Benton R E, Gersh B J
Department of Medicine, Georgetown University Medical Center, Washington, DC 20007, USA.
South Med J. 1998 Feb;91(2):133-7. doi: 10.1097/00007611-199802000-00002.
Heparin-induced thrombocytopenia (HIT) is classified as two distinct entities: HIT I and HIT II. HIT I is mild thrombocytopenia that occurs in approximately 25% of patients within the first 5 days of starting therapy and is clinically benign. HIT II is a syndrome of severe thrombocytopenia and thrombosis that occurs 6 days to 14 days into therapy in about 2% of patients and is associated with considerable morbidity and mortality. The severe form of HIT appears to be due to antibodies directed against a complex of heparin and platelet factor 4 (PF4) that leads to platelet activation, endothelial injury, and thrombosis. Treatment is problematic, but heparin administration must be immediately discontinued. In uncontrolled trials, agents such as warfarin, hirudin, and danaparoid have shown some efficacy. Early recognition by monitoring daily platelet counts during therapy may decrease the incidence of thrombosis.
肝素诱导的血小板减少症(HIT)分为两种不同类型:I型HIT和II型HIT。I型HIT是轻度血小板减少症,约25%的患者在开始治疗的前5天内出现,临床症状良性。II型HIT是一种严重血小板减少症和血栓形成综合征,约2%的患者在治疗6天至14天出现,与相当高的发病率和死亡率相关。严重形式的HIT似乎是由于针对肝素与血小板第4因子(PF4)复合物的抗体导致血小板活化、内皮损伤和血栓形成。治疗存在问题,但必须立即停止使用肝素。在非对照试验中,华法林、水蛭素和达那肝素等药物已显示出一定疗效。通过在治疗期间每日监测血小板计数进行早期识别,可能会降低血栓形成的发生率。