Pub Date : 2025-11-27DOI: 10.1016/j.idnow.2025.105216
É. Piet , F. Bastides , J. Leporrier , O. Robineau , É. Estrabaud , V. Pourcher , L. Slama
Background
Complementarily to immuno-virological control of people living with HIV (PLWH), quality of life (QoL) has become a priority in patient care.
Methods
OCTAVE® is a self-administered questionnaire comprising 42 questions categorized in eight items: HIV treatment, mental & physical health, sleep, sexuality, emotional well-being, comorbidities and social/professional life. It was developed for use in routine clinical practice, the objective being to identify possible QoL alterations in people living with HIV.
Outcomes
Thirty-nine physicians completed the survey, and 380 PLWH filled out the self-administered questionnaire. All in all, QoL alterations were detected in 44 % of respondents (mean 2.1 (SD = 1.2) per PLWH). For physicians, these findings prompted planned clinical interventions in 70 % of PLWH, predominantly regarding sleep, sexual health and emotional well-being. Of note, 11 % of the reported QoL alterations were attributed to antiretroviral therapy.
Conclusion
In routine clinical practice OCTAVE®, appears to be an effective means of detecting QoL impairments in people living with HIV, and it is likely to reinforce clinical management of potential QoL issues.
{"title":"Detecting quality of life alterations in people living with HIV: Development and evaluation of the OCTAVE® self-questionnaire","authors":"É. Piet , F. Bastides , J. Leporrier , O. Robineau , É. Estrabaud , V. Pourcher , L. Slama","doi":"10.1016/j.idnow.2025.105216","DOIUrl":"10.1016/j.idnow.2025.105216","url":null,"abstract":"<div><h3>Background</h3><div>Complementarily to immuno-virological control of people living with HIV (PLWH), quality of life (QoL) has become a priority in patient care.</div></div><div><h3>Methods</h3><div>OCTAVE® is a self-administered questionnaire comprising 42 questions categorized in eight items: HIV treatment, mental & physical health, sleep, sexuality, emotional well-being, comorbidities and social/professional life. It was developed for use in routine clinical practice, the objective being to identify possible QoL alterations in people living with HIV.</div></div><div><h3>Outcomes</h3><div>Thirty-nine physicians completed the survey, and 380 PLWH filled out the self-administered questionnaire. All in all, QoL alterations were detected in 44 % of respondents (mean 2.1 (SD = 1.2) per PLWH). For physicians, these findings prompted planned clinical interventions in 70 % of PLWH, predominantly regarding sleep, sexual health and emotional well-being. Of note, 11 % of the reported QoL alterations were attributed to antiretroviral therapy.</div></div><div><h3>Conclusion</h3><div>In routine clinical practice OCTAVE®, appears to be an effective means of detecting QoL impairments in people living with HIV, and it is likely to reinforce clinical management of potential QoL issues.</div></div>","PeriodicalId":13539,"journal":{"name":"Infectious diseases now","volume":"56 2","pages":"Article 105216"},"PeriodicalIF":2.2,"publicationDate":"2025-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145632743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-26DOI: 10.1016/j.idnow.2025.105207
Haripriya C K , Deepak Vasudevan Sajini , Nehala Subeer T , Fathima Shahadiya K , Hiba Najeem
{"title":"Primary Amoebic Meningoencephalitis: A Silent Killer from natural water sources","authors":"Haripriya C K , Deepak Vasudevan Sajini , Nehala Subeer T , Fathima Shahadiya K , Hiba Najeem","doi":"10.1016/j.idnow.2025.105207","DOIUrl":"10.1016/j.idnow.2025.105207","url":null,"abstract":"","PeriodicalId":13539,"journal":{"name":"Infectious diseases now","volume":"56 1","pages":"Article 105207"},"PeriodicalIF":2.2,"publicationDate":"2025-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145616057","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-25DOI: 10.1016/j.idnow.2025.105201
Nicole Enslinger , Stefan Glöckner , Stefan Hagel , Oliwia Makarewicz , Mathias Pletz , Sara Madzgalla
{"title":"Lack of synergy between amoxicillin and cefazolin against Enterococcus faecalis: Reassessment of a proposed empirical regimen for infective endocarditis","authors":"Nicole Enslinger , Stefan Glöckner , Stefan Hagel , Oliwia Makarewicz , Mathias Pletz , Sara Madzgalla","doi":"10.1016/j.idnow.2025.105201","DOIUrl":"10.1016/j.idnow.2025.105201","url":null,"abstract":"","PeriodicalId":13539,"journal":{"name":"Infectious diseases now","volume":"56 1","pages":"Article 105201"},"PeriodicalIF":2.2,"publicationDate":"2025-11-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145616058","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-21DOI: 10.1016/j.idnow.2025.105200
J. NTWARI , R. NDIAYE , L. MWISENEZA , Y. HABIMANA , E. SERUYANGE , O. SEBATUNZI , P. MIGAMBI , JP. RWABIHAMA , S. GALLIEN
Introduction
Multidrug-resistant tuberculosis (MDR-TB) is a significant public health challenge in Rwanda.
