Pub Date : 2025-02-01DOI: 10.1016/j.rmed.2025.107942
Júlia M. Saporiti DDS, MSc, PhD student, Thiago A. de Holanda DDS, MSc, PhD, Gabriela G. Torino DDS, MSc, PhD student, Noéli Boscato DDS, MSc, PhD
Purpose
This scoping review aimed to map research on factors associated with obstructive sleep apnoea (OSA) in children and adolescents undergoing overnight polysomnography (PSG) and questionnaire-based diagnostic assessments.
Methods
Searches were conducted in three electronic databases up to May 2023, including nine observational studies, including 3482 individuals.
Results
Among the included studies, nine reported on sex, six on obesity, five on tonsillar hypertrophy, three on mouth breathing, two on allergic rhinitis, and three on smoking exposure. The sample comprised 3482 children, with subsets analyzed for sex (n = 3482), obesity (n = 2752), and tonsillar hypertrophy (n = 794). Meta-analysis demonstrated a significantly higher prevalence of OSA in males compared to females [P < 0.0001; I2 = 49 %], with a pooled relative risk (RR) of 1.15 (95 % confidence interval [CI]: 1.07–1.23). Associations were found between obesity and OSA [RR: 1.42; 95 % CI: 1.20–1.68; P = 0.02; I2 = 61 %], and tonsillar size and OSA [RR: 1.61; 95 % CI: 1.35–1.92; P = 0.06; I2 = 60 %].
Conclusion
Considering the study's limitations, these findings underscore the importance of considering sex, obesity, and tonsillar size when evaluating OSA in children and adolescents.
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Pub Date : 2025-02-01DOI: 10.1016/j.rmed.2025.107951
Pinar Kucukdemirci Kaya, Remzi Iscimen
Purpose
Myasthenia-gravis and Guillain-Barre-syndrome are two of the most common causes of acute and reversible neuromuscular-respiratory-failure(ARNRF), both may worsen respiratory-failure and need for invasive-mechanical-ventilation(IMV) for long-periods due to muscle-weakness. However, approitive IMV-mode for ARNRF patients that better gas-exchange and weaning in ARNRF remain unclear.
Materials and methods
Critically-ill-patiens with IMV due to ARNRF, who could meet the weaning-criterias (after intubation for more than 7-days; difficult-weaning), between 2013, and 2023 were included in the study. IMV-settings, simultaneous arterial-blood-gas (ABG) analyses, and prognosis were recorded for each patient on relevant days.
Results
Sixty-critically-ill-patients with ARNRF who defined as difficult-weaning were included in the study. When different IMV-modes were used in the same patient, simultaneous ABG results were compared for each ventilation-mode. It was determined that the partial-pressure-of-oxygen/fraction of inspired-oxygen-ratios were significantly higher and partial-carbon-dioxide-levels were significantly lower when critically-ill-patients were ventilated with the biphasic-positive-airway-pressure-ventilation(BIPAP) (95 % CI: [0.641–1.41]; p < .001; 95 % CI: [-1.05-.351]; p < .001, respectively). Length-of-time-until-weaning was significantly shorter in BIPAP-mode for each patient in the study group(95 % CI: [0.717–0.188]; p < .001). Moreover, weaning-success was statistically higher in patients with ARNRF were ventilated with BIPAP one-week-before spontenous-breathing-trial (95 % CI [1.026–21.65]; p = .046) than with all other IMV-modes.
Conclusion
According to our findings, when BIPAP was selected as the IMV-settings, gas exchange was improved,and weaning-success was higher in critically-ill-patients with ARNRF.
{"title":"Management of mechanical ventilation and weaning in critically ill patients with neuromuscular disorders","authors":"Pinar Kucukdemirci Kaya, Remzi Iscimen","doi":"10.1016/j.rmed.2025.107951","DOIUrl":"10.1016/j.rmed.2025.107951","url":null,"abstract":"<div><h3>Purpose</h3><div>Myasthenia-gravis and Guillain-Barre-syndrome are two of the most common causes of acute and reversible neuromuscular-respiratory-failure(ARNRF), both may worsen respiratory-failure and need for invasive-mechanical-ventilation(IMV) for long-periods due to muscle-weakness. However, approitive IMV-mode for ARNRF patients that better gas-exchange and weaning in ARNRF remain unclear.</div></div><div><h3>Materials and methods</h3><div>Critically-ill-patiens with IMV due to ARNRF, who could meet the weaning-criterias (after intubation for more than 7-days; difficult-weaning), between 2013, and 2023 were included in the study. IMV-settings, simultaneous arterial-blood-gas (ABG) analyses, and prognosis were recorded for each patient on relevant days.</div></div><div><h3>Results</h3><div>Sixty-critically-ill-patients with ARNRF who defined as difficult-weaning were included in the study. When different IMV-modes were used in the same patient, simultaneous ABG results were compared for each ventilation-mode. It was determined that the partial-pressure-of-oxygen/fraction of inspired-oxygen-ratios were significantly higher and partial-carbon-dioxide-levels were significantly lower when critically-ill-patients were ventilated with the biphasic-positive-airway-pressure-ventilation(BIPAP) (95 % CI: [0.641–1.41]; <em>p</em> < .001; 95 % CI: [-1.05-.351]; <em>p</em> < .001, respectively). Length-of-time-until-weaning was significantly shorter in BIPAP-mode for each patient in the study group(95 % CI: [0.717–0.188]; <em>p</em> < .001). Moreover, weaning-success was statistically higher in patients with ARNRF were ventilated with BIPAP one-week-before spontenous-breathing-trial (95 % CI [1.026–21.65]; <em>p</em> = .046) than with all other IMV-modes.</div></div><div><h3>Conclusion</h3><div>According to our findings, when BIPAP was selected as the IMV-settings, gas exchange was improved,and weaning-success was higher in critically-ill-patients with ARNRF.</div></div>","PeriodicalId":21057,"journal":{"name":"Respiratory medicine","volume":"237 ","pages":"Article 107951"},"PeriodicalIF":3.5,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143010727","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 : 2025-02-01DOI: 10.1016/j.rmed.2025.107950
Patrick Stafler , Benjamin Rothschild , Yulia Gendler , Emmanuelle Seguier-Lipszyc , Simona Tyroler , Orith Waisbourd-Zinman , Meir Mei-Zahav , Dario Prais , Vered Shkalim Zemer
Background
Morbid obesity in adolescents impacts respiratory function, often leading to reduced lung volume and obstructive ventilatory defects. However, standard spirometric values frequently remain within normal ranges.
