Mulenga Veronica, Ford Deborah, Walker A Sarah, Mwenya Darlington, Mwansa James, Sinyinza Frederick, Lishimpi Kennedy, Nunn Andrew, Gillespie Stephen, Zumla Ali, Chintu Chifumbe, Gibb Diana M
University Teaching Hospital, Lusaka, Zambia.
AIDS. 2007 Jan 2;21(1):77-84. doi: 10.1097/QAD.0b013e3280114ed7.
Cotrimoxazole prophylaxis reduces morbidity and mortality in HIV-1-infected children, but mechanisms for these benefits are unclear.
CHAP was a randomized trial comparing cotrimoxazole prophylaxis with placebo in HIV-infected children in Zambia where background bacterial resistance to cotrimoxazole is high. We compared causes of mortality and hospital admissions, and antibiotic use between randomized groups.
Of 534 children (median age, 4.4 years; 32% 1-2 years), 186 died and 166 had one or more hospital admissions not ending in death. Cotrimoxazole prophylaxis was associated with lower mortality, both outside hospital (P = 0.01) and following hospital admission (P = 0.005). The largest excess of hospital deaths in the placebo group was from respiratory infections [22/56 (39%) placebo versus 10/35 (29%) cotrimoxazole]. By 2 years, the cumulative probability of dying in hospital from a serious bacterial infection (predominantly pneumonia) was 7% on cotrimoxazole and 12% on placebo (P = 0.08). There was a trend towards lower admission rates for serious bacterial infections in the cotrimoxazole group (19.1 per 100 child-years at risk versus 28.5 in the placebo group, P = 0.09). Despite less total follow-up due to higher mortality, more antibiotics (particularly penicillin) were prescribed in the placebo group in year one [6083 compared to 4972 days in the cotrimoxazole group (P = 0.05)].
Cotrimoxazole prophylaxis appears to mainly reduce death and hospital admissions from respiratory infections, supported further by lower rates of antibiotic prescribing. As such infections occur at high CD4 cell counts and are common in Africa, the role of continuing cotrimoxazole prophylaxis after starting antiretroviral therapy requires investigation.
复方新诺明预防可降低HIV-1感染儿童的发病率和死亡率,但其获益机制尚不清楚。
CHAP是一项随机试验,在赞比亚对HIV感染儿童进行复方新诺明预防与安慰剂对照研究,当地对复方新诺明的背景细菌耐药率很高。我们比较了随机分组之间的死亡原因、住院情况及抗生素使用情况。
534名儿童(中位年龄4.4岁;32%为1 - 2岁)中,186人死亡,166人有一次或多次非致死性住院。复方新诺明预防与较低死亡率相关,包括院外死亡率(P = 0.01)和住院后死亡率(P = 0.005)。安慰剂组医院死亡中超额最多的是呼吸道感染[56例中有22例(39%)为安慰剂组,35例中有10例(29%)为复方新诺明组]。到2年时,因严重细菌感染(主要是肺炎)在医院死亡的累积概率,复方新诺明组为7%,安慰剂组为12%(P = 0.08)。复方新诺明组严重细菌感染的住院率有降低趋势(每100儿童年风险为19.1例,安慰剂组为28.5例,P = 0.09)。尽管由于死亡率较高总随访时间较短,但在第一年安慰剂组使用了更多抗生素(尤其是青霉素)[复方新诺明组为4972天,安慰剂组为6083天(P = 0.05)]。
复方新诺明预防似乎主要降低呼吸道感染导致的死亡和住院率,抗生素处方率较低进一步支持了这一点。由于此类感染发生在CD4细胞计数较高时且在非洲很常见,开始抗逆转录病毒治疗后继续使用复方新诺明预防的作用需要研究。