Effect of intranasal sufentanil on acute post-traumatic pain in the emergency department: a randomised controlled trial

被引:1
|
作者
Malinverni, Stefano [1 ,3 ]
Kreps, Bernard [2 ]
Lucaccioni, Thibault [1 ]
Bouazza, Fatima-Zohra [1 ]
Bartiaux, Magali [1 ]
Plumacker, Alain [1 ]
Pascu, Andreea [1 ]
Towo, Pierre Youatou [1 ]
机构
[1] Univ Libre Bruxelles, Emergency Dept, CHU St Pierre, Brussels, Belgium
[2] Clin St Jean, Emergency Dept, Brussels, Belgium
[3] CHU St Pierre, Emergency Med, B-1000 Brussels, Belgium
关键词
analgesia; pain management; extremity; extremities; ANALGESIA; SCORE;
D O I
10.1136/emermed-2023-213353
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background Intranasal sufentanil is a potent opioid which can be used in patients with traumatic injuries presenting to the ED. Although previous studies have demonstrated the superiority of intranasal sufentanil over intravenous morphine in terms of pain relief, its clinical superiority in patients with traumatic injuries receiving adequate multimodal analgesia with acetaminophen and non-steroidal anti-inflammatory drugs is uncertain. We compared pain relief offered by intranasal sufentanil with that offered by oral and intravenous opioids in patients with acute traumatic injuries also receiving a specified regimen of non-opioid treatment.Methods In this single-centre, open-label, parallel-group, randomised controlled superiority trial conducted between January 2020 and February 2022, trauma patients presenting to the ED with a pain score of >= 7 on a visual analogue scale (VAS) were randomised to receive either intranasal sufentanil or other oral/intravenous opioids alongside oral/intravenous acetaminophen and non-steroidal anti-inflammatory drugs. The primary outcome was reduction in VAS score 15-20 min after randomisation.Results An intention-to-treat analysis included 170 out of 205 patients screened for inclusion. The intranasal sufentanil group (83 patients) showed a significantly greater reduction in pain when compared with the oral/intravenous opioid group (87 patients) 15-20 min after randomisation (reduction in VAS score 3.0 (IQR 1.7-5.0) vs 1.5 (IQR 0.9-3.0); p<0.001). Similarly, a greater reduction in pain was observed in the intranasal sufentanil group 60 min after randomisation (5.0 (IQR 3.0-7.0) vs 3.0 (IQR 2.0-5.3); p<0.001). However, side effects were more frequent in the intervention group (71.1% vs 23%; p<0.001).Conclusions Intranasal sufentanil was associated with more effective pain relief than oral/intravenous opioids in patients with traumatic injuries treated with coanalgesia. Intranasal sufentanil could be considered for the management of pain in patients with traumatic injuries associated with severe pain.
引用
收藏
页码:83 / 88
页数:6
相关论文
共 50 条
  • [41] Effect of Voluntary Exercise on Endogenous Pain Control Systems and Post-traumatic Headache in Mice
    Bharadwaj, Vimala N.
    Sahbaie, Peyman
    Shi, Xiaoyou
    Irvine, Karen-Amanda
    Yeomans, David C.
    Clark, J. David
    JOURNAL OF PAIN, 2023, 24 (10) : 1859 - 1874
  • [42] Acupuncture for post anaesthetic recovery and postoperative pain: study protocol for a randomised controlled trial
    Fleckenstein, Johannes
    Baeumler, Petra I.
    Gurschler, Caroline
    Weissenbacher, Tobias
    Simang, Michael
    Annecke, Thorsten
    Geisenberger, Thomas
    Irnich, Dominik
    TRIALS, 2014, 15
  • [43] Effect of Sufentanil Combined with Gabapentin on Acute Postoperative Pain in Patients Undergoing Intraspinal Tumor Resection: Study Protocol for a Randomized Controlled Trial
    Zhang, Yuan
    Yue, Hongli
    Qin, Yirui
    Wang, Jiajing
    Zhao, Chenyang
    Cheng, Miao
    Han, Bo
    Han, Ruquan
    Cui, Weihua
    JOURNAL OF PAIN RESEARCH, 2022, 15 : 2619 - 2628
  • [44] Safety of nurse-directed triage intranasal fentanyl protocol for acute pain management in a European pediatric emergency department: A retrospective observational analysis
    Romano, F.
    Wendelspiess, M.
    Mansour, R.
    Abplanalp-Marti, O.
    Starvaggi, C.
    Holzner, F.
    Steiner, I.
    Keitel, K.
    FRONTIERS IN PEDIATRICS, 2023, 11
  • [45] Sub dissociative dose of ketamine with haloperidol versus fentanyl on pain reduction in patients with acute pain in the emergency department; a randomized clinical trial
    Moradi, Mohammad Matin
    Moradi, Mohammad Mobin
    Safaie, Arash
    Baratloo, Alireza
    Payandemehr, Pooya
    AMERICAN JOURNAL OF EMERGENCY MEDICINE, 2022, 54 : 165 - 171
  • [46] The effect of provision of pain management advice on patient satisfaction with their pain management: a pilot, randomised, controlled trial (pain advice trial)
    Taylor, David McD
    Johnson, Olivia Grover
    Lee, Marina
    Ding, Juen Li
    Ashok, Aadith
    EMERGENCY MEDICINE JOURNAL, 2016, 33 (07) : 453 - 457
  • [47] Acupuncture effect on thermal tolerance and electrical pain threshold: a randomised controlled trial
    Amand, Marc
    Nguyen-Huu, Florence
    Balestra, Costantino
    ACUPUNCTURE IN MEDICINE, 2011, 29 (01) : 47 - 50
  • [48] Out-of-Hospital Intranasal Ketamine as an Adjunct to Fentanyl for the Treatment of Acute Traumatic Pain: A Randomized Clinical Trial
    McMullan, Jason T.
    Droege, Christopher A.
    Chard, Kathleen M.
    Otten, Edward J.
    Hart, Kim Ward
    Lindsell, Christopher J.
    Strilka, Richard J.
    ANNALS OF EMERGENCY MEDICINE, 2024, 84 (04) : 363 - 373
  • [49] EASIER trial (Erector-spinAe analgeSia for hepatopancreaticobiliary pain In the Emergency Room): a single-centre open-label cohort-based randomised controlled trial analysing the efficacy of the ultrasound-guided erector-spinae plane block compared with intravenous morphine in the treatment of acute hepatopancreaticobiliary pain in the emergency department
    David, Sandeep Nathanael
    Murali, Vignesh
    Kattumala, Pradeep Daniel
    Abhilash, Kundavaram Paul Prabhakar
    Thomas, Ajith
    Chowdury, Sudipta Dhar
    Karuppusami, Reka
    EMERGENCY MEDICINE JOURNAL, 2024, 41 (10) : 588 - 594
  • [50] Protocol for a double blind, randomised placebo-controlled trial using ondansetron to reduce vomiting in children receiving intranasal fentanyl and inhaled nitrous oxide for procedural sedation in the emergency department (the FON trial)
    Fauteux-Lamarre, Emmanuelle
    Babl, Franz E.
    Davidson, Andrew J.
    Legge, Donna
    Lee, Katherine J.
    Palmer, Greta M.
    Hopper, Sandy M.
    BMJ PAEDIATRICS OPEN, 2018, 2 (01)