Objectives
We hypothesized that Lung Clearance Index (LCI) is a more sensitive marker for detecting airway dysfunction in adolescents with morbid obesity than conventional lung function tests.
Methods
A prospective single-center cohort study evaluated adolescents with morbid obesity undergoing laparoscopic sleeve gastrectomy (LSG). Assessments included fractional exhaled nitric oxide, multiple breath washout, spirometry, plethysmography, diffusion capacity, and a 6-min walk test, conducted pre- and post-surgery.
Results
Seventeen adolescents (mean age 17.1 years, BMI 45.5 kg/m2) were studied. Pre-surgery, LCI was slightly elevated (mean 7, SD ± 0.7), other lung function measures were normal. LCI correlated with BMI (r = 0.637, p = 0.014), no correlation was found between FEV1 and BMI (r = −0.083, p = 0.752). Post-surgery, mean LCI fell from 7 (±0.7) to 6.5 (±0.7), p = 0.009. The pre-operatively observed correlation between LCI and BMI was no longer present post-operatively (r = 0.362, p = 0.225). LCI changes (r = 0.676, p = 0.011) correlated with BMI changes, whilst FEV1 did not (r = 0.160, p = 0.540).
Conclusions
LCI appeared to be a more sensitive marker than conventional spirometry for detecting airway dysfunction in adolescents with morbid obesity. Significant post-surgery improvements suggested enhanced ventilation homogeneity. LCI may detect subtle airway changes in this population, and be potentially valuable for both clinical assessment and research.
背景:青少年病态肥胖影响呼吸功能,常导致肺容量减少和阻塞性通气缺陷。然而,标准肺活量值经常保持在正常范围内。目的:我们假设肺清除率指数(LCI)是一种比常规肺功能测试更敏感的检测青少年病态肥胖气道功能障碍的指标。方法:一项前瞻性单中心队列研究评估了接受腹腔镜袖式胃切除术(LSG)的病态肥胖青少年。评估包括在术前和术后进行的分数呼出一氧化氮、多次呼吸冲洗、肺活量测定、体积脉搏图、扩散能力和6分钟步行测试。结果:17例青少年(平均年龄17.1岁,体重指数45.5 kg/m2)。术前LCI轻度升高(平均7,SD±0.7),其他肺功能指标正常。LCI与BMI相关(r = 0.637, p = 0.014), FEV1与BMI无相关性(r = -0.083, p = 0.752)。术后平均LCI由7(±0.7)降至6.5(±0.7),p = 0.009。术前观察到的LCI与BMI之间的相关性在术后不再存在(r = 0.362, p = 0.225)。LCI变化(r = 0.676, p = 0.011)与BMI变化相关,而FEV1变化与BMI变化无关(r = 0.160, p = 0.540)。结论:LCI似乎是一个比传统肺活量测定法更敏感的标志物,用于检测青少年病态肥胖的气道功能障碍。术后显著改善提示通气均匀性增强。LCI可以检测到这一人群气道的细微变化,对临床评估和研究都有潜在的价值。
{"title":"Lung clearance index: A sensitive measure of airway function improvement in adolescents after weight loss from bariatric surgery","authors":"Patrick Stafler , Benjamin Rothschild , Yulia Gendler , Emmanuelle Seguier-Lipszyc , Simona Tyroler , Orith Waisbourd-Zinman , Meir Mei-Zahav , Dario Prais , Vered Shkalim Zemer","doi":"10.1016/j.rmed.2025.107950","DOIUrl":"10.1016/j.rmed.2025.107950","url":null,"abstract":"<div><h3>Background</h3><div>Morbid obesity in adolescents impacts respiratory function, often leading to reduced lung volume and obstructive ventilatory defects. However, standard spirometric values frequently remain within normal ranges.</div></div><div><h3>Objectives</h3><div>We hypothesized that Lung Clearance Index (LCI) is a more sensitive marker for detecting airway dysfunction in adolescents with morbid obesity than conventional lung function tests.</div></div><div><h3>Methods</h3><div>A prospective single-center cohort study evaluated adolescents with morbid obesity undergoing laparoscopic sleeve gastrectomy (LSG). Assessments included fractional exhaled nitric oxide, multiple breath washout, spirometry, plethysmography, diffusion capacity, and a 6-min walk test, conducted pre- and post-surgery.</div></div><div><h3>Results</h3><div>Seventeen adolescents (mean age 17.1 years, BMI 45.5 kg/m<sup>2</sup>) were studied. Pre-surgery, LCI was slightly elevated (mean 7, SD ± 0.7), other lung function measures were normal. LCI correlated with BMI (r = 0.637, p = 0.014), no correlation was found between FEV<sub>1</sub> and BMI (r = −0.083, p = 0.752). Post-surgery, mean LCI fell from 7 (±0.7) to 6.5 (±0.7), p = 0.009. The pre-operatively observed correlation between LCI and BMI was no longer present post-operatively (r = 0.362, p = 0.225). LCI changes (r = 0.676, p = 0.011) correlated with BMI changes, whilst FEV<sub>1</sub> did not (r = 0.160, p = 0.540).</div></div><div><h3>Conclusions</h3><div>LCI appeared to be a more sensitive marker than conventional spirometry for detecting airway dysfunction in adolescents with morbid obesity. Significant post-surgery improvements suggested enhanced ventilation homogeneity. LCI may detect subtle airway changes in this population, and be potentially valuable for both clinical assessment and research.</div></div>","PeriodicalId":21057,"journal":{"name":"Respiratory medicine","volume":"237 ","pages":"Article 107950"},"PeriodicalIF":3.5,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143010774","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 : 2025-02-01DOI: 10.1016/j.rmed.2024.107921
Kabadi Alisha A, Yang Jenny Z, Fernandes Timothy M
