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Functional capacity and quality of life after telerehabilitation in post-tuberculosis lung disease: a randomized controlled trial. 结核性肺病患者远程康复后的功能能力和生活质量:一项随机对照试验
IF 3 4区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2026-02-02 eCollection Date: 2026-01-01 DOI: 10.36416/1806-3756/e20250222
Diego de Faria Magalhães Torres, Fernando Silva Guimarães, Nathanael Augusto Soares Meireles, Alexandre Pinto Cardoso, Giovanni Battista Migliori, Fernanda Carvalho de Queiroz Mello

Objective: Despite advances in diagnosis and treatment, approximately 50% of individuals affected by tuberculosis develop post-tuberculosis lung disease (PTLD), leading to functional limitations and reduced quality of life (QoL). Pulmonary rehabilitation programs have demonstrated benefits in patients with PTLD; however, access remains limited, and telerehabilitation may offer a cost-effective solution. This study sought to compare physical capacity and QoL in patients with PTLD following an eight-week telerehabilitation program.

Methods: This was a randomized controlled trial including 30 participants with confirmed PTLD. They were recruited and randomly assigned to an intervention group that received weekly telerehabilitation or a control group that received standard care. The interventions included aerobic training, breathing exercises, strength training, and stretching exercises. Physical capacity and QoL were assessed before and after the interventions by means of isokinetic dynamometry, the six-minute walk test, the five-repetition sit-to-stand test, spirometry, handgrip strength, the Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36), and the Saint George's Respiratory Questionnaire.

Results: After eight weeks, the intervention group showed significant improvements in all physical capacity parameters and QoL. Quadriceps strength correlated significantly with the physical functioning and mental health domains of the SF-36.

Conclusions: Our findings suggest that telerehabilitation is an effective approach for enhancing physical function and QoL in patients with PTLD.

目的:尽管诊断和治疗取得了进展,但大约50%的结核病患者会发展为结核后肺病(PTLD),导致功能限制和生活质量(QoL)降低。肺部康复计划已经证明对PTLD患者有益;然而,访问仍然有限,远程康复可能提供一种成本效益高的解决方案。本研究旨在比较PTLD患者在接受8周远程康复治疗后的体能和生活质量。方法:这是一项随机对照试验,包括30名确诊的PTLD患者。他们被招募并随机分配到每周接受远程康复治疗的干预组和接受标准治疗的对照组。干预措施包括有氧训练、呼吸练习、力量训练和伸展运动。通过等速动力学测量、6分钟步行测试、5次重复坐立测试、肺活量测定、握力、医学结局研究36项简短健康调查(SF-36)和圣乔治呼吸问卷评估干预前后的身体能力和生活质量。结果:干预组患者8周后各项体能指标及生活质量均有显著改善。股四头肌力量与SF-36的生理功能和心理健康领域显著相关。结论:远程康复是改善PTLD患者身体功能和生活质量的有效途径。
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引用次数: 0
Real-world evidence on diagnostic pathways and biopsy optimization for PD-L1 and molecular profiling in advanced non-small cell lung cancer: A four-year cohort analysis. 晚期非小细胞肺癌PD-L1的诊断途径和活检优化的现实证据和分子谱:一项为期四年的队列分析。
IF 3 4区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2026-02-02 eCollection Date: 2026-01-01 DOI: 10.36416/1806-3756/e20250188
Luís Vaz Rodrigues, Joana Oliveira, Joana Duarte, Luis Taborda-Barata, Vitor Sousa, Rosa Cordovilla

Objective: Efficient diagnostic pathways in advanced non-small cell lung cancer (NSCLC) are crucial for timely treatment initiation and improved outcomes. This study evaluated the impact of diagnostic delays and the role of minimally invasive techniques in biomarker assessment and survival in a real-world clinical cohort.

Methods: A retrospective cohort study was conducted involving 205 patients with advanced NSCLC diagnosed between January 2020 and December 2023. Diagnostic procedures included EBUS/EUS-B, transthoracic biopsy, and surgical biopsy. The time-to-diagnostic procedure, time-to-therapy, and survival were analyzed using multivariate models.