Methods
This retrospective study aimed to describe the epidemiological characteristics, diagnostic approaches, and treatment outcomes of MDR-TB cases between July 1, 2019 and June 30, 2023.
Results
Among 23,476 tuberculosis cases diagnosed in Rwanda, 227 (0.96 %) were confirmed as MDR-TB. Key findings include male predominance (80.6 %) and a mean age of 39.6 years. Pulmonary tuberculosis accounted for 96.9 % of cases, and 20.3 % of patients were co-infected with HIV. The GeneXpert molecular diagnostic test − the first-line diagnostic tool − demonstrated a sensitivity of 92.9 % for detecting resistance to rifampicin and isoniazid. The overall therapeutic success rate was 93.5 %, with a mortality rate of 5.3 % in evaluable cases (82.4 %). Risk factors for mortality included HIV co-infection and malnutrition (BMI < 18.5 kg/m2).
Conclusion
These findings underscore the importance of robust diagnostic and treatment strategies to control MDR-TB in Rwanda.
{"title":"Epidemiology and outcomes of multidrug-resistant tuberculosis in Rwanda","authors":"J. NTWARI , R. NDIAYE , L. MWISENEZA , Y. HABIMANA , E. SERUYANGE , O. SEBATUNZI , P. MIGAMBI , JP. RWABIHAMA , S. GALLIEN","doi":"10.1016/j.idnow.2025.105200","DOIUrl":"10.1016/j.idnow.2025.105200","url":null,"abstract":"<div><h3>Introduction</h3><div>Multidrug-resistant tuberculosis (MDR-TB) is a significant public health challenge in Rwanda.</div></div><div><h3>Methods</h3><div>This retrospective study aimed to describe the epidemiological characteristics, diagnostic approaches, and treatment outcomes of MDR-TB cases between July 1, 2019 and June 30, 2023.</div></div><div><h3>Results</h3><div>Among 23,476 tuberculosis cases diagnosed in Rwanda, 227 (0.96 %) were confirmed as MDR-TB. Key findings include male predominance (80.6 %) and a mean age of 39.6 years. Pulmonary tuberculosis accounted for 96.9 % of cases, and 20.3 % of patients were co-infected with HIV. The GeneXpert molecular diagnostic test − the first-line diagnostic tool − demonstrated a sensitivity of 92.9 % for detecting resistance to rifampicin and isoniazid. The overall therapeutic success rate was 93.5 %, with a mortality rate of 5.3 % in evaluable cases (82.4 %). Risk factors for mortality included HIV co-infection and malnutrition (BMI < 18.5 kg/m<sup>2</sup>).</div></div><div><h3>Conclusion</h3><div>These findings underscore the importance of robust diagnostic and treatment strategies to control MDR-TB in Rwanda.</div></div>","PeriodicalId":13539,"journal":{"name":"Infectious diseases now","volume":"56 1","pages":"Article 105200"},"PeriodicalIF":2.2,"publicationDate":"2025-11-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145587451","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The aim of this study was to evaluate the performances of Anyplex® MTB/NTM Real-time Detection and Xpert MTB/RIF Ultra for tuberculosis (TB) disease in people living with Human Immunodeficiency Virus (PLHIV) with low CD4 + T lymphocyte cell (CD4) count.
Patients and methods
A retrospective observational study included respiratory and non-respiratory specimens from PLHIV stratified based on their CD4 count (<200 vs. ≥ 200 cells/µL) using Anyplex® MTB/NTM Real-time Detection or Xpert® MTB/RIF Ultra.
