Pub Date : 2025-12-31eCollection Date: 2025-01-01DOI: 10.2147/HIV.S545278
Mimi Zhai, Yamin Li, Jianhai Long, Yunxia Li, Xianyang Lei
Aim: To develop and conduct a preliminary evaluation of a digital salutogenic intervention-"Towards the Sun"-aimed at enhancing sense of coherence (SOC) and improving health outcomes among newly diagnosed HIV-positive men who have sex with men (MSM).
Methods: The initial intervention draft was developed using the systematic Intervention Mapping (IM) process, informed by preliminary research, literature review, and evidence-based needs assessment. Two rounds of expert panel review were then conducted to refine the draft, followed by a feasibility assessment among newly diagnosed HIV-positive MSM.
Results: The final digital intervention consisted of a five-stage, eight-week program, focusing on stress management, resource activation, and meaning exploration to strengthen the three dimensions of SOC. After review by 8 experts, the mean importance ratings of the intervention items were all above 4 and the coefficients of variation (CV) were less than 0.20, indicating consensus. A pilot study involving 7 newly diagnosed MSM demonstrated feasibility: SOC-13 scores increased, levels of stress and depression decreased, and participants reported high satisfaction with the overall content, especially the modules on self-acceptance and resource orientation.
Conclusion: This digital salutogenic intervention demonstrated good feasibility, user acceptance, and preliminary effectiveness among newly diagnosed HIV-positive MSM. As a strengths-based and innovative digital solution, it warrants further validation and dissemination in larger samples and randomized controlled designs.
Reporting guidelines: The study followed the TIDieR (Template for Intervention Description and Replication) Checklist.
{"title":"Development and Feasibility of \"Towards the Sun\": A Digital Salutogenic Intervention to Enhance Sense of Coherence and Health Outcomes Among Newly Diagnosed HIV-Positive MSM.","authors":"Mimi Zhai, Yamin Li, Jianhai Long, Yunxia Li, Xianyang Lei","doi":"10.2147/HIV.S545278","DOIUrl":"10.2147/HIV.S545278","url":null,"abstract":"<p><strong>Aim: </strong>To develop and conduct a preliminary evaluation of a digital salutogenic intervention-\"Towards the Sun\"-aimed at enhancing sense of coherence (SOC) and improving health outcomes among newly diagnosed HIV-positive men who have sex with men (MSM).</p><p><strong>Methods: </strong>The initial intervention draft was developed using the systematic Intervention Mapping (IM) process, informed by preliminary research, literature review, and evidence-based needs assessment. Two rounds of expert panel review were then conducted to refine the draft, followed by a feasibility assessment among newly diagnosed HIV-positive MSM.</p><p><strong>Results: </strong>The final digital intervention consisted of a five-stage, eight-week program, focusing on stress management, resource activation, and meaning exploration to strengthen the three dimensions of SOC. After review by 8 experts, the mean importance ratings of the intervention items were all above 4 and the coefficients of variation (CV) were less than 0.20, indicating consensus. A pilot study involving 7 newly diagnosed MSM demonstrated feasibility: SOC-13 scores increased, levels of stress and depression decreased, and participants reported high satisfaction with the overall content, especially the modules on self-acceptance and resource orientation.</p><p><strong>Conclusion: </strong>This digital salutogenic intervention demonstrated good feasibility, user acceptance, and preliminary effectiveness among newly diagnosed HIV-positive MSM. As a strengths-based and innovative digital solution, it warrants further validation and dissemination in larger samples and randomized controlled designs.</p><p><strong>Reporting guidelines: </strong>The study followed the TIDieR (Template for Intervention Description and Replication) Checklist.</p>","PeriodicalId":46555,"journal":{"name":"HIV AIDS-Research and Palliative Care","volume":"17 ","pages":"419-431"},"PeriodicalIF":1.8,"publicationDate":"2025-12-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12766161/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145913404","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-17eCollection Date: 2025-01-01DOI: 10.2147/HIV.S528859
Alexy Inciarte, Celia Miralles, Ana Silva-Klug, Boris Revollo, Miguel García Deltoro, Joaquín Portilla, Antonio Antela, Manuel Ángel Castaño Carracedo, Cristina De Álvaro, Johanna Ramroth, Ana González-Cordón, Josep Mallolas
Background: Bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) is a single-tablet regimen recommended as first-line HIV treatment in international guidelines. This analysis aimed to assess the effectiveness and safety of B/F/TAF in real-world Spanish clinical practice.
Methods: This was an analysis of the Spanish subset from the BICSTaR study in treatment-naïve (TN) and treatment-experienced (TE) people with HIV who started treatment between November 2019 and July 2021 (European study registration: EUPAS22185). The primary endpoint was virologic suppression (HIV-1 RNA <50 copies/mL); additional endpoints included CD4 cell count changes, treatment persistence, adverse events, weight changes, and the 36-Item Short Form Survey mental and physical component summary (MCS/PCS) scores at 12 months.
Results: In total, 249 people with HIV initiated B/F/TAF treatment (62 TN, 187 TE). At 12 months, virologic suppression was achieved by 86% of TN and 98% of TE participants, with 91% of those TE participants with baseline HIV-1 RNA ≥50 copies/µL achieving suppression. Median CD4 count increased by 296 cells/µL in TN (p<0.001) and 12 cells/µL in TE (p=0.302) participants. Persistence at 12 months was high in all participants, with 95% still on treatment. Overall, none of TN and less than 3% of TE participants discontinued B/F/TAF due to drug-related adverse events, all of which were mild or moderate. Median weight increase was 2.9 kg in TN (p<0.001) and 1.0 kg in TE (p<0.001) participants. Median MCS scores improved in the TN group (8.4-point increase, p<0.001) but not in the TE group (0.4-point increase, p=0.767), while PCS scores remained stable both among TN and TE.