Results: The time interval to the first diagnostic procedure independently predicted mortality (HR=1.66; p=0.016). EBUS and EUS-B achieved significantly shorter diagnostic times (median 8 and 5 days, respectively) compared to transthoracic (20.5 days) and surgical (24.5 days) biopsies. These endoscopic techniques were also associated with shorter time intervals to systemic therapy initiation (p=0.011). Minimally invasive approaches provided sufficient tissue for complete morphological, immunohistochemical, and molecular profiling in most cases, with no significant differences in adequacy among procedures. Patients with actionable mutations had a 44% lower mortality risk (HR=0.56; p=0.013), while high PD-L1 expression was associated with a 56% reduction in mortality risk (HR=0.44; p=0.003).

Conclusions: Minimally invasive techniques, particularly EBUS and EUS-B, shortened diagnostic delays, ensured adequate biomarker sampling, and enabled earlier initiation of systemic therapy. Since the time-to-diagnosis was independently associated with survival, these approaches may have indirectly contributed to improved outcomes. Our findings highlight the importance of streamlining diagnostic pathways and expanding access to endoscopic methods to optimize care in advanced NSCLC.

目的:有效的晚期非小细胞肺癌(NSCLC)诊断途径对于及时开始治疗和改善预后至关重要。本研究在现实世界的临床队列中评估了诊断延迟的影响以及微创技术在生物标志物评估和生存中的作用。方法:对2020年1月至2023年12月诊断的205例晚期NSCLC患者进行回顾性队列研究。诊断方法包括EBUS/EUS-B、经胸活检和手术活检。使用多变量模型分析诊断时间、治疗时间和生存率。结果:第一次诊断手术的时间间隔独立预测死亡率(HR=1.66; p=0.016)。与经胸活检(20.5天)和手术活检(24.5天)相比,EBUS和EUS-B的诊断时间明显缩短(中位分别为8天和5天)。这些内镜技术也与较短的开始全身治疗的时间间隔相关(p=0.011)。在大多数情况下,微创方法提供了足够的组织进行完整的形态学、免疫组织化学和分子谱分析,不同方法在充分性方面没有显著差异。具有可操作突变的患者死亡风险降低44% (HR=0.56, p=0.013),而高PD-L1表达与死亡风险降低56%相关(HR=0.44, p=0.003)。结论:微创技术,特别是EBUS和EUS-B,缩短了诊断延迟,确保了足够的生物标志物采样,并使全身治疗能够更早开始。由于诊断时间与生存率独立相关,这些方法可能间接有助于改善预后。我们的研究结果强调了简化诊断途径和扩大内窥镜方法对优化晚期非小细胞肺癌护理的重要性。
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引用次数: 0
The importance of incorporating CFTR modulator therapy into the Brazilian public health system: one year of advances in cystic fibrosis care. 将CFTR调节剂治疗纳入巴西公共卫生系统的重要性:囊性纤维化治疗的一年进展
IF 3 4区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2026-02-02 DOI: 10.36416/1806-3756/e20250180
Renata Wrobel Folescu Cohen, Patrícia Fernandes Barreto Machado Costa, Katty Anne Carvalho Marins, Célia Regina Moutinho de Miranda Chaves, Tania Wrobel Folescu
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引用次数: 0
Step-by-step protocol for robotic cytoreductive surgery and hyperthermic intrathoracic chemotherapy. 一步一步的机器人细胞减少手术和胸内热化疗方案。
IF 3 4区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2026-02-02 DOI: 10.36416/1806-3756/e20250291
Paula Duarte D'Ambrosio, Gustavo Schvartsman, Bernard Marcel Barban, Ricardo Mingarini Terra
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引用次数: 0
Diagnostic performance, molecular analysis, and complications in CT-guided percutaneous biopsies of lung nodules with 20-gauge needles. 20号针ct引导下经皮肺结节活检的诊断表现、分子分析及并发症。
IF 3 4区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2026-02-02 DOI: 10.36416/1806-3756/e20250158
Priscila Mina Falsarella, Andre Dubinco, Marcelo da Rosa Bortot, Paulo Vidal Campregher, Renée Zon Filippi, Antonio Rahal Junior, Rodrigo Gobbo Garcia
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引用次数: 0
Reference equation for measurement of the maximal dynamic inspiratory muscle pressure index (S-Index) in healthy Brazilian adults. 巴西健康成人最大动态吸气肌压力指数(S-Index)测量的参考方程。
IF 3 4区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2026-02-02 eCollection Date: 2026-01-01 DOI: 10.36416/1806-3756/e20240312
Luis Felipe da Fonseca Reis, Cleber da Penha, Pamela do Carmo Dosso da Silva, Aline Oliveira Martins Soares de Mendonça, Ana Carolina Sebastião da Silva, Clara Pinto Diniz, Flavia Mazzoli-Rocha, Arthur de Sá Ferreira, Agnaldo José Lopes

Objectives: Several equations for calculating maximal inspiratory pressure (MIP) have been validated for the Brazilian population; however, none exist for maximal dynamic inspiratory muscle pressure (S-Index).

