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Cancer pain management in the emergency department: a multicenter prospective observational trial of the Comprehensive Oncologic Emergencies Research Network (CONCERN)

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Abstract

Purpose

Many patients with cancer seek care for pain in the emergency department (ED). Prospective research on cancer pain in this setting has historically been insufficient. We conducted this study to describe the reported pain among cancer patients presenting to the ED, how pain is managed, and how pain may be associated with clinical outcomes.

Methods

We conducted a multicenter cohort study on adult patients with active cancer presenting to 18 EDs in the USA. We reported pain scores, response to medication, and analgesic utilization. We estimated the associations between pain severity, medication utilization, and the following outcomes: 30-day mortality, 30-day hospital readmission, and ED disposition.

Results

The study population included 1075 participants. Those who received an opioid in the ED were more likely to be admitted to the hospital and were more likely to be readmitted within 30 days (OR 1.4 (95% CI: 1.11, 1.88) and OR 1.56 (95% CI: 1.17, 2.07)), respectively. Severe pain at ED presentation was associated with increased 30-day mortality (OR 2.30, 95% CI: 1.05, 5.02), though this risk was attenuated when adjusting for clinical factors (most notably functional status).

Conclusions

Patients with severe pain had a higher risk of mortality, which was attenuated when correcting for clinical characteristics. Those patients who required opioid analgesics in the ED were more likely to require admission and were more at risk of 30-day hospital readmission. Future efforts should focus on these at-risk groups, who may benefit from additional services including palliative care, hospice, or home-health services.

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Acknowledgments

The Comprehensive Oncologic Emergencies Research Network (CONCERN) Network supported this study with scientific review and suggestions on the study design and conduct. Additional information about CONCERN is available at https://epi.grants.cancer.gov/concern/. Nonniekaye Shelburne, MS, CRNP, AOCN, and the Epidemiology and Genomics Research Program within the National Cancer Institute’s Division of Cancer Control and Population Science, Bethesda, Maryland, assisted with study design, data management, and ongoing support of the research network. We thank the study participants, research staff, and medical centers who have provided data for this study.

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Correspondence to Christopher J. Coyne.

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Conflict of interest

Dr. Baugh has worked as a consultant and advisory board member for Janssen Pharmaceuticals, Nabriva Therapeutics, Salix Pharmaceuticals, and Vapotherm; has previously received research funding from Janssen Pharmaceuticals and Boehringer Ingelheim; and has served as an advisory board member and as a paid speaker for Roche Diagnostics. Dr. Yeung is the principal investigator of an investigator-initiated clinical trial supported by DepoMed and a retrospective clinical study supported by Bristol-Myers Squibb through ARISTA-USA (BMS/Pfizer American Thrombosis Investigator Initiated Research Program). Dr. Yeung participated in an advisory panel for Celgene. Dr. Henning receives research support from Baxter and provides consulting services to CytoVale.

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This study was approved by all participating institutional review boards.

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All patients provided written consent and signed a HIPPA waiver prior to participation.

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Coyne, C.J., Reyes-Gibby, C.C., Durham, D.D. et al. Cancer pain management in the emergency department: a multicenter prospective observational trial of the Comprehensive Oncologic Emergencies Research Network (CONCERN). Support Care Cancer 29, 4543–4553 (2021). https://doi.org/10.1007/s00520-021-05987-3

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