HOW I TREAT IDIOPATHICHOW I TREAT IDIOPATHIC ...ocw.usu.ac.id/course/download/1110000096... ·...
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HOW I TREAT IDIOPATHICHOW I TREAT IDIOPATHICHOW I TREAT IDIOPATHIC HOW I TREAT IDIOPATHIC THROMBOCYTOPENIC PURPURATHROMBOCYTOPENIC PURPURA
Dauglas B. Cines, James B Bussel. Dauglas B. Cines, James B Bussel. Blood Oktober 2005:106(7):2244Blood Oktober 2005:106(7):2244--22512251
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INTRODUCTION
TO SET FORTH APROACH TO MANAGING ADULTS TO SET FORTH APROACH TO MANAGING ADULTS PRIMARY (AUTOIMMUNE) ITP FROM ASH & THE BRITISH PRIMARY (AUTOIMMUNE) ITP FROM ASH & THE BRITISH ( )( )COMMITTEE FOR STANDARDS IN HAEMATOLOGY COMMITTEE FOR STANDARDS IN HAEMATOLOGY GENERAL HAEMATOLOG Y TASK FORCEGENERAL HAEMATOLOG Y TASK FORCE :
1.WHO DEVELOPS ITP ?1.WHO DEVELOPS ITP ?2.HOW DIAGNOSIS ITP ?2.HOW DIAGNOSIS ITP ?3 WHO WE TREAT ITP3 WHO WE TREAT ITP3.WHO WE TREAT ITP3.WHO WE TREAT ITP4.ITP AND PREGNANCY4.ITP AND PREGNANCY
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WHO DEVELOPS ITP ?
TYPICAL ITP : ADULT WOMANTYPICAL ITP : ADULT WOMANAGE : BETWEEN 18 AND 40 YEARS AGE : BETWEEN 18 AND 40 YEARS
TWO PUBLICATION HAVE QUESTIONED THISTWO PUBLICATION HAVE QUESTIONED THISTWO PUBLICATION HAVE QUESTIONED THIS TWO PUBLICATION HAVE QUESTIONED THIS PERCEPTION : PERCEPTION :
DENMARK (SURVEY) DENMARK (SURVEY) THE FEMALETHE FEMALE MALE RATIO =1 7 : 1MALE RATIO =1 7 : 1--THE FEMALETHE FEMALE--MALE RATIO =1. 7 : 1MALE RATIO =1. 7 : 1
--MEDIAN AT DIAGNOSIS 56 YEARSMEDIAN AT DIAGNOSIS 56 YEARS
ENGLAND (PROSPECTIVE COHORT)ENGLAND (PROSPECTIVE COHORT)(PLATELET (PLT) < 50.000X10(PLATELET (PLT) < 50.000X1099/L/L
--THE FEMALETHE FEMALE--MALE RATIO =1.2 : 1MALE RATIO =1.2 : 1--HIGHEST >60 YEARSHIGHEST >60 YEARS
Frederiksen H, Schmidt. The Incidence of Idiophatic Thrombocytopenic Purpura in Adult Increase with age. ASH 1999: 909-913 (1)
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Cines D.B. Blanchette V.S. Immune Thrombocytopenic. N Engl J Med. March,2002:995-1008George JN, el Harake MA, Aster RH. Thrombocytopenia due to enhanced platelet destruction By immunologic mechanism, in Beutler E, Litchmann MA, Coller BS, Kipps TJ. (eds): William Hematology Ne York NY McGra Hill 1995:p1315
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HOW WE DIAGNOSE ITPHOW WE DIAGNOSE ITP
-- DIAGNOSIS OF EXCLUSION DIAGNOSIS OF EXCLUSION -- ESSENSIAL ELEMEN : ISOLATED THROMBOCYTOPENIA,ESSENSIAL ELEMEN : ISOLATED THROMBOCYTOPENIA,ESSENSIAL ELEMEN : ISOLATED THROMBOCYTOPENIA, ESSENSIAL ELEMEN : ISOLATED THROMBOCYTOPENIA,
PERIFERAL SMEAR (UNREMARKABLE), PERIFERAL SMEAR (UNREMARKABLE), -- PHYSICAL EXAMINATION (BLEEDING CONSISTENT PHYSICAL EXAMINATION (BLEEDING CONSISTENT
WITH PLT COUNT)WITH PLT COUNT)WITH PLT COUNT)WITH PLT COUNT)
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Stasi R, Provan D. Management of Immune Thrombocytopenic Purpura in AdultMayo Clin Proc. 2004;79:504-522
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-- BMP (RUTINE)BMP (RUTINE)TYPICAL PATIENT 60 YEARSTYPICAL PATIENT 60 YEARS> TYPICAL PATIENT >60 YEARS> TYPICAL PATIENT >60 YEARS
