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NG GI NGUY C
d ng
AVK
Cc ch t AVK ( nh gi tc d ng b ng INR) Giao thoa v i cc y u t ng mu ph thu c Vit.K (II, VII, IX, X, protein C v S) Fenprocoumon (Marcoumar) Warfarine (Marevan) Acenocoumarol (Sintrom) Phenindione (Pindione) Ch t i khng: Vit. K Ph c h p Prothrombin (PPSB: Prothrombin, Proconvertin, y u t Stuart, hemophilia B)
American Heart Association/American College of Cardiology Foundation Guide to Warfarin Therapy - 2010 BN c nguy c huy t kh i thuyn t c th p
(khng c huy t kh i-thuyn t c TM g n y, Rung nh - Li u warfarin c th gi m 4 - 5 ngy tr khi ph u thu t). n thu n...): c ph u thu t (INR 1.3 - 1.5
- Li u duy tr c a warfarin c dng tr l i sau ph u thu t cng v i li u th p heparin (5000 U) ho c LMWH tim DD m i 12g n u c n thi t.
- Heparine tr c ph u thu t v i li u d phng 5000 U (ho c LMWH 3000 U) tim DD m i 12g. -Heparin (ho c LMWH) v i li u d phng c th c cho l i 12g sau ph u thu t cng v i warfarin v ti p t c trong 4-5 ngy n khi INR t yu c u. N u BN c nguy c cao ch y mu sau ph u thu t th heparin ho c LMWH c th tri n h n 24g ho c lu h n.
-Heparin li u i u tr (15 000 U m i 12g TDD) ho c LMWH (100 U/kg m i 12g TDD), ng ng 24g tr c ph u thu t. - Tr ng h p c n ch ng ng m nh tr c ph u thu t: heparin v i li u t n cng (1300 U/h) chuy n TM lin t c v ng ng 5g tr c ph u thu t, aPTT c th tr v m c c b n tr c ph u thu t. Heparin ho c LMWH c th c dng l i v i li u d phng 12g sau ph u thu t cng v i warfarin v ti p t c cho n khi INR t y uc u
Ng ng AVK bao lu tr
c ph u thu t ?
Fenprocoumon (Marcoumar) 10 ngy (t1/2: 4-7 ngy) Warfarin (Marevan) 7 ngy (t1/2: 20-60 gi ) Acenocoumarol (Sintrom) 4 ngy (t1/2: 8-11 gi )
Unfractionated Heparin
Advantages
Immediate anticoagulation Multiple sites of action in coagulation cascade Long history of successful clinical use Readily monitored by aPTT and ACT
Disadvantages
Indirect thrombin inhibitor so does not inhibit clot-bound thrombin Nonspecific binding to: Serine proteases Endothelial cells (can lead to variability in level of anticoagulation) Reduced effect in ACS Inhibited by PF-4 Causes platelet aggregation Nonlinear pharmacokinetics Risk of HIT
Hirsh J, et al. Circulation. 2001;103:2994-3018. aPTT = activated partial thromboplastin time; ACT = activated coagulation time; PF-4 = platelet factor 4; HIT = heparin-induced thrombocytopenia.
Low-Molecular-Weight Heparin
Advantages
Increased anti-Xa to anti-IIa activity p inhibits thrombin generation more effectively Induces release of TFPI vs UFH Not neutralized by platelet factor 4 Less binding to plasma proteins (eg, acutephase reactant proteins) p more consistent anticoagulation Lower rate of HIT vs UFH Lower fibrinogen levels Easy to administer (SC administration) Long history of clinical studies and experience, FDA-approved indications Monitoring typically unnecessary
Disadvantages
Indirect thrombin inhibitor Less reversible Difficult to monitor (no aPTT or ACT) Renally cleared Long half-life Risk of HIT
Hirsh J, et al. Circulation. 2001;103:2994-3018. TFPI = tissue factor pathway inhibitor; UFH = unfractionated heparin; SC = subcutaneous; aPTT = activated partial thromboplastin time; ACT = activated coagulation time.
THU C KHNG TI U C U
Acetylsalicylic acid (ASA) Aspirine Thienopyridines Ticlopidin Clopidogrel Prasugrel i khng th th GP IIB/IIIA Abciximab Eptifibatide Tirofiban
Thu c khng TC v ch y mu trong khi ph u thu t Thienopyridines T ng ch y mu v c n chuy n mu trong PT tim Ng ng tr c khi ph u thu t Dng l i cng s m cng t t Tr ng h p c bi t: H i ch ng vnh c p, v a m i t stent MV
V n
thu t.
Ng ng thu c clopidogrel v chuy n sang thu c khng ti u c u tc d ng ng n hay thu c khng thrombin . Ng ng clopidogrel v dng l i sau ph u thu t.
Brilakis.E.S et al: Perioperative management of patients with coronary stent. JACC 2007, 49: 2145-2150.
V n
Ti p t c hai thu c ch ng ti u c u trong v sau th thu t: - B nh nhn tr i qua ph u thu t s m sau t stent ( nguy c huy t kh i cao). - Nh ng th thu t c th c m mu t i ch nh nh r ng,ph u thu t da, th y tinh th . - C n tham kh o cc ph u thu t vin l ng gi nguy c ch y mu c a ph u thu t, qua cn nh c gi a l i ch v nguy c c a vi c dng thu c. - Khng p d ng cho ph u thu t n u ch y mu d n n h u qu nghim tr ng (PT th n kinh)
Brilakis.E.S et al: Perioperative management of patients with coronary stent. JACC 2007, 49: 2145-2150.
V n
Ng ng thu c clopidogrel v chuy n dng thu c khng ti u c u tc d ng ng n hay thu c ch ng ng: ng dng l c ch glycoprotein IIb/IIIa hay antithrombin. antithrombin.
-Thu c th
- Dng l i clopidogrel cng s m cng t t sau ph u thu t. t. - Th ng dng khi ph i ph u thu t s m (cc PT c nguy c ch y mu cao) sau t stent v c n ph i ng ng clopidogrel. cao) clopidogrel.
Brilakis.E.S et al: Perioperative management of patients with coronary stent. JACC 2007, 49: 2145-2150.
V n
v nguy c
c ny v nguy c
Ng ng Clopidogrel lc no ?
- Thay th b ng LMWH:
Nguy c cao: li u t n cng 100ui/kg x 2/ngy TDD Nguy c trung bnh: li u trung gian 3000ui x 2/ngy TDD Nguy c th p: li u d phng 50ui/kg x 1/ngy TDD
K T LU N 2: Thu c khng ti u c u
Aspirine: - D phng tin pht: ng ng 5-7 ngy - D phng th pht: khng c n ng ng, ngo i tr PT th n kinh, cc khoang kn Clopidogrel: - Ng ng 5 ngy - Thay b ng cc thu c c ch GP IIB/IIIA tr ng l ng phn t th p ho c LMWH
K T LU N 3:
Nguy c huy t kh i cao: Ph i h p ASA v i c ch GPIIB/IIIA Ph i h p LMWH v i c ch GPIIB/IIIA
XIN C M N