• Pain Manag Nurs · Aug 2024

    Auricular Acupressure Adjunct Treatment for Opioid Tapering: A Randomized Pilot Feasibility Study.

    • Heather J Jackson, Micaela Arseneau, Michelle Terrell, Kim Steanson, and Mary S Dietrich.
    • Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN. Electronic address: Heather.jackson@vumc.org.
    • Pain Manag Nurs. 2024 Aug 26.

    PurposeOpioid medications are necessary in the treatment of critically ill infants; however. prolonged use may lead to withdrawal syndrome. The purpose of this study was to assess feasibility of delivering an acupressure protocol for the treatment of iatrogenic withdrawal in a pediatric cardiac intensive care unit as well as impact and acceptance of acupressure as an adjunct treatment.DesignRandomized pilot feasibility trial.MethodsAcupressure stickers were applied and rotated to one ear every 1-3 days until withdrawal symptoms improved.ResultsThere were no serious adverse events, with only one reported incident of skin irritation. Recruiting benchmarks were exceeded. Weaning phases were significantly shorter in the acupressure group (medians 6.0 vs 22.0 respectively, p = .025, d = 0.90) and the control group used skin-to-skin contact as a comfort measure significantly more than the acupressure group (42.9% vs 6.3%, p = .18). Acupressure was accepted by parents, with an overall 96.2% rating their experience as positive, as measured by the Parent Client Satisfaction Questionnaire. The majority of health care providers (n = 19) were supportive, with 71.9% agreeing or completely agreeing acupressure is an acceptable adjunct for the treatment of withdrawal symptoms; 26.8% were neutral, as measured by the Acceptability of Intervention Measure, Intervention Appropriateness Measure, and Feasibility of Intervention Measure.ConclusionsAcupressure was found to be safe, feasible, and accepted by health care providers in a pediatric cardiac intensive care setting.Clinical ImplicationsThese findings support future research with larger sample sizes to improve clinical treatment of infants physically dependent on sedative medications.Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.

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