BMC Infectious Diseases最新文献

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Comparison of cefiderocol and colistin-based regimens for the treatment of severe infections caused by carbapenem-resistant Acinetobacter baumannii: a systematic review with meta-analysis and trial sequential analysis 耐碳青霉烯类鲍曼不动杆菌引起的严重感染的治疗方案中头孢克肟方案和可乐定方案的比较:荟萃分析和试验序列分析的系统综述
IF 3.7 3区 医学
BMC Infectious Diseases Pub Date : 2024-09-13 DOI: 10.1186/s12879-024-09899-5
Yangyang Zhan, Wenchao Mao, Changyun Zhao, Difan Lu, Changqin Chen, Weihang Hu, Qi Yang
{"title":"Comparison of cefiderocol and colistin-based regimens for the treatment of severe infections caused by carbapenem-resistant Acinetobacter baumannii: a systematic review with meta-analysis and trial sequential analysis","authors":"Yangyang Zhan, Wenchao Mao, Changyun Zhao, Difan Lu, Changqin Chen, Weihang Hu, Qi Yang","doi":"10.1186/s12879-024-09899-5","DOIUrl":"https://doi.org/10.1186/s12879-024-09899-5","url":null,"abstract":"There are multiple antibiotic regimens for the treatment of carbapenem-resistant Acinetobacter baumannii (CRAB) in clinical practice. We conducted this meta-analysis to compare the efficacy and safety of cefiderocol-based regimens and colistin-based regimens in the treatment of CRAB infections. Two authors independently searched the PubMed, Web of Science, Embase, and Cochrane databases from their establishment to April 15, 2024, to search for randomized controlled trials (RCTs) or cohort studies, and compared the clinical efficacy and safety of cefiderocol-based regimens and colistin-based regimens in the treatment of CRAB infections. The Newcastle Ottawa Scale (NOS) checklist was used to evaluate the quality of the included studies. The primary outcome was all-cause mortality, and subgroup analysis was conducted on the basis of the site of infection and the risk of bias in the studies. Trial sequential analysis (TSA) was then conducted. Six observational studies were included, with 251 cases in the cefiderocol-based group and 372 cases in the colistin-based group. Compared to the colistin-based group, the cefiderocol-based group had lower all-cause mortality (RR = 0.71, 95% CI: 0.54–0.92, P = 0.01) and 30-day mortality (RR = 0.64, 95% CI: 0.43–0.95, P = 0.03). However, for the 14-day and 28-day mortality rates, there was no statistically significant difference between two groups. According to the subgroup analysis, among patients with bloodstream infection (BSI), the cefiderocol-based group had lower all-cause mortality, but it did not reduce the mortality of ventilator-associated pneumonia (VAP) patients. The result of TSA showed that our conclusions are reliable. There was no significant statistical difference in the microbiological cure rate, clinical cure rate, or duration of hospitalization. In addition, the cefiderocol-based group did not have an increased incidence of acute kidney injury (AKI). Compared with the colistin-based regimens, the cefiderocol-based regimens were significantly associated with a lower risk of mortality in CRAB-infected patients, especially for patients with BSI. However, they did not show any advantages in terms of the clinical cure rate or microbiological cure rate, nor did they reduce the incidence of AKI. CRD42023487213.","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":null,"pages":null},"PeriodicalIF":3.7,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142223384","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Significant drop in serum C-reactive protein in patients with solid neoplasia and bacterial infection is associated with a better prognosis and identifies candidates for short-course antibiotic therapy 实体瘤和细菌感染患者血清 C 反应蛋白的显著下降与较好的预后有关,并可确定接受短程抗生素治疗的候选者
IF 3.7 3区 医学
BMC Infectious Diseases Pub Date : 2024-09-13 DOI: 10.1186/s12879-024-09544-1
Guilherme Monteiro de Barros, Isabela Nascimento Borges, Cecilia Gómez Ravetti, Paulo Henrique Diniz, Samuel Rosa Ferreira, Lara Hemerly De Mori, Rafael Castro, Getúlio H. Okamura, Felipe Gatto, Vandack Nobre