Methods: This cross-sectional study was conducted at two centers following approval by the institutional ethics committee. Healthy Brazilian adults were sequentially randomized to assess either the MIP or S-Index. Pulmonary function (spirometry), peripheral muscle strength (handgrip strength of the dominant upper limb - HGdUL), and physical activity level (IPAQ) were also evaluated. The S-Index and MIP values were reported as absolute values and compared using the Wilcoxon paired test. Multiple linear regression was used to develop reference equations. Lower limits of normality (LLNs) were stratified by sex and age using Z-scores, providing cut-off points to define inspiratory muscle weakness via the S-Index Deviation Score (SDS).

Results: The final sample comprised 214 eutrophic volunteers, 50% men, with a mean age of 43.1 ± 15.0 years. The median MIP was significantly higher than the median S-Index (97.2 [96.7-112.0] vs. 92.5 [80.0-105.0] cmH2O; p<0.001). The predicted equation for the S-Index, which used age, sex, and HGdUL as predictors, was: S-Index = 69.72 + 10.765×sex (men = 1; women = 0) - 0.211×age + 0.797×HGdUL. Additionally, the LLNs and cut-off points for ventilatory muscle weakness by sex and age group were established.

Conclusions: This study provides the first reference values for the S-Index in healthy, eutrophic Brazilian adults, including LLNs and cut-off points for diagnosing ventilatory muscle weakness.

目的:几个计算最大吸气压力(MIP)的公式已经在巴西人群中得到验证;而最大动态吸气肌压力(s指数)则不存在。方法:经机构伦理委员会批准,本横断面研究在两个中心进行。健康的巴西成年人依次随机评估MIP或s指数。肺功能(肺活量测定法)、外周肌力(优势上肢握力- HGdUL)和体力活动水平(IPAQ)也进行了评估。s指数和MIP值作为绝对值报告,并使用Wilcoxon配对检验进行比较。采用多元线性回归建立参考方程。使用z分数对正常下限(lln)按性别和年龄分层,通过s指数偏差评分(SDS)提供定义吸气肌无力的截止点。结果:最终样本包括214名富营养化志愿者,其中50%为男性,平均年龄为43.1±15.0岁。中位MIP显著高于中位s指数(97.2 [96.7-112.0]vs. 92.5 [80.0-105.0] cmH2O)。结论:本研究为健康、富营养化的巴西成年人的s指数提供了第一个参考值,包括lln和诊断通气肌无力的分界点。
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引用次数: 0
Impact of new regimens and drugs on rifampin-resistant tuberculosis management in Mexico. 新方案和药物对墨西哥耐利福平结核病管理的影响。
IF 3 4区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-12-12 eCollection Date: 2025-01-01 DOI: 10.36416/1806-3756/e20250131
Marcela Muñoz-Torrico, Rafael Laniado-Laborín, Jorge Rojas-Serrano, Eduardo Becerril-Vargas, Wendy Cinecio-Chávez, Fátima Leticia Luna-López, Luis Armando Narvaez-Díaz, Roberto Rentería-Gamez, Mariela Segura Del Pilar, Nallely Saavedra, Julio César Magaña, Lia D'Ambrosio, Rosella Centis, José Antonio Caminero, Giovanni Battista Migliori

Objective: To compare the former tuberculosis treatment regimen including one fluoroquinolone (ofloxacin, levofloxacin, or moxifloxacin) and a second-line injectable drug (amikacin, kanamycin, or capreomycin) plus three to five oral drugs (regimen 1) with the current regimen including the three WHO group A drugs (regimen 2) in terms of efficacy and safety at two tuberculosis referral centers in Mexico.

