TY - JOUR KW - Airway Extubation KW - Anesthesia, General/adverse effects KW - Case-Control Studies KW - Child KW - Female KW - Humans KW - Male KW - Naloxone/therapeutic use KW - Narcotic Antagonists/therapeutic use KW - Postoperative Period KW - Respiratory Insufficiency/drug therapy KW - Retrospective Studies KW - Analgesics KW - General anesthesia KW - Hypoventilation KW - Narcotic Antagonists KW - Postoperative complications KW - Surgery AU - Vinay K. Donempudi AU - Juraj Sprung AU - Toby N. Weingarten A1 - AB - PURPOSE: Excessive narcotization in pediatric surgical patients has not been well characterized. This report describes the use of postoperative naloxone in pediatric patients. METHODS: Pediatric surgical patients from January 1, 2010, through June 30, 2016, who underwent general anesthesia and received naloxone within 48 h postoperatively were identified and matched 1:1 with controls by age, sex, and procedure. Cases and controls underwent retrospective chart review. RESULTS: Forty-seven patients received naloxone, with a rate of 2.0 (95% CI 1.5-2.7) per 1000 anesthetics. Indications were respiratory depression (n = 19), facilitating extubation (n = 15), and reversing sedation (n = 13), and 44 cases received naloxone in a monitored environment. The median (interquartile range) naloxone dose was 4.0 (2.0-23.5) mcg/kg, and five patients (11%) later required subsequent naloxone treatments. Their characteristics were similar to controls, including opioid medications, except cases that had signs of respiratory depression before naloxone administration. The outcomes were similar, although more cases were admitted to the intensive care unit before naloxone administration. One patient died 13 days postoperatively of unrelated causes. CONCLUSION: Postoperative naloxone administration in pediatric patients is rare. The observation that most administrations occurred in a monitored setting implies that at-risk patients had been appropriately identified and kept under closer surveillance. AD - Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, 200 First St SW, Rochester, MN, 55905, USA.; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, 200 First St SW, Rochester, MN, 55905, USA.; Department of Anesthesiology and Perioperative Medicine, Mayo Clinic, 200 First St SW, Rochester, MN, 55905, USA. weingarten.toby@mayo.edu. BT - Pediatric surgery international C5 - Healthcare Disparities; Opioids & Substance Use CP - 3 CY - Germany DO - 10.1007/s00383-017-4212-2 IS - 3 JF - Pediatric surgery international LA - eng M1 - Journal Article N2 - PURPOSE: Excessive narcotization in pediatric surgical patients has not been well characterized. This report describes the use of postoperative naloxone in pediatric patients. METHODS: Pediatric surgical patients from January 1, 2010, through June 30, 2016, who underwent general anesthesia and received naloxone within 48 h postoperatively were identified and matched 1:1 with controls by age, sex, and procedure. Cases and controls underwent retrospective chart review. RESULTS: Forty-seven patients received naloxone, with a rate of 2.0 (95% CI 1.5-2.7) per 1000 anesthetics. Indications were respiratory depression (n = 19), facilitating extubation (n = 15), and reversing sedation (n = 13), and 44 cases received naloxone in a monitored environment. The median (interquartile range) naloxone dose was 4.0 (2.0-23.5) mcg/kg, and five patients (11%) later required subsequent naloxone treatments. Their characteristics were similar to controls, including opioid medications, except cases that had signs of respiratory depression before naloxone administration. The outcomes were similar, although more cases were admitted to the intensive care unit before naloxone administration. One patient died 13 days postoperatively of unrelated causes. CONCLUSION: Postoperative naloxone administration in pediatric patients is rare. The observation that most administrations occurred in a monitored setting implies that at-risk patients had been appropriately identified and kept under closer surveillance. PP - Germany PY - 2018 SN - 1437-9813; 0179-0358 SP - 335 EP - 341 EP - T1 - Pediatric patients receiving naloxone within 48 h of anesthesia: a case-control study T2 - Pediatric surgery international TI - Pediatric patients receiving naloxone within 48 h of anesthesia: a case-control study U1 - Healthcare Disparities; Opioids & Substance Use U2 - 29124404 U3 - 10.1007/s00383-017-4212-2 VL - 34 VO - 1437-9813; 0179-0358 Y1 - 2018 Y2 - Mar ER -