Department of Anesthesia, Assiut University Faculty of Medicine, Assiut, Egypt.
Department of Obstetrics and Gynecology, Assiut University Faculty of Medicine, Assiut, Egypt.
Korean J Anesthesiol. 2019 Feb;72(1):47-52. doi: 10.4097/kja.d.18.00132. Epub 2018 Sep 18.
Postoperative nausea and vomiting (PONV) is a common complication following laparascopic surgery. This study compared the effect of intraperitoneal versus intravenous dexamethasone for reducing PONV after gynecological laparoscopic surgeries.
Eighty adult female patients, American Society of Anesthesiologists physical status I-II, scheduled for gynecological laparoscopic surgery were randomized to receive 8 mg dexamethasone intravenously (IV) (n = 40) or intraperitoneally (IP) (n = 40). The primary outcome was the PONV incidence during the first 24 h after laparoscopy. Secondary outcomes included visual analogue scale (VAS) pain scores, total rescue analgesic consumption during the first 24 h postoperatively, the need for rescue antiemetic drugs, and the incidence of complications that may accompany these medications.
Eleven women (27.5%) in the IV group, versus only 3 (7.5%) women in the IP group, experienced nausea during the first 24 h postlaparoscopy (P = 0.037). However, 5 patients (12.5%) in the IV group, versus only 2 patients (5.0%) in the IP group, experienced vomiting (P = 0.424). No statistically significant differences were seen in the severity of nausea or the need for rescue antiemetics. The IV group had a higher rate of side-effects than the IP group (27.5% vs. 7.5%, P = 0.037). Headache and dizziness were common side effects in the IV dexamethasone group. The groups did not differ significantly in terms of mean VAS score for pain and total meperidine consumption during the first 24 h postoperatively.
Intraperitoneal dexamethasone at a dose of 8 mg at the end of gynecological laparoscopy reduces the incidence of postoperative nausea.
术后恶心和呕吐(PONV)是腹腔镜手术后的常见并发症。本研究比较了腹腔内与静脉内给予地塞米松对减少妇科腹腔镜手术后 PONV 的效果。
80 名美国麻醉医师协会身体状况 I-II 的成年女性患者,计划行妇科腹腔镜手术,随机分为静脉内(IV)(n = 40)或腹腔内(IP)(n = 40)接受 8mg 地塞米松。主要结局是腹腔镜手术后 24 小时内 PONV 的发生率。次要结局包括视觉模拟评分(VAS)疼痛评分、术后 24 小时内总解救镇痛药物消耗、需要解救止吐药物以及可能伴随这些药物的并发症的发生率。
IV 组有 11 名女性(27.5%)在腹腔镜术后 24 小时内出现恶心,而 IP 组只有 3 名女性(7.5%)(P = 0.037)。然而,IV 组中有 5 名女性(12.5%)发生呕吐,而 IP 组只有 2 名女性(5.0%)(P = 0.424)。两组在恶心严重程度或需要解救止吐药物方面无统计学差异。IV 组的副作用发生率高于 IP 组(27.5%比 7.5%,P = 0.037)。头痛和头晕是 IV 地塞米松组常见的副作用。两组在术后 24 小时内的平均 VAS 疼痛评分和总哌替啶消耗量方面无显著差异。
妇科腹腔镜手术结束时腹腔内给予 8mg 地塞米松可降低术后恶心的发生率。