Literature DB >> 18174543

Pulmonary hypertension and cor pulmonale during severe acute chest syndrome in sickle cell disease.

Armand Mekontso Dessap1, Rusel Leon, Anoosha Habibi, Ruben Nzouakou, Françoise Roudot-Thoraval, Serge Adnot, Bertrand Godeau, Frederic Galacteros, Christian Brun-Buisson, Laurent Brochard, Bernard Maitre.   

Abstract

RATIONALE: Steady-state mild pulmonary hypertension is a risk factor for death in adults with sickle cell disease. Acute pulmonary hypertension has been reported during exercise and vasoocclusive pain crisis in these patients.
OBJECTIVES: The aim of the present study was to evaluate changes in pulmonary pressures and cardiac biomarkers during severe acute chest syndrome and their associations with mortality.
METHODS: We prospectively evaluated 70 consecutive adults who received standardized treatment in our intensive care unit for a total of 84 episodes. At admission, cardiac biomarkers were measured. Transthoracic echocardiography was performed for pulmonary hypertension assessment via measurement of tricuspid regurgitant jet velocity and was repeated when possible after resolution.
MEASUREMENTS AND MAIN RESULTS: Tricuspid jet velocity was less than 2.5 m/second in 34 (40%) of the 84 episodes, 2.5 to 2.9 m/second in 19 (23%), and 3 m/second or greater in 31 episodes (37%). Cor pulmonale occurred in 11 (13%) episodes. Tricuspid jet velocity showed significant positive correlations with B-type natriuretic peptide (rho = 0.54, P < 0.01) and cardiac troponin I (rho = 0.42, P < 0.01). Pulmonary pressures increased compared with steady state then decreased after resolution. All five patients who required invasive ventilation and all four patients who died during the immediate hospital course had jet velocity values of 3 m/second or greater. Overall mortality was 12.9% (9 patients) and survival was significantly lower in patients whose jet velocity was 3 m/second or greater during at least one episode, compared with the other patients (P < 0.01).
CONCLUSIONS: Pulmonary pressures increase during severe acute chest syndrome, and pulmonary hypertension is associated with cardiac biomarker elevation and a higher risk of death.

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Year:  2008        PMID: 18174543     DOI: 10.1164/rccm.200710-1606OC

Source DB:  PubMed          Journal:  Am J Respir Crit Care Med        ISSN: 1073-449X            Impact factor:   21.405


  48 in total

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3.  Exercise capacity and haemodynamics in patients with sickle cell disease with pulmonary hypertension treated with bosentan: results of the ASSET studies.

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4.  An unusual cause of acute cor pulmonale--significance of the 'continuous diaphragm sign'.

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7.  Hemodynamic predictors of mortality in adults with sickle cell disease.

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Review 9.  Pathophysiology and treatment of pulmonary hypertension in sickle cell disease.

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10.  Ten tips for managing critically ill patients with sickle cell disease.

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