<div><div>Exercise-induced pulmonary arterial hypertension (EiPH) is often treated with off-label use of pulmonary arterial hypertension-targeted therapy (PH-targeted therapy). Most measures of PAH severity are normal in patients with EiPH, posing challenges in evaluating for physiological improvement in patients treated for EiPH. In this study, we used non-invasive cardiopulmonary exercise testing (CPET) to assess for objective improvement in patients treated for EiPH. Fourteen patients were included in the study, diagnosed with EiPH by invasive CPET with simultaneous right heart catheterization and subsequently treated with PH-targeted therapy. Follow-up non-invasive CPET was performed to evaluate oxygen consumption (VO<sub>2</sub>, L/min) and oxygen pulse (O<sub>2</sub> pulse, ml/beat), which was defined by the ratio of VO<sub>2</sub> to heart rate (beats/min).). Adequate stroke volume augmentation was a ratio of O<sub>2</sub> pulse at anaerobic threshold (O<sub>2</sub> pulse<sub>AT</sub>) to O<sub>2</sub> pulse at rest (O<sub>2</sub> pulse<sub>R</sub>) of >2.6. The results showed a significant improvement in O<sub>2</sub> pulse and VO<sub>2</sub> at anaerobic threshold after treatment with PH-targeted therapy. In addition, O<sub>2</sub> Pulse<sub>AT</sub>:O2 Pulse<sub>R</sub> significantly improved. Patients treated for EiPH demonstrated improvement in both stroke volume augmentation and VO<sub>2</sub> measured on non-invasive CPET, supporting the use of this test to assess for objective improvement in exercise capacity for patients treated for EiPH.</div><div>Structured Abstract.</div></div><div><h3>Rationale</h3><div>Exercise-induced pulmonary arterial hypertension (EiPH) is a clinical entity characterized by exertional dyspnea. Cardiopulmonary exercise testing (CPET) can evaluate exertional limitations in EiPH patients and assess response to therapy. We describe a series of patients treated for EiPH and monitored with non-invasive CPET.</div></div><div><h3>Methods</h3><div>case series of 14 patients with EiPH treated with PH-targeted therapy. EiPH was defined by a slope of the mean pulmonary artery pressure (mPAP) vs cardiac output of >3 mmHg/L/min with a resting mPAP of <20 mmHg and pulmonary vascular resistance <3 Woods units. Oxygen pulse (O<sub>2</sub> pulse, ml/beat), a surrogate of stroke volume (SV), was measured by the ratio of oxygen consumption (VO<sub>2</sub>, L/min) to heart rate (beats/min). Adequate SV augmentation was a ratio of O<sub>2</sub> pulse at anaerobic threshold (O<sub>2</sub> pulse<sub>AT</sub>) to O<sub>2</sub> pulse at rest (O<sub>2</sub> pulse<sub>R</sub>) of >2.6.</div></div><div><h3>Results</h3><div>Patients were majority female (86 %) with a mean age of 59.1.±12.2 years, and 57 % had connective tissue diseases. Patients took PH-targeted therapy (endothelin receptor antagonist (n = 7), phosphodiesterase-5 inhibitor (n = 5) or both (n = 2)) for a median exposure of 150 days. There was no change i
运动引起的肺动脉高压(EiPH)通常通过超说明书使用肺动脉高压靶向治疗(ph靶向治疗)来治疗。EiPH患者的PAH严重程度的大多数测量是正常的,这对EiPH治疗患者的生理改善评估提出了挑战。在这项研究中,我们使用无创心肺运动试验(CPET)来评估接受EiPH治疗的患者的客观改善。14例患者被纳入研究,通过有创CPET诊断为EiPH,同时进行右心导管插管,随后接受ph靶向治疗。随访无创CPET评估耗氧量(VO2, L/min)和氧脉冲(O2脉冲,ml/beat),以VO2与心率(beats/min)之比定义。. 适当的脑卒中容积增加是指无氧阈值时的氧脉冲(O2 pulseAT)与静止时的氧脉冲(O2 pulseR)之比为>2.6。结果显示,经ph靶向治疗后,氧脉冲和无氧阈值VO2明显改善。此外,O2 PulseAT:O2 PulseR明显改善。接受EiPH治疗的患者在卒中容量增加和无创CPET测量的VO2方面均有改善,支持使用该测试来评估EiPH治疗患者运动能力的客观改善。摘要基本原理:运动性肺动脉高压(EiPH)是一种以运动性呼吸困难为特征的临床症状。心肺运动试验(CPET)可以评估EiPH患者的运动限制和对治疗的反应。我们描述了一系列接受EiPH治疗并采用无创CPET监测的患者。方法:对14例EiPH患者进行ph靶向治疗。EiPH的定义是平均肺动脉压(mPAP)与静息mPAP为2 (ml/beat)时的心输出量(bbb3mmhg /L/min)的斜率,通过耗氧量(VO2, L/min)与心率(节拍/min)的比值来衡量卒中容量(SV)。适当的SV增强是无氧阈值O2脉冲(O2 pulseAT)与静止O2脉冲(O2 pulseR)之比>2.6。结果:患者以女性为主(86%),平均年龄59.1±12.2岁,57%患有结缔组织疾病。患者接受ph靶向治疗(内皮素受体拮抗剂(n=7),磷酸二酯酶-5抑制剂(n=5)或两者(n=2)),中位暴露时间为150天。治疗后两组血氧脉冲量无明显变化。然而,O2 pulseAT(9.7±3.1 vs 7.4±3.2 ml/beat, p=0.003)、O2 pulseAT/O2 pulseR比值(2.8±0.9 vs 2.0±0.6,p=0.006)和厌氧阈值VO2(0.9±0.3 vs 0.7±0.4 ml/kg/min, p=0.04)显著增加。结论:接受ph靶向治疗的EiPH患者在无创CPET上表现出SV增强和无氧阈值VO2的改善。CPET可作为EiPH治疗患者运动能力改善的客观指标。