Conclusion: These real-world findings strongly support B/F/TAF use in TN and TE people with HIV in Spain, demonstrating high 12-month persistence and effectiveness, and mental health benefits in TN participants, with minimal adverse events.
{"title":"Effectiveness and Safety of Bictegravir/Emtricitabine/Tenofovir Alafenamide in People with HIV: A Real-World Data from the Spanish BICSTaR Cohort.","authors":"Alexy Inciarte, Celia Miralles, Ana Silva-Klug, Boris Revollo, Miguel García Deltoro, Joaquín Portilla, Antonio Antela, Manuel Ángel Castaño Carracedo, Cristina De Álvaro, Johanna Ramroth, Ana González-Cordón, Josep Mallolas","doi":"10.2147/HIV.S528859","DOIUrl":"10.2147/HIV.S528859","url":null,"abstract":"<p><strong>Background: </strong>Bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) is a single-tablet regimen recommended as first-line HIV treatment in international guidelines. This analysis aimed to assess the effectiveness and safety of B/F/TAF in real-world Spanish clinical practice.</p><p><strong>Methods: </strong>This was an analysis of the Spanish subset from the BICSTaR study in treatment-naïve (TN) and treatment-experienced (TE) people with HIV who started treatment between November 2019 and July 2021 (European study registration: EUPAS22185). The primary endpoint was virologic suppression (HIV-1 RNA <50 copies/mL); additional endpoints included CD4 cell count changes, treatment persistence, adverse events, weight changes, and the 36-Item Short Form Survey mental and physical component summary (MCS/PCS) scores at 12 months.</p><p><strong>Results: </strong>In total, 249 people with HIV initiated B/F/TAF treatment (62 TN, 187 TE). At 12 months, virologic suppression was achieved by 86% of TN and 98% of TE participants, with 91% of those TE participants with baseline HIV-1 RNA ≥50 copies/µL achieving suppression. Median CD4 count increased by 296 cells/µL in TN (p<0.001) and 12 cells/µL in TE (p=0.302) participants. Persistence at 12 months was high in all participants, with 95% still on treatment. Overall, none of TN and less than 3% of TE participants discontinued B/F/TAF due to drug-related adverse events, all of which were mild or moderate. Median weight increase was 2.9 kg in TN (p<0.001) and 1.0 kg in TE (p<0.001) participants. Median MCS scores improved in the TN group (8.4-point increase, p<0.001) but not in the TE group (0.4-point increase, p=0.767), while PCS scores remained stable both among TN and TE.</p><p><strong>Conclusion: </strong>These real-world findings strongly support B/F/TAF use in TN and TE people with HIV in Spain, demonstrating high 12-month persistence and effectiveness, and mental health benefits in TN participants, with minimal adverse events.</p>","PeriodicalId":46555,"journal":{"name":"HIV AIDS-Research and Palliative Care","volume":"17 ","pages":"407-418"},"PeriodicalIF":1.8,"publicationDate":"2025-12-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12719640/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145821621","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-12-03eCollection Date: 2025-01-01DOI: 10.2147/HIV.S558240
Ravika Khaila Arrum, Retno Hesty Maharani, Eva Krishna Sutedja, Laila Tsaqilah, Hendra Gunawan, Pati Aji Achdiat
Anogenital warts (AGW) are a common manifestation of human papillomavirus (HPV) infection, primarily caused by strains 6 and 11. According to results, mucosal HPV is transmitted through sexual contact, with risk factors including immunodeficiency, such as Human Immunodeficiency Virus (HIV). Individuals with HIV experience a higher incidence of AGW due to impaired immune function that hinders HPV clearance. There is currently no specific antiviral therapy available for HPV, although several management options exist. However, some of these treatments may cause pain and discomfort. Glycyrrhizinic acid (GA) has demonstrated potential in managing HPV infection because of its antiviral properties and minimal side effects. Despite these promising results, GA is not yet recognized as a standard therapy for AGW. This case report describes the effectiveness of Glizigen® (topical GA) combined with Viusid® (oral GA) in managing genital warts in a 28-year-old homosexual male living with HIV. The patient, examined by a dermatologist at Dr. Hasan Sadikin General Hospital, Bandung, Indonesia, presented with perianal warts that had developed over 3 months. According to the physical examination carried out, multiple flesh-colored papules were reported, while histopathological analysis showed koilocytes, and polymerase chain reaction (PCR) confirmed HPV types 6 and 11. The treatment process, carried out using topical and oral GA, was administered from August to October 2024. The improvement was reported only in smaller lesions, while larger ones persisted, leading to electrocautery scheduling. The limited response observed in this case might be influenced by the patient's low CD4+ count, which potentially affects HPV clearance. Factors such as age, number of sexual partners, circumcision status, HPV type, and anatomical location of the lesions may also have played a role.
