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Injectable treatment for adolescents living with HIV. 为感染艾滋病毒的青少年提供注射治疗。
IF 12.8 1区 医学 Q1 IMMUNOLOGY Pub Date : 2024-12-01 Epub Date: 2024-10-18 DOI: 10.1016/S2352-3018(24)00265-0
Phakamani Moyo, Damaris Nyamweya, Nyiko Kubai, Catherine Orrell, Linda-Gail Bekker
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引用次数: 0
Correction to Lancet HIV 2024; 11: e233-44. Lancet HIV 2024; 11: e233-44 更正。
IF 12.8 1区 医学 Q1 IMMUNOLOGY Pub Date : 2024-12-01 Epub Date: 2024-09-11 DOI: 10.1016/S2352-3018(24)00243-1
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引用次数: 0
Measuring and adapting to climate change in HIV programmes. 在艾滋病毒防治计划中衡量和适应气候变化。
IF 12.8 1区 医学 Q1 IMMUNOLOGY Pub Date : 2024-12-01 Epub Date: 2024-10-09 DOI: 10.1016/S2352-3018(24)00231-5
Nathan Ford, Anne Hammill
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引用次数: 0
Outcomes and gaps in HIV care for migrants in Europe. 欧洲移民艾滋病护理的成果和差距。
IF 12.8 1区 医学 Q1 IMMUNOLOGY Pub Date : 2024-12-01 Epub Date: 2024-11-07 DOI: 10.1016/S2352-3018(24)00296-0
Deniz Gökengin
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引用次数: 0
HIV-related outcomes among migrants living in Europe compared with the general population: a systematic review and meta-analysis. 居住在欧洲的移民与普通人群相比与艾滋病毒相关的结果:系统回顾和荟萃分析。
IF 12.8 1区 医学 Q1 IMMUNOLOGY Pub Date : 2024-12-01 Epub Date: 2024-11-07 DOI: 10.1016/S2352-3018(24)00210-8
Francesco Vladimiro Segala, Francesco Di Gennaro, Luisa Frallonardo, Elda De Vita, Valentina Petralia, Vitalba Sapienza, Stefano Di Gregorio, Mariangela Cormio, Roberta Novara, Giuseppina Rizzo, Mario Barbagallo, Nicola Veronese, Annalisa Saracino

Background: Compared with the general population, international migrants arriving in Europe face severe socioeconomic challenges that result in higher HIV prevalence and limited access to health care, potentially leading to negative outcomes. In this systematic review and meta-analysis, we aimed to investigate the incidence of HIV-related outcomes among international migrants arriving in Europe compared with the incidence among the general population.

Methods: We did a systematic review and meta-analysis to identify studies investigating HIV-related outcomes in migrants and the general population living with HIV in Europe. Six authors (EDV, VP, VS, SDG, MC, and RN) independently searched PubMed, Scopus, and Web of Science from database inception until July 22, 2023 (with an update on March 3, 2024), then screened titles and abstracts of all potentially eligible articles. Studies were included if they were observational studies; investigated clinical, virological, or immunological outcomes in migrants living with HIV; were conducted in Europe; had at least one control group of non-migrants living in a European country; and were in English. Titles and abstracts were screened for eligibility followed by a full-text assessment by two authors (EDV, VP, VS, SDG, MC, or RN). Data were extracted from articles using a structured Redcap form. Primary outcomes of our systematic review were (1) mortality, (2) AIDS-defining condition, (3) combined outcome of AIDS or death, (4) treatment discontinuation, (5) rate of loss to follow-up, (6) virological failure, and (7) immunological failure. Data were reported as relative risks (RRs) or odds ratios with their 95% CIs. The study is registered with PROSPERO, CRD42024501191.

Findings: Of the 1316 articles identified (1297 in the initial search and 19 in the updated search), 19 were included in our systematic review, consisting of 104 676 participants who were followed up for a mean of 79·3 months. The meta-analysis, adjusted for potential confounders, showed that migrants present similar mortality risk (RR 0·88, 95% CI 0·75-1·04), but higher risk for AIDS-defining conditions (1·23, 1·14-1·34), treatment discontinuation (2·39, 1·49-3·29), loss to follow-up (2·53, 1·41-4·53), virological failure (1·80, 1·25-2·60), and immunological failure (3·70, 2·17-12·50) compared with the general population. In subanalyses for WHO regions, people originally from the African region had higher risk for HIV-related adverse outcomes.