{"title":"Significant drop in serum C-reactive protein in patients with solid neoplasia and bacterial infection is associated with a better prognosis and identifies candidates for short-course antibiotic therapy","authors":"Guilherme Monteiro de Barros, Isabela Nascimento Borges, Cecilia Gómez Ravetti, Paulo Henrique Diniz, Samuel Rosa Ferreira, Lara Hemerly De Mori, Rafael Castro, Getúlio H. Okamura, Felipe Gatto, Vandack Nobre","doi":"10.1186/s12879-024-09544-1","DOIUrl":"https://doi.org/10.1186/s12879-024-09544-1","url":null,"abstract":"The greater predisposition to infections, as well as the possibility of a worse response to treatment, can lead to the excessive use of antimicrobials among cancer patients. C-reactive protein (CRP) has gained prominence as a tool for monitoring therapeutic responses and reducing the duration of antibiotic therapy; however, few studies have analyzed this protein in cancer patient populations. We hypothesize that cancer patients with a good response to antibiotic therapy show a faster decline in serum CRP levels, which would allow us to identify candidates for short-course treatments. To evaluate the behavior of serum CRP levels among adult cancer patients using antibiotic therapy, and its association with the duration of this treatment, therapeutic response, and clinical recurrence. This work consisted of a retrospective study with cancer patients admitted to a university hospital between September 2018 and December 2019. Adults (age ≥ 18 years) who underwent at least one course of antibiotic therapy were included. CRP behavior over the first 7 days of treatment was classified as: i) good response: when the CRP value on the fifth day of therapy reached 50% or less of the peak value detected in the first 48 h of treatment, and ii) poor response: Maintenance, within the same interval, of a CRP value > 50% of the peak value in the first 48 h. The duration of antibiotic therapy was categorized as up to seven full days or more. Outcomes were assessed by events that occurred during the 30 days of hospitalization or until hospital discharge. Primary outcome: Clinical recurrence of the index infection. Secondary outcomes: i) Death from any cause; ii) microbiological recurrence; iii) therapeutic response; iv) colitis associated with Clostridioides difficile; and v) isolation of multi-resistant bacteria, whether in clinical or surveillance samples. The final analysis consisted of 212 patients, with a median age (IQ) of 59.2 (48 – 67) years old and a predominance of females (65%), who were hypertensive (35%), smokers (21%), and diabetics (17.8%). There was no difference in clinical recurrence between the two groups (8.1% vs. 12.2%; p = 0.364), with a lower 30-day mortality in the good CRP response group (32.2% vs. 14.5%; p = 0.002). Despite the tendency towards a lower occurrence of other secondary outcomes in the good response group, these differences were not statistically significant. In the poor CRP response group, outcomes like clinical recurrence, mortality, and therapeutic response were significantly worse, regardless of the duration of antibiotic treatment. In this study, cancer patients with a good CRP response during antibiotic therapy presented lower mortality and a higher proportion of satisfactory therapeutic responses. CRP can be a useful tool when combined with other clinical information in optimizing the duration of antimicrobial treatment in a hospitalized cancer population.\u0000","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":null,"pages":null},"PeriodicalIF":3.7,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142223338","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Correction: Common subclinical hypothyroidism during Whipple’s disease 更正:惠普尔病期间常见的亚临床甲状腺功能减退症
IF 3.7 3区 医学
BMC Infectious Diseases Pub Date : 2024-09-13 DOI: 10.1186/s12879-024-09907-8
Jean-Christophe Lagier, Florence Fenollar, Jacques Chiaroni, Christophe Picard, Christiane Oddoze, Laurent Abi-Rached, Didier Raoult
{"title":"Correction: Common subclinical hypothyroidism during Whipple’s disease","authors":"Jean-Christophe Lagier, Florence Fenollar, Jacques Chiaroni, Christophe Picard, Christiane Oddoze, Laurent Abi-Rached, Didier Raoult","doi":"10.1186/s12879-024-09907-8","DOIUrl":"https://doi.org/10.1186/s12879-024-09907-8","url":null,"abstract":"<p>Following publication of the original article [1], an error was identified in the ethics agreement number from the Ethics Committee of the Institut Fédératif de Recherche IFR48, Faculty of Medicine, Marseille France.</p><p> The Ethical Statement should read:</p><p> Informed consent was obtained from all the participating patients in the study. The study was conducted as part of normal care, without supplementary patient’s samples. The study was approved by the Ethics Committee of the Institut Fédératif de Recherche IFR48, Faculty of Medicine, Marseille France (agreement number 13-028-02).