Hospitalization for pain in patients with sickle cell disease treated with sildenafil for elevated TRV and low exercise capacity

Author:

Machado Roberto F.1,Barst Robyn J.2,Yovetich Nancy A.3,Hassell Kathryn L.4,Kato Gregory J.5,Gordeuk Victor R.6,Gibbs J. Simon R.7,Little Jane A.8,Schraufnagel Dean E.1,Krishnamurti Lakshmanan9,Girgis Reda E.10,Morris Claudia R.11,Rosenzweig Erika B.2,Badesch David B.4,Lanzkron Sophie10,Onyekwere Onyinye6,Castro Oswaldo L.6,Sachdev Vandana6,Waclawiw Myron A.12,Woolson Rob3,Goldsmith Jonathan C.13,Gladwin Mark T.1415,

Affiliation:

1. University of Illinois, Chicago, IL;

2. Columbia University, New York, NY;

3. Rho Inc, Chapel Hill, NC;

4. University of Colorado, Denver, CO;

5. Cardiovascular and Pulmonary Branch, National Heart, Lung and Blood Institute (NHLBI), National Institutes of Health (NIH), Bethesda, MD;

6. Howard University, Washington, DC;

7. National Heart & Lung Institute, Imperial College London;

8. Albert Einstein College of Medicine, Bronx, NY;

9. Children's Hospital of Pittsburgh, Pittsburgh, PA;

10. Johns Hopkins University, Baltimore, MD;

11. Children's Hospital & Research Center Oakland, Oakland, CA;

12. Office of Biostatistics Research, NHLBI, Bethesda, MD;

13. NHLBI, NIH, Bethesda, MD; and

14. Division of Pulmonary, Allergy and Critical Care Medicine and

15. the Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, PA

Abstract

Abstract In adults with sickle cell disease (SCD), an increased tricuspid regurgitation velocity (TRV) by Doppler echocardiography is associated with increased morbidity and mortality. Although sildenafil has been shown to improve exercise capacity in patients with pulmonary arterial hypertension, it has not been evaluated in SCD. We therefore sought to determine whether sildenafil could improve exercise capacity in SCD patients with increased TRV and a low exercise capacity. A TRV ≥ 2.7 m/s and a 6-minute walk distance (6MWD) between 150 and 500 m were required for enrollment in this 16-week, double-blind, placebo-controlled sildenafil trial. After 74 of the screened subjects were randomized, the study was stopped early due to a higher percentage of subjects experiencing serious adverse events in the sildenafil arm (45% of sildenafil, 22% of placebo, P = .022). Subject hospitalization for pain was the predominant cause for this difference: 35% with sildenafil compared with 14% with placebo (P = .029). There was no evidence of a treatment effect on 6MWD (placebo-corrected effect −9 m; 95% confidence interval [95% CI] −56-38; P = .703), TRV (P = .503), or N-terminal pro-brain natriuretic peptide (P = .410). Sildenafil appeared to increase hospitalization rates for pain in patients with SCD. This study is registered at www.clinicaltrials.gov as NCT00492531.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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