肛门生殖器疣(AGW)是人类乳头瘤病毒(HPV)感染的一种常见表现,主要由6和11株引起。根据研究结果,粘膜HPV是通过性接触传播的,其危险因素包括免疫缺陷,如人类免疫缺陷病毒(HIV)。由于免疫功能受损阻碍了HPV的清除,HIV感染者的AGW发病率更高。虽然存在几种管理选择,但目前尚无针对HPV的特异性抗病毒治疗方法。然而,其中一些治疗方法可能会引起疼痛和不适。甘草酸(GA)已证明在管理HPV感染的潜力,因为它的抗病毒特性和最小的副作用。尽管有这些令人鼓舞的结果,GA尚未被认为是AGW的标准治疗方法。本病例报告描述了Glizigen®(外用GA)联合Viusid®(口服GA)治疗一名28岁男同性恋艾滋病毒感染者生殖器疣的有效性。患者经印度尼西亚万隆Dr. Hasan Sadikin总医院皮肤科医生检查后,出现了3个多月的肛周疣。体检报告多发肉色丘疹,组织病理学分析显示为角质细胞,聚合酶链反应(PCR)证实为HPV 6型和11型。治疗过程于2024年8月至10月进行,使用局部和口服GA。据报道,这种改善只发生在较小的病变中,而较大的病变持续存在,这导致了电灼治疗的安排。在本病例中观察到的有限反应可能受到患者CD4+计数低的影响,这可能会影响HPV清除。年龄、性伴侣数量、包皮环切状况、HPV类型和病变的解剖位置等因素也可能起作用。
{"title":"Clinical Experience and Pitfalls in Using Glycyrrhizic Acid for Treating Anogenital Warts in an HIV-Infected Patient in Indonesia: A Case Report.","authors":"Ravika Khaila Arrum, Retno Hesty Maharani, Eva Krishna Sutedja, Laila Tsaqilah, Hendra Gunawan, Pati Aji Achdiat","doi":"10.2147/HIV.S558240","DOIUrl":"10.2147/HIV.S558240","url":null,"abstract":"<p><p>Anogenital warts (AGW) are a common manifestation of human papillomavirus (HPV) infection, primarily caused by strains 6 and 11. According to results, mucosal HPV is transmitted through sexual contact, with risk factors including immunodeficiency, such as Human Immunodeficiency Virus (HIV). Individuals with HIV experience a higher incidence of AGW due to impaired immune function that hinders HPV clearance. There is currently no specific antiviral therapy available for HPV, although several management options exist. However, some of these treatments may cause pain and discomfort. Glycyrrhizinic acid (GA) has demonstrated potential in managing HPV infection because of its antiviral properties and minimal side effects. Despite these promising results, GA is not yet recognized as a standard therapy for AGW. This case report describes the effectiveness of Glizigen<sup>®</sup> (topical GA) combined with Viusid<sup>®</sup> (oral GA) in managing genital warts in a 28-year-old homosexual male living with HIV. The patient, examined by a dermatologist at Dr. Hasan Sadikin General Hospital, Bandung, Indonesia, presented with perianal warts that had developed over 3 months. According to the physical examination carried out, multiple flesh-colored papules were reported, while histopathological analysis showed koilocytes, and polymerase chain reaction (PCR) confirmed HPV types 6 and 11. The treatment process, carried out using topical and oral GA, was administered from August to October 2024. The improvement was reported only in smaller lesions, while larger ones persisted, leading to electrocautery scheduling. The limited response observed in this case might be influenced by the patient's low CD4+ count, which potentially affects HPV clearance. Factors such as age, number of sexual partners, circumcision status, HPV type, and anatomical location of the lesions may also have played a role.</p>","PeriodicalId":46555,"journal":{"name":"HIV AIDS-Research and Palliative Care","volume":"17 ","pages":"399-406"},"PeriodicalIF":1.8,"publicationDate":"2025-12-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12683253/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145716360","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-27eCollection Date: 2025-01-01DOI: 10.2147/HIV.S499721
Noluthando Seangloria May, J-D Wagner, Uchenna Benedine Okafor
Introduction: The Joint United Nations Programme on HIV and AIDS (UNAIDS) aims for 95% ART adherence to achieve global viral suppression against HIV/AIDS, which is a major health issue worldwide, especially in southern Africa. This study investigated ART non-adherence among adult HIV-positive clients in the Amahlathi sub-district of the Eastern Cape, South Africa.
Methods: A cross-sectional study of 400 HIV/AIDS-positive persons (PLWHA) was undertaken at multiple facilities. A Survey was used to collect data, while medical records were used to ascertain the viral load. Responses were captured on an ordinal adherence scale and triangulated with viral load records from patient files. Univariate, bivariate, and multiple logistic regression analyses were performed to determine factors associated with ART non-adherence, and 95% CIs reported.
Results: The ART non-adherence rate was 28%. In the bivariate analysis (odds ratio [OR]), living with children (OR = 2.59), living with parents (OR = 4.12), alcohol use (OR = 2.08), HIV non-disclosure to family (OR = 0.31), non-sharing of HIV status to partner (OR = 0.41), staying with partners (OR = 0.41), taking treatment regimen II (OR = 5.74), taking ART doses twice a day (OR = 4.80), use of traditional medicine (OR = 2.83), and missed dosage (OR = 3.98) were associated with non-ART adherence. Multivariate analysis revealed that young age (<30-40 years) (AOR = 0.95; 95% CI: 0.93-0.98), female sex (AOR = 0.41; 95% CI: 0.21-0.77), partner HIV disclosure (AOR = 0.49; 95% CI: 0.26-0.92), and use of traditional medicine (AOR = 2.45; 95% CI: 1.05-5.68) were independent predictors of ART adherence.
Conclusion: ART adherence remains below UNAIDS targets in the study area. Tailored interventions that address traditional medicine use, strengthen partner disclosure support, and provide adherence counseling for young adults and men are urgently needed. Future programs could integrate digital adherence monitoring and reminder systems as practical tools to enhance treatment outcomes.