</p><ol data-track-component=\"outbound reference\" data-track-context=\"references section\"><li data-counter=\"1.\"><p>Lagier. et al. BMC Infect Dis. 2014:14:370. https://doi.org/10.1186/1471-2334-14-370</p></li></ol><p>Download references<svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-download-medium\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></p><h3>Authors and Affiliations</h3><ol><li><p>Faculté de Médecine, Aix Marseille Université, URMITE, UM63, CNRS 7278, IRD 198, INSERM 1095, 27 Bd Jean Moulin, Marseille, 13005, France</p><p>Jean-Christophe Lagier, Florence Fenollar, Laurent Abi-Rached & Didier Raoult</p></li><li><p>UMR 7268 (ADES), Aix-Marseille Université, CNRS, EFS, 51 Bd Pierre Dramard, Marseille, 13916, France</p><p>Jacques Chiaroni & Christophe Picard</p></li><li><p>Laboratoire de Biochimie, APHM, CHU Timone, Marseille, 13005, France</p><p>Christiane Oddoze</p></li><li><p>Laboratoire d’Analyse, Centre National de la Recherche Scientifique, Topologie, Probabilités – Unité Mixte de Recherche 7353, Equipe ATIP, Aix-Marseille Université, Marseille, 13331, France</p><p>Laurent Abi-Rached</p></li></ol><span>Authors</span><ol><li><span>Jean-Christophe Lagier</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Florence Fenollar</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Jacques Chiaroni</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Christophe Picard</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Christiane Oddoze</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Laurent Abi-Rached</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Didier Raoult</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li></ol><h3>Corresponding author</h3><p>Correspondence to Didier Raoult.</p><h3>Publishe","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":null,"pages":null},"PeriodicalIF":3.7,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142223336","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mycoplasma pneumonia in a patient with X-linked agammaglobulinemia 一名 X 连锁丙种球蛋白血症患者的支原体肺炎
IF 3.7 3区 医学
BMC Infectious Diseases Pub Date : 2024-09-13 DOI: 10.1186/s12879-024-09743-w
Bowen Dai, Shujuan Han, Yuanfang Shen, Zhi Li, Shouhang Chen, Zhuangzhuang Wang, Yan Yuan, Ruyu Zhang, Chenyu Wang, Jiaying Zheng, Qiujing Liang, Qingmei Wang, Yaodong Zhang, Xiaolong Zhang, Fang Wang, Yuefei Jin
{"title":"Mycoplasma pneumonia in a patient with X-linked agammaglobulinemia","authors":"Bowen Dai, Shujuan Han, Yuanfang Shen, Zhi Li, Shouhang Chen, Zhuangzhuang Wang, Yan Yuan, Ruyu Zhang, Chenyu Wang, Jiaying Zheng, Qiujing Liang, Qingmei Wang, Yaodong Zhang, Xiaolong Zhang, Fang Wang, Yuefei Jin","doi":"10.1186/s12879-024-09743-w","DOIUrl":"https://doi.org/10.1186/s12879-024-09743-w","url":null,"abstract":"X-linked agammaglobulinemia (XLA), also referred to as Bruton’s tyrosine kinase deficiency, is a rare genetic disorder that affects the immune system. We conducted genetic analysis on patients suffering from immunodeficiency by utilizing Next-Generation Sequencing techniques, as well as their closest relatives, to facilitate accurate diagnosis, offer genetic counseling services, and enhance our comprehension of XLA.","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":null,"pages":null},"PeriodicalIF":3.7,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142223337","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Epidemiological characteristics of human rabies cases reported by sites in China from 2006 to 2022 2006 年至 2022 年中国各地点报告的人感染狂犬病病例的流行病学特征
IF 3.7 3区 医学
BMC Infectious Diseases Pub Date : 2024-09-13 DOI: 10.1186/s12879-024-09864-2
Jia-Jia Liu, Na Zhang, Shu-Jun Ding, Zeng-Qiang Kou, Xiao-Yan Tao, Wu-Yang Zhu
