Pub Date : 2025-10-22DOI: 10.1136/bmjresp-2025-003413
Lowie E G W Vanfleteren, Delphine Vauterin, Lies Lahousse
Background: While anti-interleukin (IL) 5 therapy has been shown to be efficacious to reduce exacerbation rates (ERs) in patients with severe eosinophilic asthma and might also benefit patients with coexisting chronic obstructive pulmonary disease (COPD), it is unknown whether anti-IL5 therapy reduces all types of exacerbations in heterogeneous (smoking) real-life patients.
Methods: Adults initiating mepolizumab or benralizumab between 2017 and 2019 were identified in Belgian nationwide data. The ER in the year before anti-IL5 therapy initiation was compared to the year after. Exacerbations were classified as severe (hospitalised) exacerbations or moderate (outpatient) exacerbations treated with antibiotics, oral corticosteroids (OCS) or the combination.
Results: Among 807 patients initiating anti-IL5 therapy, severe ER was 40±4 exacerbations per 100 patient years pretreatment versus 17±3 post-treatment initiation (p<0.001, relative risk reduction (RRR) -56%, number needed to treat (NNT)=4) and significantly reduced both in patients without COPD (n=616, ERpre=15±2, ERpost=6±1, p<0.001, NNT=11) as with coexisting COPD (n=191, ERpre=119±12, ERpost=53±9, p<0.001, NNT=2). For moderate exacerbations, ERs were significantly reduced for all types of exacerbations in both patients with or without COPD, except for OCS only-treated exacerbations in patients with coexisting COPD (p=0.288). Current smoking reduced anti-IL5 effectiveness on OCS-treated exacerbations (NNT >1), although current smokers with coexisting COPD still had a great reduction in hospitalisations (ERpre=152±23, ER post=55±18, p<0.001, NNT=1, RRR=-64%).
Conclusions: In this nationwide cohort study, treatment targeting eosinophilic inflammation was significantly associated with reduced moderate and severe exacerbations, with seemingly less impact on corticosteroid-treated exacerbations in (current smoking) patients with coexisting COPD, but still a large number of hospitalisations were prevented.
{"title":"Real-life impact of anti-IL5 therapy on exacerbation types in patients with obstructive lung disease.","authors":"Lowie E G W Vanfleteren, Delphine Vauterin, Lies Lahousse","doi":"10.1136/bmjresp-2025-003413","DOIUrl":"10.1136/bmjresp-2025-003413","url":null,"abstract":"<p><strong>Background: </strong>While anti-interleukin (IL) 5 therapy has been shown to be efficacious to reduce exacerbation rates (ERs) in patients with severe eosinophilic asthma and might also benefit patients with coexisting chronic obstructive pulmonary disease (COPD), it is unknown whether anti-IL5 therapy reduces all types of exacerbations in heterogeneous (smoking) real-life patients.</p><p><strong>Methods: </strong>Adults initiating mepolizumab or benralizumab between 2017 and 2019 were identified in Belgian nationwide data. The ER in the year before anti-IL5 therapy initiation was compared to the year after. Exacerbations were classified as severe (hospitalised) exacerbations or moderate (outpatient) exacerbations treated with antibiotics, oral corticosteroids (OCS) or the combination.</p><p><strong>Results: </strong>Among 807 patients initiating anti-IL5 therapy, severe ER was 40±4 exacerbations per 100 patient years pretreatment versus 17±3 post-treatment initiation (p<0.001, relative risk reduction (RRR) -56%, number needed to treat (NNT)=4) and significantly reduced both in patients without COPD (n=616, ER<sub>pre</sub>=15±2, ER<sub>post</sub>=6±1, p<0.001, NNT=11) as with coexisting COPD (n=191, ER<sub>pre</sub>=119±12, ER<sub>post</sub>=53±9, p<0.001, NNT=2). For moderate exacerbations, ERs were significantly reduced for all types of exacerbations in both patients with or without COPD, except for OCS only-treated exacerbations in patients with coexisting COPD (p=0.288). Current smoking reduced anti-IL5 effectiveness on OCS-treated exacerbations (NNT >1), although current smokers with coexisting COPD still had a great reduction in hospitalisations (ER<sub>pre</sub>=152±23, ER <sub>post</sub>=55±18, p<0.001, NNT=1, RRR=-64%).</p><p><strong>Conclusions: </strong>In this nationwide cohort study, treatment targeting eosinophilic inflammation was significantly associated with reduced moderate and severe exacerbations, with seemingly less impact on corticosteroid-treated exacerbations in (current smoking) patients with coexisting COPD, but still a large number of hospitalisations were prevented.</p>","PeriodicalId":9048,"journal":{"name":"BMJ Open Respiratory Research","volume":"12 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12551499/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145353697","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-22DOI: 10.1136/bmjresp-2024-003131
Uday Rallabhandi, Clark Walker, Ann Davis, J W Hollingsworth
Background: The inherent unpredictability of COVID-19 has compelled clinicians to seek early predictors of in-hospital mortality. This study explored the association between mechanical power and in-hospital mortality in mechanically ventilated COVID-19 patients and provides an evidence-based foundation for mortality prediction.
Study design and methods: A multi-centre, retrospective analysis of 600 mechanically ventilated COVID-19 patients aged 18-98 years at 16 Texas Health Resources hospitals between 2020 and 2023 was conducted. Peak inspiratory pressure, static compliance, plateau pressure, driving pressure and mechanical power were analysed for association with in-hospital mortality. Mechanical power was further categorised to provide clinicians with a straightforward approach for mortality prediction.
Results: The overall in-hospital mortality was 57% (53% to 60%). All five parameters were strongly associated with mortality after adjusting for confounders. In the first 24-hours of mechanical ventilation, 72 patients with mechanical power below 10 J/min had a mortality of 31% (20% to 42%), 159 patients with mechanical power between 10 J/min and 15 J/min had a mortality of 47% (39% to 55%), and 369 patients with mechanical power greater than 15 J/min had a mortality of 66% (61% to 71%). Patients still intubated on day 7 had a 2.1% increase in mortality for each J/min increase in mechanical power.
