• 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

土耳其心内科医生和肺科医生肺动脉高压知识、态度和实践模式评估。

Assessment of Knowledge, Attitude, and Practice Patterns in Pulmonary Arterial Hypertension among Cardiologists and Pulmonologists: Evidence from Turkey.

机构信息

Department of Immunology and Allergy, Ordu University Education and Research Hospital, Ordu 52200, Türkiye.

Department of Cardiology, Haseki Training and Research Hospital, University of Health Sciences, Istanbul 34265, Türkiye.

出版信息

Medicina (Kaunas). 2023 Oct 20;59(10):1869. doi: 10.3390/medicina59101869.

DOI:10.3390/medicina59101869
PMID:37893587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10608633/
Abstract

: Pulmonary arterial hypertension (PAH) is a rare chronic disease of the small pulmonary arteries that causes right heart failure and death. Accurate management of PAH is necessary to decrease morbidity and mortality. Understanding current practices and perspectives on PAH is important. For this purpose, we intended to determine physicians' knowledge, attitudes, and practice patterns in adult pulmonary arterial hypertension (PAH) in Turkey. : Between January and February 2022, an online questionnaire was sent via e-mail to all cardiologists and pulmonologists who were members of the Turkish Society of Cardiology (TSC) and the Turkish Thoracic Society (TTS). : A total of 200 physicians (122 pulmonologists and 78 cardiologists) responded to the questionnaire. Cardiologists were more frequently involved in the primary diagnosis and treatment of PAH than pulmonologists (37.2% vs. 23.8%, = 0.042). More than half of the physicians had access to right heart catheterization. In mild/moderate PAH patients with a negative vasoreactivity test, the monotherapy option was most preferred (82.8%) and endothelin receptor antagonists (ERAs) were the most preferred group in these patients (73%). ERAs plus phosphodiesterase-5 inhibitors (PDE-5 INH) were the most preferred (69%) combination therapy, and prostacyclin analogues plus PDE-5 INH was preferred by only pulmonologists. : Overall, clinical management of patients with PAH complied with guideline recommendations. Effective clinical management of PAH in specialized centers that having right heart catheterization achieve better outcomes.

摘要

肺动脉高压(PAH)是一种罕见的肺小动脉慢性疾病,可导致右心衰竭和死亡。准确管理 PAH 对于降低发病率和死亡率非常重要。了解当前 PAH 的实践和观点很重要。为此,我们旨在确定土耳其成人肺动脉高压(PAH)医生的知识、态度和实践模式。

在 2022 年 1 月至 2 月期间,通过电子邮件向土耳其心脏病学会(TSC)和土耳其胸科学会(TTS)的所有心脏病专家和肺科医生发送了在线问卷。

共有 200 名医生(122 名肺科医生和 78 名心脏病专家)回答了问卷。与肺科医生相比,心脏病专家更频繁地参与 PAH 的初步诊断和治疗(37.2%比 23.8%, = 0.042)。超过一半的医生可以进行右心导管检查。在血管反应性试验阴性的轻度/中度 PAH 患者中,首选单一疗法(82.8%),这些患者中内皮素受体拮抗剂(ERA)是最受欢迎的药物(73%)。ERA 加磷酸二酯酶-5 抑制剂(PDE-5 INH)是最受欢迎的(69%)联合治疗方案,只有肺科医生更喜欢前列环素类似物加 PDE-5 INH。

