دورية أكاديمية

Adolescents and Young Adults With Sickle Cell Disease: Nociplastic Pain and Pain Catastrophizing as Predictors of Pain Interference and Opioid Consumption.

التفاصيل البيبلوغرافية
العنوان: Adolescents and Young Adults With Sickle Cell Disease: Nociplastic Pain and Pain Catastrophizing as Predictors of Pain Interference and Opioid Consumption.
المؤلفون: Kuisell C; Independent Researcher, Dumfries, VA., Ploutz-Snyder R; University of Michigan School of Nursing., Williams DA; University of Michigan Medical School, Ann Arbor, MI., Voepel-Lewis T; University of Michigan School of Nursing., Hutchinson RJ; University of Michigan Medical School, Ann Arbor, MI., Dudding KM; University of Alabama at Birmingham School of Nursing, Birmingham, AL., Bridges C; University of Alabama at Birmingham School of Nursing, Birmingham, AL., Lavoie Smith EM; University of Alabama at Birmingham School of Nursing, Birmingham, AL.
المصدر: The Clinical journal of pain [Clin J Pain] 2023 Jul 01; Vol. 39 (7), pp. 326-333. Date of Electronic Publication: 2023 Jul 01.
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 8507389 Publication Model: Electronic Cited Medium: Internet ISSN: 1536-5409 (Electronic) Linking ISSN: 07498047 NLM ISO Abbreviation: Clin J Pain Subsets: MEDLINE
أسماء مطبوعة: Publication: Hagerstown, MD : Lippincott Williams & Wilkins
Original Publication: [New York, N.Y.] : Raven Press, [c1985-
مواضيع طبية MeSH: Analgesics, Opioid*/therapeutic use , Anemia, Sickle Cell*/complications, Humans ; Adolescent ; Young Adult ; Pain Measurement ; Pain/etiology ; Pain/complications ; Catastrophization
مستخلص: Objectives: Some patients with sickle cell disease (SCD) have features of nociplastic pain. While research suggests that many patients with nociplastic pain consume more opioids due to opioid nonresponsiveness, little is known about the impact of nociplastic pain and pain catastrophizing on opioid consumption and pain interference among adolescents and young adults (AYA) with SCD. The purpose of this study was to (1) characterize nociplastic pain and pain catastrophizing among AYA with SCD, and (2) determine whether these characterizations are associated with subsequent opioid consumption and pain interference 1 month after characterization.
Methods: Participants completed surveys characterizing nociplastic pain and catastrophizing at a routine clinic visit (baseline). Thereafter, participants received weekly text messages that included pain interference and opioid consumption surveys. Multipredictor 2-part models were used to evaluate the predictive relationships between baseline characterizations and subsequent pain interference, and opioid consumption.
Results: Forty-eight AYA aged 14 to 35 completed baseline measures. Twenty-five percent of participants had scores suggestive of nociplastic pain. Greater nociplastic pain features significantly increased the odds of consuming opioids (odds ratio=1.2) and having greater interference from pain (odds ratio=1.46). Regression analyses found that greater baseline nociplastic pain characteristics were significantly associated with opioid consumption (β=0.13) and pain interference (β=0.061); whereas higher pain catastrophizing scores predicted less opioid consumption (β=-0.03) and less pain interference (β=-0.0007).
Discussion: In this sample of AYA with SCD, features of nociplastic pain predicted higher subsequent opioid consumption and pain interference. Being aware of nociplastic pain features in patients with SCD may better guide individualized pain management.
Competing Interests: Funding for this study was provided by the Hillman Advancing Early Research Opportunities Grant (The Rita & Alex Hillman Foundation, New York, NY), Rackham Graduate Student Research Grant (Rackham Graduate School, University of Michigan, Ann Arbor, MI), and the University of Michigan School of Nursing New Investigator Award (Ann Arbor, MI). C.K. received funding from the National Institute of Nursing Research (T32 NR016914). The authors declare no conflict of interest.
(Copyright © 2023 Wolters Kluwer Health, Inc. All rights reserved.)
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معلومات مُعتمدة: T32 NR016914 United States NR NINR NIH HHS
المشرفين على المادة: 0 (Analgesics, Opioid)
تواريخ الأحداث: Date Created: 20230421 Date Completed: 20230623 Latest Revision: 20240702
رمز التحديث: 20240702
مُعرف محوري في PubMed: PMC10330104
DOI: 10.1097/AJP.0000000000001119
PMID: 37083638
قاعدة البيانات: MEDLINE
الوصف
تدمد:1536-5409
DOI:10.1097/AJP.0000000000001119