THORAX胸腔

THORAX(英文缩写 THORAX),ISSN 0040-6376,eISSN 1468-3296,中文译名:胸腔 是一本学术期刊。本页汇总该期刊的最新影响因子、分区信息以及最新收录于 PubMed 的文献,帮助您快速了解期刊全貌。

2026 年数据 · 影响因子
9.100
JCR 分区
Q1
CAS 分区
B1
近一年发文量
344
本站 PubMed 收录统计

发文量统计区间:2025-09-27 至 2026-09-27,按本站收录文献的发表日期统计。

ISSN: 0040-6376 · eISSN: 1468-3296 · 缩写: THORAX ·中文: 胸腔

期刊介绍

选择期刊介绍栏目

期刊简介

Thorax 是呼吸医学与胸部疾病领域的国际权威期刊,由英国胸科学会等机构支持,发表呼吸系统、重症监护、胸外科及胸部影像相关的高质量临床与转化研究。读者群涵盖呼吸科医师、重症医学专家、胸外科医生、流行病学家及基础研究人员,尤其关注能改变临床实践或深化疾病机制认识的工作。

研究方向

主要方向包括哮喘、慢阻肺、间质性肺病、肺部感染、肺癌、肺血管病、呼吸衰竭与机械通气、睡眠呼吸障碍及胸外科。论文类型以原创临床研究、系统综述、荟萃分析、方法学与转化研究为主,兼有评论、病例报告和指南解读。

期刊特色

研究取向强调临床相关性、方法严谨性和多学科交叉,偏好大样本队列、随机对照试验及机制明确的转化研究。论文通常数据扎实、统计规范,对临床决策有直接参考价值。适合呼吸与危重症领域临床医生、科研人员及研究生阅读和投稿。

投稿难度

投稿难度较高,对创新性、样本量、统计分析和临床意义均有严格要求。建议在投稿前明确科学问题,完善研究设计,充分预实验或内部验证,并参考近期同主题论文的深度与格式。不能仅凭分区判断是否容易录用,需结合自身数据质量与期刊定位综合评估。

历年影响因子趋势

JCR 数据年份影响因子JCR 分区
20219.203Q1
202210.000Q1
20239.000Q1
20247.700Q1
20259.100Q1

THORAX 最新收录文献

  1. JCR分区: Q1 CAS分区: B1 影响因子: 9.1

    1. Pulmonary embolism: from diagnosis to prognosis.

    1. 肺栓塞:从诊断到预后
    作者:
    Ken Kuljit S Parhar, Kevin J Solverson
    期刊:
    日期:
    2026-09-24

    该文献暂无摘要。

  2. JCR分区: Q1 CAS分区: B1 影响因子: 9.1
  3. JCR分区: Q1 CAS分区: B1 影响因子: 9.1

    3. {"_":"PM, O and survival gains from China's clean air actions among patients with lung cancer: a 20-year registry-based cohort study in Beijing.","sub":["2.5","3"]}

    作者:
    Lei Yang, Ning Kang, Tao Xue, Ning Wang, Shuo Liu, Huichao Li, Xi Zhang, Lili Cao, Xiaolin Ma, Shaohua Ma, Jiafu Ji, Tong Zhu
    期刊:
    日期:
    2026-09-23

    In recent years, China has experienced declining fine particulate matter (PM) levels but rising ozone (O) levels. We aimed to examine the independent and joint associations of long-term exposure to PM and O with all-cause mortality among patients with lung cancer and to estimate potential survival gains. We included 172 845 lung cancer patients diagnosed in 2003-2022 from the Beijing Cancer Registry. Three-year average pre-diagnosis PM and O were assigned using the ChinaHighAirPollutants dataset. Cox proportional hazards models were used to estimate associations of PM and O with mortality. Joint exposure-response patterns were examined using a two-dimensional tensor-product spline and quantified by the multiplicative interaction index. Model-estimated avoided deaths and extended expected lifespan (EEL) were calculated using counterfactual simulations based on 2013 exposure levels. Both PM and O were associated with increased mortality among patients with lung cancer, with HRs of 1.111 for PM (95% CI 1.083 to 1.140) and 1.117 for O (95% CI 1.070 to 1.166) per 10 μg/m increase. A significant multiplicative interaction was observed between PM and O, with statistically significant positive interactions mainly occurring at higher O concentrations (>105 µg/m). During 2016-2022, reductions in pre-diagnosis PM exposure were associated with 13 229 model-estimated avoided deaths and a 7.8-month increase in 5-year EEL. However, O and the PM-O interaction offset approximately 40% of these benefits. PM reduction was associated with substantial survival gains among lung cancer patients, but rising O and pollutant interactions partly offset these benefits, supporting coordinated multipollutant control.

