Mallolas J, Zamora L, Gatell J M, Miró J M, Vernet E, Valls M E, Soriano E, SanMiguel J G
Infectious Disease Service, Hospital Clinic, Faculty of Medicine, University of Barcelona, Spain.
AIDS. 1993 Jan;7(1):59-64.
To compare the efficacy and tolerance of monthly aerosolized pentamidine versus cotrimoxazole versus dapsone plus pyrimethamine to prevent the initial episodes of Pneumocystis carinii pneumonia (PCP) in HIV-infected patients.
An open randomized clinical trial.
HIV-infected patients (n = 331) with CD4 cell counts < 200 x 10(6)/l or with AIDS but without a history of PCP or cerebral toxoplasmosis (CT) were randomized to receive pentamidine (300 mg every 4 weeks), cotrimoxazole (160/800 mg 3 days a week) or dapsone plus pyrimethamine (100 and 25 mg weekly). If immunoglobulin G (IgG) antibodies to Toxoplasma were present, patients in the first two groups were randomized further to 25 mg pyrimethamine per week or to no treatment.
The mean follow-up was 313 days (range, 30-670 days). The three groups were homogeneous for age, sex, risk group for HIV infection, initial CD4 cell count and mean follow-up. PCP developed in 16 patients, with an estimated cumulative probability of 5.3% at 1 year of follow-up. The PCP rate per year of observation, using an intention-to-treat analysis, was 5.6% [95% confidence interval (CI), 0.9-10.3], 3% (95% CI, 0-6.3) and 8.3% (95% CI, 2.8-13.8) in the groups treated with pentamidine, cotrimoxazole and dapsone plus pyrimethamine, respectively (P > 0.05). Moderate or severe side-effects were observed in one patient on pentamidine, 10 on cotrimoxazole and nine on dapsone plus pyrimethamine (P < 0.05); the study drug had to be discontinued in no, 10 and six patients, respectively (P < 0.05). Neither cotrimoxazole alone nor pyrimethamine combined with dapsone or cotrimoxazole prevented initial episodes of toxoplasmosis among patients with IgG antibodies to Toxoplasma gondii.
Low-dose thrice-weekly cotrimoxazole or weekly dapsone plus pyrimethamine was not significantly worse (differences > 15% would have been detected with 90% certainty) than monthly aerosolized pentamidine in preventing a first episode of PCP in patients at high risk, but aerosolized pentamidine was better tolerated.
比较每月雾化吸入喷他脒、复方新诺明、氨苯砜加乙胺嘧啶预防HIV感染患者卡氏肺孢子虫肺炎(PCP)初发的疗效及耐受性。
开放随机临床试验。
331例CD4细胞计数<200×10⁶/L或患有艾滋病但无PCP或脑弓形虫病(CT)病史的HIV感染患者被随机分为接受喷他脒(每4周300mg)、复方新诺明(每周3天,每次160/800mg)或氨苯砜加乙胺嘧啶(每周分别为100mg和25mg)治疗组。若存在抗弓形虫免疫球蛋白G(IgG)抗体,则前两组患者进一步随机分为每周25mg乙胺嘧啶治疗组或不治疗组。
平均随访313天(范围30 - 670天)。三组在年龄、性别、HIV感染风险组、初始CD4细胞计数及平均随访时间方面具有同质性。16例患者发生PCP,随访1年时估计累积发生率为5.3%。采用意向性分析,喷他脒组、复方新诺明组和氨苯砜加乙胺嘧啶组每年观察到的PCP发生率分别为5.6%[95%置信区间(CI),0.9 - 10.3]、3%(95%CI,0 - 6.3)和8.3%(95%CI,2.8 - 13.8)(P>0.05)。喷他脒组有1例患者出现中度或重度副作用,复方新诺明组有10例,氨苯砜加乙胺嘧啶组有9例(P<0.05);研究药物分别在喷他脒组0例、复方新诺明组10例和氨苯砜加乙胺嘧啶组6例患者中停用(P<0.05)。单独使用复方新诺明或乙胺嘧啶联合氨苯砜或复方新诺明均不能预防抗弓形虫IgG抗体阳性患者的弓形虫病初发。
在预防高危患者首次发生PCP方面,低剂量每周三次的复方新诺明或每周一次的氨苯砜加乙胺嘧啶并不比每月雾化吸入喷他脒显著差(若差异>15%,则有90%的把握度可检测到),但雾化吸入喷他脒耐受性更好。