{"title":"Epidemiological characteristics of human rabies cases reported by sites in China from 2006 to 2022","authors":"Jia-Jia Liu, Na Zhang, Shu-Jun Ding, Zeng-Qiang Kou, Xiao-Yan Tao, Wu-Yang Zhu","doi":"10.1186/s12879-024-09864-2","DOIUrl":"https://doi.org/10.1186/s12879-024-09864-2","url":null,"abstract":"Rabies is an incessant public health threat in China. The Ministry of Health implemented the Central Payment for Rabies Prevention and Control Project to assist with rabies prevention and control in a few representative provinces in 2006. Data on human rabies cases reported by the National Infectious Disease Reporting Information Management System and national surveillance sites from 2006 to 2022 were collected, and statistical and multivariate analyses were then used to assess the effectiveness of current prevention and control efforts. During 2006–2022, a total of 2025 human rabies cases were collected by the national surveillance sites, with incidence rates far above the national average, but the incidence rate was consistent with the national trend. Human rabies cases demonstrated a dual peak distribution in terms of exposure and onset dates, with the peak exposure dates falling mostly in the spring and summer and the peak onset dates occurring mostly in the summer and autumn. Three danger categories are shown by the geographical distribution: high, medium and low. Dogs had a high infection rate (86.93%), with own domesticated dogs accounting for the majority of infections. The rates of post-exposure prophylaxis are not constant. The median incubation period was 71 days. Various measures and policies implemented by the government have played a key role in reducing the incidence of rabies. To effectively prevent and control the resurgence of epidemics and halt the spread of the virus among host animals, it is imperative to prioritize and implement a robust dog management system, accelerate research and development of animal vaccines and improve the level of post-exposure prophylaxis.","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":null,"pages":null},"PeriodicalIF":3.7,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142223385","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Self-reported exposure to blood and body fluids and serological evidence of lifetime exposure to hepatitis B virus among health care workers in Ghana: a cross-sectional study 加纳医护人员自我报告的血液和体液接触情况以及终生接触乙型肝炎病毒的血清学证据:一项横断面研究
IF 3.7 3区 医学
BMC Infectious Diseases Pub Date : 2024-09-13 DOI: 10.1186/s12879-024-09703-4
Vivian Efua Senoo-Dogbey, Ellen Eyi Klutsey
{"title":"Self-reported exposure to blood and body fluids and serological evidence of lifetime exposure to hepatitis B virus among health care workers in Ghana: a cross-sectional study","authors":"Vivian Efua Senoo-Dogbey, Ellen Eyi Klutsey","doi":"10.1186/s12879-024-09703-4","DOIUrl":"https://doi.org/10.1186/s12879-024-09703-4","url":null,"abstract":"In Sub-Saharan Africa alone, about 40–65% of Hepatitis B Virus infections among HCWs were a result of percutaneous occupational exposures to contaminated blood and body fluids of patients. Occupational exposure to blood and body fluids among healthcare workers is on the rise in Ghana. However, the relationship between self-reported exposures to blood and body fluids suspected to be contaminated with the hepatitis B virus and actual serological evidence of exposure remains unknown. The aim of the study however was to assess the self-reported exposure to HBV as against the serological evidence of lifetime exposure to HBV and associated factors among Ghanaian HCWs. The study was a cross-sectional analytical survey that involved 340 HCWs who were recruited using a simple random sampling procedure from six cadres of staff from five districts in Greater Accra. The participants were surveyed using a validated instrument and 5mls of venous blood was aseptically withdrawn for qualitative detection of Anti-HBc. SPSS version 23.0 was used to analyze the data to obtain proportions, odds ratios and their corresponding confidence intervals with the level of significance set at 0.05. The response rate was 94% with Nurses and Doctors in the majority with a mean age of 35.6 ± 7.2. Self-reported exposure to HBV was 63% whereas lifetime exposure to HBV (Anti-HBc) prevalence was 8.2% (95% CI = 5.0-11.0%). Females were 60% less likely to be exposed to HBV (aOR = 0.4; 95% CI = 0.1–0.9) than their male counterparts. HCWs without training in the prevention of blood-borne infections had almost three times higher odds of being exposed to HBV in their lifetime (aOR = 2.6; 95% CI = 1.0-6.4). The findings of this study suggest that self-reported exposure to HBV-contaminated biological materials was high with a corresponding high lifetime exposure to HBV. The female gender was protective of anti-HBc acquisition. Apart from direct interventions for preventing occupational exposures to HBV in the healthcare setting, periodic training of all categories of healthcare workers in infection prevention techniques could significantly reduce exposure to the Hepatitis B virus.","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":null,"pages":null},"PeriodicalIF":3.7,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142223383","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Correction: TgVax452, an epitope-based candidate vaccine targeting Toxoplasma gondii tachyzoite-specific SAG1-related sequence (SRS) proteins: immunoinformatics, structural simulations and experimental evidence-based approaches 更正:TgVax452 是一种基于表位的候选疫苗,其靶标是弓形虫迅殖体特异性 SAG1 相关序列 (SRS) 蛋白:免疫信息学、结构模拟和基于实验证据的方法
