Journal of Microbiology Immunology and Infection最新文献

{"title":"Uropathogens and clinical manifestations of pyuria-negative urinary tract infections in young infants: A single center cross-sectional study","authors":"","doi":"10.1016/j.jmii.2024.05.008","DOIUrl":"10.1016/j.jmii.2024.05.008","url":null,"abstract":"<div><h3>Background</h3><p>Urine leukocyte count under microscopy is one of the most frequently used routine screening tests for urinary tract infection (UTI). Nevertheless, it is observed that pyuria is lacking in 10-25% of children with UTI. This study aims to determine the factors related to pyuria-negative UTI in young infants aged under four months old.</p></div><div><h3>Method</h3><p>This retrospective cross-sectional study was conducted on 157 patients aged under 4 months old with UTI. All subjects had paired urinalysis and urine culture, which were collected via transurethral catheterization. According to the results of their urinalysis, the patients were then classified as UTI cases with pyuria and UTI cases without pyuria. The clinical characteristics and outcomes of both groups were analyzed.</p></div><div><h3>Result</h3><p>Among the 157 UTI patients, the prevalence of pyuria-negative UTI was 44%. Significant risk factors associated with pyuria-negative UTI included non-<em>E.coli</em> pathogens, younger age, shorter duration of fever prior to hospital visit, lower white blood cell (WBC) count upon hospital visit, and absence of microscopic hematuria.</p></div><div><h3>Conclusions</h3><p>We found that non-<em>E.coli</em> uropathogens were the strongest factor related to pyuria-negative UTI. The absence of pyuria cannot exclude the diagnosis of UTI in young infants, and it’s reasonable to perform both urinalysis and urine culture as a part of the assessment of febrile or ill-looking young infants.</p></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"57 4","pages":"Pages 609-616"},"PeriodicalIF":4.5,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1684118224000859/pdfft?md5=b13341597d85c72cd86aa1416d1d6f05&pid=1-s2.0-S1684118224000859-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141254955","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Clinical characteristics and risk factors of severe human parainfluenza virus infection in hospitalized children","authors":"","doi":"10.1016/j.jmii.2024.05.002","DOIUrl":"10.1016/j.jmii.2024.05.002","url":null,"abstract":"<div><h3>Background</h3><p>Human parainfluenza viruses (HPIVs) commonly cause childhood respiratory illness requiring hospitalization in Taiwan. This study aimed to investigate clinical severity and identify risk factors predisposing to severe disease in hospitalized children with HPIV infection.</p></div><div><h3>Methods</h3><p>We included hospitalized patients with lab-confirmed HPIV infection from 2007 to 2018 and collected their demographic and clinical characteristics. Patients with ventilator support, intravenous inotropic agents, and extracorporeal membrane oxygenation were defined as severe cases.</p></div><div><h3>Results</h3><p>There were 554 children hospitalized for HPIV infection. The median age was 1.2 years; 518 patients had non-severe HPIV infection, whereas 36 patients (6.5%) had severe HPIV infection. 266 (48%) patients had underlying diseases, and 190 patients (34.3%) had bacterial co-detection. Children with severe HPIV infection were more likely to have bacterial co-detection than those without (52.8% vs 33.0%, <em>p</em> = 0.02). Patients with lung patch or consolidation had more invasive bacterial co-infection or co-detection than those without patch or consolidation (43% vs 33%, <em>p</em> = 0.06). Patients with neurological disease (adjusted OR 4.77, 95% CI 1.94–11.68), lung consolidation/patch (adjusted OR 6.64, 95% CI 2.80–15.75), and effusion (adjusted OR 11.59, 95% CI 1.52–88.36) had significantly higher risk to have severe HPIV infection.</p></div><div><h3>Conclusion</h3><p>Neurological disease and lung consolidation/patch or effusion were the most significant predictors of severe HPIV infection.