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  1. Article ; Online: Ketamine Compared With Morphine for Out-of-Hospital Analgesia for Patients With Traumatic Pain: A Randomized Clinical Trial.

    Le Cornec, Clément / Le Pottier, Marion / Broch, Hélène / Marguinaud Tixier, Alexandre / Rousseau, Emmanuel / Laribi, Said / Janière, Charles / Brenckmann, Vivien / Guillerm, Anne / Deciron, Florence / Kabbaj, Amine / Jenvrin, Joël / Péré, Morgane / Montassier, Emmanuel

    JAMA network open

    2024  Volume 7, Issue 1, Page(s) e2352844

    Abstract: Importance: Pain is a common out-of-hospital symptom among patients, and opioids are often prescribed. Research suggests that overprescribing for acute traumatic pain is still prevalent, even when limits restricting opioid prescriptions have been ... ...

    Abstract Importance: Pain is a common out-of-hospital symptom among patients, and opioids are often prescribed. Research suggests that overprescribing for acute traumatic pain is still prevalent, even when limits restricting opioid prescriptions have been implemented. Ketamine hydrochloride is an alternative to opioids in adults with out-of-hospital traumatic pain.
    Objective: To assess the noninferiority of intravenous ketamine compared with intravenous morphine sulfate to provide pain relief in adults with out-of-hospital traumatic pain.
    Design, setting, and participants: The Intravenous Subdissociative-Dose Ketamine Versus Morphine for Prehospital Analgesia (KETAMORPH) study was a multicenter, single-blind, noninferiority randomized clinical trial comparing ketamine hydrochloride (20 mg, followed by 10 mg every 5 minutes) with morphine sulfate (2 or 3 mg every 5 minutes) in adult patients with out-of-hospital trauma and a verbal pain score equal to or greater than 5. Enrollment occurred from November 23, 2017, to November 26, 2022, in 11 French out-of-hospital emergency medical units.
    Interventions: Patients were randomly assigned to ketamine (n = 128) or morphine (n = 123).
    Main outcomes and measures: The primary outcome was the between-group difference in mean change in verbal rating scale pain scores measured from the time before administration of the study drug to 30 minutes later. A noninferiority margin of 1.3 was chosen.
    Results: A total of 251 patients were randomized (median age, 51 [IQR, 34-69] years; 111 women [44.9%] and 140 men [55.1%] among the 247 with data available) and were included in the intention-to-treat population. The mean pain score change was -3.7 (95% CI, -4.2 to -3.2) in the ketamine group compared with -3.8 (95% CI, -4.2 to -3.4) in the morphine group. The difference in mean pain score change was 0.1 (95% CI, -0.7 to 0.9) points. There were no clinically meaningful differences for vital signs between the 2 groups. The intravenous morphine group had 19 of 113 (16.8% [95% CI, 10.4%-25.0%]) adverse effects reported (most commonly nausea [12 of 113 (10.6%)]) compared with 49 of 120 (40.8% [95% CI, 32.0%-49.6%]) in the ketamine group (most commonly emergence phenomenon [24 of 120 (20.0%)]). No adverse events required intervention.
    Conclusions and relevance: In the KETAMORPH study of patients with out-of-hospital traumatic pain, the use of intravenous ketamine compared with morphine showed noninferiority for pain reduction. In the ongoing opioid crisis, ketamine administered alone is an alternative to opioids in adults with out-of-hospital traumatic pain.
    Trial registration: ClinicalTrials.gov Identifier: NCT03236805.
    MeSH term(s) Adult ; Aged ; Female ; Humans ; Male ; Middle Aged ; Acute Pain ; Analgesia ; Analgesics, Opioid/therapeutic use ; Hospitals ; Ketamine/therapeutic use ; Morphine/therapeutic use ; Single-Blind Method
    Chemical Substances Analgesics, Opioid ; Ketamine (690G0D6V8H) ; Morphine (76I7G6D29C)
    Language English
    Publishing date 2024-01-02
    Publishing country United States
    Document type Equivalence Trial ; Journal Article ; Multicenter Study ; Randomized Controlled Trial
    ISSN 2574-3805
    ISSN (online) 2574-3805
    DOI 10.1001/jamanetworkopen.2023.52844
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Is intravenously administered, subdissociative-dose KETAmine non-inferior to MORPHine for prehospital analgesia (the KETAMORPH study): study protocol for a randomized controlled trial.

