Literature DB >> 24440340

Supine changes in lung function correlate with chronic respiratory failure in myotonic dystrophy patients.

Mathias Poussel1, Pierre Kaminsky2, Pierre Renaud3, Julien Laroppe3, Lelia Pruna2, Bruno Chenuel3.   

Abstract

Quality of life and prognosis of patients with myotonic dystrophy type 1 (MD1) often depend on the degree of lung function impairment. This study was designed to assess the respective prevalence of ventilatory restriction, hypoxaemia and hypercapnia in MD1 patients and to determine whether postural changes in lung function could contribute to the early diagnosis of poor respiratory outcome. Fifty-eight patients (42.6±12.9 years) with MD1 were prospectively evaluated from April 2008 to June 2010 to determine their supine and upright lung function and arterial blood gases. The prevalence of ventilatory restriction was 36% and increased with the severity of muscular disability (from 7.7% to 70.6%). The prevalence of hypoxaemia and hypercapnia was 37.9% and 25.9%, respectively. Multiple regression analysis showed that the supine fall in FEV1 was the only variable associated with ventilatory restriction, hypoxaemia and hypercapnia. Our data indicate that supine evaluation of lung function could be helpful to predict poor respiratory outcome, which is closely correlated with hypoxaemia and/or hypercapnia.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Hypercapnia; Hypoxaemia; Lung function; Myotonic dystrophy; Ventilatory restriction

Mesh:

Year:  2014        PMID: 24440340     DOI: 10.1016/j.resp.2014.01.006

Source DB:  PubMed          Journal:  Respir Physiol Neurobiol        ISSN: 1569-9048            Impact factor:   1.931


  6 in total

Review 1.  Myotonic dystrophy.

Authors:  Charles A Thornton
Journal:  Neurol Clin       Date:  2014-06-06       Impact factor: 3.806

Review 2.  Sleep Complaints, Sleep and Breathing Disorders in Myotonic Dystrophy Type 2.

Authors:  Andrea Romigi; Michelangelo Maestri; Carmine Nicoletta; Giuseppe Vitrani; Marco Caccamo; Gabriele Siciliano; Enrica Bonanni; Diego Centonze; Alessandro Sanduzzi
Journal:  Curr Neurol Neurosci Rep       Date:  2019-02-09       Impact factor: 5.081

Review 3.  Myotonic Dystrophies: Targeting Therapies for Multisystem Disease.

Authors:  Samantha LoRusso; Benjamin Weiner; W David Arnold
Journal:  Neurotherapeutics       Date:  2018-10       Impact factor: 7.620

4.  Noninvasive assessment of respiratory muscle strength and activity in Myotonic dystrophy.

Authors:  Morgana de Araújo Evangelista; Fernando Augusto Lavezzo Dias; Mário Emílio Teixeira Dourado Júnior; George Carlos do Nascimento; Antonio Sarmento; Lucien Peroni Gualdi; Andrea Aliverti; Vanessa Resqueti; Guilherme Augusto de Freitas Fregonezi
Journal:  PLoS One       Date:  2017-06-08       Impact factor: 3.240

Review 5.  Respiratory management of patients with neuromuscular disease: current perspectives.

Authors:  Gerald Pfeffer; Marcus Povitz
Journal:  Degener Neurol Neuromuscul Dis       Date:  2016-11-18

6.  The effect of body position on pulmonary function: a systematic review.

Authors:  Shikma Katz; Nissim Arish; Ariel Rokach; Yacov Zaltzman; Esther-Lee Marcus
Journal:  BMC Pulm Med       Date:  2018-10-11       Impact factor: 3.317

  6 in total

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