Interpretation: Compared with the non-migrant population, migrants living in Europe with HIV face higher risks for progression to AIDS, loss to follow-up, treatment discontinuation, and virological and immunological failure. Interventions aimed to improve HIV care among migrants living in Europe are urgently needed.

Funding: None.

背景:与普通人群相比,抵达欧洲的国际移民面临着严峻的社会经济挑战,这导致了较高的 HIV 感染率和有限的医疗途径,从而可能导致负面结果。在本系统综述和荟萃分析中,我们旨在调查抵达欧洲的国际移民中与艾滋病相关的结果的发生率,并与普通人群的发生率进行比较:我们进行了系统回顾和荟萃分析,以确定调查欧洲移民和普通艾滋病病毒感染者艾滋病相关结果的研究。六位作者(EDV、VP、VS、SDG、MC 和 RN)独立检索了 PubMed、Scopus 和 Web of Science 数据库,检索时间从数据库开始到 2023 年 7 月 22 日(2024 年 3 月 3 日更新),然后筛选了所有可能符合条件的文章的标题和摘要。纳入的研究必须是观察性研究;调查了感染艾滋病病毒的移民的临床、病毒学或免疫学结果;在欧洲进行;至少有一个居住在欧洲国家的非移民对照组;并且使用英语。对文章标题和摘要进行资格筛选,然后由两名作者(EDV、VP、VS、SDG、MC 或 RN)进行全文评估。使用结构化 Redcap 表格从文章中提取数据。系统综述的主要结果包括:(1) 死亡率;(2) 艾滋病定义病症;(3) 艾滋病或死亡的综合结果;(4) 治疗中断;(5) 随访损失率;(6) 病毒学失败;(7) 免疫学失败。数据以相对风险 (RR) 或几率比及其 95% CIs 的形式报告。该研究已在 PROSPERO 注册,注册号为 CRD42024501191:在已确定的 1316 篇文章中(1297 篇为初始搜索,19 篇为更新搜索),19 篇被纳入我们的系统性综述,其中包括 104 676 名参与者,他们的平均随访时间为 79-3 个月。经调整潜在混杂因素后进行的荟萃分析表明,与普通人群相比,移民的死亡风险相似(RR 0-88,95% CI 0-75-1-04),但出现艾滋病定义病症(1-23,1-14-1-34)、中断治疗(2-39,1-49-3-29)、失去随访(2-53,1-41-4-53)、病毒学失败(1-80,1-25-2-60)和免疫学失败(3-70,2-17-12-50)的风险较高。在对世卫组织地区进行的子分析中,来自非洲地区的人出现与艾滋病毒相关的不良后果的风险更高:与非移民人群相比,居住在欧洲的艾滋病病毒感染者面临着更高的风险,包括发展为艾滋病、失去随访、中断治疗以及病毒学和免疫学失败。迫切需要采取干预措施,改善欧洲移民的艾滋病护理:无。
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引用次数: 0
Cost-effectiveness of lenacapavir for PrEP in Africa. 来那卡韦用于非洲 PrEP 的成本效益。
IF 12.8 1区 医学 Q1 IMMUNOLOGY Pub Date : 2024-11-01 Epub Date: 2024-09-20 DOI: 10.1016/S2352-3018(24)00242-X
Dvora Joseph Davey, Lise Jamieson
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引用次数: 0
Health impact, budget impact, and price threshold for cost-effectiveness of lenacapavir for HIV pre-exposure prophylaxis in eastern and southern Africa: a modelling analysis. 来那卡韦用于东部和南部非洲艾滋病暴露前预防的健康影响、预算影响和成本效益价格阈值:模型分析。
IF 12.8 1区 医学 Q1 IMMUNOLOGY Pub Date : 2024-11-01 Epub Date: 2024-09-20 DOI: 10.1016/S2352-3018(24)00239-X
Linxuan Wu, David Kaftan, Rachel Wittenauer, Cory Arrouzet, Nishali Patel, Arden L Saravis, Brian Pfau, Edinah Mudimu, Anna Bershteyn, Monisha Sharma
<p><strong>Background: </strong>Injectable lenacapavir administered every 6 months is a promising product for HIV pre-exposure prophylaxis (PrEP). We aimed to estimate the health and budget impacts and threshold price at which lenacapavir could be cost-effective in eastern and southern Africa.</p><p><strong>Methods: </strong>We adapted an agent-based network model, EMOD-HIV, to simulate lenacapavir scale-up in Zimbabwe, South Africa, and western Kenya from 2026 to 2035. Uptake assumptions were informed by a literature review of PrEP product preferences. In the main analysis, we varied lenacapavir coverage by subgroup: female sex workers (40% coverage); male clients of female sex workers (40%); adolescent girls and young women aged 15-24 years with more than one sexual partner (32%); women aged 25 years and older with more than one sexual partner (36%); and males with more than one sexual partner (32%). We also assessed a higher coverage scenario (64-76% across subgroups) and scenarios of expanding lenacapavir use, varying from concentrated among those at highest HIV risk to broader coverage including those at medium HIV risk. We estimated the maximum per-dose lenacapavir price that achieved cost-effectiveness (<US$500 per disability-adjusted life-year averted), infections averted, and 5-year budget impact, compared with daily oral PrEP only.