• 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

基层医疗医生对主要间质性肺疾病的认知。

Awareness towards the main ILD among primary care physicians.

作者信息

Silva Mariana, Fernandes Amélia, Pereira Ana Rita, Madanelo Sofia, Clemêncio Tatiana, Ferreira Pedro Gonçalo

机构信息

Unidade de Cuidados de Saúde Personalizados Anadia II, Anadia.

Unidade de Saúde Familiar Vale do Cértima, Oliveira do Bairro.

出版信息

Multidiscip Respir Med. 2022 Apr 26;17(1):848. doi: 10.4081/mrm.2022.848. eCollection 2022 Jan 12.

DOI:10.4081/mrm.2022.848
PMID:35558644
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9088858/
Abstract

BACKGROUND

Interstitial lung diseases (ILDs) comprise a group of multiple entities sharing some clinical, functional, and radiological similarities. In many countries primary care setting has been devoid of pre- and post-graduate educational interventions focused on basic knowledge on ILD. This, along with usual nonspecificity of symptoms at presentation, may contribute to diagnostic delay in this disease setting.

METHODS

We designed a study questionnaire to assess the level of awareness on basic diagnostic and management aspects of core ILDs - idiopathic pulmonary fibrosis (IPF), hypersensitivity pneumonitis, sarcoidosis, connective tissue disease related-ILD, and drug-induced ILD - among primary care physicians (GPs) from five "ACeS Baixo Vouga" health centres and to perceive possible weaknesses. Differences in awareness between GPs under 45 and over 45 yearsold were also assessed.

RESULTS

Globally, 69% of questions were correctly answered but only 21.9% of GPs considered to have a satisfactory self-perceived level of knowledge on ILD. Except sarcoidosis (p=0.017) and some isolated questions on other diseases, no significant differences were found between physicians below 45 years and above. Though, there was a trend to higher awareness in the younger group. The best awareness was seen in sarcoidosis. IPF questions had the worst performance and only 48.5% of GPs recognized the importance of velcro-type crackles in suggesting a possible diagnosis.

CONCLUSION

Specific attention should be devoted to educational interventions directed to GPs on basic notions on the main ILDs. This could improve the usual diagnostic delay in many ILDs, as a timely diagnosis is essential for an early treatment and prolonged patient survival.

摘要

背景

间质性肺疾病(ILDs)是一组在临床、功能和放射学方面有一些相似之处的多种疾病。在许多国家,基层医疗环境缺乏针对ILD基础知识的研究生前和研究生教育干预措施。这一点,再加上疾病表现时症状通常缺乏特异性,可能导致这种疾病的诊断延迟。

方法

我们设计了一项研究问卷,以评估来自五个“ACeS Baixo Vouga”健康中心的基层医疗医生(全科医生)对核心ILDs——特发性肺纤维化(IPF)、过敏性肺炎、结节病、结缔组织病相关ILD和药物性ILD——的基本诊断和管理方面的认知水平,并找出可能存在的薄弱环节。我们还评估了45岁以下和45岁以上全科医生在认知方面的差异。

结果

总体而言,69%的问题回答正确,但只有21.9%的全科医生认为自己对ILD的认知水平令人满意。除结节病(p = 0.017)和关于其他疾病的一些个别问题外,45岁以下和45岁以上的医生之间没有发现显著差异。不过,年轻组的认知水平有更高的趋势。对结节病的认知最好。IPF相关问题的表现最差,只有48.5%的全科医生认识到捻发音在提示可能诊断方面的重要性。

结论

应特别关注针对全科医生的关于主要ILDs基本概念的教育干预措施。这可以改善许多ILDs常见的诊断延迟情况,因为及时诊断对于早期治疗和延长患者生存期至关重要。

相似文献

1
Awareness towards the main ILD among primary care physicians.基层医疗医生对主要间质性肺疾病的认知。
Multidiscip Respir Med. 2022 Apr 26;17(1):848. doi: 10.4081/mrm.2022.848. eCollection 2022 Jan 12.
2
Advances with pharmacotherapy for the treatment of interstitial lung disease.间质肺疾病治疗的药物治疗进展。
Expert Opin Pharmacother. 2022 Mar;23(4):483-495. doi: 10.1080/14656566.2021.2016697. Epub 2021 Dec 15.
3
Nintedanib in patients with progressive fibrosing interstitial lung diseases-subgroup analyses by interstitial lung disease diagnosis in the INBUILD trial: a randomised, double-blind, placebo-controlled, parallel-group trial.尼达尼布治疗进行性肺纤维化间质性肺疾病患者- INBUILD 试验中按间质性肺疾病诊断的亚组分析:一项随机、双盲、安慰剂对照、平行组试验。
Lancet Respir Med. 2020 May;8(5):453-460. doi: 10.1016/S2213-2600(20)30036-9. Epub 2020 Mar 5.
4
A cohort study of Danish patients with interstitial lung diseases: burden, severity, treatment and survival.一项针对丹麦间质性肺疾病患者的队列研究:负担、严重程度、治疗与生存情况。
Dan Med J. 2015 Apr;62(4):B5069.
5
Auscultation of Velcro Crackles is Associated With Usual Interstitial Pneumonia.听诊发现的捻发音与普通型间质性肺炎相关。
Medicine (Baltimore). 2016 Feb;95(5):e2573. doi: 10.1097/MD.0000000000002573.
6
Organisation of diagnosis and treatment of idiopathic pulmonary fibrosis and other interstitial lung diseases in the Nordic countries.北欧国家特发性肺纤维化及其他间质性肺疾病的诊断与治疗组织
Eur Clin Respir J. 2015 Jul 1;2. doi: 10.3402/ecrj.v2.28348. eCollection 2015.
7
Integrated approach to bronchoalveolar lavage cytology to distinguish interstitial lung diseases.综合支气管肺泡灌洗液细胞学检查鉴别间质性肺疾病。
Eur J Intern Med. 2021 Jul;89:76-80. doi: 10.1016/j.ejim.2021.04.005. Epub 2021 Apr 28.
8
Interstitial lung diseases in Saudi Arabia: A single-center study.沙特阿拉伯的间质性肺疾病:一项单中心研究。
Ann Thorac Med. 2013 Jan;8(1):33-7. doi: 10.4103/1817-1737.105717.
9
CCL18 in serum, BAL fluid and alveolar macrophage culture supernatant in interstitial lung diseases.血清、BAL 液和肺泡巨噬细胞培养上清液中的 CCL18 在间质性肺疾病中的作用。
Respir Med. 2013 Sep;107(9):1444-52. doi: 10.1016/j.rmed.2013.06.004. Epub 2013 Jul 5.
10
Spectrum of interstitial lung diseases at a tertiary center in a developing country: A study of 803 subjects.发展中国家一家三级医疗中心的间质性肺疾病谱:一项对803名受试者的研究。
PLoS One. 2018 Feb 8;13(2):e0191938. doi: 10.1371/journal.pone.0191938. eCollection 2018.

