) 'ith multitude o# or$an dys#unction .

    "eo0/aic paraeters Criteria for hypotension drop in sys$ 4:% -'!!hg fro! #aseline or

    ,E'(F'!!hg or =.: ,F'!!hg

    Hypotension does not equate to shock often

    Shock Oftenhappens prior to hypotension

    Shock !ay happen despite nor!al 4: & conversely 4: !ay #e low

    without shock #eing present

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    Syste!ic "issue :erfusion

    Cardiac >utput7C>9

    Heart ate7H9

    StrokeVolu!e

    7SV9

    :reload .fterload Contractility

    Syste!ic Vascularesistance 7SV9

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    Differe/tiatio/ of s1oc+Differe/tiatio/ of s1oc+

    %ar0ioe/ic "po-o*eic Septic

    Pu*se pressure G G

    Diasto*ic pr G G GGG

    E>treities Cool Cool War! initially8 coollater

    Nai*e0 2*oo0retur/ Slow Slow apid

    @$P G G

    Respirator creps III ++ ++

    S5 S Ga**op III ++ ++

    %1est ra0iorap1 /arge heart8pul!onary ede!a

    Di!inished cardiacsie

    6or!al8unlesspneu!onia present

    I0e/tifie0 site ofi/fectio/

    ++ ++ III

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    %ar0ioe/ic s1oc+%ar0ioe/ic s1oc+

    evasculariation i!!ediately is the definitivecare 7TIME IS MUSCLE 9

    62V support 7when he!odyna!ically sa#le &

    cooperative 9 =echanical ventilation even in nor!al

    o5ygenation status with resp distress7to unload

    resp$ !uscle workload9 & utiliation of low C>

    #y vital organs 2nitial therapy of hypotension

    A//

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    %ARDIGENI% S"%K ? Approac1%ARDIGENI% S"%K ? Approac1

    V 26A.C" W2"H HJ:>";6S2>6

    Aluid #olus *1'+1''=/ 7over '+1!inutes9

    .6"$W.// 26A.C" W2"H HJ:>";6S2>6 Aluid challenge ''+*1'=/7over '+1!inutes9

    Static test

    Clinical end points7H 4: vein

    co!pressi#ility urine output9

    CV::CW:CK:2CC>

    D/aic testi/

    :assive leg raise testing7pulsepressure variation9

    ;nd e5piratory occlusion

    testing

    *cho & + o# ! diameter

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    %ar0ioe/ic s1oc+%ar0ioe/ic s1oc+

    6>.D;6./26; S" L 1=CBS(="7-$0=/(H92A 4:,0'==HB

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    "aper & stop inotropic supports7dopa!ine & do#uta!ine 9 if4: i!proved % #aseline level for that patient(=.: %F1!!hg

    "aper noradrenaline once reached 1!cgs(!t dosage

    IF BP N# IMPR$ED

    Start

    EPINEP"RINE( c7t )

    Uptitrate to a>iu EPINEP"RINE ? 56cs7t

    %$% LINE $asopressors & i/otropic supports 48;1ours71i1 0oses

    SI#E ? I@$ (# MNI#R %$P )

    AR#ERIAL LINE Epi/ep1ri/e 7 Nora0 4

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    Ne3er Sepsis 0efi/itio/86

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    Seue/tia* ora/ fai*ure assesse/t(SFA Score)Seue/tia* ora/ fai*ure assesse/t(SFA Score)

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    SEP#I% S"%KSEP#I% S"%K

    Secure the air3a & 2reat1i/ + septic shock patient

    F*ui0 resuscitatio/ + wide #ore 7F B9+ *'+3'!l(kg

    crystalloids over -'+F' !inutes with careful vitals !onitoring

    RES%UE P#IMIA#IN S#ABILIA#IN DEES%ALA#IN

    Rescue 1''!l #olus over 1!inutes(FLUID BOLUS)

    ptiiatio/ ''+*''!l over 1+' !inutes(FLUID CHALLENGE)

    no longer life threatening8 to opti!ise tissue perfusionSta2i*iatio/ !aintenance fluids for ongoing nor!al fluid loss in

    renal8B28 insensi#le loss

    Deesca*atio/ stage of negative fluid #alance if warranted #y signs

    & sy!pto!s

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    FLUID ADMINIS#RA#INFLUID ADMINIS#RA#IN

    #ARGE#S IN FLUID #"ERAP'

    :ulse volu!e8 o5i!etry 8=.: %F1!!hg & :ulse

    pressure variation

    "arget CV: N+'c!7non ventilated9( '+*c! H*>7ventilated 9

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    $ASPRESSR & IN#RPES ?

