Therapeutic Advances in Infectious Disease最新文献

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The role and prospects of skin microbiota in dermatosis. 皮肤微生物群在皮肤病中的作用及展望。
IF 3.8
Therapeutic Advances in Infectious Disease Pub Date : 2025-06-14 eCollection Date: 2025-01-01 DOI: 10.1177/20499361251333562
Yuanyuan Chen, Zhijian Yao, Zhuren Ruan, Gao Wei, Wenjun Zheng, Xianghui Li
{"title":"The role and prospects of skin microbiota in dermatosis.","authors":"Yuanyuan Chen, Zhijian Yao, Zhuren Ruan, Gao Wei, Wenjun Zheng, Xianghui Li","doi":"10.1177/20499361251333562","DOIUrl":"10.1177/20499361251333562","url":null,"abstract":"<p><p>The skin microbiota is crucial in defending against toxic, solar, and pathogenic assaults, yet it can also precipitate dermatosis when its equilibrium is disrupted. The composition and distribution of various microorganisms within the skin maintain a dynamic balance, modulating the barrier function and the immune system, thereby constituting the skin microbiota. This microbiota not only offers new insights into pathological microbe-host interactions and associated dermatoses but also inspires innovative therapeutic strategies that promise high efficacy and reduced symptomatology. In this review, we synthesize recent advancements in the field of skin microbiota, focusing on its relationship with dermatosis and the application of microbiota-based therapies in skin diseases. Our aim is to scrutinize the current understanding of the skin microbiota's role, ranging from a protective barrier to a causative agent of dermatosis.</p>","PeriodicalId":46154,"journal":{"name":"Therapeutic Advances in Infectious Disease","volume":"12 ","pages":"20499361251333562"},"PeriodicalIF":3.8,"publicationDate":"2025-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12171259/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144318357","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}
引用次数: 0
Plastic bronchitis in a man living with advanced HIV and disseminated Kaposi sarcoma: case report and discussion. 塑胶支气管炎的男性生活与晚期艾滋病毒和播散性卡波西肉瘤:病例报告和讨论。
IF 3.8
Therapeutic Advances in Infectious Disease Pub Date : 2025-06-08 eCollection Date: 2025-01-01 DOI: 10.1177/20499361251342883
Lindsey Robertson, Pamela Gorejena-Chidawanyika, Margaret Borok
{"title":"Plastic bronchitis in a man living with advanced HIV and disseminated Kaposi sarcoma: case report and discussion.","authors":"Lindsey Robertson, Pamela Gorejena-Chidawanyika, Margaret Borok","doi":"10.1177/20499361251342883","DOIUrl":"10.1177/20499361251342883","url":null,"abstract":"<p><p>A 33-year-old man living with advanced HIV with a histologically confirmed diagnosis of Kaposi sarcoma presented during a SARS-CoV-2 outbreak with worsening shortness of breath. He was treated for confirmed SARS CoV-2 infection with minimal symptomatic response, and whilst undergoing KS treatment on the ward developed the rare complication of plastic bronchitis. He had a prolonged hospital admission undergoing treatment for his Kaposi sarcoma and plastic bronchitis whilst being evaluated for concurrent opportunistic infections.</p>","PeriodicalId":46154,"journal":{"name":"Therapeutic Advances in Infectious Disease","volume":"12 ","pages":"20499361251342883"},"PeriodicalIF":3.8,"publicationDate":"2025-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12146592/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144259021","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}
引用次数: 0
Determinants of health-related quality of life in drug-susceptible tuberculosis patients in Ghana: a prospective observational study. 加纳药物敏感结核病患者健康相关生活质量的决定因素:一项前瞻性观察研究
IF 3.8
Therapeutic Advances in Infectious Disease Pub Date : 2025-06-08 eCollection Date: 2025-01-01 DOI: 10.1177/20499361251343143
Richard Delali Agbeko Djochie, Berko Panyin Anto, Mercy Naa Aduele Opare-Addo
