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Letter to the editor on “Effectiveness, safety and patient-reported outcomes of emtricitabine/tenofovir alafenamide-based regimens for the treatment of HIV-1 infection: Final 24-month results from the prospective German TAFNES cohort study” 致编辑的关于“基于恩曲他滨/替诺福韦阿拉芬胺方案治疗HIV-1感染的有效性、安全性和患者报告的结果:来自前瞻性德国TAFNES队列研究的最后24个月结果”的信。
IF 3.2 3区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2025-10-13 DOI: 10.1111/hiv.70071
Joaquín Borrás-Blasco, Alejandro Valcuende-Rosique, Silvia Cornejo-Uixeda
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引用次数: 0
Predictors of discontinuing injectable cabotegravir/rilpivirine and virologic outcomes after resuming oral antiretroviral therapy 恢复口服抗逆转录病毒治疗后停止注射卡波特韦/利匹韦林和病毒学结果的预测因素。
IF 3.2 3区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2025-10-12 DOI: 10.1111/hiv.70128
Tali Faggiano, Jeffrey Yin, Nimish Patel, Afsana Karim, Kari Abulhosn, Laura Bamford, Lucas Hill

Objective

Evaluate factors associated with discontinuation of long-acting injectable (LAI) cabotegravir/rilpivirine (CAB/RPV) and describe virologic outcomes in those that returned to oral antiretroviral therapy (ART).

Methods

This is a retrospective cohort study at a single-centre primary care HIV clinic. Included were adults who received at least one injection of LAI CAB/RPV between April 2021 and March 2024. Characteristics were compared between those that continued LAI CAB/RPV and those that discontinued treatment during the study period. HIV viral load (VL) outcomes were evaluated in those that returned to oral ART and included the most recent VL in the range of 1–24 weeks, 24–48 weeks and the most recently documented VL through September 2024.

Results

A total of 92 and 346 patients were included in the discontinuation and continuation cohorts, respectively. Being male sex assigned at birth and having psychiatric disease was associated with continuing LAI CAB/RPV, whereas having active substance use and being on a multi-class regimen prior to initiation of LAI CAB/RPV was associated with discontinuation. In those with VL data after resuming oral ART, the percentage of those with HIV VL <50 copies per mL up to 24 weeks (n = 58) was 91.4%, up to 48 weeks (n = 53) was 90.6%, and using the most recent documented VL (n = 74) was 91.9%.

Conclusions

High viral suppression rates were observed in those that returned to oral therapy after discontinuing LAI CAB/RPV. Individuals with substance use demonstrated a higher rate of LAI discontinuation, despite the potential benefit from LAIs in this population.

目的:评估长效注射卡博特格拉韦/利匹韦林(CAB/RPV)停药的相关因素,并描述那些恢复口服抗逆转录病毒治疗(ART)的患者的病毒学结果。方法:这是一项在单中心初级保健HIV诊所进行的回顾性队列研究。研究对象是在2021年4月至2024年3月期间至少接受过一次LAI CAB/RPV注射的成年人。比较在研究期间继续进行LAI CAB/RPV和停止治疗的患者的特征。对那些重新接受口服抗逆转录病毒治疗的患者的HIV病毒载量(VL)结果进行评估,包括最近的VL(1-24周,24-48周)和最近记录的VL(截至2024年9月)。结果:分别有92例和346例患者被纳入停药组和继续治疗组。出生时性别为男性且患有精神疾病与持续LAI CAB/RPV相关,而在开始LAI CAB/RPV之前,有活性物质使用和正在进行多类治疗方案与中断相关。结论:在停用LAI CAB/RPV后恢复口服治疗的患者中,观察到较高的病毒抑制率。有药物使用的个体显示出更高的LAI停药率,尽管LAI在这一人群中有潜在的益处。
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引用次数: 0
“I cry alone because I'm so exhausted”: Family caregivers' perspectives on mHealth support in paediatric HIV care in Indonesia “我一个人哭,因为我太累了”:家庭照顾者对印度尼西亚儿科艾滋病毒护理中移动医疗支持的看法。
IF 3.2 3区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2025-10-12 DOI: 10.1111/hiv.70126
Syamikar Baridwan Syamsir, Agus Setiawan, Dhea Natashia, Nyimas Heny Purwati,  Astuti, Rian Adi Pamungkas

Objectives

Family caregivers of children living with HIV (CLHIV) in Indonesia navigate complex emotional and caregiving responsibilities amid stigma, isolation and limited support. This study aimed to explore the lived experiences of family caregivers in caring for children with HIV and to understand their perspectives on the potential use of mobile health (mHealth) applications to support paediatric HIV care in Indonesia.

Methods

A qualitative descriptive study was conducted using semi-structured interviews with fifteen purposively selected family caregivers at a national infectious disease referral hospital in Jakarta. Data were collected between June and August 2024, and analysed using conventional content analysis to inductively identify key themes.

Results

Three overarching themes were identified: (1) The Silent Burden of Caregiving, encompassing stigma, fear of disclosure, emotional fatigue and uncertainty about the child's future, (2) Supportive and Enabling Conditions, reflecting the role of social and spiritual support alongside interest in mHealth applications and their desired features, and (3) Barriers to Digital Technology Use, highlighting concerns over privacy, confidentiality and limited digital literacy.

Conclusions

Caregiving for a child with HIV is emotionally taxing and often undertaken in silence. mHealth applications may offer meaningful support when designed to be user-informed, culturally relevant and integrated with broader psychosocial services. Contextualized digital solutions have the potential to enhance HIV care outcomes in low-resource settings.

目的:印度尼西亚感染艾滋病毒(CLHIV)儿童的家庭照顾者在耻辱、孤立和有限的支持中处理复杂的情感和照顾责任。本研究旨在探讨家庭照顾者在照顾感染艾滋病毒的儿童方面的生活经验,并了解他们对潜在使用移动医疗(mHealth)应用程序支持印度尼西亚儿科艾滋病毒护理的看法。方法:采用半结构化访谈对雅加达一家国家传染病转诊医院的15名家庭护理人员进行定性描述性研究。数据收集于2025年6月至8月之间,并使用传统的内容分析来归纳确定关键主题。结果:确定了三个总体主题:(1)照顾的无声负担,包括耻辱,对披露的恐惧,情感疲劳和对孩子未来的不确定性;(2)支持和启用条件,反映了社会和精神支持的作用,以及对移动健康应用程序及其期望功能的兴趣;(3)数字技术使用的障碍,突出对隐私,保密性和有限数字素养的担忧。结论:照顾感染艾滋病毒的儿童在情感上很费力,而且往往是在沉默中进行的。如果移动医疗应用程序的设计与用户相关,与文化相关,并与更广泛的社会心理服务相结合,则可以提供有意义的支持。情境化的数字解决方案有可能在资源匮乏的环境中提高艾滋病毒护理结果。
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引用次数: 0
Antiretroviral treatment in people living with HIV with late diagnosis initiating ART with DTG/3TC or BIC/TAF/FTC: A real-world cohort analysis 晚期诊断的艾滋病病毒感染者使用DTG/3TC或BIC/TAF/FTC开始抗逆转录病毒治疗:现实世界队列分析
IF 3.2 3区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2025-10-07 DOI: 10.1111/hiv.70119
Gundolf Schuettfort, Jan Borch, Alfonso Cabello, Maria Crusells, Miguel Górgolas, Eva Herrmann, Carmen Hidalgo-Tenorio, Juan Lopez, Rafael Mican, Roser Navarro-Soler, Eugenia Negredo, Sebastian Noe, Jordi Puig, Federico Pulido, Rosario Serrao, Juergen Rockstroh, Sergio Rodriguez, Christoph Stephan, Miguel Torralba, Diva Trigo, Maria Vehreschild, Annette E. Haberl

Objective

To investigate the efficacy and safety of first-line antiretroviral treatment (ART) with 2DR dolutegravir/lamivudine (DTG/3TC) versus 3DR bictegravir/tenofovir alafenamide/emtricitabine (BIC/TAF/FTC) in persons with low CD4 cell counts and/or an AIDS-defining disease.