Conclusion: Mechanical power in the first 24 hours of mechanical ventilation in COVID-19 patients is associated with in-hospital mortality and is useful for clinical prognostication.
{"title":"Mechanical power is an early predictor of mortality in mechanically ventilated patients with COVID-19.","authors":"Uday Rallabhandi, Clark Walker, Ann Davis, J W Hollingsworth","doi":"10.1136/bmjresp-2024-003131","DOIUrl":"10.1136/bmjresp-2024-003131","url":null,"abstract":"<p><strong>Background: </strong>The inherent unpredictability of COVID-19 has compelled clinicians to seek early predictors of in-hospital mortality. This study explored the association between mechanical power and in-hospital mortality in mechanically ventilated COVID-19 patients and provides an evidence-based foundation for mortality prediction.</p><p><strong>Study design and methods: </strong>A multi-centre, retrospective analysis of 600 mechanically ventilated COVID-19 patients aged 18-98 years at 16 Texas Health Resources hospitals between 2020 and 2023 was conducted. Peak inspiratory pressure, static compliance, plateau pressure, driving pressure and mechanical power were analysed for association with in-hospital mortality. Mechanical power was further categorised to provide clinicians with a straightforward approach for mortality prediction.</p><p><strong>Results: </strong>The overall in-hospital mortality was 57% (53% to 60%). All five parameters were strongly associated with mortality after adjusting for confounders. In the first 24-hours of mechanical ventilation, 72 patients with mechanical power below 10 J/min had a mortality of 31% (20% to 42%), 159 patients with mechanical power between 10 J/min and 15 J/min had a mortality of 47% (39% to 55%), and 369 patients with mechanical power greater than 15 J/min had a mortality of 66% (61% to 71%). Patients still intubated on day 7 had a 2.1% increase in mortality for each J/min increase in mechanical power.</p><p><strong>Conclusion: </strong>Mechanical power in the first 24 hours of mechanical ventilation in COVID-19 patients is associated with in-hospital mortality and is useful for clinical prognostication.</p>","PeriodicalId":9048,"journal":{"name":"BMJ Open Respiratory Research","volume":"12 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12551554/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145353531","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-22DOI: 10.1136/bmjresp-2025-003329
Sarah Blau, Martin Mücke, Michaela Hesse, Julia Sellin, Gabriele Gradl, Martin Schulz, Gülay Ateş
Background: Inhalers are essential for managing asthma and chronic obstructive pulmonary disease; however, their environmental effects vary significantly. Pressurised metered-dose inhalers (pMDIs) contain potent greenhouse gases (GHGs), resulting in a much higher carbon footprint (CF) than non-propellant inhalers (NPIs). Consequently, reducing the use of pMDIs is seen as an important contribution to reduce the healthcare sector's effect on climate change. This study analyses inhaler dispensing trends in Germany, estimates their resulting CF and quantifies the potential GHG savings from increased NPI use.
Methods: Dispensing data at the expense of statutory health insurances, covering nearly 90% of the German population, were analysed from 2013 to 2022 across three age groups. Annual dispensing shares and CF estimates based on life cycle assessment-derived CF values were calculated for four inhaler types: pMDIs with hydrofluorocarbon (HFC)-134a, pMDIs with HFC-227ea, dry powder inhalers (DPIs), and soft mist inhalers (SMIs). Two scenario calculations estimated the potential GHG savings.
Results: Between 2013 and 2022, the total number of dispensed defined daily doses of inhalers increased by 14%, with no significant shift towards lower-emission inhalers (2013, 55% NPIs; 2022, 52% NPIs). Consequently, the total CF increased from 459 kilotonnes of carbon dioxide equivalent (kt CO2eq) in 2013 to 525 kt CO2eq in 2022 (+14%). More than 95% of the inhaler-related CF was attributable to pMDIs. A GHG-saving scenario assuming 85% NPI use among patients aged 10-79 years projected an annual CF reduction of 55% (288 kt CO2eq).
Conclusion: Despite climate neutrality goals, inhaler-related CF has continued to rise because of stable pMDI usage rates. The substantial potential for GHG reduction highlights the necessity and feasibility of a sustainable change in clinical prescription practice. Our insights could support the promotion of climate-friendly inhalers across other European countries with similar prescription patterns.