Results
In PLHIV with low CD4 count (<200 cells/µL), Anyplex demonstrated comparable sensitivity (81.4 % vs. 81.8 %) and specificity (78.7 % vs. 78.5 %) to Xpert for MTC detection in respiratory samples, but lower sensitivity (81.8 % vs. 100 %) and higher specificity (83.3 % vs. 66.6 %) than Xpert in non-respiratory samples.
Conclusions
Whereas the two methodologies showed similar MTC diagnostic performance in respiratory samples from PLHIV with low CD4 levels, Anyplex showed higher specificity and lower sensitivity than Xpert in non-respiratory samples.
{"title":"Diagnostic performances of Anyplex MTB/NTM Real-time detection vs Xpert® MTB/RIF Ultra for tuberculosis among people living with human immunodeficiency virus with low CD4 count","authors":"Alina Gaxiola-Castro, Samantha Flores-Treviño, Paola Bocanegra-Ibarias, Mariana Ramírez-Yáñez, Eduardo-Pérez-Alba, Adrián Camacho-Ortiz","doi":"10.1016/j.idnow.2025.105191","DOIUrl":"10.1016/j.idnow.2025.105191","url":null,"abstract":"<div><h3>Objectives</h3><div>The aim of this study was to evaluate the performances of Anyplex® MTB/NTM Real-time Detection and Xpert MTB/RIF Ultra for tuberculosis (TB) disease in people living with Human Immunodeficiency Virus (PLHIV) with low CD4 + T lymphocyte cell (CD4) count.</div></div><div><h3>Patients and methods</h3><div>A retrospective observational study included respiratory and non-respiratory specimens from PLHIV stratified based on their CD4 count (<200 vs. ≥ 200 cells/µL) using Anyplex® MTB/NTM Real-time Detection or Xpert® MTB/RIF Ultra.</div></div><div><h3>Results</h3><div>In PLHIV with low CD4 count (<200 cells/µL), Anyplex demonstrated comparable sensitivity (81.4 % vs. 81.8 %) and specificity (78.7 % vs. 78.5 %) to Xpert for MTC detection in respiratory samples, but lower sensitivity (81.8 % vs. 100 %) and higher specificity (83.3 % vs. 66.6 %) than Xpert in non-respiratory samples.</div></div><div><h3>Conclusions</h3><div>Whereas the two methodologies showed similar MTC diagnostic performance in respiratory samples from PLHIV with low CD4 levels, Anyplex showed higher specificity and lower sensitivity than Xpert in non-respiratory samples.</div></div>","PeriodicalId":13539,"journal":{"name":"Infectious diseases now","volume":"56 1","pages":"Article 105191"},"PeriodicalIF":2.2,"publicationDate":"2025-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145563509","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-19DOI: 10.1016/j.idnow.2025.105190
Klinger Soares Faico-Filho , Ana Helena Sita Perosa , Nancy Bellei
{"title":"Epidemiological and clinical insights into respiratory syncytial virus among hospitalized adults and healthcare workers in Brazil: A retrospective study","authors":"Klinger Soares Faico-Filho , Ana Helena Sita Perosa , Nancy Bellei","doi":"10.1016/j.idnow.2025.105190","DOIUrl":"10.1016/j.idnow.2025.105190","url":null,"abstract":"","PeriodicalId":13539,"journal":{"name":"Infectious diseases now","volume":"56 1","pages":"Article 105190"},"PeriodicalIF":2.2,"publicationDate":"2025-11-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145563581","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-15DOI: 10.1016/j.idnow.2025.105189
Rhythm Sharma , Abhishek Walia , Dinesh Lakhanpal
Human metapneumovirus (hMPV), a negative-sense RNA virus in the Pneumoviridae family, has emerged as a major yet under-recognized cause of acute respiratory infections worldwide. Since its identification in 2001, hMPV has shown steady genetic evolution into genotypes A and B, with newer sublineages such as A2.2.1, A2.2.2, and B2 currently detected across continents. A recent global rise in hMPV detections, detailed in reports from China, Europe, and the USA, likely reflects both expanded testing and the re-establishment of seasonal circulation following the COVID-19 pandemic. Co-infections with respiratory viruses, including RSV and influenza, contribute to severe clinical outcomes and hospital burden. Multiplex RT-PCR remains the most sensitive and widely used diagnostic method for detection of hMPV, outperforming conventional PCR approaches, while metagenomic sequencing and CRISPR-based assays are primarily research tools. Diagnostic sensitivity also varies with sample source, and access to advanced technologies remains globally uneven. Despite its growing clinical impact, no approved antiviral is available. Promising candidates, including monoclonal antibodies against the fusion protein, siRNA therapies, and mRNA-based vaccines, are in the early stages of development. This review encompasses recent evidence on hMPV epidemiology, molecular evolution, diagnostic approaches, and therapeutic and vaccine development, underscoring a need for sustained surveillance, equitable diagnostic capacity, and proactive vaccine research more effectively addressing a largely overlooked respiratory pathogen.
