Journal article
Health disparities and treatment approaches in portopulmonary hypertension and idiopathic pulmonary arterial hypertension: an analysis of the Pulmonary Hypertension Association Registry
Pulmonary circulation, Vol.11(3), pp.1-10
05/17/2021
DOI: 10.1177/20458940211020913
PMCID: PMC8186121
PMID: 34158918
Abstract
Compared to idiopathic pulmonary arterial hypertension (IPAH), patients with portopulmonary hypertension (POPH) have worse survival. Health disparities may contribute to these differences but have not been studied. We sought to compare socioeconomic factors in patients with POPH and IPAH and to determine whether socioeconomic status and/or POPH diagnosis were associated with treatment and health-care utilization. We performed a cross-sectional study of adults enrolled in the Pulmonary Hypertension Association Registry. Patients with IPAH (n = 344) and POPH (n = 57) were compared. Compared with IPAH, patients with POPH were less likely to be college graduates (19.6% vs. 34.9%, p = 0.02) and more likely to be unemployed (54.7% vs. 30.5%, p < 0.001) and have an annual household income below poverty level (45.7% vs. 19.0%, p < 0.001). Patients with POPH had similar functional class, quality of life, 6-min walk distance, and mean pulmonary arterial pressure with a higher cardiac index. Compared with IPAH, patients with POPH were less likely to receive combination therapy (46.4% vs. 62.2%, p = 0.03) and endothelin receptor antagonists (28.6% vs. 55.1%, p < 0.001) at enrollment with similar treatment at follow-up. Patients with POPH had more emergency department visits (1.7 ± 2.1 vs. 0.9 ± 1.2, p = 0.009) and hospitalizations in the six months preceding enrollment (1.5 ± 2.1 vs. 0.8 ± 1.1, p = 0.02). Both POPH diagnosis and lower education level were independently associated with a higher number of emergency department visits. Compared to IPAH, patients with POPH have lower socioeconomic status, are less likely to receive initial combination therapy and endothelin receptor antagonists but have similar treatment at follow-up, and have increased health-care utilization.
Details
- Title: Subtitle
- Health disparities and treatment approaches in portopulmonary hypertension and idiopathic pulmonary arterial hypertension: an analysis of the Pulmonary Hypertension Association Registry
- Creators
- Hilary M. DuBrock - Mayo Clinic Rochester, MNCharles D. Burger - Mayo Clinic in FloridaSonja D. Bartolome - The University of Texas Southwestern Medical CenterJeremy P. Feldman - Arizona Pain SpecialistsD. Dunbar Ivy - University of DenverErika B. Rosenzweig - Columbia UniversityJeffrey S. Sager - Cottage HealthKenneth W. Presberg - Medical College of WisconsinStephen C. Mathai - Johns Hopkins UniversityMatthew R. Lammi - Louisiana State University Health Sciences Center New OrleansJames R. Klinger - Brown UniversityMichael Eggert - Cardiovascular Institute HospitalTeresa De Marco - University of California, San FranciscoJean M. Elwing - University of CincinnatiDavid Badesch - University of DenverTodd M. Bull - University of DenverLinda M. Cadaret - University of IowaGautam Ramani - University of Maryland, BaltimoreThenappan Thenappan - University of MinnesotaH. James Ford - University of North Carolina at Chapel HillNadine Al-Naamani - University of PennsylvaniaMarc A. Simon - University of PittsburghSula Mazimba - University of VirginiaJames R. Runo - University of Wisconsin–MadisonMurali Chakinala - Washington University in St. LouisEvelyn M. Horn - Cornell UniversityJohn J. Ryan - University of UtahRobert P. Frantz - Mayo Clinic Rochester, MNMichael J. Krowka - Mayo Clinic Rochester, MNPHAR Investigators
- Resource Type
- Journal article
- Publication Details
- Pulmonary circulation, Vol.11(3), pp.1-10
- DOI
- 10.1177/20458940211020913
- PMID
- 34158918
- PMCID
- PMC8186121
- NLM abbreviation
- Pulm Circ
- ISSN
- 2045-8932
- eISSN
- 2045-8940
- Publisher
- SAGE Publications
- Language
- English
- Date published
- 05/17/2021
- Academic Unit
- Cardiovascular Medicine; Internal Medicine
- Record Identifier
- 9984359570702771
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