Literature DB >> 16304281

Factors associated with dyspnea in adult patients with sickle cell disease.

Christophe Delclaux1, Françoise Zerah-Lancner, Dora Bachir, Anoosha Habibi, Jean-Luc Monin, Bertrand Godeau, Frédéric Galacteros.   

Abstract

OBJECTIVE: The aim of this prospective study was to determine the cardiorespiratory factors associated with dyspnea in patients with sickle cell SS-hemoglobin disease, with a specific interest in lung vascular involvement. MEASUREMENTS: Forty-nine patients (29 women and 20 men; mean [+/- SD] age: women, 29 +/- 6 years; men, 31 +/- 11 years) underwent direct evaluations (Borg scale evaluation during a 6-min walk test) and indirect evaluations (modified Medical Research Council [MRC]score) of their dyspnea, pulmonary function tests (PFTs) [spirometry, volumes, diffusing capacity of the lung for carbon monoxide (Dlco), diffusing capacity of the alveolar-capillary membrane, and pulmonary capillary blood volume measurements], echocardiography, and biological evaluation.
RESULTS: Thirty-four patients complained of significant breathlessness (MRC score, > 1). Indirect and direct evaluations of dyspnea were correlated. PFT results depicted a very mild restrictive pattern (mean total pulmonary capacity, 86 +/- 11% predicted) and an impairment of Dlco (mean Dlco corrected for the degree of anemia, 69 +/- 13% predicted). The statistical analysis demonstrated that dyspnea and exercise performance were closely linked to indexes of Dlco but not with any echocardiographic or biological measure including anemia. Nevertheless, only approximately 25% of the variability was explained by these associations. Despite having a similar history of vasoocclusive crisis events, women had more severe anemia, dyspnea, decreases in Dlco (corrected for the degree of anemia), and a higher capillary blood volume (corrected for alveolar volume) than men.
CONCLUSION: Lung vascular disease contributes to dyspnea and the exercise limitation of patients with sickle cell disease. A sequential assessment of Dlco would therefore constitute one of the objective functional end points for follow-up studies of these patients.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 16304281     DOI: 10.1378/chest.128.5.3336

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  11 in total

1.  Recurrent, severe wheezing is associated with morbidity and mortality in adults with sickle cell disease.

Authors:  Robyn T Cohen; Anusha Madadi; Morey A Blinder; Michael R DeBaun; Robert C Strunk; Joshua J Field
Journal:  Am J Hematol       Date:  2011-08-02       Impact factor: 10.047

2.  Pattern of Lung Function Is Not Associated with Prior or Future Morbidity in Children with Sickle Cell Anemia.

Authors:  Robyn T Cohen; Robert C Strunk; Mark Rodeghier; Carol L Rosen; Fenella Jane Kirkham; Jane Kirkby; Michael R DeBaun
Journal:  Ann Am Thorac Soc       Date:  2016-08

3.  Abnormal pulmonary function in adults with sickle cell anemia.

Authors:  Elizabeth S Klings; Diego F Wyszynski; Vikki G Nolan; Martin H Steinberg
Journal:  Am J Respir Crit Care Med       Date:  2006-03-23       Impact factor: 21.405

Review 4.  How I treat hypoxia in adults with hemoglobinopathies and hemolytic disorders.

Authors:  Evans M Machogu; Roberto F Machado
Journal:  Blood       Date:  2018-09-11       Impact factor: 22.113

5.  Lung function and six-minute walk test performance in individuals with sickle cell disease.

Authors:  Daniela G Ohara; Gualberto Ruas; Isabel A P Walsh; Shamyr S Castro; Mauricio Jamami
Journal:  Braz J Phys Ther       Date:  2014 Jan-Feb       Impact factor: 3.377

6.  Relationship between pulmonary and cardiac abnormalities in sickle cell disease: implications for the management of patients.

Authors:  Maria Christina Paixão Maioli; Andrea Ribeiro Soares; Ricardo Bedirian; Ursula David Alves; Cirlene de Lima Marinho; Agnaldo José Lopes
Journal:  Rev Bras Hematol Hemoter       Date:  2015-12-11

7.  Respiratory resistance and reactance in adults with sickle cell anemia: Correlation with functional exercise capacity and diagnostic use.

Authors:  Cirlene de Lima Marinho; Maria Christina Paixão Maioli; Jorge Luis Machado do Amaral; Agnaldo José Lopes; Pedro Lopes de Melo
Journal:  PLoS One       Date:  2017-12-08       Impact factor: 3.240

8.  Relationship between ventilation heterogeneity and exercise intolerance in adults with sickle cell anemia.

Authors:  A J Lopes; C L Marinho; U D Alves; C E A Gonçalves; P O Silva; E C Botelho; R Bedirian; A R Soares; M C P Maioli
Journal:  Braz J Med Biol Res       Date:  2017-07-20       Impact factor: 2.590

9.  Cardiorespiratory pathogenesis of sickle cell disease in a mouse model.

Authors:  Jun Ren; Xiuqing Ding; Marie Trudel; John J Greer; Joanna E MacLean
Journal:  Sci Rep       Date:  2017-08-17       Impact factor: 4.379

10.  Salbutamol Worsens the Autonomic Nervous System Dysfunction of Children With Sickle Cell Disease.

Authors:  Plamen Bokov; Houmam El Jurdi; Isabelle Denjoy; Claudine Peiffer; Noria Medjahdi; Laurent Holvoet; Malika Benkerrou; Christophe Delclaux
Journal:  Front Physiol       Date:  2020-02-26       Impact factor: 4.566

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.