{"title":"Determinants of health-related quality of life in drug-susceptible tuberculosis patients in Ghana: a prospective observational study.","authors":"Richard Delali Agbeko Djochie, Berko Panyin Anto, Mercy Naa Aduele Opare-Addo","doi":"10.1177/20499361251343143","DOIUrl":"10.1177/20499361251343143","url":null,"abstract":"<p><strong>Background: </strong>Tuberculosis (TB) affects patients' quality of life due to symptoms and social stigma, especially in low-income settings like Ghana. However, data on factors influencing health-related quality of life (HRQOL) in such environments are limited. Identifying these factors is essential for improving treatment outcomes through holistic care.</p><p><strong>Objective: </strong>This study determined the impact of sociodemographic and clinical factors on HRQOL at treatment initiation, and monitored changes until the end of treatment.</p><p><strong>Design: </strong>Prospective observational study.</p><p><strong>Methods: </strong>A cohort of 378 newly diagnosed patients with drug-susceptible TB (mean age: 45.3 ± 15.1 years) was followed across eight hospitals in the Ashanti and Eastern regions of Ghana. Patients received first-line antitubercular treatment, and HRQOL was assessed at baseline, month 2, and month 6 using an interviewer-administered SF-12v2 questionnaire. Associations between HRQOL and sociodemographic or clinical factors were examined using Chi-square or Fisher's exact tests, while logistic regression was used to estimate crude and adjusted odds ratios (<i>p</i> < 0.05).</p><p><strong>Results: </strong>At baseline, 78.8% of participants had impaired physical HRQOL, and 25.7% were at risk of depression. At treatment completion, physical HRQOL impairment remained high (59.5%), with 15.0% still at risk of depression. Only 44.7% showed clinically significant improvement in physical HRQOL, while 39.8% improved in mental HRQOL. Employment, HIV-positive status, and alcohol use were associated with poorer mental HRQOL. Extrapulmonary TB patients demonstrated better physical HRQOL at both the beginning and end of treatment but exhibited poorer mental HRQOL at treatment completion. Widowed participants improved mentally despite poorer baseline health, while married individuals had better physical HRQOL. Higher education correlated with better baseline mental health but lower odds of significant HRQOL improvement.</p><p><strong>Conclusion: </strong>Sociodemographic and clinical factors significantly influenced HRQOL in drug-susceptible TB patients after 6 months of treatment. These findings underscore the importance of targeted mental health support during and after treatment to improve patient well-being.</p>","PeriodicalId":46154,"journal":{"name":"Therapeutic Advances in Infectious Disease","volume":"12 ","pages":"20499361251343143"},"PeriodicalIF":3.8,"publicationDate":"2025-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12146591/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144259020","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}
引用次数: 0
Inability-to-walk-unaided-a single WHO danger sign predicts in-hospital mortality in people with HIV under routine care conditions in a low-resource setting. 无法独立行走——世卫组织的一个危险标志,可预测在资源匮乏环境中常规护理条件下艾滋病毒感染者的住院死亡率。
IF 3.8
Therapeutic Advances in Infectious Disease Pub Date : 2025-06-05 eCollection Date: 2025-01-01 DOI: 10.1177/20499361251341385
Ethel Rambiki, Agness Thawani, Davis Kapenga, Chikaiko Malunda, Boniface Mseke, Patrick Mpesi, Prakash Ganesh, Hans-Michael Steffen, Tom Heller, Claudia Wallrauch
{"title":"Inability-to-walk-unaided-a single WHO danger sign predicts in-hospital mortality in people with HIV under routine care conditions in a low-resource setting.","authors":"Ethel Rambiki, Agness Thawani, Davis Kapenga, Chikaiko Malunda, Boniface Mseke, Patrick Mpesi, Prakash Ganesh, Hans-Michael Steffen, Tom Heller, Claudia Wallrauch","doi":"10.1177/20499361251341385","DOIUrl":"10.1177/20499361251341385","url":null,"abstract":"<p><strong>Background: </strong>People with advanced HIV admitted to hospitals are at high risk of mortality. Serious illness can be identified using WHO-defined danger signs (\"WHO score\") or bedside scores like the quick Sequential Organ Failure Assessment (qSOFA) score.</p><p><strong>Objectives: </strong>The study aimed at assessing clinical parameters as predictors of in-hospital mortality for people with HIV (PWH) admitted for routine medical care.</p><p><strong>Study design: </strong>A prospective observational study of all PWH admitted to medical wards at Kamuzu Central Hospital, Lilongwe, Malawi.