{"title":"Stroke volume augmentation improves with PH-targeted therapy in patients with exercise-induced pulmonary hypertension","authors":"Kabadi Alisha A, Yang Jenny Z, Fernandes Timothy M","doi":"10.1016/j.rmed.2024.107921","DOIUrl":"10.1016/j.rmed.2024.107921","url":null,"abstract":"<div><div>Exercise-induced pulmonary arterial hypertension (EiPH) is often treated with off-label use of pulmonary arterial hypertension-targeted therapy (PH-targeted therapy). Most measures of PAH severity are normal in patients with EiPH, posing challenges in evaluating for physiological improvement in patients treated for EiPH. In this study, we used non-invasive cardiopulmonary exercise testing (CPET) to assess for objective improvement in patients treated for EiPH. Fourteen patients were included in the study, diagnosed with EiPH by invasive CPET with simultaneous right heart catheterization and subsequently treated with PH-targeted therapy. Follow-up non-invasive CPET was performed to evaluate oxygen consumption (VO<sub>2</sub>, L/min) and oxygen pulse (O<sub>2</sub> pulse, ml/beat), which was defined by the ratio of VO<sub>2</sub> to heart rate (beats/min).). Adequate stroke volume augmentation was a ratio of O<sub>2</sub> pulse at anaerobic threshold (O<sub>2</sub> pulse<sub>AT</sub>) to O<sub>2</sub> pulse at rest (O<sub>2</sub> pulse<sub>R</sub>) of >2.6. The results showed a significant improvement in O<sub>2</sub> pulse and VO<sub>2</sub> at anaerobic threshold after treatment with PH-targeted therapy. In addition, O<sub>2</sub> Pulse<sub>AT</sub>:O2 Pulse<sub>R</sub> significantly improved. Patients treated for EiPH demonstrated improvement in both stroke volume augmentation and VO<sub>2</sub> measured on non-invasive CPET, supporting the use of this test to assess for objective improvement in exercise capacity for patients treated for EiPH.</div><div>Structured Abstract.</div></div><div><h3>Rationale</h3><div>Exercise-induced pulmonary arterial hypertension (EiPH) is a clinical entity characterized by exertional dyspnea. Cardiopulmonary exercise testing (CPET) can evaluate exertional limitations in EiPH patients and assess response to therapy. We describe a series of patients treated for EiPH and monitored with non-invasive CPET.</div></div><div><h3>Methods</h3><div>case series of 14 patients with EiPH treated with PH-targeted therapy. EiPH was defined by a slope of the mean pulmonary artery pressure (mPAP) vs cardiac output of >3 mmHg/L/min with a resting mPAP of <20 mmHg and pulmonary vascular resistance <3 Woods units. Oxygen pulse (O<sub>2</sub> pulse, ml/beat), a surrogate of stroke volume (SV), was measured by the ratio of oxygen consumption (VO<sub>2</sub>, L/min) to heart rate (beats/min). Adequate SV augmentation was a ratio of O<sub>2</sub> pulse at anaerobic threshold (O<sub>2</sub> pulse<sub>AT</sub>) to O<sub>2</sub> pulse at rest (O<sub>2</sub> pulse<sub>R</sub>) of >2.6.</div></div><div><h3>Results</h3><div>Patients were majority female (86 %) with a mean age of 59.1.±12.2 years, and 57 % had connective tissue diseases. Patients took PH-targeted therapy (endothelin receptor antagonist (n = 7), phosphodiesterase-5 inhibitor (n = 5) or both (n = 2)) for a median exposure of 150 days. There was no change i","PeriodicalId":21057,"journal":{"name":"Respiratory medicine","volume":"237 ","pages":"Article 107921"},"PeriodicalIF":3.5,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142882767","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 : 2025-02-01DOI: 10.1016/j.rmed.2025.107939
Hye Jin Jang , Yu Min Seong , Jihyeon Jeong , Jin-Young Huh , Jin-Ho Kim , Kyung Hoon Kim , Joo Hun Park , Won-Il Choi
Introduction
Ca2+ signaling in fibroblasts would be one of the important mediators of lung fibrosis.
This study investigated the relationship between calcium channel blocker usage and the risk of developing interstitial lung disease and idiopathic pulmonary fibrosis.
Material and methods
This cohort study used data from the Korean National Health Screening Cohort spanned from January 1, 2004, to December 31, 2015. The study included 394,142 participants. CCB usage, as a time-dependent variable assessed every two years, was categorized by medication status (ever-users and never-users) and further divided into five groups based on cumulative defined daily dose: <182.5, 182.5–365.0, 365.0–547.5, and ≥547.5. Incidence rates of ILD and IPF among CCB users compared to never-users, analyzed using time-dependent Cox regression models.
Results
The incidence rates were 27.7 per 100,000 person-years for ILD and 15.0 per 100,000 person-years for IPF among never-users, compared to 19.5 per 100,000 person-years for ILD and 13.9 per 100,000 person-years for IPF among ever-users. The adjusted hazard ratios (aHRs) were 0.68 [95 % confidence interval (CI), 0.55–0.83] for ILD and 0.69 (95 % CI, 0.54–0.88) for IPF. Increasing categories of CCB usage were significantly associated with a lower risk of ILD [aHRs: 1.23 (95 % CI, 0.97–1.56), 1.20 (0.85–1.71), 0.49 (0.30–0.81), and 0.27(0.19–0.39)] and IPF [aHRs: 1.21 (95 % confidence interval, 0.89–1.64), 1.45 (0.96–2.20), 0.83 (0.52–1.33), and 0.25 (0.16–0.38)], compared to never-users.
Conclusions
This study found that individuals using CCBs had a significantly lower risk of interstitial lung disease and idiopathic pulmonary fibrosis compared to never-users in a dose-response manner.
