Acupuncture vs intravenous morphine in the management of acute pain in the ED - 02/11/16
Abstract |
Background |
Acupuncture is one of the oldest techniques to treat pain and is commonly used for a large number of indications. However, there is no sufficient evidence to support its application in acute medical settings.
Methods |
This was a prospective, randomized trial of acupuncture vs morphine to treat ED patients with acute onset moderate to severe pain.
Primary outcome consists of the degree of pain relief with significant pain reduction defined as a pain score reduction ≥50% of its initial value. We also analyzed the pain reduction time and the occurrence of short-term adverse effects. We included in the protocol 300 patients with acute pain: 150 in each group.
Results |
Success rate was significantly different between the 2 groups (92% in the acupuncture group vs 78% in the morphine group P<.001). Resolution time was 16±8 minutes in the acupuncture group vs 28±14 minutes in the morphine group (P<.005). Overall, 89 patients (29.6%) experienced minor adverse effects: 85 (56.6%) in morphine group and 4 (2.6%) in acupuncture group (P<.001). No major adverse effects were recorded during the study protocol. In patients with acute pain presenting to the ED, acupuncture was associated with more effective and faster analgesia with better tolerance.
Conclusion |
This article provides an update on one of the oldest pain relief techniques (acupuncture) that could find a central place in the management of acute care settings. This should be considered especially in today's increasingly complicated and polymedicated patients to avoid adverse drug reactions.
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☆ | Study registration: The protocol was registered at clinicaltrials.gov under: NCT02460913. |
☆☆ | Funding: The authors declare that no funding sources were provided. |
★ | Conflict of interest: The authors declare that they have no conflict of interest. |
★★ | Author contributions: HB and SN conceived the study, and designed the trial. SN, HB, WB, RB, MHG, HB, and KB supervised the conduct of the trial and data collection. HB was the acupuncturist of the study. HB, NB, NF, and MAM undertook recruitment of patients and managed the data, including quality control. SN, HB, NB, and MHG performed statistical analysis and analyzed the data. SN drafted the manuscript. HB and NB revised the manuscript. SN takes the responsibility for the paper as a whole. This study was supported in part by the Tunisian Ministry of Scientific Research. |
Vol 34 - N° 11
P. 2112-2116 - novembre 2016 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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