</p><p><strong>Methods: </strong>WHO danger signs and qSOFA score were determined at the first encounter, CD4 count tests were performed, and discharge outcomes were recorded. The discriminatory power of different scores for predicting in-hospital mortality was assessed using the area under receiver-operating-characteristic curves (AUROCs).</p><p><strong>Results: </strong>From November 2022 to May 2023, 401 adults aged ⩾18 years were admitted. Advanced HIV disease (CD4 < 200 cells/mm<sup>3</sup>) was present in 55.2% (95% CI 50.2-60.2). Overall, in-hospital mortality was 25.7% (95% CI 21.3-30.0). Neither sex, age, CD4 count, nor BMI < 18.5 was significantly associated with mortality. Both the WHO score and qSOFA score were significantly associated with increasing mortality. AUROC for WHO score and qSOFA were 0.68 (95% CI 0.61-0.75) and 0.71 (95% CI 0.64-0.78), respectively. Including BMI or CD4 did not significantly improve AUROC. Using only the individual danger sign \"inability-to-walk-unaided\" yielded a similar AUROC of 0.68 (95% CI 0.61-0.75).</p><p><strong>Conclusion: </strong>Increasing WHO danger sign scores were associated with in-hospital mortality; adding BMI or CD4 did not improve predictive accuracy. Notably, the predictive information derived from a single parameter-inability-to-walk-unaided-was as effective as the complete WHO score and was easier to obtain. Given the challenges in comprehensive vital sign recording, this simple measure may prove valuable in triaging PWH admitted to hospitals in resource-limited settings such as Malawi.</p>","PeriodicalId":46154,"journal":{"name":"Therapeutic Advances in Infectious Disease","volume":"12 ","pages":"20499361251341385"},"PeriodicalIF":3.8,"publicationDate":"2025-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12141800/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144250215","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}
引用次数: 0
Kidney impairment in HIV: an insight into the burden and associated factors among adults on antiretroviral therapy in Zambia. A retrospective cross-sectional study. 艾滋病毒肾损害:深入了解赞比亚成人抗逆转录病毒治疗的负担和相关因素。回顾性横断面研究。
IF 3.8
Therapeutic Advances in Infectious Disease Pub Date : 2025-06-05 eCollection Date: 2025-01-01 DOI: 10.1177/20499361251340795
Matenge Mutalange, Lukundo Siame, Chilala Cheelo, Sepiso K Masenga, Benson M Hamooya
{"title":"Kidney impairment in HIV: an insight into the burden and associated factors among adults on antiretroviral therapy in Zambia. A retrospective cross-sectional study.","authors":"Matenge Mutalange, Lukundo Siame, Chilala Cheelo, Sepiso K Masenga, Benson M Hamooya","doi":"10.1177/20499361251340795","DOIUrl":"10.1177/20499361251340795","url":null,"abstract":"<p><strong>Background: </strong>Kidney disease, ranging from asymptomatic kidney impairment to end-stage renal disease, remains a public health concern globally. Kidney diseases have been shown to be a significant cause of mortality and morbidity among people living with HIV (PLWH). However, there is limited data on the burden and risk factors for kidney impairment in resource-limited settings.</p><p><strong>Objectives: </strong>This study aimed to determine the prevalence and factors associated with kidney impairment among PLWH receiving antiretroviral therapy (ART) at a tertiary hospital in Zambia.</p><p><strong>Design: </strong>This was a retrospective cross-sectional study.</p><p><strong>Methods: </strong>This study consisted of 374 PLWH aged ⩾18 years and on ART for ⩾ 6 months. We obtained clinical, laboratory, and demographic characteristics from a study that focused on metabolic syndrome among PLWH. Kidney impairment was defined as having an estimated glomerular filtration rate (eGFR) of <60 ml/min/1.73 m<sup>2</sup>. Data was analyzed using STATA version 15. Multivariable logistic regression was used to ascertain factors associated with kidney impairment.</p><p><strong>Results: </strong>The median age among the study participants was 44 years, and the majority were females, 63.4% (<i>n</i> = 237). The prevalence of kidney impairment was 10.7% (<i>n</i> = 40. After accounting for duration on ART, sex and blood pressure (systolic and diastolic), older age and being on a Dolutegravir (DTG) and tenofovir disoproxil fumarate/lamivudine (TDF/3TC) based regimen was positively associated with kidney impairment (adjusted odds ratio (aOR) 1.09; 95% CI: 1.05, 1.14, <i>p</i> < 0.001) and (aOR 2.44; 95% CI: 1.02, 5.79, <i>p</i> = 0.043), respectively.