TY - JOUR
T1 - Predicting the Need for Upfront Combination Therapy in Pulmonary Arterial Hypertension
AU - Bajwa, Abubakr A.
AU - Qureshi, Tauseef
AU - Shujaat, Adil
AU - Seeram, Vandana
AU - Jones, Lisa M.
AU - Al-Saffar, Farah
AU - Cury, James D.
N1 - Publisher Copyright:
© 2015 The Author(s).
PY - 2015/7/19
Y1 - 2015/7/19
N2 - Background: Combination therapy is commonly used for pulmonary arterial hypertension (PAH) treatment. We aimed to identify factors that may predict the need for future combination therapy. Methods: We conducted a retrospective chart review of consecutive patients with PAH in an aim to describe baseline clinical, echocardiogram, and hemodynamic characteristics of patients who eventually required combination therapy during the course of their disease and compared them to the ones who were maintained on monotherapy. Results: The monotherapy group was followed for an average of 31.8±18.8 months and the combination therapy group was followed for an average of 28.7 ± 13.6 months. Among the 71 patients analyzed, a significantly higher number of patients who eventually required combination therapy belonged to World Health Organization functional class 3 (45% vs 37%) and 4 (23% vs 0) at baseline, compared with those on monotherapy (P < .05). Combination group also had a higher Registry to Evaluate Early And Long-term PAH Disease Management (REVEAL) PAH risk score at presentation. End of 6-minute walk test (6MWT), oxygen saturation (SpO2) was also lower in the combination therapy group, 86% ± 8% versus 91% ± 7% (P < .05). Patients who eventually required combination therapy were more frequently noticed to have right ventricular enlargement, right atrial enlargement, and had a higher resting estimated right ventricular systolic pressure (RVSP). Right heart catheterization-derived hemodynamics data at baseline showed that the combination therapy group had a higher mean pulmonary artery (PA) pressure, lower pulmonary capillary wedge pressure, lower cardiac output, and higher pulmonary vascular resistance (PVR). Onunivariate analysis, only PVR≥300 dyne·s/cm5, mean PA pressure of≥40mmHg, estimated RVSP≥60mmHg, PAH risk score≥10, and end of6MWTsaturation of≤90% were of significance. Conclusion: Patients with PAH who require combination therapy in the course of their disease have worse hemodynamics, PAH risk score, functional class, and end of 6MWT oxygen saturation at the time of presentation compared to patients maintained on monotherapy.
AB - Background: Combination therapy is commonly used for pulmonary arterial hypertension (PAH) treatment. We aimed to identify factors that may predict the need for future combination therapy. Methods: We conducted a retrospective chart review of consecutive patients with PAH in an aim to describe baseline clinical, echocardiogram, and hemodynamic characteristics of patients who eventually required combination therapy during the course of their disease and compared them to the ones who were maintained on monotherapy. Results: The monotherapy group was followed for an average of 31.8±18.8 months and the combination therapy group was followed for an average of 28.7 ± 13.6 months. Among the 71 patients analyzed, a significantly higher number of patients who eventually required combination therapy belonged to World Health Organization functional class 3 (45% vs 37%) and 4 (23% vs 0) at baseline, compared with those on monotherapy (P < .05). Combination group also had a higher Registry to Evaluate Early And Long-term PAH Disease Management (REVEAL) PAH risk score at presentation. End of 6-minute walk test (6MWT), oxygen saturation (SpO2) was also lower in the combination therapy group, 86% ± 8% versus 91% ± 7% (P < .05). Patients who eventually required combination therapy were more frequently noticed to have right ventricular enlargement, right atrial enlargement, and had a higher resting estimated right ventricular systolic pressure (RVSP). Right heart catheterization-derived hemodynamics data at baseline showed that the combination therapy group had a higher mean pulmonary artery (PA) pressure, lower pulmonary capillary wedge pressure, lower cardiac output, and higher pulmonary vascular resistance (PVR). Onunivariate analysis, only PVR≥300 dyne·s/cm5, mean PA pressure of≥40mmHg, estimated RVSP≥60mmHg, PAH risk score≥10, and end of6MWTsaturation of≤90% were of significance. Conclusion: Patients with PAH who require combination therapy in the course of their disease have worse hemodynamics, PAH risk score, functional class, and end of 6MWT oxygen saturation at the time of presentation compared to patients maintained on monotherapy.
KW - cardiovascular disease
KW - combination therapy
KW - predictors
KW - pulmonary arterial hypertension
UR - https://www.scopus.com/pages/publications/84931363703
U2 - 10.1177/1074248414568195
DO - 10.1177/1074248414568195
M3 - Article
C2 - 25613465
AN - SCOPUS:84931363703
SN - 1074-2484
VL - 20
SP - 395
EP - 400
JO - Journal of Cardiovascular Pharmacology and Therapeutics
JF - Journal of Cardiovascular Pharmacology and Therapeutics
IS - 4
ER -