02__SIROSIS HEPATIS

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    Liver Cirrhosis

    Dr. Soegiarto Gani, SpPD

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    Causes of Cirrhosis Viral hepatitis; B, D, and C

    Alcohol

    Metabolic

    Haemochromatosis

    Wilsons disease

    lpha!"!antitr#psin deficienc#

    Chronic biliary obstruction

    $%trahepatic &iliar# o&struction

    'ntrahepatic &iliar# o&struction

    Venous outflow obstruction

    (eno!occlusive disease

    )udd!Chiari s#ndrome

    Cardiac failure Autoimmune chronic active hepatitis

    Drug and toxins

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    Complications of Cirrhosis

    Variceal bleeding

    Ascites, refractory ascites

    Hepatorenal syndrome

    Hepatic encephalopathy

    Spontaneous bacterial peritonitis Hepatocelluler carcinoma

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    Causes of death

    Variceal hemorrhage

    pontaneous bacterial peritonitis

    epsis

    !iver failure

    "epatic coma #unctional renal failure

    "epatocelluler carcinoma

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    Continuing Liver damage

    Nodular regeneration

    Fibrosis

    Increased sinusoidal

    pressure

    Portal Hypertension

    Splancnic vasodilatation Increased gastroesophageal

    collateral

    Formation of

    oesophagogastric varices

    Decreased effective bloodvolume

    Variceal rupture

    Variceal bleeding

    Increased sodium retention

    scites

    Portal H#pertension S#ndrome

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    (ariceal )leeding

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    A.A. Bleeding from varises is reported in about 20 60Bleeding from varises is reported in about 20 60

    % of case whit cirrhosis.% of case whit cirrhosis.

    B.B. Mortality of the first bleeding episode is around 0Mortality of the first bleeding episode is around 0%%

    !.!. "p to #0 % $f atient &hoo do not receive"p to #0 % $f atient &hoo do not receive

    treatment die within ' year of the initial bleedingtreatment die within ' year of the initial bleedingepisodeepisode

    reventime measure rationalto avoid developmentreventime measure rationalto avoid developmentof (arices and bleeding )rimary proplylaris*.of (arices and bleeding )rimary proplylaris*.

    +he ,fforts in preventing bleeding seems to be+he ,fforts in preventing bleeding seems to becrucial )secondary- prophylais*crucial )secondary- prophylais*

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    !onsensus in ortal /ypertension Baveno !onsensus in ortal /ypertension Baveno

    Monitoring for the 1evelopment of (arices in the

    ortal /ypertensive atient.'. All cirrhotic patients should be screened for thepresence of varices at the time of the initialdiagnosis of cirrhosis.

    2. n compensated patients without varices- endoscopy

    should be repeated at 23 year intervals toevaluate the development of varices.

    3. n compensated patients with small varices-endoscopyshould be repeated at 2 year intervals to

    evaluate progression of varices.4. +here is no indication for subse5uent evaluationsonce large varices are detected.

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    Algorithm for cirrhosis $ithout Bleeding

    Algorithm ForCirrhosis Without

    BleedingCirrhosis

    !stablished

    Reguler Interval

    Usually one week

    "pper !ndoscopy

    %o varices mall or Medium

    VaricesLarge Varices

    #bserve#bserve

    $% & ' years !valuation(Primary )leeding

    Prophyla*is

    %on electne Bloc&ers

    'and (or long actmy %itrates) !igation

    (2 3 years Evaluation)

    lgorithm *or )leeding Cirrhotis

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    lgorithm *or )leeding Cirrhotis

    Algorithm #or

    Bleeding CirrhotisResuscitaeBegin Octreotide

    (or Vasopressin)

    Early endoscopy

    on!"ortal

    #ypertensiveCause

    Gastric (arices Esop$agel

    Varices"ortal

    #ypertensive

    %astropat$y

    +reat appropriatelyContinue octreotide * days)egin beta,bloc-er .hen stable

    )and ligation or in+ection

    Sclerotheraph#

    )allon amponade

    -e&leeding o re&leeding

    '$unt ($ild )

    *i"''+ or,iver transplantation ($ild B or )

    ontinue treat-ent

    "reventation o. Re&leeding Pharmacological +reatment/ Ligation /Sclerotheraphy

    Reguler Interval

    Usually one week

    Repeated Endoscopy

    3 0 -ont$

    Eradication

    '$unt ($ild )

    *I"'' or ,iver transplantation($ild B or )

    Re&leeding

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    Dosis dan cara pem&erian o&at!o&at vasoatif pada

    perdarahan varises+bat Cara pemberian Dosis !ama

    pemberianVasopressin

    'V) -

    %itroglyserin

    '%.)

