Effect of Intravenous Ondansetron on Spinal Anaesthesia-Induced Hypotension During Caesarean Section
DOI:
https://doi.org/10.61919/jhrr.v4i2.1120Keywords:
Ondansetron, hypotension, spinal anaesthesia, caesarean section, maternal health, elective caesarean deliveryAbstract
Background: Spinal anaesthesia has become the preferred method for elective caesarean sections due to its simplicity, speed, and reliability. However, a significant challenge with this technique is maternal hypotension, which can lead to nausea, vomiting, and decreased cardiac output, necessitating effective preventive measures. Ondansetron, a 5-HT3 receptor antagonist, is commonly used to prevent nausea and vomiting, and recent studies suggest its potential efficacy in reducing hypotension during spinal anaesthesia.
Objective: To compare the frequency of hypotension during spinal anaesthesia for elective caesarean delivery between two groups: one receiving intravenous ondansetron and the other receiving normal saline as a placebo.
Methods: This randomized controlled trial was conducted at the Department of Anaesthesia, Combined Military Hospital Sialkot, over six months (May 6, 2016, to November 6, 2016). A total of 60 pregnant women scheduled for elective caesarean delivery under spinal anaesthesia, aged 18-35 years, classified as ASA I or II, and carrying a singleton pregnancy at 37-42 weeks, were included. Exclusion criteria included contraindications to spinal anaesthesia, history of heart or lung disease, known hypersensitivity to the study medication, diabetes with blood sugar >180 mg/dl, hypertension with blood pressure >160/90 mmHg, morbid obesity, and fetal abnormalities. Participants were randomly assigned to Group A (intervention) receiving 4 mg ondansetron intravenously in 10 ml saline 5 minutes before spinal anaesthesia, or Group B (control) receiving 10 ml saline intravenously. Baseline vitals, including heart rate, mean arterial pressure, systolic and diastolic blood pressure, were recorded. Spinal anaesthesia was administered using a 25-gauge needle with 2.5 ml of hyperbaric 0.5% bupivacaine solution. Hypotension was managed with intravenous bolus of 100 mcg phenylephrine and 100 ml normal saline. Data were analyzed using SPSS version 25.0, with qualitative variables compared using chi-square tests and significance set at p ≤ 0.05.
Results: The mean age of participants was 27.95±5.68 years, and the mean BMI was 24.12±3.30 kg/m². Baseline systolic blood pressure averaged 129.00±11.24 mmHg, diastolic blood pressure 71.67±6.99 mmHg, and mean arterial pressure 114.67±7.93 mmHg. In Group A, 8 out of 30 participants (26.7%) experienced hypotension compared to 17 out of 30 participants (56.7%) in Group B (p=0.036). Stratification by age revealed a significant difference in hypotension incidence in participants >26 years (p=0.028). No significant differences were observed when stratified by BMI <24 kg/m² (p=0.056) and >24 kg/m² (p=0.300).
Conclusion: Administration of 4 mg intravenous ondansetron 5 minutes prior to spinal anaesthesia for elective caesarean delivery significantly reduces the frequency of hypotension compared to placebo, especially in patients older than 26 years. Ondansetron appears to be a practical and cost-effective prophylactic measure against spinal anaesthesia-induced hypotension, warranting further large-scale, multi-centre trials to validate these findings.
Downloads
References
Trabelsi W, Romdhani C, Elaskri H, Sammoud W, Bensalah M, Labbene I, Ferjani M. Effect of Ondansetron on the Occurrence of Hypotension and on Neonatal Parameters During Spinal Anesthesia for Elective Caesarean Section: A Prospective, Randomized, Controlled, Double-Blind Study. Anesthesiology Research and Practice. 2015;2015:158061. doi:10.1155/2015/158061
Randa AS, Sohair AM, Ahmed S, Mustafa MH. Comparative Study Between Two Doses of Intravenous Ondansetron on Maternal Haemodynamics During Elective Caesarean Delivery Under Spinal Anaesthesia. Med J Cairo Univ. 2021;89(June):543-51. doi:10.21608/mjcu.2021.167845
Herbosa GA, Tho NN, Gapay AA, Lorsomradee S, Thang CQ. Consensus on the Southeast Asian Management of Hypotension Using Vasopressors and Adjunct Modalities During Cesarean Section Under Spinal Anesthesia. J Anesth Analg Crit Care. 2022;2(1):56. PMID:37386598; PMCID.
Bhiwal AK, Chauhan K, Choudhary S, Bhatt HA, Gupta S. Intravenous Ondansetron to Prevent Hypotension During Cesarean Section Under Spinal Anaesthesia. J Obstet Anaesth Crit Care. 2021;11(1):15-9.