{"title":"Inhaler use and their carbon footprint in Germany: a 10-year analysis (2013-2022).","authors":"Sarah Blau, Martin Mücke, Michaela Hesse, Julia Sellin, Gabriele Gradl, Martin Schulz, Gülay Ateş","doi":"10.1136/bmjresp-2025-003329","DOIUrl":"10.1136/bmjresp-2025-003329","url":null,"abstract":"<p><strong>Background: </strong>Inhalers are essential for managing asthma and chronic obstructive pulmonary disease; however, their environmental effects vary significantly. Pressurised metered-dose inhalers (pMDIs) contain potent greenhouse gases (GHGs), resulting in a much higher carbon footprint (CF) than non-propellant inhalers (NPIs). Consequently, reducing the use of pMDIs is seen as an important contribution to reduce the healthcare sector's effect on climate change. This study analyses inhaler dispensing trends in Germany, estimates their resulting CF and quantifies the potential GHG savings from increased NPI use.</p><p><strong>Methods: </strong>Dispensing data at the expense of statutory health insurances, covering nearly 90% of the German population, were analysed from 2013 to 2022 across three age groups. Annual dispensing shares and CF estimates based on life cycle assessment-derived CF values were calculated for four inhaler types: pMDIs with hydrofluorocarbon (HFC)-134a, pMDIs with HFC-227ea, dry powder inhalers (DPIs), and soft mist inhalers (SMIs). Two scenario calculations estimated the potential GHG savings.</p><p><strong>Results: </strong>Between 2013 and 2022, the total number of dispensed defined daily doses of inhalers increased by 14%, with no significant shift towards lower-emission inhalers (2013, 55% NPIs; 2022, 52% NPIs). Consequently, the total CF increased from 459 kilotonnes of carbon dioxide equivalent (kt CO<sub>2</sub>eq) in 2013 to 525 kt CO<sub>2</sub>eq in 2022 (+14%). More than 95% of the inhaler-related CF was attributable to pMDIs. A GHG-saving scenario assuming 85% NPI use among patients aged 10-79 years projected an annual CF reduction of 55% (288 kt CO<sub>2</sub>eq).</p><p><strong>Conclusion: </strong>Despite climate neutrality goals, inhaler-related CF has continued to rise because of stable pMDI usage rates. The substantial potential for GHG reduction highlights the necessity and feasibility of a sustainable change in clinical prescription practice. Our insights could support the promotion of climate-friendly inhalers across other European countries with similar prescription patterns.</p>","PeriodicalId":9048,"journal":{"name":"BMJ Open Respiratory Research","volume":"12 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-10-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12551470/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145353576","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: High blood or sputum eosinophil counts are linked to poor clinical outcomes in chronic obstructive pulmonary disease (COPD), yet the value of combining both for the assessment of clinical prognosis remains unclear. In this study, we explore the value of combined blood and sputum eosinophil counts for assessing COPD outcomes.
Methods: Patients were divided into four groups by blood (≥300 cells/µL) and sputum (≥3%) eosinophil counts (low blood and low sputum, low blood and high sputum, high blood and low sputum, high blood and high sputum). Spirometry, questionnaires, CT scans, impulse oscillometry, blood laboratory tests and induced sputum tests were performed at baseline. Spirometry and follow-up questionnaires were performed annually. Poisson regression was used to compute the relative risk (RR) for acute exacerbation. The mixed-effects model was used to assess annual lung function decline.
Results: Compared with the low blood and low sputum eosinophils group, the high blood and high sputum eosinophils group had poorer lung function, more severe airway resistance and worse emphysema and air trapping at baseline. The high blood and high sputum eosinophils group had higher risks of cough (adjusted OR=1.87, 95% CI 1.20 to 2.92, p=0.006) and wheezing (adjusted OR=2.19, 95% CI 1.32 to 3.64, p=0.002). The low blood and high sputum eosinophils group had higher risks of phlegm (adjusted OR=1.53, 95% CI 1.04 to 2.24, p=0.029) and dyspnoea (adjusted OR=1.68, 95% CI 1.13 to 2.50, p=0.010). The high blood and high sputum eosinophils group demonstrated higher total (adjusted RR=1.36, 95% CI 1.15 to 1.60, p<0.001) and moderate-to-severe (adjusted RR=1.42, 95% CI 1.14 to 1.76, p=0.001) exacerbation risks. There was no significant difference in annual lung function decline among the groups.
Conclusion: Elevated blood and sputum eosinophil counts are linked to worse lung function and a higher exacerbation risk in patients with COPD.
背景:高血或痰嗜酸性粒细胞计数与慢性阻塞性肺疾病(COPD)的不良临床结局有关,但将两者结合评估临床预后的价值尚不清楚。在这项研究中,我们探讨了血液和痰嗜酸性粒细胞联合计数在评估COPD预后方面的价值。方法:按血(≥300个细胞/µL)和痰(≥3%)嗜酸性粒细胞计数(低血低痰、低血高痰、高血低痰、高血高痰)将患者分为4组。在基线时进行肺活量测定、问卷调查、CT扫描、脉冲振荡测定、血液实验室检查和诱导痰检查。每年进行肺活量测定和随访问卷调查。泊松回归计算急性加重的相对危险度(RR)。混合效应模型用于评估肺功能的年下降。结果:与低血、低痰嗜酸性粒细胞组相比,高血、高痰嗜酸性粒细胞组在基线时肺功能较差,气道阻力更严重,肺气肿和空气潴留更严重。高血、高痰嗜酸性粒细胞组发生咳嗽(校正OR=1.87, 95% CI 1.20 ~ 2.92, p=0.006)和喘息(校正OR=2.19, 95% CI 1.32 ~ 3.64, p=0.002)的风险较高。低血高痰嗜酸性粒细胞组痰多(校正OR=1.53, 95% CI 1.04 ~ 2.24, p=0.029)和呼吸困难(校正OR=1.68, 95% CI 1.13 ~ 2.50, p=0.010)的风险较高。高血和高痰嗜酸性粒细胞组表现出更高的总(调整后RR=1.36, 95% CI 1.15至1.60)。结论:血和痰嗜酸性粒细胞计数升高与COPD患者肺功能恶化和加重风险增加有关。
{"title":"Assessment of the clinical prognosis of patients with chronic obstructive pulmonary disease using combined blood and sputum eosinophil counts.","authors":"Jieqi Peng, Xiaohui Wu, Xiang Wen, Zhishan Deng, Fan Wu, Qi Wan, Gaoying Tang, Kunning Zhou, Lifei Lu, Cuiqiong Dai, Shengtang Chen, Changli Yang, Yongqing Huang, Shuqing Yu, Pixin Ran, Yumin Zhou","doi":"10.1136/bmjresp-2025-003161","DOIUrl":"10.1136/bmjresp-2025-003161","url":null,"abstract":"<p><strong>Background: </strong>High blood or sputum eosinophil counts are linked to poor clinical outcomes in chronic obstructive pulmonary disease (COPD), yet the value of combining both for the assessment of clinical prognosis remains unclear. In this study, we explore the value of combined blood and sputum eosinophil counts for assessing COPD outcomes.</p><p><strong>Methods: </strong>Patients were divided into four groups by blood (≥300 cells/µL) and sputum (≥3%) eosinophil counts (low blood and low sputum, low blood and high sputum, high blood and low sputum, high blood and high sputum). Spirometry, questionnaires, CT scans, impulse oscillometry, blood laboratory tests and induced sputum tests were performed at baseline. Spirometry and follow-up questionnaires were performed annually. Poisson regression was used to compute the relative risk (RR) for acute exacerbation. The mixed-effects model was used to assess annual lung function decline.