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Lung Function and Safety Outcomes in Patients With Moderate-to-Severe COPD Treated With Ensifentrine 恩西芬汀治疗中重度COPD患者的肺功能和安全性结局
Pub Date : 2025-12-01 Epub Date: 2025-09-02 DOI: 10.1016/j.chpulm.2025.100210
Diego J. Maselli MD , Jessica Bon MD , Tara Rheault PhD, MPH , Amy Dixon PharmD , Daniel Reyner DrPH , Kathleen Rickard MD , Michael G. Lester MD

Background

Despite the use of maintenance therapies, many patients with COPD continue to experience persistent symptoms and impaired lung function. Ensifentrine is a novel, first-in-class selective dual inhibitor of phosphodiesterase (PDE) 3 and PDE4 with demonstrated nonsteroidal antiinflammatory activity and bronchodilatory effects.

Research Question

Does ensifentrine improve lung function among patients with COPD?

Study Design and Methods

This prespecified, pooled analysis of the phase 3, multicenter, randomized, double-anonymized, placebo-controlled Ensifentrine as a Novel Inhaled Nebulized COPD Therapy (ENHANCE-1 [NCT04535986] and ENHANCE-2 [NCT04542057]) trials evaluated the effect of ensifentrine on lung function and safety outcomes. The trials included patients 40 to 80 years of age with symptomatic moderate-to-severe COPD who received 3 mg twice-daily ensifentrine or placebo for 24 weeks.

Results

The pooled analysis included 975 patients treated with ensifentrine and 574 patients who received placebo. Ensifentrine significantly improved average FEV1 area under the curve over 12 hours at week 12 from baseline vs placebo (least squares [LS] mean difference, 90 mL). Rapid improvements in peak FEV1 were observed with ensifentrine treatment as early as day 1 (LS mean difference, 154 mL), which were sustained through week 24 compared with placebo (LS mean difference, 135 mL) (P < .0001 for all time points). Ensifentrine also demonstrated significant improvements across all other lung function parameters, including average FEV1 area under the curve from administration time to 4 hours (LS mean difference, 137 mL at week 12; P < .0001 for all time points), FEV1 area under the curve from 6 hours to 12 hours (LS mean difference, 59 mL at week 12; P < .0001), morning trough FEV1 (LS mean difference, 42 mL at week 12; P < .001), and evening trough FEV1 (LS mean difference, 56 mL at week 12; P < .0001). Ensifentrine was well tolerated, with adverse event rates similar to placebo.

Interpretation

Ensifentrine demonstrated early, sustained, and clinically significant improvements in lung function in a broad population and across all subgroups of patients with symptomatic moderate-to-severe COPD.
背景:尽管使用了维持治疗,许多COPD患者仍然经历持续的症状和肺功能受损。Ensifentrine是一种新型的,一流的选择性磷酸二酯酶(PDE) 3和PDE4双重抑制剂,具有非甾体抗炎活性和支气管扩张作用。研究问题:恩西芬碱能改善COPD患者的肺功能吗?研究设计和方法:这项预先指定的、多中心、随机、双匿名、安慰剂对照的3期试验(ENHANCE-1 [NCT04535986]和ENHANCE-2 [NCT04542057])的合并分析评估了Ensifentrine作为一种新型吸入雾化COPD治疗药物对肺功能和安全性的影响。这些试验包括40至80岁的有症状的中重度COPD患者,他们接受每日两次3毫克的恩西芬汀或安慰剂治疗,持续24周。结果合并分析包括975名接受恩西芬汀治疗的患者和574名接受安慰剂治疗的患者。与安慰剂相比,在第12周的12小时内,恩西芬汀显著改善了曲线下平均FEV1面积(最小二乘[LS]平均差值,90 mL)。早在第1天,就观察到埃西芬汀治疗对FEV1峰值的快速改善(LS平均差值为154 mL),与安慰剂(LS平均差值为135 mL)相比,这种改善持续到第24周(所有时间点的P <; 0.0001)。Ensifentrine还演示了所有其他显著改善肺功能参数,包括平均FEV1曲线下面积的管理时间4小时(LS平均差,在第12周137毫升;P & lt;。所有的时间点),FEV1曲线下面积的6小时至12小时(LS平均差,在第12周59毫升;P & lt;。),早上槽FEV1 (LS平均差,在第12周42毫升;P & lt;措施),和晚上槽FEV1 (LS平均差,在第12周56毫升;P < .0001)。恩西芬汀耐受性良好,不良事件发生率与安慰剂相似。在广泛的人群和有症状的中重度COPD患者的所有亚组中,恩西芬汀显示出早期、持续和临床显著的肺功能改善。
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引用次数: 0
Does a Patient-Centered Informational Video Impact Real-World Perception of Lung Cancer Screening Among At-Risk Veterans? 以患者为中心的信息视频是否会影响高危退伍军人对肺癌筛查的真实感知?
Pub Date : 2025-12-01 Epub Date: 2025-04-08 DOI: 10.1016/j.chpulm.2025.100169
Norah N. Zaza MD , Eduardo Lopez-Gutierrez BS , Dominic J. Vitello MD , Jessica Gardner BS , Thanh-Huyen T. Vu MD, PhD , Eleanor Riviera MSN , Sayyed Hamidi MD , Israel Rubinstein MD , Howard S. Gordon MD , David J. Bentrem MD
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引用次数: 0
Improved Risk Stratification Prior to Major Pulmonary Resection by Combining Peak Oxygen Uptake and Ventilatory Efficiency in a 9-Field Matrix 在9场矩阵中结合峰值摄氧量和通气效率改善大肺切除术前的风险分层
Pub Date : 2025-12-01 Epub Date: 2025-07-24 DOI: 10.1016/j.chpulm.2025.100192
Karolina Kristenson MD, PhD , Johan Hylander MD , Miklós Boros MD , Éva Tamás MD, PhD , Gabriel Högström MD, PhD , Kristofer Hedman MD, PhD

