Assisted Reproduction Unit, Andrology Laboratory, Health Sciences University, Adana City Training and Research Hospital, Adana, Turkiye.
Emergency Medicine Clinic, Health Sciences University, Adana City Training and Research Hospital, Adana, Turkiye.
J Coll Physicians Surg Pak. 2024 Feb;34(2):160-165. doi: 10.29271/jcpsp.2024.02.160.
To evaluate the analgaesic efficacy of tenoxicam and dexketoprofen in patients admitted to the Emergency Medicine (EM) Clinic with severe acute pain due to primary dysmenorrhea (PD).
Randomised-controlled trial. Place and Duration of the Study: Emergency Medicine Clinic, Health Sciences University, Adana City Training and Research Hospital, Adana, Turkiye, from January to December 2022.
Patients presenting with PD, were divided into two groups of 60 each, administered 50 mg dexketoprofen and 20 mg tenoxicam intravenously. Visual analogue scale (VAS) scores were recorded at the 15th, 30th, 60th, and 120th minutes. VAS scores and ΔVAS scores were compared with the effectiveness of drugs, the need for rescue drugs and its side-effects.
Intravenous (IV) dexketoprofen was administered to 60 of the patients and IV tenoxicam was administered to another 60. At the time of admission, mean VAS scores of the patients were 8.8 ± 0.9 for the dexketoprofen group and 8.6 ± 0.8 for the tenoxicam group. The VAS scores of the dexketoprofen group were found to be statistically significantly lower after 30 minutes with lower need for rescue analgaesics. ΔVAS scores of the dexketoprofen group were statistically significantly higher from the 30th minute.
According to the VAS scoring, IV dexketoprofen was a more effective drug than IV tenoxicam in patients who were admitted to the EM clinic with severe pain due to PD.
Dexketoprofen, Primary dysmenorrhea, VAS score.
评估酮咯酸和右旋酮洛芬在因原发性痛经(PD)而到急诊医学(EM)诊所就诊的严重急性疼痛患者中的镇痛效果。
随机对照试验。研究地点和时间:土耳其阿德南市训练与研究医院,阿德亚曼健康科学大学急诊医学科,2022 年 1 月至 12 月。
将因 PD 就诊的患者分为两组,每组 60 例,分别静脉注射 50mg 右旋酮洛芬和 20mg 酮咯酸。在第 15、30、60 和 120 分钟记录视觉模拟评分(VAS)。比较药物的有效性、需要抢救药物及其副作用。
静脉注射(IV)右旋酮洛芬治疗 60 例患者,静脉注射酮咯酸治疗另 60 例患者。入院时,右旋酮洛芬组患者的平均 VAS 评分为 8.8±0.9,酮咯酸组为 8.6±0.8。右旋酮洛芬组的 VAS 评分在 30 分钟后明显降低,需要使用抢救性镇痛药的比例更低。右旋酮洛芬组的 ΔVAS 评分从第 30 分钟开始显著升高。
根据 VAS 评分,与 IV 酮咯酸相比,IV 右旋酮洛芬在因 PD 而到 EM 诊所就诊的严重疼痛患者中更有效。
右旋酮洛芬;原发性痛经;VAS 评分。