{"title":"Factors Associated with Non-Adherence to Antiretroviral Therapy: A Health-Facility-Based Cross-Sectional Study in the Amahlathi Sub-District of the Eastern Cape, South Africa.","authors":"Noluthando Seangloria May, J-D Wagner, Uchenna Benedine Okafor","doi":"10.2147/HIV.S499721","DOIUrl":"10.2147/HIV.S499721","url":null,"abstract":"<p><strong>Introduction: </strong>The Joint United Nations Programme on HIV and AIDS (UNAIDS) aims for 95% ART adherence to achieve global viral suppression against HIV/AIDS, which is a major health issue worldwide, especially in southern Africa. This study investigated ART non-adherence among adult HIV-positive clients in the Amahlathi sub-district of the Eastern Cape, South Africa.</p><p><strong>Methods: </strong>A cross-sectional study of 400 HIV/AIDS-positive persons (PLWHA) was undertaken at multiple facilities. A Survey was used to collect data, while medical records were used to ascertain the viral load. Responses were captured on an ordinal adherence scale and triangulated with viral load records from patient files. Univariate, bivariate, and multiple logistic regression analyses were performed to determine factors associated with ART non-adherence, and 95% CIs reported.</p><p><strong>Results: </strong>The ART non-adherence rate was 28%. In the bivariate analysis (odds ratio [OR]), living with children (OR = 2.59), living with parents (OR = 4.12), alcohol use (OR = 2.08), HIV non-disclosure to family (OR = 0.31), non-sharing of HIV status to partner (OR = 0.41), staying with partners (OR = 0.41), taking treatment regimen II (OR = 5.74), taking ART doses twice a day (OR = 4.80), use of traditional medicine (OR = 2.83), and missed dosage (OR = 3.98) were associated with non-ART adherence. Multivariate analysis revealed that young age (<30-40 years) (AOR = 0.95; 95% CI: 0.93-0.98), female sex (AOR = 0.41; 95% CI: 0.21-0.77), partner HIV disclosure (AOR = 0.49; 95% CI: 0.26-0.92), and use of traditional medicine (AOR = 2.45; 95% CI: 1.05-5.68) were independent predictors of ART adherence.</p><p><strong>Conclusion: </strong>ART adherence remains below UNAIDS targets in the study area. Tailored interventions that address traditional medicine use, strengthen partner disclosure support, and provide adherence counseling for young adults and men are urgently needed. Future programs could integrate digital adherence monitoring and reminder systems as practical tools to enhance treatment outcomes.</p>","PeriodicalId":46555,"journal":{"name":"HIV AIDS-Research and Palliative Care","volume":"17 ","pages":"385-397"},"PeriodicalIF":1.8,"publicationDate":"2025-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12669060/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145670219","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose: HIV infection is one of the most important health, social, and economic issues of humanity today and one of the greatest concerns and dilemmas in many countries around the world. It is a multifaceted issue with biological, social, and psychological consequences that affect the individual and social lives of those infected. The aim of this study was to investigate the palliative needs of people living with HIV in Illness trajectory in Iran.
Patients and methods: This study was of qualitative type. Purposeful sampling was used to select the participants from the People living with HIV, their caregivers, and professionals in this field. 27 participants were interviewed. The main data collection instrument was semi-structured interview with open questions. Additionally, the collected data were analyzed via inductive content analysis method.
Results: Data analysis resulted in 4 main categories, including providing essential information, social facilities, psychological rehabilitation, and healthcare services.
Conclusion: People living with HIV and their caregivers face diverse needs on the path of living with this disease. Therefore, controlling HIV infection is impossible without understanding the needs of patients and their caregivers and planning to meet these needs. Study findings provide an opportunity for HIV planners and policymakers.
{"title":"Palliative Needs of People Living with HIV in Illness Trajectory.","authors":"Asma Baniasad, Ghoncheh Raheb, Kian Norouzi Tabrizi, Maryam Latifian","doi":"10.2147/HIV.S559858","DOIUrl":"10.2147/HIV.S559858","url":null,"abstract":"<p><strong>Purpose: </strong>HIV infection is one of the most important health, social, and economic issues of humanity today and one of the greatest concerns and dilemmas in many countries around the world. It is a multifaceted issue with biological, social, and psychological consequences that affect the individual and social lives of those infected. The aim of this study was to investigate the palliative needs of people living with HIV in Illness trajectory in Iran.</p><p><strong>Patients and methods: </strong>This study was of qualitative type. Purposeful sampling was used to select the participants from the People living with HIV, their caregivers, and professionals in this field. 27 participants were interviewed. The main data collection instrument was semi-structured interview with open questions. Additionally, the collected data were analyzed via inductive content analysis method.</p><p><strong>Results: </strong>Data analysis resulted in 4 main categories, including providing essential information, social facilities, psychological rehabilitation, and healthcare services.</p><p><strong>Conclusion: </strong>People living with HIV and their caregivers face diverse needs on the path of living with this disease. Therefore, controlling HIV infection is impossible without understanding the needs of patients and their caregivers and planning to meet these needs. Study findings provide an opportunity for HIV planners and policymakers.</p>","PeriodicalId":46555,"journal":{"name":"HIV AIDS-Research and Palliative Care","volume":"17 ","pages":"373-383"},"PeriodicalIF":1.8,"publicationDate":"2025-11-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12642784/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145606864","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-04eCollection Date: 2025-01-01DOI: 10.2147/HIV.S548947
Nobert Moris Kasibante, Nelson Tokema, Alfred Douglas Kilama, Michael Mpuuga, Ivaan Pitua, Jerom Okot, Felix Bongomin
Background: Dolutegravir (DTG), an integrase-strand transfer inhibitor approved by WHO in 2019 as part of first-line HIV treatment, has been linked to weight gain; however, data on this and its associated factors remain limited.
Objective: This study aimed to determine the prevalence of weight gain and associated factors among people living with HIV (PLHIV) on DTG-based antiretroviral therapy (ART) regimens.