{"title":"Association between calcium channel blocker use and the risk of interstitial lung disease and idiopathic pulmonary fibrosis: A longitudinal cohort study","authors":"Hye Jin Jang , Yu Min Seong , Jihyeon Jeong , Jin-Young Huh , Jin-Ho Kim , Kyung Hoon Kim , Joo Hun Park , Won-Il Choi","doi":"10.1016/j.rmed.2025.107939","DOIUrl":"10.1016/j.rmed.2025.107939","url":null,"abstract":"<div><h3>Introduction</h3><div>Ca2+ signaling in fibroblasts would be one of the important mediators of lung fibrosis.</div><div>This study investigated the relationship between calcium channel blocker usage and the risk of developing interstitial lung disease and idiopathic pulmonary fibrosis.</div></div><div><h3>Material and methods</h3><div>This cohort study used data from the Korean National Health Screening Cohort spanned from January 1, 2004, to December 31, 2015. The study included 394,142 participants. CCB usage, as a time-dependent variable assessed every two years, was categorized by medication status (ever-users and never-users) and further divided into five groups based on cumulative defined daily dose: <182.5, 182.5–365.0, 365.0–547.5, and ≥547.5. Incidence rates of ILD and IPF among CCB users compared to never-users, analyzed using time-dependent Cox regression models.</div></div><div><h3>Results</h3><div>The incidence rates were 27.7 per 100,000 person-years for ILD and 15.0 per 100,000 person-years for IPF among never-users, compared to 19.5 per 100,000 person-years for ILD and 13.9 per 100,000 person-years for IPF among ever-users. The adjusted hazard ratios (aHRs) were 0.68 [95 % confidence interval (CI), 0.55–0.83] for ILD and 0.69 (95 % CI, 0.54–0.88) for IPF. Increasing categories of CCB usage were significantly associated with a lower risk of ILD [aHRs: 1.23 (95 % CI, 0.97–1.56), 1.20 (0.85–1.71), 0.49 (0.30–0.81), and 0.27(0.19–0.39)] and IPF [aHRs: 1.21 (95 % confidence interval, 0.89–1.64), 1.45 (0.96–2.20), 0.83 (0.52–1.33), and 0.25 (0.16–0.38)], compared to never-users.</div></div><div><h3>Conclusions</h3><div>This study found that individuals using CCBs had a significantly lower risk of interstitial lung disease and idiopathic pulmonary fibrosis compared to never-users in a dose-response manner.</div></div>","PeriodicalId":21057,"journal":{"name":"Respiratory medicine","volume":"237 ","pages":"Article 107939"},"PeriodicalIF":3.5,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142927912","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 : 2025-02-01DOI: 10.1016/j.rmed.2025.107947
Dongyuan Wang , Lijuan Hua , Wenxue Bai , Mengyao Guo , Yongman Lv , Dong Kuang , Hanxiong Guan , Jun Yu , Qi Wang , Zhipeng Hao , Wei Sun , Ni Zhang , Kaiyan Li , Hui Xu , Min Xie
Objectives
Previous studies suggest peripheral blood immune cells associate with the progression and prognosis of lung cancer. The main purpose of this study was to explore the association of peripheral immune cell and its dynamics with the growth of pulmonary nodules.
Materials and method
Of 9280 subjects whom had blood cell counts and chest CT scan in health check-up, 1068 participants were enrolled with the incidental pulmonary nodules of above 5 mm in diameter and subsequently followed up for 2 years. The pulmonary nodules were identified as growth based on the increase of at least 2 mm in the diameters within the two years. The relationships of pulmonary nodules growth with peripheral immune cell dynamics and clinical variables were analyzed using univariable inter-group comparison and multivariable logistic regression analyses.
Results
During the two years, 116 (10.9 %) of 1068 participants had the growth pulmonary nodules. Overall, emphysema, nodule diameter and non-solid characteristics associated with the growth of nodules. In the subgroup of pure solid nodules, high baseline eosinophil percentage (OR 1.220; 95 % CI 1.009–1.474; P = 0.040) and the increase of neutrophil count (OR 3.805; 95 % CI 1.027–14.093; P = 0.045) were significant risk factors for the nodule growth. In the subgroup of solid-predominant nodules, the increase of lymphocyte was associated with a lower risk of growth (OR 0.039; 95 % CI 0.002–0.839; P = 0.038).
Conclusions
High baseline eosinophil and increase of neutrophil were associated with the growth of pure solid pulmonary nodules. The decrease of lymphocyte related to the growth of solid-predominant nodules.