{"title":"Human metapneumovirus: an underdiagnosed public health threat","authors":"Rhythm Sharma , Abhishek Walia , Dinesh Lakhanpal","doi":"10.1016/j.idnow.2025.105189","DOIUrl":"10.1016/j.idnow.2025.105189","url":null,"abstract":"<div><div>Human metapneumovirus (hMPV), a negative-sense RNA virus in the <em>Pneumoviridae</em> family, has emerged as a major yet under-recognized cause of acute respiratory infections worldwide. Since its identification in 2001, hMPV has shown steady genetic evolution into genotypes A and B, with newer sublineages such as A2.2.1, A2.2.2, and B2 currently detected across continents. A recent global rise in hMPV detections, detailed in reports from China, Europe, and the USA, likely reflects both expanded testing and the re-establishment of seasonal circulation following the COVID-19 pandemic. Co-infections with respiratory viruses, including RSV and influenza, contribute to severe clinical outcomes and hospital burden. Multiplex RT-PCR remains the most sensitive and widely used diagnostic method for detection of hMPV, outperforming conventional PCR approaches, while metagenomic sequencing and CRISPR-based assays are primarily research tools. Diagnostic sensitivity also varies with sample source, and access to advanced technologies remains globally uneven. Despite its growing clinical impact, no approved antiviral is available. Promising candidates, including monoclonal antibodies against the fusion protein, siRNA therapies, and mRNA-based vaccines, are in the early stages of development. This review encompasses recent evidence on hMPV epidemiology, molecular evolution, diagnostic approaches, and therapeutic and vaccine development, underscoring a need for sustained surveillance, equitable diagnostic capacity, and proactive vaccine research more effectively addressing a largely overlooked respiratory pathogen.</div></div>","PeriodicalId":13539,"journal":{"name":"Infectious diseases now","volume":"56 1","pages":"Article 105189"},"PeriodicalIF":2.2,"publicationDate":"2025-11-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145534378","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Tick-borne encephalitis (TBE), which is caused by the tick-borne encephalitis virus (TBEV), is primarily transmitted to humans through Ixodes bites of infected ticks of the genus Ixodes and, more rarely, by the consumption of contaminated dairy products. TBEV encompasses three main subtypes with distinct degrees of severity and clinical courses: European (TBEV-Eu), Siberian (TBEV-Sib), and Far Eastern (TBEV-FE). Over the past decade, TBE epidemiology has significantly changed in Europe, with increasing incidence in endemic countries and the discovery of new human case foci and areas of virus circulation. This emergence involves many factors of which the impacts are not easily determined. While most TBEV-Eu infections are asymptomatic, some patients develop signs of central nervous system involvement that can be severe (meningitis, encephalitis). While the mortality rate in humans is low (< 2 %), post-infectious sequelae (cognitive and/or motor) can occur in up to 40 % of cases. While TBE treatment is symptomatic, several antiviral treatments are under study. The emergence of TBEV in Europe, particularly in France, represents a significant public health issue. This review provides an up-to-date overview of the latest data concerning TBE, focusing on the epidemiology and clinical, diagnostic, and therapeutic aspects of this emerging infection.
