Literature DB >> 32139456

Physiological predictors of survival in patients with sarcoidosis-associated pulmonary hypertension: results from an international registry.

Oksana A Shlobin1, Vasilis Kouranos2, Scott D Barnett3, Esam H Alhamad4, Daniel A Culver5, Joseph Barney6, Francis C Cordova7, Eva M Carmona8, Mary Beth Scholand9, Marlies Wijsenbeek10, Sivagini Ganesh11, Elyse E Lower12, Peter J Engel13, John Wort2, Laura Price2, Athol U Wells2, Steven D Nathan3, Robert P Baughman12.   

Abstract

INTRODUCTION: Sarcoidosis-associated pulmonary hypertension (SAPH) is associated with reduced survival in single-centre studies. The international Registry for SAPH (ReSAPH) with long-term follow-up was established to enrich our knowledge of this complication of sarcoidosis. This analysis aims to elucidate factors associated with reduced transplant-free survival in SAPH patients.
METHODS: ReSAPH contains prospectively collected outcomes of SAPH patients since the time of registry enrolment. Information analysed includes right heart catheterisation data, pulmonary function testing, chest radiography, Scadding stage and 6-min walk distance (6MWD), among others. Cox regression models were used to identify independent predictors of transplant-free survival.
RESULTS: Data from 215 patients followed for a mean±sd 2.5±1.9 years were available for analysis. In the 159 precapillary patients, the Kaplan-Meier-adjusted 1-, 3- and 5-year transplant-free survival was 89.2%, 71.7% and 62.0%, respectively. Kaplan-Meier-adjusted 1-, 3- and 5-year transplant-free survival in the incident group was 83.5%, 70.3% and 58.3%, respectively, and in the prevalent group was 94.7%, 72.2% and 66.3%, respectively. Patients with reduced diffusing capacity of the lung for carbon monoxide (D LCO) (<35% predicted) and 6MWD <300 m in the precapillary cohort had significantly worse transplant-free survival. Reduced 6MWD and preserved forced expiratory volume (FEV1)/forced vital capacity (FVC) ratio were identified as independent risk factors for reduced transplant-free survival in the precapillary cohort.
CONCLUSION: Reduced D LCO (<35% pred) and 6MWD (<300 m) at the time of registry enrolment were associated with reduced transplant-free survival in the overall precapillary cohort. Preserved FEV1/FVC ratio was identified as an independent risk factor for worsened outcomes.
Copyright ©ERS 2020.

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Year:  2020        PMID: 32139456     DOI: 10.1183/13993003.01747-2019

Source DB:  PubMed          Journal:  Eur Respir J        ISSN: 0903-1936            Impact factor:   16.671


  9 in total

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3.  Predictors of Mortality in Patients with Interstitial Lung Disease-Associated Pulmonary Hypertension.

Authors:  Esam H Alhamad; Joseph G Cal; Nuha N Alrajhi; Waleed M Alharbi
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5.  Healthcare resource utilization and quality of life in patients with sarcoidosis-associated pulmonary hypertension.

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6.  Riociguat for Sarcoidosis-Associated Pulmonary Hypertension: Results of a 1-Year Double-Blind, Placebo-Controlled Trial.

Authors:  Robert P Baughman; Oksana A Shlobin; Rohit Gupta; Peter J Engel; Jeffrey I Stewart; Elyse E Lower; Franck F Rahaghi; Joyce Zeigler; Steven D Nathan
Journal:  Chest       Date:  2021-08-04       Impact factor: 9.410

7.  Management of Pulmonary Hypertension Due to Chronic Lung Disease.

Authors:  Jordan Sugarman; Jason Weatherald
Journal:  Methodist Debakey Cardiovasc J       Date:  2021-07-01

Review 8.  A Comprehensive Review of Sarcoidosis Diagnosis and Monitoring for the Pulmonologist.

Authors:  Andrea S Melani; Albano Simona; Martina Armati; Miriana d'Alessandro; Elena Bargagli
Journal:  Pulm Ther       Date:  2021-06-06

9.  Prevalence of Sarcoidosis-Associated Pulmonary Hypertension: A Systematic Review and Meta-Analysis.

Authors:  Shijie Zhang; Xiang Tong; Tianli Zhang; Dongguang Wang; Sitong Liu; Lian Wang; Hong Fan
Journal:  Front Cardiovasc Med       Date:  2022-01-17
  9 in total

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