    Le Cornec, Clément / Lariby, Said / Brenckmann, Vivien / Hardouin, Jean Benoit / Ecoffey, Claude / Le Pottier, Marion / Fradin, Philippe / Broch, Hélène / Kabbaj, Amine / Auffret, Yannick / Deciron, Florence / Longo, Céline / Javaudin, François / Le Bastard, Quentin / Jenvrin, Joël / Montassier, Emmanuel

    Trials

    2018  Volume 19, Issue 1, Page(s) 260

    Abstract: Background: Acute pain is a common condition among prehospital patients and prompt management is pivotal. Opioids are the most frequently analgesics used in the prehospital setting. However, opioids are highly addictive, and some patients may develop ... ...

    Abstract Background: Acute pain is a common condition among prehospital patients and prompt management is pivotal. Opioids are the most frequently analgesics used in the prehospital setting. However, opioids are highly addictive, and some patients may develop opioid dependence, even when they are exposed to brief opioid treatments. Therefore, alternative non-opioid analgesia should be developed to manage pain in the prehospital setting. Used at subdissociative doses, ketamine, a noncompetitive N-methyl-D-aspartate and glutamate receptor antagonist, provides analgesic effects accompanied by preservation of protective airway reflexes. In this context, we will carry out a randomized controlled, open-label, multicenter trial to compare a subdissociative dose of ketamine to morphine to provide pain relief in the prehospital setting, in patients with traumatic and non-traumatic pain.
    Methods/design: This will be a multicenter, single-blind, randomized controlled trial. Consecutive adults will be enrolled in the prehospital setting if they experience moderate to severe, acute, non-traumatic and traumatic pain, defined as a numeric rating scale score greater or equal to 5. Patients will be randomized to receive ketamine or morphine by intravenous push. The primary outcome will be the between-group difference in mean change in numeric rating scale pain scores measured from the time before administration of the study medication to 30 min later.
    Discussion: This upcoming randomized clinical trial was design to assess the efficacy and safety of ketamine, an alternative non-opiate analgesia, to manage non-traumatic and traumatic pain in the prehospital setting. We aim to provide evidence to change prescribing practices to reduce exposition to opioids and the subsequent risk of addiction.
    Trial registration: ClinicalTrials.gov, ID: NCT03236805 . Registered on 2 August 2017.
    MeSH term(s) Acute Pain/diagnosis ; Acute Pain/physiopathology ; Acute Pain/prevention & control ; Acute Pain/psychology ; Administration, Intravenous ; Analgesics, Opioid/administration & dosage ; Analgesics, Opioid/adverse effects ; Anesthetics, Dissociative/administration & dosage ; Anesthetics, Dissociative/adverse effects ; Emergency Medical Services/methods ; France ; Humans ; Ketamine/administration & dosage ; Ketamine/adverse effects ; Morphine/administration & dosage ; Morphine/adverse effects ; Multicenter Studies as Topic ; Pain Management/adverse effects ; Pain Management/methods ; Pain Measurement ; Randomized Controlled Trials as Topic ; Single-Blind Method ; Time Factors ; Treatment Outcome
    Chemical Substances Analgesics, Opioid ; Anesthetics, Dissociative ; Ketamine (690G0D6V8H) ; Morphine (76I7G6D29C)
    Language English
    Publishing date 2018-05-02
    Publishing country England
    Document type Clinical Trial Protocol ; Journal Article
    ZDB-ID 2040523-6
    ISSN 1745-6215 ; 1468-6694 ; 1468-6708
    ISSN (online) 1745-6215 ; 1468-6694
    ISSN 1468-6708
    DOI 10.1186/s13063-018-2634-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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