Route of oxytocin administration for preventing blood loss at caesarean section: a systematic review with meta-analysis.

BMJ Open

Reproductive Health and Research, UNDP/UNFPA/UNICEF/WHO/World Bank Special Programme of Research, Development and Research Training in Human Reproduction (HRP), World Health Organization, Geneva, Switzerland.

Published: September 2021

AI Article Synopsis

  • * Three randomized controlled trials with 180 women compared intramyometrial (IMY) oxytocin to intravenous oxytocin; results showed negligible differences in various outcomes, though IMY oxytocin might reduce nausea/vomiting and slightly decrease blood loss.
  • * The study concluded that there is low to very low certainty evidence regarding the effectiveness of IMY versus intravenous oxytocin for blood loss prevention during caesarean sections, highlighting the need for more research, including potential intr

Article Abstract

Objectives: Assess the effects of different routes of prophylactic oxytocin administration for preventing blood loss at caesarean section (CS).

Design: Systematic review and meta-analysis.

Methods: Medline, EMBASE, CINAHL, Cochrane Library, BVS, SciELO and Global Index Medicus were searched through 24 May 2020 for randomised controlled trials (RCTs) comparing different routes of prophylactic oxytocin administration during CS. Study selection, data extraction and quality assessment were conducted by two investigators independently. We pooled results in fixed effects meta-analyses and calculated average risk ratio (RR), mean difference (MD) and 95% CI. We used GRADE to assess the overall quality of evidence for each outcome.

Results: Three trials (180 women) were included in the review. All studies compared intramyometrial (IMY) versus intravenous oxytocin in women having prelabour CS. IMY compared with intravenous oxytocin administration may result in little or no difference in the incidence of postpartum haemorrhage (RR 0.14, 95% CI 0.01 to 2.70; N=100 participants; 1 RCT), hypotension (RR 1.00, 95% CI 0.29 to 3.45; N=40; 1 RCT), headache (RR 3.00, 95% CI 0.13 to 69.52; N=40; 1 RCT) or facial flushing (RR 0.50, 95% CI 0.05 to 5.08; N=40; 1 RCT); IMY oxytocin may reduce nausea/vomiting (RR 0.13, 95% CI 0.02 to 0.69; N=140; 2 RCTs). We are very uncertain about the effect IMY versus intravenous oxytocin on the need for additional uterotonics (RR 0.82; 95% CI 0.25 to 2.69; N=140; 2 RCTs). IMY oxytocin may reduce blood loss slightly (MD -57.40 mL, 95% CI -101.71 to -13.09; N=40; 1 RCT).

Conclusions: There is limited, low to very low certainty evidence on the effects of IMY versus intravenous oxytocin at CS for preventing blood loss. The evidence is insufficient to support choosing one route over another. More trials, including studies that assess intramuscular oxytocin administration, are needed on this relevant question.

Prospero Registration Number: CRD42020186797.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449971PMC
http://dx.doi.org/10.1136/bmjopen-2021-051793DOI Listing

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