Methods: We conducted a retrospective cohort study of PLHIV at St. Mary's Hospital Lacor between January 2020 and December 2021. Charts were reviewed for demographic and clinical data at baseline, at 6 months and at 12 months. Weight gain was defined as a ≥5% increase in weight from baseline at 6 months. Bivariate analysis followed by stepwise multivariable logistic regression was used to identify independent predictors of weight gain. Data were analyzed using STATA 17.
Results: A total of 432 participants were included, 83.8% of whom were female. The median age was 44 years (IQR: 37.0-49.5). Most (97.0%) programmatically switched to DTG-based regimens. The prevalence of weight gain (defined as ≥5% increase from baseline) at 6 months was 7.4% (n=32/432) and 16.5% (n=31/187) at 12 months. Mean weight at baseline and 6 months was comparable (61.0 kg vs 60.0 kg, p=0.108), but a statistically significant increase in weight (p<0.001) and BMI (p<0.001) was observed from baseline to 12 months. On bivariate analysis, lower baseline WHO stage (p=0.048) and viral load <1000 copies/mL (p=0.009) were associated with weight gain; however, no factor remained significantly associated in multivariable analysis.
Conclusion: Weight gain occured in approximately 1 in 14 participants at 6 months and 1 in 6 participants at 12 months post-DTG initiation. WHO stage I and lower viral load were associated with weight gain on bivariate analysis, though not independently on multivariable analysis. Routine weight and cardiovascular risk monitoring is recommended. A prospective study is warranted.
背景:Dolutegravir (DTG)是一种整合酶链转移抑制剂,于2019年被世卫组织批准作为一线艾滋病毒治疗的一部分,与体重增加有关;然而,关于这一点及其相关因素的数据仍然有限。目的:本研究旨在确定基于dtg的抗逆转录病毒治疗(ART)方案的HIV感染者(PLHIV)体重增加的患病率及其相关因素。方法:我们于2020年1月至2021年12月在Lacor圣玛丽医院进行了一项PLHIV回顾性队列研究。回顾了基线、6个月和12个月时的人口学和临床数据。体重增加定义为6个月时体重较基线增加≥5%。采用双变量分析和逐步多变量逻辑回归来确定体重增加的独立预测因素。使用STATA 17分析数据。结果:共纳入432名受试者,其中女性占83.8%。中位年龄44岁(IQR: 37.0 ~ 49.5)。大多数(97.0%)有计划地切换到基于dtg的方案。6个月时体重增加(定义为比基线增加≥5%)的患病率为7.4% (n=32/432), 12个月时为16.5% (n=31/187)。基线和6个月的平均体重相当(61.0 kg vs 60.0 kg, p=0.108),但体重有统计学意义上的显著增加(结论:dtg开始后6个月和12个月,14名参与者中约有1名体重增加。在双变量分析中,世卫组织I期和较低的病毒载量与体重增加有关,但在多变量分析中不是独立的。建议进行常规体重和心血管风险监测。有必要进行前瞻性研究。
{"title":"Prevalence of Weight Gain and Associated Factors Among People Living with HIV 6- and 12-Months Post Dolutegravir-Based Anti-Retroviral Regimen Initiation in Gulu, Uganda; A Hospital-Based Retrospective Cohort Study.","authors":"Nobert Moris Kasibante, Nelson Tokema, Alfred Douglas Kilama, Michael Mpuuga, Ivaan Pitua, Jerom Okot, Felix Bongomin","doi":"10.2147/HIV.S548947","DOIUrl":"10.2147/HIV.S548947","url":null,"abstract":"<p><strong>Background: </strong>Dolutegravir (DTG), an integrase-strand transfer inhibitor approved by WHO in 2019 as part of first-line HIV treatment, has been linked to weight gain; however, data on this and its associated factors remain limited.</p><p><strong>Objective: </strong>This study aimed to determine the prevalence of weight gain and associated factors among people living with HIV (PLHIV) on DTG-based antiretroviral therapy (ART) regimens.</p><p><strong>Methods: </strong>We conducted a retrospective cohort study of PLHIV at St. Mary's Hospital Lacor between January 2020 and December 2021. Charts were reviewed for demographic and clinical data at baseline, at 6 months and at 12 months. Weight gain was defined as a ≥5% increase in weight from baseline at 6 months. Bivariate analysis followed by stepwise multivariable logistic regression was used to identify independent predictors of weight gain. Data were analyzed using STATA 17.</p><p><strong>Results: </strong>A total of 432 participants were included, 83.8% of whom were female. The median age was 44 years (IQR: 37.0-49.5). Most (97.0%) programmatically switched to DTG-based regimens. The prevalence of weight gain (defined as ≥5% increase from baseline) at 6 months was 7.4% (n=32/432) and 16.5% (n=31/187) at 12 months. Mean weight at baseline and 6 months was comparable (61.0 kg vs 60.0 kg, p=0.108), but a statistically significant increase in weight (p<0.001) and BMI (p<0.001) was observed from baseline to 12 months. On bivariate analysis, lower baseline WHO stage (p=0.048) and viral load <1000 copies/mL (p=0.009) were associated with weight gain; however, no factor remained significantly associated in multivariable analysis.</p><p><strong>Conclusion: </strong>Weight gain occured in approximately <b>1 in 14 participants at 6 months</b> and <b>1 in 6 participants at 12 months</b> post-DTG initiation. WHO stage I and lower viral load were associated with weight gain on bivariate analysis, though not independently on multivariable analysis. Routine weight and cardiovascular risk monitoring is recommended. A prospective study is warranted.</p>","PeriodicalId":46555,"journal":{"name":"HIV AIDS-Research and Palliative Care","volume":"17 ","pages":"361-372"},"PeriodicalIF":1.8,"publicationDate":"2025-11-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12595951/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145483463","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Purpose: Oral candidiasis remains prevalent in HIV patients, with growing concern over antifungal resistance. This study aimed to identify Candida species in HIV patients with oral candidiasis and assess the antifungal susceptibility of the predominant species.
