• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

巴基斯坦一家三级护理中心的结缔组织病相关性间质性肺疾病与特发性肺纤维化的对比分析。

Comparative analysis of connective tissue disease-associated interstitial lung disease and idiopathic pulmonary fibrosis from a tertiary care centre in Pakistan.

机构信息

Department of Medicine, The Aga Khan University, Karachi, Pakistan.

Department of Health Sciences, The University of York, York, United Kingdom.

出版信息

J Pak Med Assoc. 2021 Oct;71(10):2330-2334. doi: 10.47391/JPMA.01-107.

DOI:10.47391/JPMA.01-107
PMID:34974565
Abstract

OBJECTIVE

To compare the characteristics of connective tissue disease-associated interstitial lung disease with idiopathic pulmonary fibrosis at a tertiary care hospital.

METHODS

The retrospective study was conducted at the Aga Khan University Hospital, Karachi, and comprised demographical, clinical and radiological data of patients with interstitial lung disease between October 2016 and October 2017 accessed through the outpatient data registry. Data was compared in terms of characteristics and key features of patients with connective tissue disease-associated interstitial lung disease with those of idiopathic pulmonary fibrosis. Statistical analysis was done using STATA 12.

RESULTS

Of the 184 patients, 52(29.3%) had connective tissue disease-associated interstitial lung disease and 62(35%) had idiopathic pulmonary fibrosis. The most prevalent conditions among connective tissue disease-associated interstitial lung disease patients were rheumatoid arthritis 22(42.3%) and scleroderma 13(25%). Compared to patients with idiopathic pulmonary fibrosis, those with connective tissue disease-associated interstitial lung disease were predominantly younger (p<0.001) and female (p<0.001). History of gastroesophageal reflux disease was also significantly lower in connective tissue disease-associated interstitial lung disease (p=0.05).

CONCLUSIONS

Connective tissue disease-associated interstitial lung disease patients were found to be younger and predominantly female compared to patients of idiopathic pulmonary fibrosis.

摘要

目的

在一家三级保健医院比较结缔组织病相关性间质性肺疾病与特发性肺纤维化的特征。

方法

该回顾性研究在卡拉奇的阿迦汗大学医院进行,纳入了 2016 年 10 月至 2017 年 10 月通过门诊数据登记系统获取的间质性肺疾病患者的人口统计学、临床和影像学数据。比较了结缔组织病相关性间质性肺疾病患者与特发性肺纤维化患者的特征和关键特征。使用 STATA 12 进行统计分析。

结果

在 184 名患者中,52 名(29.3%)患有结缔组织病相关性间质性肺疾病,62 名(35%)患有特发性肺纤维化。结缔组织病相关性间质性肺疾病患者中最常见的疾病是类风湿关节炎 22 例(42.3%)和硬皮病 13 例(25%)。与特发性肺纤维化患者相比,结缔组织病相关性间质性肺疾病患者主要更年轻(p<0.001)和女性(p<0.001)。结缔组织病相关性间质性肺疾病患者的胃食管反流病病史也明显较低(p=0.05)。

结论

与特发性肺纤维化患者相比,结缔组织病相关性间质性肺疾病患者更年轻,主要为女性。

相似文献

1
Comparative analysis of connective tissue disease-associated interstitial lung disease and idiopathic pulmonary fibrosis from a tertiary care centre in Pakistan.巴基斯坦一家三级护理中心的结缔组织病相关性间质性肺疾病与特发性肺纤维化的对比分析。
J Pak Med Assoc. 2021 Oct;71(10):2330-2334. doi: 10.47391/JPMA.01-107.
2
Spectrum of interstitial lung disease from a tertiary care hospital in Karachi.来自卡拉奇一家三级医疗医院的间质性肺疾病谱
J Pak Med Assoc. 2017 Jul;67(7):1065-1069.
3
Comparison of the diagnostic criteria for progressive pulmonary fibrosis in connective tissue disease related interstitial lung disease.结缔组织病相关间质性肺疾病中进行性肺纤维化诊断标准的比较
Respir Med. 2023 Jun;212:107242. doi: 10.1016/j.rmed.2023.107242. Epub 2023 Apr 7.
4
Comparison of characteristics of connective tissue disease-associated interstitial lung diseases, undifferentiated connective tissue disease-associated interstitial lung diseases, and idiopathic pulmonary fibrosis in Chinese Han population: a retrospective study.中国汉族人群中结缔组织病相关间质性肺疾病、未分化结缔组织病相关间质性肺疾病和特发性肺纤维化的特征比较:一项回顾性研究
Clin Dev Immunol. 2013;2013:121578. doi: 10.1155/2013/121578. Epub 2013 Sep 19.
5
Evaluation of progressive pulmonary fibrosis in non-idiopathic pulmonary fibrosis-interstitial lung diseases: a cross-sectional study.非特发性肺纤维化-间质性肺疾病进展性肺纤维化的评估:一项横断面研究。
BMC Pulm Med. 2024 Aug 22;24(1):403. doi: 10.1186/s12890-024-03226-z.
6
Connective Tissue Disease Associated Interstitial Lung Disease.结缔组织病相关间质性肺疾病。
Immunol Allergy Clin North Am. 2023 May;43(2):229-244. doi: 10.1016/j.iac.2023.01.005. Epub 2023 Mar 3.
7
Survival and outcomes after lung transplantation for non-scleroderma connective tissue-related interstitial lung disease.非硬皮病相关结缔组织病所致间质性肺疾病肺移植后的生存和结局。
J Heart Lung Transplant. 2017 Jul;36(7):763-769. doi: 10.1016/j.healun.2016.12.013. Epub 2016 Dec 31.
8
Acute exacerbations of fibrosing interstitial lung disease associated with connective tissue diseases: a population-based study.与结缔组织疾病相关的纤维性间质性肺疾病的急性加重:一项基于人群的研究。
BMC Pulm Med. 2019 Nov 14;19(1):215. doi: 10.1186/s12890-019-0960-1.
9
Baseline characteristics and comorbidities in the CAnadian REgistry for Pulmonary Fibrosis.加拿大肺纤维化注册研究中的基线特征和合并症。
BMC Pulm Med. 2019 Nov 27;19(1):223. doi: 10.1186/s12890-019-0986-4.
10
An analysis of connective tissue disease-associated interstitial lung disease at a US Tertiary Care Center: better survival in patients with systemic sclerosis.美国三级保健中心结缔组织病相关间质性肺疾病分析:系统性硬化症患者的生存率更好。
J Rheumatol. 2011 Apr;38(4):693-701. doi: 10.3899/jrheum.100675. Epub 2011 Feb 1.