</p></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"57 4","pages":"Pages 573-579"},"PeriodicalIF":4.5,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1684118224000793/pdfft?md5=b892a8c7d40e01549460f2e0a7f647e7&pid=1-s2.0-S1684118224000793-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141288960","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Nonbacterial thrombotic endocarditis mimics acute infective endocarditis in a woman with endometrial cancer","authors":"","doi":"10.1016/j.jmii.2024.02.006","DOIUrl":"10.1016/j.jmii.2024.02.006","url":null,"abstract":"","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"57 4","pages":"Pages 665-667"},"PeriodicalIF":4.5,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1684118224000422/pdfft?md5=e4e040c813e092260303657e857d46f0&pid=1-s2.0-S1684118224000422-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139998345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Efficacy of short- versus prolonged-courses of antimicrobial therapy for carbapenem-resistant Klebsiella pneumoniae bloodstream infections: A propensity score-matched cohort study","authors":"","doi":"10.1016/j.jmii.2024.05.010","DOIUrl":"10.1016/j.jmii.2024.05.010","url":null,"abstract":"<div><h3>Background</h3><p>As limited antibiotic options are available for the treatment of carbapenem-resistant <em>Klebsiella pneumoniae</em> (CRKP) bloodstream infections (BSIs), the optimal treatment duration for CRKP BSIs is unclear. Our objective was to investigate whether short courses (6–10 days) are as effective as prolonged courses (≥11 days) of active antibiotic therapy for CRKP BSIs.</p></div><div><h3>Methods</h3><p>A retrospective cohort study comprising adults with monomicrobial CRKP BSI receiving a short or prolonged course of <em>in vitro</em> active therapy at a medical center was conducted between 2010 and 2021. Comparisons of two therapeutic strategies were assessed by the logistic regression model and propensity score analysis. The primary endpoint was 30-day crude mortality. Secondary outcomes included recurrent BSIs, the emergence of multidrug-resistant organisms and candidemia during hospitalization after completing antibiotic therapy for CRKP BSIs.</p></div><div><h3>Results</h3><p>Of 263 eligible adults, 160 (60.8%) were male, and the median (interquartile range) age was 69.0 (53.0–76.0) years. Common comorbidities included diabetes (143 patients, 54.4%), malignancy (75, 28.5%), cerebrovascular accident (58, 22.1%), and hemodialysis (49, 18.6%). The 30-day mortality rate was 8.4% (22 patients). Of 84 propensity score well-balanced matched pairs, the 30-day mortality was similar in the short-course and prolonged-course group (6.0% and 7.1%, respectively; <em>P</em> = 1.00). However, there were less episodes candidemia in the short-course group (1.2% versus 13.1%; odds ratio, 0.08; 95% confidence interval, 0.01–0.63; <em>P</em> = 0.005).</p></div><div><h3>Conclusion</h3><p>Short courses of active therapy for CRKP BSIs demonstrate comparable clinical outcomes to prolonged courses and are associated with a lower risk of subsequent candidemia.</p></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"57 4","pages":"Pages 594-600"},"PeriodicalIF":4.5,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1684118224001026/pdfft?md5=abb0875112dd70097610e7f6f8b55122&pid=1-s2.0-S1684118224001026-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141254644","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"The multicenter real-world report of the efficacies of 14-day esomeprazole-based and rabeprazole-based high-dose dual therapy in first-line Helicobacter pylori eradication in Taiwan","authors":"","doi":"10.1016/j.jmii.2024.02.009","DOIUrl":"10.1016/j.jmii.2024.02.009","url":null,"abstract":"<div><h3>Background</h3><p>High-dose dual therapy (HDDT) using proton-pump inhibitors (PPI) and amoxicillin attracted attention for its simplicity and lower adverse event profile. Besides, vonoprazan is not available worldwide. This real-world study aims to compare the efficacy of esomeprazole-based and rabeprazole-based HDDT regimens and to identify clinical factors influencing outcomes.