Methods: This was a retrospective study based on a review of the clinical records of all consecutive rifampin-resistant or multidrug-resistant tuberculosis (RR/MDR-TB) patients treated from January of 2010 to October of 2023. Patients included were microbiologically confirmed cases of RR/MDR-TB with pulmonary involvement and who received at least 30 days of regimen 1 or regimen 2. Outcomes and adverse events were classified in accordance with WHO definitions.

Results: One hundred and twenty-six RR/MDR-TB patients met the inclusion criteria. Of those, 87 were treated with regimen 1 and 39 received regimen 2. Success rates were not significantly different between the two groups of patients, although those treated with the oral regimen including bedaquiline from regimen 2 had higher success rates. Regimen 2 patients experienced a shorter time to culture conversion, and the regimen length was shortened accordingly, the median duration being 16.1 months [IQR, 15-17.3 months]. In patients receiving the all-oral regimen 2, adverse events were significantly associated with a history of type 2 diabetes mellitus (OR = 15.4; 95% CI, 2.73-87.29; p = 0.002) and were mainly related to linezolid use.

Conclusions: Oral regimens appear to be effective, although toxicity to linezolid requires strict patient monitoring.

目的:比较墨西哥两家结核病转诊中心以前采用一种氟喹诺酮类药物(氧氟沙星、左氧氟沙星或莫西沙星)和一种二线注射药物(阿米卡星、卡那霉素或卷曲霉素)加三到五种口服药物(方案1)的结核病治疗方案与目前采用的包括三种WHO a类药物(方案2)的结核病治疗方案的疗效和安全性。方法:这是一项回顾性研究,基于2010年1月至2023年10月期间所有连续治疗的利福平耐药或耐多药结核病(RR/MDR-TB)患者的临床记录。纳入的患者是微生物学证实的耐药/耐多药结核病病例,并伴有肺部受累,并且接受了至少30天的方案1或方案2。根据世卫组织的定义对结果和不良事件进行分类。结果:126例耐药/耐多药结核病患者符合纳入标准。其中87人接受方案1,39人接受方案2。两组患者的成功率无显著差异,但口服方案包括方案2的贝达喹啉治疗的成功率更高。方案2患者到培养转化时间较短,方案长度相应缩短,中位持续时间为16.1个月[IQR, 15-17.3个月]。在接受全口服方案2的患者中,不良事件与2型糖尿病史显著相关(OR = 15.4; 95% CI, 2.73-87.29; p = 0.002),主要与利奈唑胺的使用有关。结论:口服方案似乎是有效的,尽管对利奈唑胺的毒性需要严格的患者监测。
{"title":"Impact of new regimens and drugs on rifampin-resistant tuberculosis management in Mexico.","authors":"Marcela Muñoz-Torrico, Rafael Laniado-Laborín, Jorge Rojas-Serrano, Eduardo Becerril-Vargas, Wendy Cinecio-Chávez, Fátima Leticia Luna-López, Luis Armando Narvaez-Díaz, Roberto Rentería-Gamez, Mariela Segura Del Pilar, Nallely Saavedra, Julio César Magaña, Lia D'Ambrosio, Rosella Centis, José Antonio Caminero, Giovanni Battista Migliori","doi":"10.36416/1806-3756/e20250131","DOIUrl":"https://doi.org/10.36416/1806-3756/e20250131","url":null,"abstract":"<p><strong>Objective: </strong>To compare the former tuberculosis treatment regimen including one fluoroquinolone (ofloxacin, levofloxacin, or moxifloxacin) and a second-line injectable drug (amikacin, kanamycin, or capreomycin) plus three to five oral drugs (regimen 1) with the current regimen including the three WHO group A drugs (regimen 2) in terms of efficacy and safety at two tuberculosis referral centers in Mexico.</p><p><strong>Methods: </strong>This was a retrospective study based on a review of the clinical records of all consecutive rifampin-resistant or multidrug-resistant tuberculosis (RR/MDR-TB) patients treated from January of 2010 to October of 2023. Patients included were microbiologically confirmed cases of RR/MDR-TB with pulmonary involvement and who received at least 30 days of regimen 1 or regimen 2. Outcomes and adverse events were classified in accordance with WHO definitions.</p><p><strong>Results: </strong>One hundred and twenty-six RR/MDR-TB patients met the inclusion criteria. Of those, 87 were treated with regimen 1 and 39 received regimen 2. Success rates were not significantly different between the two groups of patients, although those treated with the oral regimen including bedaquiline from regimen 2 had higher success rates. Regimen 2 patients experienced a shorter time to culture conversion, and the regimen length was shortened accordingly, the median duration being 16.1 months [IQR, 15-17.3 months]. In patients receiving the all-oral regimen 2, adverse events were significantly associated with a history of type 2 diabetes mellitus (OR = 15.4; 95% CI, 2.73-87.29; p = 0.002) and were mainly related to linezolid use.</p><p><strong>Conclusions: </strong>Oral regimens appear to be effective, although toxicity to linezolid requires strict patient monitoring.</p>","PeriodicalId":14845,"journal":{"name":"Jornal Brasileiro De Pneumologia","volume":"51 5","pages":"e20250131"},"PeriodicalIF":3.0,"publicationDate":"2025-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145794092","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Development and preliminary tests of a portable volumetric capnograph for outpatient use. 门诊用便携式容量测量仪的研制和初步试验。
IF 3 4区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-12-12 eCollection Date: 2025-01-01 DOI: 10.36416/1806-3756/e20250136
Francisco Ubaldo Vieira Junior, Denilson Antônio Marques, Natalie Camila Dos Reis Silva, Maria Ângela Gonçalves de Oliveira Ribeiro, Marcos Melo Moreira, Ilma Aparecida Paschoal, Isadora Minuzzi Vieira, Eduardo Tavares Costa

