Department of Epidemiology of Microbial Diseases, Yale School of Public Health, New Haven, CT.
Department of Global Health, University of Washington, Seattle, WA.
J Acquir Immune Defic Syndr. 2020 Dec 15;85(5):643-650. doi: 10.1097/QAI.0000000000002497.
To assist the Malawi Ministry of Health to evaluate 2 competing strategies for scale-up of isoniazid preventive therapy (IPT) among HIV-positive adults receiving antiretroviral therapy.
Malawi.
We used a multidistrict, compartmental model of the Malawi tuberculosis (TB)/HIV epidemic to compare the anticipated health impacts of 6-month versus continuous IPT programs over a 12-year horizon while respecting a US$10.8 million constraint on drug costs in the first 3 years.
The 6-month IPT program could be implemented nationwide, whereas the continuous IPT alternative could be introduced in 14 (of the 27) districts. By the end of year 12, the continuous IPT strategy was predicted to avert more TB cases than the 6-month alternative, although not statistically significant (2368 additional cases averted; 95% projection interval [PI], -1459 to 5023). The 6-month strategy required fewer person-years of IPT to avert a case of TB or death than the continuous strategy. For both programs, the mean reductions in TB incidence among people living with HIV by year 12 were expected to be <10%, and the cumulative numbers of IPT-related hepatotoxicity to exceed the number of all-cause deaths averted in the first 3 years.
With the given budgetary constraint, the nationwide implementation of 6-month IPT would be more efficient and yield comparable health benefits than implementing a continuous IPT program in fewer districts. The anticipated health effects associated with both IPT strategies suggested that a combination of different TB intervention strategies would likely be required to yield a greater impact on TB control in settings such as Malawi, where antiretroviral therapycoverage is relatively high.
为了协助马拉维卫生部评估两种竞争策略,以扩大接受抗逆转录病毒治疗的艾滋病毒阳性成年人的异烟肼预防治疗(IPT)。
马拉维。
我们使用马拉维结核病(TB)/艾滋病毒流行的多地区、隔室模型,在尊重前 3 年药物成本 1080 万美元限制的情况下,比较了 6 个月与连续 IPT 方案在 12 年期间的预期健康影响。
6 个月的 IPT 方案可以在全国范围内实施,而连续 IPT 方案可以在 27 个区中的 14 个区实施。到第 12 年末,连续 IPT 策略预计将避免更多的结核病病例,尽管没有统计学意义(避免 2368 例额外病例;95%预测区间[PI],-1459 至 5023)。与连续策略相比,6 个月的策略需要更少的 IPT 人年来避免结核病或死亡病例。对于这两种方案,到第 12 年,艾滋病毒感染者的结核病发病率预计将降低不到 10%,并且累积的 IPT 相关肝毒性病例数将超过前 3 年避免的所有原因死亡人数。
在给定的预算限制下,在全国范围内实施 6 个月的 IPT 将比在较少的地区实施连续 IPT 方案更有效,并产生可比的健康效益。这两种 IPT 策略的预期健康效果表明,在马拉维等抗逆转录病毒治疗覆盖率相对较高的环境中,可能需要结合不同的结核病干预策略,以对结核病控制产生更大的影响。