目的:以往的研究表明,外周血免疫细胞与肺癌的进展和预后有关。本研究的主要目的是探讨外周免疫细胞及其动力学与肺结节生长的关系。材料与方法:9280例体检时进行血细胞计数和胸部CT扫描的受试者中,1068例偶发肺结节直径大于5mm,随访2年。肺结节在两年内直径增加至少2mm即为生长。采用单变量组间比较和多变量logistic回归分析肺结节生长与外周血免疫细胞动力学及临床变量的关系。结果:在两年中,1068名参与者中有116名(10.9%)患有生长性肺结节。总的来说,肺气肿、结节直径和非实性特征与结节的生长有关。在纯实性结节亚组中,基线嗜酸性粒细胞百分比高(OR 1.220;95% ci 1.009-1.474;P= 0.040),中性粒细胞计数增加(OR 3.805;95% ci 1.027-14.093;P= 0.045)是结节生长的显著危险因素。在固体结节亚组中,淋巴细胞的增加与较低的生长风险相关(OR 0.039;95% ci 0.002-0.839;P = 0.038)。结论:高基线嗜酸性粒细胞和中性粒细胞增加与纯实性肺结节的生长有关。淋巴细胞的减少与实性结节的生长有关。
{"title":"Peripheral blood immune cell dynamics associate with growth of incidental indeterminate pulmonary nodules","authors":"Dongyuan Wang , Lijuan Hua , Wenxue Bai , Mengyao Guo , Yongman Lv , Dong Kuang , Hanxiong Guan , Jun Yu , Qi Wang , Zhipeng Hao , Wei Sun , Ni Zhang , Kaiyan Li , Hui Xu , Min Xie","doi":"10.1016/j.rmed.2025.107947","DOIUrl":"10.1016/j.rmed.2025.107947","url":null,"abstract":"<div><h3>Objectives</h3><div>Previous studies suggest peripheral blood immune cells associate with the progression and prognosis of lung cancer. The main purpose of this study was to explore the association of peripheral immune cell and its dynamics with the growth of pulmonary nodules.</div></div><div><h3>Materials and method</h3><div>Of 9280 subjects whom had blood cell counts and chest CT scan in health check-up, 1068 participants were enrolled with the incidental pulmonary nodules of above 5 mm in diameter and subsequently followed up for 2 years. The pulmonary nodules were identified as growth based on the increase of at least 2 mm in the diameters within the two years. The relationships of pulmonary nodules growth with peripheral immune cell dynamics and clinical variables were analyzed using univariable inter-group comparison and multivariable logistic regression analyses.</div></div><div><h3>Results</h3><div>During the two years, 116 (10.9 %) of 1068 participants had the growth pulmonary nodules. Overall, emphysema, nodule diameter and non-solid characteristics associated with the growth of nodules. In the subgroup of pure solid nodules, high baseline eosinophil percentage (OR 1.220; 95 % CI 1.009–1.474; <em>P</em> = 0.040) and the increase of neutrophil count (OR 3.805; 95 % CI 1.027–14.093; <em>P</em> = 0.045) were significant risk factors for the nodule growth. In the subgroup of solid-predominant nodules, the increase of lymphocyte was associated with a lower risk of growth (OR 0.039; 95 % CI 0.002–0.839; <em>P</em> = 0.038).</div></div><div><h3>Conclusions</h3><div>High baseline eosinophil and increase of neutrophil were associated with the growth of pure solid pulmonary nodules. The decrease of lymphocyte related to the growth of solid-predominant nodules.</div></div>","PeriodicalId":21057,"journal":{"name":"Respiratory medicine","volume":"237 ","pages":"Article 107947"},"PeriodicalIF":3.5,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142953015","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 : 2025-02-01DOI: 10.1016/j.rmed.2024.107914
Shivang Sharma , Stephen J. Kuperberg
Mounier–Kuhn syndrome (MKS) or tracheobronchomegaly is an uncommon disease of the central airways. It is characterized by pathological dilatation of the trachea and main bronchi and inevitably leads to recurrent respiratory infections, bronchiectasis, hospitalizations, and results in considerable morbidity and mortality. Despite numerous case reports, there is a shortage of evidence on clinical outcomes and limited data on interventions, thus presenting a significant gap in the literature. Fortunately, new strategies and increasing clinical experience have improved the clinical approach, diagnostic workup, classification, and management of MKS. Articles in English, Spanish, and French were searched from databases, including Pubmed, Google Scholar, Medline, and SCOPUS, using the terms “Mounier–Kuhn syndrome,” “Tracheomegaly,” “Tracheobronchomegaly,” and “Bronchomegaly,” without date restrictions. A total of 360 articles with the aforementioned syntax were indexed on Pubmed. This state-of-the-art review attempts to fill a void in the current literature by summarizing the current scientific knowledge and highlighting novel interventional strategies in the management of Mounier Kuhn Syndrome.
{"title":"State-of-the-art narrative review: Mounier–Kuhn syndrome and tracheobronchomegaly","authors":"Shivang Sharma , Stephen J. Kuperberg","doi":"10.1016/j.rmed.2024.107914","DOIUrl":"10.1016/j.rmed.2024.107914","url":null,"abstract":"<div><div>Mounier–Kuhn syndrome (MKS) or tracheobronchomegaly is an uncommon disease of the central airways. It is characterized by pathological dilatation of the trachea and main bronchi and inevitably leads to recurrent respiratory infections, bronchiectasis, hospitalizations, and results in considerable morbidity and mortality. Despite numerous case reports, there is a shortage of evidence on clinical outcomes and limited data on interventions, thus presenting a significant gap in the literature. Fortunately, new strategies and increasing clinical experience have improved the clinical approach, diagnostic workup, classification, and management of MKS. Articles in English, Spanish, and French were searched from databases, including Pubmed, Google Scholar, Medline, and SCOPUS, using the terms “Mounier–Kuhn syndrome,” “Tracheomegaly,” “Tracheobronchomegaly,” and “Bronchomegaly,” without date restrictions. A total of 360 articles with the aforementioned syntax were indexed on Pubmed. This state-of-the-art review attempts to fill a void in the current literature by summarizing the current scientific knowledge and highlighting novel interventional strategies in the management of Mounier Kuhn Syndrome.</div></div>","PeriodicalId":21057,"journal":{"name":"Respiratory medicine","volume":"237 ","pages":"Article 107914"},"PeriodicalIF":3.5,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142876487","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 : 2025-02-01DOI: 10.1016/j.rmed.2024.107922
Airi Hasegawa , Kazuya Tone , Yuri Baba , Zenya Saito , Takuya Akutsu , Takaaki Kitayama , Shunsuke Inaki , Mina Gochi , Takashi Yaguchi , Koichi Makimura , Masamichi Takagi , Jun Araya
Background
Pulmonary nocardiosis is a rare opportunistic infection, with approximately 15 % of patients being immunocompetent. The isolation rate of Nocardia spp. has recently increased, indicating rising clinical concern. This study aimed to summarize computed tomography (CT) findings, evaluate treatment outcomes, and improve disease recognition.
Methods
We retrospectively analyzed 12 pulmonary nocardiosis cases recorded over 10 years in three hospitals, excluding two unclear cases. All pathogens were detected on smears and isolated from respiratory specimens.
