Remifentanil for Carboprost-Induced Adverse Reactions During Cesarean Delivery Under Combined Spinal-Epidural Anesthesia

Chang-Na Wei; Xiang-Yang Chang; Jin-Hua Dong; Qing-He Zhou

doi:10.3389/fphar.2020.00980

Remifentanil for Carboprost-Induced Adverse Reactions During Cesarean Delivery Under Combined Spinal-Epidural Anesthesia

Front Pharmacol. 2020 Jun 30:11:980. doi: 10.3389/fphar.2020.00980. eCollection 2020.

Authors

Chang-Na Wei¹, Xiang-Yang Chang¹, Jin-Hua Dong², Qing-He Zhou³

Affiliations

¹ Department of Anesthesia, Jiaxing University Affiliated Women and Children Hospital, Jiaxing, China.
² Department of Obstetrics, Jiaxing University Affiliated Women and Children Hospital, Jiaxing, China.
³ Department of Anesthesia, Affiliated Hospital of Jiaxing University, Jiaxing, China.

Abstract

Purpose: Carboprost may induce adverse reactions when used to treat postpartum hemorrhage. We aimed to explore the effects of intravenous infusion of low-dose remifentanil to prevent such reactions.

Methods: We enrolled parturient patients scheduled for elective cesarean section. Anesthesiologist administered combined spinal epidurals at the L3/4 interspace, with 0.5% hyperbaric bupivacaine subarachnoid space injections (1.5-2.5 ml). We randomly divided parturient patients, administered carboprost during surgery, into the remifentanil group (group R) and the control group (group C). Patients in group R received an intravenous target-controlled infusion of remifentanil (target effect-site concentration, 1.5 ng/ml) simultaneously with a carboprost tromethamine injection (250 µg). Patients in group C received a normal saline infusion with carboprost. We recorded and analyzed the incidence of carboprost-related adverse reactions (vomiting, nausea, chest congestion, flushing, hypertension, tachycardia, cough, and shivering), and assessed patient comfort using a numerical rating scale ([NRS], on which 0 was very uncomfortable and 10 was very comfortable).

Results: After applying inclusion and exclusion criteria, we conducted statistical analysis of the data from 70 women. The incidence of vomiting was significantly lower in group R than in group C (14.3 vs. 51.4%, p < 0.01); and the incidence of nausea, chest congestion, facial flushing, and hypertension were significantly lower in group R than in group C (all p < 0.01). Furthermore, the patients' comfort scores were significantly higher in group R than in group C (8.0 ± 1.8 vs. 3.6 ± 2.1, p < 0.01).

Conclusion: Our results demonstrate that an intravenous low-dose remifentanil infusion can effectively prevent carboprost-related adverse reactions during cesarean delivery under combined spinal and epidural anesthesia.

Clinical trial registration: We pre-registered this study at http://www.chictr.org.cn/showproj.aspx?proj=27707 (ChiCTR1800016292).

Keywords: adverse reaction; carboprost; cesarean delivery; intraspinal anesthesia; remifentanil.