Background

Cardiopulmonary exercise testing (CPET) has a pivotal role in preoperative evaluation of patients before lung cancer surgery. As surgical and perioperative practice and functional diagnostics continuously evolve, it may be time to reevaluate and refine the use of CPET in this setting.

Research Question

Can risk assessment with CPET before lung cancer surgery be improved by combining 2 established CPET variables (percent predicted peak oxygen uptake [Vo2peak], and ventilatory efficiency, measured by minute ventilation [V˙E]/carbon dioxide elimination [Vco2] slope) while using recently suggested optimal threshold values for these variables?

Study Design and Methods

Single-center, retrospective analysis of 208 patients with lung cancer who underwent preoperative CPET in 2008 to 2020. The main outcome was any major pulmonary complication (MPC) or death within 30 days of surgery. We combined previously suggested threshold values of percent predicted Vo2peak and V˙E/Vco2 slope, defined with a focus on high sensitivity and specificity. For each measure, patients were categorized into 3 groups based on these thresholds, yielding a proposed 9-field matrix for risk assessment. The frequency of complications between groups was compared using the χ2 test.

Results

Overall, 29 patients (14%) suffered an MPC and 3 died. The frequency of complications differed between groups based on the 9-field matrix in patients who underwent lobectomy or pulmectomy (P < .001). No patient with both favorable percent predicted Vo2peak and V˙E/Vco2 slope values experienced MPC or death, whereas worsening values in both percent predicted Vo2peak and V˙E/Vco2 slope were associated with an increasing frequency of adverse outcomes.

Interpretation

The proposed 9-field matrix for risk assessment was able to demonstrate a synergistic effect between V˙E/Vco2 slope and percent predicted Vo2peak for identifying patients who suffered major pulmonary complications or death within 30 days of cancer lobectomy or pulmectomy. These results further improve and help nuance risk assessment in these patients.
背景:心肺运动试验(CPET)在肺癌手术前患者的术前评估中具有关键作用。随着手术和围手术期实践以及功能诊断的不断发展,可能是时候重新评估和完善CPET在这种情况下的应用了。研究问题:结合两个已建立的CPET变量(预测峰值摄氧量百分比[Vo2peak]和通气效率,通过分钟通气[V˙E]/二氧化碳消除[Vco2]斜率测量),并使用最近建议的这些变量的最佳阈值,是否可以改善肺癌手术前CPET的风险评估?研究设计与方法对2008年至2020年行术前CPET的208例肺癌患者进行单中心回顾性分析。主要观察结果为手术30天内的肺部并发症(MPC)或死亡。我们将先前提出的预测vo2峰值百分比阈值和V˙E/Vco2斜率相结合,以高灵敏度和特异性为重点。对于每项测量,根据这些阈值将患者分为3组,产生一个建议的9字段矩阵用于风险评估。两组患者并发症发生率比较采用χ2检验。结果29例(14%)患者发生MPC, 3例死亡。在肺叶切除术和肺叶切除术患者中,基于9场基质的并发症发生率在两组之间存在差异(P < .001)。预测vo2峰值和V˙E/Vco2斜率值均为有利的患者没有发生MPC或死亡,而预测vo2峰值和V˙E/Vco2斜率值均为恶化的患者与不良结局的频率增加有关。提出的9场风险评估矩阵能够证明V˙E/Vco2斜率和预测vo2峰值百分比之间的协同效应,用于识别患有主要肺部并发症或在癌症肺叶切除术或肺叶切除术后30天内死亡的患者。这些结果进一步改善并有助于这些患者的风险评估。
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引用次数: 0
Communication of Lung Cancer Screening Results 肺癌筛查结果的交流
Pub Date : 2025-12-01 Epub Date: 2025-05-24 DOI: 10.1016/j.chpulm.2025.100183
Elena Vlachos DO , John Dell’Italia PhD , Kristina Crothers MD , Nicholas Maurice MD , Nichole T. Tanner MD, MSCR
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引用次数: 0
Association of Pulse Dose Corticosteroids With Outcomes Among Patients With Acute Exacerbations of Idiopathic Pulmonary Fibrosis 特发性肺纤维化急性加重患者脉冲剂量皮质类固醇与预后的关系
Pub Date : 2025-12-01 Epub Date: 2025-08-18 DOI: 10.1016/j.chpulm.2025.100207
Divya A. Shankar MD , Nicholas A. Bosch MD , S. Reza Jafarzadeh DVM, MPVM, PhD , Mari-Lynn Drainoni PhD, MEd , Renda Soylemez Wiener MD, MPH , Kevin C. Wilson MD , Finn J. Hawkins MBBCh , Konstantinos-Dionysios Alysandratos MD, PhD , Allan J. Walkey MD , Anica C. Law MD

