Literature DB >> 7458733

Evaluation of pulmonary function in neuromuscular disease.

R C Griggs, K M Donohoe, M J Utell, D Goldblatt, R T Moxley.   

Abstract

Pulmonary function tests were performed on 40 patients with neuromuscular disease. The maximum expiratory pressure was the most sensitive indicator of weakness and was decreased in 87% of adult patients. A comparison of Stead-Wells, electronic (Vanguard), and bellows spirometry (Vitalor) indicated an excellent correlation between the Stead-Wells and electronic devices. The bellows spirometer consistently underestimated volumes, particularly in severely weak patients.

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Year:  1981        PMID: 7458733     DOI: 10.1001/archneur.1981.00510010035004

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


  13 in total

1.  Nocturnal sleep and oxygen balance in Duchenne muscular dystrophy. A clinical and polygraphic 2-year follow-up study.

Authors:  R Manni; C Zucca; C A Galimberti; A Ottolini; I Cerveri; C Bruschi; M C Zoia; G Lanzi; A Tartara
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1991       Impact factor: 5.270

2.  Breathing patterns and HbSaO2 changes during nocturnal sleep in patients with Duchenne muscular dystrophy.

Authors:  R Manni; A Ottolini; I Cerveri; C Bruschi; M C Zoia; G Lanzi; A Tartara
Journal:  J Neurol       Date:  1989-10       Impact factor: 4.849

Review 3.  Respiratory involvement in inherited primary muscle conditions.

Authors:  N Shahrizaila; W J M Kinnear; A J Wills
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-10       Impact factor: 10.154

4.  Respiratory muscle and pulmonary function in polymyositis and other proximal myopathies.

Authors:  N M Braun; N S Arora; D F Rochester
Journal:  Thorax       Date:  1983-08       Impact factor: 9.139

Review 5.  Respiratory assessment in centronuclear myopathies.

Authors:  Barbara K Smith; Melissa Goddard; Martin K Childers
Journal:  Muscle Nerve       Date:  2014-08-05       Impact factor: 3.217

6.  Evaluation of a clinical implementation of a respiratory muscle training group during spinal cord injury rehabilitation.

Authors:  Anja M Raab; Jörg Krebs; Claudio Perret; Mirjam Pfister; Maria Hopman; Gabi Mueller
Journal:  Spinal Cord Ser Cases       Date:  2018-04-27

7.  Being ambulatory does not secure respiratory functions of Duchenne patients.

Authors:  Barış Ekici; Yakup Ergül; Burak Tatlı; Feride Bilir; Fatih Binboğa; Ayşe Süleyman; Zeynep Tamay; Mine Calışkan; Nermin Güler
Journal:  Ann Indian Acad Neurol       Date:  2011-07       Impact factor: 1.383

Review 8.  Pulmonary rehabilitation in patients with neuromuscular disease.

Authors:  Seong-Woong Kang
Journal:  Yonsei Med J       Date:  2006-06-30       Impact factor: 2.759

9.  Respiratory muscle strength and cough capacity in patients with Duchenne muscular dystrophy.

Authors:  Seong-Woong Kang; Yeoun-Seung Kang; Hong-Seok Sohn; Jung-Hyun Park; Jae-Ho Moon
Journal:  Yonsei Med J       Date:  2006-04-30       Impact factor: 2.759

10.  Effects of yoga breathing exercises on pulmonary function in patients with Duchenne muscular dystrophy: an exploratory analysis.

Authors:  Marcos Rojo Rodrigues; Celso Ricardo Fernandes Carvalho; Danilo Forghieri Santaella; Geraldo Lorenzi-Filho; Suely Kazue Nagahashi Marie
Journal:  J Bras Pneumol       Date:  2014 Mar-Apr       Impact factor: 2.624

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