Mermin Jonathan, Lule John, Ekwaru John Paul, Malamba Samuel, Downing Robert, Ransom Ray, Kaharuza Frank, Culver David, Kizito Francis, Bunnell Rebecca, Kigozi Aminah, Nakanjako Damalie, Wafula Winnie, Quick Robert
CDC-Uganda, Global AIDS Program, National Center for HIV, STD and TB Prevention, National Center for Infectious Diseases; Centers for Disease Control and Prevention, Atlanta, GA, USA.
Lancet. 2004;364(9443):1428-34. doi: 10.1016/S0140-6736(04)17225-5.
Prophylaxis with co-trimoxazole (trimethoprim-sulphamethoxazole) is recommended for people with HIV infection or AIDS but is rarely used in Africa. We assessed the effect of such prophylaxis on morbidity, mortality, CD4-cell count, and viral load among people with HIV infection living in rural Uganda, an area with high rates of bacterial resistance to co-trimoxazole.
Between April, 2001, and March, 2003, we enrolled, and followed up with weekly home visits, 509 individuals with HIV-1 infection and their 1522 HIV-negative household members. After 5 months of follow-up, HIV-positive participants were offered daily co-trimoxazole prophylaxis (800 mg trimethoprim, 160 mg sulphamethoxazole) and followed up for a further 1.5 years. We assessed rates of malaria, diarrhoea, hospital admission, and death.
Co-trimoxazole was well tolerated with rare (<2% per person-year) adverse reactions. Even though rates of resistance in diarrhoeal pathogens were high (76%), co-trimoxazole prophylaxis was associated with a 46% reduction in mortality (hazard ratio 0.54 [95% CI 0.35-0.84], p=0.006) and lower rates of malaria (multivariate incidence rate ratio 0.28 [0.19-0.40], p<0.0001), diarrhoea (0.65 [0.53-0.81], p<0.0001), and hospital admission (0.69 [0.48-0.98], p=0.04). The annual rate of decline in CD4-cell count was less during prophylaxis than before (77 vs 203 cells per microL, p<0.0001), and the annual rate of increase in viral load was lower (0.08 vs 0.90 log(10) copies per mL, p=0.01).
Daily co-trimoxazole prophylaxis was associated with reduced morbidity and mortality and had beneficial effects on CD4-cell count and viral load. Co-trimoxazole prophylaxis is a readily available, effective intervention for people with HIV infection in Africa.
对于感染HIV或患艾滋病的人群,推荐使用复方新诺明(甲氧苄啶 - 磺胺甲恶唑)进行预防,但在非洲很少使用。我们评估了在乌干达农村地区对感染HIV的人群进行这种预防措施对发病率、死亡率、CD4细胞计数及病毒载量的影响,该地区对复方新诺明的细菌耐药率很高。
在2001年4月至2003年3月期间,我们招募了509名HIV - 1感染者及其1522名HIV阴性家庭成员,并通过每周上门访视进行随访。在随访5个月后,为HIV阳性参与者提供每日复方新诺明预防治疗(800mg甲氧苄啶,160mg磺胺甲恶唑),并继续随访1.5年。我们评估了疟疾、腹泻、住院及死亡的发生率。
复方新诺明耐受性良好,不良反应发生率低(每人每年<2%)。尽管腹泻病原体的耐药率很高(76%),但复方新诺明预防治疗使死亡率降低了46%(风险比0.54 [95%可信区间0.35 - 0.84],p = 0.006),疟疾、腹泻及住院发生率也较低(多变量发病率比分别为0.28 [0.19 - 0.40],p < 0.0001;0.65 [0.53 - 0.81],p < 0.0001;0.69 [0.48 - 0.98],p = 0.04)。预防治疗期间CD4细胞计数的年下降率低于治疗前(分别为每微升77个细胞和203个细胞,p < 0.0001),病毒载量的年增长率也较低(分别为每毫升0.08 log(10)拷贝和0.90 log(10)拷贝,p = 0.01)。
每日复方新诺明预防治疗可降低发病率和死亡率,并对CD4细胞计数及病毒载量有有益影响。复方新诺明预防治疗是非洲HIV感染者可随时获得的有效干预措施。