Drew R H
Division of Infectious Diseases, Duke University Medical Center, Durham, NC 27710.
Ann Pharmacother. 1993 Dec;27(12):1510-8. doi: 10.1177/106002809302701218.
To review the pharmacotherapy of disseminated histoplasmosis (DH) in patients with AIDS. The article provides an overview of the pathophysiology, epidemiology, clinical presentation and diagnosis of this disease. Clinical trials reporting intervention with antifungal therapy are reviewed, with an emphasis on efficacy and toxicity of these agents.
A MEDLINE search from 1976 to the present was performed to identify pertinent biomedical literature, including reviews.
All available reviews and clinical trials in AIDS patients were evaluated, as were all available case series and interventional clinical trials.
DH in patients with HIV infection is an AIDS-defining opportunistic infection caused by Histoplasma capsulatum. It is most frequently observed in HIV-infected patients living in or traveling to endemic regions. The clinical presentation most often includes fever and weight loss, but may be complicated by comorbid illness such as other opportunistic infections. Diagnosis is best established by histologic examination of peripheral blood smear or bone marrow aspirate, or isolation of the organism in cultures of blood, bone marrow, and respiratory secretions. Serologic examinations may provide supportive diagnostic information. Detection of histoplasma polysaccharide antigen (HPA) in serum or urine may prove to be a promising approach for the rapid diagnosis and therapeutic monitoring of DH in AIDS patients. In contrast to immunocompetent hosts, high relapse rates are reported after therapy in AIDS patients. Therefore, initial (induction) therapy is routinely followed by long-term (maintenance) therapy to prevent relapse. Issues regarding the selection, dosage, and duration of therapy, as well as prophylaxis of patients at highest risk, still need to be addressed by controlled clinical trials.
Amphotericin B is presently the drug of choice for induction therapy. Maintenance therapy with either amphotericin B or an oral azole antifungal agent active against H. capsulatum is necessary to prevent relapse. Itraconazole, a triazole antifungal agent, may provide effective alternative therapy for both induction and maintenance treatment of DH.
回顾艾滋病患者播散性组织胞浆菌病(DH)的药物治疗。本文概述了该疾病的病理生理学、流行病学、临床表现及诊断。对报告抗真菌治疗干预情况的临床试验进行了综述,重点关注这些药物的疗效和毒性。
进行了一项从1976年至今的MEDLINE检索,以识别相关的生物医学文献,包括综述。
评估了所有关于艾滋病患者的可用综述和临床试验,以及所有可用的病例系列和干预性临床试验。
HIV感染患者的DH是由荚膜组织胞浆菌引起的一种定义艾滋病的机会性感染。它最常见于生活在或前往流行地区的HIV感染患者中。临床表现最常包括发热和体重减轻,但可能因合并其他机会性感染等疾病而复杂化。通过外周血涂片或骨髓穿刺的组织学检查,或在血液、骨髓和呼吸道分泌物培养中分离出该病原体,可最佳地确立诊断。血清学检查可提供支持性诊断信息。血清或尿液中组织胞浆菌多糖抗原(HPA)的检测可能被证明是艾滋病患者DH快速诊断和治疗监测的一种有前景的方法。与免疫功能正常的宿主相比,艾滋病患者治疗后复发率较高。因此,初始(诱导)治疗后通常接着进行长期(维持)治疗以预防复发。关于治疗的选择、剂量和持续时间以及对高危患者的预防等问题,仍需要通过对照临床试验来解决。
两性霉素B目前是诱导治疗的首选药物。使用两性霉素B或对荚膜组织胞浆菌有活性的口服唑类抗真菌剂进行维持治疗对于预防复发是必要的。三唑类抗真菌剂伊曲康唑可能为DH的诱导和维持治疗提供有效的替代疗法。