A hemodynamic study of pulmonary hypertension in sickle cell disease
- PMID: 21732836
- DOI: 10.1056/NEJMoa1005565
A hemodynamic study of pulmonary hypertension in sickle cell disease
Abstract
Background: The prevalence and characteristics of pulmonary hypertension in adults with sickle cell disease have not been clearly established.
Methods: In this prospective study, we evaluated 398 outpatients with sickle cell disease (mean age, 34 years) at referral centers in France. All patients underwent Doppler echocardiography, with measurement of tricuspid-valve regurgitant jet velocity. Right heart catheterization was performed in 96 patients in whom pulmonary hypertension was suspected on the basis of a tricuspid regurgitant jet velocity of at least 2.5 m per second. Pulmonary hypertension was defined as a mean pulmonary arterial pressure of at least 25 mm Hg.
Results: The prevalence of a tricuspid regurgitant jet velocity of at least 2.5 m per second was 27%. In contrast, the prevalence of pulmonary hypertension as confirmed on catheterization was 6%. The positive predictive value of echocardiography for the detection of pulmonary hypertension was 25%. Among the 24 patients with confirmed pulmonary hypertension, the pulmonary-capillary wedge pressure was 15 mm Hg or less (indicating precapillary pulmonary hypertension) in 11 patients. Patients with confirmed pulmonary hypertension were older and had poorer functional capacity and higher levels of N-terminal pro-brain natriuretic peptide than other patients. In contrast, patients who had a tricuspid regurgitant jet velocity of at least 2.5 m per second without pulmonary hypertension and patients with a tricuspid regurgitant jet velocity of less than 2.5 m per second had similar clinical characteristics.
Conclusions: In this study of adults with sickle cell disease, the prevalence of pulmonary hypertension as confirmed on right heart catheterization was 6%. Echocardiographic evaluation alone had a low positive predictive value for pulmonary hypertension. (Funded by the French Ministry of Health and Assistance Publique-Hôpitaux de Paris; ClinicalTrials.gov number, NCT00434902.).
Comment in
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Pulmonary hypertension in sickle cell disease.N Engl J Med. 2011 Oct 27;365(17):1645-6; author reply 1648-9. doi: 10.1056/NEJMc1109130. N Engl J Med. 2011. PMID: 22029996 No abstract available.
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Pulmonary hypertension in sickle cell disease.N Engl J Med. 2011 Oct 27;365(17):1646; author reply 1648-9. doi: 10.1056/NEJMc1109130. N Engl J Med. 2011. PMID: 22029997 No abstract available.
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Pulmonary hypertension in sickle cell disease.N Engl J Med. 2011 Oct 27;365(17):1646-7; author reply 1648-9. doi: 10.1056/NEJMc1109130. N Engl J Med. 2011. PMID: 22029998 No abstract available.
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Pulmonary hypertension in sickle cell disease.N Engl J Med. 2011 Oct 27;365(17):1647; author reply 1648-9. doi: 10.1056/NEJMc1109130. N Engl J Med. 2011. PMID: 22029999 No abstract available.
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Pulmonary hypertension in sickle cell disease.N Engl J Med. 2011 Oct 27;365(17):1647-8. doi: 10.1056/NEJMc1109130. N Engl J Med. 2011. PMID: 22030000 No abstract available.
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Prevalence, risk factors and mortality of pulmonary hypertension defined by right heart catheterization in patients with sickle cell disease.Expert Rev Hematol. 2011 Dec;4(6):593-6. doi: 10.1586/ehm.11.66. Expert Rev Hematol. 2011. PMID: 22077523 No abstract available.
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Outcomes in elderly intensive care unit patients, pulmonary hypertension in sickle cell disease, and total liquid ventilation for therapeutic hypothermia after cardiac arrest in rabbits.Am J Respir Crit Care Med. 2012 Feb 15;185(4):453-4. doi: 10.1164/rccm.201109-1608RR. Am J Respir Crit Care Med. 2012. PMID: 22336678 Free PMC article. No abstract available.
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