Maddix D S, Tallian K B, Mead P S
Pharmacy Service (119), VA Medical Center, San Francisco, CA 94121.
Ann Pharmacother. 1994 Nov;28(11):1250-4. doi: 10.1177/106002809402801108.
To discuss the mechanism of action, in vitro and in vivo activity, pharmacokinetics, clinical trials, adverse effects, drug interactions, and dosage guidelines of rifabutin.
Pertinent literature published between 1982 and 1993 was identified via a MEDLINE search. Published proceedings of selected conferences were also reviewed.
Selected basic science, microbiologic, and pharmacokinetic articles were evaluated. Because only limited data regarding rifabutin were available in the literature, all clinical trials involving the use of rifabutin in the prevention of Mycobacterium avium complex (MAC) infection in AIDS patients were reviewed.
Rifabutin is a rifamycin derivative that was approved recently for the prevention of disseminated MAC disease in patients with advanced HIV infection. The drug has in vitro and in vivo activity against gram-positive bacteria, gram-negative bacteria, and mycobacteria. Two prospective, randomized, double-blind, placebo-controlled, multicenter trials demonstrated that rifabutin decreased the progression to MAC bacteremia in AIDS patients by about 50 percent. Adverse effects that resulted in the discontinuation of rifabutin prophylaxis occurred in 16 percent of patients. Rifabutin induces hepatic enzymes to a lesser extent than does rifampin, but dosage adjustment of drugs that are known to interact with rifampin may be required.
Rifabutin is the only drug shown to be effective in the prevention of MAC bacteremia in AIDS patients; therefore, it should be made available as a formulary agent. It may be reasonable to delay initiation of rifabutin prophylaxis until CD4 lymphocyte counts are less than 75-50/mm3.
探讨利福布汀的作用机制、体内外活性、药代动力学、临床试验、不良反应、药物相互作用及剂量指南。
通过医学文献数据库检索1982年至1993年间发表的相关文献。还查阅了选定会议的发表论文集。
对选定的基础科学、微生物学和药代动力学文章进行评估。由于文献中关于利福布汀的数据有限,因此对所有涉及利福布汀用于预防艾滋病患者鸟分枝杆菌复合体(MAC)感染的临床试验进行了综述。
利福布汀是一种利福霉素衍生物,最近被批准用于预防晚期HIV感染患者的播散性MAC病。该药物对革兰氏阳性菌、革兰氏阴性菌和分枝杆菌具有体内外活性。两项前瞻性、随机、双盲、安慰剂对照、多中心试验表明,利福布汀可使艾滋病患者发生MAC菌血症的进展降低约50%。16%的患者出现导致停用利福布汀预防治疗的不良反应。利福布汀诱导肝酶的程度比利福平小,但可能需要对已知与利福平相互作用的药物进行剂量调整。
利福布汀是唯一被证明对预防艾滋病患者MAC菌血症有效的药物;因此,应将其作为一种处方药物提供。在CD4淋巴细胞计数低于75 - 50/mm3之前延迟开始利福布汀预防治疗可能是合理的。