Literature DB >> 2753240

Central ventilatory dysfunction in myelodysplasia: an independent determinant of survival.

R M Hays1, R A Jordan, J F McLaughlin, R E Nickel, L D Fisher.   

Abstract

Central ventilatory dysfunction (CVD) is a significant complication of myelodysplasia with Arnold-Chiari type II defect. The records of 616 patients with myelodysplasia were reviewed and CVD was documented in 35 cases (5.7 per cent): it was the single most common cause of death in this population. There was no significant association between CVD and level of lesion, severity of hydrocephalus, hemorrhage or infection. The effects of CVD may be variable, with some patients having spontaneous remission and others having severe, often fatal, disruption of ventilation.

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Year:  1989        PMID: 2753240     DOI: 10.1111/j.1469-8749.1989.tb04005.x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  3 in total

1.  Apnea associated with Chiari malformation: medullary hemorrhage revealed by MRI.

Authors:  S Nomura; T Akimura; Y Eguchi; Y Shiroyama; H Ito; T Saito
Journal:  Childs Nerv Syst       Date:  1993-09       Impact factor: 1.475

2.  Central Hypoventilation Syndromes.

Authors:  Christopher Cielo; Carole L Marcus
Journal:  Sleep Med Clin       Date:  2014-03-01

3.  Central Alveolar Hypoventilation Syndromes.

Authors:  Hiren Muzumdar; Raanan Arens
Journal:  Sleep Med Clin       Date:  2008-12-01
  3 in total

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