{"title":"Tick-borne encephalitis: An ancient pathology, but a current emergence in Europe","authors":"Baptiste Hoellinger , Assilina Parfut , Maëlle Grisard , Sandra Martin-Latil , Julie Denis , Olivier Augereau , Guillaume Gregorowicz , Martin Martinot , Yves Hansmann , Aurélie Velay","doi":"10.1016/j.idnow.2025.105187","DOIUrl":"10.1016/j.idnow.2025.105187","url":null,"abstract":"<div><div>Tick-borne encephalitis (TBE), which is caused by the tick-borne encephalitis virus (TBEV), is primarily transmitted to humans through Ixodes bites of infected ticks of the genus Ixodes and, more rarely, by the consumption of contaminated dairy products. TBEV encompasses three main subtypes with distinct degrees of severity and clinical courses: European (TBEV-Eu), Siberian (TBEV-Sib), and Far Eastern (TBEV-FE). Over the past decade, TBE epidemiology has significantly changed in Europe, with increasing incidence in endemic countries and the discovery of new human case foci and areas of virus circulation. This emergence involves many factors of which the impacts are not easily determined. While most TBEV-Eu infections are asymptomatic, some patients develop signs of central nervous system involvement that can be severe (meningitis, encephalitis). While the mortality rate in humans is low (<<!--> <!-->2 %), post-infectious sequelae (cognitive and/or motor) can occur in up to 40 % of cases. While TBE treatment is symptomatic, several antiviral treatments are under study. The emergence of TBEV in Europe, particularly in France, represents a significant public health issue. This review provides an up-to-date overview of the latest data concerning TBE, focusing on the epidemiology and clinical, diagnostic, and therapeutic aspects of this emerging infection.</div></div>","PeriodicalId":13539,"journal":{"name":"Infectious diseases now","volume":"56 1","pages":"Article 105187"},"PeriodicalIF":2.2,"publicationDate":"2025-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145534424","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-08DOI: 10.1016/j.idnow.2025.105186
Robert Cohen, Odile Launay, Catherine Weil-Olivier, Pierre Bakhache, Pierre Bégué, Marie-Aliette Dommergues, Véronique Dufour, Joël Gaudelus, Isabelle Hau, Didier Pinquier, Georges Thiebault, Franck Thollot, François Vie le Sage, Corinne Levy, Maeva Lefebvre, Hervé Haas
{"title":"Toward a simplified vaccination schedule in France: How can the tools we possess be put to better use?","authors":"Robert Cohen, Odile Launay, Catherine Weil-Olivier, Pierre Bakhache, Pierre Bégué, Marie-Aliette Dommergues, Véronique Dufour, Joël Gaudelus, Isabelle Hau, Didier Pinquier, Georges Thiebault, Franck Thollot, François Vie le Sage, Corinne Levy, Maeva Lefebvre, Hervé Haas","doi":"10.1016/j.idnow.2025.105186","DOIUrl":"10.1016/j.idnow.2025.105186","url":null,"abstract":"","PeriodicalId":13539,"journal":{"name":"Infectious diseases now","volume":"55 8","pages":"Article 105186"},"PeriodicalIF":2.2,"publicationDate":"2025-11-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145488488","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-11-05DOI: 10.1016/j.idnow.2025.105185
Andreas Chiabi , Sankara Nykam , Kate Kan , Cecilia Fomenky , Lucas M. Tanlaka , Franklin N. Ngueiwoh , Christabelle Ewane , Vanessa M. Fozao , Denis Nsame
Objectives
Cameroon adopted dolutegravir-based regimen in 2020 as the first-line treatment of HIV infection, as recommended by the World Health Organization on the basis of efficacy, high genetic barriers to drug resistance, low toxicity, and low cost. Our main objective was to evaluate the efficacy of dolutegravir-based regimen among HIV-infected children.
Patients and methods
We performed a retrospective hospital-based cohort study over a 5-month period at the pediatric day care unit of Bamenda Regional Hospital among HIV-infected children aged 3–15 years. Data was collected using a predesigned questionnaire and was analyzed with SPSS v.27.0 using the appropriate statistical test. P-values < 0.05 were considered statistically significant.
Results
We included 207 participants: 139 in the efavirenz (EFV) group and 68 in the dolutegravir (DTG) group. The mean viral load was lower in the DTG group than in the EFV group with mean viral load differences of 3,679 copies/ml, 2,245 copies/ml, and 3,207 copies/ml at 6 months, 12 months, and 24 months, respectively. The viral load suppression rate was higher in the DTG group than in the EFV group at 6 months (63.2 % vs 51.1 %, p = 0.099), at 12 months (80.9 % vs 64.7 %, p = 0.017), and at 24 months (83.8 % vs 70.5 %, p = 0.038). Children on DTG achieved virologic suppression quicker than children on EFV (9 months vs 10 months, p = 0.178).