</p><p><strong>Findings: </strong>In the main analysis, lenacapavir was projected to achieve from 1·6% (95% uncertainty interval [UI] 1·5-1·8) to 4·0% (3·4-5·1) population coverage across settings and to avert from 12·3% (5·4-19·5) to 18·0% (11·0-22·9) of infections over 10 years. The maximum price per dose was highest in South Africa ($106·28 [95% UI 95·72-115·87]), followed by Zimbabwe ($21·15 [17·70-24·89]), and lowest in western Kenya ($16·58 [15·44-17·70]). The 5-year budget impact was US$507·25 million (95% UI 436·14-585·42) in South Africa, $16·80 million (13·95-22·64) in Zimbabwe, and $4·09 million (3·86-4·30) in western Kenya. In the higher coverage scenario, lenacapavir distribution was projected to reach from 3·2% (95% UI 2·9-3·6) to 8·1% (6·8-10·5) population coverage and to avert from 21·2% (95% UI 14·7-18·5) to 33·3% (28·5-36·9) of HIV infections across settings over 10 years. Price thresholds were lower than in the main analysis: $88·34 (95% UI 83·02-94·19) in South Africa, $17·71 (15·61-20·05) in Zimbabwe, and $14·78 (14·33-15·30) in western Kenya. The 5-year budget impact was higher than the main analysis: $835·29 million (95% UI 736·98-962·98) in South Africa, $29·50 million (24·62-39·52) in Zimbabwe, and $7·45 million (7·11-7·85) in western Kenya. Expanding lenacapavir coverage resulted in higher HIV infections averted but lower price thresholds than scenarios of concentrated use among those with highest HIV risk.</p><p><strong>Interpretation: </strong>Our findings suggest that lenacapavir could avert substantial HIV incidence and that price thresholds and budget impacts vary by setting and
背景:每6个月注射一次的来那那韦是一种很有前景的艾滋病暴露前预防(PrEP)产品。我们旨在估算来那卡韦在东部和南部非洲对健康和预算的影响以及具有成本效益的阈值价格:我们对基于代理的网络模型EMOD-HIV进行了调整,以模拟2026年至2035年在津巴布韦、南非和肯尼亚西部扩大来那卡韦的情况。关于PrEP产品偏好的文献综述为我们提供了摄入量假设。在主要分析中,我们按以下亚群对来那那韦的覆盖率进行了调整:女性性工作者(覆盖率为 40%);女性性工作者的男性客户(40%);有一个以上性伴侣的 15-24 岁少女和年轻女性(32%);有一个以上性伴侣的 25 岁及以上女性(36%);有一个以上性伴侣的男性(32%)。我们还评估了覆盖率较高的方案(各亚群覆盖率为64%-76%)以及扩大来那卡韦使用范围的方案,从集中在HIV高危人群到覆盖范围更广(包括HIV中等风险人群)不等。我们估算了可实现成本效益的来那卡韦最高单剂量价格(结果显示,每毫升来那卡韦价格为1.5美元):在主要分析中,预计来那卡韦在不同环境下的人群覆盖率为1-6%(95%不确定区间[UI] 1-5-1-8)至4-0%(3-4-5-1),在10年内可避免12-3%(5-4-19-5)至18-0%(11-0-22-9)的感染。南非的每剂最高价格最高(106-28 美元 [95% UI 95-72-115-87]),其次是津巴布韦(21-15 美元 [17-70-24-89]),肯尼亚西部最低(16-58 美元 [15-44-17-70])。南非的 5 年预算影响为 5.07-25 亿美元(95% UI 为 4.36-14-585-42 美元),津巴布韦为 1,600-8,000 万美元(13-95-22-64 美元),肯尼亚西部为 400-0900 万美元(3-86-4-30 美元)。在覆盖率较高的情况下,预计来那卡韦的分布将达到3-2%(95% UI 2-9-3-6)到8-1%(6-8-10-5)的人口覆盖率,并在10年内避免21-2%(95% UI 14-7-18-5)到33-3%(28-5-36-9)的HIV感染。价格阈值低于主要分析:南非为 88-34 美元(95% UI 83-02-94-19),津巴布韦为 17-71 美元(15-61-20-05),肯尼亚西部为 14-78 美元(14-33-15-30)。5年预算影响高于主要分析:南非为8.35-29亿美元(95% UI 736-98-962-98),津巴布韦为2,900-5,000万美元(24-62-39-52),肯尼亚西部为700-4500万美元(7-11-7-85)。扩大来那卡韦的覆盖范围可避免更多的艾滋病感染,但与集中在艾滋病风险最高人群中使用的方案相比,价格阈值较低:我们的研究结果表明,来那卡韦可避免大量艾滋病感染,价格阈值和预算影响因环境和覆盖范围而异。这些结果可为有关来那那韦定价和资源规划的政策审议提供参考:比尔及梅琳达-盖茨基金会
{"title":"Health impact, budget impact, and price threshold for cost-effectiveness of lenacapavir for HIV pre-exposure prophylaxis in eastern and southern Africa: a modelling analysis.","authors":"Linxuan Wu, David Kaftan, Rachel Wittenauer, Cory Arrouzet, Nishali Patel, Arden L Saravis, Brian Pfau, Edinah Mudimu, Anna Bershteyn, Monisha Sharma","doi":"10.1016/S2352-3018(24)00239-X","DOIUrl":"10.1016/S2352-3018(24)00239-X","url":null,"abstract":"&lt;p&gt;&lt;strong&gt;Background: &lt;/strong&gt;Injectable lenacapavir administered every 6 months is a promising product for HIV pre-exposure prophylaxis (PrEP). We aimed to estimate the health and budget impacts and threshold price at which lenacapavir could be cost-effective in eastern and southern Africa.