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接受齐多夫定治疗的晚期人类免疫缺陷病毒病患者鸟分枝杆菌复合群感染的发病率和自然史。齐多夫定流行病学研究组。

Incidence and natural history of Mycobacterium avium-complex infections in patients with advanced human immunodeficiency virus disease treated with zidovudine. The Zidovudine Epidemiology Study Group.

作者信息

Chaisson R E, Moore R D, Richman D D, Keruly J, Creagh T

机构信息

Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205.

出版信息

Am Rev Respir Dis. 1992 Aug;146(2):285-9. doi: 10.1164/ajrccm/146.2.285.

Abstract

To determine the incidence and natural history of Mycobacterium avium-complex infections in persons with advanced human immunodeficiency virus (HIV) infection, we studied a multicenter cohort of 1,020 persons with acquired immunodeficiency syndrome (AIDS) or the AIDS-related complex (ARC) and CD4 cell count < 0.250 x 10(9)/L initially treated with zidovudine between April 1987 and April 1988. M. avium-complex infections developed in 123 (12%) patients during follow-up, with a 2-yr actuarial risk of 19%. Patients with an initial diagnosis of Pneumocystis carinii pneumonia were more likely to develop M. avium-complex infections than patients with an initial diagnosis of another opportunistic disease or of ARC (p = 0.002). Individuals developing M. avium-complex infections had lower baseline CD4 cell counts, hematocrits, lymphocyte counts, and total white blood cell counts than those who did not develop M. avium-complex infection. During follow-up, individuals who developed M. avium-complex infections were more likely to have severe anemia, to experience zidovudine dose reductions, and to die than were patients without M. avium-complex (p < 0.001). By proportional hazards analysis, a baseline CD4 cell count < 0.100 x 10(9)/L, development of severe anemia, P. carinii pneumonia during follow-up, and zidovudine dose interruption were significantly associated with subsequently developing M. avium-complex infection. A proportional hazards analysis of survival showed that M. avium-complex infection, severe anemia, zidovudine dose interruption, occurrence of an opportunistic infection, CD4 cell count < 0.100 x 10(9)/L, baseline AIDS diagnosis, and transfusion independently predicted an increased risk of death.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

为确定晚期人类免疫缺陷病毒(HIV)感染者中鸟分枝杆菌复合群感染的发病率及自然病程,我们研究了一个多中心队列,该队列由1020例获得性免疫缺陷综合征(AIDS)或AIDS相关综合征(ARC)患者组成,其初始CD4细胞计数<0.250×10⁹/L,于1987年4月至1988年4月期间接受齐多夫定初始治疗。在随访期间,123例(12%)患者发生了鸟分枝杆菌复合群感染,2年精算风险为19%。初始诊断为卡氏肺孢子虫肺炎的患者比初始诊断为其他机会性疾病或ARC的患者更易发生鸟分枝杆菌复合群感染(p = 0.002)。发生鸟分枝杆菌复合群感染的个体,其基线CD4细胞计数、血细胞比容、淋巴细胞计数及总白细胞计数均低于未发生该感染的个体。随访期间,发生鸟分枝杆菌复合群感染的个体比未发生该感染的患者更易出现严重贫血、经历齐多夫定剂量减少及死亡(p < 0.001)。通过比例风险分析,基线CD4细胞计数<0.100×10⁹/L、发生严重贫血、随访期间发生卡氏肺孢子虫肺炎及齐多夫定剂量中断与随后发生鸟分枝杆菌复合群感染显著相关。生存的比例风险分析显示,鸟分枝杆菌复合群感染、严重贫血、齐多夫定剂量中断、机会性感染的发生、CD4细胞计数<0.100×10⁹/L、基线AIDS诊断及输血独立预测死亡风险增加。(摘要截短于250字)

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