Department of Obstetrics and Gynecology, Tampere University Hospital, PL 2000, 33521, Tampere, Finland.
Faculty of Medicine and Life Sciences, University of Tampere, Tampere, Finland.
Arch Gynecol Obstet. 2019 Oct;300(4):903-909. doi: 10.1007/s00404-019-05260-3. Epub 2019 Aug 17.
The optimal postoperative analgesia after cesarean section (CS) remains to be determined. The primary objective of this study was to assess whether oral oxycodone provides the same or better pain control and satisfaction with pain relief as oxycodone given intravenously using a patient-controlled analgesia (PCA) infusion device. The secondary objectives were to compare the gastrointestinal symptoms and postsurgical recovery of the two groups.
This prospective randomized trial was conducted at a University Hospital between February 2015 and June 2017. Altogether 270 CS patients were randomly assigned to receive postoperative oxycodone pain relief by IV PCA (n = 133) or orally (n = 137). Pain control and satisfaction with pain treatment were assessed by a numeric rating scale (NRS) at 2, 4, 8, and 24 h postoperatively.
No differences were found in NRS pain scores or satisfaction between the groups except at 24 h pain when coughing; there was a statistically significant difference favoring the IV PCA group (p = 0.006). In the IV PCA group, the patients experienced more nausea at 4 h (p = 0.001) and more vomiting at 8 h (p = 0.010). Otherwise, postoperative recovery was similar in both groups. The equianalgesic dose of oxycodone was significantly smaller in the oral group (p = 0.003).
This study indicates that oral oxycodone provides pain control and satisfaction with pain relief equal to IV oxycodone PCA for postoperative analgesia after cesarean section. Satisfaction with pain treatment was high in both groups, and both methods were well tolerated. Early nausea was less common with oral medication.
剖宫产术后的最佳镇痛效果仍有待确定。本研究的主要目的是评估口服羟考酮与静脉使用患者自控镇痛(PCA)输注装置给予羟考酮相比,是否能提供相同或更好的疼痛控制和缓解疼痛的满意度。次要目的是比较两组的胃肠道症状和术后恢复情况。
这是一项在 2015 年 2 月至 2017 年 6 月期间在一所大学医院进行的前瞻性随机试验。共有 270 名剖宫产患者被随机分为静脉 PCA 组(n=133)和口服组(n=137)接受术后羟考酮镇痛。通过数字评分量表(NRS)在术后 2、4、8 和 24 小时评估疼痛控制和疼痛治疗的满意度。
两组患者的 NRS 疼痛评分或满意度均无差异,但在咳嗽时 24 小时疼痛方面存在统计学差异,静脉 PCA 组更优(p=0.006)。在静脉 PCA 组,患者在 4 小时时更易出现恶心(p=0.001),在 8 小时时更易出现呕吐(p=0.010)。其他方面,两组的术后恢复情况相似。口服组的羟考酮等效剂量明显较小(p=0.003)。
本研究表明,口服羟考酮可提供与静脉 PCA 给予羟考酮相似的剖宫产术后镇痛效果。两组患者对疼痛治疗的满意度均较高,两种方法均耐受良好。口服药物早期恶心较少见。