Conclusion
Children on dolutegravir had good viral load suppression compared with children on efavirenz.
目标:喀麦隆根据世界卫生组织基于疗效、高耐药遗传屏障、低毒性和低成本的建议,于2020年采用以多替格雷韦为基础的方案作为艾滋病毒感染的一线治疗方法。我们的主要目的是评估以盐酸多替替韦为基础的治疗方案对感染艾滋病毒的儿童的疗效。患者和方法:我们在巴门达地区医院儿科日托部对3-15岁 岁的艾滋病毒感染儿童进行了为期5个月的回顾性医院队列研究。使用预先设计的问卷收集数据,并使用SPSS v.27.0进行分析,使用适当的统计检验。p值 结果:我们纳入了207名参与者:139名在依非韦伦(EFV)组,68名在多鲁特韦(DTG)组。DTG组的平均病毒载量低于EFV组,在6 个月、12 个月和24 个月时的平均病毒载量分别为3,679拷贝/ml、2,245拷贝/ml和3,207拷贝/ml。的病毒载量壳体组抑制率高于EFV小组6 个月(63.2 vs 51.1 % % p = 0.099), 12个月(80.9 vs 64.7 % % p = 0.017),并在24 月(83.8 vs 70.5 % % p = 0.038)。DTG组患儿比EFV组患儿更快达到病毒学抑制(9 个月vs 10 个月,p = 0.178)。结论:与依非韦伦相比,多替格拉韦对儿童病毒载量有较好的抑制作用。
{"title":"Efficacy of dolutegravir-based regimen in HIV-infected children in a treatment center in a regional health facility in Cameroon","authors":"Andreas Chiabi , Sankara Nykam , Kate Kan , Cecilia Fomenky , Lucas M. Tanlaka , Franklin N. Ngueiwoh , Christabelle Ewane , Vanessa M. Fozao , Denis Nsame","doi":"10.1016/j.idnow.2025.105185","DOIUrl":"10.1016/j.idnow.2025.105185","url":null,"abstract":"<div><h3>Objectives</h3><div>Cameroon adopted dolutegravir-based regimen in 2020 as the first-line treatment of HIV infection, as recommended by the World Health Organization on the basis of efficacy, high genetic barriers to drug resistance, low toxicity, and low cost. Our main objective was to evaluate the efficacy of dolutegravir-based regimen among HIV-infected children.</div></div><div><h3>Patients and methods</h3><div>We performed a retrospective hospital-based cohort study over a 5-month period at the pediatric day care unit of Bamenda Regional Hospital among HIV-infected children aged 3–15 years. Data was collected using a predesigned questionnaire and was analyzed with SPSS v.27.0 using the appropriate statistical test. P-values < 0.05 were considered statistically significant.</div></div><div><h3>Results</h3><div>We included 207 participants: 139 in the efavirenz (EFV) group and 68 in the dolutegravir (DTG) group. The mean viral load was lower in the DTG group than in the EFV group with mean viral load differences of 3,679<!--> <!-->copies/ml, 2,245<!--> <!-->copies/ml, and 3,207<!--> <!-->copies/ml at 6 months, 12 months, and 24 months, respectively. The viral load suppression rate was higher in the DTG group than in the EFV group at 6 months (63.2 % vs 51.1 %, <em>p</em> = 0.099), at 12 months (80.9 % vs 64.7 %, <em>p</em> = 0.017), and at 24 months (83.8 % vs 70.5 %, <em>p</em> = 0.038). Children on DTG achieved virologic suppression quicker than children on EFV (9 months vs 10 months, <em>p</em> = 0.178).</div></div><div><h3>Conclusion</h3><div>Children on dolutegravir had good viral load suppression compared with children on efavirenz.</div></div>","PeriodicalId":13539,"journal":{"name":"Infectious diseases now","volume":"55 8","pages":"Article 105185"},"PeriodicalIF":2.2,"publicationDate":"2025-11-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145470766","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}