在乌干达中部通过地段质量保证抽样评估抗逆转录病毒疗法服务提供模式。

IF 1.5 Q4 INFECTIOUS DISEASES HIV AIDS-Research and Palliative Care Pub Date : 2024-09-06 eCollection Date: 2024-01-01 DOI:10.2147/HIV.S475258
Semei Christopher Mukama, Jane Senyondo Nakawesi, Dedrix Stephenson Bindeeba, Simon Ezajobo, Andrew Mugisa, Catherine Senyimba, Eve Namitala, Robert Onzima D D M Anguyo, Simon Peter Katongole, Barbara Mukasa
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引用次数: 0

摘要

背景:本研究评估了人类免疫缺陷病毒(HIV)/获得性免疫缺陷综合征(AIDS)差异化服务提供模式(DSDMs)的有效性和响应性,这些服务提供模式旨在提高抗逆转录病毒疗法(ART)的可及性和患者的治疗效果,同时解决结核病(TB)-HIV整合问题,研究重点是目前在乌干达实施的五个DSDMs中的四个:2023 年 3 月 7 日至 23 日,我们采用地段质量保证抽样法在乌干达中部的八个地区进行了描述性横断面调查。我们随机抽取了 2668 名患者,这些患者在基于设施的个体管理(FBIM)模式下接受抗逆转录病毒疗法至少 1 年,或在非 FBIM DSDM 模式下接受抗逆转录病毒疗法至少 1 年。我们通过对患者进行访谈、查阅抗逆转录病毒疗法和 DSDM 登记簿中的记录以及抗逆转录病毒疗法卡来收集数据。我们对数据进行了比例分析,比较了社区客户主导的抗逆转录病毒疗法分配模式(CCLAD)、社区药品分配点模式(CDDP)和快速通道药品补充模式(FTDR)与标准护理模式(FBIM)之间选定的抗逆转录病毒疗法结果和响应性指标。抗逆转录病毒疗法的结果变量包括:保留在抗逆转录病毒疗法第一线的患者、在最后一次医疗机构就诊时处于世界卫生组织临床 1 期的患者、在过去 12 个月中未提出 CD4 请求的患者、病毒载量抑制、坚持抗逆转录病毒疗法的患者,以及报告在过去 6 个月中未出现艾滋病相关症状的患者。结核病护理变量包括使用强化病例发现表进行结核病筛查和结核病检测呈阳性的患者。响应性变量包括:抗逆转录病毒疗法补液的旅行时间、抗逆转录病毒疗法补液的旅行距离、抗逆转录病毒疗法补液期间的便利性和灵活性、抗逆转录病毒疗法补液的旅行费用、对在抗逆转录病毒疗法补液点就诊的恐惧、服务前的等待时间、服务时间的充足性、拥挤程度和感染风险、社会支持、应对抗逆转录病毒疗法治疗挑战的能力、艾滋病病毒感染状况的披露以及获得服务的障碍。非 FBIM DSDM 与 FBIM 之间指标比例的 95% 置信区间无重叠表示比例差异有统计学意义,否则无意义:与 FBIM 模型相比,CCLAD 和 CDDP DSDM 中坚持抗逆转录病毒疗法、病毒载量得到抑制、结核病发病率较低的抗逆转录病毒疗法患者比例更高。此外,与 FBIM 模式中的患者相比,更多的 CCLAD 和 CDDP 患者表示接受抗逆转录病毒疗法所需的旅行时间和距离更短。与 FBIM 模式相比,更多的 CCLAD 和 CDDP 患者还表示抗逆转录病毒疗法补药时间安排灵活、交通费用降低、隐私问题减少、与艾滋病毒/艾滋病相关的污名减少、等待时间缩短、服务效率提高、抗逆转录病毒疗法取药点的拥堵减少、同伴支持增强、解决问题的协助改善以及艾滋病毒感染状况披露增加。在减少 CD4 检测请求的比例、病毒载量抑制以及客户报告的比例方面,FTDR 模式优于 FBIM;FTDR 模式缩短了旅行时间,降低了交通成本,减少了对隐私的担忧,缩短了等待时间,提高了服务效率。与 CDDP 和 FTDR 相比,FBIM 有更高比例的受试者坚持一线抗逆转录病毒疗法:以社区为基础的 DSDM 既能满足患者的需求,又不影响患者接受抗逆转录病毒疗法的效果。虽然 FTDR 对接受抗逆转录病毒疗法的患者也表现出较高的有效性和响应性,但仍有进一步改进的潜力。抗逆转录病毒疗法项目的规划者和实施者应同时考虑需求方和供应方的创新,以保持 DSDM 的持续性。
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Evaluating Antiretroviral Therapy Service Delivery Models Through Lot Quality Assurance Sampling in Central Uganda.