    SEP#I% S"%K

    $ASPRESSR & IN#RPES ?

    SEP#I% S"%K

    Which Vasopressors to start withOOOOOOOOO

    6>+;:26;:H26; ?

    D>:.=26; ?

    D>42C; ?

    o, hich dru$ as second line/rescue therapy

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    S"%Ke0 HS"%Ke0 H6>.D;6./26; S" L 1=CBS(="7-$0=/(H9

    2A 4:,0'==HB

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    t "aper vasopressin L '$1units(hour

    2f =.: % F1!!hg

    %$% LINE $asopressors & i/otropic supports 48;1ours71i1 0oses

    AR#ERIAL LINE $asopressi/ i/0icatio/ 7 Nora0 4"2C>S";>2DS

    .DP

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    ' N# DPAMINE INS#EAD F NRAD' N# DPAMINE INS#EAD F NRAD

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    Stu0iesStu0ies

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    Stro/ recoe/0atio/sStro/ recoe/0atio/s

    Cardiogenic shock + 6orepinephine as first line vasopressor

    6orepinephrine stline vasopressor agent for septic shock

    Do#uta!ine 2n septic shock for low cardiac output state despite volu!eresuscitation

    ;pinephrine infusion anaphylactic shock not responding to 2= or 2V #olusepinephrine

    ;pinephrine is the stline agent in hypotension after C.4B$

    6or epinephrine stline vasopressor for undifferentiated shock notresponding to fluid therapy

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    %o/0itio/a* recoe/0atio/s%o/0itio/a* recoe/0atio/s

    Cardiogenic shock do#uta!ine ad!inistration if inotropedee!ed necessary

    outine vasopressor use in hypovole!ic shock notreco!!ended

    Vasopressin for he!orrhagic or hypovole!ic shock ifvasopressor dee!ed necessary

    Qnown or suspected H>C= or dyna!ic outflow o#structionpts avoid inotropic agents $use vasopressors @udiciously

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    %o/0itio/a* recoe/0atio/s%o/0itio/a* recoe/0atio/s

    >#structive shock not reponding to specifiedtreat!ent8vasopressor should #e initiated

    Vasopressin catechola!ine refractory septic shock

    6orad stchoice for distri#utive shock due to hepaticfailure

    Short ter! vasopressor infusion ,+*hours throughperipheral line co!plications unlikely

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    #rou2*es1ooti/7%1ec+*ists 0uri/

    I/otropes & Pressors support

    #rou2*es1ooti/7%1ec+*ists 0uri/

    I/otropes & Pressors support

    2s the patient appropiately !onitored

    Had the early use of vasopressors falsely elevated CV: & !asked hypovole!ia

    .re the vasopressors !i5ed in correct dose

    Vasopressor(inotropes & fluid tu#ing connected in separate line

    Check out whether three way port directed properly for flow

    624: intervals kept every '!inutes(2nvasive !onitoring .+line positioned( flushedqhour

    Cardiac !onitors connected properly for specific patients

    :rior filled pressor agents #efore ongoing supports e!pty

    Drug na!e(Concentration & colour code la#elling of the various line done

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    #a+e 1oe poi/ts#a+e 1oe poi/ts

    $asopressi/ ? co/trai/0icate0 i/ %%F pts.(3ater rete/tio/ & se0after*oa0 )

    $asopressi/ 2o3e* isc1eia & *actic aci0osis

    I/otropes & -asopressor 3o/t 3or+ i/ aci0ic state( p" :.< )

    I/otropes receptor 2i/0i/ affi/it a*tere0 2 teperature &co/ce/tratio/

    %*assica* i/0icatio/ of so0a 2icar2 ? p":.< to a+e pressors

    3or+

    Do /ot i-e so0a 2icar2 i/ case of *actic aci0osis

    E*e-ate0 *actate ? ar+er of ipaire0 o>e/ 0e*i-er7uti*iatio/

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    REFEREN%ESREFEREN%ES

    42"2SH P>A .6.;S"H;S2. C.6.D2.6 P>A ;=;B;6CJ =;D2C26;

    >Q >A ;=;B;6CJ =;D2C26;

    .=;2C.6 :H.=C2S" .SS>C2."2>6 C2"2C./C.; D>Q

    :C2;"J >A 26";6S2V; C.;

    =;D2C26; 2SCC= P>

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