Background

Corticosteroids are a mainstay of treatment for acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF), but dosing practices vary. We leveraged between-hospital variation in propensity to administer pulse dose corticosteroids to determine the association between pulse dose corticosteroids and patient outcomes in AE-IPF.

Research Question

Do outcomes differ for hospitalized patients who recieve pulse dose corticosteroids vs low dose corticosteroids for AE-IPF?

Study Design and Methods

We designed an instrumental variable study informed by a target trial framework using the Premier Healthcare Database (2016-2022). We identified adults ≥ 50 years of age with AE-IPF who received a dose of IV methylprednisolone within 2 days of admission. Our exposure of interest was receipt of pulse dose methylprednisolone (≥ 250 mg); our instrument was admission to a hospital with high use of pulse dosing. We assessed association with in-hospital death/discharge to hospice and discharge home without invasive mechanical ventilation. In subgroup analyses, we tested for interaction with unit of admission (admission to ICU/intermediate care units vs ward units).

Results

We identified 3,049 patients with AE-IPF at 177 US hospitals (pulse dose: n = 1,094; low dose: n = 1,955). Patients who received a pulse dose vs low dose had a risk difference for death/hospice of 1.2% (95% CI, −6.0% to 8.5%); for discharge home without invasive mechanical ventilation, this was 5.3% (95% CI, −2.6% to 13.1%). In subgroup analysis, receipt of pulse dosing was associated with differential risk of death/hospice by admission unit (risk difference: ICU/intermediate care: 26.3%; 95% CI, 10.1%-42.6% vs ward units: 0.1%; 95% CI, −11.1% to 11.3%; P interaction = .009), but not with differential risk of discharge home without invasive mechanical ventilation (P interaction = .18).

