Demographic, hemodynamic characteristics, and therapeutic trends of pulmonary hypertension patients: The Pulmonary Hypertension Mexican registry (REMEHIP)

Author:

Jerjes‐Sánchez Carlos12ORCID,Ramírez‐Rivera Alicia3ORCID,Hernandez Nayeli Zayas4,Cueto Robledo Guillermo5ORCID,García‐Aguilar Humberto6ORCID,Gutiérrez‐Fajardo Pedro7ORCID,Seoane García de León Mario8,Moreno Hoyos‐Abril Francisco9ORCID,Ernesto Beltrán Gámez Miguel10ORCID,Elizalde Jose11,Fccp Tomás Pulido4ORCID,Sandoval Julio8ORCID,

Affiliation:

1. Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud Monterrey Nuevo Leon Mexico

2. Instituto de Cardiología y Medicina Vascular, TecSalud San Pedro Garza Garcia Nuevo Leon Mexico

3. Unidad de Investigación Clínica en Medicina S.C. Monterrey Nuevo Leon Mexico

4. Instituto Nacional de Cardiología Ignacio Chavez Mexico City Mexico

5. Hospital General de México Mexico City Mexico

6. Centro Médico Nacional 20 de noviembre, ISSSTE Mexico City Mexico

7. Cardiotest, Laboratorio de Ecocardiografía Guadalajara Jalisco Mexico

8. Centro Médico ABC Mexico City Mexico

9. Hospital Universitario “Dr. José E. González” UANL Monterrey Nuevo Leon Mexico

10. Hospital Angeles de Tijuana Tijuana Baja California Mexico

11. Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán Mexico City Mexico

Abstract

AbstractData on demographic characteristics and therapeutic approaches in Latin American pulmonary arterial hypertension (PAH) patients are scarce. Pulmonary Hypertension Mexican registry (REMEHIP) is a multicenter Mexican registry of adult and pediatric patients, including prevalent and incident cases. Objective: assess clinical characteristics, treatment trends, and in‐hospital outcomes. Inclusion: age >2 years, diagnosis of pulmonary hypertension (PH) (groups 1 and 4), right heart catheterization with mPAP ≥25 mmHg, PWP ≤ 15 mmHg, and PVR > 3 Wood unit (WU). We included 875 PH patients, 619 adults, 133 pediatric idiopathic PAH (IPAH), and 123 chronic thromboembolic pulmonary hypertension (CTEPH) patients. We enrolled 48.4% of the incident and 51.6% of the prevalent adult and pediatric patients. PAH adults: age 43 ± 15, females 81.9%, functional class (FC) (I/II) 66.5%, 6‐min walk distance (6MWD) 378 ± 112 m, mPAP 57.3 ± 19.0 mmHg, confidence interval (CI) 3.3 ± 1.5 L/min/m2, PVR 12.0 ± 8.1 WU. PAH pediatrics: age 9 ± 5, females 51.1%, FC (I/II) 85.5%, 6MWD 376 ± 103 m, mPAP 49.7 ± 13.4 mmHg, CI 2.6 ± 0.9 L/min/m2, PVR 16.4 ± 13.5 WU. CTEPH: age 44 ± 17, females 56.1%, FC (I/II) 65.5%, 6MWD 369 ± 126 m, mPAP 49.7 ± 13.4 mmHg, CI 2.6 ± 0.9 L/min/m2, PVR 10.5 + 6.5 WU. When we analyzed the IPAH group separately, it sustained a high functional class I/II incidence. REMEHIP shows better functional class in young females with severe PAH than in American and European patients. Also, PAH pediatric patients had a better functional class than other registries. However, our registry also shows that our population's access to specific pharmacologic treatments is still far from optimal.

Publisher

Wiley

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