引用本文的文献

1
Incidence and prevalence of asthma, chronic obstructive pulmonary disease and interstitial lung disease between 2004 and 2023: harmonised analyses of longitudinal cohorts across England, Wales, South-East Scotland and Northern Ireland.2004年至2023年间哮喘、慢性阻塞性肺疾病和间质性肺疾病的发病率和患病率:对英格兰、威尔士、苏格兰东南部和北爱尔兰纵向队列的统一分析
Thorax. 2025 Jun 16;80(7):466-477. doi: 10.1136/thorax-2024-222699.
2
Patient-centered care in pulmonary fibrosis: access, anticipate, and act.肺纤维化中的以患者为中心的护理:获得、预见和行动。
Respir Res. 2024 Nov 1;25(1):395. doi: 10.1186/s12931-024-02997-7.
3
The Role of Macrophages in Connective Tissue Disease-Associated Interstitial Lung Disease: Focusing on Molecular Mechanisms and Potential Treatment Strategies.巨噬细胞在结缔组织病相关间质性肺疾病中的作用:聚焦于分子机制和潜在治疗策略。
Int J Mol Sci. 2023 Jul 26;24(15):11995. doi: 10.3390/ijms241511995.
4
Early Diagnosis and Treatment of Idiopathic Pulmonary Fibrosis: A Narrative Review.特发性肺纤维化的早期诊断与治疗:一篇叙述性综述
Pulm Ther. 2023 Jun;9(2):177-193. doi: 10.1007/s41030-023-00216-0. Epub 2023 Feb 11.

本文引用的文献

1
Decrements of body mass index are associated with poor outcomes of idiopathic pulmonary fibrosis patients.体重指数下降与特发性肺纤维化患者的不良预后相关。
PLoS One. 2019 Oct 4;14(10):e0221905. doi: 10.1371/journal.pone.0221905. eCollection 2019.
2
Idiopathic pulmonary fibrosis and GERD: links and risks.特发性肺纤维化与胃食管反流病:关联与风险
Ther Clin Risk Manag. 2019 Sep 5;15:1081-1093. doi: 10.2147/TCRM.S184291. eCollection 2019.
3
Risk factors for diagnostic delay in idiopathic pulmonary fibrosis.特发性肺纤维化的诊断延迟的危险因素。
Respir Res. 2019 May 24;20(1):103. doi: 10.1186/s12931-019-1076-0.
4
Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline.特发性肺纤维化诊断。美国胸科学会/欧洲呼吸学会/日本呼吸学会/拉丁美洲胸科学会临床实践指南。
Am J Respir Crit Care Med. 2018 Sep 1;198(5):e44-e68. doi: 10.1164/rccm.201807-1255ST.
5
The Clinical Significance of Body Weight Loss in Idiopathic Pulmonary Fibrosis Patients.特发性肺纤维化患者体重减轻的临床意义。
Respiration. 2018;96(4):338-347. doi: 10.1159/000490355. Epub 2018 Aug 21.
6
Idiopathic pulmonary fibrosis: pathogenesis and management.特发性肺纤维化:发病机制与治疗。
Respir Res. 2018 Feb 22;19(1):32. doi: 10.1186/s12931-018-0730-2.
7
Idiopathic pulmonary fibrosis.特发性肺纤维化。
Nat Rev Dis Primers. 2017 Oct 20;3:17074. doi: 10.1038/nrdp.2017.74.
8
Effectiveness of pulmonary rehabilitation in patients with interstitial lung disease of different etiology: a multicenter prospective study.不同病因间质性肺疾病患者肺康复治疗的有效性:一项多中心前瞻性研究。
BMC Pulm Med. 2017 Oct 10;17(1):130. doi: 10.1186/s12890-017-0476-5.
9
An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline: Treatment of Idiopathic Pulmonary Fibrosis. An Update of the 2011 Clinical Practice Guideline.美国胸科学会/欧洲呼吸学会/日本呼吸学会/拉丁美洲胸科学会特发性肺纤维化临床实践指南:治疗。对 2011 年临床实践指南的更新。
Am J Respir Crit Care Med. 2015 Jul 15;192(2):e3-19. doi: 10.1164/rccm.201506-1063ST.
10
Idiopathic pulmonary fibrosis and sleep disorders: no longer strangers in the night.特发性肺纤维化与睡眠障碍:不再是夜间的陌生人。
Eur Respir Rev. 2015 Jun;24(136):327-39. doi: 10.1183/16000617.00009114.