Interpretation

We observed no significant benefit or harm associated with the receipt of pulse dose corticosteroids for patients with AE-IPF. However, in the subgroup of patients admitted to ICU/intermediate care, there was an increased risk of in-hospital death/discharge to hospice. Future studies should explore the use of pulse vs low-dose corticosteroids in critically ill populations with AE-IPF.
背景:皮质类固醇是特发性肺纤维化急性加重(AE-IPF)的主要治疗方法,但剂量不同。我们利用医院间使用脉冲剂量皮质类固醇倾向的差异来确定脉冲剂量皮质类固醇与AE-IPF患者预后之间的关系。AE-IPF住院患者接受脉冲剂量糖皮质激素治疗与低剂量糖皮质激素治疗的结果是否不同?研究设计和方法我们设计了一项工具变量研究,该研究采用了Premier Healthcare数据库(2016-2022)的目标试验框架。我们确定了≥50岁患有AE-IPF的成年人,他们在入院2天内接受了一剂静脉注射甲基强的松龙。我们感兴趣的暴露是接受脉冲剂量甲基强的松龙(≥250 mg);我们的仪器被送入一家脉冲剂量使用率很高的医院。我们评估了院内死亡/出院到临终关怀和出院回家无创机械通气的相关性。在亚组分析中,我们测试了入院单位(ICU/中级护理单位与病房)的相互作用。结果:我们在美国177家医院鉴定了3049例AE-IPF患者(脉冲剂量:n = 1094;低剂量:n = 1955)。接受脉冲剂量与低剂量的患者死亡/临终关怀的风险差异为1.2% (95% CI, - 6.0%至8.5%);对于无创机械通气出院的患者,这一比例为5.3% (95% CI,−2.6%至13.1%)。在亚组分析中,接受脉冲剂量与住院单位的死亡/临终关怀差异风险相关(风险差异:ICU/中级护理:26.3%;95% CI, 10.1%-42.6%;病房单位:0.1%;95% CI, - 11.1%至11.3%;P交互作用= 0.009),但与无创机械通气出院的差异风险无关(P交互作用= 0.18)。解释:我们观察到对AE-IPF患者接受脉冲剂量皮质类固醇没有显著的益处或危害。然而,在ICU/中级护理患者亚组中,住院死亡/出院至临终关怀的风险增加。未来的研究应探讨在AE-IPF危重患者中使用脉冲糖皮质激素与低剂量糖皮质激素的对比。
{"title":"Association of Pulse Dose Corticosteroids With Outcomes Among Patients With Acute Exacerbations of Idiopathic Pulmonary Fibrosis","authors":"Divya A. Shankar MD ,&nbsp;Nicholas A. Bosch MD ,&nbsp;S. Reza Jafarzadeh DVM, MPVM, PhD ,&nbsp;Mari-Lynn Drainoni PhD, MEd ,&nbsp;Renda Soylemez Wiener MD, MPH ,&nbsp;Kevin C. Wilson MD ,&nbsp;Finn J. Hawkins MBBCh ,&nbsp;Konstantinos-Dionysios Alysandratos MD, PhD ,&nbsp;Allan J. Walkey MD ,&nbsp;Anica C. Law MD","doi":"10.1016/j.chpulm.2025.100207","DOIUrl":"10.1016/j.chpulm.2025.100207","url":null,"abstract":"<div><h3>Background</h3><div>Corticosteroids are a mainstay of treatment for acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF), but dosing practices vary. We leveraged between-hospital variation in propensity to administer pulse dose corticosteroids to determine the association between pulse dose corticosteroids and patient outcomes in AE-IPF.</div></div><div><h3>Research Question</h3><div>Do outcomes differ for hospitalized patients who recieve pulse dose corticosteroids vs low dose corticosteroids for AE-IPF?</div></div><div><h3>Study Design and Methods</h3><div>We designed an instrumental variable study informed by a target trial framework using the Premier Healthcare Database (2016-2022). We identified adults ≥ 50 years of age with AE-IPF who received a dose of IV methylprednisolone within 2 days of admission. Our exposure of interest was receipt of pulse dose methylprednisolone (≥ 250 mg); our instrument was admission to a hospital with high use of pulse dosing. We assessed association with in-hospital death/discharge to hospice and discharge home without invasive mechanical ventilation. In subgroup analyses, we tested for interaction with unit of admission (admission to ICU/intermediate care units vs ward units).</div></div><div><h3>Results</h3><div>We identified 3,049 patients with AE-IPF at 177 US hospitals (pulse dose: n = 1,094; low dose: n = 1,955). Patients who received a pulse dose vs low dose had a risk difference for death/hospice of 1.2% (95% CI, −6.0% to 8.5%); for discharge home without invasive mechanical ventilation, this was 5.3% (95% CI, −2.6% to 13.1%). In subgroup analysis, receipt of pulse dosing was associated with differential risk of death/hospice by admission unit (risk difference: ICU/intermediate care: 26.3%; 95% CI, 10.1%-42.6% vs ward units: 0.1%; 95% CI, −11.1% to 11.3%; <em>P</em> interaction = .009), but not with differential risk of discharge home without invasive mechanical ventilation (<em>P</em> interaction = .18).</div></div><div><h3>Interpretation</h3><div>We observed no significant benefit or harm associated with the receipt of pulse dose corticosteroids for patients with AE-IPF. However, in the subgroup of patients admitted to ICU/intermediate care, there was an increased risk of in-hospital death/discharge to hospice. Future studies should explore the use of pulse vs low-dose corticosteroids in critically ill populations with AE-IPF.</div></div>","PeriodicalId":94286,"journal":{"name":"CHEST pulmonary","volume":"3 4","pages":"Article 100207"},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145747465","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Long-Term Prognosis of Resected Stage 1 Lung Adenocarcinoma With Radiomics, Regionality, and Histopathologic Correlation 切除的1期肺腺癌的放射组学、地域性和组织病理学相关性的长期预后
Pub Date : 2025-12-01 Epub Date: 2025-01-22 DOI: 10.1016/j.chpulm.2025.100139
Abdelmohaymin Abdalla MBBS , Srinivasan Rajagopalan PhD , Tobias Peikert MD , Jennifer M. Boland MD , Nan Zhang MS , Brain Bartholmai MD , Cyril Varghese MD

