PMID- 29491750 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20240313 IS - 1551-6776 (Print) IS - 2331-348X (Electronic) IS - 1551-6776 (Linking) VI - 23 IP - 1 DP - 2018 Jan-Feb TI - Sedation Protocol During Bevacizumab Intravitreal Injection in Preterm Infants With Retinopathy of Prematurity. PG - 34-40 LID - 10.5863/1551-6776-23.1.34 [doi] AB - OBJECTIVES: This study describes outcomes of intravenous (IV) analgesics and sedatives for bedside intravitreal bevacizumab injections for retinopathy of prematurity. METHODS: This retrospective study included infants receiving intravitreal bevacizumab injections between January 2012 and May 2016. Infants were excluded if bevacizumab was administered under general anesthesia or for incomplete records. Data collection included demographics, sedation and analgesia regimen, and cardiopulmonary adverse events (AEs). The primary objective was to identify the median doses of the IV analgesics and sedatives. The secondary objectives included the number of patients with cardiopulmonary AEs and those with procedure success, defined as procedure completion without interruption and absence of interventions. RESULTS: Fifteen infants were included. Fourteen (93.3%) were initiated on a fentanyl infusion at a median of 2 mcg/kg/hr (IQR, 2-3.6), and 12 (80%) received midazolam infusions at a median of 0.06 mg/kg/hr. All patients received at least 1 IV neuromuscular blocker dose just prior to the procedure. Only 2 patients (13.3%) required an increase in their fentanyl or midazolam infusions. Procedure success was achieved in 13 patients (86.7%). Five patients (33.3%) experienced 1 cardiopulmonary AE. One patient (6.7%) had a delay in the procedure, and 1 patient (6.7%) required naloxone. Despite this, the procedure was completed in all patients. CONCLUSIONS: Most received fentanyl and midazolam infusions with a dose of vecuronium just prior to the procedure. Thirteen (86.7%) met the criteria for procedure success. One-third experienced a cardiopulmonary AE. Future studies are needed to identify the optimal agents and route of administration for this procedure. FAU - Miller, Jamie L AU - Miller JL FAU - Johnson, Peter N AU - Johnson PN FAU - Harkey, Kari AU - Harkey K FAU - Siatkowski, R Michael AU - Siatkowski RM LA - eng PT - Journal Article PL - United States TA - J Pediatr Pharmacol Ther JT - The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG JID - 101089851 PMC - PMC5823490 OTO - NOTNLM OT - bevacizumab OT - fentanyl OT - midazolam OT - neonatal intensive care unit OT - retinopathy of prematurity COIS- Disclosure Dr Jamie Miller is on the speaker's bureau for Chiesi, USA, Inc. The rest of the authors declare no conflicts or financial interest in any product or service mentioned in the manuscript, including grants, equipment, medications, employment, gifts, and honoraria. The authors had full access to all the data in the study and take responsibility for the integrity of the data and the accuracy of the data analysis. EDAT- 2018/03/02 06:00 MHDA- 2018/03/02 06:01 PMCR- 2018/01/01 CRDT- 2018/03/02 06:00 PHST- 2018/03/02 06:00 [entrez] PHST- 2018/03/02 06:00 [pubmed] PHST- 2018/03/02 06:01 [medline] PHST- 2018/01/01 00:00 [pmc-release] AID - 10.5863/1551-6776-23.1.34 [doi] PST - ppublish SO - J Pediatr Pharmacol Ther. 2018 Jan-Feb;23(1):34-40. doi: 10.5863/1551-6776-23.1.34.