</p><p><strong>Results: </strong>Compared with the low blood and low sputum eosinophils group, the high blood and high sputum eosinophils group had poorer lung function, more severe airway resistance and worse emphysema and air trapping at baseline. The high blood and high sputum eosinophils group had higher risks of cough (adjusted OR=1.87, 95% CI 1.20 to 2.92, p=0.006) and wheezing (adjusted OR=2.19, 95% CI 1.32 to 3.64, p=0.002). The low blood and high sputum eosinophils group had higher risks of phlegm (adjusted OR=1.53, 95% CI 1.04 to 2.24, p=0.029) and dyspnoea (adjusted OR=1.68, 95% CI 1.13 to 2.50, p=0.010). The high blood and high sputum eosinophils group demonstrated higher total (adjusted RR=1.36, 95% CI 1.15 to 1.60, p<0.001) and moderate-to-severe (adjusted RR=1.42, 95% CI 1.14 to 1.76, p=0.001) exacerbation risks. There was no significant difference in annual lung function decline among the groups.</p><p><strong>Conclusion: </strong>Elevated blood and sputum eosinophil counts are linked to worse lung function and a higher exacerbation risk in patients with COPD.</p>","PeriodicalId":9048,"journal":{"name":"BMJ Open Respiratory Research","volume":"12 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12542751/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145343156","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-20DOI: 10.1136/bmjresp-2025-003506
Irene Mommers, Sumaira Mubarik, Job F M van Boven, Jens H Bos, Maarten J Bijlsma, Eelko Hak
Background: Antibiotics are widely used to manage acute asthma exacerbations, despite little evidence for their effectiveness. This study assesses the added value of antibiotics alongside oral corticosteroids (OCSs) in treating asthma exacerbations.
Methods: This retrospective cohort study included individuals from the Netherlands between 1994 and 2022 from the IADB.nl pharmacy dispensing database. Individuals had to be 16-45 years old, use inhaled asthma medication and have a first recorded prednisone/prednisolone (OCS) dispense of ≥30 mg/day for 3-14 days. Patients were compared regarding treatment failure (a new dispense of OCS or antibiotics, 15-30 days after initial dispense), based on whether or not they were dispensed antibiotics (AB) alongside their first recorded OCS dispense. Regression analyses with inverse probability of treatment weighting were used to adjust for various confounders.
Results: Of the 5401 individuals included, 38% received antibiotics alongside the first-recorded OCS dispense, with a decreasing trend from 47% in 2009 to 24% in 2020. The OR for treatment failure was 1.36 (95% CI 0.81 to 2.16) for AB+OCS versus OCS-only. The HR for a new exacerbation within 31-365 days of follow-up was 1.20 (95% CI 0.92 to 1.56) for AB+OCS versus OCS-only. The lack of beneficial effect of AB was consistent across subcohorts.
Conclusions: This study found no reduction in treatment failure, nor in risk of subsequent exacerbation, from adding AB to OCS for treating acute asthma exacerbations. We suggest that antibiotics should not be used in primary care settings to treat acute asthma exacerbation unless there are clear signs of bacterial infection.
背景:抗生素被广泛用于治疗急性哮喘发作,尽管很少有证据表明其有效性。本研究评估了抗生素与口服皮质类固醇(OCSs)治疗哮喘加重的附加价值。方法:这项回顾性队列研究包括1994年至2022年间来自荷兰IADB的个体。Nl药房调剂数据库。受试者年龄必须在16-45岁之间,使用吸入性哮喘药物,并且首次记录强的松/强的松(OCS)配药≥30mg /天,持续3-14天。根据患者是否在首次记录的OCS配药的同时配药抗生素(AB),比较患者的治疗失败情况(首次配药后15-30天的OCS或抗生素新配药)。采用处理加权逆概率回归分析来调整各种混杂因素。结果:在纳入的5401名患者中,38%的患者在首次记录的OCS处方中同时使用抗生素,从2009年的47%下降到2020年的24%。AB+OCS治疗失败的OR为1.36 (95% CI 0.81 - 2.16)。在31-365天的随访中,AB+OCS与仅OCS的新加重的HR为1.20 (95% CI 0.92至1.56)。AB缺乏有益效果在各个亚群中是一致的。结论:本研究发现,在OCS中加入AB治疗急性哮喘加重,既没有降低治疗失败,也没有降低随后加重的风险。我们建议,除非有明显的细菌感染迹象,否则初级保健机构不应使用抗生素治疗急性哮喘加重。
{"title":"Real-world effectiveness of antibiotics in addition to oral corticosteroids for managing asthma exacerbations in adults.","authors":"Irene Mommers, Sumaira Mubarik, Job F M van Boven, Jens H Bos, Maarten J Bijlsma, Eelko Hak","doi":"10.1136/bmjresp-2025-003506","DOIUrl":"10.1136/bmjresp-2025-003506","url":null,"abstract":"<p><strong>Background: </strong>Antibiotics are widely used to manage acute asthma exacerbations, despite little evidence for their effectiveness. This study assesses the added value of antibiotics alongside oral corticosteroids (OCSs) in treating asthma exacerbations.</p><p><strong>Methods: </strong>This retrospective cohort study included individuals from the Netherlands between 1994 and 2022 from the IADB.nl pharmacy dispensing database. Individuals had to be 16-45 years old, use inhaled asthma medication and have a first recorded prednisone/prednisolone (OCS) dispense of ≥30 mg/day for 3-14 days. Patients were compared regarding treatment failure (a new dispense of OCS or antibiotics, 15-30 days after initial dispense), based on whether or not they were dispensed antibiotics (AB) alongside their first recorded OCS dispense. Regression analyses with inverse probability of treatment weighting were used to adjust for various confounders.</p><p><strong>Results: </strong>Of the 5401 individuals included, 38% received antibiotics alongside the first-recorded OCS dispense, with a decreasing trend from 47% in 2009 to 24% in 2020. The OR for treatment failure was 1.36 (95% CI 0.81 to 2.16) for AB+OCS versus OCS-only. The HR for a new exacerbation within 31-365 days of follow-up was 1.20 (95% CI 0.92 to 1.56) for AB+OCS versus OCS-only. The lack of beneficial effect of AB was consistent across subcohorts.</p><p><strong>Conclusions: </strong>This study found no reduction in treatment failure, nor in risk of subsequent exacerbation, from adding AB to OCS for treating acute asthma exacerbations. We suggest that antibiotics should not be used in primary care settings to treat acute asthma exacerbation unless there are clear signs of bacterial infection.</p>","PeriodicalId":9048,"journal":{"name":"BMJ Open Respiratory Research","volume":"12 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12542710/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145342753","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Bronchiolitis is associated with asthma persisting until adulthood. While bronchial hyper-reactivity (BHR) is a hallmark of asthma, its occurrence and characteristics after bronchiolitis have been less studied. We aimed to study if BHR differed between young adults hospitalised for bronchiolitis in infancy and control subjects with no such history. Further, we sought to study whether any association between asthma and BHR differed between these two groups.