    V/ i0v infus

    %./

    percutaneus,

    bolus

    V/

    1,233(menit

    24 5am

    6erlipressin i0v, bolus 7 mg(2 5am

    selama 72824

    5am pertama,

    &emudian 9

    mg( 2 5am

    78* hari

    omatostatin i0v bolus dan

    infus

    7*1 ug dii&uti

    7*18*11 ug(5am

    78* hari

    +ctreotide i0v, bolus dan

    infus

    *1 ug dii&uti

    *1 ug(5am

    78* hari

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    Spontaneus )acterialis

    Peritonitis

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    Cirrhotic patients at high ris of S)P

    Hospitali/ed cirrhotic patients 0ith ascites and lo0 ascitic

    fluid total protein 12 " g3dl4

    Cirrhotic patients 0ith gastrointestinal hemorrhage

    Cirrhotic patients 0ith lo0 ascitic fluid total protein 12 "

    g3dL4 and 3 or high serum &iliru&in 156.7 mg3dl4

    Survivors of an episode of S)P.

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    Pasien sirosis hati dengan asites

    Nyeri perut panas 0e1ala menyertai2Syo-3 perdarahan3 gangguan

    -esadaran3 gangguan

    motilitas3 hipotensi3 dll

    simtomati-4

    Pungsi asites

    Pungsi asites2peri-sa2 P5N

    6ultur

    Sel P5N 7 '89 Sel P5N : '89

    )5NN

    $)a-terasites 5onomi-robial

    Non,Neutrosisti-(

    6ultur ; 5onomi-robial

    P)S

    6ultur ; 5onomi-robial

    "langi pungsi

    '< 1am

    Diagnosis Peritonitis )aterialis Spontan

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    P)S simtomati- Profila-sis P)S

    #flo-sasinSiproflo-sasin

    Dosis standar

    8,= hari

    ntibioti- pilihan 2

    Sefota-sim %,' gram/hari selama 8,= hari

    mo-sisilin;sam -lavulanat selama 8,= hari

    Parasentesis ulang setelah '< 1am

    antibioti-

    Sel P5N Sel P5N

    0anti antibioti-ntibioti-

    diterus-an

    Penatalasanaan Peritonitis )aterialis Spontan

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    H$P8-$9L S:9D-8;$

    P h i f H l S d

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    Cirrhosis

    Splanchnic vasodilatation

    rterial underfilling

    )aroreceptor,mediated

    activation of systemic

    Vasoconstriction factors

    >enal vasoconstriction

    Hepatorenal syndrome

    >educed renal

    vasodilator factors

    Increased intrarenal

    vasoconstriction

    factors

    Sinusoidal portal

    hypertension

    Pathogenesis of Hepatorenal S#ndrome

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    H$P8C$LL

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    reatment of HCC depends on

    1. Local resources2. Stage of the disease

    3. Presence of cirrhosis

    Liver ransplantation

    Hepatic resection treatment of choice for the

    fe0 patients 0ith HCC and normal liver.

    rans rterial Chemo $m&oli/ation

    C#tostatica

    'nterferon

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    *ive #ears survival of pts 0ith HCC treated

    transplantation in =6 $uropeans centers &et0een ">== and

    +une ">>?

    :ndication to transplantation atients Alive

    HCC 0ith Cirrhosis @A" ?A

    HCC 0ithout cirrhosis ??A @?

    Cirrhosis 0ith HCC "BA 7?

    p .?

    from $uropean ransplantation -egister

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    E$S';P

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