Institut für Immunologie und Transfusionsmedizin, Ernst-Moritz-Arndt Universität, Greifswald, Germany.
Am Heart J. 2010 Aug;160(2):362-9. doi: 10.1016/j.ahj.2010.05.026.
Heparin-induced thrombocytopenia (HIT) is caused by anti-platelet factor 4/heparin (PF4/H) immunoglobulin (Ig) G antibodies, which activate platelets. In some patients, anti-PF4/H antibodies are already detectable before cardiac surgery. Whether preoperative presence of antibodies confers adverse prognosis and which particular antibody classes (IgG, IgA, IgM) might be implicated are unknown.
We prospectively screened 591 patients undergoing cardiopulmonary bypass surgery for heparin-dependent antibodies by PF4/H immunoassay (separately for IgG, IgA, and IgM) and platelet activation test at preoperative baseline and at days 6 and 10. All patients received heparin or low-molecular-weight heparin postsurgery regardless of antibody status and were followed for postoperative complications, frequency of HIT, length of hospital stay, and 30-day mortality.
Anti-PF4/H antibodies of any class were detected at preoperative baseline in 128 (21.7%) of 591 patients: IgG n = 44 (7.4%), IgA n = 36 (6.1%), and IgM n = 79 (13.4%); some patients had >1 antibody class. Neither IgG nor IgA was a risk factor for any adverse outcome parameter. However, preoperative presence of IgM antibodies was associated with an increased risk for nonthromboembolic complications (all complications combined: hazard ratio 1.73, 95% CI 1.15-2.61) and a longer in-hospital stay (P = .02), but without evidence for increased risk of thrombotic complications or subsequent HIT.
Patients with preoperative anti-PF4/H antibodies of IgG and IgA class are not at increased risk for thrombotic or nonthrombotic adverse events, whereas those with baseline anti-PF4/H IgM had an increased risk of nonthrombotic adverse outcomes but not of subsequent HIT or thrombosis. Because IgM antibodies do not cause HIT, they could represent a surrogate marker for other heparin-independent risk factors.
肝素诱导的血小板减少症(HIT)是由抗血小板因子 4/肝素(PF4/H)免疫球蛋白(Ig)G 抗体引起的,该抗体可激活血小板。在某些患者中,在心脏手术前就已经可以检测到抗 PF4/H 抗体。术前存在抗体是否会导致不良预后,以及哪些特定的抗体类别(IgG、IgA、IgM)可能与此相关,目前尚不清楚。
我们前瞻性地筛选了 591 名接受体外循环手术的患者,通过 PF4/H 免疫测定(分别检测 IgG、IgA 和 IgM)和血小板激活试验,在术前基线、第 6 天和第 10 天检测肝素依赖性抗体。所有患者术后均接受肝素或低分子肝素治疗,无论抗体状态如何,并随访术后并发症、HIT 发生率、住院时间和 30 天死亡率。
在 591 名患者中,术前基线检测到任何类别的抗 PF4/H 抗体 128 例(21.7%):IgG 44 例(7.4%)、IgA 36 例(6.1%)和 IgM 79 例(13.4%);一些患者存在 >1 种抗体类别。IgG 和 IgA 均不是任何不良结局参数的危险因素。然而,术前 IgM 抗体的存在与非血栓栓塞性并发症的风险增加相关(所有并发症合并:危险比 1.73,95%CI 1.15-2.61)和住院时间延长(P =.02),但没有证据表明血栓形成并发症或随后的 HIT 风险增加。
术前 IgG 和 IgA 类抗 PF4/H 抗体的患者发生血栓或非血栓不良事件的风险没有增加,而基线时抗 PF4/H IgM 抗体的患者发生非血栓不良事件的风险增加,但随后发生 HIT 或血栓形成的风险没有增加。由于 IgM 抗体不会引起 HIT,它们可能是其他肝素非依赖性危险因素的替代标志物。