  4. JCR分区: Q1 CAS分区: B1 影响因子: 9.1

    4. Effects of obstructive sleep apnoea treatment on cardiovascular and sleep health in bed partners: the sleep partners clinical trial.

    作者:
    Sara Q C Giampá, Sofia F Furlan, Thiago A Macedo, Fernanda Csg Cruz, Mayara L Cabrini, Silvana de Barros, Indira Fb Azam, Valéria A Costa-Hong, Paulo Hs Fernandes, Luiz A Bortolotto, Geraldo Lorenzi-Filho, Luciano F Drager
    期刊:
    日期:
    2026-09-22

    It remains unclear whether obstructive sleep apnoea (OSA) and its treatment influence cardiovascular and sleep health in bed partners. In this placebo-controlled trial, patients with moderate/severe OSA who had bed partners were randomly assigned to receive continuous positive airway pressure (CPAP) or placebo (nasal strips). At baseline and after 3 months, the bed partners underwent clinical evaluation, endothelial function (flow-mediated dilation, FMD), 24-hour ambulatory blood pressure (BP) monitoring, sleep questionnaires and 1-week wrist actigraphy. A total of 63 couples were recruited (34 patients randomised to CPAP and 29 to nasal strips). At baseline, bed partners showed impaired FMD and a higher frequency of long sleep latency, fragmented sleep, short sleep duration and poor sleep quality. Mean adherence to CPAP and nasal strips in OSA patients was 5.7±1.7 hours and 93.1%±12.6%, respectively. Compared with placebo, bed partners of patients assigned to CPAP did not change FMD (Δ: -0.94% (6.03%; 2.24%) vs Δ: -3.27% (-6.50%; 1.76%), p=0.67). However, significant differences were observed for 24-hour systolic BP (CPAP: -0.85±5.22 mm Hg; placebo: +3.14±8.00 mm Hg; p=0.03), daytime systolic BP (CPAP: -1.2±5.5 mm Hg; placebo: +3.8±8.8 mm Hg; p=0.01) and night-time heart rate (CPAP: -3±6 bpm; placebo: +2±7 bpm; p=0.01). They improved sleep quality (p=0.02), decreased daytime sleepiness (p=0.01), time awake after sleep onset (CPAP: -4.71±20.32 min; placebo: +7.36±17.51 min; p=0.002) and number of awakenings (CPAP: -0.97±9.42; placebo: +2.83±9.14; p=0.02). In a stratified analysis by CPAP adherence, endothelial function in bed partners was preserved with optimal use (≥6 hours/night), but worsened with lower adherence (p=0.03). OSA treatment did not improve endothelial function in bed partners but prevented BP increases, alongside improvements in sleep quality, daytime sleepiness and sleep fragmentation. NCT03011294.

  5. JCR分区: Q1 CAS分区: B1 影响因子: 9.1

    5. Inequalities in chronic respiratory disease: working towards policy change?

    作者:
    Ruth Costello, Rosalind Eggo
    期刊:
    日期:
    2026-09-22

    该文献暂无摘要。

  6. JCR分区: Q1 CAS分区: B1 影响因子: 9.1

    6. Systematic misclassification of lung function in Indian adolescents using GLI-2012 reference equations: evidence from the multicity APEAL cohort.