</p><p><strong>Conclusion: </strong>The prevalence of kidney impairment was common among adult PLWH and was significantly associated with older age and the use of a DTG and TDF/3TC-based regimen. There is a need to regularly monitor kidney function among people with HIV, especially older people who are on a DTG and TDF/3TC-based regimen.</p>","PeriodicalId":46154,"journal":{"name":"Therapeutic Advances in Infectious Disease","volume":"12 ","pages":"20499361251340795"},"PeriodicalIF":3.8,"publicationDate":"2025-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12141796/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144250216","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}
引用次数: 0
Differences in antimicrobial resistance gene abundance and microbial diversity of the gut microbiome in patients on antibiotics enrolled in a clinical trial. 临床试验中抗生素患者肠道微生物组的耐药基因丰度和微生物多样性差异
IF 3.8
Therapeutic Advances in Infectious Disease Pub Date : 2025-06-05 eCollection Date: 2025-01-01 DOI: 10.1177/20499361251337597
Adam G Stewart, Patrick N A Harris, Rikki M A Graham, Amy V Jennison, Sanmarie Schlebusch, Asha Kakkanat, Tiffany Harris-Brown, David L Paterson, Brian M Forde
{"title":"Differences in antimicrobial resistance gene abundance and microbial diversity of the gut microbiome in patients on antibiotics enrolled in a clinical trial.","authors":"Adam G Stewart, Patrick N A Harris, Rikki M A Graham, Amy V Jennison, Sanmarie Schlebusch, Asha Kakkanat, Tiffany Harris-Brown, David L Paterson, Brian M Forde","doi":"10.1177/20499361251337597","DOIUrl":"10.1177/20499361251337597","url":null,"abstract":"<p><strong>Background: </strong>Understanding how the gut microbiome adapts on exposure to individual antibiotics, with respect to antimicrobial resistance gene (ARG) enrichment, is important.</p><p><strong>Objectives: </strong>To characterise the changes that occur in the gut microbiome of patients enrolled in an antibiotic clinical trial and to propose methods in which to embed gut microbiome analysis into clinical trials.</p><p><strong>Design: </strong>This was a prospective cohort study of hospitalised patients who were successfully enrolled and randomised into two clinical trials between January 2021 to December 2021.</p><p><strong>Methods: </strong>Adult patients admitted to the hospital with a bloodstream infection have been randomised to receive either benzylpenicillin, ampicillin, cefazolin, ceftriaxone, piperacillin-tazobactam or meropenem at a single institution. Faecal specimens were collected at enrolment and every second day until discharge. Each specimen underwent DNA sequencing to determine microbial diversity and ARG abundance.</p><p><strong>Results: </strong>Ten patients (including six females) were included. DNA concentration and sampling quality were markedly lower for rectal swabs compared to stool samples. Relative abundance of <i>Enterococcus faecium</i> was increased in individual patients where treatment included ampicillin, meropenem and piperacillin-tazobactam. Piperacillin-tazobactam also increased the abundance of key beta-lactamase genes (<i>bla</i> <sub>SHV-100</sub>, <i>bla</i> <sub>OXA-392</sub>, <i>bla</i> <sub>CMY-18</sub>). Ampicillin increased the abundance of <i>bla</i> <sub>TEM-1A</sub>. There were no extended-spectrum beta-lactamase (ESBL) or carbapenemase genes detected in our study. The presence of key anaerobes such as <i>Clostridium</i> and <i>Bifidobacterium</i> species appeared to play an important role in colonisation resistance of <i>E. faecium</i> and <i>Clostridioides difficile</i>.</p><p><strong>Conclusion: </strong>Differential changes in anaerobic bacterial genera on exposure to antibiotics may be a key determinant of colonisation resistance. The pre-analytical phase of microbiome analysis is a critical factor in data quality and interpretation.</p>","PeriodicalId":46154,"journal":{"name":"Therapeutic Advances in Infectious Disease","volume":"12 ","pages":"20499361251337597"},"PeriodicalIF":3.8,"publicationDate":"2025-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12144387/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144250214","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}
