Postoperative Pain Management in Rhinoplasty: A Double Blind Randomized Controlled Trial.
Abstract
[BACKGROUND] There is inadequate evidence for the utilization of nonnarcotic pain medications for postoperative pain management following rhinoplasty.
[OBJECTIVE] To compare the effectiveness of opioid and non-opioid medications for postoperative pain control in rhinoplasty as measured by a visual analog scale (VAS) on postoperative days 0-5.
[METHODS] In this double-blind randomized controlled clinical trial, adult patients who underwent primary rhinoplasty at a tertiary center were enrolled from August 2019 to October 2024. Patients were randomized to receive either a combination of acetaminophen (325 mg) and hydrocodone (5 mg) or acetaminophen (325 mg) and ibuprofen (200 mg), 1-2 tablets every 4 h for five postoperative days. Tramadol (50 mg) was prescribed for breakthrough pain.
[RESULTS] A total of 130 patients (65 per group) completed the study. The average age (SD) was 32 (10.7) years. The majority were women (77%), White (68%), and underwent combined functional and aesthetic rhinoplasty (52%). There was no difference detected in mean postoperative pain (VAS) scores recorded on postoperative days 0-5, between treatment groups ( = 0.156). Among side effects, only itchiness was significantly higher ( = 0.001) in the hydrocodone-acetaminophen group.
[CONCLUSION] This trial demonstrates a lack of difference between opioid and non-opioid pain medications in postoperative pain control after rhinoplasty.
[OBJECTIVE] To compare the effectiveness of opioid and non-opioid medications for postoperative pain control in rhinoplasty as measured by a visual analog scale (VAS) on postoperative days 0-5.
[METHODS] In this double-blind randomized controlled clinical trial, adult patients who underwent primary rhinoplasty at a tertiary center were enrolled from August 2019 to October 2024. Patients were randomized to receive either a combination of acetaminophen (325 mg) and hydrocodone (5 mg) or acetaminophen (325 mg) and ibuprofen (200 mg), 1-2 tablets every 4 h for five postoperative days. Tramadol (50 mg) was prescribed for breakthrough pain.
[RESULTS] A total of 130 patients (65 per group) completed the study. The average age (SD) was 32 (10.7) years. The majority were women (77%), White (68%), and underwent combined functional and aesthetic rhinoplasty (52%). There was no difference detected in mean postoperative pain (VAS) scores recorded on postoperative days 0-5, between treatment groups ( = 0.156). Among side effects, only itchiness was significantly higher ( = 0.001) in the hydrocodone-acetaminophen group.
[CONCLUSION] This trial demonstrates a lack of difference between opioid and non-opioid pain medications in postoperative pain control after rhinoplasty.
추출된 의학 개체 (NER)
| 유형 | 영어 표현 | 한국어 / 풀이 | UMLS CUI | 출처 | 등장 |
|---|---|---|---|---|---|
| 시술 | rhinoplasty
|
코성형술 | dict | 6 | |
| 약물 | acetaminophen
|
C0000970
acetaminophen
|
scispacy | 1 | |
| 약물 | hydrocodone
|
C0020264
hydrocodone
|
scispacy | 1 | |
| 약물 | ibuprofen
|
C0020740
ibuprofen
|
scispacy | 1 | |
| 약물 | Tramadol
|
C0040610
tramadol
|
scispacy | 1 | |
| 약물 | hydrocodone-acetaminophen
|
C0717367
acetaminophen / hydrocodone
|
scispacy | 1 | |
| 약물 | non-opioid pain
|
scispacy | 1 | ||
| 약물 | [BACKGROUND]
|
scispacy | 1 | ||
| 약물 | [OBJECTIVE]
|
scispacy | 1 | ||
| 약물 | non-opioid
|
scispacy | 1 | ||
| 약물 | [RESULTS] A
|
scispacy | 1 | ||
| 질환 | Postoperative Pain
|
C0030201
Pain, Postoperative
|
scispacy | 1 | |
| 질환 | pain
|
C0030193
Pain
|
scispacy | 1 | |
| 질환 | itchiness
|
C3840668
Itchiness
|
scispacy | 1 | |
| 기타 | patients
|
scispacy | 1 | ||
| 기타 | women
|
scispacy | 1 |
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