    作者:
    Priya Samdarshi, Padukudru Anand Mahesh, Swapnali Patil, Anant Mohan, George D'Souza, Rajesh Thimmulappa, Twinkle Agrawal, Jayaraj Biligere Siddaiah, Harish Chandra Phuleria
    期刊:
    日期:
    2026-09-22

    Accurate spirometric interpretation depends on appropriate reference equations. The Global Lung Function Initiative (GLI-2012) equations are widely used internationally, but South Asian populations were sparsely represented in their derivation and their applicability in Indian adolescents remains uncertain. We performed a cross-sectional analysis of baseline data from the multicity Air Pollution Exposure on Adolescents' Lungs cohort. Healthy, non-smoking school-going adolescents aged 11-14 years from Delhi, Mumbai, Bengaluru and Mysuru underwent spirometry using standardised American Thoracic Society/European Respiratory Society procedures. GLI-2012 z-scores for forced expiratory volume in 1 s (FEV), forced vital capacity (FVC) and FEV/FVC were calculated using the Asian reference category. Fit was assessed using mean z-scores and the proportion below the lower limit of normal (LLN; z<-1.645). Among 4175 adolescents (2148 males), mean z-scores were -2.44 (SD 1.27) for FEV, -1.34 (0.93) for FVC and -0.78 (1.11) for FEV/FVC, all well outside the accepted ±0.5 range for adequate fit. Overall, 74.6% were below the LLN for FEV, 36.8% for FVC and 19.3% for FEV/FVC, compared with the expected 5% in a well-calibrated healthy population. The leftward shift in z-score distributions was consistent across sex, city, age, height and body mass index strata. GLI-2012 equations, as currently applied in the absence of South Asian-specific references, demonstrated substantial calibration mismatch relative to this cohort of Indian adolescents and risk major overclassification of low lung function. Population-specific validation and recalibration are needed before routine clinical or epidemiological use in this population.

  7. JCR分区: Q1 CAS分区: B1 影响因子: 9.1

    7. Associations between accelerated lung function decline and cardiovascular outcomes: a systematic review.

    作者:
    Jiaxin Li, Yaoyao Qian, Jennifer Perret, Jingwen Zhang, Nur Sabrina Idrose, Xin Dai, Anurika P De Silva, Shyamali C Dharmage, Caroline J Lodge, Dinh S Bui
    期刊:
    日期:
    2026-09-22

    Emerging evidence suggests that lung function decline may be linked to cardiovascular disease (CVD), but this has not been synthesised to date. This review aims to synthesise the current evidence on accelerated lung function decline and cardiovascular outcomes. We systematically searched MEDLINE, Embase and PubMed from inception to May 2026 for studies evaluating longitudinal changes in lung function in adults in relation to CVD. Study quality was assessed using the Risk Of Bias In Non-randomised Studies of Exposure tool, and findings were synthesised narratively. Of 6772 studies identified from the search, 15 publications met the inclusion criteria: 12 general population cohorts, 2 occupational cohorts and 1 chronic obstructive pulmonary disease (COPD) cohort. In the general/occupational population, accelerated lung function decline was consistently associated with increased cardiovascular risk, with a uniformly positive directional trend and HRs ranging from 1.07 to 1.36 for forced expiratory volume in 1 s (FEV₁) and 1.06 to 1.33 for forced vital capacity. Similar trends were observed for CVD-related biomarkers, risk factors and subclinical cardiovascular phenotypes (eg, HRs 1.04-1.66 for accelerated FEV decline). Potential effect modifiers of these associations such as smoking were reported. However, the association between accelerated lung function decline and CVD mortality in the general population remains inconclusive. In two occupational cohorts, lung function decline was associated with higher CVD mortality risk (HRs 2.05-2.59). In ageing populations, tracking the rate of lung function decline may help identify not only those at risk of COPD but also those at risk of CVD.

  8. JCR分区: Q1 CAS分区: B1 影响因子: 9.1

    8. International epidemiology of antimicrobial resistance in people living with chronic lung infection.

    作者:
    Ollie Pitts, Chiara Premuda, ZhiLing Yuan, Mattia Nigro, Till Othmer, Nikolas Johl, Arafa Aboelhassan, Safaa Eid, Sarah Hashem, Noha Khalil, Michael Behnke, Oto Melter, Pavel Drevinek, Rishi Dhillon, Irfan Shafiq, Nilüfer Acet-Öztürk, Ozge Aydin Guclu, Daniela Girelli, Jamie Duckers, Wang Chun Kwok, Stefano Aliberti, Andrea Gramegna, Stephanie Thee, Frederick Frost, Anand Shah
    期刊:
    日期:
    2026-09-21

