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Biomedical subjects

R J McBride

Publications and source records attributed to R J McBride.

At least 19 recordsLinked to original sources
PubMed1994

Onset and duration of action and hemodynamic effects of rocuronium bromide under balanced and volatile anesthesia.

The onset and duration of action, and hemodynamic effects of rocuronium bromide 0.6 or 0.9 mg kg-1 were studied in 4 groups of 10 patients each during anesthesia with nitrous oxide in oxygen and fentanyl or halothane. Neuromuscular block was monitored using mechanomyography and train-of-four (TOF) stimulation. The mean time to onset of complete neuromuscular block was 55 s with the 0.6 mg kg-1 dose during both anesthetic techniques. The times to recovery of T1 (first response in the TOF stimulation) to 25 and 90% of control and to the recovery of the TOF ratio to 0.7 were 36, 45 and 54 min respectively during narcotic anesthesia, and 35, 54 and 58 min during halothane anesthesia. Complete block with the 0.9 mg kg-1 dose occurred in 50, and 52 s respectively in the fentanyl and halothane groups. The recovery of T1 to 25% occurred in 49 and 52 min, to 90% in 66 and 71 min and to TOF ratio of 0.7 in 72 and 79 min respectively during balanced and halothane anesthesia. There were no significant changes in heart rate or mean arterial pressure during the 5 min following administration of either dose of rocuronium during balanced or halothane anesthesia. A separate group of 10 patients received 0.9 mg kg-1 of rocuronium during anesthesia with nitrous oxide, oxygen and isoflurane. Complete block occurred in an average time of 45 s in these patients with 25% recovery of T1 in 53 min.(ABSTRACT TRUNCATED AT 250 WORDS)

Adolescent↗
PubMed1984

Prevention of intracranial hypertension during laryngoscopy and endotracheal intubation. Use of a second dose of thiopentone.

In nine patients, with preoperative ICP monitoring, anaesthesia was induced with thiopentone 5 mg kg-1 given over 1 min, followed by pancuronium 0.1 mg kg-1. After manual hyperventilation with nitrous oxide and oxygen for 3 min they were given thiopentone 2.5 mg kg-1 over 30 s (phase 1); 30 s later laryngoscopy was performed and topical analgesia administered to the larynx. Endotracheal intubation was performed 1 min after spraying the cords (phase 2). The measurements continued for a further 5 min during which the patients were mechanically ventilated (phase 3). ICP and intra-arterial pressure were recorded. Although there was a significant decrease (P less than 0.05) in MAP at the end of the second dose of thiopentone, there were no other significant changes in ICP, MAP or PaCO2 throughout the study. In two patients there were transient decreases in cerebral perfusion pressure to less than 60 mm Hg. Although MAP increased in five of the patients during laryngoscopy and intubation, there was no increase in ICP, showing that the MAP was still within the autoregulatory limits.

Adult↗
PubMed1981

Partition coefficients of some aromatic alcohols in an n-heptane/water system and their relationship to minimum inhibitory concentration against Pseudomonas aeruginosa and Staphylococcus aureus.

The partition coefficients of the homologous series of aromatic alcohols were determined in an n-heptane/water system. The minimum inhibitory concentrations of benzyl alcohol, 2-phenylethanol, 3-phenylpropanol, 4-phenylbutanol and 5-phenylpentanol were elucidated against Pseudomonas aeruginosa and Staphylococcus aureus. The linear relationship log1/C = a log P + b postulated by Hansch was found to apply.

Alcohols↗
PubMed1979

A study of the plasma concentrations of lorazepam in mother and neonate.

A standard dose of lorazepam 2.5 mg was given i.v. to two groups of mothers: (a) before surgical induction of labour and (b) at the beginning of the second stage of labour. A group of non-pregnant women was studied as control. Plasma concentrations of lorazepam were measured by gas-liquid chromatography, in the mothers before delivery, and in the mother and neonate at delivery and 24 and 48 h thereafter. Concentrations at delivery in the neonates were similar to those in the mothers in group (a), but significantly less in group (b). Fetal concentration rarely exceeded that in the mother. Measurements after delivery indicated that the neonates were able to metabolize lorazepam at the same rate as the mothers. Of the 22 neonates studied only one had an Apgar score of less than 8 at 5 min and this score was 10 at 10 min.

Adult↗