引用次数: 0
Spatiotemporal analysis of tuberculosis drug resistance and associated risk factors in Tanzania. 坦桑尼亚结核病耐药性及相关危险因素的时空分析。
IF 3.8
Therapeutic Advances in Infectious Disease Pub Date : 2025-06-01 eCollection Date: 2025-01-01 DOI: 10.1177/20499361251339576
Bwire Wilson Bwire, Maurice C Y Mbago, Amina S Msengwa
{"title":"Spatiotemporal analysis of tuberculosis drug resistance and associated risk factors in Tanzania.","authors":"Bwire Wilson Bwire, Maurice C Y Mbago, Amina S Msengwa","doi":"10.1177/20499361251339576","DOIUrl":"10.1177/20499361251339576","url":null,"abstract":"<p><strong>Background: </strong>The prevalence of tuberculosis (TB) multi-drug resistance is increasing worldwide, including in Tanzania. This trend hinders the attainment of sustainable development goal number three as it increases the number of cases of the disease and treatment costs. Fewer cases of drug resistance have been reported over time, making it necessary to demand models that can handle an excessive number of zero counts. This study employed the zero-inflated Poisson (ZIP) models suitable for such data to assess drug resistance patterns.</p><p><strong>Objective: </strong>To examine the TB drug resistance spatiotemporal risk patterns and associated risk factors using health facility case notification data.</p><p><strong>Design: </strong>A retrospective cohort study utilizing TB drug resistance case notification data from the District Health Information System 2 for Tanzania Mainland between 2018 and 2020.</p><p><strong>Methods: </strong>The study was conducted in Tanzania Mainland and utilized TB drug resistance case data from 184 councils. Six hundred fifty-two (652) TB drug resistance cases were analyzed using the Bayesian ZIP spatiotemporal model to identify high-risk areas and risk factors for TB drug resistance. The deviance information criterion guided model selection.</p><p><strong>Results: </strong>The findings revealed a higher prevalence of drug resistance among males (65.2%), individuals aged 35-49 years (33.7%), persons living without HIV (66.4%) and new TB cases (70.7%). Spatiotemporal modelling indicated significant relationships between drug resistance and sex, age, TB treatment history and HIV status. Males were 1.4 times more likely to develop drug resistance than females. Children aged 0-4 and 5-14 years were 25 and 8.3 times less likely to develop drug resistance than adults aged 35-49. Persons living with HIV and those with unknown HIV status were 1.2 and 3.4 times less likely to develop drug resistance, respectively, than persons living without HIV. Individuals with a previous TB treatment history were three times more likely to develop drug resistance compared to new cases.</p><p><strong>Conclusion: </strong>The Bayesian ZIP spatiotemporal models provide critical insights by identifying high-risk populations and areas, enabling targeted interventions to control multi-drug resistant TB. The study further concludes that resistance to anti-TB drugs is highly associated with sex, age and previous treatment history. To mitigate its spread and impact, the study recommends strengthening awareness campaigns on adherence to treatment guidelines and understanding the risk factors associated with TB drug resistance.</p>","PeriodicalId":46154,"journal":{"name":"Therapeutic Advances in Infectious Disease","volume":"12 ","pages":"20499361251339576"},"PeriodicalIF":3.8,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12130660/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144217237","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}
引用次数: 0
The weekend effect in critically ill patients with severe infections in Japanese intensive care units: a multicenter retrospective cohort study. 日本重症监护病房重症感染危重患者的周末效应:一项多中心回顾性队列研究
IF 3.8
Therapeutic Advances in Infectious Disease Pub Date : 2025-05-28 eCollection Date: 2025-01-01 DOI: 10.1177/20499361241292626
