Literature DB >> 11468332

Postural change of forced vital capacity predicts some respiratory symptoms in ALS.

J Varrato1, A Siderowf, P Damiano, S Gregory, D Feinberg, L McCluskey.   

Abstract

The detection of respiratory muscle weakness in ALS is necessary to plan initiation of noninvasive positive pressure ventilation and begin discussion of advanced directives. The authors measured the erect seated and supine forced vital capacity (FVC) in 38 patients with ALS and 15 controls. The supine FVC is significantly lower and the erect--supine FVC difference is significantly greater in patients with complaints of dyspnea, orthopnea, and daytime fatigue.

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Year:  2001        PMID: 11468332     DOI: 10.1212/wnl.57.2.357

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  14 in total

1.  Home mechanical ventilation: a Canadian Thoracic Society clinical practice guideline.

Authors:  Douglas A McKim; Jeremy Road; Monica Avendano; Steve Abdool; Fabien Cote; Nigel Duguid; Janet Fraser; Fracois Maltais; Debra L Morrison; Colleen O'Connell; Basil J Petrof; Karen Rimmer; Robert Skomro
Journal:  Can Respir J       Date:  2011 Jul-Aug       Impact factor: 2.409

2.  Mandibuloptosis as a cause of supine choking in a patient with amyotrophic lateral sclerosis.

Authors:  Michito Namekawa; Hiroto Ito; Tomoaki Kameda; Imaharu Nakano
Journal:  J Neurol       Date:  2012-01-25       Impact factor: 4.849

Review 3.  [Residual neuromuscular blockades. Clinical consequences, frequency and avoidance strategies].

Authors:  T Fuchs-Buder; M Eikermann
Journal:  Anaesthesist       Date:  2006-01       Impact factor: 1.041

4.  Prognosis of amyotrophic lateral sclerosis with respiratory onset.

Authors:  Christen L Shoesmith; Karen Findlater; Ann Rowe; Michael J Strong
Journal:  J Neurol Neurosurg Psychiatry       Date:  2006-11-06       Impact factor: 10.154

Review 5.  Measures and markers in amyotrophic lateral sclerosis.

Authors:  Merit Cudkowicz; Muhammad Qureshi; Jeremy Shefner
Journal:  NeuroRx       Date:  2004-04

Review 6.  Symptom Management and End-of-Life Care in Amyotrophic Lateral Sclerosis.

Authors:  Carlayne E Jackson; April L McVey; Stacy Rudnicki; Mazen M Dimachkie; Richard J Barohn
Journal:  Neurol Clin       Date:  2015-11       Impact factor: 3.806

7.  Respiratory and nutritional support in amyotrophic lateral sclerosis.

Authors:  Namita A Goyal; Tahseen Mozaffar
Journal:  Curr Treat Options Neurol       Date:  2014-02       Impact factor: 3.598

8.  How respiratory muscle strength correlates with cough capacity in patients with respiratory muscle weakness.

Authors:  Jung Hyun Park; Seong-Woong Kang; Sang Chul Lee; Won Ah Choi; Dong Hyun Kim
Journal:  Yonsei Med J       Date:  2010-05       Impact factor: 2.759

Review 9.  Practice parameter update: the care of the patient with amyotrophic lateral sclerosis: drug, nutritional, and respiratory therapies (an evidence-based review): report of the Quality Standards Subcommittee of the American Academy of Neurology.

Authors:  R G Miller; C E Jackson; E J Kasarskis; J D England; D Forshew; W Johnston; S Kalra; J S Katz; H Mitsumoto; J Rosenfeld; C Shoesmith; M J Strong; S C Woolley
Journal:  Neurology       Date:  2009-10-13       Impact factor: 9.910

Review 10.  Mechanical ventilation for amyotrophic lateral sclerosis/motor neuron disease.

Authors:  Aleksandar Radunovic; Djillali Annane; Muhammad K Rafiq; Ruth Brassington; Naveed Mustfa
Journal:  Cochrane Database Syst Rev       Date:  2017-10-06
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