Journal of Midwifery and Reproductive Health

Journal of Midwifery and Reproductive Health

The impact of Low- versus High-Dose Oxytocin Infusion on Maternal Hematologic and Hemodynamic Parameters after Vaginal Delivery: A Randomized Triple-Blind Clinical Trial

Document Type : Original Research Article

Authors
1 BSc Community Midwife, Royal London Hospital, Barts Health NHS Trust, London, United Kingdom
2 Assistant Professor, Department of Epidemiology and Biostatistics, Neyshabur University of Medical Sciences, Neyshabur, Iran
3 Medical Student, Students Research Committee, Neyshabur University of Medical Sciences, Neyshabur, Iran
4 Assistant Professor, Fellowship of Maternal-Fetal Medicine, Neyshabur University of Medical Sciences, Neyshabur, Iran
5 Assistant Professor, Department of Midwifery, School of Nursing and Midwifery, Neyshabur University of Medical Sciences, Neyshabur, Iran
Abstract
Background & aim: Postpartum hemorrhage is a major cause of maternal mortality. Although oxytocin is routinely used for prevention, optimal dose balancing uterine efficacy and maternal hemodynamic stability remains uncertain. This trial compared the impact of low-dose versus high-dose oxytocin infusion on maternal hematologic and hemodynamic parameters after vaginal delivery.Methods: This randomized, triple-blind clinical trial was conducted on 60 primiparous women undergoing vaginal delivery at a teaching hospital affiliated with Neyshabur University of Medical Sciences, Neyshabour, Iran in 2024. Participants were randomly allocated 1:1 to low-dose (10 IU) or high-dose (60 IU) oxytocin infusion immediately after delivery. Hemoglobin and hematocrit were measured at admission and six hours postpartum. Blood pressure and heart rate were monitored for two hours postpartum. Data were analyzed using linear mixed-effects models.
Results: Participants had a median age of 21 years (interquartile range, 19.25–25.50 years), with similar baseline characteristics between groups. Maternal heart rate and body temperature showed no significant differences in two groups (P > 0.05). Although transient changes in systolic and diastolic blood pressure occurred at 15 minutes postpartum, mixed-effects analysis showed no dose-dependent effects (P > 0.05). Hemoglobin and hematocrit decreased significantly from admission to six hours postpartum in both groups (p < 0.001), with no significant between-group differences.
Conclusion: Low- and high-dose oxytocin infusion resulted in comparable maternal hemodynamic and hematologic outcomes during the early postpartum period. These findings support using the lowest effective dose to maintain uterine contraction while minimizing potential adverse effects.
Keywords
Subjects

