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The use of Short-Acting Relaxants in E.C.T.

Published online by Cambridge University Press:  08 February 2018

A. B. Monro
Affiliation:
Long Grove Hospital, Epsom
Anne K. Kirkland
Affiliation:
Long Grove Hospital, Epsom
A. Gillie
Affiliation:
Long Grove Hospital, Epsom
D. L. M. McNeill
Affiliation:
Long Grove Hospital, Epsom

Extract

Since the introduction of curare to modify the contractions in E.C.T., the use of relaxants has become standard psychiatric practice. These substances reduce the risk of fractures and enable treatment to be given to patients who would otherwise be denied it owing to risks arising from concomitant physical disease. During recent years great efforts have been made to simplify the technique of muscle relaxation, in particular to evolve a method which is short in duration, free from undesirable side-effects and easy in use. In this short paper we give a description of our experience with three drugs recently introduced, namely, Suxamethonium Bromide or Brevidil “M” which we used in 111 treatments, Suxethonium Bromide or Brevidil “E” (70 treatments), and Suxamethonium Chloride or Scoline (653 treatments). These choline succinic ester derivatives have similar characteristics which can be considered together.

Type
Part I.—Original Articles
Copyright
Copyright © Royal College of Psychiatrists, 1953 

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References

Bovet, D., Bovet-Nitti, F., Guarino, S., and Longo, V. G., R.C. 1st sup. San., 1949a, 12, 810.Google Scholar
Iidem and Marotta, M., ibid., 1949b, 12, 106.Google Scholar
Iidem and Fusco, R., Arch. Int. Pharmacodyn., 1951, 88, 1.Google Scholar
Idem, R.C. 1st sup. San., 1949, 12, 138.Google Scholar
Castillo, J. C., and De Beer, E. J., J. Pharmacol., 1950b, 99, 458.Google Scholar
Ginzel, K. H., Klupp, H., and Werner, G., Arch. Int. Pharmacodyn., 1951a, 86, 385.Google Scholar
Iidem, ibid., 1951b, 87, 79.Google Scholar
Iidem, ibid., 1951c, 87, 351.Google Scholar
Iidem, Arch. exp. Path. Pharmak., 1951d, 213, 453.CrossRefGoogle Scholar
Iidem, Sci. pharm., 1951e, 19, 164.Google Scholar
Glick, D., J. biol. Chem., 1941, 137, 357.CrossRefGoogle Scholar
Hurley, M. J., and Monro, A. B., Brit. med. J., 1952, i, 1027.Google Scholar
Thesleff, S., Nord. Med., 1951, 46, 1045.Google Scholar
Von Dardel, O., and Thesleff, S., ibid., 46, 1038.Google Scholar
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