Background

The discovery of adenocarcinoma (AC) spectrum nodules often leads to a pathway of ongoing radiologic observation, tissue biopsy, ablative therapies, or surgical excision. This complex decision-making process may be aided by machine learning. The Score Indicative of Lung Cancer Aggression was developed and validated as an evolution of previously developed radiomics models to predict the degree of histologic tumor invasion in AC and to predict patient survival. We now investigate if radiomics classification can help predict long-term outcomes after stage I AC resection. Secondarily, we explore if the geographic location of stage 1 AC nodules correlates with local invasion or long-term outcomes.

Research Question

Can radiomics predict long-term outcomes in stage 1 lung adenocarcinoma after curative surgical resection?

Study Design and Methods

A total of 196 patients with early stage AC who underwent curative surgical resection were studied over a follow-up median period of 12 years. Kaplan-Meier analysis of disease-free survival was performed on patients whose index nodule was categorized by radiomics. Local invasion of tumor was analyzed using radiomics and histopathologic assessment. The correlation of these metrics relating to the nodule’s geographic location was explored. Finally, disease-free survival analysis based on the location of the index nodule was performed.

Results

Patients whose stage I AC nodules were classified as poor before resection by our radiomics tool had worse long-term prognosis (> 5 years) than those classified as intermediate or good. AC nodules in lower lung regions were proportionately more invasive than nodules in the upper lung regions, both based on radiomics and histopathologic review. However, that did not translate to a disease-free survival advantage for upper lobe nodules that were resected.

Interpretation

Our results indicate that radiomics helps prognosticate long-term outcomes in patients with resected stage I AC. Furthermore, histopathologic invasion detected by radiomics seems to vary depending on geographic location of the nodule in the lung.
背景:腺癌(AC)谱结节的发现通常需要持续的放射学观察、组织活检、消融治疗或手术切除。这种复杂的决策过程可能会得到机器学习的帮助。肺癌侵袭评分(Score indication of Lung Cancer Aggression)是在先前开发的放射组学模型的基础上发展而来的,用于预测AC的组织学肿瘤侵袭程度和预测患者生存。我们现在研究放射组学分类是否可以帮助预测I期AC切除术后的长期预后。其次,我们探讨了1期AC结节的地理位置是否与局部侵袭或长期预后相关。放射组学能否预测一期肺腺癌根治性手术切除后的长期预后?研究设计和方法共对196例接受根治性手术切除的早期AC患者进行了为期12年的随访研究。通过放射组学对指数结节进行分类的患者进行Kaplan-Meier无病生存分析。采用放射组学和组织病理学分析肿瘤的局部浸润情况。探讨了这些指标与结节地理位置的相关性。最后,根据指标结节的位置进行无病生存分析。结果放疗组学工具将I期AC结节分类为切除前不良的患者远期预后(5年)较分类为中等或良好的患者差。根据放射组学和组织病理学检查,下肺区域的AC结节比上肺区域的结节更具侵袭性。然而,这并不能转化为切除上肺叶结节的无病生存优势。我们的研究结果表明,放射组学有助于预测切除的I期AC患者的长期预后。此外,放射组学检测到的组织病理学侵袭似乎取决于肺中结节的地理位置。
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引用次数: 0
Lung Ultrasound for Predicting Resolution of Transient Tachypnea of the Newborn 肺超声预测新生儿短暂性呼吸急促的缓解
Pub Date : 2025-12-01 Epub Date: 2025-09-30 DOI: 10.1016/j.chpulm.2025.100216
Amanjot Kaur MD , Deeksha Gupta MD, DM , Mayank Priyadarshi MD, DM , Suman Chaurasia MD, PhD , Poonam Singh MD, DNB , Nowneet Kumar Bhat MD , Sriparna Basu MD, FRCPCH

Background

Transient tachypnea of the newborn (TTN) is a self-limited condition, but can persist for prolonged durations. None of the existing tools can accurately predict the timing of TTN resolution.

Research Question

In term and late preterm neonates (population), can lung ultrasound (LUS) score (index test) predict delayed resolution of TTN, defined as persistence of respiratory distress beyond 6 hours of age (disease), monitored with Downes score (reference test)?