Materials and methods: A cross-sectional study was conducted at a referral hospital in West Java, Indonesia, involving 30 HIV patients aged ≥18 years, with no prior antifungal therapy and a confirmed diagnosis of oral candidiasis. Oral rinse samples were collected and cultured on CHROMagar Candida for species identification and CFU/mL quantification. Antifungal activity was assessed using disk diffusion against nystatin, fluconazole, itraconazole, and voriconazole. Inhibition zone diameters were recorded, while categorical susceptibility interpretation was applied only to fluconazole and voriconazole based on CLSI guidelines. The Friedman test and Fisher's exact test were used, with p < 0.05 considered statistically significant.
Results: Candida (C). albicans was the predominant species (100%), consistent with previous findings. Non-Candida albicans Candida (NCAC) species, including C. glabrata (10%), C. krusei (3.3%), and C. tropicalis (3.3%), were also identified, aligning with reports of emergence. Inhibition zone diameters varied significantly (p < 0.001). Voriconazole had the widest zone (34.0 ± 10.7 mm), followed by fluconazole (33.0 ± 9.3 mm), itraconazole (29.5 ± 5.5 mm), and nystatin (27.9 ± 5.0 mm). For fluconazole and voriconazole, categorical interpretation showed 90.0% and 86.7% susceptibility, respectively, with no significant difference (p = 1.00). Since no interpretive breakpoints exist for nystatin and itraconazole, only inhibition zone diameters were reported.
Conclusion: C. albicans predominated, with fluconazole and voriconazole showing high susceptibility, while nystatin and itraconazole demonstrated inhibition zones but could not be categorically interpreted due to the absence of established breakpoints. Routine species identification and susceptibility testing remain essential to guide therapy and monitor emerging resistance in immunocompromised populations, highlighting the need for further validation studies.
{"title":"Evaluation of Antifungal Activity Against <i>Candida albicans</i> Isolates From HIV-Positive Patients with Oral Candidiasis in a Major Referral Hospital, West Java, Indonesia.","authors":"Yuliana, Irna Sufiawati, Intan Mauli Warma Dewi, Yovita Hartantri","doi":"10.2147/HIV.S536437","DOIUrl":"10.2147/HIV.S536437","url":null,"abstract":"<p><strong>Purpose: </strong>Oral candidiasis remains prevalent in HIV patients, with growing concern over antifungal resistance. This study aimed to identify <i>Candida</i> species in HIV patients with oral candidiasis and assess the antifungal susceptibility of the predominant species.</p><p><strong>Materials and methods: </strong>A cross-sectional study was conducted at a referral hospital in West Java, Indonesia, involving 30 HIV patients aged ≥18 years, with no prior antifungal therapy and a confirmed diagnosis of oral candidiasis. Oral rinse samples were collected and cultured on CHROMagar <i>Candida</i> for species identification and CFU/mL quantification. Antifungal activity was assessed using disk diffusion against nystatin, fluconazole, itraconazole, and voriconazole. Inhibition zone diameters were recorded, while categorical susceptibility interpretation was applied only to fluconazole and voriconazole based on CLSI guidelines. The Friedman test and Fisher's exact test were used, with p < 0.05 considered statistically significant.</p><p><strong>Results: </strong><i>Candida</i> (<i>C</i>). <i>albicans</i> was the predominant species (100%), consistent with previous findings. Non<i>-Candida albicans Candida</i> (NCAC) species, including <i>C. glabrata</i> (10%), <i>C. krusei</i> (3.3%), and <i>C. tropicalis</i> (3.3%), were also identified, aligning with reports of emergence. Inhibition zone diameters varied significantly (p < 0.001). Voriconazole had the widest zone (34.0 ± 10.7 mm), followed by fluconazole (33.0 ± 9.3 mm), itraconazole (29.5 ± 5.5 mm), and nystatin (27.9 ± 5.0 mm). For fluconazole and voriconazole, categorical interpretation showed 90.0% and 86.7% susceptibility, respectively, with no significant difference (p = 1.00). Since no interpretive breakpoints exist for nystatin and itraconazole, only inhibition zone diameters were reported.</p><p><strong>Conclusion: </strong><i>C. albicans</i> predominated, with fluconazole and voriconazole showing high susceptibility, while nystatin and itraconazole demonstrated inhibition zones but could not be categorically interpreted due to the absence of established breakpoints. Routine species identification and susceptibility testing remain essential to guide therapy and monitor emerging resistance in immunocompromised populations, highlighting the need for further validation studies.</p>","PeriodicalId":46555,"journal":{"name":"HIV AIDS-Research and Palliative Care","volume":"17 ","pages":"351-360"},"PeriodicalIF":1.8,"publicationDate":"2025-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12570985/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145410490","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-02eCollection Date: 2025-01-01DOI: 10.2147/HIV.S492850
Matthew D Mara, Cynthia Miguel, Nina H Lin, Curt G Beckwith, Michelle Henshaw
Background: Mail-in saliva samples are a participant-centered means of monitoring patients' oral and overall health that may help to reduce unnecessary medical trips and more efficiently use provider time. The use and acceptability of mail-in saliva samples have been studied in high-risk populations; however, it has not been studied in cohorts of people living with HIV (PLWH).
Objective: To investigate the feasibility of PLWHs' willingness to provide mail-in saliva samples, 900 saliva collection kits were mailed to a randomized sample of PLWH across two urban and diverse clinics in the Northeast United States in 2019-2020.
