The need to differentiate at re-engagement: lessons from South Africa and Zimbabwe's re-engagement algorithms

IF 4.6 1区 医学 Q2 IMMUNOLOGY
Lynne S. Wilkinson, Helen Bygrave, Musa Manganye, Chiedza Mupanguri, Anna Grimsrud
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Fortunately, many individuals are self-motivated to return to care. However, their timely re-engagement often depends on removing barriers and introducing valued facilitators [<span>6, 7</span>]. Data from Malawi and South Africa show that the majority of people attempt return within 3 months of missing a scheduled appointment, but more country-specific time-to-return data is needed [<span>8, 9</span>].</p><p>Disengagement occurs across the HIV care cascade, with proportionally more people disengaging during early ART but greater numbers disengaging thereafter. In mature, generalised HIV epidemics, disengagement is common among all population groups, reinforcing the need for broad, scalable approaches that improve re-engagement outcomes [<span>3</span>].</p><p>Re-engagement involves two main intervention categories: tracing to encourage return, and enhancing the return experience to reduce interruption length and repeat disengagement [<span>5</span>]. 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Accelerating access to less-intensive differentiated service delivery (DSD) can reduce client burden and help prevent future interruptions [<span>6, 7</span>]. Frequent clinical visits should be reserved for when clinically necessary.</p><p>Ministries of health are starting to implement guidance on managing people returning to care, focusing on respectful care and a shift away from one-size-fits-all intensified clinical management, with its monthly appointments and multiple adherence counselling sessions. Differentiating care pathways identify individuals who are simply “late” for their scheduled visit, with no or only a brief treatment interruption, and who can continue routine care, including in DSD models. They also identify those who require further assessment. Two key assessments at return guide further differentiation. First, clinical stability, assessed through signs of opportunistic infections, mental health concerns, AHD or an elevated viral load prior to disengagement. 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Clinically unstable individuals, regardless of interruption duration, require a repeat CD4 test to identify AHD and their follow-up schedule is determined by need. Clinically stable individuals are assessed for time since the missed appointment, with CD4 testing required for those missing for more than 90 days. Those missing appointments by 29–90 days are managed similarly to individuals 28 days or less late. Both clinically unstable and “more than 90 days late” groups require a follow-up viral load test after 3 months and a 3-month ART refill unless earlier clinical care is needed. A month later, if suppressed, they are offered DSD enrolment.</p><p>Piloting an earlier version in nine health facilities revealed that engaged leadership, provider empathy and alignment with existing workflows were critical for successful adoption [<span>13</span>].</p><p>Zimbabwe defines re-engagement as stopping ART after a missed visit. 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引用次数: 0

Abstract

As HIV epidemics mature, effectively addressing interruptions in antiretroviral therapy (ART) becomes increasingly critical to reducing morbidity, mortality and transmission [1-3]. Prolonged disengagement from ART places significant demands on health systems, including the need to manage advanced HIV disease (AHD), higher rates of hospitalisation and preventable new HIV acquisitions.

Disengagement from HIV care is the result of individual, interpersonal and/or structural vulnerabilities combined with life disruptions, such as unexpected travel, that impact a person's ability to remain in care [4, 5]. Fortunately, many individuals are self-motivated to return to care. However, their timely re-engagement often depends on removing barriers and introducing valued facilitators [6, 7]. Data from Malawi and South Africa show that the majority of people attempt return within 3 months of missing a scheduled appointment, but more country-specific time-to-return data is needed [8, 9].

Disengagement occurs across the HIV care cascade, with proportionally more people disengaging during early ART but greater numbers disengaging thereafter. In mature, generalised HIV epidemics, disengagement is common among all population groups, reinforcing the need for broad, scalable approaches that improve re-engagement outcomes [3].

Re-engagement involves two main intervention categories: tracing to encourage return, and enhancing the return experience to reduce interruption length and repeat disengagement [5]. This viewpoint focuses on the latter by removing barriers and adapting service delivery to support re-engagement.