Design

Retrospective, multicentre, multinational study.

Methods

We conducted a retrospective, multicentre, multinational analysis to investigate the virological response and discontinuation rate in people living with HIV starting first-line ART with a CD4 cell count <200/μL and/or an AIDS-defining condition. Proportions of discontinuations were compared using univariate analysis. Virological response was analyzed using FDA snapshot analysis (HIV-1 RNA <50 copies/mL at week 48).

Results

Two hundred and fifty-nine people who were diagnosed late with HIV were included in the study. Sixty-nine of them were started on 2DR DTG/3TC and 190 on 3DR BIC/TAF/FTC. After matching 1 to 1 (matching criteria: age, sex, CD4 cell count, HI-viral load, Centers for Disease Control and Prevention (CDC) stage, n = 62 per group), the mean baseline CD4 cell count was 121/μL (standard deviation [SD] 65), including 21% presenting with an AIDS-defining condition. 96.2% and 91.8% of people living with HIV on 2DR and 3DR, respectively, had a viral load <50 copies/mL at week 48 (p = 0.244). No significant differences in discontinuation rates were observed at week 48 (5.5% in the 2DR and 9.4% in the 3DR group; p = 0.301).

Conclusion

In a European cohort of people diagnosed late with HIV who started first-line ART either with 2DR DTG/3TC or 3DR BIC/TAF/FTC, there were no significant differences in virological response and discontinuation rates after 48 weeks of treatment. With respect to the relatively small sample size and the inherent constraints of the study design, the possibility of establishing causal inference remains limited, and prospective studies are needed to further investigate on this topic.

