Literature DB >> 1859007

The neuromuscular effects of ORG9426 in patients receiving balanced anesthesia.

F F Foldes1, H Nagashima, H D Nguyen, W S Schiller, M M Mason, Y Ohta.   

Abstract

In searching for a nondepolarizing muscle relaxant with intermediate duration but more rapid onset of action than the presently available compounds, the neuromuscular and circulatory effects of ORG9426 were investigated in two studies in humans receiving fentanyl, droperidol, thiopental, and nitrous oxide-oxygen anesthesia. Eighty patients, randomly assigned to one of four groups of 20 each, received 0.12, 0.16, 0.20, or 0.24 mg/kg ORG9426. In the first study, the doses (in milligrams per kilogram) of ORG9426 that caused 50% (ED50), 90% (ED90), or 95% (ED95) neuromuscular block were determined by the individual dose-response method; they were 0.170, 0.268, and 0.305 mg/kg, respectively. In the second study, after induction of anesthesia, patients received 0.6 mg/kg (about 2 x ED95) of ORG9426, either in a single bolus (group 1) or in two unequal (0.1 and 0.5 mg/kg) increments 4 min apart (group 2). After the administration of 0.6 mg/kg ORG9426, maximal neuromuscular block developed in 1.5 +/- 0.12 min in group 1 and in 1.2 +/- 0.14 min in group 2. Patients tracheas were intubated after development of the maximal neuromuscular effect of the intubating dose and after the recording of heart rate and systolic and diastolic blood pressure. There was no difference in the clinical duration of the intubating doses, which were 40.0 +/- 3.2 (15-73) min in group 1 and 39.3 +/- 2.4 (19-57) min in group 2.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1991        PMID: 1859007     DOI: 10.1097/00000542-199108000-00004

Source DB:  PubMed          Journal:  Anesthesiology        ISSN: 0003-3022            Impact factor:   7.892


  29 in total

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Review 2.  Clinical pharmacokinetics of the newer neuromuscular blocking drugs.

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Authors:  H Shiraishi; H Suzuki; T Suzuki; N Katsumata; S Ogawa
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4.  Interactions between ORG9426 and other non-depolarizing neuromuscular blocking agents in rats in vivo.

Authors:  K Watanabe
Journal:  J Anesth       Date:  1992-07       Impact factor: 2.078

5.  The role of the amino acid residue at alpha1:189 in the binding of neuromuscular blocking agents to mouse and human muscle nicotinic acetylcholine receptors.

Authors:  P G Purohit; R J Tate; E Pow; D Hill; J G Connolly
Journal:  Br J Pharmacol       Date:  2007-02-12       Impact factor: 8.739

Review 6.  Newer neuromuscular blocking agents: how do they compare with established agents?

Authors:  H J Sparr; T M Beaufort; T Fuchs-Buder
Journal:  Drugs       Date:  2001       Impact factor: 9.546

7.  Survey of neuromuscular monitoring and assessment of postoperative residual neuromuscular block in a postoperative anaesthetic care unit.

Authors:  Xu Feng Lin; Christine Yoke Kuen Yong; May Un Sam Mok; Poopalalingam Ruban; Patrick Wong
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8.  Accelerated onset of rocuronium.

Authors:  R K Mirakhur
Journal:  Can J Anaesth       Date:  1995-05       Impact factor: 5.063

9.  Haemodynamic effects of rocuronium during fentanyl anaesthesia: comparison with vecuronium.

Authors:  E P McCoy; V R Maddineni; P Elliott; R K Mirakhur; I W Carson; R A Cooper
Journal:  Can J Anaesth       Date:  1993-08       Impact factor: 5.063

Review 10.  Newer neuromuscular blocking drugs. An overview of their clinical pharmacology and therapeutic use.

Authors:  R K Mirakhur
Journal:  Drugs       Date:  1992-08       Impact factor: 9.546

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