What is the recommended dosing regimen of Epidosin (valethamate bromide) for a woman in active first‑stage labour who has no severe hepatic or renal disease, no hypersensitivity to anticholinergic agents, and no evidence of uterine rupture or fetal distress?

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Epidosin (Valethamate Bromide) Dosing for Labour

Epidosin (valethamate bromide) should be administered at 8 mg intramuscularly when cervical dilatation reaches 3–4 cm in active first‑stage labour, repeated every hour for a maximum of three doses (total 24 mg). 1, 2

Standard Dosing Protocol

  • Initial dose: 8 mg intramuscularly at 3–4 cm cervical dilatation 1, 2
  • Repeat dosing: 8 mg every hour 1, 2
  • Maximum doses: Three injections (total 24 mg over 2–3 hours) 1, 2
  • Timing: Begin administration only after establishing active labour with regular contractions and cervical dilatation of at least 3–4 cm 1, 2

Expected Clinical Effects

  • Cervical dilatation rate: Increases to approximately 1.86–2.4 cm/hour (compared to 1.0–1.9 cm/hour without medication) 1, 2
  • Duration of first stage: Reduces by approximately 60–90 minutes compared to no intervention 1, 3, 4
  • Injection‑to‑delivery interval: Approximately 206–221 minutes (3.4–3.7 hours) 1, 2
  • Normal vertex delivery rate: Not significantly affected by valethamate administration 3, 4

Common Side Effects to Monitor

Maternal effects that occur transiently with valethamate include: 1, 2

  • Maternal tachycardia (most common)
  • Fetal tachycardia
  • Facial flushing
  • Dry mouth

These side effects are more frequent with valethamate than with alternative antispasmodics like drotaverine, though no serious maternal or neonatal adverse events have been reported in clinical trials. 1, 2, 3

Important Clinical Caveats

Do not administer if:

  • Cervical dilatation is less than 3 cm (not yet in active labour) 1, 2
  • Evidence of fetal distress is present 3
  • Uterine rupture or dehiscence is suspected 3
  • Known hypersensitivity to anticholinergic agents exists 3

Monitoring requirements:

  • Assess maternal heart rate before each dose and 15–30 minutes after administration 1, 2
  • Monitor fetal heart rate continuously during labour 3
  • Document cervical dilatation progress hourly 1, 2

Comparative Efficacy Context

While valethamate bromide is effective for labour augmentation, evidence from head‑to‑head trials demonstrates that drotaverine hydrochloride produces faster cervical dilatation (3.0 cm/hour versus 2.4 cm/hour) and shorter injection‑to‑delivery intervals (183 minutes versus 207 minutes) with fewer side effects. 1, 2 However, valethamate remains a reasonable option when drotaverine is unavailable, as it still significantly reduces first‑stage labour duration compared to no intervention (reduction of 65–74 minutes). 3, 4

The overall quality of evidence supporting antispasmodics in labour is low to moderate, with significant heterogeneity across studies and inconsistent reporting of maternal and neonatal safety outcomes. 3, 4 Nevertheless, the consistent finding across multiple trials is that valethamate accelerates cervical dilatation without increasing operative delivery rates. 3, 4

References

Research

Drotaverine hydrochloride vs. valethamate bromide in acceleration of labor.

International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics, 2001

Research

Antispasmodics for labour.

The Cochrane database of systematic reviews, 2013

Research

Antispasmodics for labour.

The Cochrane database of systematic reviews, 2012

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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