Literature DB >> 2920577

Patient and family participation in the management of respiratory failure in Duchenne's muscular dystrophy.

I Gilgoff1, W Prentice, A Baydur.   

Abstract

Mechanical ventilation is now considered a therapeutic option for respiratory failure associated with Duchenne's muscular dystrophy (DMD). Through the monitoring of forced vital capacity and PCO2, prediction of impending respiratory failure is possible. This knowledge allows the patient to choose institution of mechanical ventilation before acute respiratory failure or no intervention and preparation for a natural death. To assist patients and families in this decision making, a special clinic was established. Thirty adolescent boys with DMD were followed up. Eighteen boys reached the end stage of their disease. Three died of cardiac failure. Prediction of respiratory failure was possible in 14 of the remaining 15; 11 of the 15 were able to make educated choices regarding respirator assistance or a natural death. The clinic has shown that in the majority of cases, when properly educated, patients and families can be active participants in life-and-death decisions.

Entities:  

Keywords:  Death and Euthanasia; Professional Patient Relationship; Rancho Los Amigos Medical Center (Downey, Calif.)

Mesh:

Year:  1989        PMID: 2920577     DOI: 10.1378/chest.95.3.519

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


  4 in total

1.  Long term non-invasive ventilation in the community for patients with musculoskeletal disorders: 46 year experience and review.

Authors:  A Baydur; E Layne; H Aral; N Krishnareddy; R Topacio; G Frederick; W Bodden
Journal:  Thorax       Date:  2000-01       Impact factor: 9.139

2.  Muscle fiber type-predominant promoter activity in lentiviral-mediated transgenic mouse.

Authors:  Tomohiro Suga; En Kimura; Yuka Morioka; Masahito Ikawa; Sheng Li; Katsuhisa Uchino; Yuji Uchida; Satoshi Yamashita; Yasushi Maeda; Jeffrey S Chamberlain; Makoto Uchino
Journal:  PLoS One       Date:  2011-03-18       Impact factor: 3.240

3.  Skeletal muscle fibrosis in the mdx/utrn+/- mouse validates its suitability as a murine model of Duchenne muscular dystrophy.

Authors:  Kelly M Gutpell; William T Hrinivich; Lisa M Hoffman
Journal:  PLoS One       Date:  2015-01-21       Impact factor: 3.240

4.  Improvement of survival in Duchenne Muscular Dystrophy: retrospective analysis of 835 patients.

Authors:  Luigia Passamano; Antonella Taglia; Alberto Palladino; Emanuela Viggiano; Paola D'Ambrosio; Marianna Scutifero; Maria Rosaria Cecio; Vito Torre; Francesco DE Luca; Esther Picillo; Orlando Paciello; Giulio Piluso; Gerardo Nigro; Luisa Politano
Journal:  Acta Myol       Date:  2012-10
  4 in total

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