目的:探讨2DR度替格拉韦/拉米夫定(DTG/3TC)与3DR比替格拉韦/替诺福韦/恩曲他滨(BIC/TAF/FTC)一线抗逆转录病毒治疗(ART)在CD4细胞计数低和/或艾滋病定义疾病患者中的疗效和安全性。设计:回顾性、多中心、多国研究。方法:我们进行了一项回顾性、多中心、多国分析,通过CD4细胞计数调查艾滋病毒感染者开始一线抗逆转录病毒治疗的病毒学反应和停药率。结果:259名被诊断为晚期艾滋病毒感染者纳入了研究。其中69人开始使用2DR DTG/3TC, 190人开始使用3DR BIC/TAF/FTC。1比1匹配后(匹配标准:年龄、性别、CD4细胞计数、hi病毒载量、疾病控制与预防中心(CDC)分期,每组n = 62),平均基线CD4细胞计数为121/μL(标准差[SD] 65),其中21%呈现艾滋病定义状态。结论:在一个欧洲队列中,诊断为晚期艾滋病毒的人开始一线抗逆转录病毒治疗时使用2DR DTG/3TC或3DR BIC/TAF/FTC, 48周治疗后病毒学反应和停药率没有显著差异。由于样本量相对较小,且研究设计的固有约束,建立因果推理的可能性仍然有限,需要前瞻性研究对该主题进行进一步研究。
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引用次数: 0
BHIVA guidelines on the management of HIV in pregnancy and the postpartum period 2025 BHIVA关于妊娠期和产后艾滋病毒管理的指南2025
IF 3.2 3区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2025-10-05 DOI: 10.1111/hiv.70091
Laura Byrne
<p>Writing group members </p><p><b>Contents</b></p><p><b>1 Introduction 1762</b></p><p>1.2 Key changes in the current guidelines 1763</p><p>1.3 Scope and purpose 1763</p><p>1.4 Methodology 1763</p><p>1.4.1 Guideline development process 1763</p><p>1.4.2 Involvement of people living with HIV 1764</p><p>1.4.3 Dissemination and implementation 1764</p><p>1.4.4 Inclusive language 1764</p><p>1.4.5 Guideline updates and date of next review 1764</p><p>1.5 Supporting women/people living with HIV during pregnancy and the postpartum period 1765</p><p>1.6 References 1765</p><p><b>2 Summary of recommendations 1765</b></p><p>From Section 4.2 Managing women/people who decline HIV screening in pregnancy 1765</p><p>From Section 4.5 Preventing HIV acquisition during pregnancy and infant feeding from a partner living with HIV 1766</p><p>From Section 6.1 The antenatal HIV MDT 1766</p><p>From Section 6.2 Supporting emotional and psychological wellbeing 1766</p><p>From Section 6.3 Supporting social wellbeing 1766</p><p>From Section 6.4 Screening for domestic abuse in pregnancy 1766</p><p>From Section 6.6 Pregnancy care in specific populations living with HIV 1766</p><p>From Section 7.1 Sexual health screening 1766</p><p>From Section 8.1 What ART to start in women/people who may become pregnant and continue in those who are pregnant 1767</p><p>From Section 8.2 ART dosing in pregnancy 1769</p><p>From Section 8.3.1 Regimens for first-line ART in pregnancy 1769</p><p>From Section 8.4 When to start ART in pregnancy 1770</p><p>From Section 8.5 Laboratory monitoring of ART in pregnancy 1770</p><p>From Section 8.6 HIV-2 1770</p><p>From Section 8.7.1 Presenting late in pregnancy (>28 weeks) not on ART 1770</p><p>From Section 8.7.2 Presenting in labour or after spontaneous rupture of membranes (SROM) (term and pre-term) 1771</p><p>From Section 8.7.3 Management of pregnant women/people with viraemia on ART 1771</p><p>From Section 9.1.3 Investigation and monitoring 1771</p><p>From Section 9.1.5 Antiviral treatment 1772</p><p>From Section 9.1.7 Obstetric management of HIV/HBV co-infection 1772</p><p>From Section 9.1.8 Management of neonates born to women/people with HIV/HBV co-infection 1772</p><p>From Section 9.2.2 Diagnosis and monitoring 1772</p><p>From Section 9.2.3 Antiviral treatment 1772</p><p>From Section 9.2.4 HBV vaccination 1772</p><p>From Section 9.2.5 Mode of delivery 1772</p><p>From Section 9.3 HAV vaccination 1773</p><p>From Section 10.1 Antenatal management 1773</p><p>From Section 10.2 Invasive prenatal testing 1773</p><p>From Section 10.4 External cephalic version (ECV) 1773</p><p>From Section 10.5 Fetal surveillance 1773</p><p>From Section 10.6 Management of term SROM 1773</p><p>From Section 10.7 Management of preterm prelabour rupture of membranes (PPROM) 1773</p><p>From Section 10.8 Preterm labour 1774</p><p>From Section 10.9 Mode of delivery 1774</p><p>From Section 10.10 Timing of birth 1774</p><p>From Section 10.11 Intrapartum management 1774</p
编写组成员内容1简介17621.2当前指南的主要变化17631.3范围和目的17631.4方法17631.4.1指南制定过程17631.4.2艾滋病毒感染者的参与17641.4.3传播和实施17641.4.4包容性语言17641.4.5指南更新和下次评审日期17641.5孕期和产后支持妇女/艾滋病毒感染者17651.6参考文献17652摘要第4.2节管理怀孕期间拒绝接受艾滋病毒筛查的妇女/人群第4.5节预防怀孕期间感染艾滋病毒和由携带艾滋病毒的伴侣喂养婴儿第6.1节产前艾滋病毒MDT第6.2节支持情感和心理健康第6.3节支持社会福祉第6.4节筛查怀孕期间家庭暴力第6.6节特定人群的妊娠护理艾滋病毒感染者1766来自第7.1节性健康筛查1766来自第8.1节可能怀孕的妇女/人群应开始何种抗逆转录病毒治疗1767来自第8.2节妊娠期抗逆转录病毒剂量1769来自第8.3.1节妊娠期一线抗逆转录病毒治疗方案1769来自第8.4节妊娠期何时开始抗逆转录病毒治疗1770来自第8.5节妊娠期抗逆转录病毒治疗的实验室监测1770来自第8.6节HIV-2 1770来自第8.7.1节妊娠晚期(28周)未出现来自第8.7.2节分娩时或自发破膜(SROM)后(足月和早产);来自第8.7.3节孕妇/病毒血症患者的ART 1771治疗;来自第9.1.3节调查和监测;来自第9.1.5节抗病毒治疗;来自第9.1.7节HIV/HBV合并感染的产科管理;来自第9.1.8节HIV/HBV合并感染妇女/患者所生新生儿的管理;来自第9.2.2节诊断和诊断监测来自第9.2.3节抗病毒治疗来自第9.2.4节乙肝疫苗接种来自第9.2.5节分娩方式来自第9.3节甲肝病毒疫苗接种来自第10.1节产前管理来自第10.2节有创产前检查来自第10.5节胎儿监测来自第10.6节足月管理来自第10.7节早产产前膜破裂(PPROM)的管理来自第9.2.3节第10.8节早产第10.9节分娩方式第10.10节分娩时机第10.11节产中管理第11.1节婴儿PNP第11.1.8节HIV-2节分娩时间第11.1.9节母乳喂养/母乳喂养期间PNP持续时间和PEP第11.2节免疫接种第11.3节诊断或排除HIV第11.4节诊断为HIV的婴儿的管理和乙型肺囊虫肺炎的预防来自第11.6节暴露于艾滋病毒的艾滋病毒阴性儿童来自第12.1节婴儿喂养决策来自第12.2节通过母乳/母乳传播艾滋病毒来自第12.3节配方奶粉(和其他替代)喂养与英国的艾滋病毒来自第12.3.1节支持妇女/艾滋病毒感染者使用配方奶粉喂养来自第12.4节抑制泌乳来自第12.5节联合王国的母乳/母乳喂养和艾滋病毒1777第12.5.1节支持联合王国妇女/人母乳/母乳喂养1778第12.6节母乳/母乳喂养期间可检测到的艾滋病毒载量的管理1778第12.7节混合喂养和艾滋病毒1778第13.1节ART 1778第13.2节产后坚持ART治疗和保留护理1778第13.3节产后心理健康需求评估1778第13.4节避孕1779第13.5节宫颈细胞学1779第13.6节支持服务和干预措施来自第13.8节伴侣和大龄儿童的检测英国妊娠期艾滋病毒的流行病学和传播风险3.1英国的垂直传播17803.2参考文献17814艾滋病毒筛查和预防妊娠期感染艾滋病毒17814.1 IDPS计划17814.2管理妊娠期拒绝艾滋病毒筛查的妇女/人17824.3妊娠期艾滋病毒重新检测17834.4产前转诊途径17834.5预防怀孕期间感染艾滋病毒和从感染艾滋病毒的伴侣那里喂养婴儿17834.6参考文献17845孕前建议17855.1补充叶酸17855.2优化孕前健康17855.3参考文献17866怀孕期间的情感、心理和社会健康17866.1产前艾滋病毒MDT 17866.2支持情感和心理健康17876.3支持社会福利17886.4筛查怀孕期间的家庭虐待17886。 5管理怀孕期间艾滋病毒状况信息17896.6特定艾滋病毒感染者的妊娠护理17896.6.1妇女/少数族裔社区的人17906.6.2妇女/移民身份不安全的人17906.6.3跨性别者和性别多样化的人17906.7参考文献17917孕妇/艾滋病毒感染者的感染筛查和免疫接种17937.1性健康筛查17937.2单纯疱疹病毒(HSV) 179747.3孕期免疫接种17947.4妊娠期抗逆转录病毒药物使用的现状和妊娠结局17968.1在可能怀孕的妇女/人群中开始何种抗逆转录病毒药物治疗,并在妊娠期继续治疗17968.1.1妊娠期转换17998.1.2妊娠期安全性的证据17998.1.3个体化和以个人为中心的护理18008.1.4数据有限的锚定药物18008.1.5转换后的病毒载量监测18008.2妊娠期抗逆转录病毒药物剂量18008.2.1 NRTI骨密度18018.2.2 inis 18018.2.3非核苷类逆转录酶抑制剂(NNRTIs) 18038.2.4 PIs 18038.2.5口服两药方案18048.2.6长效注射治疗18048.2.7其他药物18048.3妊娠期开始何种抗逆转录病毒治疗18048.3.1妊娠期一线抗逆转录病毒治疗方案18058.3.2妊娠期病毒抑制的证据18058.3.3因数据有限而不推荐的方案18068.3.4不再推荐的方案18068.3.5病毒学控制者18068.4何时开始抗逆转录病毒治疗决定何时开始抗逆转录病毒治疗需要考虑的因素。