</p></div><div><h3>Methods</h3><p>A retrospective study enrolled 346 <em>Helicobacter pylori</em>-infected naïve patients from January 2016 to August 2023. Patients were assigned to either a 14-day esomeprazole-based HDDT (EA-14; esomeprazole 40 mg t.i.d. and amoxicillin 750 mg q.i.d. for 14 days, n = 173) or a 14-day rabeprazole-based HDDT (RA-14; rabeprazole 20 mg and amoxicillin 750 mg q.i.d. for 14 days, n = 173).</p></div><div><h3>Results</h3><p>Five patients from the EA-14 group and 10 from the RA-14 group were lost to follow-up, resulting in 168 and 163 patients for the per-protocol (PP) analysis, respectively. Eradication rates for the EA-14 and RA-14 groups were 90.2% and 80.9% (P = 0.014) in intention-to-treat (ITT) analysis; and 92.9% and 85.9% (P = 0.039) in PP analysis. Adverse event rates were similar between the two groups (11.9% vs 11.7%, P = 0.944). In multiple logistic regression analysis, age≧60 was associated with eradication failure (P = 0.046) and a trend of significance for smoking (P = 0.060) in the EA-14 group but not in the RA-14 group. A trend of significance was also observed for eradication regimens (EA-14 vs RA-14) (P = 0.071).</p><p>The antibiotic resistance rates were amoxicillin (2.3%), clarithromycin (14.7%), metronidazole (40.3%), and dual resistance to clarithromycin and metronidazole (7.0%).</p></div><div><h3>Conclusions</h3><p>Esomeprazole-based HDDT achieved over 90% eradication rates but rabeprazole-based HDDT, which failed.</p></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"57 4","pages":"Pages 601-608"},"PeriodicalIF":4.5,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S168411822400046X/pdfft?md5=4638e74156369d0757b9d92ac88058ba&pid=1-s2.0-S168411822400046X-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140068945","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Changing epidemic patterns of infectious diseases during and after COVID-19 pandemic in Taiwan","authors":"Ping-Ing Lee ,&nbsp;Po-Ren Hsueh ,&nbsp;Jen-Hsiang Chuang ,&nbsp;Ming-Tsan Liu","doi":"10.1016/j.jmii.2024.07.002","DOIUrl":"10.1016/j.jmii.2024.07.002","url":null,"abstract":"<div><p>Mitigation measures aimed at curbing the transmission of the severe acute respiratory syndrome coronavirus 2 effectively suppressed the occurrence of many respiratory infections other than coronavirus disease 2019. Several infections experienced a resurgence following the relaxation of non-pharmaceutical interventions, surpassing pre-pandemic levels in Taiwan. This phenomenon, known as immune debt, primarily affected respiratory infections in young children, including respiratory syncytial virus (RSV) infection. Infections transmitted by means other than droplets or contact did not exhibit significant changes in their epidemic patterns, such as varicella and Japanese encephalitis. Alterations in seasonality were noted for RSV infection and influenza, and these changes are also linked to immune debt. The recent emergence of severe pediatric pneumonia in northern China may be associated with immune debt and the rise of macrolide-resistant <em>Mycoplasma pneumoniae</em> associated with severe illness.</p></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"57 5","pages":"Pages 685-690"},"PeriodicalIF":4.5,"publicationDate":"2024-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1684118224001130/pdfft?md5=c69b0558b96f5f83d6eced5752ef4a3f&pid=1-s2.0-S1684118224001130-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141762965","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Twelve-month effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide in treatment-naïve and treatment-experienced people with HIV: Findings from the Asia cohort of the BICSTaR study","authors":"Yu-Ting Tseng ,&nbsp;Chia-Jui Yang ,&nbsp;Yeon-Sook Kim ,&nbsp;Jun Yong Choi ,&nbsp;Chen Seong Wong ,&nbsp;Kuan-Yeh Lee ,&nbsp;Jeong-a Lee ,&nbsp;Jack Chang ,&nbsp;Rebecca Harrison ,&nbsp;Andrea Marongiu ,&nbsp;Sun Hee Lee ,&nbsp;Chien-Ching Hung","doi":"10.1016/j.jmii.2024.07.003","DOIUrl":"10.1016/j.jmii.2024.07.003","url":null,"abstract":"<div><h3>Background</h3><p>The ongoing, observational BICSTaR (BICtegravir Single Tablet Regimen) cohort study is evaluating real-world effectiveness and safety of bictegravir/emtricitabine/tenofovir alafenamide (B/F/TAF) in people with HIV across 14 countries over 24 months. We present 12-month data from the BICSTaR Asia cohort.