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Clinical Investigations: PULMONARY CIRCULATION |

Hemodynamics and Survival in Patients With Pulmonary Arterial Hypertension Related to Systemic Sclerosis*

Steven M. Kawut, MD; Darren B. Taichman, MD, PhD; Christine L. Archer-Chicko, MSN, CRNP; Harold I. Palevsky, MD, FCCP; Stephen E. Kimmel, MD, MSCE
Author and Funding Information

*From the Pulmonary Vascular Disease Program (Drs. Taichman and Palevsky, and Ms. Archer-Chinko), Pulmonary, Allergy, and Critical Care Division (Dr. Kawut), Cardiovascular Division and the Center for Clinical Epidemiology and Biostatistics (Dr. Kimmel), University of Pennsylvania School of Medicine, Philadelphia, PA.

Correspondence to: Steven Kawut, MD; Pulmonary Hypertension Center, Division of Pulmonary, Allergy, and Critical Care Medicine, Columbia University College of Physicians and Surgeons, 622 W 168th St, New York, NY 10032; e-mail: SK2097@columbia.edu



Chest. 2003;123(2):344-350. doi:10.1378/chest.123.2.344
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Study objectives: The goal of this study was to determine whether the survival of patients with pulmonary hypertension related to systemic sclerosis (SScPH) was different from that of patients with other forms of pulmonary arterial hypertension.

Design: Retrospective cohort study.

Setting: Tertiary care medical center.

Patients: Our cohort was composed of 33 patients with pulmonary hypertension that is sporadic, familial, or related to anorexigen use (PPH) and 22 patients with SScPH who underwent initial pulmonary artery catheterization and vasodilator study at our center between January 1997 and June 2001.

Measurements and results: Patients with SScPH had somewhat lower percentage of predicted lung volumes than patients with PPH (total lung capacity, 80% vs 92%; p = 0.06) and had lower percentage of predicted diffusion capacity of the lung for carbon monoxide (42% vs 68%; p = 0.0002). Right atrial pressure, pulmonary artery pressure, and cardiac index were similar between the groups. Patients with SScPH and PPH were treated with usual medical therapies, such as digoxin, warfarin, and continuous IV epoprostenol. Despite these similarities, the risk of death in patients with SScPH was higher than in patients with PPH (unadjusted hazard ratio, 2.9; 95% confidence interval, 1.1 to 7.8; p = 0.03). This increased risk appeared to persist after adjustment for a variety of demographic, hemodynamic, or treatment variables.

Conclusions: Despite having similar hemodynamics, patients with SScPH have a higher risk of death than patients with PPH. Future studies of the mechanism and therapy of pulmonary arterial hypertension should focus on the distinctions between the different forms of this disease.

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