HIV programmes must first recognise that ART interruptions are common and prioritise facilitating easy, quick and sustained re-engagement [3]. Some individuals fear returning due to concerns about disappointing healthcare workers and experiencing punitive actions [6, 10, 11]. Respectful care for returning clients can reduce fear and promote timely return. Re-engagement guidance should emphasise same-day ART provision, avoiding multiple visits [7] or transfer documentation collection [11]. Long waiting times and penalisation for missed appointments should be monitored and penalisation [6, 7]. People re-engaging in care commonly previously struggled with frequent appointments, inconvenient locations and long wait times. Accelerating access to less-intensive differentiated service delivery (DSD) can reduce client burden and help prevent future interruptions [6, 7]. Frequent clinical visits should be reserved for when clinically necessary.

Ministries of health are starting to implement guidance on managing people returning to care, focusing on respectful care and a shift away from one-size-fits-all intensified clinical management, with its monthly appointments and multiple adherence counselling sessions. Differentiating care pathways identify individuals who are simply “late” for their scheduled visit, with no or only a brief treatment interruption, and who can continue routine care, including in DSD models. They also identify those who require further assessment. Two key assessments at return guide further differentiation. First, clinical stability, assessed through signs of opportunistic infections, mental health concerns, AHD or an elevated viral load prior to disengagement. Second, time since the missed appointment which indicates potential interruption duration and AHD risk.

To illustrate how these programmatic considerations have been applied, we highlight the national re-engagement algorithms of South Africa and Zimbabwe—the first two countries to formalise differentiated re-engagement pathways in national guidelines – offering valuable lessons for other settings. These are shown in Figure 1.

South Africa defines re-engagement as missing an appointment and returning to care unwell or by more than 28 days [12]. Their algorithm (Panel A) distinguishes routine from re-engagement care [12]. People late by 28 days or less continue or enrol in DSD models. The viral load testing schedule remains unchanged. Those missing appointments for more than 28 days or self-identifying as unwell undergo a clinical assessment and, unless clinically indicated, continue or restart ART on the same day. Clinically unstable individuals, regardless of interruption duration, require a repeat CD4 test to identify AHD and their follow-up schedule is determined by need. Clinically stable individuals are assessed for time since the missed appointment, with CD4 testing required for those missing for more than 90 days. Those missing appointments by 29–90 days are managed similarly to individuals 28 days or less late. Both clinically unstable and “more than 90 days late” groups require a follow-up viral load test after 3 months and a 3-month ART refill unless earlier clinical care is needed. A month later, if suppressed, they are offered DSD enrolment.

Piloting an earlier version in nine health facilities revealed that engaged leadership, provider empathy and alignment with existing workflows were critical for successful adoption [13].

Zimbabwe defines re-engagement as stopping ART after a missed visit. A clinical assessment is required for everyone re-engaging to differentiate between those who are clinically stable and unstable (Panel B) [14]. For clinically stable individuals, those who are less than 3 months late are re-initiated within 7 days and (re)enrolled in DSD models after receiving adherence counselling sessions. The viral load testing schedules remain unchanged. Clinically unstable individuals include those who are unwell, have an elevated viral load within the past 12 months or have significant psychosocial challenges. They require a follow-up CD4 if the last viral load exceeded 1000 copies/ml, with their appointment schedule tailored to clinical needs. For all individuals more than 3 months late, CD4 counts are repeated to assess for AHD. Those with a CD4 count above 200 cells/mm3 follow the standard ART initiation schedule, with follow-up clinical reviews after 1, 3 and 6 months—after which a viral load test is done. At the subsequent visit, suppressed individuals are offered DSD models, including 6-month ART refills.