</p></div><div><h3>Methods</h3><p>Data were pooled from retrospective and prospective cohorts of antiretroviral therapy (ART)-naïve (hereafter, TN) and ART-experienced (hereafter, TE) people with HIV (aged ≥21 years) receiving B/F/TAF in routine clinical care in the Republic of Korea, Singapore, and Taiwan. Analyses included effectiveness (primary endpoint: HIV-1 RNA &lt;50 copies/ml, missing = excluded analysis), CD4 count, CD4/CD8 ratio, safety, treatment persistence, and patient-reported outcomes (prospective group).</p></div><div><h3>Results</h3><p>The analysis population included 328 participants (80 retrospective, 248 prospective; 65 TN, 263 TE). Participants were predominantly male (96.9% TN, 93.2% TE) with ≥1 comorbidity (52.3% TN, 57.8% TE); median age (years) was 31 (TN) and 42 (TE). Following 12 months of B/F/TAF, HIV-1 RNA was &lt;50 copies/ml in 98.2% (54/55) of TN and 97.0% (227/234) of TE participants. Median (Q1, Q3) CD4 cell count increased by +187 (119, 291) cells/μl in the TN group (p &lt; 0.001) and remained stable (+8 [–91, 110] cells/μl) in the TE group. B/F/TAF persistence was high in the prospective group, with 1/34 (2.9%) TN and 5/214 (2.3%) TE participants discontinuing treatment within 12 months. Drug-related adverse events occurred in 5.8% (19/328) of participants, leading to treatment discontinuation in 0.6% (2/328).</p></div><div><h3>Conclusions</h3><p>Real-world evidence from BICSTaR supports the effectiveness, safety and tolerability of B/F/TAF in people with HIV in Asia.</p></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"57 5","pages":"Pages 760-770"},"PeriodicalIF":4.5,"publicationDate":"2024-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1684118224001142/pdfft?md5=81f8de64e84ca34d88fa8240c4e57522&pid=1-s2.0-S1684118224001142-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141696209","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"A sbiT-sbiRS-gloIo regulatory circuit is involved in oxidative stress tolerance of Stenotrophomonas maltophilia","authors":"Cheng-Mu Wu ,&nbsp;Yi-Tzu Lee ,&nbsp;Hsu-Feng Lu ,&nbsp;Yen-Ling Lin ,&nbsp;Tsuey-Ching Yang","doi":"10.1016/j.jmii.2024.07.005","DOIUrl":"10.1016/j.jmii.2024.07.005","url":null,"abstract":"<div><p>The <em>sbiT</em>-<em>sbiR</em>-<em>sbiS</em> operon of <em>Stenotrophomonas maltophilia</em> encodes an inner-membrane protein SbiT and a SbiS-SbiR two-component regulatory system. A <em>sbiT</em> mutant displayed a growth defect in LB agar. Mechanism studies revealed that <em>sbiT</em> deletion resulted in SbiSR activation and <em>gloIo</em> upregulation, which increased intracellular ROS level and caused growth defect.</p></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"57 5","pages":"Pages 827-831"},"PeriodicalIF":4.5,"publicationDate":"2024-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1684118224001154/pdfft?md5=c9eae1eba1b4d76d478d661a2ba2c616&pid=1-s2.0-S1684118224001154-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141691979","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Respiratory viral infections and Kawasaki disease: A molecular epidemiological analysis","authors":"Kentaro Marutani ,&nbsp;Kenji Murata ,&nbsp;Yumi Mizuno ,&nbsp;Sagano Onoyama ,&nbsp;Takayuki Hoshina ,&nbsp;Kenichiro Yamamura ,&nbsp;Kenji Furuno ,&nbsp;Yasunari Sakai ,&nbsp;Junji Kishimoto ,&nbsp;Koichi Kusuhura ,&nbsp;Toshiro Hara","doi":"10.1016/j.jmii.2024.07.001","DOIUrl":"10.1016/j.jmii.2024.07.001","url":null,"abstract":"<div><h3>Background/Purpose</h3><p>Recent large-scale epidemiological studies have revealed significant temporal associations between certain viral infections and the subsequent development of Kawasaki disease (KD). Despite these associations, definitive laboratory evidence linking acute or recent viral infections to KD cases remains elusive. The objective of this study is to employ a molecular epidemiological approach to investigate the temporal association between viral infections and the development of KD.</p></div><div><h3>Methods</h3><p>We analyzed 2460 patients who underwent the FilmArray® Respiratory Panel test between April 2020 and September 2021.