IF 3.7 3区 医学
BMC Infectious Diseases Pub Date : 2024-09-13 DOI: 10.1186/s12879-024-09881-1
Hamidreza Majidiani, Mohammad M. Pourseif, Bahareh Kordi, Mohammad-Reza Sadeghi, Alireza Najafi
{"title":"Correction: TgVax452, an epitope-based candidate vaccine targeting Toxoplasma gondii tachyzoite-specific SAG1-related sequence (SRS) proteins: immunoinformatics, structural simulations and experimental evidence-based approaches","authors":"Hamidreza Majidiani, Mohammad M. Pourseif, Bahareh Kordi, Mohammad-Reza Sadeghi, Alireza Najafi","doi":"10.1186/s12879-024-09881-1","DOIUrl":"https://doi.org/10.1186/s12879-024-09881-1","url":null,"abstract":"<p><b>Correction: BMC Infectious Diseases (2024) 24:886</b></p><p><b>https://doi.org/10.1186/s12879-024-09807-x</b></p><p>Following publication of the original article [1], we have been notified that due to a misunderstanding in proof corrections, there are some corrections needed in the affiliations.</p><p>Originally published affiliations in the authorship line: Hamidreza Majidiani1,2*†, Mohammad M. Pourseif3,4,5*†, Bahareh Kordi5, Mohammad-Reza Sadeghi3,6 and Alireza Najafi7,8.</p><p>Correct affiliations: Hamidreza Majidiani1,2*†, Mohammad M. Pourseif3,4,5*†, Bahareh Kordi6, Mohammad-Reza Sadeghi3,7 and Alireza Najafi8.</p><p>The original article has been corrected.</p><ol data-track-component=\"outbound reference\" data-track-context=\"references section\"><li data-counter=\"1.\"><p>Majidiani et al. BMC Infectious Diseases (2024) 24:886 https://doi.org/10.1186/s12879-024-09807-x</p></li></ol><p>Download references<svg aria-hidden=\"true\" focusable=\"false\" height=\"16\" role=\"img\" width=\"16\"><use xlink:href=\"#icon-eds-i-download-medium\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"></use></svg></p><span>Author notes</span><ol><li><p>Hamidreza Majidiani and Mohammad M. Pourseif contributed equally to this study as co-first authors.</p></li></ol><h3>Authors and Affiliations</h3><ol><li><p>Healthy Aging Research Centre, Neyshabur University of Medical Sciences, Neyshabur, Iran</p><p>Hamidreza Majidiani</p></li><li><p>Department of Basic Medical Sciences, Neyshabur University of Medical Sciences, Neyshabur, Iran</p><p>Hamidreza Majidiani</p></li><li><p>Research Center for Pharmaceutical Nanotechnology (RCPN), Biomedicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran</p><p>Mohammad M. Pourseif & Mohammad-Reza Sadeghi</p></li><li><p>Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran</p><p>Mohammad M. Pourseif</p></li><li><p>Engineered Biomaterial Research Center (EBRC), Khazar University, Baku, Azerbaijan</p><p>Mohammad M. Pourseif</p></li><li><p>Department of Agricultural Science, Technical and Vocational University (TVU), Tehran, Iran</p><p>Bahareh Kordi</p></li><li><p>Department of Molecular Medicine, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran</p><p>Mohammad-Reza Sadeghi</p></li><li><p>Faculty of Veterinary Medicine, University of Tabriz, Tabriz, Iran</p><p>Alireza Najafi</p></li></ol><span>Authors</span><ol><li><span>Hamidreza Majidiani</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Mohammad M. Pourseif</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Bahareh Kordi</span>View author publications<p>You can also search for this author in <span>PubMed<span> </span>Google Scholar</span></p></li><li><span>Mohammad-Reza Sadeghi</span>View author publications<p>You can also search f","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":null,"pages":null},"PeriodicalIF":3.7,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142223382","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Molecular detection of OXA-48 and NDM-1 carbapenemase genes among clinical isolates of Klebsiella pneumoniae recovered from patients attending a private tertiary hospital in Southwestern Nigeria 从尼日利亚西南部一家私立三级医院就诊患者中分离出的肺炎克雷伯氏菌临床分离株中分子检测 OXA-48 和 NDM-1 碳青霉烯酶基因
IF 3.7 3区 医学