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Methods: &lt;/strong&gt;We adapted an agent-based network model, EMOD-HIV, to simulate lenacapavir scale-up in Zimbabwe, South Africa, and western Kenya from 2026 to 2035. Uptake assumptions were informed by a literature review of PrEP product preferences. In the main analysis, we varied lenacapavir coverage by subgroup: female sex workers (40% coverage); male clients of female sex workers (40%); adolescent girls and young women aged 15-24 years with more than one sexual partner (32%); women aged 25 years and older with more than one sexual partner (36%); and males with more than one sexual partner (32%). We also assessed a higher coverage scenario (64-76% across subgroups) and scenarios of expanding lenacapavir use, varying from concentrated among those at highest HIV risk to broader coverage including those at medium HIV risk. We estimated the maximum per-dose lenacapavir price that achieved cost-effectiveness (&lt;US$500 per disability-adjusted life-year averted), infections averted, and 5-year budget impact, compared with daily oral PrEP only.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Findings: &lt;/strong&gt;In the main analysis, lenacapavir was projected to achieve from 1·6% (95% uncertainty interval [UI] 1·5-1·8) to 4·0% (3·4-5·1) population coverage across settings and to avert from 12·3% (5·4-19·5) to 18·0% (11·0-22·9) of infections over 10 years. The maximum price per dose was highest in South Africa ($106·28 [95% UI 95·72-115·87]), followed by Zimbabwe ($21·15 [17·70-24·89]), and lowest in western Kenya ($16·58 [15·44-17·70]). The 5-year budget impact was US$507·25 million (95% UI 436·14-585·42) in South Africa, $16·80 million (13·95-22·64) in Zimbabwe, and $4·09 million (3·86-4·30) in western Kenya. In the higher coverage scenario, lenacapavir distribution was projected to reach from 3·2% (95% UI 2·9-3·6) to 8·1% (6·8-10·5) population coverage and to avert from 21·2% (95% UI 14·7-18·5) to 33·3% (28·5-36·9) of HIV infections across settings over 10 years. Price thresholds were lower than in the main analysis: $88·34 (95% UI 83·02-94·19) in South Africa, $17·71 (15·61-20·05) in Zimbabwe, and $14·78 (14·33-15·30) in western Kenya. The 5-year budget impact was higher than the main analysis: $835·29 million (95% UI 736·98-962·98) in South Africa, $29·50 million (24·62-39·52) in Zimbabwe, and $7·45 million (7·11-7·85) in western Kenya. Expanding lenacapavir coverage resulted in higher HIV infections averted but lower price thresholds than scenarios of concentrated use among those with highest HIV risk.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Interpretation: &lt;/strong&gt;Our findings suggest that lenacapavir could avert substantial HIV incidence and that price thresholds and budget impacts vary by setting and ","PeriodicalId":48725,"journal":{"name":"Lancet Hiv","volume":" ","pages":"e765-e773"},"PeriodicalIF":12.8,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11519315/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142308845","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Injectable PrEP comes to southern Africa. 注射式 PrEP 进入南部非洲。
IF 12.8 1区 医学 Q1 IMMUNOLOGY Pub Date : 2024-11-01 DOI: 10.1016/S2352-3018(24)00274-1
Roger Pebody
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引用次数: 0
HIV incidence in people receiving government-subsidised pre-exposure prophylaxis in Australia: a whole-of-population retrospective cohort study. 澳大利亚接受政府补贴的暴露前预防治疗人群中的艾滋病毒感染率:一项全人群回顾性队列研究。
IF 12.8 1区 医学 Q1 IMMUNOLOGY Pub Date : 2024-11-01 Epub Date: 2024-09-27 DOI: 10.1016/S2352-3018(24)00213-3
Nicholas A Medland, Hamish McManus, Benjamin R Bavinton, Doug Fraser, Michael W Traeger, Andrew E Grulich, Mark A Stoove, Skye McGregor, Jonathan M King, Dash Heath-Paynter, Rebecca J Guy

