Literature DB >> 3547120

Management of end stage respiratory failure in Duchenne muscular dystrophy.

J R Bach, J O'Brien, R Krotenberg, A S Alba.   

Abstract

There were 31 Duchenne patients placed on overnight mouth intermittent positive pressure ventilation for severe respiratory insufficiency at the average age of 19.9 years. Most patients had vital capacities less than 200 cc at their last evaluations. Of these, 23 patients are alive at the average age of 27 years and live in the community, although they are dependent on assisted ventilation 24 hours a day. There were 8 patients who died at the average age of 30 years. Although normocapnic during the day, the presence of symptomatic nocturnal hypoventilation or pCO2 over 55 mmHg documented by continuous overnight capnograph study indicates the need for introducing overnight respiratory assistance. Mouth intermittent positive pressure ventilation alone or in combination with other techniques of ventilatory assistance can prolong life while allowing optimal function, attainment of higher levels of education, and home management of patients with Duchenne muscular dystrophy.

Entities:  

Mesh:

Year:  1987        PMID: 3547120     DOI: 10.1002/mus.880100212

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  24 in total

1.  Spinal muscular atrophy--type I.

Authors:  M K M Hardart; R D Truog
Journal:  Arch Dis Child       Date:  2003-10       Impact factor: 3.791

2.  Living with a ventilator.

Authors:  I S Gilgoff
Journal:  West J Med       Date:  1991-05

3.  Accuracy of tidal volume delivered by home mechanical ventilation during mouthpiece ventilation: A bench evaluation.

Authors:  Adam Ogna; Helene Prigent; Line Falaize; Karl Leroux; Dante Santos; Isabelle Vaugier; David Orlikowski; Frederic Lofaso
Journal:  Chron Respir Dis       Date:  2016-07-08       Impact factor: 2.444

4.  2015 William Allan Award.

Authors:  Kay E Davies
Journal:  Am J Hum Genet       Date:  2016-03-03       Impact factor: 11.025

Review 5.  Respiratory care in muscular dystrophy.

Authors:  J Z Heckmatt
Journal:  Br Med J (Clin Res Ed)       Date:  1987-10-24

6.  Widening gap in age at muscular dystrophy-associated death between blacks and whites, 1986-2005.

Authors:  Aileen Kenneson; Ajay Vatave; Richard Finkel
Journal:  Neurology       Date:  2010-09-14       Impact factor: 9.910

7.  Liberation and mortality outcomes in pediatric long-term ventilation: A qualitative systematic review.

Authors:  Candice M Foy; Monica L Koncicki; Jeffrey D Edwards
Journal:  Pediatr Pulmonol       Date:  2020-08-12

8.  Outcome of non-invasive positive pressure ventilation in paediatric neuromuscular disease.

Authors:  S Katz; H Selvadurai; K Keilty; M Mitchell; I MacLusky
Journal:  Arch Dis Child       Date:  2004-02       Impact factor: 3.791

Review 9.  Aberrant NLRP3 Inflammasome Activation Ignites the Fire of Inflammation in Neuromuscular Diseases.

Authors:  Christine Péladeau; Jagdeep K Sandhu
Journal:  Int J Mol Sci       Date:  2021-06-04       Impact factor: 5.923

10.  Deep Learning of Ultrasound Imaging for Evaluating Ambulatory Function of Individuals with Duchenne Muscular Dystrophy.

Authors:  Ai-Ho Liao; Jheng-Ru Chen; Shi-Hong Liu; Chun-Hao Lu; Chia-Wei Lin; Jeng-Yi Shieh; Wen-Chin Weng; Po-Hsiang Tsui
Journal:  Diagnostics (Basel)       Date:  2021-05-27
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.