BMJ · 1976 · 47 citations · 16 references
MedicineAnesthesiologyPharmacologyAnesthesiaClinical PharmacologyPerioperative PharmacologyCardiac MedicationsCardiac PharmacotherapyCardiovascular Drug SafetyCardiovascular Effects Of AnesthesiaPharmacokinetics In SurgeryAcute Myocardial Infarction DiagnosisCirculatory DisordersDose Regimen DesignDose Regimen SelectionInfusion Rate AdjustmentMyocardial Infarction PharmacotherapyPost-myocardial Infarction PharmacotherapyVentricular Conduction
Plasma lignocaine concentrations were measured during and after lignocaine infusions administered for suppressing ventricular dysrhythmias. Twenty-four patients with a primary diagnosis of acute myocardial infarction without gross circulatory disturbance received, after a bolus of lignocaine, either 4 mg/min for 30 minutes, 2 mg/min for two hours, then 1 mg/min thereafter or 1 mg/min throughout. The higher dose regimen produced continous therapeutic levels of lignocaine, which were achieved only after four hours by the lower dose. On the other hand, in patients who had undergone cardiac surgery and who had circulatory and heptic dysfunction the lower dose regimen achieved therapeutic levels early. The plasma half life was longer in the surgical group (P less than 0.02). The higher initial infusion rate is recommended for patients with acute myocardial infarction without gross circulatory impairment.
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Lidocaine in the Prevention of Primary Ventricular Fibrillation
K. I. Lie, Hein J.J. Wellens, F J van Capelle et al. · New England Journal of Medicine · 1974 · 443 citations
Medicine, Cardiology, Pharmacology +13
ACUTE PHASE OF MYOCARDIAL INFARCTION
A.A.J. Adgey, J S Geddes, S W Webb et al. · The Lancet · 1971 · 232 citations
VENTRICULAR FIBRILLATION COMPLICATING ACUTE MYOCARDIAL INFARCTION
D.M. Lawrie, Michael R. Higgins, M J Godman et al. · The Lancet · 1968 · 225 citations