Background: HIV pre-exposure prophylaxis (PrEP) is highly effective and has been government subsidised in Australia since April, 2018. We examined HIV incidence over 5 years in a retrospective observational cohort of people who had received subsidised PrEP.

Methods: Linked de-identified dispensing records for all government-subsidised oral PrEP, HIV antiretroviral therapy (ART), and hepatitis C treatment were used. We included all people dispensed subsidised PrEP from April 1, 2018, to March 31, 2023, and examined records up to Sept 30, 2023. Exposure was measured from date of first PrEP prescription and days covered by PrEP calculated for individuals based on quantity and date supplied. Assuming that HIV was diagnosed 30 days before ART initiation, we imputed the date of acquisition as the midpoint between the diagnosis and the later of the last PrEP prescription or 6 months before the diagnosis. We calculated HIV incidence and its predictors using Poisson regression.

Findings: We included 66 206 people dispensed PrEP: 64 757 (97·8%) were men; median age was 33 years (IQR 27-43). 207 people acquired HIV, with an overall incidence of 1·07 per 1000 person-years (95% CI 0·93-1·23). Incidence was 2·61 per 1000 person-years among those dispensed PrEP once only. Using this group as a comparator, those with 60% or more days covered by PrEP had a 78·5% reduction in incidence (0·56 per 1000 person-years, p<0·0001) and those with less than 60% days covered had a 61·6% reduction (0·99 per 1000 person-years, p=0·0045). Independent predictors of HIV acquisition were a record of hepatitis C treatment (9·83 per 1000 person-years, adjusted incident rate ratio [aIRR] 8·70, 95% CI 4·86-15·56), only attending prescribers outside of areas with a high estimated prevalence of gay men (1·66 per 1000 person-years, aIRR 1·50, 1·08-2·09), age 18-29 years (1·33 per 1000 person-years, aIRR 1·56, 1·11-2·21), and earlier year of first PrEP.

Interpretation: The low observed incidence of HIV among people receiving government-subsidised PrEP highlights the success of a national programme of oral PrEP scale-up in achieving sustained reduction in community HIV transmission. However, incidence varied greatly, indicating that more research is needed to understand why people were not taking PrEP at times of risk and emphasising the need for new interventions focused on this population to achieve elimination of HIV transmission. Individuals dispensed PrEP once only and less frequent users might benefit from more support.

Funding: None.

