Literature DB >> 624106

Succinylcholine sensitivity in a Nova Scotia family.

J J Candy, M J McQueen.   

Abstract

Succinylcholine apnoea is usually the result of a delay in hydrolysis of the injected muscle relaxant due to the presence of an inherited defect in the enzyme cholinesterase. This report presents a Nova Scotia family in whom several members had "difficulty in breathing" following anaesthesia. Subsequent investigations revealed the presence of several phenotypes of the enzyme cholinesterase including individuals who were homozygous for the atypical cholinesterase genes. The frequency of occurrence and significance of the various phenotypes are discussed, together with their management and recommendations for family screening.

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Year:  1978        PMID: 624106     DOI: 10.1007/bf03006785

Source DB:  PubMed          Journal:  Can Anaesth Soc J        ISSN: 0008-2856


  4 in total

Review 1.  PHARMACOGENETICS AND ANESTHESIA.

Authors:  W KALOW
Journal:  Anesthesiology       Date:  1964 May-Jun       Impact factor: 7.892

2.  A comparison of optical and manometric methods for the assay of human serum cholinesterase.

Authors:  W KALOW; H A LINDSAY
Journal:  Can J Biochem Physiol       Date:  1955-07

3.  Case history number 92: Prolonged apnea after succinylcholine in a dental outpatient.

Authors:  R G McLaren; E A Moffitt
Journal:  Anesth Analg       Date:  1976 Sep-Oct       Impact factor: 5.108

4.  Differentiation of serum cholinesterase variants by succinyldicholine inhibition.

Authors:  J King; D Griffin
Journal:  Br J Anaesth       Date:  1973-05       Impact factor: 9.166

  4 in total
  1 in total

1.  Abnormal enzyme phenotype (E1a E1f): normal response to succinylcholine.

Authors:  M J McQueen; F Lepinskie; R D Strickland; A Trimble
Journal:  Can Anaesth Soc J       Date:  1979-03
  1 in total

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