Methods: This Norwegian historical cohort study included 186 young adults hospitalised for respiratory syncytial virus positive or negative bronchiolitis in infancy during 1996-2001 and 139 matched control subjects. BHR was assessed at 17-20 years by methacholine provocation tests and recorded as dose-response slopes (DRS). Outcomes were analysed by mixed effects regression models.
Results: DRS was higher in the post-bronchiolitis group than in the control group (regression coefficient (β) 0.37; 95% CI 0.01 to 0.73; p=0.045). In both groups combined, current asthma was positively associated with DRS (β 0.98; 95% CI 0.50 to 1.45; p<0.001). Stratified analyses showed that the effect (β) of asthma on BHR was 0.80 (95% CI 0.21 to 1.38; p=0.008) in the post-bronchiolitis group and 1.40 (95% CI 0.58 to 2.23; p=0.001) in the control group. The difference in the association between asthma and BHR across the two groups was not statistically significant (p=0.191 for interaction).
Conclusions: BHR at age 17-20 years was higher in subjects hospitalised for bronchiolitis in infancy than in control subjects. The association between asthma and BHR was not found to differ between the post-bronchiolitis group and the control group, although a possible stronger association in the control group may warrant further study.
背景:毛细支气管炎与哮喘相关,持续到成年。虽然支气管高反应性(BHR)是哮喘的标志,但其在细支气管炎后的发生和特征研究较少。我们的目的是研究在婴儿期因毛细支气管炎住院的年轻人和没有这种病史的对照组之间的BHR是否存在差异。此外,我们试图研究哮喘和BHR之间的关联在这两组之间是否存在差异。方法:这项挪威历史队列研究纳入了1996-2001年期间因呼吸道合胞病毒阳性或阴性毛细支气管炎住院的186名年轻成年人和139名匹配的对照组。采用甲胆碱激发试验评估17-20岁时的BHR,并记录剂量-反应斜率(DRS)。结果采用混合效应回归模型进行分析。结果:毛细支气管炎后组DRS高于对照组(回归系数(β) 0.37;95% CI 0.01 ~ 0.73;p = 0.045)。两组合并后,当前哮喘与DRS呈正相关(β 0.98; 95% CI 0.50 - 1.45)。结论:在17-20岁时,因婴儿期细支气管炎住院的受试者的BHR高于对照组。哮喘和BHR之间的相关性在毛细支气管炎后组和对照组之间没有发现差异,尽管在对照组中可能存在更强的相关性,这值得进一步研究。
{"title":"Bronchial hyper-reactivity in young adults after hospitalisation for bronchiolitis in infancy.","authors":"Karen Galta Sørensen, Knut Øymar, Ingvild Dalen, Thomas Halvorsen, Ingvild Bruun Mikalsen","doi":"10.1136/bmjresp-2024-002881","DOIUrl":"10.1136/bmjresp-2024-002881","url":null,"abstract":"<p><strong>Background: </strong>Bronchiolitis is associated with asthma persisting until adulthood. While bronchial hyper-reactivity (BHR) is a hallmark of asthma, its occurrence and characteristics after bronchiolitis have been less studied. We aimed to study if BHR differed between young adults hospitalised for bronchiolitis in infancy and control subjects with no such history. Further, we sought to study whether any association between asthma and BHR differed between these two groups.</p><p><strong>Methods: </strong>This Norwegian historical cohort study included 186 young adults hospitalised for respiratory syncytial virus positive or negative bronchiolitis in infancy during 1996-2001 and 139 matched control subjects. BHR was assessed at 17-20 years by methacholine provocation tests and recorded as dose-response slopes (DRS). Outcomes were analysed by mixed effects regression models.</p><p><strong>Results: </strong>DRS was higher in the post-bronchiolitis group than in the control group (regression coefficient (β) 0.37; 95% CI 0.01 to 0.73; p=0.045). In both groups combined, current asthma was positively associated with DRS (β 0.98; 95% CI 0.50 to 1.45; p<0.001). Stratified analyses showed that the effect (β) of asthma on BHR was 0.80 (95% CI 0.21 to 1.38; p=0.008) in the post-bronchiolitis group and 1.40 (95% CI 0.58 to 2.23; p=0.001) in the control group. The difference in the association between asthma and BHR across the two groups was not statistically significant (p=0.191 for interaction).</p><p><strong>Conclusions: </strong>BHR at age 17-20 years was higher in subjects hospitalised for bronchiolitis in infancy than in control subjects. The association between asthma and BHR was not found to differ between the post-bronchiolitis group and the control group, although a possible stronger association in the control group may warrant further study.</p>","PeriodicalId":9048,"journal":{"name":"BMJ Open Respiratory Research","volume":"12 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12542717/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145343180","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-20DOI: 10.1136/bmjresp-2025-003307
Jeongha Mok, Dawoon Jeong, Hojoon Sohn, Saerom Kim, Seung Won Lee, Young Ae Kang
Background: We assessed the coverage of molecular drug susceptibility testing (mDST) among patients with pulmonary multidrug/rifampicin-resistant tuberculosis (MDR/RR-TB) in South Korea and identified factors influencing the lack of mDST implementation.
