Assessment of Opioid Use and Analgesic Requirements After Endoscopic Sinus Surgery: A Randomized Clinical Trial.
Acetaminophen
/ administration & dosage
Adolescent
Adult
Aged
Aged, 80 and over
Analgesics, Non-Narcotic
/ administration & dosage
Analgesics, Opioid
/ administration & dosage
Drug Therapy, Combination
Endoscopy
Female
Humans
Ibuprofen
/ administration & dosage
Male
Middle Aged
Oxycodone
/ administration & dosage
Pain Measurement
Pain, Postoperative
/ diagnosis
Prospective Studies
Rhinitis
/ surgery
Rhinoplasty
/ methods
Sinusitis
/ surgery
Treatment Outcome
Young Adult
Journal
JAMA otolaryngology-- head & neck surgery
ISSN: 2168-619X
Titre abrégé: JAMA Otolaryngol Head Neck Surg
Pays: United States
ID NLM: 101589542
Informations de publication
Date de publication:
01 09 2021
01 09 2021
Historique:
pubmed:
6
8
2021
medline:
3
11
2021
entrez:
5
8
2021
Statut:
ppublish
Résumé
The opioid epidemic has generated interest in optimizing opioid prescribing after common surgeries. Recent studies have shown a broad range of analgesic prescription patterns following endoscopic sinus surgery (ESS). To compare the efficacy of different analgesic regimens after ESS. This multi-institutional, nonblinded randomized clinical trial was conducted at 6 tertiary centers across the US and Canada and included participants who underwent ESS for acute or chronic rhinosinusitis. The study was conducted from March 2019 to March 2020, and the data were analyzed in November to December 2020. All participants received acetaminophen, 650 mg, as the first-line analgesic. From there, patients were randomized to either oxycodone rescue (oxycodone, 5 mg, as second-line therapy) or ibuprofen rescue (ibuprofen, 600 mg, as second-line therapy, with oxycodone, 5 mg, reserved for breakthrough pain). Baseline characteristics and disease severity were collected at enrollment. Medication logs, pain scores, and epistaxis measures were collected until postoperative day 7. The primary outcome was the postoperative visual analog scale score for pain. Brief Pain Inventory Pain Severity and Pain Interference Scores were also collected. A total of 118 patients were randomized (62 [52.5%] oxycodone rescue, 56 [47.5%] ibuprofen rescue; mean [SD] age, 46.7 [16.3] years; 44 women [44.0%]; 83 White [83.0%], 7 Black [7.0%], and 7 Asian individuals [7.0%]). After exclusions for loss to follow-up and noncompliance, 51 remained in the oxycodone rescue group and 49 in the ibuprofen rescue group. The groups had similar demographic characteristics and disease severity. Thirty-two (63%) in the oxycodone rescue group had adequate pain management with acetaminophen only, while 19 (37%) consumed at least 1 oxycodone dose. In the ibuprofen rescue group, 18 (16%) required only acetaminophen, 28 (57%) used only acetaminophen and ibuprofen, and the remaining 13 (26%) consumed 1 or more oxycodone doses. The groups had similar average acetaminophen (9.69 vs 7.96 doses; difference, 1.73; 95% CI, -1.37 to 4.83) and oxycodone (1.89 vs 0.77 doses; difference, 1.13; 95% CI, -0.11 to 2.36) use. Both groups had similar postoperative visual analog scale scores. A subanalysis that compared opioids users with nonusers showed clinically significant lower pain scores in nonusers at multiple postoperative points. In this randomized clinical trial, most patients who underwent ESS could be treated postoperatively using a nonopioid regimen of either acetaminophen alone or acetaminophen and ibuprofen. Ibuprofen as a second-line therapy did not reduce overall narcotic consumption, but the overall narcotic use was low in both groups. ClinicalTrials.gov Identifier: NCT03783702.
Identifiants
pubmed: 34351376
pii: 2782827
doi: 10.1001/jamaoto.2021.1839
pmc: PMC8343514
doi:
Substances chimiques
Analgesics, Non-Narcotic
0
Analgesics, Opioid
0
Acetaminophen
362O9ITL9D
Oxycodone
CD35PMG570
Ibuprofen
WK2XYI10QM
Banques de données
ClinicalTrials.gov
['NCT03783702']
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM
Pagination
811-819Commentaires et corrections
Type : CommentIn