随机对照研究中发现,与以依非韦伦为基础的方案相比,抗逆转录病毒疗法对抗逆转录病毒疗法的病毒学应答更强18078.4.3英国从INSTI时代开始的抗逆转录病毒疗法对抗逆转录病毒疗法的病毒学应答数据18088.5妊娠期抗逆转录病毒疗法的实验室监测18088.6 HIV-2 18098.6.1妊娠期开始抗逆转录病毒疗法的风险18098.6.2妊娠期开始抗逆转录病毒疗法对HIV-2病毒载量持续≤50拷贝/mL的孕妇/接受抗逆转录病毒疗法的管理携带可检测到的HIV-2病毒载量18108.6.5婴儿PNP 18108.6.6婴儿喂养18108.7处理妊娠期间的特殊情况18108.7.1在妊娠晚期(&gt;28周)未接受抗逆转录病毒疗法18108.7.2在分娩时或在自发破膜(rom)后(足月和早产)出现18118.7.3在抗逆转录病毒疗法18127.3孕妇/病毒血症患者的管理妊娠期恶心呕吐和妊娠呕吐的情况下处理抗逆转录病毒疗法18158.8参考文献18159 HIV和肝炎合并感染18209.1 HBV 18209.1.1背景与流行病学18209.1.2 HIV/HBV合并感染的影响18209.1.3调查与监测18209.1.4急性HBV感染18219.1.5抗病毒治疗18219.1.6 HIV/HBV合并感染的并发症18229.1.7 HIV/HBV合并感染的产科管理18229.1.8 HIV/HBV合并感染妇女/患者新生儿管理18239.1.8 HCV 18239.2.1背景与流行病学18239.2.2诊断与监测18249.2.3抗病毒治疗治疗方法18249.2.4 HBV疫苗接种18259.2.5分娩方式18259.2.6 HIV/H
{"title":"BHIVA guidelines on the management of HIV in pregnancy and the postpartum period 2025","authors":"Laura Byrne","doi":"10.1111/hiv.70091","DOIUrl":"https://doi.org/10.1111/hiv.70091","url":null,"abstract":"&lt;p&gt;Writing group members\u0000 &lt;/p&gt;&lt;p&gt;&lt;b&gt;Contents&lt;/b&gt;&lt;/p&gt;&lt;p&gt;&lt;b&gt;1 Introduction 1762&lt;/b&gt;&lt;/p&gt;&lt;p&gt;1.2 Key changes in the current guidelines 1763&lt;/p&gt;&lt;p&gt;1.3 Scope and purpose 1763&lt;/p&gt;&lt;p&gt;1.4 Methodology 1763&lt;/p&gt;&lt;p&gt;1.4.1 Guideline development process 1763&lt;/p&gt;&lt;p&gt;1.4.2 Involvement of people living with HIV 1764&lt;/p&gt;&lt;p&gt;1.4.3 Dissemination and implementation 1764&lt;/p&gt;&lt;p&gt;1.4.4 Inclusive language 1764&lt;/p&gt;&lt;p&gt;1.4.5 Guideline updates and date of next review 1764&lt;/p&gt;&lt;p&gt;1.5 Supporting women/people living with HIV during pregnancy and the postpartum period 1765&lt;/p&gt;&lt;p&gt;1.6 References 1765&lt;/p&gt;&lt;p&gt;&lt;b&gt;2 Summary of recommendations 1765&lt;/b&gt;&lt;/p&gt;&lt;p&gt;From Section 4.2 Managing women/people who decline HIV screening in pregnancy 1765&lt;/p&gt;&lt;p&gt;From Section 4.5 Preventing HIV acquisition during pregnancy and infant feeding from a partner living with HIV 1766&lt;/p&gt;&lt;p&gt;From Section 6.1 The antenatal HIV MDT 1766&lt;/p&gt;&lt;p&gt;From Section 6.2 Supporting emotional and psychological wellbeing 1766&lt;/p&gt;&lt;p&gt;From Section 6.3 Supporting social wellbeing 1766&lt;/p&gt;&lt;p&gt;From Section 6.4 Screening for domestic abuse in pregnancy 1766&lt;/p&gt;&lt;p&gt;From Section 6.6 Pregnancy care in specific populations living with HIV 1766&lt;/p&gt;&lt;p&gt;From Section 7.1 Sexual health screening 1766&lt;/p&gt;&lt;p&gt;From Section 8.1 What ART to start in women/people who may become pregnant and continue in those who are pregnant 1767&lt;/p&gt;&lt;p&gt;From Section 8.2 ART dosing in pregnancy 1769&lt;/p&gt;&lt;p&gt;From Section 8.3.1 Regimens for first-line ART in pregnancy 1769&lt;/p&gt;&lt;p&gt;From Section 8.4 When to start ART in pregnancy 1770&lt;/p&gt;&lt;p&gt;From Section 8.5 Laboratory monitoring of ART in pregnancy 1770&lt;/p&gt;&lt;p&gt;From Section 8.6 HIV-2 1770&lt;/p&gt;&lt;p&gt;From Section 8.7.1 Presenting late in pregnancy (&gt;28 weeks) not on ART 1770&lt;/p&gt;&lt;p&gt;From Section 8.7.2 Presenting in labour or after spontaneous rupture of membranes (SROM) (term and pre-term) 1771&lt;/p&gt;&lt;p&gt;From Section 8.7.3 Management of pregnant women/people with viraemia on ART 1771&lt;/p&gt;&lt;p&gt;From Section 9.1.3 Investigation and monitoring 1771&lt;/p&gt;&lt;p&gt;From Section 9.1.5 Antiviral treatment 1772&lt;/p&gt;&lt;p&gt;From Section 9.1.7 Obstetric management of HIV/HBV co-infection 1772&lt;/p&gt;&lt;p&gt;From Section 9.1.8 Management of neonates born to women/people with HIV/HBV co-infection 1772&lt;/p&gt;&lt;p&gt;From Section 9.2.2 Diagnosis and monitoring 1772&lt;/p&gt;&lt;p&gt;From Section 9.2.3 Antiviral treatment 1772&lt;/p&gt;&lt;p&gt;From Section 9.2.4 HBV vaccination 1772&lt;/p&gt;&lt;p&gt;From Section 9.2.5 Mode of delivery 1772&lt;/p&gt;&lt;p&gt;From Section 9.3 HAV vaccination 1773&lt;/p&gt;&lt;p&gt;From Section 10.1 Antenatal management 1773&lt;/p&gt;&lt;p&gt;From Section 10.2 Invasive prenatal testing 1773&lt;/p&gt;&lt;p&gt;From Section 10.4 External cephalic version (ECV) 1773&lt;/p&gt;&lt;p&gt;From Section 10.5 Fetal surveillance 1773&lt;/p&gt;&lt;p&gt;From Section 10.6 Management of term SROM 1773&lt;/p&gt;&lt;p&gt;From Section 10.7 Management of preterm prelabour rupture of membranes (PPROM) 1773&lt;/p&gt;&lt;p&gt;From Section 10.8 Preterm labour 1774&lt;/p&gt;&lt;p&gt;From Section 10.9 Mode of delivery 1774&lt;/p&gt;&lt;p&gt;From Section 10.10 Timing of birth 1774&lt;/p&gt;&lt;p&gt;From Section 10.11 Intrapartum management 1774&lt;/p","PeriodicalId":13176,"journal":{"name":"HIV Medicine","volume":"26 11","pages":"1757-1880"},"PeriodicalIF":3.2,"publicationDate":"2025-10-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/hiv.70091","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145426268","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Perceived disabling physical pain and suicidal ideation in aging people living with HIV cured of hepatitis C: A multi-center survey in France (ANRS CO13 HEPAVIH) 感知致残性身体疼痛和自杀意念的老年丙型肝炎病毒感染者治愈:法国多中心调查(ANRS CO13 HEPAVIH)。
IF 3.2 3区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2025-10-01 DOI: 10.1111/hiv.70121
Tangui Barré, Clémence Ramier, Camelia Protopopescu, Philippe Sogni, Karine Ory, Tounes Saidi, Sophie Abgrall, Sylvie Brégigeon-Ronot, Patrizia Carrieri, Fabienne Marcellin, the ANRS CO13 HEPAVIH Study Group