Methods: This retrospective study included patients with pulmonary MDR/RR-TB who initiated tuberculosis (TB) treatment between January 2015 and September 2021. Data were obtained from the K-TB-N cohort, an integrated national TB database linking three datasets. We assessed mDST coverage, temporal trends and factors associated with the lack of mDST implementation. mDST was defined as the use of the Xpert MTB/RIF assay or line probe assay (LPA) for isoniazid and rifampicin (first-line LPA).
Results: In total, 4637 patients were included in the analysis. Of the 4637 patients, 1342 (28.9%) did not undergo mDST; whereas, 3295 (71.1%) underwent mDST. Over the study period, a statistically significant annual increase in mDST coverage was observed, escalating from 49.1% in 2015 to 96.9% in 2021 (p<0.001). Throughout the study, the coverage of the Xpert MTB/RIF assay remained lower than that of LPA (22.1% vs 64.2%, p<0.001). Multivariable logistic regression analysis identified several factors independently associated with a decreased likelihood of mDST being conducted, including TB treatment initiation in secondary general hospitals, small hospitals or primary clinics, as well as in non-public-private mix (PPM) participating institutions. In addition, transfers between PPM-participating and non-participating institutions during the treatment period and sputum acid-fast bacilli smear-negative status were significantly associated with lower mDST uptake.
Conclusion: Although the increasing mDST coverage is a positive development, further efforts are needed to achieve nationwide and universal implementation, particularly for the Xpert MTB/RIF assay, in South Korea.
背景:我们评估了韩国肺部多药/利福平耐药结核病(MDR/ rp - tb)患者分子药敏试验(mDST)的覆盖率,并确定了影响mDST实施不足的因素。方法:这项回顾性研究纳入了2015年1月至2021年9月期间开始结核病(TB)治疗的肺部MDR/RR-TB患者。数据来自K-TB-N队列,这是一个连接三个数据集的综合国家结核病数据库。我们评估了mDST覆盖率、时间趋势和与mDST实施缺乏相关的因素。mDST定义为使用Xpert MTB/RIF法或线探针法(LPA)检测异烟肼和利福平(一线LPA)。结果:共纳入4637例患者。在4637例患者中,1342例(28.9%)未接受mDST;3295例(71.1%)行mDST。在研究期间,观察到mDST覆盖率的统计显着年度增长,从2015年的49.1%上升到2021年的96.9% (p结论:尽管mDST覆盖率的增加是一个积极的发展,但需要进一步努力实现全国和普遍实施,特别是在韩国的Xpert MTB/RIF检测。
{"title":"Nationwide coverage of molecular drug susceptibility testing in patients with pulmonary multidrug/rifampicin-resistant tuberculosis in South Korea: a retrospective cohort study (2015-2021).","authors":"Jeongha Mok, Dawoon Jeong, Hojoon Sohn, Saerom Kim, Seung Won Lee, Young Ae Kang","doi":"10.1136/bmjresp-2025-003307","DOIUrl":"10.1136/bmjresp-2025-003307","url":null,"abstract":"<p><strong>Background: </strong>We assessed the coverage of molecular drug susceptibility testing (mDST) among patients with pulmonary multidrug/rifampicin-resistant tuberculosis (MDR/RR-TB) in South Korea and identified factors influencing the lack of mDST implementation.</p><p><strong>Methods: </strong>This retrospective study included patients with pulmonary MDR/RR-TB who initiated tuberculosis (TB) treatment between January 2015 and September 2021. Data were obtained from the K-TB-N cohort, an integrated national TB database linking three datasets. We assessed mDST coverage, temporal trends and factors associated with the lack of mDST implementation. mDST was defined as the use of the Xpert MTB/RIF assay or line probe assay (LPA) for isoniazid and rifampicin (first-line LPA).</p><p><strong>Results: </strong>In total, 4637 patients were included in the analysis. Of the 4637 patients, 1342 (28.9%) did not undergo mDST; whereas, 3295 (71.1%) underwent mDST. Over the study period, a statistically significant annual increase in mDST coverage was observed, escalating from 49.1% in 2015 to 96.9% in 2021 (p<0.001). Throughout the study, the coverage of the Xpert MTB/RIF assay remained lower than that of LPA (22.1% vs 64.2%, p<0.001). Multivariable logistic regression analysis identified several factors independently associated with a decreased likelihood of mDST being conducted, including TB treatment initiation in secondary general hospitals, small hospitals or primary clinics, as well as in non-public-private mix (PPM) participating institutions. In addition, transfers between PPM-participating and non-participating institutions during the treatment period and sputum acid-fast bacilli smear-negative status were significantly associated with lower mDST uptake.</p><p><strong>Conclusion: </strong>Although the increasing mDST coverage is a positive development, further efforts are needed to achieve nationwide and universal implementation, particularly for the Xpert MTB/RIF assay, in South Korea.</p>","PeriodicalId":9048,"journal":{"name":"BMJ Open Respiratory Research","volume":"12 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-10-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12551535/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145343217","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Chronic respiratory diseases, particularly chronic obstructive pulmonary disease (COPD), are the eighth leading cause of death in Taiwan. Although COPD management has advanced in the previous two decades, mortality trends remain unclear. The present study analysed COPD mortality rates in Taiwan from 2002 to 2022.
