Change in Pediatric Adenotonsillectomy Postoperative Visit Patterns After Opioid Food and Drug Administration Warning

Author:

Cohen Naiomi1,Schissler Kathryn2,Jeter Justin3,Stathas Adam4,Lozano Juan5,Dave Sandeep6,Lowe David1

Affiliation:

1. Department of Pediatric Emergency Medicine, Nicklaus Children's Hospital, Miami, FL

2. Department of Pediatric Emergency Medicine, Connecticut Children's, University of Connecticut School of Medicine, Hartford, CT

3. Pediatric Associates, Miami, FL

4. Department of Medical Education, Nicklaus Children's Hospital, Miami, FL

5. Division of Medical and Population Health Sciences Education and Research, College of Medicine, Florida International University, Miami, FL

6. Division of Pediatric Otolaryngology, Nicklaus Children's Hospital, Miami, FL

Abstract

Study Objective This study aimed to determine the association between opioid prescriptions given after tonsillectomy with adenoidectomy (T + A) and pain-related return visit rates in pediatric patients. Determine association between Food and Drug Administration (FDA) black box warning against opioid use in this population and pain-related return visit rates. Methods This was a single-institution retrospective cohort study of pediatric patients who underwent T + A between April 2012 and December 2015 and had return visits to the emergency department or urgent care center. Data were obtained from the hospital electronic warehouse using International Classification of Diseases-9/10 procedure codes. Odds ratios (ORs) with 95% confidence intervals (CIs) for return visits were calculated. Multivariate logistic regression analysis was used to measure association between opioid prescriptions and return visit rates as well as FDA warning and return visit rates adjusting for confounders. Results There were 4778 patients who underwent T + A, median age, 5 years. Of these, 752 (15.7%) had return visits. Pain-related return visits were higher in patients who received opioid prescriptions (adjusted OR, 1.31; 95% CI, 1.09–1.57). After FDA warning, opioids were prescribed at a lower rate (47.9%) compared with previous (98.6%) (OR, 0.01; 95% CI, 0.008–0.02). Pain-related return visits were lower after FDA warning (OR, 0.73; 95% CI, 0.61–0.87). Steroid prescription rate increased after FDA warning (OR, 415; 95% CI, 197–874). Conclusions Opioid prescriptions were associated with higher pain-related return visits after T + A, whereas issuance of FDA black box warning against codeine use was associated with lower pain-related return visits. Our data suggest that the black box warning potentially had unintended benefits in pain management and health care usage.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine,Emergency Medicine,Pediatrics, Perinatology and Child Health

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