Department of Anesthesia and Critical Care Medicine, Cairo University, Cairo, Egypt.
BMC Anesthesiol. 2024 Jun 7;24(1):202. doi: 10.1186/s12871-024-02571-0.
We aimed to compare the analgesic effects of intravenous ibuprofen to ketorolac after open abdominal hysterectomy.
This randomized double-blinded controlled trial included adult women scheduled for elective open abdominal hysterectomy. Participants were randomized to receive either 30 mg ketorolac (n = 50) or 800 mg ibuprofen (n = 50) preoperatively, then every 8 h postoperatively for 24 h. All participants received paracetamol 1 gm/6 h. Rescue analgesic was given if the visual analogue scale (VAS) for pain assessment was > 3. The primary outcome was the mean postoperative dynamic VAS during the first 24 h. Secondary outcomes were static VAS, intraoperative fentanyl consumption, postoperative morphine consumption, time to independent movement, and patient's satisfaction.
Forty-six patients in the ibuprofen group and fifty patients in the ketorolac group were analyzed. The 24-h dynamic and static VAS were similar in the two groups. The median (quartiles) dynamic VAS was 1.1 (0.9, 1.9) in the ibuprofen group versus 1.0 (0.7, 1.3) in the ketorolac group, P-value = 0.116; and the median (quartiles) static VAS was 0.9 (0.6, 1.3) in the ibuprofen group versus 0.7 (0.4, 1.1) in the ketorolac group, P-value = 0.113. The intra- and postoperative analgesic requirements were also similar in the two groups. However, patient satisfaction was slightly higher in the ketorolac group than that in the ibuprofen group (median [quartiles]: 6 [5, 7] versus 5 [4, 7], respectively), P-value: 0.009.
The two drugs, intravenous ibuprofen and ketorolac produced similar analgesic profile in patients undergoing open abdominal hysterectomy receiving multimodal analgesic regimen. NCT05610384, Date of registration: 09/11/2022 CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT05610384. https://clinicaltrials.gov/ct2/show/NCT05610384.
本研究旨在比较静脉注射布洛芬和酮洛酸在开腹子宫切除术患者中的镇痛效果。
这是一项随机、双盲、对照临床试验,纳入了择期行开腹子宫切除术的成年女性。参与者被随机分为两组,分别接受 30mg 酮洛酸(n=50)或 800mg 布洛芬(n=50)术前用药,然后每 8 小时用药一次,持续 24 小时。所有患者均给予 1g 对乙酰氨基酚,每 6 小时一次。如果疼痛评估的视觉模拟量表(VAS)>3,则给予解救性镇痛。主要结局为术后 24 小时内的平均动态 VAS。次要结局包括静态 VAS、术中芬太尼用量、术后吗啡用量、独立活动时间和患者满意度。
在布洛芬组和酮洛酸组中,分别有 46 例和 50 例患者进行了分析。两组 24 小时动态和静态 VAS 相似。布洛芬组的 24 小时动态 VAS 中位数(四分位距)为 1.1(0.9,1.9),酮洛酸组为 1.0(0.7,1.3),P 值=0.116;布洛芬组的静态 VAS 中位数(四分位距)为 0.9(0.6,1.3),酮洛酸组为 0.7(0.4,1.1),P 值=0.113。两组的围术期镇痛需求也相似。然而,酮洛酸组患者满意度略高于布洛芬组(中位数[四分位距]:6[5,7]与 5[4,7],P 值:0.009)。
在接受多模式镇痛方案的开腹子宫切除术患者中,静脉注射布洛芬和酮洛酸产生了相似的镇痛效果。NCT05610384,注册日期:2022 年 9 月 11 日。临床试验注册:ClinicalTrials.gov 标识符:NCT05610384。https://clinicaltrials.gov/ct2/show/NCT05610384。