Clinical studies of induction agents. XV. A comparison of the cumulative effects of thiopentone, methohexitone and propidid.

SUMMARY Thiopentone, methohexitone and propanidid have been given by intermittent dosage as main agent for a series of body surface operations. The requirements over the first hour show a marked falling off with the barbiturates but little decline with propanidid. This supports the experimental findings that propanidid is rapidly destroyed in the body whereas the other agents are translocated into storage depots.

[1]  T. Howells,et al.  AN INTRODUCTION TO FBA.1420, A NEW NON-BARBITURATE INTRAVENOUS ANAESTHETIC. , 1964, British journal of anaesthesia.

[2]  J. Dundee,et al.  CLINICAL STUDIES OF INDUCTION AGENTS. IX. A COMPARATIVE STUDY OF A NEW EUGENOL DERIVATIVE, FBA.1420, WITH G.29.505 AND STANDARD BARBITURATES. , 1964, British journal of anaesthesia.

[3]  L. C. Mark,et al.  Physiologic Disposition of Methohexital in Man , 1963, Anesthesiology.

[4]  J. Dundee,et al.  The influence of phenothiazine premedication on methohexitone dosage , 1963 .

[5]  J. Dundee CLINICAL STUDIES OF INDUCTION AGENTS III: THE RELATIONSHIP BETWEEN DURATION OF ANAESTHESIA AND DOSAGE WITH G.29.505 , 1962 .

[6]  M. keeri-Szanto DRUG CONSUMPTION DURING THIOPENTONE-NITROUS OXIDE-RELAXANT ANAESTHESIA: THE PREPARATION AND INTERPRETATION OF TIME/DOSE CURVES , 1960 .

[7]  H. L. Price A DYNAMIC CONCEPT OF THE DISTRIBUTION OF THIOPENTAL IN THE HUMAN BODY , 1960, Anesthesiology.

[8]  J. Dundee,et al.  A clinical trial of thiamylal as an intravenous anaesthetic in 1,750 cases. , 1955, British journal of anaesthesia.

[9]  M. keeri-Szanto Anaesthetic dosage in thiopental-curare-nitrous oxide anaesthesia, using a thiopental-curare mixture , 1955 .

[10]  J. Wyngaarden,et al.  ANESTHETIC PROPERTIES OF SODIUM 5-ALLYL-5-(1-METHYLBUTYL)-2-THIOBARBITURATE (SURITAL) AND CERTAIN OTHER THIOBARBITURATES IN DOGS , 1949 .

[11]  I. Podlesch,et al.  Klinische Erfahrungen mit Propanidid , 1965 .

[12]  H. Kreuscher Zur Straßenverkehrstüchtigkeit nach Anwendung von Propanidid , 1965 .

[13]  K. Horatz,et al.  Die intravenöse Kurznarkose mit dem neuen Phenoxyessigsäurederivat Propanidid (Epontol , 1965 .