Introduction

Suicidal ideation (SI) is highly prevalent among people living with HIV (PWH) and those with chronic hepatitis C virus (HCV) infection. Individuals with long-term HIV–HCV co-infection face specific health challenges, including heightened physical pain. We aimed to assess whether disabling physical pain is associated with SI in aging PWH who have been cured of HCV, after controlling for potential correlates or confounders such as depression and psychoactive substance use.

Methods

We analysed data from HCV-cured PWH who participated in a multi-center cross-sectional survey embedded within the French ANRS CO13 HEPAVIH cohort. We performed a multivariable logistic regression model with SI (score >0 for the ninth item of the Patient Health Questionnaire-9) as the outcome. Disabling physical pain was assessed using an answer ≥'very much' to the third item from the WHOQOL-HIV BREF questionnaire.

Results

Study population comprised 396 HCV-cured PWH (73.2% male), among whom 17.7% reported SI and 11.9% reported disabling physical pain. Participants reporting disabling physical pain had a three-fold higher risk of SI (adjusted odds ratio [95% confidence interval]: 3.07 [1.29–7.34]), after adjustment for depression (5.52 [2.66–11.43]), substance use, and lower social relationships-related quality of life (0.72 [0.64–0.80]).

Conclusions

These findings highlight that disabling physical pain should be systematically addressed among PWH cured of HCV, given its independent association with SI. Routine HIV follow-up care should integrate systematic screening for pain, mental health problems, and lack of social support. Timely referral to specialized services may help prevent future suicidal behaviours in this population.

导读:自杀意念(SI)在HIV感染者(PWH)和慢性丙型肝炎病毒感染者(HCV)中非常普遍。长期HIV-HCV合并感染的个体面临特定的健康挑战,包括身体疼痛加剧。我们的目的是在控制了潜在的相关因素或混杂因素(如抑郁和精神活性物质使用)后,评估致残性身体疼痛是否与HCV治愈的老年PWH中的SI相关。方法:我们分析了参加法国ANRS CO13 HEPAVIH队列多中心横断面调查的hcv治愈PWH的数据。我们以SI(患者健康问卷-9的第九项得分为b>)为结果进行了多变量逻辑回归模型。使用WHOQOL-HIV BREF问卷第三项的答案≥“very much”来评估致残性身体疼痛。结果:研究人群包括396名hcv治愈的PWH(73.2%为男性),其中17.7%报告SI, 11.9%报告致残性身体疼痛。在调整抑郁(5.52[2.66-11.43])、物质使用和较低的社会关系相关生活质量(0.72[0.64-0.80])后,报告致残性身体疼痛的参与者发生SI的风险高出三倍(调整优势比[95%置信区间]:3.07[1.29-7.34])。结论:这些发现强调,鉴于其与SI的独立关联,应系统地解决PWH治愈的HCV致残性身体疼痛。常规艾滋病毒随访护理应结合疼痛、心理健康问题和缺乏社会支持的系统筛查。及时转诊到专门服务机构可能有助于预防这一人群未来的自杀行为。
{"title":"Perceived disabling physical pain and suicidal ideation in aging people living with HIV cured of hepatitis C: A multi-center survey in France (ANRS CO13 HEPAVIH)","authors":"Tangui Barré,&nbsp;Clémence Ramier,&nbsp;Camelia Protopopescu,&nbsp;Philippe Sogni,&nbsp;Karine Ory,&nbsp;Tounes Saidi,&nbsp;Sophie Abgrall,&nbsp;Sylvie Brégigeon-Ronot,&nbsp;Patrizia Carrieri,&nbsp;Fabienne Marcellin,&nbsp;the ANRS CO13 HEPAVIH Study Group","doi":"10.1111/hiv.70121","DOIUrl":"10.1111/hiv.70121","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Introduction</h3>\u0000 \u0000 <p>Suicidal ideation (SI) is highly prevalent among people living with HIV (PWH) and those with chronic hepatitis C virus (HCV) infection. Individuals with long-term HIV–HCV co-infection face specific health challenges, including heightened physical pain. We aimed to assess whether disabling physical pain is associated with SI in aging PWH who have been cured of HCV, after controlling for potential correlates or confounders such as depression and psychoactive substance use.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We analysed data from HCV-cured PWH who participated in a multi-center cross-sectional survey embedded within the French ANRS CO13 HEPAVIH cohort. We performed a multivariable logistic regression model with SI (score &gt;0 for the ninth item of the Patient Health Questionnaire-9) as the outcome. Disabling physical pain was assessed using an answer ≥'very much' to the third item from the WHOQOL-HIV BREF questionnaire.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Study population comprised 396 HCV-cured PWH (73.2% male), among whom 17.7% reported SI and 11.9% reported disabling physical pain. Participants reporting disabling physical pain had a three-fold higher risk of SI (adjusted odds ratio [95% confidence interval]: 3.07 [1.29–7.34]), after adjustment for depression (5.52 [2.66–11.43]), substance use, and lower social relationships-related quality of life (0.72 [0.64–0.80]).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>These findings highlight that disabling physical pain should be systematically addressed among PWH cured of HCV, given its independent association with SI. Routine HIV follow-up care should integrate systematic screening for pain, mental health problems, and lack of social support. Timely referral to specialized services may help prevent future suicidal behaviours in this population.</p>\u0000 </section>\u0000 </div>","PeriodicalId":13176,"journal":{"name":"HIV Medicine","volume":"27 1","pages":"106-119"},"PeriodicalIF":3.2,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/hiv.70121","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145199200","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Impact on weight of a Doravirine switch in people living with HIV 多拉韦林转换对艾滋病毒感染者体重的影响
IF 3.2 3区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2025-09-30 DOI: 10.1111/hiv.70123
Nina Garofoli, Philippe Flandre, Jean-Paul Vincensini, Quentin Richier, Priscille Couture, Karine Lacombe, Gilles Pialoux, Jean-Luc Meynard

Background and Objective

Doravirine is among the first-line recommended treatments for people living with HIV (PLHIV) in the 2025 EACS guidelines. As opposed to tenofovir alafenamide or anti-integrase, its use was not associated with weight gain in clinical trials, but limited data are currently available in real life. In this cohort study, we investigated weight variation in PLHIV switching to doravirine.

Methods

A retrospective cohort analysis was conducted in two Parisian hospitals, including all PLHIV switching to doravirine between January 2019 and September 2022. Body Mass Index (BMI) variation was calculated from 48 months before to 36 months after the switch.