Results
The mean age was 73.0 ± 12.9 years, with 9 men and 6 smokers. Among the included patients, 8 had underlying pulmonary diseases, 4 had non-pulmonary diseases, and 3 were on steroids. The most common species were N. cyriacigeorgica and N. nova. CT findings included cavitary, consolidation/infiltrative, and nodular-bronchiectatic (NB) patterns. The NB pattern, particularly common in immunocompetent patients, was associated with significantly better treatment outcomes than non-NB patterns (Fisher's exact test, p = 0.0476). All isolates were susceptible to trimethoprim/sulfamethoxazole. Eight patients recovered with appropriate antimicrobial therapy, while two patients died.
Conclusions
Pulmonary nocardiosis presented three CT patterns, with the NB pattern being the most frequent and showing favorable treatment outcomes, especially in immunocompetent patients. While Nocardia spp. can develop in patients with preexisting bronchiectasis, it may also independently cause bronchiectasis. Nocardia infection should be considered as a differential diagnosis in patients exhibiting the NB pattern, resembling that of nontuberculous mycobacterial pulmonary diseases.
{"title":"Nodular-bronchiectatic pattern in pulmonary nocardiosis: Immune status and treatment outcomes in a multicenter retrospective study","authors":"Airi Hasegawa , Kazuya Tone , Yuri Baba , Zenya Saito , Takuya Akutsu , Takaaki Kitayama , Shunsuke Inaki , Mina Gochi , Takashi Yaguchi , Koichi Makimura , Masamichi Takagi , Jun Araya","doi":"10.1016/j.rmed.2024.107922","DOIUrl":"10.1016/j.rmed.2024.107922","url":null,"abstract":"<div><h3>Background</h3><div>Pulmonary nocardiosis is a rare opportunistic infection, with approximately 15 % of patients being immunocompetent. The isolation rate of <em>Nocardia</em> spp. has recently increased, indicating rising clinical concern. This study aimed to summarize computed tomography (CT) findings, evaluate treatment outcomes, and improve disease recognition.</div></div><div><h3>Methods</h3><div>We retrospectively analyzed 12 pulmonary nocardiosis cases recorded over 10 years in three hospitals, excluding two unclear cases. All pathogens were detected on smears and isolated from respiratory specimens.</div></div><div><h3>Results</h3><div>The mean age was 73.0 ± 12.9 years, with 9 men and 6 smokers. Among the included patients, 8 had underlying pulmonary diseases, 4 had non-pulmonary diseases, and 3 were on steroids. The most common species were <em>N. cyriacigeorgica</em> and <em>N. nova</em>. CT findings included cavitary, consolidation/infiltrative, and nodular-bronchiectatic (NB) patterns. The NB pattern, particularly common in immunocompetent patients, was associated with significantly better treatment outcomes than non-NB patterns (Fisher's exact test, <em>p</em> = 0.0476). All isolates were susceptible to trimethoprim/sulfamethoxazole. Eight patients recovered with appropriate antimicrobial therapy, while two patients died.</div></div><div><h3>Conclusions</h3><div>Pulmonary nocardiosis presented three CT patterns, with the NB pattern being the most frequent and showing favorable treatment outcomes, especially in immunocompetent patients. While <em>Nocardia</em> spp. can develop in patients with preexisting bronchiectasis, it may also independently cause bronchiectasis. <em>Nocardia</em> infection should be considered as a differential diagnosis in patients exhibiting the NB pattern, resembling that of nontuberculous mycobacterial pulmonary diseases.</div></div>","PeriodicalId":21057,"journal":{"name":"Respiratory medicine","volume":"237 ","pages":"Article 107922"},"PeriodicalIF":3.5,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142897245","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 : 2025-02-01DOI: 10.1016/j.rmed.2025.107948
R.J. van Kalsbeek , E.A.M. Feijen , D. Bresters , L.C.M. Kremer , S.M.F. Pluijm , O.A. Asogwa , E.van Dulmen-den Broeder , M.M. van den Heuvel-Eibrink , G.O. Janssens , W.J. Tissing , J.J. Loonen , S.J.C.M.M. Neggers , H.J.H. van der Pal , C.M. Ronckers , J.C. Teepen , A.C.H. de Vries , M. Louwerens , M. van der Heiden-van der Loo , S.M.P.J. Prevaes , A.B. Versluys
Background
Treatment for childhood cancer may increase the risk of long-term pulmonary complications and dysfunction. Pulmonary surveillance is recommended after established pulmonary toxic exposures, including bleomycin, busulfan, carmustine (BCNU), lomustine (CCNU), radiotherapy to a field exposing the lungs, and pulmonary surgery. However, the role of cyclophosphamide as a pulmonary toxic agent is debated.
Aim
To establish whether cyclophosphamide is associated with late pulmonary dysfunction among survivors of childhood cancer.
Methods
In this multicenter Dutch Childhood Cancer Survivor Study (DCCSS)-LATER 2 PULM sub-study, we included 828 survivors with a median follow-up of 26.6 years, treated with cyclophosphamide and/or established pulmonary toxic treatment, or neither. Pulmonary function tests were used to measure the primary outcomes of diffusion impairment (diffusing capacity for carbon monoxide (DLCO) z-score), restriction (total lung capacity (TLC) z-score), and obstruction (forced expiratory volume in the first second/forced vital capacity (FEV1/FVC) z-score). Secondary outcomes comprised chronic cough, recurrent respiratory tract infections, shortness of breath, and supplemental oxygen need.
Results
Diffusion and restrictive abnormalities were highly prevalent among those treated with established pulmonary toxic treatment, with cyclophosphamide (41.0 % and 50.4 %, respectively) and without (34.3 % and 41.9 %, respectively), and occurred less frequently in survivors treated with cyclophosphamide only (12.9 % and 7.3 %, respectively) or in survivor controls (9.9 % and 12.4 %, respectively). In multivariable analyses, cyclophosphamide did not have a clinically relevant effect on the primary or secondary outcomes.
Conclusions
This study suggests that cyclophosphamide is not associated with clinically relevant pulmonary dysfunction in long-term childhood cancer survivors.