总体而言,PAH 患者的临床管理符合指南建议。在有右心导管检查的专门中心进行有效的 PAH 临床管理可获得更好的结果。

相似文献

1
Assessment of Knowledge, Attitude, and Practice Patterns in Pulmonary Arterial Hypertension among Cardiologists and Pulmonologists: Evidence from Turkey.土耳其心内科医生和肺科医生肺动脉高压知识、态度和实践模式评估。
Medicina (Kaunas). 2023 Oct 20;59(10):1869. doi: 10.3390/medicina59101869.
2
Phosphodiesterase 5 inhibitors for pulmonary hypertension.用于治疗肺动脉高压的磷酸二酯酶5抑制剂。
Cochrane Database Syst Rev. 2019 Jan 31;1(1):CD012621. doi: 10.1002/14651858.CD012621.pub2.
3
Hemodynamic Response to Treatment and Outcomes in Pulmonary Hypertension Associated With Interstitial Lung Disease Versus Pulmonary Arterial Hypertension in Systemic Sclerosis: Data From a Study Identifying Prognostic Factors in Pulmonary Hypertension Associated With Interstitial Lung Disease.特发性肺纤维化相关肺动脉高压与系统性硬化症相关肺动脉高压患者治疗后血流动力学反应及结局比较:特发性肺纤维化相关肺动脉高压预后因素研究数据。
Arthritis Rheumatol. 2021 Feb;73(2):295-304. doi: 10.1002/art.41512. Epub 2020 Dec 29.
4
Switching to riociguat versus maintenance therapy with phosphodiesterase-5 inhibitors in patients with pulmonary arterial hypertension (REPLACE): a multicentre, open-label, randomised controlled trial.在肺动脉高压患者中,改用利奥西呱与使用磷酸二酯酶-5抑制剂进行维持治疗的对比研究(REPLACE):一项多中心、开放标签、随机对照试验。
Lancet Respir Med. 2021 Jun;9(6):573-584. doi: 10.1016/S2213-2600(20)30532-4. Epub 2021 Mar 24.
5
Advances in targeted therapy for pulmonary arterial hypertension in children.儿童肺动脉高压靶向治疗的进展
Eur J Pediatr. 2023 May;182(5):2067-2076. doi: 10.1007/s00431-022-04750-y. Epub 2022 Dec 17.
6
Predictors of the response to phosphodiesterase-5 inhibitors in pulmonary arterial hypertension: an analysis of the Spanish registry.肺动脉高压对磷酸二酯酶-5 抑制剂反应的预测因素:西班牙登记处的分析。
Respir Res. 2023 Sep 15;24(1):223. doi: 10.1186/s12931-023-02531-1.
7
Incremental burden of disease in patients diagnosed with pulmonary arterial hypertension receiving monotherapy and combination vasodilator therapy.接受单药治疗和联合血管扩张剂治疗的肺动脉高压患者的疾病增量负担。
Adv Ther. 2014 Feb;31(2):168-79. doi: 10.1007/s12325-014-0094-z. Epub 2014 Jan 22.
8
Combination Therapy in Pulmonary Arterial Hypertension-Targeting the Nitric Oxide and Prostacyclin Pathways.肺动脉高压的联合治疗-靶向一氧化氮和前列环素通路。
J Cardiovasc Pharmacol Ther. 2021 Sep;26(5):453-462. doi: 10.1177/10742484211006531. Epub 2021 Apr 9.
9
Assessment of Risk of Disease Progression in Pulmonary Arterial Hypertension: Insights from an International Survey of Clinical Practice.肺动脉高压疾病进展风险评估:国际临床实践调查的见解。
Adv Ther. 2019 Sep;36(9):2351-2363. doi: 10.1007/s12325-019-01030-4. Epub 2019 Jul 16.
10
Positive Vasoreactivity Testing in Pulmonary Arterial Hypertension: Therapeutic Consequences, Treatment Patterns, and Outcomes in the Modern Management Era.肺动脉高压的血管反应性阳性检测:现代管理时代的治疗后果、治疗模式和结局。
Circulation. 2024 May 14;149(20):1549-1564. doi: 10.1161/CIRCULATIONAHA.122.063821. Epub 2024 Apr 12.

本文引用的文献

1
2022 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension.2022年欧洲心脏病学会/欧洲呼吸学会肺动脉高压诊断和治疗指南。
Eur Heart J. 2022 Oct 11;43(38):3618-3731. doi: 10.1093/eurheartj/ehac237.
2
Real-world treatment patterns, healthcare resource utilization, and cost among adults with pulmonary arterial hypertension in the United States.美国肺动脉高压成年患者的真实世界治疗模式、医疗资源利用及成本
Pulm Circ. 2022 Jun 8;12(2):e12090. doi: 10.1002/pul2.12090. eCollection 2022 Apr.
3
Diagnosis and Treatment of Pulmonary Arterial Hypertension: A Review.
肺动脉高压的诊断与治疗:综述
JAMA. 2022 Apr 12;327(14):1379-1391. doi: 10.1001/jama.2022.4402.
4
Epidemiology of pulmonary arterial hypertension and chronic thromboembolic pulmonary hypertension: identification of the most accurate estimates from a systematic literature review.肺动脉高压和慢性血栓栓塞性肺动脉高压的流行病学:通过系统文献综述确定最准确的估计值。
Pulm Circ. 2021 Jan 7;11(1):2045894020977300. doi: 10.1177/2045894020977300. eCollection 2021 Jan-Mar.
5
Combination Therapy with Oral Treprostinil for Pulmonary Arterial Hypertension. A Double-Blind Placebo-controlled Clinical Trial.口服曲前列尼尔联合治疗肺动脉高压的疗效。一项双盲安慰剂对照临床试验。
Am J Respir Crit Care Med. 2020 Mar 15;201(6):707-717. doi: 10.1164/rccm.201908-1640OC.
6
Treatment patterns, healthcare resource utilization, and healthcare costs among patients with pulmonary arterial hypertension in a real-world US database.美国真实世界数据库中肺动脉高压患者的治疗模式、医疗资源利用及医疗费用
Pulm Circ. 2019 Jan-Mar;9(1):2045894018816294. doi: 10.1177/2045894018816294. Epub 2018 Nov 13.
7
Lung transplantation for idiopathic pulmonary arterial hypertension on intraoperative and postoperatively prolonged extracorporeal membrane oxygenation provides optimally controlled reperfusion and excellent outcome.特发性肺动脉高压患者行肺移植,术中及术后长时间体外膜肺氧合可提供最佳控制的再灌注,获得极佳的预后。
Eur J Cardiothorac Surg. 2018 Jan 1;53(1):178-185. doi: 10.1093/ejcts/ezx212.
8
An international physician survey of pulmonary arterial hypertension management.一项关于肺动脉高压管理的国际医生调查。
Pulm Circ. 2016 Sep;6(3):338-46. doi: 10.1086/688058.
9
Combination therapy versus monotherapy for pulmonary arterial hypertension: a meta-analysis.联合治疗与单药治疗肺动脉高压的疗效比较:一项荟萃分析。
Lancet Respir Med. 2016 Apr;4(4):291-305. doi: 10.1016/S2213-2600(16)00027-8. Epub 2016 Feb 27.
10
Selexipag for the Treatment of Pulmonary Arterial Hypertension.塞乐西帕用于肺动脉高压的治疗。
N Engl J Med. 2015 Dec 24;373(26):2522-33. doi: 10.1056/NEJMoa1503184.