In an evaluation of the AHD screening component across 70 facilities, 23% of re-engaging clients received CD4 testing, with 41% of those tested having CD4 < 200 cells/mm3. Staff shortages and commodity constraints posed challenges, particularly for point-of-care CD4 testing, while facilities trained on the use of the algorithm, conducted screening more confidently [15].

The South African and Zimbabwean algorithm-based differentiated pathways for re-engagement offer scalable approaches to facilitating efficient and durable return to care. By ensuring minimal disruption to individuals’ lives through accelerated access to extended ART refills and less-intensive DSD, these approaches reduce the burden for clinically stable clients while ensuring necessary oversight for those with increased clinical needs, including AHD. Importantly, they ensure the re-engagement process is person-centred, with a focus on enhancing the return experience and mitigating barriers that may lead to prolonged or future interruptions. These adaptable approaches allow healthcare systems to address individual needs while optimising resources for broader population coverage.

The authors declare that they have no conflict of interest.

The concept for this commentary was developed by LSW, HB and AG. LSW wrote the first draft. All authors contributed and approved the final version.

Abstract Image

重新接触时需要区分:来自南非和津巴布韦重新接触算法的教训
随着艾滋病毒流行的成熟,有效解决抗逆转录病毒治疗(ART)中断问题对于降低发病率、死亡率和传播变得越来越重要[1-3]。长期脱离抗逆转录病毒治疗对卫生系统提出了重大要求,包括需要管理晚期艾滋病毒疾病、更高的住院率和可预防的新发艾滋病毒感染。脱离艾滋病毒护理是个人、人际和/或结构脆弱性与生活中断(如意外旅行)相结合的结果,这些因素影响了一个人继续接受护理的能力[4,5]。幸运的是,许多人都是自我激励回到护理。然而,他们的及时重新参与往往取决于消除障碍和引入有价值的促进者[6,7]。来自马拉维和南非的数据显示,大多数人在错过预定的约会后3个月内试图返回,但需要更多具体国家的返回时间数据[8,9]。脱离治疗发生在整个艾滋病毒护理级联中,在早期抗逆转录病毒治疗期间脱离治疗的人数比例更高,但此后脱离治疗的人数更多。在成熟的、普遍的艾滋病毒流行病中,脱离接触在所有人口群体中都很普遍,因此需要采取广泛的、可扩展的办法,以改善重新参与的结果[10]。重新参与包括两个主要的干预类别:追踪以鼓励返回,以及增强返回体验以减少中断时间和重复脱离。该观点通过消除障碍和调整服务交付以支持重新参与来关注后者。艾滋病毒规划必须首先认识到抗逆转录病毒治疗中断是常见的,并优先考虑促进容易、快速和持续的重新参与。一些人害怕返回,因为担心失望的医护人员和经历惩罚行动[6,10,11]。尊重和照顾回头客可以减少恐惧,促进及时回头客。重新参与指导应强调当天提供抗逆转录病毒治疗,避免多次访问bb1或转移文件收集bb1。长时间的等待和错过预约的惩罚应该受到监控和惩罚[6,7]。以前,重新接受治疗的人通常要面对频繁的预约、不方便的地点和漫长的等待时间。加速获得低密集差异化服务交付(DSD)可以减轻客户负担,并有助于防止未来的中断[6,7]。频繁的临床访问应保留到临床需要时。