Results: 73/900 (8%) packages were returned to study personnel, with 100% (73/73) containing saliva deemed usable for analysis. 55/900 (6%) of packages were returned to the study team undeliverable. Further information may be gained from investigating the influence of personalized test results, health literacy, the requirement of the oral health survey, and study compensation that may affect an individual's motivation to participate in the study.
Conclusion: While findings suggest limited feasibility of mail-in saliva collection without personalized test results in a cohort of PLWH in terms of response rate, all returned saliva samples were usable for analysis suggesting that addressing potential barriers may improve response rates and the feasibility of using mail-in salivary diagnostics to monitor disease progression in PLWH in future studies.
{"title":"Determining the Feasibility of a Mail-In Saliva Sample Protocol for Persons Living with HIV in Two Urban Northeast United States Clinics.","authors":"Matthew D Mara, Cynthia Miguel, Nina H Lin, Curt G Beckwith, Michelle Henshaw","doi":"10.2147/HIV.S492850","DOIUrl":"10.2147/HIV.S492850","url":null,"abstract":"<p><strong>Background: </strong>Mail-in saliva samples are a participant-centered means of monitoring patients' oral and overall health that may help to reduce unnecessary medical trips and more efficiently use provider time. The use and acceptability of mail-in saliva samples have been studied in high-risk populations; however, it has not been studied in cohorts of people living with HIV (PLWH).</p><p><strong>Objective: </strong>To investigate the feasibility of PLWHs' willingness to provide mail-in saliva samples, 900 saliva collection kits were mailed to a randomized sample of PLWH across two urban and diverse clinics in the Northeast United States in 2019-2020.</p><p><strong>Results: </strong>73/900 (8%) packages were returned to study personnel, with 100% (73/73) containing saliva deemed usable for analysis. 55/900 (6%) of packages were returned to the study team undeliverable. Further information may be gained from investigating the influence of personalized test results, health literacy, the requirement of the oral health survey, and study compensation that may affect an individual's motivation to participate in the study.</p><p><strong>Conclusion: </strong>While findings suggest limited feasibility of mail-in saliva collection without personalized test results in a cohort of PLWH in terms of response rate, all returned saliva samples were usable for analysis suggesting that addressing potential barriers may improve response rates and the feasibility of using mail-in salivary diagnostics to monitor disease progression in PLWH in future studies.</p>","PeriodicalId":46555,"journal":{"name":"HIV AIDS-Research and Palliative Care","volume":"17 ","pages":"337-349"},"PeriodicalIF":1.8,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12500845/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145253115","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-09-27eCollection Date: 2025-01-01DOI: 10.2147/HIV.S509460
Joseph Fabian Inyang, Jimin James Sontyo, Ayokunle Bello, Kabiru Suru Usman, Tosin Awele Idaboh, Doreen Magaji, Moses Katbi
Introduction: There is limited research on factors impacting viral load suppression among children and adolescents living with HIV (CALHIV) in low-income countries. The objective of the study was to determine and analyze factors affecting HIV viral suppression levels among CALHIV enrolled in the Integrated Child Health and Social Services Activity (ICHSSA 4) Orphans and Vulnerable Children (OVC) project in Northeast Nigeria.
Methodology: The study adopted a descriptive cross-sectional research design for the study. The study involved collecting data among 847 CALHIV aged 0 to 17 years, enrolled in USAID-supported healthcare facilities across 9 Local Government Areas (LGAs) in Adamawa, Bauchi, and Taraba States. Prevalence of viral load suppression was described by child/adolescent, caregiver-related factors. Mixed-effects multivariable logistic regression models were fitted to explore the factors associated with viral load suppression.
Results: CALHIV enrolled on the ICHSSA-4 project >2 years (92.7%) had better suppression levels compared to those 1 year and less (7.1%). About 94.5% of CALHIV who adhered to prescribed ARV medication were transitioned to pediatric ARV optimal regimen achieved viral suppression. Psychosocial factors such as the presence of treatment support person, enrolment in an age-appropriate support group, and positive HIV disclosure status also impacted viral load suppression positively. The sociodemographic, health/clinical, and psychosocial factors affecting viral load in CALHIV enrolled on the project were found to be statistically significant (p < 0.05).
Conclusion: The study found that factors such as CSO OVC services provided to households, adherence support, food sufficiency in the household, attendance at support groups, treatment literacy and other social services influence viral load suppression. Identifying these factors can help monitor and improve treatment outcomes among CALHIV enrolled in an OVC programs and surely accelerate progress towards achieving the UNAIDS 3rd 95 goal.