Results

Between January 2019 and December 2022, 300 patients were included, with 220 men (73%) and 185 (62%) patients born in France. The main antiretroviral combination before the switch was TAF/FTC/BIC (n = 47, 16%), and after the switch, doravirine with TDF and 3TC (n = 202, 67%). Twenty-eight patients (9.3%) discontinued doravirine after a median duration of 17.5 months. At 12 and 24 months after the switch, the median BMI variation was 0.0 kg/m2, and this variation remained unchanged regardless of the pre-switch treatment. These results were less pronounced in subgroups of patients originating from sub-Saharan Africa (+0.2 and +0.4 kg/m2) and in women (+0.3 and 0.5 kg/m2).

Conclusion

Switching to doravirine led to a weight stabilisation, without reversal of the previously gained weight. In PLHIV at higher risk of weight gain, there was still a slight increase in BMI after the doravirine switch.

背景和目的:在2025年EACS指南中,多拉韦林是HIV感染者(PLHIV)的一线推荐治疗之一。与替诺福韦alafenamide或抗整合酶相反,在临床试验中,它的使用与体重增加无关,但目前在现实生活中可获得的数据有限。在这项队列研究中,我们调查了PLHIV改用多拉韦林后的体重变化。方法:在巴黎两家医院进行回顾性队列分析,包括2019年1月至2022年9月期间所有改用多拉韦林的PLHIV患者。身体质量指数(BMI)的变化计算从48个月前到36个月后的转换。结果:在2019年1月至2022年12月期间,纳入了300例患者,其中220例男性(73%)和185例(62%)出生在法国。切换前以TAF/FTC/BIC联合治疗为主(n = 47, 16%),切换后以doravirine联合TDF和3TC联合治疗为主(n = 202, 67%)。28名患者(9.3%)在中位持续时间17.5个月后停用多拉韦林。在转换后的12个月和24个月,BMI的中位数变化为0.0 kg/m2,无论转换前的治疗如何,这一变化都保持不变。这些结果在撒哈拉以南非洲患者亚组(+0.2和+0.4 kg/m2)和女性(+0.3和0.5 kg/m2)中不太明显。结论:改用多拉韦林导致体重稳定,未逆转先前增加的体重。在体重增加风险较高的PLHIV患者中,在改用多拉韦林后,BMI仍有轻微增加。
{"title":"Impact on weight of a Doravirine switch in people living with HIV","authors":"Nina Garofoli,&nbsp;Philippe Flandre,&nbsp;Jean-Paul Vincensini,&nbsp;Quentin Richier,&nbsp;Priscille Couture,&nbsp;Karine Lacombe,&nbsp;Gilles Pialoux,&nbsp;Jean-Luc Meynard","doi":"10.1111/hiv.70123","DOIUrl":"10.1111/hiv.70123","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Background and Objective</h3>\u0000 \u0000 <p>Doravirine is among the first-line recommended treatments for people living with HIV (PLHIV) in the 2025 EACS guidelines. As opposed to tenofovir alafenamide or anti-integrase, its use was not associated with weight gain in clinical trials, but limited data are currently available in real life. In this cohort study, we investigated weight variation in PLHIV switching to doravirine.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>A retrospective cohort analysis was conducted in two Parisian hospitals, including all PLHIV switching to doravirine between January 2019 and September 2022. Body Mass Index (BMI) variation was calculated from 48 months before to 36 months after the switch.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Between January 2019 and December 2022, 300 patients were included, with 220 men (73%) and 185 (62%) patients born in France. The main antiretroviral combination before the switch was TAF/FTC/BIC (<i>n</i> = 47, 16%), and after the switch, doravirine with TDF and 3TC (<i>n</i> = 202, 67%). Twenty-eight patients (9.3%) discontinued doravirine after a median duration of 17.5 months. At 12 and 24 months after the switch, the median BMI variation was 0.0 kg/m<sup>2</sup>, and this variation remained unchanged regardless of the pre-switch treatment. These results were less pronounced in subgroups of patients originating from sub-Saharan Africa (+0.2 and +0.4 kg/m<sup>2</sup>) and in women (+0.3 and 0.5 kg/m<sup>2</sup>).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusion</h3>\u0000 \u0000 <p>Switching to doravirine led to a weight stabilisation, without reversal of the previously gained weight. In PLHIV at higher risk of weight gain, there was still a slight increase in BMI after the doravirine switch.</p>\u0000 </section>\u0000 </div>","PeriodicalId":13176,"journal":{"name":"HIV Medicine","volume":"27 1","pages":"136-145"},"PeriodicalIF":3.2,"publicationDate":"2025-09-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/hiv.70123","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145191706","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Diagnostic accuracy of the WHO clinical staging system for detection of immunologically defined advanced HIV disease: A systematic review and meta-analysis WHO临床分期系统检测免疫定义的晚期HIV疾病的诊断准确性:系统回顾和荟萃分析。
IF 3.2 3区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2025-09-26 DOI: 10.1111/hiv.70122
Hussein H. Twabi, Akitoshi Ueno, Josephine Ives, Ross Murtagh, Madalo Mukoka, Seyed Alireza Mortazavi, David S. Lawrence, Augustine T. Choko, Robina Semphere, Kelvin Balakasi, Ajay Rangaraj, Nathan Ford, Joseph N. Jarvis, Peter MacPherson

Introduction

People with advanced HIV disease face high risks of severe illness and death. CD4 testing enables timely diagnosis and appropriate care, yet access remains limited in many settings. This review investigated the diagnostic accuracy of the WHO clinical staging for identifying advanced HIV disease.

Methods

We conducted a systematic review and meta-analysis of studies published between 1 January 1998 and 1 May 2024 that assessed both WHO clinical staging and CD4 counts in people living with HIV aged 5 years and older (PROSPERO: CRD42024558372). We pooled sensitivity and specificity estimates of WHO Stage 3/4 for detecting advanced HIV disease (CD4 <200 cells/μL) using bivariate random-effects meta-analysis. Risk of bias was assessed using QUADAS-2, and certainty of evidence was appraised using Grading of Recommendations, Assessment, Development, and Evaluations (GRADE).

Results

Of 15,194 studies screened, 335 relevant studies were identified, from which 25 were included in evidence synthesis and 21 in the meta-analysis. Most studies were from the WHO African (19/25) and South-East Asian (5/25) regions. Risk of bias was moderate to high in 88% of studies, primarily due to issues with clinical staging assessment. Pooled sensitivity and specificity of WHO Stage 3/4 were 60.7% (95% CI: 48.0%–72.1%) and 72.4% (95% CI: 61.4%–81.3%), respectively. Specificity was significantly higher outside the African region (p < 0.001). In a population of 100,000 people living with HIV with 30% advanced HIV disease prevalence, WHO staging would miss 11,700 true advanced HIV disease cases and misclassify 19,600.

Conclusions

WHO clinical staging alone shows low accuracy for detecting advanced HIV disease, risking both missed diagnoses and overtreatment. CD4 testing remains essential for accurately identifying and managing advanced HIV disease.

