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适应低流行国家有效和高效儿科 HIV 病例发现策略:在埃塞俄比亚高风险进入点就诊的儿童检测用风险筛查工具。

Adapting strategies for effective and efficient pediatric HIV case finding in low prevalence countries: risk screening tool for testing children presenting at high-risk entry points in Ethiopia.

机构信息

Centers for Disease Control and Prevention, US Embassy Entoto Road, P.O.B 1014, Addis Ababa, Ethiopia.

Centers for Disease Control and Prevention, Atlanta, Georgia, USA.

出版信息

BMC Infect Dis. 2022 May 20;22(1):480. doi: 10.1186/s12879-022-07460-w.

DOI:10.1186/s12879-022-07460-w
PMID:35596158
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9121612/
Abstract

BACKGROUND

Implementing effective and efficient case-finding strategies is crucial to increasing pediatric antiretroviral therapy coverage. In Ethiopia, universal HIV testing is conducted for children presenting at high-risk entry points including malnutrition treatment, inpatient wards, tuberculosis (TB) clinics, index testing for children of positive adults, and referral of orphans and vulnerable children (OVC); however, low positivity rates observed at inpatient, malnutrition and OVC entry points warrant re-assessing current case-finding strategies. The aim of this study is to develop HIV risk screening tool applicable for testing children presenting at inpatient, malnutrition and OVC entry points in low-HIV prevalence settings.

METHODS

The study was conducted from May 2017-March 2018 at 29 public health facilities in Amhara and Addis Ababa regions of Ethiopia. All children 2-14 years presenting to five high-risk entry points including malnutrition treatment, inpatient wards, tuberculosis (TB) clinics, index testing for children of positive adults, and referral of orphans and vulnerable children (OVC) were enrolled after consent. Data were collected from registers, medical records, and caregiver interviews. Screening tools were constructed using predictors of HIV positivity as screening items by applying both logistic regression and an unweighted method. Sensitivity, specificity and number needed to test (NNT) to identify one new child living with HIV (CLHIV) were estimated for each tool.

RESULTS

The screening tools had similar sensitivity of 95%. However, the specificities of tools produced by logistic regression methods (61.4 and 65.6%) which are practically applicable were higher than those achieved by the unweighted method (53.6). Applying these tools could result in 58‒63% reduction in the NNT compared to universal testing approach while maintaining the overall number of CLHIV identified.

CONCLUSION

The screening tools developed using logistic regression method could significantly improve HIV testing efficiency among children presenting to malnutrition, inpatient, and OVC entry points in Ethiopia while maintaining case identification. These tools are simplified to practically implement and can potentially be validated for use at various entry points. HIV programs in low-prevalence countries can also further investigate and optimize these tools in their settings.

摘要

背景

实施有效和高效的病例发现策略对于提高儿科抗逆转录病毒治疗的覆盖率至关重要。在埃塞俄比亚,对在包括营养不良治疗、住院病房、结核病 (TB) 诊所、成人阳性儿童的索引检测以及孤儿和弱势儿童 (OVC) 转介在内的高风险进入点出现的儿童进行普遍的 HIV 检测;然而,在住院、营养不良和 OVC 进入点观察到的低阳性率需要重新评估当前的病例发现策略。本研究旨在为在低 HIV 流行地区在住院、营养不良和 OVC 进入点就诊的儿童开发适用于 HIV 风险筛查的工具。

方法

该研究于 2017 年 5 月至 2018 年 3 月在埃塞俄比亚阿姆哈拉和亚的斯亚贝巴地区的 29 个公共卫生机构进行。所有 2-14 岁在五个高风险进入点就诊的儿童,包括营养不良治疗、住院病房、结核病 (TB) 诊所、成人阳性儿童的索引检测和孤儿和弱势儿童 (OVC) 的转介,在同意后都被纳入研究。数据来自登记册、病历和护理人员访谈。筛查工具是使用 HIV 阳性预测因子作为筛查项目,通过应用逻辑回归和非加权方法构建的。为每个工具估计了识别一个新的 HIV 阳性儿童 (CLHIV) 的敏感性、特异性和需要检测的数量 (NNT)。

结果

筛查工具的敏感性相似,为 95%。然而,逻辑回归方法产生的工具的特异性(61.4%和 65.6%)在实际应用中较高,高于非加权方法的特异性(53.6%)。与普遍检测方法相比,应用这些工具可使 NNT 降低 58%至 63%,同时保持识别的 CLHIV 总数。

结论

使用逻辑回归方法开发的筛查工具可以显著提高埃塞俄比亚在营养不良、住院和 OVC 进入点就诊的儿童的 HIV 检测效率,同时保持病例发现。这些工具已经简化,可以实际实施,并且有可能在各个进入点得到验证。低流行国家的 HIV 项目也可以在其环境中进一步研究和优化这些工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a10/9121612/22c746299b32/12879_2022_7460_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a10/9121612/70a2b5e530c7/12879_2022_7460_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a10/9121612/22c746299b32/12879_2022_7460_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a10/9121612/70a2b5e530c7/12879_2022_7460_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6a10/9121612/22c746299b32/12879_2022_7460_Fig2_HTML.jpg

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