Hyogo Prefectural Awaji Hospital, Sumoto, Hyogo, Japan.
Clin Appl Thromb Hemost. 2013 Jan-Feb;19(1):73-8. doi: 10.1177/1076029612436676. Epub 2012 Feb 16.
A retrospective study was performed to elucidate the characteristics of heparin-induced thrombocytopenia (HIT) in newly treated hemodialysis (HD) patients who essentially required anticoagulation with unfractionated heparin (UFH). Seventy-eight patients suspected of having HIT within 3 months of starting HD with UFH were selected for this study. Their platelet counts were routinely followed, and anti-PF4/heparin complex antibodies (HIT antibodies) were measured with enzyme-linked immunosorbent assay (ELISA) until the titer became negative. The characteristics of thrombocytopenia were a platelet count of ≤150 × 10(9)/L and/or decrease of ≥30% and as caused by the intermittent use (3 times/a week) of UFH during HD. Fifty-five patients showed unexpected clotting in the extracorporeal circuit and/or arteriovenous fistula (AVF) thrombosis, while 23 patients had neither of these complications. The patients were classified into HD-related and non-HD-related thrombus groups. The impact of various combinations of the 3 clinical factors (thrombocytopenia, timing, and HD-related thrombus) and the results of ELISA as a laboratory factor were examined. A combination of 2 platelet factors (thrombocytopenia and timing) and ELISA positivity did not reveal the presence of HIT, while a combination of the 3 clinical factors and a positive ELISA improved the accuracy of HIT diagnosis. The findings on the 4-factor combination were supported by high rates of seroconversion in a serotonin release assay. Combining appropriate clinical factors and a positive ELISA may lead to the proper management of HD patients suspected of having HIT. In conclusion, while HD patients showed a drop of ≤150 × 10(9)/L or ≥30% on days 7 to 30, unexpected clotting in the circuit and/or AVF thrombosis was considered as a sign of HIT development.
一项回顾性研究阐明了新开始接受血液透析(HD)治疗且需要使用未分级肝素(UFH)抗凝的患者中肝素诱导的血小板减少症(HIT)的特征。本研究纳入了 78 例在开始使用 UFH 后 3 个月内怀疑患有 HIT 的患者。常规监测他们的血小板计数,并通过酶联免疫吸附试验(ELISA)检测抗 PF4/肝素复合物抗体(HIT 抗体),直至效价转为阴性。血小板减少症的特征为血小板计数≤150×10(9)/L 和/或下降≥30%,并由 HD 期间间歇性使用 UFH(每周 3 次)引起。55 例患者出现体外循环和/或动静脉瘘(AVF)血栓形成中意料之外的凝血,而 23 例患者均无这些并发症。将患者分为与 HD 相关和非 HD 相关血栓形成组。检查了各种组合的 3 个临床因素(血小板减少症、时间和与 HD 相关的血栓形成)和作为实验室因素的 ELISA 结果的影响。血小板因素(血小板减少症和时间)和 ELISA 阳性的 2 个组合并不能显示 HIT 的存在,而 3 个临床因素和 ELISA 阳性的组合则提高了 HIT 诊断的准确性。4 个因素组合的结果得到了在 5-羟色胺释放试验中高比例的血清转化的支持。将适当的临床因素与 ELISA 阳性相结合可能导致对疑似患有 HIT 的 HD 患者进行适当的管理。总之,当 HD 患者在第 7 至 30 天内血小板计数下降≤150×10(9)/L 或下降≥30%时,体外循环中意料之外的凝血和/或 AVF 血栓形成被认为是 HIT 发展的迹象。