    Antimicrobial resistance (AMR) is a global threat for people with chronic lung infection; however, international AMR epidemiology in bronchiectasis and cystic fibrosis (CF) is poorly characterised. In this study, we retrospectively analyse international longitudinal AMR epidemiology in bronchiectasis and CF. Microbiology data were analysed from 110 323 respiratory samples in 19 143 individuals with bronchiectasis or CF across 11 cities, eight countries, three continents between 2011 and 2024. Longitudinal AMR prevalence, multidrug-resistant (MDR) and extensively drug-resistant (XDR) prevalence and multiple antibiotic resistance (MAR) index were analysed by disease and country. Pilot analysis of concurrent/disjoint resistance in antimicrobial pairs and triplets in regional datasets was performed to inform combination or cyclical antimicrobial choice. Geographic AMR differences were noted across pathogens in bronchiectasis and CF with increased resistance in central/southern Europe and increased resistance in Hong Kong. MDR burden was high in emergent pathogens (CF: MDR 32.6%; XDR 12.4%; bronchiectasis: MDR 39.2%; XDR 4.9%) and (CF: MDR 22.7%; XDR 15.6%; bronchiectasis: MDR 13.4%; XDR 1.5%). A longitudinal rise in AMR was seen in bronchiectasis across four centres for antipseudomonal aminoglycosides (p<0.001; OR/year 1.44; 95% CI 1.24 to 1.67), fluoroquinolones (p=0.002; OR/year 1.13; 95% CI 1.05 to 1.23), cephalosporins (p=0.005; OR/year 1.17; 95% CI 1.05 to 1.30), penicillins with beta-lactamase inhibitor (p=0.02; OR/year 1.18; 95% CI 1.03 to 1.35) and carbapenems (p=0.048; OR/year 1.11; 95% CI 1.00 to 1.23). Rising longitudinal AMR was seen for cephalosporins (p=0.01; OR/year 1.32; 95% CI 1.06 to 1.65) and carbapenems (p=0.04; OR/year 1.64; 95% CI 1.03 to 2.62). A significant increase in AMR, as measured by the MAR index, was observed in individuals with residual culture-positive CF receiving triple cystic fibrosis transmembrane conductance regulator (CFTR) modulator therapy (p<0.001). Strong concurrent resistance was noted in bronchiectasis across regions with geographic variation in disjoint antimicrobial pair resistance. We show a significant increasing international AMR burden in bronchiectasis and CF, with geographic variation and persistence post-CFTR modulator therapy.

  9. JCR分区: Q1 CAS分区: B1 影响因子: 9.1

    9. Generational changes in lung function in adults from several world regions: results from the Burden of Obstructive Lung Disease study.

    9. 全球多个地区成年人肺功能的代际变化:阻塞性肺疾病负担研究的结果
    作者:
    Jixuan Ma, Peter G J Burney, David M Mannino, Christer Janson, Thorarinn Gíslason, Daniel O Obaseki, Rain Jõgi, Valentina Quintero Santofimio, James Potts, Abdul Rashid, Gregory E Erhabor, Rune Nielsen, Ali Kocabas, Asaad Nafees, Rana Ahmed, Meriam Denguezli, Cristina Barbara, Joao Cardoso, Herminia Brites Dias, Fátima Rodrigues, Dhiraj Agarwal, Sanjay Juvekar, Frits M E Franssen, Terence Seemungal, Kevin Mortimer, Mohammed El Biaze, Padukudru Anand Mahesh, Parvaiz Koul, Michael Studnicka, Andre F S Amaral
    期刊:
    日期:
    2026-09-18

    This study estimated birth cohort effects on lung function using BOLD (Burden of Obstructive Lung Disease) data from 28 569 adults born between 1902 and 1976 across 41 sites in 34 countries. Forced vital capacity (FVC), forced expiratory volume in 1 s (FEV) and the FEV/FVC increased across successive birth cohorts in both high-income countries (HICs) and low- and middle-income countries (LMICs), with mean values rising steadily with later birth year. In fully adjusted models, FVC increased by 21.4 mL, FEV by 24.6 mL and FEV/FVC by 0.25% per birth year. These positive associations were consistent across sex, smoking status and country-income subgroups (HICs and LMICs).

  10. JCR分区: Q1 CAS分区: B1 影响因子: 9.1

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