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Hemodynamic trajectories and outcomes in patients with pulmonary arterial hypertension.
Amsallem, Myriam; Bagherzadeh, Shadi P; Boulate, David; Sweatt, Andrew J; Kudelko, Kristina T; Sung, Yon K; Feinstein, Jeffrey A; Fadel, Elie; Mercier, Olaf; Denault, Andre; Haddad, Francois; Zamanian, Roham.
Afiliación
  • Amsallem M; Division of Cardiovascular Medicine, Stanford University, Stanford, CA, USA.
  • Bagherzadeh SP; Stanford Cardiovascular Institute, Stanford University, Stanford, CA, USA.
  • Boulate D; Division of Cardiovascular Medicine, Stanford University, Stanford, CA, USA.
  • Sweatt AJ; INSERM UMR S 999, Hôpital Marie Lannelongue, Le Plessis-Robinson, France.
  • Kudelko KT; Division of Pulmonary and Critical Care Medicine, Stanford University, Stanford, CA, USA.
  • Sung YK; Vera Moulton Wall Center for Pulmonary Vascular Disease at Stanford, CA, USA.
  • Feinstein JA; Division of Pulmonary and Critical Care Medicine, Stanford University, Stanford, CA, USA.
  • Fadel E; Vera Moulton Wall Center for Pulmonary Vascular Disease at Stanford, CA, USA.
  • Mercier O; Division of Pulmonary and Critical Care Medicine, Stanford University, Stanford, CA, USA.
  • Denault A; Vera Moulton Wall Center for Pulmonary Vascular Disease at Stanford, CA, USA.
  • Haddad F; Department of Pediatrics (Cardiology), and by courtesy Bioengineering, Stanford University, Stanford, CA, USA.
  • Zamanian R; INSERM UMR S 999, Hôpital Marie Lannelongue, Le Plessis-Robinson, France.
Pulm Circ ; 10(4): 2045894020941343, 2020.
Article en En | MEDLINE | ID: mdl-33335708
The relative pulmonary to systemic pressure ratio (mean pulmonary arterial pressure/mean arterial pressure) has been proven to be valuable in cardiac surgery. Little is known on the prognostic value of baseline and trajectory of mean pulmonary arterial pressure/mean arterial pressure in pulmonary arterial hypertension. Patients with confirmed idiopathic, familial, drug and toxins, or connective tissue disease-related pulmonary arterial hypertension and at least one complete right heart catheterization were included and prospectively followed-up for 5.9 ± 4.03 years. Correlates of the primary end point (i.e. death or lung transplant need) during follow-up were determined using Cox regression modeling. Results showed that among the 308 patients included, 187 had at least one follow-up catheterization (median time between catheterizations: 2.16 (1.16-3.19) years). In the total cohort (mean age 47.3 ± 14.9 years, 82.8% of female and 58.1% in New York Heart Association class 3 or 4), mean pulmonary arterial pressure/mean arterial pressure (1.38 (1.07-1.77)) was associated with outcome (p = 0.01). Mean pulmonary arterial pressure/mean arterial pressure was incremental to a basic model (including right atrial pressure, systolic blood pressure, New York Heart Association class 3 or 4, and connective tissue disease) for outcome prediction, while mean pulmonary arterial pressure was not. In the 187 patients with a follow-up catheterization, both delta mean pulmonary arterial pressure and delta mean pulmonary arterial pressure/mean arterial pressure were associated with outcome (1.32 (1.11-1.58) and 1.31 (1.1-1.57) respectively, p < 0.01). Mean pulmonary arterial pressure and mean pulmonary arterial pressure/mean arterial pressure were both incremental to the basic model, while worsening in mean pulmonary arterial pressure or mean pulmonary arterial pressure/mean arterial pressure did not reach significance. In conclusion, mean pulmonary arterial pressure/mean arterial pressure at baseline prognosticates long-term outcome with a significant, albeit modest, incremental value to basic variables.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Pulm Circ Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Pulm Circ Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos