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Disseminated disease due to Mycobacterium avium complex in AIDS

机译:艾滋病中鸟分枝杆菌复合物引起的传播性疾病

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We retrospectively analysed 46 cases of disseminated infection with Mycobacterium avium complex (MAC) within a cohort of 702 HIV-infected patients in Edinburgh. Clinical features were compared with case-matched controls (AIDS cases without disseminated MAC), and survival and progression times were controlled for confounding variables that influence survival. Disseminated MAC was diagnosed antemortem in 18% of AIDS patients, and was the AIDS-defining diagnosis in 6% of all AIDS cases. Concomitant colonization of respiratory and gastrointestinal tracts was common (61% and 48%, respectively). In 58% of cases, CD4+ counts were < 10 cells/mm~3 (median 6 cells/mm~3). Weight loss, anaemia, leucopenia, and elevated liver transamin-ases and alkaline phosphatase were significantly more common among cases than controls. Therapy was given in 74%, and not tolerated in 32%. Following AIDS diagnosis, disseminated MAC incidence was 14% at one year, 25% at 2 years and 36% at 3 years. Median survival after disseminated MAC diagnosis was 6 months, with shorter survival in untreated cases. However, overall survival from AIDS diagnosis was not significantly different between patients who did or did not develop disseminated MAC. Disseminated MAC contributes significantly to AIDS morbidity, and its incidence increases with prolonged AIDS survival. Although survival following diagnosis is short, the development of disseminated MAC in AIDS probably does not affect overall survival. In cohorts with a low incidence, an alternative to prophylaxis might be surveillance and early diagnosis.
机译:我们回顾性分析了爱丁堡的702名HIV感染患者队列中的46例鸟分枝杆菌复合物(MAC)传播性感染。将临床特征与病例匹配的对照(没有传播性MAC的AIDS病例)进行比较,并控制生存和进展时间以控制影响生存的混杂变量。播散性MAC在18%的AIDS患者中被诊断为死前,在6%的AIDS患者中是定义AIDS的诊断。呼吸道和胃肠道的同时定植是常见的(分别为61%和48%)。在58%的病例中,CD4 +计数<10个细胞/ mm〜3(中位数为6个细胞/ mm〜3)。体重减轻,贫血,白血球减少以及肝转氨酶和碱性磷酸酶升高明显高于对照组。有74%的人接受了治疗,有32%的人没有接受治疗。艾滋病诊断后,一年中的传播性MAC发生率分别为14%,2年为25%和3年为36%。播散性MAC诊断后的中位生存期为6个月,未治疗病例的生存期较短。但是,在有或没有发展为弥散性MAC的患者之间,从AIDS诊断得出的总体生存率没有显着差异。传播的MAC显着增加了AIDS的发病率,并且其发病率随着AIDS存活时间的延长而增加。尽管诊断后的生存期很短,但在艾滋病中传播性MAC的发展可能不会影响总体生存期。在低发病率人群中,预防和预防的替代方法可能是监测和早期诊断。

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