Teiko Kawahigashi, Taisuke Jo, Tetsuya Komuro, Jan De Waele, Liesbet De Bus, Akihiro Takaba, Akira Kuriyama, Atsuko Kobayashi, Chie Tanaka, Hideki Hashi, Hideki Hashimoto, Hiroshi Nashiki, Mami Shibata, Masafumi Kanamoto, Masashi Inoue, Satoru Hashimoto, Shinshu Katayama, Shinsuke Fujiwara, Shinya Kameda, Shunsuke Shindo, Taketo Suzuki, Toshiomi Kawagishi, Yasumasa Kawano, Yoshihito Fujita, Yoshiko Kida, Yuya Hara, Hideki Yoshida, Shigeki Fujitani, Hiroshi Koyama
{"title":"The weekend effect in critically ill patients with severe infections in Japanese intensive care units: a multicenter retrospective cohort study.","authors":"Teiko Kawahigashi, Taisuke Jo, Tetsuya Komuro, Jan De Waele, Liesbet De Bus, Akihiro Takaba, Akira Kuriyama, Atsuko Kobayashi, Chie Tanaka, Hideki Hashi, Hideki Hashimoto, Hiroshi Nashiki, Mami Shibata, Masafumi Kanamoto, Masashi Inoue, Satoru Hashimoto, Shinshu Katayama, Shinsuke Fujiwara, Shinya Kameda, Shunsuke Shindo, Taketo Suzuki, Toshiomi Kawagishi, Yasumasa Kawano, Yoshihito Fujita, Yoshiko Kida, Yuya Hara, Hideki Yoshida, Shigeki Fujitani, Hiroshi Koyama","doi":"10.1177/20499361241292626","DOIUrl":"10.1177/20499361241292626","url":null,"abstract":"<p><strong>Background: </strong>Reduced or delayed access to medical resources on weekends could lead to worsening outcomes, in critically ill infected patients requiring intensive care unit (ICU) admission.</p><p><strong>Objective: </strong>To investigate the \"weekend effect,\" on critically ill infected patients in Japanese ICUs for the first time.</p><p><strong>Design: </strong>Multicenter retrospective cohort study.</p><p><strong>Methods: </strong>We examined data from Japanese ICU patients participating in the DIANA study, a multicenter international observational cohort study. This prospective investigation enrolled critically ill patients with infections admitted to the ICU. The primary endpoint was successful discharge from the ICU within 28 days of admission. Outcome measures were evaluated through both univariate and covariate Cox regression analyses, providing hazard ratios (HRs) along with estimated 95% confidence intervals (CIs).</p><p><strong>Results: </strong>Out of the 276 patients enrolled in the DIANA study across 31 facilities, 208 patients (75.4%) meeting the inclusion criteria were included in the analysis. The weekday ICU admission group comprised 156 patients (75.0%), while the weekend ICU admission group comprised 52 patients (25.0%). In the multivariate Cox regression analysis, there were no statistically significant differences observed in the rates of ICU discharge alive within 28 days and 14 days (28 days, HR: 0.94, 95% CI: 0.63-1.40; 14 days, HR: 0.97, 95% CI: 0.64-1.48). Furthermore, the overall ICU mortality rates at 28 days and 14 days after ICU admission did not show statistical significance between patients admitted on weekends and those admitted on weekdays (ICU mortality, 28 days: 13.5% vs 11.5%, <i>p</i> = 0.806; 14 days: 7.7% vs 10.9%, <i>p</i> = 0.604).</p><p><strong>Conclusion: </strong>The rates of ICU discharge alive within 28 days after ICU admission did not differ significantly between weekday and weekend admissions, both in the unadjusted and adjusted analyses. Moreover, further well-designed studies are warranted to thoroughly assess this effect.</p>","PeriodicalId":46154,"journal":{"name":"Therapeutic Advances in Infectious Disease","volume":"12 ","pages":"20499361241292626"},"PeriodicalIF":3.8,"publicationDate":"2025-05-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12120283/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144181814","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}
引用次数: 0
Antimicrobial resistance with a focus on antibacterial, antifungal, antimalarial, and antiviral drugs resistance, its threat, global priority pathogens, prevention, and control strategies: a review. 抗微生物药物耐药性,重点是抗菌、抗真菌、抗疟疾和抗病毒药物耐药性,其威胁,全球重点病原体,预防和控制策略:综述
IF 3.8
Therapeutic Advances in Infectious Disease Pub Date : 2025-05-23 eCollection Date: 2025-01-01 DOI: 10.1177/20499361251340144
Wubetu Yihunie Belay, Melese Getachew, Bantayehu Addis Tegegne, Zigale Hibstu Teffera, Abebe Dagne, Tirsit Ketsela Zeleke, Samuel Agegnew Wondm, Rahel Belete Abebe, Abebaw Abie Gedif, Abebe Fenta, Getasew Yirdaw, Adane Tilahun, Yibeltal Aschale
