The IKONIA Cohort: A Tertiary Center’s Five-Year Experience in Pulmonary Hypertension Management

IF 2.2 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Yakup Alsancak, Oznur Keskin, Ahmet Taha Sahin, Sefa Tatar, Ahmet Seyfeddin Gurbuz, Mehmet Akif Duzenli
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Abstract

Aim and Background: Pulmonary hypertension (PH) is a progressive disease that significantly impacts patient morbidity and mortality. The recent ESC/ERS Guidelines classify PH into five groups, emphasizing the need for specific treatment in certain subgroups. This study presents a 5-year follow-up of patients diagnosed with precapillary PH at our center, aiming to analyze treatment outcomes and associated clinical characteristics.

Methods: This single-center retrospective cohort study included 65 patients diagnosed with precapillary PH between January 2018 and January 2024. Comprehensive assessments including medical history, echocardiography, and laboratory tests were performed. Treatment efficacy was evaluated through echocardiographic and laboratory parameter changes.

Results: The cohort primarily consisted of patients with idiopathic pulmonary arterial hypertension, and 40% received combination therapy. Notable improvements were observed in pulmonary artery pressure, tricuspid regurgitant velocity, and hemodynamic parameters. Despite therapeutic intervention, a mortality rate of 15.4% was recorded, highlighting the complexity of PH management.

Conclusion: This study underscores the multifaceted nature of PH and the importance of a multidisciplinary approach for optimal diagnosis and management. While combination therapy shows promise in improving patient outcomes, the persistent mortality rate emphasizes the need for enhanced awareness and early diagnosis in PH.

IKONIA队列:第三中心在肺动脉高压管理方面的五年经验
目的与背景:肺动脉高压(Pulmonary hypertension, PH)是一种影响患者发病率和死亡率的进行性疾病。最近的ESC/ERS指南将PH分为五组,强调需要对某些亚组进行特殊治疗。本研究对我中心诊断为毛细血管前PH的患者进行了为期5年的随访,旨在分析治疗结果和相关临床特征。方法:该单中心回顾性队列研究纳入了2018年1月至2024年1月诊断为毛细血管前PH的65例患者。进行了包括病史、超声心动图和实验室检查在内的综合评估。通过超声心动图和实验室参数变化评价治疗效果。结果:该队列主要由特发性肺动脉高压患者组成,其中40%接受联合治疗。肺动脉压、三尖瓣反流速度和血流动力学参数均有显著改善。尽管进行了治疗干预,但记录的死亡率为15.4%,突出了PH管理的复杂性。结论:本研究强调了PH的多面性和多学科方法对最佳诊断和管理的重要性。虽然联合治疗有望改善患者的预后,但持续的死亡率强调需要提高对PH的认识和早期诊断。
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来源期刊
CiteScore
5.30
自引率
0.00%
发文量
274
审稿时长
3-8 weeks
期刊介绍: IJCP is a general medical journal. IJCP gives special priority to work that has international appeal. IJCP publishes: Editorials. IJCP Editorials are commissioned. [Peer reviewed at the editor''s discretion] Perspectives. Most IJCP Perspectives are commissioned. Example. [Peer reviewed at the editor''s discretion] Study design and interpretation. Example. [Always peer reviewed] Original data from clinical investigations. In particular: Primary research papers from RCTs, observational studies, epidemiological studies; pre-specified sub-analyses; pooled analyses. [Always peer reviewed] Meta-analyses. [Always peer reviewed] Systematic reviews. From October 2009, special priority will be given to systematic reviews. [Always peer reviewed] Non-systematic/narrative reviews. From October 2009, reviews that are not systematic will be considered only if they include a discrete Methods section that must explicitly describe the authors'' approach. Special priority will, however, be given to systematic reviews. [Always peer reviewed] ''How to…'' papers. Example. [Always peer reviewed] Consensus statements. [Always peer reviewed] Short reports. [Always peer reviewed] Letters. [Peer reviewed at the editor''s discretion] International scope IJCP publishes work from investigators globally. Around 30% of IJCP articles list an author from the UK. Around 30% of IJCP articles list an author from the USA or Canada. Around 45% of IJCP articles list an author from a European country that is not the UK. Around 15% of articles published in IJCP list an author from a country in the Asia-Pacific region.
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