Methods: COPD mortality and population data were obtained from Taiwan's National Health Statistics and the Ministry of the Interior's Demographic Yearbook. For comparison, global COPD mortality data were sourced from the WHO mortality database. A joinpoint analysis was conducted to assess trends in age-specific and age-standardised mortality rates across sex, region or country.
Results: From 2002 to 2022, Taiwan had 100 147 deaths attributed to COPD. The age-standardised mortality rate decreased with an annual average percentage change (AAPC) of -3.79%, which was more pronounced in women (AAPC: -4.28%) than in men (AAPC: -3.79%). The largest decline occurred from 2016 to 2022, with an AAPC of -7.70%. Most COPD-related deaths occurred among older individuals, with significant reductions in mortality rates observed among men aged ≥60 years and among women aged ≥50 years. A downward trend in COPD mortality rates was noted in most counties from 2016 to 2022, although patterns varied. The overall COPD mortality rate has declined in most countries since 2002, including Taiwan, which ranks third in Asia in terms of reductions in COPD mortality rates during this period.
Conclusion: From 2002 to 2022, COPD mortality rates in Taiwan declined considerably across sexes and regions, although patterns varied. In Asia, Taiwan's reduction in the rate of COPD mortality ranks third behind those of the Republic of Korea and Singapore. The reductions observed in COPD mortality rates in Taiwan may be attributable to tobacco control initiatives and nationwide COPD care programmes.
{"title":"Chronic obstructive pulmonary disease mortality rate trends in Taiwan, 2002-2022: a joinpoint regression analysis.","authors":"Ching-Hsiung Lin, Yi-Rong Li, Shu-O Chiang, Hao-Chien Wang, Meng-Chih Lin, Shih-Lung Cheng, Chong-Jen Yu","doi":"10.1136/bmjresp-2024-002719","DOIUrl":"10.1136/bmjresp-2024-002719","url":null,"abstract":"<p><strong>Background: </strong>Chronic respiratory diseases, particularly chronic obstructive pulmonary disease (COPD), are the eighth leading cause of death in Taiwan. Although COPD management has advanced in the previous two decades, mortality trends remain unclear. The present study analysed COPD mortality rates in Taiwan from 2002 to 2022.</p><p><strong>Methods: </strong>COPD mortality and population data were obtained from Taiwan's National Health Statistics and the Ministry of the Interior's Demographic Yearbook. For comparison, global COPD mortality data were sourced from the WHO mortality database. A joinpoint analysis was conducted to assess trends in age-specific and age-standardised mortality rates across sex, region or country.</p><p><strong>Results: </strong>From 2002 to 2022, Taiwan had 100 147 deaths attributed to COPD. The age-standardised mortality rate decreased with an annual average percentage change (AAPC) of -3.79%, which was more pronounced in women (AAPC: -4.28%) than in men (AAPC: -3.79%). The largest decline occurred from 2016 to 2022, with an AAPC of -7.70%. Most COPD-related deaths occurred among older individuals, with significant reductions in mortality rates observed among men aged ≥60 years and among women aged ≥50 years. A downward trend in COPD mortality rates was noted in most counties from 2016 to 2022, although patterns varied. The overall COPD mortality rate has declined in most countries since 2002, including Taiwan, which ranks third in Asia in terms of reductions in COPD mortality rates during this period.</p><p><strong>Conclusion: </strong>From 2002 to 2022, COPD mortality rates in Taiwan declined considerably across sexes and regions, although patterns varied. In Asia, Taiwan's reduction in the rate of COPD mortality ranks third behind those of the Republic of Korea and Singapore. The reductions observed in COPD mortality rates in Taiwan may be attributable to tobacco control initiatives and nationwide COPD care programmes.</p>","PeriodicalId":9048,"journal":{"name":"BMJ Open Respiratory Research","volume":"12 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12530367/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145298323","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-10-14DOI: 10.1136/bmjresp-2025-003526
Anthony A Laverty, Nicholas S Hopkinson
Background: Health is a fundamental issue in politics and an area where governments hold significant levers of influence. Countries in Europe have seen increased support for populist political parties, with some evidence linking support for these parties to health metrics. We aimed to establish if there is an association between health metrics and patterns of voting in England, particularly in relation to a recently established political party, Reform UK, in the 2024 general election.
Methods: We conducted a cross sectional ecological study with data from all constituencies in England (n=543). We conducted Pearson correlations and linear regression between the proportion of eligible votes for Reform UK and estimated prevalence of 20 common non-communicable diseases, including obesity, chronic obstructive pulmonary disease (COPD), asthma, type 2 diabetes and depression.
Results: Constituencies electing Reform members of parliament (MPs) (n=5/543) had the highest average prevalence of asthma (7.44%) and COPD (2.85%). Across the country, adjusting for age, sex and deprivation, a 10% increase in the party's vote share was associated with a +0.261% (95% CI 0.213% to 0.309%) prevalence of COPD, a +0.113% (95% CI 0.026% to 0.201%) prevalence of asthma and a +1.479% (95% CI 1.239% to 1.720%) increase in obesity prevalence.
Conclusions: At a constituency level, poor health, in particular conditions associated with breathlessness, was associated with a greater proportion of votes for Reform UK.