</p></div><div><h3>Results</h3><p>Following the application of inclusion criteria, 2402 patients were categorized into KD (n = 148), respiratory tract infection (n = 1524), and control groups (n = 730). The KD group exhibited higher positive rates for respiratory syncytial virus (RSV), human rhinovirus/enterovirus (hRV/EV), parainfluenza virus (PIV) 3, and adenovirus (AdV) compared to the control group. Additionally, coinfections involving two or more viruses were significantly more prevalent in the KD group. Notably, RSV-positive, hRV/EV-positive, and PIV3-positive KD patients exhibited a one-month delay in peak occurrence compared to non-KD patients positive for corresponding viruses. In contrast, AdV-positive KD cases did not show a one-month delay in peak occurrence. Moreover, anti-RSV, anti-PIV3, and anti-AdV antibody-positive rates or antibody titers were higher in RSV-, PIV3-, and AdV-positive KD cases, respectively, compared to non-KD cases with the same viral infections.</p></div><div><h3>Conclusion</h3><p>Recent infection with RSV, PIV3, or AdV, occasionally in conjunction with other viruses, may contribute to the pathogenesis of KD as infrequent complications.</p></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"57 5","pages":"Pages 691-699"},"PeriodicalIF":4.5,"publicationDate":"2024-07-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1684118224001129/pdfft?md5=fe77a6df805b421c26b7bce8ad6e5685&pid=1-s2.0-S1684118224001129-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141689508","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}

{"title":"Risk of severe dengue during secondary infection: A population-based cohort study in Taiwan","authors":"Hsin-I Shih ,&nbsp;Yu-Ching Wang ,&nbsp;Yu-Ping Wang ,&nbsp;Chia-Yu Chi ,&nbsp;Yu-Wen Chien","doi":"10.1016/j.jmii.2024.07.004","DOIUrl":"10.1016/j.jmii.2024.07.004","url":null,"abstract":"<div><h3>Background</h3><p>Dengue poses a significant public health concern. Secondary dengue infections with different dengue virus (DENV) serotypes have been linked to an increased risk of severe dengue. This study aimed to assess the risk of severe dengue during secondary infection in Taiwan.</p></div><div><h3>Methods</h3><p>A retrospective cohort study was conducted using Taiwan's National Health Insurance Research Database to identify dengue cases with secondary dengue infection born after 1944 from 2014 to 2015. Ten matched patients with primary infection were selected as controls using propensity score matching for each secondary dengue infection case. The odds ratio (OR) for severe dengue in secondary versus primary infections was calculated using conditional logistic regression.</p></div><div><h3>Results</h3><p>This study included 357 cases with secondary dengue infection and 3570 matched controls. The risk of severe dengue was found to be 7.8% in individuals with secondary infection, compared to 3.8% in those with primary dengue infection. Secondary infection significantly increased the risk of severe dengue (OR 2.13, 95% CI: 1.40–3.25, P = 0.0004). Notably, a significant association between secondary infection and severe dengue was observed only when the interval between the first and secondary infection was greater than two years (OR 3.19, 95% CI 2.04–5.00, P &lt; 0.0001).</p></div><div><h3>Conclusion</h3><p>Secondary dengue infection significantly increases the risk of severe disease in Taiwan, particularly when the interval between infections is over two years.</p><p>Healthcare professionals should maintain heightened vigilance for individuals with a history of previous dengue infection, particularly if their initial diagnosis was more than two years prior.</p></div>","PeriodicalId":56117,"journal":{"name":"Journal of Microbiology Immunology and Infection","volume":"57 5","pages":"Pages 730-738"},"PeriodicalIF":4.5,"publicationDate":"2024-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1684118224001166/pdfft?md5=4e156297f003b43f14839f3ea1e1a71d&pid=1-s2.0-S1684118224001166-main.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141635970","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}