Ayorinde BT, Buczkowski P, Brown J, Shah J, Buggy DJ. Evaluation of Pre-Emptive Intramuscular Phenylephrine and Ephedrine for Reduction of Spinal Anesthesia-Induced Hypotension During Caesarean Section. Br J Anaesth. 2001;86(3):372-6.
Sahoo T, SenDasgupta C, Goswami A, Hazra A. Reduction in Spinal-Induced Hypotension With Ondansetron in Parturients Undergoing Cesarean Section: A Double-Blind Randomized, Placebo-Controlled Study. Obstet Anesth Dig. 2013;33(1):31-2.
Marciniak A, Owczuk R, Wujtewicz M, Preis K, Majdyło K. The Influence of Intravenous Ondansetron on Maternal Blood Haemodynamics After Spinal Anesthesia for Caesarean Section: A Double-Blind, Placebo-Controlled Study. Ginekol Pol. 2015;86(6).
El Khouly NI, Meligy AM. Randomized Controlled Trial Comparing Ondansetron and Placebo for the Reduction of Spinal Anesthesia-Induced Hypotension During Elective Cesarean Delivery in Egypt. Int J Gynaecol Obstet. 2016;135(2):205-9.
Devkota K, Adhikari K, Pradhan B. Effect of Intravenous Ondansetron for Prevention of Spinal Anesthesia Induced Hypotension During Cesarean Section. J Coll Med Sci Nepal. 2021;17(4):289-97. doi:10.3126/jcmsn.v17i4.41651
Xiao F, Wei C, Chang X, Zhang Y, Xue L, Shen H, Kee WD, Chen X. A Prospective, Randomized, Double-Blinded Study of the Effect of Intravenous Ondansetron on the Effective Dose in 50% of Subjects of Prophylactic Phenylephrine Infusions for Preventing Spinal Anesthesia–Induced Hypotension During Cesarean Delivery. Anesth Analg. 2020;131(2):564-9. doi:10.1213/ANE.0000000000004534
Hou XM, Chen YJ, Lai L, Liu K, Shen QH. Ondansetron Reduces the Incidence of Hypotension After Spinal Anesthesia: A Systematic Review and Meta-Analysis. Pharmaceuticals. 2022;15(12):1588. doi:10.3390/ph15121588 PMCIDPMID:36559039
Gao L, Zheng G, Han J, Wang Y, Zheng J. Effects of Prophylactic Ondansetron on Spinal Anesthesia-Induced Hypotension: A Meta-Analysis. Int J Obstet Anesth. 2015;24(4):335-43. doi:10.1016/j.ijoa.2015.08.012
Ortiz-Gómez JR, Palacio-Abizanda FJ, Morillas-Ramirez F, Fornet-Ruiz I, Lorenzo-Jiménez A, Bermejo-Albares ML. The Effect of Intravenous Ondansetron on Maternal Haemodynamics During Elective Caesarean Delivery Under Spinal Anesthesia: A Double-Blind, Randomised, Placebo-Controlled Trial. Int J Obstet Anesth. 2014;23(2):138-43. doi:10.1016/j.ijoa.2014.01.005
Tatikonda CM, Rajappa GC, Rath P, Abbas M, Madhapura VS, Gopal NV. Effect of Intravenous Ondansetron on Spinal Anesthesia-Induced Hypotension and Bradycardia: A Randomized Controlled Double-Blinded Study. Anesth Essays Res. 2019;13(2):340-6.
Mendonça FT, Crepaldi Junior LC, Gersanti RC, de Araújo KC. Effect of Ondansetron on Spinal Anesthesia-Induced Hypotension in Non-Obstetric Surgeries: A Randomised, Double-Blind and Placebo-Controlled Trial. Braz J Anesthesiol. 2021;71:233-40. doi:10.1016/j.bjane.2020.12.028
Ali DC, Naveed M, Gordon A, Majeed F, Saeed M, Ogbuke MI, Atif M, Zubair HM, Changxing L. β-Adrenergic Receptor, an Essential Target in Cardiovascular Diseases. Heart Fail Rev. 2020;25:343-54. doi:10.1007/s10741-019-09825-x
Elvir-Lazo OL, White PF, Yumul R, Eng HC. Management Strategies for the Treatment and Prevention of Postoperative/Postdischarge Nausea and Vomiting: An Updated Review. F1000Research. 2020;9.
Malaki M. Ondansetron and Arrhythmia: An Adverse Effect, Medical Error, or Insufficient Guidelines. J Pharm Negative Results. 2020;11(1):75-6.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2024 Hafsa Nazir, Muhammad Abdul Rehman, Muhammad Arslan Zahid, Pervaiz Ali, Qurat Ul Ain Arshad, Nighat Begum
This work is licensed under a Creative Commons Attribution 4.0 International License.