Study Design and Methods

In this prospective study, term and late preterm neonates requiring neonatal ICU admission with a diagnosis of TTN were included. Respiratory distress was monitored with hourly Downes score, and resolution was noted when Downes score was 0 in the neonate not requiring any respiratory support. Baseline characteristics, physiological monitoring, respiratory support parameters, and LUS clips were recorded within 2 hours of age and compared between early and delayed resolution groups. LUS findings were neither revealed to the treating team, nor used in the management of neonates. LUS scoring was later performed by blinded assessors.

Results

Among 113 enrolled neonates, 37 (32.7%) had delayed resolution of TTN. The mean birth weight and gestation were lower in the delayed resolution group, along with a higher requirement for resuscitation at birth. The median LUS score was significantly higher in the delayed (7; interquartile range, 5.5-9) compared with the early resolution group (4; interquartile range, 2-5.5). The diagnostic accuracy of LUS score was determined by receiver operating characteristic curve analysis (area under the curve, 0.84; 95% CI, 0.76-0.92; P < .01). An LUS score ≥ 6 was considered an optimal cutoff for prediction of delayed TTN resolution (sensitivity, 73%; 95% CI, 56-86; specificity, 80%; 95% CI, 70-89).

Interpretation

LUS is a promising tool to predict delayed resolution of TTN. Early prediction of TTN resolution may guide decision for neonatal ICU admission and help avoid unnecessary admissions in cases likely to resolve within 6 hours.
背景:新生儿短暂性呼吸急促(TTN)是一种自限性疾病,但可以持续较长时间。现有的工具都不能准确预测TTN分辨率的时间。研究问题:在足月和晚期早产儿(人群)中,肺超声(LUS)评分(指数测试)能否预测TTN的延迟缓解,TTN的定义是呼吸窘迫持续超过6小时(疾病),用唐斯评分(参考测试)监测?研究设计和方法在这项前瞻性研究中,纳入了诊断为TTN需要新生儿ICU住院的足月和晚期早产儿。采用每小时唐斯评分监测呼吸窘迫,当唐斯评分为0时,不需要任何呼吸支持的新生儿呼吸窘迫得到缓解。在2小时内记录基线特征、生理监测、呼吸支持参数和LUS剪辑,并比较早期和延迟消退组。LUS的发现既没有透露给治疗小组,也没有用于新生儿的管理。LUS评分随后由盲法评估员进行。结果113例新生儿中,37例(32.7%)出现TTN延迟消退。延迟解决组的平均出生体重和妊娠期较低,出生时对复苏的要求较高。延迟组的中位LUS评分(7分,四分位范围5.5-9)明显高于早期解决组(4分,四分位范围2-5.5)。LUS评分的诊断准确性通过受试者工作特征曲线分析确定(曲线下面积,0.84;95% CI, 0.76-0.92; P < 0.01)。LUS评分≥6被认为是预测延迟TTN分辨率的最佳截止值(敏感性,73%;95% CI, 56-86;特异性,80%;95% CI, 70-89)。解释lus是预测TTN延迟分辨率的一种很有前途的工具。TTN解决的早期预测可以指导新生儿ICU入院的决定,并有助于避免可能在6小时内解决的病例不必要的入院。
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引用次数: 0
Rapid Metagenomic Sequencing of Bronchoalveolar Lavage Fluid for Diagnosis of Infection in Patients With Hematologic Malignancies and Pulmonary Complications 支气管肺泡灌洗液快速宏基因组测序诊断血液学恶性肿瘤和肺部并发症患者感染
Pub Date : 2025-12-01 Epub Date: 2025-05-30 DOI: 10.1016/j.chpulm.2025.100173
Matthew K. Hensley MD, MPH, Khaled Sayed PhD, Ghady Haidar MD, Xiaohong Wang RN, Panayiotis V. Benos PhD, Sawa Ito MD, PhD, Annie Im MD, Emily Geramita MD, PhD, Warren Shlomchik MD, Barbara Methé PhD, Charles Dela Cruz MD, PhD, Alison Morris MD, MS, Georgios D. Kitsios MD, PhD

Background

Diagnosing pulmonary complications (PCs) in hematologic malignancies remains challenging due to insensitive conventional microbiologic testing (CMT) and overlapping clinical manifestations of infectious and noninfectious pulmonary complications. For these reasons, empirical antimicrobials and immunosuppression (eg, corticosteroids) are used for prolonged periods.

Research Question

How does metagenomic sequencing of the lower respiratory tract compare with conventional microbiologic testing among patients with hematologic malignancy?

Study Design and Methods

Prospective proof-of-concept cohort study of 30 adult inpatients with hematologic malignancies and PCs who underwent bronchoscopy for suspected lower respiratory tract infection.

