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A Randomized Controlled Trial of an Emergency Department Intervention for Patients with Chronic Noncancer Pain.
Ringwalt, Chris; Shanahan, Meghan; Wodarski, Stephanie; Jones, Jennifer; Schaffer, Danielle; Fusaro, Angela; Paulozzi, Len; Garrettson, Mariana; Ford, Marsha.
Afiliación
  • Ringwalt C; Injury Prevention Research Center, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Shanahan M; Injury Prevention Research Center, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Wodarski S; Carolinas Medical Center, Charlotte, North Carolina.
  • Jones J; Injury Prevention Research Center, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Schaffer D; Carolinas Medical Center, Charlotte, North Carolina.
  • Fusaro A; Carolinas Medical Center, Charlotte, North Carolina.
  • Paulozzi L; National Center for Injury Prevention and Control, Centers for Disease Control and Prevention, Atlanta, Georgia.
  • Garrettson M; Injury Prevention Research Center, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Ford M; Carolinas Medical Center, Charlotte, North Carolina.
J Emerg Med ; 49(6): 974-83, 2015 Dec.
Article en En | MEDLINE | ID: mdl-26423915
BACKGROUND: Emergency Departments (EDs) are beginning to notify their physicians of patients reporting chronic noncancer pain (CNCP) who frequent EDs, and are suggesting that the physicians not prescribe opioids to these patients. OBJECTIVES: We hypothesized that this intervention would reduce both the number of opioids prescribed to these patients by their ED physicians and the number of these patients' return visits to the ED. METHODS: We conducted a randomized controlled trial of this intervention in 13 electronically linked EDs. Patients eligible for the study were characterized by CNCP, lacked evidence of sickle cell anemia and suicide ideation, and made frequent (>10) visits to the EDs over a 12-month period. We randomly assigned 411 of these patients to either an intervention group or a control group. Our intervention comprised both an alert placed in eligible patients' medical files and letters sent to the patients and their community-based providers. The alert suggested that physicians decline requests for opioid analgesic prescriptions and instead refer these patients to community-based providers to manage their ongoing pain. RESULTS: During the 12 months after randomization, patients in the intervention and control groups averaged 11.9 and 16.6 return visits, and received prescriptions for opioids on 16% and 26% of those visits, respectively. Altogether, patients in the intervention group made 1033 fewer return visits to the EDs in the follow-up year than those in the control group. CONCLUSION: This intervention constitutes a promising practice that EDs should consider to reduce the number of visits made by frequent visitors with CNCP.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pautas de la Práctica en Medicina / Servicio de Urgencia en Hospital / Dolor Crónico / Analgésicos Opioides Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Male País/Región como asunto: America do norte Idioma: En Revista: J Emerg Med Asunto de la revista: MEDICINA DE EMERGENCIA Año: 2015 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Pautas de la Práctica en Medicina / Servicio de Urgencia en Hospital / Dolor Crónico / Analgésicos Opioides Tipo de estudio: Clinical_trials Límite: Adult / Female / Humans / Male País/Región como asunto: America do norte Idioma: En Revista: J Emerg Med Asunto de la revista: MEDICINA DE EMERGENCIA Año: 2015 Tipo del documento: Article