Background: This study evaluated the effectiveness and responsiveness of differentiated Human Immunodeficiency Virus (HIV)/Acquired Immuno-Deficiency Syndrome (AIDS) service delivery models (DSDMs) implemented to enhance antiretroviral therapy (ART) access and outcomes for patients while addressing Tuberculosis (TB)-HIV integration, focusing on four of the five DSDMs currently implemented in Uganda.

Methodology: A descriptive cross-sectional survey was conducted in eight districts of central Uganda using Lot Quality Assurance Sampling approach from 7th to 23rd March 2023. We randomly sampled 2668 patients who have been on ART for at least 1 year in a Facility-Based Individual Management (FBIM) model or in a non-FBIM DSDM for at least one year. Data were collected through patient interviews and review of records in ART and DSDM registers as well as ART cards. We analyzed the data in proportions, comparing the selected ART outcome and responsiveness indicators between Community Client Led ART Distribution (CCLAD), Community Drugs Distribution Point (CDDP) and Fast-Track Drug Refill (FTDR) DSDMs with the standard care (FBIM) model. The ART outcome variables include patients retained in the 1st line of the ART regimen, patients in World Health Organization clinical stage 1 during the last facility visit, patients who had no CD4 request during the past 12 months, viral load suppression, ART adherence, and patients who reported that they did not experience HIV/AIDS-related symptoms in the past 6 months. The variables on TB care include screening for TB using the intensified case finding form and patients tested positive for TB. Responsiveness variables include the perceived; travel time for ART refill, travel distance for ART refill, convenience and flexibility during ART refill, cost of travel for ART refill, fear of being seen at ART refill point, waiting time before service, adequacy of service time, crowding and risk of infections, social support, ability to address ART treatment challenges, HIV status disclosure and barriers to access. Non-overlap in 95% confidence interval in indicator proportion between non-FBIM DSDM and FBIM means a statistically significant difference in proportion, or otherwise non-significant.

Results: Higher proportions of ART patients in the CCLAD and CDDP DSDMs adhered to ART, had suppressed viral load, and a lower TB prevalence than those in FBIM model. Additionally, more CCLAD and CDDP clients reported shorter travel time and distance to access ART than their counterparts in the FBIM model. Compared to FBIM model, higher proportions of those in CCLAD and CDDP also reported flexibility in ART refill scheduling, reduced transport costs, fewer privacy concerns, less HIV/AIDS-related stigma, shorter waiting times, more efficient services, decreased congestion at ART pickup sites, enhanced peer support, improved problem-solving assistance, and increased HIV status disclosure. The FTDR model outperformed FBIM in proportions with fewer requests for CD4 testing, viral load suppression, as well as proportions of clients who reported; shorter travel time, lower transportation cost, decreased privacy concerns, shorter waiting time, and efficient service provision. Compared to both CDDP and FTDR, the FBIM had a higher proportion of clients remain on the first-line ART regimen.

Conclusion: Community-based DSDMs show responsiveness to clients' needs without compromising the effectiveness of ART care for patients. Although FTDR also demonstrates high effectiveness and responsiveness for clients on ART, there is potential for further improvement. Planners and implementers of ART programs should consider both demand- and supply-side innovations to sustain the continuation of DSDMs.

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CiteScore
3.00
自引率
6.70%
发文量
61
审稿时长
16 weeks
期刊介绍: About Dove Medical Press Dove Medical Press Ltd is part of Taylor & Francis Group, the Academic Publishing Division of Informa PLC. We specialize in the publication of Open Access peer-reviewed journals across the broad spectrum of science, technology and especially medicine. Dove Medical Press was founded in 2003 with the objective of combining the highest editorial standards with the ''best of breed'' new publishing technologies. We have offices in Manchester and London in the United Kingdom, representatives in Princeton, New Jersey in the United States, and our editorial offices are in Auckland, New Zealand. Dr Scott Fraser is our Medical Director based in the UK. He has been in full time clinical practice for over 20 years as well as having an active research interest.
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