2008 至 2017 年韩国慢性阻塞性肺病患病率和死亡率的全国趋势。

IF 3.6 3区 医学 Q1 RESPIRATORY SYSTEM BMJ Open Respiratory Research Pub Date : 2024-06-18 DOI:10.1136/bmjresp-2024-002391
Sun-Hyung Kim, Jong Eun Park, Bumhee Yang, So Young Kim, Yeon Yong Kim, Jong Hyock Park
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引用次数: 0

摘要

背景:韩国现有的慢性阻塞性肺病(COPD)研究缺乏全人口覆盖,依赖于较小的样本量。因此,本研究旨在调查整个韩国人口中慢性阻塞性肺病的患病率和死亡率:这项连续横断面研究使用了国家数据库,将国家健康信息数据库(2008-2017 年)与死亡原因统计联系起来。通过诊断代码(国际疾病分类-10:J41-J44)或与慢性阻塞性肺病相关的住院史来识别慢性阻塞性肺病患者,重点关注 40 岁及以上的成年人。计算的 2008-2017 年患病率和死亡率既包括粗略指标,也包括年龄标准化和性别标准化指标。一个多变量泊松回归模型利用2017年的数据估算了慢性阻塞性肺病与全因死亡率和特定原因死亡率之间的关系,并给出了发病率比(IRR)和95% CIs:从2008年(7.9%)到2017年(16.7%),经年龄调整的慢性阻塞性肺病发病率在男女两性中均有显著增长。慢性阻塞性肺病组的糖尿病、高血压、血脂异常、缺血性心脏病、癌症、骨质疏松症和肺结核患病率均高于无慢性阻塞性肺病组(P 均为讨论值):我们的研究表明,慢性阻塞性肺病的患病率正从 2009 年的 9.2% 逐步上升至 2018 年的 16.7%。此外,在总死亡率(全因)方面,慢性阻塞性肺病组明显高于非慢性阻塞性肺病组。慢性阻塞性肺病患者的死亡率远高于总死亡率,但正在逐渐下降。
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National trend in the prevalence and mortality of COPD in South Korea from 2008 to 2017.

Background: Existing studies on chronic obstructive pulmonary disease (COPD) in Korea lack full population coverage, relying on small sample sizes. Therefore, this study aims to investigate the prevalence and mortality of COPD in the entire Korean population.

Methods: This serial cross-sectional study used national databases, linking the National Health Information Database (2008-2017) with Causes of Death Statistics. Identification of individuals with COPD used diagnostic codes (International Classification of Diseases-10: J41-J44) or a history of COPD-related hospitalisation, focusing on adults aged 40 and above. Prevalence and mortality rates, calculated for 2008-2017, encompassed both crude and age-standardised and sex-standardised measures. A multivariate Poisson regression model estimated the association between COPD and all-cause and cause-specific mortality, presenting incidence rate ratios (IRRs) and 95% CIs, using data from the year 2017.

Results: Age-adjusted COPD prevalence exhibited a notable increase from 2008 (7.9%) to 2017 (16.7%) in both sexes. The prevalences of diabetes mellitus, hypertension, dyslipidaemia, ischaemic heart disease, cancer, osteoporosis and tuberculosis were higher in the COPD group than in the group without COPD (p for all <0.001). The incidence of stroke and myocardial infarction (p for all <0.001) and overall mortality were higher in the COPD group (adjusted IRR 1.23, 95% CI 1.22 to 1.24, p<0.001). In particular, incidence rate and risk of mortality due to lung cancer were higher than that of those without COPD compared with other cancer types (adjusted IRR 2.51, 95% CI 2.42 to 2.60, p<0.001). It was significantly higher the incidence rate and risk of mortality among group with COPD than those without COPD in lower respiratory disease (adjusted IRR 16.62, 95% CI 15.07 to 18.33, p<0.001), asthma (adjusted IRR 6.41, 95% CI 5.47 to 7.51, p<0.001) and bronchiectasis (adjusted IRR 11.77, 95% CI 7.59 to 18.26, p<0.001), respectively.

Discussion: Our study showed that the prevalence of COPD is gradually increasing from 9.2% in 2009 to 16.7% in 2018. Furthermore, in overall (all-cause) mortality, it was significantly higher in group with COPD than in group without COPD. The mortality rate of group with COPD was much higher than the overall mortality rate but is gradually decreasing.

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来源期刊
BMJ Open Respiratory Research
BMJ Open Respiratory Research RESPIRATORY SYSTEM-
CiteScore
6.60
自引率
2.40%
发文量
95
审稿时长
12 weeks
期刊介绍: BMJ Open Respiratory Research is a peer-reviewed, open access journal publishing respiratory and critical care medicine. It is the sister journal to Thorax and co-owned by the British Thoracic Society and BMJ. The journal focuses on robustness of methodology and scientific rigour with less emphasis on novelty or perceived impact. BMJ Open Respiratory Research operates a rapid review process, with continuous publication online, ensuring timely, up-to-date research is available worldwide. The journal publishes review articles and all research study types: Basic science including laboratory based experiments and animal models, Pilot studies or proof of concept, Observational studies, Study protocols, Registries, Clinical trials from phase I to multicentre randomised clinical trials, Systematic reviews and meta-analyses.
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