{"title":"Factors Impacting Viral Load Suppression in Children and Adolescents Living with HIV Enrolled in an Orphans and Vulnerable Children Program in Northeast Nigeria.","authors":"Joseph Fabian Inyang, Jimin James Sontyo, Ayokunle Bello, Kabiru Suru Usman, Tosin Awele Idaboh, Doreen Magaji, Moses Katbi","doi":"10.2147/HIV.S509460","DOIUrl":"10.2147/HIV.S509460","url":null,"abstract":"<p><strong>Introduction: </strong>There is limited research on factors impacting viral load suppression among children and adolescents living with HIV (CALHIV) in low-income countries. The objective of the study was to determine and analyze factors affecting HIV viral suppression levels among CALHIV enrolled in the Integrated Child Health and Social Services Activity (ICHSSA 4) Orphans and Vulnerable Children (OVC) project in Northeast Nigeria.</p><p><strong>Methodology: </strong>The study adopted a descriptive cross-sectional research design for the study. The study involved collecting data among 847 CALHIV aged 0 to 17 years, enrolled in USAID-supported healthcare facilities across 9 Local Government Areas (LGAs) in Adamawa, Bauchi, and Taraba States. Prevalence of viral load suppression was described by child/adolescent, caregiver-related factors. Mixed-effects multivariable logistic regression models were fitted to explore the factors associated with viral load suppression.</p><p><strong>Results: </strong>CALHIV enrolled on the ICHSSA-4 project >2 years (92.7%) had better suppression levels compared to those 1 year and less (7.1%). About 94.5% of CALHIV who adhered to prescribed ARV medication were transitioned to pediatric ARV optimal regimen achieved viral suppression. Psychosocial factors such as the presence of treatment support person, enrolment in an age-appropriate support group, and positive HIV disclosure status also impacted viral load suppression positively. The sociodemographic, health/clinical, and psychosocial factors affecting viral load in CALHIV enrolled on the project were found to be statistically significant (p < 0.05).</p><p><strong>Conclusion: </strong>The study found that factors such as CSO OVC services provided to households, adherence support, food sufficiency in the household, attendance at support groups, treatment literacy and other social services influence viral load suppression. Identifying these factors can help monitor and improve treatment outcomes among CALHIV enrolled in an OVC programs and surely accelerate progress towards achieving the UNAIDS 3rd 95 goal.</p>","PeriodicalId":46555,"journal":{"name":"HIV AIDS-Research and Palliative Care","volume":"17 ","pages":"323-335"},"PeriodicalIF":1.8,"publicationDate":"2025-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12489023/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145233635","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: In recent years, China has seen a rapid rise in the HIV epidemic, especially among college students. However, the uptake of HIV testing was low. This study aimed to explore the factors influencing the acceptance of voluntary counseling and testing (VCT) among sexually active college students, in order to provide scientific evidence for the prevention and control of HIV infection on campus.
Methods: A cross-sectional study was completed at 13 colleges in 11 cities by stratified cluster random sampling. We formulated a questionnaire to collect information on demographic characteristics, sexual behaviors, sexual attitudes, HIV-relevant knowledge, and HIV/AIDS interventions. The chi-square test was performed to compare composition ratios. Single-factor logistic regression and multivariate regression analyses were performed to determine the influencing factors.
Results: This study included 3873 college students with sexual experience, of whom 199 had received VCT, accounting for 5.14%. The results of the multivariate logistic regression analysis demonstrated that the participants who were age ≥ 22 (OR = 2.11, 95% CI: 1.36-3.29), had casual sex in the past year (OR = 1.75, 95% CI: 1.21-2.52), had received a lecture or health education class on HIV/AIDS at school (OR = 1.80, 95% CI: 1.07-3.02), had received school information on HIV testing (OR = 2.15, 95% CI: 1.32-3.50), and had received a school-based HIV risk self-assessment in the last year (OR = 3.47, 95% CI: 2.40-5.03) were inclined to receive VCT.
Conclusion: The findings revealed that college students who had received health education about AIDS or acquired HIV testing information on campus were inclined to receive VCT, especially those who had engaged in high-risk sexual behaviors. Regarding HIV prevention among college students, it is recommended that health education related to AIDS be conducted regularly on campus and that HIV testing be promoted to increase the testing rate.
{"title":"Analysis of Factors Influencing the Acceptance of Voluntary Counseling and Testing Among Sexually Active College Students in Zhejiang Province, China.","authors":"Jiajin He, Xin Zhou, Lingjuan Chen, Qiaoqin Ma, Liebo Zhu, Junfang Lou, Lianqi Zha, Jieyun Lou, Nan Zheng, Weiyong Chen","doi":"10.2147/HIV.S539563","DOIUrl":"10.2147/HIV.S539563","url":null,"abstract":"<p><strong>Background: </strong>In recent years, China has seen a rapid rise in the HIV epidemic, especially among college students. However, the uptake of HIV testing was low. This study aimed to explore the factors influencing the acceptance of voluntary counseling and testing (VCT) among sexually active college students, in order to provide scientific evidence for the prevention and control of HIV infection on campus.</p><p><strong>Methods: </strong>A cross-sectional study was completed at 13 colleges in 11 cities by stratified cluster random sampling. We formulated a questionnaire to collect information on demographic characteristics, sexual behaviors, sexual attitudes, HIV-relevant knowledge, and HIV/AIDS interventions. The chi-square test was performed to compare composition ratios. Single-factor logistic regression and multivariate regression analyses were performed to determine the influencing factors.</p><p><strong>Results: </strong>This study included 3873 college students with sexual experience, of whom 199 had received VCT, accounting for 5.14%. The results of the multivariate logistic regression analysis demonstrated that the participants who were age ≥ 22 (OR = 2.11, 95% CI: 1.36-3.29), had casual sex in the past year (OR = 1.75, 95% CI: 1.21-2.52), had received a lecture or health education class on HIV/AIDS at school (OR = 1.80, 95% CI: 1.07-3.02), had received school information on HIV testing (OR = 2.15, 95% CI: 1.32-3.50), and had received a school-based HIV risk self-assessment in the last year (OR = 3.47, 95% CI: 2.40-5.03) were inclined to receive VCT.</p><p><strong>Conclusion: </strong>The findings revealed that college students who had received health education about AIDS or acquired HIV testing information on campus were inclined to receive VCT, especially those who had engaged in high-risk sexual behaviors. Regarding HIV prevention among college students, it is recommended that health education related to AIDS be conducted regularly on campus and that HIV testing be promoted to increase the testing rate.</p>","PeriodicalId":46555,"journal":{"name":"HIV AIDS-Research and Palliative Care","volume":"17 ","pages":"313-321"},"PeriodicalIF":1.8,"publicationDate":"2025-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12452958/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145132185","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}