导言:艾滋病毒晚期患者面临严重疾病和死亡的高风险。CD4检测可实现及时诊断和适当护理,但在许多情况下获得检测的机会仍然有限。本综述调查了世卫组织临床分期识别晚期HIV疾病的诊断准确性。方法:我们对1998年1月1日至2024年5月1日发表的研究进行了系统回顾和荟萃分析,这些研究评估了5岁及以上艾滋病毒感染者的WHO临床分期和CD4计数(PROSPERO: CRD42024558372)。结果:在筛选的15,194项研究中,确定了335项相关研究,其中25项纳入证据综合,21项纳入荟萃分析。大多数研究来自世卫组织非洲(19/25)和东南亚(5/25)区域。88%的研究偏倚风险为中等至高,主要是由于临床分期评估的问题。WHO 3/4期的合并敏感性和特异性分别为60.7% (95% CI: 48.0% ~ 72.1%)和72.4% (95% CI: 61.4% ~ 81.3%)。结论:世卫组织单独的临床分期显示,检测晚期艾滋病毒疾病的准确性较低,存在漏诊和过度治疗的风险。CD4检测对于准确识别和管理晚期艾滋病毒疾病仍然至关重要。
{"title":"Diagnostic accuracy of the WHO clinical staging system for detection of immunologically defined advanced HIV disease: A systematic review and meta-analysis","authors":"Hussein H. Twabi,&nbsp;Akitoshi Ueno,&nbsp;Josephine Ives,&nbsp;Ross Murtagh,&nbsp;Madalo Mukoka,&nbsp;Seyed Alireza Mortazavi,&nbsp;David S. Lawrence,&nbsp;Augustine T. Choko,&nbsp;Robina Semphere,&nbsp;Kelvin Balakasi,&nbsp;Ajay Rangaraj,&nbsp;Nathan Ford,&nbsp;Joseph N. Jarvis,&nbsp;Peter MacPherson","doi":"10.1111/hiv.70122","DOIUrl":"10.1111/hiv.70122","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Introduction</h3>\u0000 \u0000 <p>People with advanced HIV disease face high risks of severe illness and death. CD4 testing enables timely diagnosis and appropriate care, yet access remains limited in many settings. This review investigated the diagnostic accuracy of the WHO clinical staging for identifying advanced HIV disease.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>We conducted a systematic review and meta-analysis of studies published between 1 January 1998 and 1 May 2024 that assessed both WHO clinical staging and CD4 counts in people living with HIV aged 5 years and older (PROSPERO: CRD42024558372). We pooled sensitivity and specificity estimates of WHO Stage 3/4 for detecting advanced HIV disease (CD4 &lt;200 cells/μL) using bivariate random-effects meta-analysis. Risk of bias was assessed using QUADAS-2, and certainty of evidence was appraised using Grading of Recommendations, Assessment, Development, and Evaluations (GRADE).</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>Of 15,194 studies screened, 335 relevant studies were identified, from which 25 were included in evidence synthesis and 21 in the meta-analysis. Most studies were from the WHO African (19/25) and South-East Asian (5/25) regions. Risk of bias was moderate to high in 88% of studies, primarily due to issues with clinical staging assessment. Pooled sensitivity and specificity of WHO Stage 3/4 were 60.7% (95% CI: 48.0%–72.1%) and 72.4% (95% CI: 61.4%–81.3%), respectively. Specificity was significantly higher outside the African region (<i>p</i> &lt; 0.001). In a population of 100,000 people living with HIV with 30% advanced HIV disease prevalence, WHO staging would miss 11,700 true advanced HIV disease cases and misclassify 19,600.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>WHO clinical staging alone shows low accuracy for detecting advanced HIV disease, risking both missed diagnoses and overtreatment. CD4 testing remains essential for accurately identifying and managing advanced HIV disease.</p>\u0000 </section>\u0000 </div>","PeriodicalId":13176,"journal":{"name":"HIV Medicine","volume":"27 1","pages":"120-135"},"PeriodicalIF":3.2,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145148991","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
People living with HIV on modern antiretrovirals do not display a pro-atherogenic lipid profile and have similar body composition compared to healthy controls 与健康对照组相比,接受现代抗逆转录病毒治疗的艾滋病毒感染者没有显示出促动脉粥样硬化的脂质特征,并且具有相似的身体组成。
IF 3.2 3区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2025-09-24 DOI: 10.1111/hiv.70118
S. Savinelli, A. Heeney, W. Tinago, A. A. Garcia Leon, P. McGettrick, A. G. Cotter, I. Walsh, M. Fitzgibbon, C. A. Sabin, P. W. G. Mallon, E. R. Feeney, the HIV UPBEAT study group

Objectives

Alterations in lipids and apolipoproteins contribute to cardiovascular disease (CVD) and are common in people with HIV. The aim of our study was to compare lipid profiles and body composition between people with and without HIV and to explore whether any associations with HIV could be explained by socio-demographic, clinical characteristics and body composition.

Methods

Cross-sectional analysis of a cohort study enrolling people with HIV and HIV-negative controls. Apolipoproteins [ApoB-100, ApoA1, Lp(a)] were analysed by immunoturbidimetry. Lipids (total cholesterol [TC], low-density lipoprotein [LDL], high-density lipoprotein [HDL]), clinical/demographic data and dual-energy X-ray absorptiometry (DXA)-measured body composition parameters were collected. Between-group differences were assessed with Student's T-test. Linear regression models assessed associations of lipids and apolipoproteins with HIV status and associations with socio-demographic, clinical characteristics and body composition.

Results

We included 108 people with HIV on treatment (93.5% with viral suppression) and 96 controls. People with HIV were younger, more likely to be male, with obesity, of African ethnicity, smokers and with a higher representation of CVD, hypertension, diabetes and statin use. ApoB-100, TC, HDL and LDL were significantly lower in people with HIV, with no between-group difference in ApoA, Lp(a) and body composition. HIV infection remained independently associated with lower TC and LDL after adjustment for possible confounders.

Conclusions

People with HIV from a contemporary cohort had lower pro-atherogenic lipid parameters compared to controls, and no differences in body composition between people with HIV and controls were observed. Traditional risk factors for CVD and chronic inflammation might have a greater impact than dyslipidaemia itself on the increased CVD risk in people with HIV.