卫生部正在开始实施关于管理重返护理人员的指导,重点是尊重护理,并从千篇一律的强化临床管理转变为每月预约和多次坚持咨询会议。区分护理路径可以识别那些只是“迟到”的患者,没有或只有短暂的治疗中断,以及可以继续常规护理的患者,包括在DSD模型中。他们还确定了那些需要进一步评估的人。回报的两个关键评估指导进一步区分。首先,临床稳定性,通过机会性感染、精神健康问题、多动症或脱离接触前病毒载量升高的迹象来评估。第二,错过预约后的时间,这表明潜在的中断持续时间和AHD风险。为了说明这些规划考虑是如何应用的,我们重点介绍了南非和津巴布韦的国家再参与算法——这两个国家最早在国家指导方针中正式确定了差异化的再参与途径——为其他国家提供了宝贵的经验。如图1所示。南非对“重新聘用”的定义是:缺席一次约会,身体不适,或逾期28天以上。他们的算法(图A)区分了常规护理和再参与护理[12]。迟到28天或更少的人继续或参加DSD模型。病毒载量测试计划保持不变。那些错过预约超过28天或自认为身体不适的人接受临床评估,除非临床指示,否则在同一天继续或重新开始抗逆转录病毒治疗。临床不稳定的个体,无论中断时间长短,都需要重复CD4检测以确定AHD,并根据需要确定随访计划。临床稳定的个体自错过预约后的时间进行评估,对于那些错过预约超过90天的人需要进行CD4检测。那些迟到29-90天的人的处理方式与迟到28天或更短时间的人类似。临床不稳定组和“延迟超过90天”组都需要在3个月后进行随访病毒载量检测,并在3个月后重新进行抗逆转录病毒治疗,除非需要早期临床护理。一个月后,如果他们被压制,他们就会被录取。 在9个卫生设施试点的早期版本表明,参与的领导、提供者的同情和与现有工作流程的一致是成功采用bbb的关键。津巴布韦将重新接触定义为在错过访问后停止抗逆转录病毒治疗。每个重新参与的人都需要进行临床评估,以区分临床稳定和不稳定(B组)[14]。对于临床稳定的个体,延迟少于3个月的患者在7天内重新开始,并在接受依从性咨询会议后(重新)入组DSD模型。病毒载量测试时间表保持不变。临床不稳定个体包括身体不适、过去12个月内病毒载量升高或有重大社会心理挑战的个体。如果最后一次病毒载量超过1000拷贝/毫升,他们需要随访CD4,并根据临床需要调整预约时间表。对于所有延迟3个月以上的个体,重复CD4计数以评估AHD。CD4细胞计数高于200细胞/mm3的患者遵循标准的ART启动计划,在1、3和6个月后进行随访临床检查,之后进行病毒载量测试。在随后的访问中,被抑制的个体被提供DSD模型,包括6个月的ART补充。在对70个设施的AHD筛查部分的评估中,23%的重新参与的客户接受了CD4检测,其中41%的被检测者CD4 &lt;200 / mm3。工作人员短缺和商品限制带来了挑战,特别是在护理点CD4检测方面,而经过算法使用培训的设施则更有信心地进行了筛查。南非和津巴布韦基于算法的差异化再参与途径提供了可扩展的方法,以促进有效和持久的重返护理。通过加速获得延长的ART补充和低强度的DSD,确保对个人生活的干扰最小化,这些方法减轻了临床稳定客户的负担,同时确保对包括AHD在内的临床需求增加的患者进行必要的监督。重要的是,他们确保再参与过程以人为本,重点是提高返回体验和减少可能导致长期或未来中断的障碍。这些适应性强的方法使医疗保健系统能够满足个人需求,同时优化资源,以扩大人口覆盖范围。作者声明他们没有利益冲突。这个解说的概念是由LSW, HB和AG开发的。LSW写了初稿。所有作者都贡献并批准了最终版本。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of the International AIDS Society
Journal of the International AIDS Society IMMUNOLOGY-INFECTIOUS DISEASES
CiteScore
8.60
自引率
10.00%
发文量
186
审稿时长
>12 weeks
期刊介绍: The Journal of the International AIDS Society (JIAS) is a peer-reviewed and Open Access journal for the generation and dissemination of evidence from a wide range of disciplines: basic and biomedical sciences; behavioural sciences; epidemiology; clinical sciences; health economics and health policy; operations research and implementation sciences; and social sciences and humanities. Submission of HIV research carried out in low- and middle-income countries is strongly encouraged.
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