Marks Kristen M, Clarke Robin M A, Bussel James B, Talal Andrew H, Glesby Marshall J
Division of Infectious Diseases, Department of Medicine, Weill Cornell Medical College, New York, NY 10065, USA.
J Acquir Immune Defic Syndr. 2009 Dec;52(5):595-9. doi: 10.1097/QAI.0b013e3181b79aff.
Before potent antiretroviral therapy, thrombocytopenia was observed frequently. Little is known about risk factors for or severity and consequences of thrombocytopenia since establishment of highly effective therapy for HIV.
We conducted a retrospective-matched case-control study of HIV-infected adult outpatients with and without thrombocytopenia to elucidate the contribution of HIV viremia, hepatitis C infection, and other potential risk factors for thrombocytopenia. Seventy-three cases with thrombocytopenia (platelet count <100 x 10(9)/L persistent for >3 months) were matched by age, sex, and first clinic visit with 73 nonthrombocytopenic controls. Risk factors and outcomes were assessed using conditional logistic regression.
Nadir platelet counts in cases were <or=50 x 10(9)/L in 58% and <or=30 x 10(9)/L in 38%. In multivariate modeling, HIV RNA >400 copies/ml, hepatitis C virus infection, and cirrhosis were significantly associated with thrombocytopenia with adjusted odds ratios of 5.3 [confidence interval (CI) 1.6-17.1, P = 0.006], 6.1 (CI 1.6-22.6, P = 0.007), and 24.0 (CI 1.7-338, P = 0.019), respectively. Thrombocytopenia was significantly associated with major bleeding events and nonbleeding-related death.
Thrombocytopenia in the era of potent antiretroviral therapy is associated with hepatitis C virus infection, cirrhosis, and uncontrolled HIV replication, and serious complications including major bleeding and death.
在强效抗逆转录病毒治疗之前,血小板减少症很常见。自从建立了针对HIV的高效治疗方法后,对于血小板减少症的危险因素、严重程度及后果了解甚少。
我们对有和没有血小板减少症的HIV感染成年门诊患者进行了一项回顾性匹配病例对照研究,以阐明HIV病毒血症、丙型肝炎感染及其他血小板减少症潜在危险因素的作用。73例血小板减少症患者(血小板计数<100×10⁹/L持续超过3个月)按年龄、性别和首次就诊情况与73例非血小板减少症对照进行匹配。使用条件逻辑回归评估危险因素和结局。
病例组的最低血小板计数在58%的患者中≤50×10⁹/L,在38%的患者中≤30×10⁹/L。在多变量模型中,HIV RNA>400拷贝/ml、丙型肝炎病毒感染和肝硬化与血小板减少症显著相关,调整后的优势比分别为5.3[置信区间(CI)1.6 - 17.1,P = 0.006]、6.1(CI 1.6 - 22.6,P = 0.007)和24.0(CI 1.7 - 338,P = 0.019)。血小板减少症与严重出血事件和非出血相关死亡显著相关。
在强效抗逆转录病毒治疗时代,血小板减少症与丙型肝炎病毒感染、肝硬化及未控制的HIV复制相关,且与包括严重出血和死亡在内的严重并发症相关。