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dc.contributor.authorDusek, Jeffery A
dc.contributor.authorKallenberg, Gene A
dc.contributor.authorHughes, Robert M
dc.contributor.authorStorrow, Alan B
dc.contributor.authorCoyne, Christopher J
dc.contributor.authorVago, David R
dc.contributor.authorNielsen, Arya
dc.contributor.authorKarasz, Alison
dc.contributor.authorKim, Ryung S
dc.contributor.authorSurdam, Jessica
dc.contributor.authorSegall, Tracy
dc.contributor.authorMcKee, M Diane
dc.date.accessioned2023-08-10T20:16:51Z
dc.date.available2023-08-10T20:16:51Z
dc.date.issued2022-03-04
dc.identifier.citationDusek JA, Kallenberg GA, Hughes RM, Storrow AB, Coyne CJ, Vago DR, Nielsen A, Karasz A, Kim RS, Surdam J, Segall T, McKee MD. Acupuncture in the emergency department for pain management: A BraveNet multi-center feasibility study. Medicine (Baltimore). 2022 Mar 4;101(9):e28961. doi: 10.1097/MD.0000000000028961. PMID: 35244059; PMCID: PMC8896475.en_US
dc.identifier.eissn1536-5964
dc.identifier.doi10.1097/MD.0000000000028961en_US
dc.identifier.pmid35244059
dc.identifier.urihttp://hdl.handle.net/20.500.14038/52404
dc.description.abstractPurpose: Pain accounts for up to 78% of emergency department (ED) patient visits and opioids remain a primary method of treatment despite risks of addiction and adverse effects. While prior acupuncture studies are promising as an alternative opioid-sparing approach to pain reduction, successful conduct of a multi-center pilot study is needed to prepare for a future definitive randomized control trial (RCT). Methods: Acupuncture in the Emergency Department for Pain Management (ACUITY) is funded by the National Center for Complementary and Integrative Health. The objectives are to: conduct a multi-center feasibility RCT, examine feasibility of data collection, develop/deploy a manualized acupuncture intervention and assess feasibility/implementation (barrier/facilitators) in 3 EDs affiliated with the BraveNet Practice Based Research Network.Adults presenting to a recruiting ED with acute non-emergent pain (e.g., musculoskeletal, back, pelvic, noncardiac chest, abdominal, flank or head) of ≥4 on a 0-10-point Numeric Rating Scale will be eligible. ED participants (n = 165) will be equally randomized to Acupuncture or Usual Care.At pre-, post-, and discharge time-points, patients will self-assess pain and anxiety using the Numeric Rating Scale. Pain, anxiety, post-ED opioid use and adverse events will be assessed at 1 and 4 weeks. Opioid utilization in the ED and discharge prescriptions will be extracted from patients' electronic medical records.Acupuncture recipients will asked to participate in a brief qualitative interview about 3 weeks after their discharge. ED providers and staff will also be interviewed about their general perspectives/experiences related to acupuncture in the ED and implementation of acupuncture in ACUITY. Results: Recruitment began on 5/3/21. As of 12/7/21: 84 patients have enrolled, the responsive acupuncture intervention has been developed and deployed, and 26 qualitative interviews have been conducted. Conclusion: Successful conduct of ACUITY will provide the necessary framework for conducting a future, multi-center, definitive RCT of acupuncture in the ED. Clinical trialsgov: NCT04880733 https://clinicaltrials.gov/ct2/show/NCT04880733.en_US
dc.language.isoenen_US
dc.relation.ispartofMedicineen_US
dc.relation.urlhttps://doi.org/10.1097/md.0000000000028961en_US
dc.rightsCopyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.en_US
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectacupunctureen_US
dc.subjectemergency departmenten_US
dc.subjectnonpharmacologicen_US
dc.subjectopioiden_US
dc.subjectpainen_US
dc.titleAcupuncture in the emergency department for pain management: A BraveNet multi-center feasibility studyen_US
dc.typeJournal Articleen_US
dc.source.journaltitleMedicine
dc.source.volume101
dc.source.issue9
dc.source.beginpagee28961
dc.source.endpage
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.source.countryUnited States
dc.identifier.journalMedicine
refterms.dateFOA2023-08-10T20:16:51Z
dc.contributor.departmentFamily Medicine and Community Healthen_US


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Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc.
This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in
any medium, provided the original work is properly cited.
Except where otherwise noted, this item's license is described as Copyright © 2022 the Author(s). Published by Wolters Kluwer Health, Inc. This is an open access article distributed under the Creative Commons Attribution License 4.0 (CCBY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.