Results

CMT identified a pathogen via culture- or polymerase chain reaction-based testing in 53% of patients. 16S sequencing demonstrated 66.7% positive and 42.9% negative concordance with CMT, while also identifying additional plausible respiratory pathogens in 59.3% of patients. Nanopore demonstrated 6.7% positive and 87.5% negative concordance with CMT and identified additional plausible respiratory pathogens in 42.3% of patients.

Interpretation

Culture-independent sequencing approaches had modest agreement with CMT when considering bacterial PCs and showed poor detection of fungal pathogens. Sequencing frequently identified additional plausible respiratory pathogens, and further validation is needed to determine if such detection represents clinically missed infections or nonpathogenic colonization.
由于常规微生物检测(CMT)不敏感以及感染性和非感染性肺部并发症的重叠临床表现,诊断血液学恶性肿瘤的肺部并发症(PCs)仍然具有挑战性。由于这些原因,经验性抗菌剂和免疫抑制(如皮质类固醇)被长期使用。研究问题:恶性血液病患者的下呼吸道宏基因组测序与常规微生物学检测比较如何?研究设计与方法前瞻性概念验证队列研究,纳入30例因怀疑下呼吸道感染而行支气管镜检查的成年恶性血液病和pc住院患者。结果scmt通过基于培养或聚合酶链反应的检测在53%的患者中鉴定出病原体。16S测序结果显示,66.7%的患者与CMT呈阳性,42.9%的患者与CMT呈阴性,同时在59.3%的患者中还发现了其他可能的呼吸道病原体。在42.3%的患者中,纳米孔与CMT的一致性为6.7%阳性和87.5%阴性,并鉴定出额外的疑似呼吸道病原体。当考虑细菌pc时,培养独立测序方法与CMT有一定的一致性,并且显示真菌病原体的检测较差。测序经常发现其他可能的呼吸道病原体,需要进一步验证,以确定这种检测是否代表临床漏诊感染或非致病性定植。
{"title":"Rapid Metagenomic Sequencing of Bronchoalveolar Lavage Fluid for Diagnosis of Infection in Patients With Hematologic Malignancies and Pulmonary Complications","authors":"Matthew K. Hensley MD, MPH,&nbsp;Khaled Sayed PhD,&nbsp;Ghady Haidar MD,&nbsp;Xiaohong Wang RN,&nbsp;Panayiotis V. Benos PhD,&nbsp;Sawa Ito MD, PhD,&nbsp;Annie Im MD,&nbsp;Emily Geramita MD, PhD,&nbsp;Warren Shlomchik MD,&nbsp;Barbara Methé PhD,&nbsp;Charles Dela Cruz MD, PhD,&nbsp;Alison Morris MD, MS,&nbsp;Georgios D. Kitsios MD, PhD","doi":"10.1016/j.chpulm.2025.100173","DOIUrl":"10.1016/j.chpulm.2025.100173","url":null,"abstract":"<div><h3>Background</h3><div>Diagnosing pulmonary complications (PCs) in hematologic malignancies remains challenging due to insensitive conventional microbiologic testing (CMT) and overlapping clinical manifestations of infectious and noninfectious pulmonary complications. For these reasons, empirical antimicrobials and immunosuppression (eg, corticosteroids) are used for prolonged periods.</div></div><div><h3>Research Question</h3><div>How does metagenomic sequencing of the lower respiratory tract compare with conventional microbiologic testing among patients with hematologic malignancy?</div></div><div><h3>Study Design and Methods</h3><div>Prospective proof-of-concept cohort study of 30 adult inpatients with hematologic malignancies and PCs who underwent bronchoscopy for suspected lower respiratory tract infection.</div></div><div><h3>Results</h3><div>CMT identified a pathogen via culture- or polymerase chain reaction-based testing in 53% of patients. 16S sequencing demonstrated 66.7% positive and 42.9% negative concordance with CMT, while also identifying additional plausible respiratory pathogens in 59.3% of patients. Nanopore demonstrated 6.7% positive and 87.5% negative concordance with CMT and identified additional plausible respiratory pathogens in 42.3% of patients.</div></div><div><h3>Interpretation</h3><div>Culture-independent sequencing approaches had modest agreement with CMT when considering bacterial PCs and showed poor detection of fungal pathogens. Sequencing frequently identified additional plausible respiratory pathogens, and further validation is needed to determine if such detection represents clinically missed infections or nonpathogenic colonization.</div></div>","PeriodicalId":94286,"journal":{"name":"CHEST pulmonary","volume":"3 4","pages":"Article 100173"},"PeriodicalIF":0.0,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145624053","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Impact of Self-Contained Underwater Breathing Apparatus Diving on French Military Divers’ Lung Function 自给式水下呼吸器潜水对法国军用潜水员肺功能的影响
Pub Date : 2025-12-01 Epub Date: 2025-03-24 DOI: 10.1016/j.chpulm.2025.100158
Justin Ulm MD, MPH , Jean-Eric Blatteau MD , Luc Aigle MD , Roman Glogowski MD , Olivier Castagna MD, PhD , Arnaud Druelle MD