Objective: To develop and validate a portable volumetric capnograph for collecting data on ventilatory mechanics during spontaneous breathing for outpatient use.

Methods: The device was developed by integrating the following commercially available sensors: a Hamilton® flow sensor (variable orifice; Hamilton Medical AG, Graubünden, Switzerland); an SDP810-125PA differential pressure sensor (Sensirion AG, Stäfa, Switzerland); and a Capnostat 5 CO2 sensor (Philips Respironics, Murrysville, PA, USA). An Arduino UNO-R3® microcontroller (Arduino, Monza, Italy) was used as an interface between the sensors and a laptop computer, and a Python application was used to acquire data at 10 ms intervals (100 Hz). Validation included static tests (flow: 0-45 L/min; partial pressure of CO2: 0-100 mmHg) and tests with five healthy volunteers (n = 115 respiratory cycles), in comparison with the reference equipment (a CO2SMO Plus® DX-8100 oxycapnograph; Philips Respironics).

Results: The static tests showed excellent linear correlation for flow and CO2 concentration. For the tests conducted with the five volunteers, no significant differences were observed between the portable volumetric capnograph and the reference equipment for any of the variables analyzed. Intracycle variability was observed in the capnography curves, reflecting the physiological characteristics of spontaneous breathing.

Conclusions: Our portable volumetric capnograph demonstrated the ability to collect accurate data on flow and partial pressure of CO2 during spontaneous breathing, with performance equivalent to that of the reference equipment. The variability in the capnography curves represents an intrinsic characteristic of spontaneous breathing that must be considered when developing algorithms for calculating physiological indicators.