BMC Infectious Diseases Pub Date : 2024-09-13 DOI: 10.1186/s12879-024-09869-x
Chisom Blossom Onyeji, Seyi Samson Enitan, Olalekan Ademola Kemiki, Abigail Chinyere Igwe, Akinbobola Ayokunle Adeniyi, Michael Unata Iduh, Grace Eleojo Itodo, Ayomide Oluwatobiloba Okuneye, Precious Oluwatosin Adamson, Mofeoluwa Favour Kolawole
{"title":"Molecular detection of OXA-48 and NDM-1 carbapenemase genes among clinical isolates of Klebsiella pneumoniae recovered from patients attending a private tertiary hospital in Southwestern Nigeria","authors":"Chisom Blossom Onyeji, Seyi Samson Enitan, Olalekan Ademola Kemiki, Abigail Chinyere Igwe, Akinbobola Ayokunle Adeniyi, Michael Unata Iduh, Grace Eleojo Itodo, Ayomide Oluwatobiloba Okuneye, Precious Oluwatosin Adamson, Mofeoluwa Favour Kolawole","doi":"10.1186/s12879-024-09869-x","DOIUrl":"https://doi.org/10.1186/s12879-024-09869-x","url":null,"abstract":"There have been increasing reports of Klebsiella pneumoniae resistant to β-lactam antibiotics. This study aimed to determine the prevalence of some selected carbapenemase genes among clinical isolates of Klebsiella pneumoniae recovered from patients attending a private tertiary hospital in Southwestern Nigeria. The study was conducted over two months (February-March 2024). A total of 50 clinical isolates of Klebsiella pneumoniae from different clinical specimens were obtained from the Medical Microbiology Department, Babcock University Teaching Hospital (BUTH). The clinical isolates were then characterized using standard microbiological procedures and were tested for susceptibility to meropenem and other classes of antibiotics according to Clinical and Laboratory Standards Institute (CLSI) guidelines. Polymerase Chain Reaction (PCR) detection for OXA-48 and NDM-1 carbapenemase genes was performed on the 50 clinical isolates. PCR analysis showed that 9 (18%) clinical isolates were positive for the OXA-48 gene, 22 (44%) were positive for the NDM-1 gene, 4 (8%) possessed both the OXA-48 and NDM-1 genes, and 23 (46%) possessed neither the OXA-48 nor NDM-1 genes. Antibiotic Susceptibility Testing (AST) revealed that all the clinical isolates were resistant to meropenem. In conclusion, this study demonstrates the presence of OXA-48 and NDM-1 genes in clinical isolates of Klebsiella pneumoniae recovered from patients attending a private tertiary hospital in Southwestern Nigeria, highlighting the role of ESBL (extended-spectrum beta-lactamase) as a major resistance mechanism alongside other mechanisms. Population-based surveillance programs should be implemented to monitor the prevalence and epidemiology of Klebsiella pneumoniae infections at the community level, facilitating early detection of outbreaks and identification of emerging antimicrobial resistance patterns. This study highlights the significant prevalence of NDM-1 and OXA-48 carbapenemase genes among Klebsiella pneumoniae clinical isolates in a private tertiary hospital in Southwestern Nigeria, with 44% and 18% of isolates harboring these genes, respectively. Notably, 46% of isolates were resistant to carbapenems despite lacking these genes, suggesting alternative resistance mechanisms. The findings underscore the urgent need for enhanced surveillance, infection control measures, and antibiotic stewardship programs to combat the spread of multidrug-resistant Klebsiella pneumoniae in healthcare settings.","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":null,"pages":null},"PeriodicalIF":3.7,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142223381","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development and evaluation of a health literacy scale for parasitic diseases 寄生虫病健康知识量表的编制与评估
IF 3.7 3区 医学
BMC Infectious Diseases Pub Date : 2024-09-13 DOI: 10.1186/s12879-024-09857-1
Yi Wang, Chengyuan Li, Yuanchun Mao, Yaobao Liu, Yanmin Mao, Jie Shao, Jianfeng Chen, Kun Yang
