Ganzer D, Gutezeit A, Mayer G, Greinacher A, Eichler P
Klinik und Poliklinik für Orthopädie, Ernst-Moritz-Arndt-Universität Greifswald.
Z Orthop Ihre Grenzgeb. 1997 Nov-Dec;135(6):543-9. doi: 10.1055/s-2008-1039743.
A life-threatening complication of the thrombembolism prophylaxis with heparin is heparin-induced thrombocytopenia (HIT) type II. HIT type II is based on immunological mechanisms. Even low, subcutaneously applied doses may produce HIT type II. In those patients, continued application may cause thromboembolic complications. The most important symptom of HIT type II is a decrease of platelets.
In a prospective study, we investigated the incidence of HIT type II within the period from 01.07.95 to 30.06.96 in orthopedic patients. We also evaluated the importance of the daily platelet count from the fifth postoperative day for the early diagnosis of HIT type II and a possible reduction of the thrombosis rate. The study included 307 patients after primary implantation of hip and knee endoprosthesis and after hip endoprosthesis replacement. All patients received 3 x 5000 IU/d of unfractionated heparin subcutaneously. Whenever there was a decrease of platelets of at least 50% in relation to the preoperative value or whenever thrombembolic complications occurred, serum was analyzed by the heparin-induced platelet activation test (HIPA).
20 patients developed HIT type II. This corresponds to an incidence of 6.5%. 10 of the HIT type II antibody positive patients (50%) developed thrombembolic complications. 3 patients (0.9%) of the group studied developed clinically symptomatic thrombembolic complications without evidence of heparin antibodies. The total risk of getting thrombembolic complications was 4.2% (13 patients). 3.3% (10 patients) of the entire group developed HIT type II antibody associated thrombembolic complications; 1 patient died. The lethality in the HIT type II antibody positive patient group amounted to 5%. The patients with HIT type II received LMW heparinoid Orgaran (AKZO-Organon, The Netherlands) or hirudin (as a clinical trial). The comparison group (retrospective study from 17.10.92 to 16.10.93) was composed of 262 patients with the same operations and equal thromboembolism prophylaxis. The platelet count was made only as part of routine diagnostic tests. 21 patients (8.0%) developed clinically symptomatic thrombembolic complications. The difference in the thrombosis rate between these two groups of patients is statistically significant. Unrecognized HIT type II is probably the reason for the high thrombembolic complication rate in the comparison group.
The daily platelet count from the fifth postoperative day and from the first day in case of reexposure to heparin is an important measure for the early diagnosis of HIT type II.
肝素用于预防血栓栓塞的一种危及生命的并发症是II型肝素诱导的血小板减少症(HIT)。II型HIT基于免疫机制。即使是皮下注射的低剂量肝素也可能引发II型HIT。对于这些患者,继续使用肝素可能会导致血栓栓塞并发症。II型HIT最重要的症状是血小板减少。
在一项前瞻性研究中,我们调查了1995年7月1日至1996年6月30日期间骨科患者中II型HIT的发生率。我们还评估了术后第五天开始每日进行血小板计数对于II型HIT早期诊断以及可能降低血栓形成率的重要性。该研究纳入了307例初次植入髋膝关节假体以及髋关节假体置换术后的患者。所有患者均接受皮下注射3×5000IU/d的普通肝素。每当血小板计数相对于术前值至少降低50%或出现血栓栓塞并发症时,均通过肝素诱导的血小板活化试验(HIPA)对血清进行分析。
20例患者发生了II型HIT。这对应于6.5%的发生率。10例II型HIT抗体阳性患者(50%)发生了血栓栓塞并发症。研究组中有3例患者(0.9%)出现了临床症状性血栓栓塞并发症,但未检测到肝素抗体。发生血栓栓塞并发症的总风险为4.2%(13例患者)。整个研究组中有3.3%(10例患者)发生了与II型HIT抗体相关的血栓栓塞并发症;1例患者死亡。II型HIT抗体阳性患者组的死亡率为5%。发生II型HIT的患者接受了低分子肝素类药物Orgaran(荷兰阿克苏诺贝尔公司生产)或水蛭素(作为一项临床试验用药)。对照组(1992年10月17日至1993年10月16日的回顾性研究)由262例接受相同手术且血栓栓塞预防措施相同的患者组成。血小板计数仅作为常规诊断检查的一部分。21例患者(8.0%)出现了临床症状性血栓栓塞并发症。这两组患者的血栓形成率差异具有统计学意义。未被识别的II型HIT可能是对照组中血栓栓塞并发症发生率高的原因。
术后第五天起每日进行血小板计数,以及再次使用肝素时从第一天起每日进行血小板计数,是II型HIT早期诊断的重要措施。