目的:开发和验证一种便携式容积容积记录仪,用于收集门诊患者自主呼吸时的通气力学数据。方法:该设备是通过集成以下市售传感器开发的:Hamilton®流量传感器(可变孔,Hamilton Medical AG, graub nden,瑞士);SDP810-125PA压差传感器(Sensirion AG, Stäfa,瑞士);Capnostat 5 CO2传感器(Philips呼吸器,Murrysville, PA, USA)。Arduino UNO-R3®微控制器(Arduino, Monza, Italy)用作传感器和笔记本电脑之间的接口,并使用Python应用程序以10毫秒的间隔(100 Hz)获取数据。验证包括静态测试(流量:0-45 L/min; CO2分压:0-100 mmHg)和5名健康志愿者的测试(n = 115个呼吸循环),并与参考设备(CO2SMO Plus®DX-8100吸氧仪;Philips呼吸器)进行比较。结果:静态试验显示流量与CO2浓度呈良好的线性相关。在对五名志愿者进行的测试中,在分析的任何变量中,便携式容积测量仪和参考设备之间没有观察到显著差异。血管造影曲线观察到周期内变异性,反映了自主呼吸的生理特征。结论:我们的便携式容积式二氧化碳记录仪能够准确收集自发呼吸过程中二氧化碳的流量和分压数据,其性能与参考设备相当。二氧化碳曲线的可变性代表了自然呼吸的内在特征,在开发计算生理指标的算法时必须考虑到这一点。
{"title":"Development and preliminary tests of a portable volumetric capnograph for outpatient use.","authors":"Francisco Ubaldo Vieira Junior, Denilson Antônio Marques, Natalie Camila Dos Reis Silva, Maria Ângela Gonçalves de Oliveira Ribeiro, Marcos Melo Moreira, Ilma Aparecida Paschoal, Isadora Minuzzi Vieira, Eduardo Tavares Costa","doi":"10.36416/1806-3756/e20250136","DOIUrl":"https://doi.org/10.36416/1806-3756/e20250136","url":null,"abstract":"<p><strong>Objective: </strong>To develop and validate a portable volumetric capnograph for collecting data on ventilatory mechanics during spontaneous breathing for outpatient use.</p><p><strong>Methods: </strong>The device was developed by integrating the following commercially available sensors: a Hamilton® flow sensor (variable orifice; Hamilton Medical AG, Graubünden, Switzerland); an SDP810-125PA differential pressure sensor (Sensirion AG, Stäfa, Switzerland); and a Capnostat 5 CO2 sensor (Philips Respironics, Murrysville, PA, USA). An Arduino UNO-R3® microcontroller (Arduino, Monza, Italy) was used as an interface between the sensors and a laptop computer, and a Python application was used to acquire data at 10 ms intervals (100 Hz). Validation included static tests (flow: 0-45 L/min; partial pressure of CO2: 0-100 mmHg) and tests with five healthy volunteers (n = 115 respiratory cycles), in comparison with the reference equipment (a CO2SMO Plus® DX-8100 oxycapnograph; Philips Respironics).</p><p><strong>Results: </strong>The static tests showed excellent linear correlation for flow and CO2 concentration. For the tests conducted with the five volunteers, no significant differences were observed between the portable volumetric capnograph and the reference equipment for any of the variables analyzed. Intracycle variability was observed in the capnography curves, reflecting the physiological characteristics of spontaneous breathing.</p><p><strong>Conclusions: </strong>Our portable volumetric capnograph demonstrated the ability to collect accurate data on flow and partial pressure of CO2 during spontaneous breathing, with performance equivalent to that of the reference equipment. The variability in the capnography curves represents an intrinsic characteristic of spontaneous breathing that must be considered when developing algorithms for calculating physiological indicators.</p>","PeriodicalId":14845,"journal":{"name":"Jornal Brasileiro De Pneumologia","volume":"51 5","pages":"e20250136"},"PeriodicalIF":3.0,"publicationDate":"2025-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145793993","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Treatment of sarcoidosis-an opinion. 结节病的治疗——一种看法。
IF 3 4区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-12-12 DOI: 10.36416/1806-3756/e20250330
Eduardo Pamplona Bethlem, Marcos de Carvalho Bethlem, Paolo Spa Gnolo
{"title":"Treatment of sarcoidosis-an opinion.","authors":"Eduardo Pamplona Bethlem, Marcos de Carvalho Bethlem, Paolo Spa Gnolo","doi":"10.36416/1806-3756/e20250330","DOIUrl":"https://doi.org/10.36416/1806-3756/e20250330","url":null,"abstract":"","PeriodicalId":14845,"journal":{"name":"Jornal Brasileiro De Pneumologia","volume":"51 5","pages":"e20250330"},"PeriodicalIF":3.0,"publicationDate":"2025-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145794028","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Gas dissection from the thorax to the abdomen. 从胸腔到腹部的气体分离。
IF 3 4区 医学 Q2 RESPIRATORY SYSTEM Pub Date : 2025-12-12 DOI: 10.36416/1806-3756/e20250184
Marina Manica Tamiozzo, Letícia Dalmolin, Mariana Manica Tamiozzo
{"title":"Gas dissection from the thorax to the abdomen.","authors":"Marina Manica Tamiozzo, Letícia Dalmolin, Mariana Manica Tamiozzo","doi":"10.36416/1806-3756/e20250184","DOIUrl":"https://doi.org/10.36416/1806-3756/e20250184","url":null,"abstract":"","PeriodicalId":14845,"journal":{"name":"Jornal Brasileiro De Pneumologia","volume":"51 5","pages":"e20250184"},"PeriodicalIF":3.0,"publicationDate":"2025-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145793944","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Jornal Brasileiro De Pneumologia
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