Classification of malignant hyperthermia-equivocal patients by 4-chloro-M-cresol.

Anesth Analg

L. Boltzmann Institute for Experimental Anaesthesiology and Research in Intensive Care Medicine, and Department of Anaesthesiology and General Intensive Care B, University of Vienna, Austria.

Published: July 1997

AI Article Synopsis

  • The study focused on the effects of 4-chloro-m-cresol (4-CmC) on muscle contractions in malignant hyperthermia (MH) equivocal (MHE) cases to clarify diagnostic ambiguities.
  • In vitro contracture tests were conducted on 35 participants, revealing that MH susceptible (MHS) muscles reacted significantly stronger to certain concentrations of 4-CmC compared to MHE halothane sensitive (MHEh) and malignant hyperthermia normal (MHN) muscles.
  • The research indicates 4-CmC might help refine MHE diagnoses, but it’s too early to rely on it fully, as MHE individuals may still have underlying genetic issues that affect their reaction to MH.

Article Abstract

To clarify the contracture response to 4-chloro-m-cresol (4-CmC) in malignant hyperthermia (MH) equivocal (MHE) muscle, we studied the effect of cumulative concentrations of 4-CmC. In vitro contracture test (IVCT) was performed in 35 probands according to the European MH test protocol. Surplus muscle bundles were exposed to 4-CmC (25-200 micromol/L), maintaining each concentration for 4 and 8 min. After 4 min exposure, the contracture increase of MH susceptible (MHS) (n = 7) muscle specimens was significantly (P = 0.05) greater at 50 micromol/L compared with either MHE halothane sensitive (MHEh) (n = 13) or MH normal (MHN) (n = 15) classified patients. Statistically significant differences (P < 0.05) were also found at 75 micromol/L. Exposure for 8 min yielded significant differences at 50 micromol/L only between MHS and MHEh. MHEh muscles revealed a dose-response curve similar to that found in MHN specimens. MHS muscles showed a significantly higher sensitivity to 4-CmC than either MHEh or MHN, and, in the probands tested so far, MHEh and MHN muscles seem to identically respond to 4-CmC, which seems to indicate a normal response in MHEh probands, implying no MH susceptibility. Therefore, 4-CmC might reduce the frequency of MHEh diagnosis based on standard halothane-caffeine IVCT. However, since MHE individuals may also represent an aberrant genetic status, with MH causing defects linked to unknown mutations, it is premature to consider 4-CmC as a solution to the diagnostic uncertainty of the true status of MHE probands. Presently, 4-CmC may provide supplementary information for a more precise phenotypic categorization of MHE individuals.

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http://dx.doi.org/10.1097/00000539-199707000-00027DOI Listing

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