{"title":"Development and evaluation of a health literacy scale for parasitic diseases","authors":"Yi Wang, Chengyuan Li, Yuanchun Mao, Yaobao Liu, Yanmin Mao, Jie Shao, Jianfeng Chen, Kun Yang","doi":"10.1186/s12879-024-09857-1","DOIUrl":"https://doi.org/10.1186/s12879-024-09857-1","url":null,"abstract":"Parasitic diseases remain a serious public health problem in China. Health education aimed at disseminating health-related knowledge and promoting healthy behaviours, plays a crucial role in the prevention and control of parasitic diseases. This study aims to develop a tool to measure the parasitic disease health literacy of residents in China. Scale development was based on qualitative and quantitative methods. Qualitative method included focus group discussions and Delphi consultations. A methodological design with multistage sampling and a pilot study was used to evaluate the questionnaire. The scale’s reliability was tested using Cronbach’s α and split-half reliability, while its construct validity was assessed using confirmatory factor analysis. The scale’s passing score was determined using the receiver operating characteristic curve. A cross-sectional survey was conducted in six districts of the prefecture of Jiangsu and residents aged 14–69 years in the participating townships were randomly selected based on their location. The health literacy indicator system for parasitic diseases included 3 first-level, 9 s-level and 23 third-level indicators. The 23-item questionnaire demonstrated good internal consistency (Cronbach’s alpha = 0.774) and split-half reliability (Spearman-Brown coefficient = 0.778). The questionnaire’s passing score was 60. A total of 990 valid questionnaires were collected from participants in three cities. The percentage of participants with health literacy regarding parasitic diseases was 15.8%. Their scores were influenced by age, income, employment, and educational level. Health literacy of parasitic diseases is an integrated indicator rather than just knowledge or behavior information. The correlation between knowledge and behavior is weak. The capacity for healthy behavior of parasitic disease is associated with the location and culture of the city. For neglected diseases, it is important for people to talk positively about their behaviors with a doctor.","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":null,"pages":null},"PeriodicalIF":3.7,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142223380","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Longevity of hybrid immunity against SARS-CoV-2 in adults vaccinated with an adenovirus-based COVID-19 vaccine 接种基于腺病毒的 COVID-19 疫苗的成年人对 SARS-CoV-2 的混合免疫力的长效性
IF 3.7 3区 医学
BMC Infectious Diseases Pub Date : 2024-09-12 DOI: 10.1186/s12879-024-09891-z
Memory Mvula, Fatima Mtonga, Jonathan Mandolo, Chisomo Jowati, Alice Kalirani, Precious Chigamba, Edwin Lisimba, Ndaona Mitole, Marah G. Chibwana, Kondwani C. Jambo
{"title":"Longevity of hybrid immunity against SARS-CoV-2 in adults vaccinated with an adenovirus-based COVID-19 vaccine","authors":"Memory Mvula, Fatima Mtonga, Jonathan Mandolo, Chisomo Jowati, Alice Kalirani, Precious Chigamba, Edwin Lisimba, Ndaona Mitole, Marah G. Chibwana, Kondwani C. Jambo","doi":"10.1186/s12879-024-09891-z","DOIUrl":"https://doi.org/10.1186/s12879-024-09891-z","url":null,"abstract":"Hybrid immunity provides better protection against COVID-19 than vaccination or prior natural infection alone. It induces high magnitude and broadly cross-reactive neutralising anti-Spike IgG antibodies. However, it is not clear how long these potent antibodies last, especially in the context of adenovirus-based COVID-19 vaccines. We conducted a longitudinal cohort study and enrolled 20 adults who had received an adenovirus-based COVID-19 vaccine before a laboratory-confirmed SARS-CoV-2 infection. We followed up the study participants for 390 days post the initial breakthrough infection. We assessed the longevity and cross-reactive breadth of serum antibodies against SARS-CoV-2 variants of concern (VOCs), including Omicron. The binding anti-Spike IgG antibodies remained within the reported putative levels for at least 360 days and were cross-neutralising against Beta, Gamma, Delta, and Omicron. During the follow up period, a median of one SARS-CoV-2 re-infection event was observed across the cohort, but none resulted in severe COVID-19. Moreover, the re-exposure events were associated with augmented anti-Spike and anti-RBD IgG antibody titres. This study confirms that hybrid immunity provides durable broadly cross-reactive antibody immunity against SARS-CoV-2 variants of concern for at least a year (360 days), and that it is further augment by SARS-CoV-2 re-exposure.","PeriodicalId":8981,"journal":{"name":"BMC Infectious Diseases","volume":null,"pages":null},"PeriodicalIF":3.7,"publicationDate":"2024-09-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142223177","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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