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Outcomes and Risk Factors of Systolic Pulmonary Artery Pressure Progression in Patients With Systemic Rheumatic Diseases: Follow-up Results from a Korean Registry

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dc.contributor.authorSeo, Mi Ryoung-
dc.contributor.authorYeo, Jina-
dc.contributor.authorRyu, Hee Jung-
dc.contributor.authorChoi, Hyo-jin-
dc.contributor.authorKo, Kwang-pil-
dc.contributor.authorBaek, Han Joo-
dc.date.available2020-12-21T00:40:49Z-
dc.date.created2020-12-15-
dc.date.issued2020-12-
dc.identifier.issn2148-5046-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/79382-
dc.description.abstractObjectives: This study aims to investigate the outcomes and risk factors associated with the progression of systolic pulmonary artery pressure (sPAP) in patients with systemic rheumatic diseases. Patients and methods: A total of 532 patients (73 males, 459 females; median age 49 years; interquartile range (IQR), 36 to 62 years) registered with the Registry of Pulmonary Hypertension Associated with Rheumatic Diseases were included. Mortality curves were constructed using the Kaplan-Meier method and comparisons were performed using the log-rank test. A paired t-test was performed to evaluate the patients with markedly elevated sPAP between baseline and follow-up. Results: The average follow-up duration was 31 months (IQR, 9 to 60 months). Of the patients, 196 had follow-up echocardiographs at least one year later. We defined the sPAP over 60 mmHg as markedly elevated. Patients in the increased sPAP above 60 mmHg at follow-up and persistently markedly elevated sPAP were associated with worse outcomes in all-cause mortality and pulmonary arterial hypertension-related mortality (p<0.001). In patients with systemic sclerosis, the majority of patients remained static within their pressure group or rose progressively: the patients with markedly elevated sPAP at follow-up were higher than those at baseline (32% versus 15%, p<0.01). In patients with mixed connective tissue disease (MCTD) or rheumatoid arthritis (RA), the majority of patients remained static within their pressure group or gradually improved: the patients with markedly elevated sPAP at follow-up were lower than those at baseline (RA=14% versus 29%, MCTD=5% versus 16%, p<0.05). Conclusion: Persistently high sPAP or increase of sPAP over 60 mmHg at follow-up was associated with increased mortality. There were some differences in the progression of sPAP according to the underlying rheumatic diseases. © 2020 Turkish League Against Rheumatism. All rights reserved.-
dc.language영어-
dc.language.isoen-
dc.publisherTurkish League Against Rheumatism (TLAR)-
dc.relation.isPartOfArchives of Rheumatology-
dc.titleOutcomes and Risk Factors of Systolic Pulmonary Artery Pressure Progression in Patients With Systemic Rheumatic Diseases: Follow-up Results from a Korean Registry-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000595829400011-
dc.identifier.doi10.46497/ArchRheumatol.2020.7812-
dc.identifier.bibliographicCitationArchives of Rheumatology, v.35, no.4, pp.558 - 567-
dc.description.isOpenAccessN-
dc.identifier.scopusid2-s2.0-85097179610-
dc.citation.endPage567-
dc.citation.startPage558-
dc.citation.titleArchives of Rheumatology-
dc.citation.volume35-
dc.citation.number4-
dc.contributor.affiliatedAuthorSeo, Mi Ryoung-
dc.contributor.affiliatedAuthorYeo, Jina-
dc.contributor.affiliatedAuthorRyu, Hee Jung-
dc.contributor.affiliatedAuthorChoi, Hyo-jin-
dc.contributor.affiliatedAuthorKo, Kwang-pil-
dc.contributor.affiliatedAuthorBaek, Han Joo-
dc.type.docTypeArticle-
dc.subject.keywordAuthorConnective tissue diseases-
dc.subject.keywordAuthorHypertension-
dc.subject.keywordAuthorPrognosis-
dc.subject.keywordAuthorPulmonary-
dc.subject.keywordAuthorRheumatic diseases-
dc.subject.keywordAuthorSystolic pulmonary artery pressure-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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