{"title":"Cyclophosphamide is not associated with clinically relevant late pulmonary dysfunction in Dutch survivors of childhood cancer – The DCCSS-LATER 2 PULM sub-study","authors":"R.J. van Kalsbeek , E.A.M. Feijen , D. Bresters , L.C.M. Kremer , S.M.F. Pluijm , O.A. Asogwa , E.van Dulmen-den Broeder , M.M. van den Heuvel-Eibrink , G.O. Janssens , W.J. Tissing , J.J. Loonen , S.J.C.M.M. Neggers , H.J.H. van der Pal , C.M. Ronckers , J.C. Teepen , A.C.H. de Vries , M. Louwerens , M. van der Heiden-van der Loo , S.M.P.J. Prevaes , A.B. Versluys","doi":"10.1016/j.rmed.2025.107948","DOIUrl":"10.1016/j.rmed.2025.107948","url":null,"abstract":"<div><h3>Background</h3><div>Treatment for childhood cancer may increase the risk of long-term pulmonary complications and dysfunction. Pulmonary surveillance is recommended after established pulmonary toxic exposures, including bleomycin, busulfan, carmustine (BCNU), lomustine (CCNU), radiotherapy to a field exposing the lungs, and pulmonary surgery. However, the role of cyclophosphamide as a pulmonary toxic agent is debated.</div></div><div><h3>Aim</h3><div>To establish whether cyclophosphamide is associated with late pulmonary dysfunction among survivors of childhood cancer.</div></div><div><h3>Methods</h3><div>In this multicenter Dutch Childhood Cancer Survivor Study (DCCSS)-LATER 2 PULM sub-study, we included 828 survivors with a median follow-up of 26.6 years, treated with cyclophosphamide and/or established pulmonary toxic treatment, or neither. Pulmonary function tests were used to measure the primary outcomes of diffusion impairment (diffusing capacity for carbon monoxide (DLCO) z-score), restriction (total lung capacity (TLC) z-score), and obstruction (forced expiratory volume in the first second/forced vital capacity (FEV1/FVC) z-score). Secondary outcomes comprised chronic cough, recurrent respiratory tract infections, shortness of breath, and supplemental oxygen need.</div></div><div><h3>Results</h3><div>Diffusion and restrictive abnormalities were highly prevalent among those treated with established pulmonary toxic treatment, with cyclophosphamide (41.0 % and 50.4 %, respectively) and without (34.3 % and 41.9 %, respectively), and occurred less frequently in survivors treated with cyclophosphamide only (12.9 % and 7.3 %, respectively) or in survivor controls (9.9 % and 12.4 %, respectively). In multivariable analyses, cyclophosphamide did not have a clinically relevant effect on the primary or secondary outcomes.</div></div><div><h3>Conclusions</h3><div>This study suggests that cyclophosphamide is not associated with clinically relevant pulmonary dysfunction in long-term childhood cancer survivors.</div></div>","PeriodicalId":21057,"journal":{"name":"Respiratory medicine","volume":"237 ","pages":"Article 107948"},"PeriodicalIF":3.5,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142966437","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 : 2025-02-01DOI: 10.1016/j.rmed.2025.107944
Filippo F. Cosini , Diego Bagnasco , Fulvio Braido , G. Walter Canonica , Giovanni Passalacqua , Elisa Testino , Manlio Milanese
Background
Global Initiative for Asthma (GINA) recently recommends clinicians to reduce inhaled corticosteroid doses in patients with severe asthma who respond positively to monoclonal antibodies (MAbs).
Objective
As we operated this reduction even before the document, we analysed our cohort of subjects on treatment with a MAbs for at least 24 months.
Methods
Data stored in our electronic archive and at the 6-month follow-up (FU) were registered and patients’ adherence to asthma therapy was derived by electronic pharmacy claim database.
Results
Sixty-three subjects were enrolled. A complete asthma remission and reduction to GINA Step 3 was obtained in 41 % and 61 % of them, respectively. Non-adherent subjects to inhaled and oral asthma therapy were 45 % of them, with a higher percentage among those in complete remission (59 % vs 33 %).
Conclusion
In our cohort, stepping down asthma therapy from 5 to 3 level in severe asthmatic patients on Mabs is without any negative consequences on asthma control, even in the case of non-adherence.
{"title":"Background therapy in severe asthma on monoclonal antibody treatment in real life","authors":"Filippo F. Cosini , Diego Bagnasco , Fulvio Braido , G. Walter Canonica , Giovanni Passalacqua , Elisa Testino , Manlio Milanese","doi":"10.1016/j.rmed.2025.107944","DOIUrl":"10.1016/j.rmed.2025.107944","url":null,"abstract":"<div><h3>Background</h3><div>Global Initiative for Asthma (GINA) recently recommends clinicians to reduce inhaled corticosteroid doses in patients with severe asthma who respond positively to monoclonal antibodies (MAbs).</div></div><div><h3>Objective</h3><div>As we operated this reduction even before the document, we analysed our cohort of subjects on treatment with a MAbs for at least 24 months.</div></div><div><h3>Methods</h3><div>Data stored in our electronic archive and at the 6-month follow-up (FU) were registered and patients’ adherence to asthma therapy was derived by electronic pharmacy claim database.</div></div><div><h3>Results</h3><div>Sixty-three subjects were enrolled. A complete asthma remission and reduction to GINA Step 3 was obtained in 41 % and 61 % of them, respectively. Non-adherent subjects to inhaled and oral asthma therapy were 45 % of them, with a higher percentage among those in complete remission (59 % vs 33 %).</div></div><div><h3>Conclusion</h3><div>In our cohort<strong>,</strong> stepping down asthma therapy from 5 to 3 level in severe asthmatic patients on Mabs is without any negative consequences on asthma control, even in the case of non-adherence.</div></div>","PeriodicalId":21057,"journal":{"name":"Respiratory medicine","volume":"237 ","pages":"Article 107944"},"PeriodicalIF":3.5,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143178988","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}