A randomized, double-blind study comparing morphine with fentanyl in prehospital analgesia - 21/08/11
, François Dolveck, MD b, Stephen W. Borron, MD, MS c, Loic Tual, MD, MS d, Vincent Van Laer, MD e, Jean-Yves Lardeur, MD f, Frédéric Lapostolle, MD a, Frédéric Adnet, MD, PhD aAbstract |
Study Objective |
The aim of this study was to compare, by a randomized double-blind method, morphine (M) and fentanyl (F) in a prehospital setting.
Methods |
Consecutive patients with severe, acute pain defined as a visual analog scale score (VASS) of 60/100 or higher were included. The M group received an initial intravenous M injection of 0.1 mg/kg then of 3 mg every 5 minutes. The F group received an initial intravenous F injection of 1 μg/kg then of 30 μg every 5 minutes. The goal of analgesia was a VASS of 30/100 or lower. The end point was the VASS measured 30 minutes after initial administration (VAS [T30]).
Results |
There were 26 patients included in the M group and 28 in the F group. Initial VASS(T0) and VASS(T30), mean (95% CI), were 83 (78-88) and 40 (28-52) in the M group and 77 (72-82) and 35 (27-43) in the F group (P = NS). Sixty-two percent of patients in the M group described analgesia as excellent or good vs 76% of those in the F group who did (P = NS). There were no differences in the incidence of side effects in the 2 groups.
Conclusion |
This study demonstrates that M and F were comparable in treating severe, acute pain in a prehospital setting during the first 30 minutes in spontaneous breathing patients.
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| ☆ | Financial support was given by the School of Medicine, Paris 13 University. |
Vol 23 - N° 2
P. 114-119 - mars 2005 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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