目的:脂质和载脂蛋白的改变与心血管疾病(CVD)有关,并且在HIV感染者中很常见。本研究的目的是比较HIV感染者和非HIV感染者的脂质特征和身体组成,并探讨是否有任何与HIV相关的因素可以用社会人口统计学、临床特征和身体组成来解释。方法:对一项纳入HIV感染者和HIV阴性对照的队列研究进行横断面分析。免疫比浊法分析载脂蛋白[ApoB-100, ApoA1, Lp(a)]。收集血脂(总胆固醇[TC]、低密度脂蛋白[LDL]、高密度脂蛋白[HDL])、临床/人口统计学数据和双能x线吸收仪(DXA)测量的身体成分参数。组间差异采用学生t检验。线性回归模型评估了脂质和载脂蛋白与HIV状态的关系,以及与社会人口统计学、临床特征和身体组成的关系。结果:我们纳入了108例接受治疗的HIV感染者(93.5%采用病毒抑制)和96例对照组。艾滋病毒感染者更年轻,更可能是男性,肥胖,非洲裔,吸烟者,心血管疾病,高血压,糖尿病和他汀类药物使用的比例更高。HIV感染者的ApoB-100、TC、HDL和LDL显著降低,ApoA、Lp(a)和体成分组间无差异。在调整了可能的混杂因素后,HIV感染仍然与较低的TC和LDL独立相关。结论:与对照组相比,来自当代队列的HIV感染者具有较低的促动脉粥样硬化脂质参数,并且在HIV感染者和对照组之间的身体组成没有观察到差异。心血管疾病和慢性炎症的传统危险因素可能比血脂异常本身对艾滋病毒感染者心血管疾病风险增加的影响更大。
{"title":"People living with HIV on modern antiretrovirals do not display a pro-atherogenic lipid profile and have similar body composition compared to healthy controls","authors":"S. Savinelli,&nbsp;A. Heeney,&nbsp;W. Tinago,&nbsp;A. A. Garcia Leon,&nbsp;P. McGettrick,&nbsp;A. G. Cotter,&nbsp;I. Walsh,&nbsp;M. Fitzgibbon,&nbsp;C. A. Sabin,&nbsp;P. W. G. Mallon,&nbsp;E. R. Feeney,&nbsp;the HIV UPBEAT study group","doi":"10.1111/hiv.70118","DOIUrl":"10.1111/hiv.70118","url":null,"abstract":"<div>\u0000 \u0000 \u0000 <section>\u0000 \u0000 <h3> Objectives</h3>\u0000 \u0000 <p>Alterations in lipids and apolipoproteins contribute to cardiovascular disease (CVD) and are common in people with HIV. The aim of our study was to compare lipid profiles and body composition between people with and without HIV and to explore whether any associations with HIV could be explained by socio-demographic, clinical characteristics and body composition.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Methods</h3>\u0000 \u0000 <p>Cross-sectional analysis of a cohort study enrolling people with HIV and HIV-negative controls. Apolipoproteins [ApoB-100, ApoA1, Lp(a)] were analysed by immunoturbidimetry. Lipids (total cholesterol [TC], low-density lipoprotein [LDL], high-density lipoprotein [HDL]), clinical/demographic data and dual-energy X-ray absorptiometry (DXA)-measured body composition parameters were collected. Between-group differences were assessed with Student's T-test. Linear regression models assessed associations of lipids and apolipoproteins with HIV status and associations with socio-demographic, clinical characteristics and body composition.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Results</h3>\u0000 \u0000 <p>We included 108 people with HIV on treatment (93.5% with viral suppression) and 96 controls. People with HIV were younger, more likely to be male, with obesity, of African ethnicity, smokers and with a higher representation of CVD, hypertension, diabetes and statin use. ApoB-100, TC, HDL and LDL were significantly lower in people with HIV, with no between-group difference in ApoA, Lp(a) and body composition. HIV infection remained independently associated with lower TC and LDL after adjustment for possible confounders.</p>\u0000 </section>\u0000 \u0000 <section>\u0000 \u0000 <h3> Conclusions</h3>\u0000 \u0000 <p>People with HIV from a contemporary cohort had lower pro-atherogenic lipid parameters compared to controls, and no differences in body composition between people with HIV and controls were observed. Traditional risk factors for CVD and chronic inflammation might have a greater impact than dyslipidaemia itself on the increased CVD risk in people with HIV.</p>\u0000 </section>\u0000 </div>","PeriodicalId":13176,"journal":{"name":"HIV Medicine","volume":"27 1","pages":"86-95"},"PeriodicalIF":3.2,"publicationDate":"2025-09-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/hiv.70118","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145130606","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"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
Sexual dysfunction care needs of gay, bisexual, and other men who have sex with men living with HIV in Montreal, Canada 加拿大蒙特利尔同性恋者、双性恋者和其他与艾滋病毒携带者发生性行为的男性的性功能障碍护理需求
IF 3.2 3区 医学 Q2 INFECTIOUS DISEASES Pub Date : 2025-09-22 DOI: 10.1111/hiv.70115
Francesco Avallone, Kim Engler, Ford Hickson, Joseph Cox, Eric Fortin, Sean Yaphe, Bertrand Lebouché

Objectives

Sexual dysfunction (SD) is common among gay, bisexual and other men who have sex with men (GBM) with HIV, yet little is known about their views on SD care. We explored these views to inform patient-centred SD care to improve care delivery and sexual health outcomes.

Methods

Semi-structured interviews were conducted in 2024 with 31 Montreal-based GBM with HIV who experienced SD in the last 5 years (reduced libido, erectile dysfunction, premature/delayed ejaculation and/or pain during sex), covering SD care experiences and preferences. Thematic analysis was applied to interview transcripts.

Results

Participants mostly reported reduced libido (83.9%) and erectile dysfunction (ED(80.6%), with over half (58.0%) experiencing multiple SDs concurrently. Themes regarding SD care experiences were (1) costs and benefits of ED medication, (2) limited benefits of testosterone replacement therapy, (3) mixed views on talk therapy (and a preference for group therapy), and (4) not seeking care due to questions of SD definition and normalcy. SD care preferences concerned both provider characteristics (identity, approach to patients and expertise) and care delivery (information provision, involvement and respect and access to diverse resources).

Conclusions

Irrespective of the approach to SD care sought (medication or talk therapy), participants experienced limited success. For some, doubts about the severity of their SD impeded help-seeking. SD care preferences for the provider (e.g., expertise) and care provided (e.g., information, patient involvement) offer paths to more patient-centred care.

目的:性功能障碍(SD)在男同性恋、双性恋和其他男男性行为者(GBM)中很常见,但他们对性功能障碍护理的看法却知之甚少。我们探讨了这些观点,为以患者为中心的可持续发展护理提供信息,以改善护理服务和性健康结果。方法:在2024年对31名在过去5年内经历过SD(性欲减退、勃起功能障碍、早泄/延迟射精和/或性交疼痛)的蒙特利尔HIV GBM患者进行半结构化访谈,涵盖SD护理经历和偏好。访谈笔录采用专题分析。结果:参与者大多报告性欲下降(83.9%)和勃起功能障碍(ED)(80.6%),超过一半(58.0%)的患者同时经历多重性勃起障碍。关于性功能障碍治疗经历的主题是(1)ED药物的成本和收益,(2)睾酮替代疗法的有限收益,(3)对谈话治疗的不同看法(以及对团体治疗的偏好),以及(4)由于性功能障碍定义和正常问题而不寻求治疗。可持续发展护理偏好涉及提供者特征(身份、对患者的态度和专业知识)和护理提供(信息提供、参与、尊重和获得各种资源)。结论:无论采用何种方法寻求SD治疗(药物治疗或谈话治疗),参与者的成功程度有限。对一些人来说,对SD严重程度的怀疑阻碍了他们寻求帮助。提供者的SD护理偏好(例如,专业知识)和所提供的护理(例如,信息,患者参与)为更加以患者为中心的护理提供了途径。
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引用次数: 0
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HIV Medicine
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