背景:卫生是政治中的一个基本问题,也是政府具有重要影响力的领域。欧洲国家对民粹主义政党的支持有所增加,一些证据将对这些政党的支持与健康指标联系起来。我们的目标是确定健康指标与英格兰投票模式之间是否存在关联,特别是与最近成立的政党“改革英国”(Reform UK)在2024年大选中的关系。方法:我们对英格兰所有选区的数据进行了横断面生态学研究(n=543)。我们在英国改革的合格投票比例与20种常见非传染性疾病的估计患病率之间进行了Pearson相关性和线性回归,包括肥胖、慢性阻塞性肺疾病(COPD)、哮喘、2型糖尿病和抑郁症。结果:选举改革派议员的选区(n=5/543)平均哮喘患病率最高(7.44%),COPD患病率最高(2.85%)。在全国范围内,调整年龄、性别和贫困因素后,该党的选票份额每增加10%,COPD患病率增加0.261% (95% CI 0.213%至0.309%),哮喘患病率增加0.113% (95% CI 0.026%至0.201%),肥胖患病率增加1.479% (95% CI 1.239%至1.720%)。结论:在选区一级,健康状况不佳,特别是与呼吸困难有关的状况,与支持改革联合王国的比例较大有关。
{"title":"What is the relationship between population health and voting patterns: an ecological study in England.","authors":"Anthony A Laverty, Nicholas S Hopkinson","doi":"10.1136/bmjresp-2025-003526","DOIUrl":"10.1136/bmjresp-2025-003526","url":null,"abstract":"<p><strong>Background: </strong>Health is a fundamental issue in politics and an area where governments hold significant levers of influence. Countries in Europe have seen increased support for populist political parties, with some evidence linking support for these parties to health metrics. We aimed to establish if there is an association between health metrics and patterns of voting in England, particularly in relation to a recently established political party, Reform UK, in the 2024 general election.</p><p><strong>Methods: </strong>We conducted a cross sectional ecological study with data from all constituencies in England (n=543). We conducted Pearson correlations and linear regression between the proportion of eligible votes for Reform UK and estimated prevalence of 20 common non-communicable diseases, including obesity, chronic obstructive pulmonary disease (COPD), asthma, type 2 diabetes and depression.</p><p><strong>Results: </strong>Constituencies electing Reform members of parliament (MPs) (n=5/543) had the highest average prevalence of asthma (7.44%) and COPD (2.85%). Across the country, adjusting for age, sex and deprivation, a 10% increase in the party's vote share was associated with a +0.261% (95% CI 0.213% to 0.309%) prevalence of COPD, a +0.113% (95% CI 0.026% to 0.201%) prevalence of asthma and a +1.479% (95% CI 1.239% to 1.720%) increase in obesity prevalence.</p><p><strong>Conclusions: </strong>At a constituency level, poor health, in particular conditions associated with breathlessness, was associated with a greater proportion of votes for Reform UK.</p>","PeriodicalId":9048,"journal":{"name":"BMJ Open Respiratory Research","volume":"12 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145290921","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}
Pub Date : 2025-10-13DOI: 10.1136/bmjresp-2024-003003
Katie Scandrett, Scott Pallett, Yemisi Takwoingi, Adam F Cunningham, Martin Dedicoat, Matthew K O'Shea
Introduction: There is significant potential for respiratory infections, such as tuberculosis (TB) and COVID-19, to overlap but little is known about such co-infection. We aimed to study the impact of active TB and latent TB on the incidence of severe COVID-19 in a large cohort of individuals in a setting of low TB endemicity.
Methods: Clinical data of patients admitted to hospital with acute SARS-CoV-2 were merged with a database of patients with a history of previous or current active TB, latent TB or healthy controls. We assessed the incidence of COVID-19 in these groups, length of hospital stay, admission to the intensive care unit (ICU) and in-hospital mortality.
Results: COVID-19 incidence among individuals with current active TB was 6.2% (12/194) and previous active TB 0.67% (30/4496). In contrast, the incidence in previously treated latent TB was 0.09% (4/4542) and among TB contacts 0.24% (34/13 391). There were similar rates of ICU admission and mortality among individuals with COVID-19 and current active TB, TB contacts and other patients. No individuals with previously treated latent TB and COVID-19 were admitted to the ICU or died.
Conclusions: Individuals with a history of latent TB seem to be at reduced risk of severe COVID-19 and have better outcomes than those with active TB and even uninfected controls. Further studies are required to understand the mechanistic basis of this observation.
{"title":"Previously treated latent tuberculosis infection is associated with less severe acute COVID-19: a cohort study.","authors":"Katie Scandrett, Scott Pallett, Yemisi Takwoingi, Adam F Cunningham, Martin Dedicoat, Matthew K O'Shea","doi":"10.1136/bmjresp-2024-003003","DOIUrl":"10.1136/bmjresp-2024-003003","url":null,"abstract":"<p><strong>Introduction: </strong>There is significant potential for respiratory infections, such as tuberculosis (TB) and COVID-19, to overlap but little is known about such co-infection. We aimed to study the impact of active TB and latent TB on the incidence of severe COVID-19 in a large cohort of individuals in a setting of low TB endemicity.</p><p><strong>Methods: </strong>Clinical data of patients admitted to hospital with acute SARS-CoV-2 were merged with a database of patients with a history of previous or current active TB, latent TB or healthy controls. We assessed the incidence of COVID-19 in these groups, length of hospital stay, admission to the intensive care unit (ICU) and in-hospital mortality.</p><p><strong>Results: </strong>COVID-19 incidence among individuals with current active TB was 6.2% (12/194) and previous active TB 0.67% (30/4496). In contrast, the incidence in previously treated latent TB was 0.09% (4/4542) and among TB contacts 0.24% (34/13 391). There were similar rates of ICU admission and mortality among individuals with COVID-19 and current active TB, TB contacts and other patients. No individuals with previously treated latent TB and COVID-19 were admitted to the ICU or died.</p><p><strong>Conclusions: </strong>Individuals with a history of latent TB seem to be at reduced risk of severe COVID-19 and have better outcomes than those with active TB and even uninfected controls. Further studies are required to understand the mechanistic basis of this observation.</p>","PeriodicalId":9048,"journal":{"name":"BMJ Open Respiratory Research","volume":"12 1","pages":""},"PeriodicalIF":3.4,"publicationDate":"2025-10-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12519662/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145285600","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}