> DON`T SHOW A ROBUST RESPONSE (PLT>50.000) > DON`T SHOW A ROBUST RESPONSE (PLT>50.000) > PRIOR SPLENECTOMY> PRIOR SPLENECTOMY> EVALUATION OF RESPONSE IVIG, anti> EVALUATION OF RESPONSE IVIG, anti--D D > POOR RESPONSE TREATMENT> POOR RESPONSE TREATMENT
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WHO WE TREATWHO WE TREAT
PLT <20.000/MM3 WITH BLEEDING MANIFESTATION OR NOTWITH BLEEDING MANIFESTATION OR NOT
10-YEAR STUDY OF 310 PT (PLT<30.000)1 HEMORRHAGIC DEATH1 HEMORRHAGIC DEATH
META-ANALYSIS OF 17 STUDIES, THE AGE ADJUSTED ,RISK OF FATAL HEMORHAGE WITH PLT <30.000
<40 Y 0 4%<40 Y 0,4%, 40-60 Y 1,2%, >60 Y 13%5Y MORTALITY 2 2 TO 47 8%5Y MORTALITY 2,2 TO 47,8%
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TREATMENT AT PRESENTATIONTREATMENT AT PRESENTATION
PRINCIPLES OF MANAGEMENT
PLT<20.000, WITH PETECHIAE OR PURPURA, THE ONSET MORE OFTEN INSIDIOUS THAN PREVIOUSLY
PLT<10.000, SEVERE CUTANEOUS BLEEDING,PROLONGE EPISTAXIS, GINGGIVA BLEEDING, OVERT HEMATURIA, OR MENORRHAGIAOR MENORRHAGIA
PLT COUNTS : 10.000-20.000, SPONTANEOUS BLEEDING30.000 TO 50.000, MAY NOT EASY BRUISING>50.000, DISCOVERED INCIDENTALLY50 000, SCO C
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PLT COUNT : ≥30.000 INITIAL GOAL OF TREATMENTINITIAL GOAL OF TREATMENT
PLT 20 000 TO 50 000PLT 20.000 TO 50.000 IMMIDIATE TH/ IS NOT REQUIRED.IN ABSENCE OF BLEEDING OR PREDISPOSING COMORBID UNCONTROLED HT, ACTIVE PEPTIC ULCER DISEASE , ANTICOAGULATION, RECENT SURGERY OR HEAD TRAUMA.SURGERY OR HEAD TRAUMA.
PLT 40.000 TO 50.000, RECOMMENDED REQUIRING ASPRIN NSAIDRECOMMENDED, REQUIRING ASPRIN, NSAID, WARFARIN, OR ATHER ANTITHROMBOTICS.
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Cines D.B. Blanchette V.S. Immune Thrombocytopenic. N Engl J Med. March,2002:995-1008
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Cines D.B. Blanchette V.S. Immune Thrombocytopenic. N Engl J Med. March,2002:995-1008
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HOSPITALIZATION AND EMERGENCY THERAPYHOSPITALIZATION AND EMERGENCY THERAPY
HOSPITALIZED :HOSPITALIZED :1.PROFOUND MUCUCUTANEOUS OR INTERNAL BLEEDING 2.PLT ≤20.000
BLEEDING & HISTORY OF SIGNIFICANT COMPLIANCERESPON TH/ HAS NOT BEEN ESTABLISHED
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REDUCE RISK OF BLEEDING (GENERAL):( )-CESSATION OF DRUG THAT IMPAIR PLT FUNCTION-CONTROL BP-MINIMIZE TRAUMA-MINIMIZE TRAUMA
-REDUCE MUCOSAL BLEEDING E AMINOCAPROIC ACID ( 100 /KB LOADING DOSEE-AMINOCAPROIC ACID ( 100mg/KB LOADING DOSE UP TO MAX OF 5 gr IV OVER 30-60 MNT FOLLOW UP BY 5 gr EVERY 6 H IV OR ORALLY (MAX DOSE=24 gr/DAY)g ( g / )
TRANEXAMIC ACID
DESMOPRESSIN ACETAT (DDAVP; 0,3 ug/KB)
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INITIAL THERAPY FOR NONEMERGENT INDICATIONSINITIAL THERAPY FOR NONEMERGENT INDICATIONS
THERE IS NO CONSENSUS OPTIMAL DURATION OF CORTICOSTEROIDCONTINUE FULL DOSE FOR 3 to 4 WEEKSTAPERRING PREDNISON SLOWLY, ONCE DOSES OF10 MG/DAY ARE REACHED10 MG/DAY ARE REACHED
RESPON RATE 50-90% STABEL REMISI 10 30%STABEL REMISI 10-30%
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PERSISTEN ITPPERSISTEN ITP
THROMBOCYTOPENIA RECURS WHEN CORTICOSTEROIDTHROMBOCYTOPENIA RECURS WHEN CORTICOSTEROID ARE TAPEREDTARGET PLT > 20.000 to 30.000
MAYOR DECISION : SPLENECTOMY
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