Background

Although acute risks concerning underwater divers are well documented, the literature regarding the long-term impacts on pulmonary function remains inconclusive. Although oxygen toxicity at high partial pressures is established for patients in intensive care, the impact of diving seems limited.

Research Question

What are the long-term effects of self-contained underwater breathing apparatus diving on pulmonary function in military divers?

Study Design and Methods

This longitudinal study used routinely collected data from Sainte-Anne Military Teaching Hospital, Toulon, France, over a 20-year follow-up period. We expressed spirometric measures as a percentage of predicted values to account for age, height, and ethnicity, and analyzed them using mixed-effects models. The impact of diving is assessed for different gas and diving apparatus. Other included variables were atopy, tobacco use, and BMI.

Results

A total of 331 divers were included (2,685 spirometric measurements), with an average follow-up of 23.9 years and 2,491 dives. Only male divers met inclusion criteria. Baseline FEV1 matched predicted values (100.00%; SD, 11.98). Every 1,000 dives, FEV1 increased by 3.21% (95% CI, 2.73-3.68; P < .001), regardless of gas or apparatus. FVC (3.02%; 95% CI, 2.52-3.53; P < .001) and forced expiratory flow when 75% of forced expiratory vital capacity has been exhaled (10.12%; 95% CI, 8.29-11.95; P < .001) increased, whereas FEV1/FVC remained stable. Each BMI point increase was associated with a 0.51% rise in FVC (P = .010) and 0.38% rise in FEV1 (P = .032), whereas each pack-year was associated with a 1.12% decline in forced expiratory flow when 75% of forced expiratory vital capacity has been exhaled (P = .005).

Interpretation

Our results show that self-contained underwater breathing apparatus diving is associated with increased pulmonary flows and volumes in this population of military divers. Prospective studies could explore the role of unmeasured confounding factors and could significantly contribute to health policies for both military and civilian divers.
尽管水下潜水者的急性风险有充分的文献记载,但关于其对肺功能的长期影响的文献尚无定论。虽然高分压下的氧毒性对重症监护病人是确定的,但潜水的影响似乎有限。研究问题自给式水下呼吸器潜水对军事潜水员肺功能的长期影响是什么?研究设计和方法本纵向研究使用了从法国土伦圣安妮军事教学医院常规收集的数据,随访20年。我们将肺活量测量值表示为预测值的百分比,以考虑年龄、身高和种族,并使用混合效应模型对其进行分析。对不同气体和潜水设备对潜水的影响进行了评估。其他包括的变量包括特应性、吸烟和身体质量指数。结果共纳入331名潜水员(肺量测量2685次),平均随访23.9年,随访2491次。只有男性潜水员符合入选标准。基线FEV1符合预测值(100.00%;SD, 11.98)。无论使用气体或设备,每1000次潜水,FEV1增加3.21% (95% CI, 2.73-3.68; P < 0.001)。用力呼气肺活量达到75%时,FVC (3.02%; 95% CI, 2.52 ~ 3.53; P < .001)和用力呼气流量(10.12%;95% CI, 8.29 ~ 11.95; P < .001)增加,而FEV1/FVC保持稳定。BMI每增加一个点,FVC增加0.51% (P = 0.010), FEV1增加0.38% (P = 0.032),而用力呼气流量每增加一个包年,当75%的用力呼气活气量被呼出时,用力呼气流量下降1.12% (P = 0.005)。我们的研究结果表明,自给式水下呼吸器潜水与这群军事潜水员的肺流量和体积增加有关。前瞻性研究可以探索未测量的混杂因素的作用,并可以为军事和民用潜水员的卫生政策做出重大贡献。
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引用次数: 0
A 40-Year-Old Woman With an Incidentally Found Semisolid Pulmonary Nodule 一位40岁女性偶然发现半实性肺结节
Pub Date : 2025-12-01 Epub Date: 2025-07-21 DOI: 10.1016/j.chpulm.2025.100195
Joseph V. Moran DO , Amar Mainra MD , Tian Sun MD , Eric R. Montgomery MD , Lauren A. Rome MD , Michael J. Walker MD
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引用次数: 0
期刊
CHEST pulmonary
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