Prognosis in Hispanic patient population with pulmonary arterial hypertension: An application of common risk stratification models

Author:

Fadah Kahtan1ORCID,Cruz Rodriguez Jose B.2ORCID,Alkhateeb Haider3,Mukherjee Debabrata3,Garcia Hernando4,Schuller Dan5,Mohammad Khan O.6,Sahay Sandeep7ORCID,Nickel Nils P.8ORCID

Affiliation:

1. Department of Internal Medicine Texas Tech University Health Sciences Center El Paso El Paso Texas USA

2. Department of Internal Medicine, Division of Cardiovascular Medicine University of California San Diego San Diego California USA

3. Department of Internal Medicine, Texas Tech University Health Sciences Center El Paso Division of Cardiovascular Medicine El Paso Texas USA

4. Department of Internal Medicine, Division of Pulmonology and Critical Care Medicine Mount Sinai Medical Center Miami Beach Florida USA

5. Department of Internal Medicine Texas Tech University Health Science Center El Paso‐ Transmountain El Paso Texas USA

6. Department of Internal Medicine, Dell Seton Medical Center University of Texas at Austin Austin Texas USA

7. Houston Methodist Hospital Lung Center Houston Methodist Hospital Houston Texas USA

8. Department of Internal Medicine, Division of Pulmonary and Critical Care Texas Tech University Health Sciences Center El Paso El Paso Texas USA

Abstract

AbstractPulmonary arterial hypertension (PAH) is a cardiovascular disease with high mortality rate. Current guidelines propose initiation and escalation of PAH‐targeted treatment based on a goal‐directed approach targeting hemodynamic, functional, and biochemical variables. This approach has been successfully validated in large Caucasian cohorts. However, given the low number of Hispanic patients enrolled in large PAH trials and registries, it is unknown if the same prognostic tools can be applied to this patient population. We analyzed a single‐center outpatient cohort that consisted of 135 Hispanic patients diagnosed with PAH. Baseline characteristics were calculated based on COMPERA, COMPERA 2.0 and REVEAL 2.0 risk scores before the initiation of PAH‐targeted therapies. The survival rate at 1 year after diagnosis was 88% for the entire cohort. The three established risk scores to predict PAH outcomes yielded similar results with reasonable discrimination of mortality in the different risk strata (all p < 0.001). Hispanic patients with PAH have a high mortality rate. Our analysis suggests that guideline proposed risk assessment at baseline yields important prognostic information in this patient population.

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine

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