1.     World Health Organization. Lifesaving solution dramatically reduces severe bleeding after childbirth. Geneva: World Health Organization; 2023 May 9. Available from: https:// www.who.int/  news/item/09-05-2023-lifesaving-solution- dramatically-reduces-severe-bleeding-after-childbirth  (accessed 1 September 2026).
2.     World Health Organization. WHO recommendations for the prevention and treatment of postpartum haemorrhage. Geneva: World Health Organization; 2012.
3.     Collaboration M-U, Knight M, Bunch K, Felker A, Patel R, Shakespeare J, et al. Saving Lives, Improving Mothers’ Care Core Report - Lessons learned to inform maternity care from the UK and Ireland Confidential Enquiries into Maternal Deaths and Morbidity 2019-21: National Perinatal Epidemiology Unit: University of Oxford; 2023.
4.     Yunas I, Islam MA, Price MJ, Melo P, Aswat A, Alam SS, et al. Prevalence of postpartum haemorrhage: a systematic review and meta-analysis. The Lancet Obstetrics, Gynaecology & Women’s Health. 2026; 2(2): e129-e139.
5.     World Health Organization. Global health agencies issue new recommendations to help end deaths from postpartum haemorrhage. Geneva: World Health Organization; 2025 Oct 5. Available from: https:// www.who.int/ news/ item/05-10-2025-global-health-agencies-issue-new-recommendations-to-help -end-deaths-from-postpartum-haemorrhage (accessed 1 September 2026).
6.     Weeks A. The prevention and treatment of postpartum haemorrhage: what do we know, and where do we go to next. An International Journal of Obstetrics & Gynaecology. 2015; 122(2): 202–210.
7.     World Health Organization. WHO recommendations: uterotonics for the prevention of postpartum haemorrhage. Geneva: World Health Organization; 2018.
8.     Escobar MF, Nassar AH, Theron G, Barnea ER, Nicholson W, Ramasauskaite D, et al. FIGO recommendations on the management of postpartum hemorrhage 2022. International Journal of Gynecology & Obstetrics. 2022; 157(S1): 3–50.
9.     Westhoff G, Cotter AM, Tolosa JE. Prophylactic oxytocin for the third stage of labour to prevent postpartum haemorrhage. Cochrane Database of Systematic Reviews. 2013; (10): Cd001808.
10.  Arrowsmith S, Wray S. Oxytocin: its mechanism of action and receptor signalling in the myometrium. Journal of Neuroendocrinology. 2014; 26(6): 356–369.
11.  Balki M, Tsen L. Oxytocin protocols for cesarean delivery. International Anesthesiology Clinics. 2014; 52(2): 48-66.
12.  Thomas JS, Koh SH, Cooper GM. Haemodynamic effects of oxytocin given as i.v. bolus or infusion on women undergoing Caesarean section. British Journal of Anaesthesia. 2007; 98(1): 116–119.
13.  Tita AT, Szychowski JM, Rouse DJ, Bean CM, Chapman V, Nothern A, et al. Higher-dose oxytocin and hemorrhage after vaginal delivery: a randomized controlled trial. Obstetrics and Gynecology. 2012; 119(2Pt 1): 293–300.
14.  Duffield A, McKenzie C, Carvalho B, Ramachandran B, Yin V, El-Sayed YY, et al. Effect of a High-Rate Versus a Low-Rate Oxytocin Infusion for Maintaining Uterine Contractility During Elective Cesarean Delivery: A Prospective Randomized Clinical Trial. Anesthesia and Analgesia. 2017; 124(3): 857–862.
15.  Shea AE, Woolfolk CL, Cahill AG, Tuuli MG, Tita AT, Srinivas SK, Caughey AB, Macones GA, Subramaniam A. Association of postpartum oxytocin dose and postpartum bleeding outcomes in nulliparous patients at term. American Journal of Obstetrics and Gynecology. 2025; 233(2): 118.e1-118.e11.
16.  Dashe JS, Bloom SL, Spong CY, Hoffman BL. Williams Obstetrics. 25th ed. New York: McGraw-Hill Education; 2018.
17.  Ministry of Health and Medical Education. National Guidelines for Midwifery and Childbirth Services. 4th ed. Tehran: Ministry of Health and Medical Education; 2024.
18.  Hébert V, D'Souza R, Santesso N, Zeraatkar D, Oltean I, Furnivall M, et al. Prophylactic oxytocin dose following vaginal birth to prevent postpartum hemorrhage: a systematic review and dose-response meta-analysis. American Journal of Obstetrics & Gynecology. 2026; 234(2): 350-389
19.   Mojibian M, Salehi E, Enjezab B, Tabatabaie A. Comparing the effectiveness of two methods of oxytocin infusion in preventing atonic uterus. Journal of Reproduction & Infertility. 2005; 6(3): 240-247.
20.   Bhattacharya S, Ghosh S, Ray D, Mallik S, Laha A. Oxytocin administration during cesarean delivery: Randomized controlled trial to compare intravenous bolus with intravenous infusion regimen. Journal of Anaesthesiology Clinical Pharmacology. 2013; 29(1): 32-35.
21.  Mohta M, Chowdhury RB, Tyagi A, Agarwal R. Efficacy of different infusion rates of oxytocin for maintaining uterine tone during elective caesarean section: A randomised double blind trial. Anaesthesia and Intensive Care. 2021; 49(3): 183–189.
22.  Mohta M, Siddiqui S, Chilkoti GT, Agarwal R. Oxytocin infusion rates for maintaining uterine tone during non-elective cesarean section in laboring patients: a randomized, controlled trial. Journal of Anesthesia. 2022; 36(4): 456–463.
23   Frölich MA, Esame A, Warren Iii WM, Owen J. High-dose oxytocin is not associated with maternal temperature elevation: a retrospective cohort study of mid-trimester pregnancy with intrauterine fetal demise. International Journal of Obstetric Anesthesia. 2011; 20(1): 30–33.