{"title":"Antimicrobial resistance with a focus on antibacterial, antifungal, antimalarial, and antiviral drugs resistance, its threat, global priority pathogens, prevention, and control strategies: a review.","authors":"Wubetu Yihunie Belay, Melese Getachew, Bantayehu Addis Tegegne, Zigale Hibstu Teffera, Abebe Dagne, Tirsit Ketsela Zeleke, Samuel Agegnew Wondm, Rahel Belete Abebe, Abebaw Abie Gedif, Abebe Fenta, Getasew Yirdaw, Adane Tilahun, Yibeltal Aschale","doi":"10.1177/20499361251340144","DOIUrl":"10.1177/20499361251340144","url":null,"abstract":"<p><p>Antimicrobial resistance (AMR) poses a significant global health threat by diminishing the effectiveness of once-powerful antimicrobial agents, leading to higher rates of illness and death, along with escalating healthcare costs. While bacterial resistance is a primary concern, resistance is also increasing against antifungal, antiparasitic, and antiviral drugs. Many of the last-resort drugs are becoming less effective due to AMR. Projections indicate that by 2050, AMR could cause up to 10 million deaths annually, making it the leading cause of death worldwide, a situation that could result in a post-antibiotic era with substantially increased morbidity and mortality. This review aims to raise awareness about the dangers of AMR and its potential to become a silent global pandemic. It begins by examining antimicrobial drugs, followed by a discussion on AMR, focusing on resistance to antibacterial, antifungal, antimalarial, and antiviral drugs, along with its effects on health, and the economy, and prioritized global pathogens. Finally, it explores preventive measures and innovative strategies to combat AMR.</p>","PeriodicalId":46154,"journal":{"name":"Therapeutic Advances in Infectious Disease","volume":"12 ","pages":"20499361251340144"},"PeriodicalIF":3.8,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12103682/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144143927","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}
引用次数: 0
Not your typical hookworm infection-a case report from the Peruvian Amazon and review of the literature. 不是典型的钩虫感染——秘鲁亚马逊地区的一份病例报告和文献综述。
IF 3.8
Therapeutic Advances in Infectious Disease Pub Date : 2025-05-19 eCollection Date: 2025-01-01 DOI: 10.1177/20499361251332148
Edgar A Ramirez-García, Ricci A Chafloque-Vasquez, Angel A Moreno-Soto, Jhosephi J Vásquez-Ascate, Marco F Paredes-Obando, Nelson Iván Agudelo Higuita, Andrés F Henao-Martínez, Carlos Franco-Paredes, Luis A Marcos, Juan C Celis Salinas, Martín Casapía-Morales
{"title":"Not your typical hookworm infection-a case report from the Peruvian Amazon and review of the literature.","authors":"Edgar A Ramirez-García, Ricci A Chafloque-Vasquez, Angel A Moreno-Soto, Jhosephi J Vásquez-Ascate, Marco F Paredes-Obando, Nelson Iván Agudelo Higuita, Andrés F Henao-Martínez, Carlos Franco-Paredes, Luis A Marcos, Juan C Celis Salinas, Martín Casapía-Morales","doi":"10.1177/20499361251332148","DOIUrl":"10.1177/20499361251332148","url":null,"abstract":"<p><p>Human hookworm infection is caused by the nematodes <i>Necator americanus</i>, <i>Ancylostoma duodenale</i>, and <i>Ancylostoma ceylanicum</i>. Iron deficiency anemia is the hallmark of chronic, moderate-to-heavy-intensity infections, promoting a vicious poverty cycle. Overt severe and acute life-threatening lower gastrointestinal hemorrhage is an extremely rare manifestation of hookworm infection, as well as finding multiple nematodes attached to the colonic mucosae. This rare hookworm presentation with hematochezia from the colon in a patient living with human immunodeficiency virus highlights the importance of physicians' awareness of this neglected tropical disease responsible for high morbidity and burden in healthcare systems of endemic regions.</p>","PeriodicalId":46154,"journal":{"name":"Therapeutic Advances in Infectious Disease","volume":"12 ","pages":"20499361251332148"},"PeriodicalIF":3.8,"publicationDate":"2025-05-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12089704/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144112092","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}
引用次数: 0
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