Intravenous versus intramuscular oxytocin injection for preventing uterine atonic primary postpartum haemorrhage in third stage of labour: A double-blind randomised controlled trial

Author:

Okaforcha Emmanuel Ikechukwu1,Eleje George Uchenna12ORCID,Ikechebelu Joseph Ifeanyichukwu12ORCID,Ezeama Chukwuemeka Okwudili12,Igbodike Emeka Philip3ORCID,Ugwu Emmanuel Onyebuchi4ORCID,Okpala Boniface Chukwuneme12ORCID,Mbachu Ikechukwu Innocent12,Umeononihu Osita Samuel12,Ogabido Chukwudi Anthony12,Onwusulu Daniel Nnaemeka12,Oguejiofor Charlotte Blanche12,Okafor Chidinma Charity5,Olisa Chinedu Lawrence1,Ikwuka David Chibuike6,Ofor Ifeanyichukwu Jude7,Okafor Chigozie Geoffrey1ORCID

Affiliation:

1. Department of Obstetrics and Gynaecology, Nnamdi Azikiwe University Teaching Hospital, Nnewi, Nigeria

2. Department of Obstetrics and Gynaecology, Nnamdi Azikiwe University, Awka, Nigeria

3. Department of Obstetrics and Gynaecology, Havana Hospital, Lagos, Nigeria

4. Department of Obstetrics and Gynaecology, University of Nigeria Teaching Hospital, Ituku-Ozalla, Nigeria

5. Department of Psychiatry, Leicestershire Partnership NHS Trust, Leicester, UK

6. Department of Medical Physiology, College of Medicine and Health Sciences, University of Rwanda, Huye, Rwanda

7. Department of Obstetrics and Gynaecology, ESUT College of Medicine, Parklane, Nigeria

Abstract

Objectives: To compare the efficacy and safety of intravenous and intramuscular oxytocin in preventing atonic primary postpartum haemorrhage in the third stage of labour. Methods: A double-blind randomised clinical study on consenting women without risk factors for primary postpartum haemorrhage in labour at term. Two hundred and thirty-two women were randomly allotted into intravenous ( n = 115) and intramuscular ( n = 117) oxytocin groups in the active management of the third stage of labour. All participants received 10 IU of oxytocin, either IV or IM, and 1 ml of water for injection as a placebo via a route alternate to that of administration of oxytocin within 1 min of the baby’s delivery. The primary outcome measures were mean postpartum blood loss and haematocrit change. Trial Registration No.: PACTR201902721929705. Results: The baseline socio-demographic and clinical characteristics were similar between the two groups ( p > 0.05). There was no statistically significant difference between the two groups with regards to the mean postpartum blood loss (254.17 ± 34.85 ml versus 249.4 ± 39.88 ml; p = 0.210), haematocrit change (2.4 (0.8%) versus 2.1 (0.6%); p = 0.412) or adverse effects ( p > 0.05). However, the use of additional uterotonics was significantly higher in the intravenous group (25 (21.73%) versus 17 (14.53%); p = 0.032). Conclusion: Although oxytocin in both study groups showed similar efficacy in terms of preventing atonic primary postpartum haemorrhage, participants who received intravenous oxytocin were more likely to require additional uterotonics to reduce their likelihood of having an atonic primary postpartum haemorrhage. However, both routes have similar side effect profiles.

Funder

borne by the researcher

Publisher

SAGE Publications

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