Results 71 to 80 of about 16,705 (111)
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Intravenous Lidocaine for Status Epilepticus
Epilepsia, 1988Summary: Intravenous lidocaine successfully controlled convulsive status epilepticus in eight patients. Lidocaine was administered, as a diazepam substitute, to elderly patients with chronic obstructive lung disease and to those patients unresponsive to the stated doses of intravenous diazepam.
J, Pascual +3 more
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Lidocaine reduces intravenous diazepam pain
The Journal of Emergency Medicine, 1985We studied 41 consecutive patients receiving intravenous (IV) diazepam in the preoperative holding area to evaluate whether low-dose IV lidocaine could ameliorate pain of the diazepam injection. In a double-blind trial we found 1 cc of 1% lidocaine effective versus placebo at lowering the incidence of pain from 80% to 5% (P less than .001) and ...
R D, Herr, L, Ampel, R, Natonson
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Anesthesia & Analgesia, 1987
La lidocaine a la dose de 1,5 mg/kg attenue les augmentations du rythme cardiaque et de la pression arterielle lorsqu'elle est administree 3 minutes avant l'intubation et n'offre pas de protection contre les modifications hemodynamiques lorsqu'elle est donnee 1, 2 ou 5 minutes avant l ...
S, Tam, F, Chung, M, Campbell
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La lidocaine a la dose de 1,5 mg/kg attenue les augmentations du rythme cardiaque et de la pression arterielle lorsqu'elle est administree 3 minutes avant l'intubation et n'offre pas de protection contre les modifications hemodynamiques lorsqu'elle est donnee 1, 2 ou 5 minutes avant l ...
S, Tam, F, Chung, M, Campbell
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Prevention of Lidocaine Aerosol-induced Bronchoconstriction with Intravenous Lidocaine
Anesthesiology, 1996Background Lidocaine applied topically provokes bronchoconstriction in persons with hyperreactive airway disease. The authors questioned whether intravenous lidocaine would prevent lidocaine-aerosol induced bronchoconstriction.
Y, Bulut, C A, Hirshman, R H, Brown
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SUNCT Syndrome Responsive to Intravenous Lidocaine
Cephalalgia, 2004Short-lasting unilateral neuralgiform headache with conjunctival injection and tearing (SUNCT) is a primary headache syndrome that has been reported to be resistant to treatment with intravenous lidocaine. We report four cases of SUNCT in whom intravenous lidocaine (1.3-3.3 mg kg−1 h−1) completely suppressed the headaches for the duration of the ...
M S, Matharu, A S, Cohen, P J, Goadsby
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Neonatal Mydriasis: Intravenous Lidocaine Adverse Reaction
Journal of Child Neurology, 2002Lidocaine (a sodium channel blocker) serves as an antiepilepsy drug in neonates. We present a neonate with a seizure disorder who acutely developed pupillary mydriasis secondary to lidocaine overdose. We suggest adding this side effect to the list of untoward effects of lidocaine and to the differential diagnosis of fixed dilated pupils in neonates ...
Itai, Berger +4 more
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Methemoglobin levels following intravenous lidocaine administration
Annals of Emergency Medicine, 1987Methemoglobin levels were obtained before and after administration of IV lidocaine in 40 cardiac patients. Patients were given a 1-mg/kg bolus of IV lidocaine hydrochloride, started on a maintenance infusion at 2.0 mg/min, and given a second bolus of lidocaine of 0.5 mg/kg 15 minutes after the initial bolus. The maintenance infusion was adjusted from 1
L D, Weiss +6 more
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Chronic pain treatment with intravenous lidocaine
Neurological Research, 1986In a few uncontrolled studies intravenous lidocaine has been used in the treatment of chronic pain. In a controlled study we used intravenous lidocaine in 18 patients with severe chronic pain states due to various but mainly neurological diseases. After the infusion of lidocaine 14 patients (78%) had significant pain relief ranging from 2 hours to 25 ...
P, Petersen +3 more
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Intravenous Lidocaine for Acute Pain Treatment
Journal of PeriAnesthesia Nursing, 2011Lidocaine’s versatility is seen in the many routes by which it can be administered. It is given topically or by infiltration for procedural pain, such as for venous punctures and laceration repairs, and is available in a topical patch formulation for peripheral types of pain, such as postherpetic neuralgia.
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