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Adoption of evidence-informed guidelines in prescribing protease inhibitors for HIV-Tuberculosis co-infected patients on rifampicin and effects on HIV treatment outcomes in Uganda

机译:采用证据知识的指导蛋白酶抑制剂对乌干达艾滋病毒治疗结果的艾滋病毒 - 结核病有关患者的规定蛋白酶抑制剂及对乌干达的影响

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We aimed to determine how emerging evidence over the past decade informed how Ugandan HIV clinicians prescribed protease inhibitors (PIs) in HIV patients on rifampicin-based tuberculosis (TB) treatment and how this affected HIV treatment outcomes. We reviewed clinical records of HIV patients aged 13?years and above, treated with rifampicin-based TB treatment while on PIs between1st—January -2013 and 30th—September—2018 from twelve public HIV clinics in Uganda. Appropriate PI prescription during rifampicin-based TB treatment was defined as; prescribing doubled dose lopinavir/ritonavir- (LPV/r 800/200?mg twice daily) and inappropriate PI prescription as prescribing standard dose LPV/r or atazanavir/ritonavir (ATV/r). Of the 602 patients who were on both PIs and rifampicin, 103 patients (17.1% (95% CI: 14.3–20.34)) received an appropriate PI prescription. There were no significant differences in the two-year mortality (4.8 vs. 5.7%, P?=?0.318), loss to follow up (23.8 vs. 18.9%, P?=?0.318) and one-year post TB treatment virologic failure rates (31.6 vs. 30.7%, P?=?0.471) between patients that had an appropriate PI prescription and those that did not. However, more patients on double dose LPV/r had missed anti-retroviral therapy (ART) days (35.9 vs 21%, P?=?0.001). We conclude that despite availability of clinical evidence, double dosing LPV/r in patients receiving rifampicin-based TB treatment is low in Uganda’s public HIV clinics but this does not seem to affect patient survival and viral suppression.
机译:我们旨在确定过去十年的新出现证据如何了解乌干达艾滋病毒临床医生如何在艾滋病毒蛋白的结核病(TB)治疗中的蛋白酶抑制剂(PIS)以及这种影响的艾滋病毒治疗结果。我们审查了13岁及以上的艾滋病毒患者的临床记录,以利福平为基础的TB治疗治疗,而PIS在乌干达的十二个公共艾滋病毒诊所(2018年1月)至2018年至2018年。基于利福平的TB处理期间的适当PI处方定义为;规定的剂量Lopinavir / Ritonavir-(LPV / R 800/200?Mg每日两次),不适当的PI处方作为规定标准剂量LPV / R或ATAZANAVIR / Ritonavir(ATV / R)。在PIS和利福平的602名患者中,103名患者(17.1%(95%(95%(95%)(95%:14.3-20.34))接受了适当的PI处方。两年死亡率没有显着差异(4.8与5.7%,p?= 0.318),丧失跟进(23.8与18.9%,p?= 0.318)和一年后TB治疗病毒学在具有适当PI处方的患者之间,失败利率(31.6 vs.30.7%,p?= 0.471)。然而,更多患者Double剂量LPV / R错过了抗逆转录病毒治疗(第35.9 Vs 21%,P?= 0.001)。我们得出结论,尽管临床证据可用,但在乌干达的公共艾滋病毒诊所接受基于利福平的TB治疗的患者的双重剂量LPV / R低,但这似乎不会影响患者的存活和病毒抑制。

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