背景:艾滋病暴露前预防疗法(PrEP)非常有效,自2018年4月起在澳大利亚开始享受政府补贴。我们对接受过补贴的 PrEP 的人群进行了回顾性观察队列,研究了 5 年内的艾滋病发病率:我们使用了所有政府补贴的口服 PrEP、HIV 抗逆转录病毒疗法 (ART) 和丙型肝炎治疗的链接式去标识配药记录。我们纳入了 2018 年 4 月 1 日至 2023 年 3 月 31 日期间所有获得补贴的 PrEP 配药者,并检查了截至 2023 年 9 月 30 日的记录。暴露时间从首次开具 PrEP 处方之日起计算,并根据提供的数量和日期计算个人的 PrEP 覆盖天数。假设在开始抗逆转录病毒疗法前 30 天诊断出 HIV,我们将感染日期推算为诊断日期与最后一次 PrEP 处方日期或诊断前 6 个月之间(以较晚者为准)的中点。我们使用泊松回归法计算了艾滋病发病率及其预测因素:我们纳入了 66 206 名获得 PrEP 处方的人:其中 64 757 人(97-8%)为男性;年龄中位数为 33 岁(IQR 27-43)。207 人感染了艾滋病毒,总发病率为每 1000 人年 1-07 例(95% CI 0-93-1-23)。在只接受过一次 PrEP 治疗的人群中,发病率为每千人年 2-61 例。以这组人群为参照,PrEP覆盖天数达到或超过60%的人群发病率降低了78%-5%(每1000人-年0-56例,p解释:在接受政府补贴的 PrEP 的人群中,观察到的艾滋病发病率较低,这突出表明口服 PrEP 的全国性推广计划在持续减少社区艾滋病传播方面取得了成功。然而,发病率差异很大,这表明需要开展更多的研究,以了解人们在风险时期不服用 PrEP 的原因,并强调需要针对这一人群采取新的干预措施,以消除艾滋病毒的传播。只配发一次 PrEP 的个人和使用频率较低的人可能会受益于更多的支持:无。
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引用次数: 0
Ending AIDS as a public health threat: the imperative for clear messaging on U=U, viral suppression, and zero risk. 消除艾滋病对公共健康的威胁:必须就 U=U、病毒抑制和零风险发出明确的信息。
IF 2.9 1区 医学 Q1 IMMUNOLOGY Pub Date : 2024-11-01 DOI: 10.1016/S2352-3018(24)00241-8
Emi E Okamoto, Florence Riako Anam, Solange Batiste, Mandisa Dukashe, Erika Castellanos, Midnight Poonkasetwattana, Bruce Richman

To end AIDS as a public health threat by 2030, we must leverage both the impactful message of U=U (undetectable equals untransmittable) and viral suppression to improve the wellbeing of individuals living with HIV, increase engagement with HIV services, and reduce barriers such as stigma, discrimination, and criminalisation. This message requires clear and unambiguous evidence-based narratives that emphasise the message that there is zero risk of sexual transmission when an undetectable viral load is maintained and negligible risk when viral suppression (as defined by 200-1000 copies per mL) is maintained. Dissemination of this information to individuals living with or affected by HIV, health-care workers, communities, the general public, and policy makers will increase awareness and credibility of this message and challenge deep-seated misperceptions. Furthermore, understanding the impact of this evidence underscores the necessity to urgently prioritise universal access to quality care, including viral load testing; leverage community leadership to address structural barriers; and monitor for ongoing success. Responsible and equitable messaging, which includes attention to women and marginalised groups, should be used to realise benefits for personal wellbeing and work towards an AIDS-free future.

要在 2030 年之前消除艾滋病这一公共卫生威胁,我们必须利用 U=U(检测不到等于不会传播)和病毒抑制这两个具有影响力的信息来改善艾滋病毒感染者的福祉,提高艾滋病毒服务的参与度,并减少污名化、歧视和定罪等障碍。这一信息需要清晰明确的循证说明,强调在保持检测不到病毒载量的情况下,性传播的风险为零;在保持病毒抑制(定义为每毫升 200-1000 拷贝)的情况下,风险可忽略不计。向艾滋病病毒感染者或患者、医护人员、社区、公众和政策制定者传播这一信息,将提高人们对这一信息的认识和可信度,并挑战根深蒂固的错误观念。此外,了解这一证据的影响突出表明,必须紧急优先普及优质护理服务,包括病毒载量检测;利用社区领导力解决结构性障碍;并监测持续取得的成功。应利用负责任和公平的信息传播,包括对妇女和边缘化群体的关注,以实现对个人福祉的惠益,并努力实现无艾滋病的未来。
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引用次数: 0
期刊
Lancet Hiv
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