Hourly Low-Dose Oral Misoprostol Solution for Induction of Labour at Term: A Prospective Observational Study from a Pakistan

Authors

  • Saba Nadeem Author
  • Iqra Aslam Author
  • Sumreen Akram Author
  • Salma Jabeen Author
  • Irum Manzoor Author

DOI:

https://doi.org/10.51985/JBUMDC2025794

Keywords:

Cesarean Section, Labor, Induced, Misoprostol, Pakistan, Pregnancy, Term

Abstract

 Objectives: To evaluate the effectiveness and short-term safety of an hourly 20 µg oral misoprostol solution protocol for
induction of labour (IOL) in primigravid term pregnancies at a Pakistani tertiary center.
Study design and setting: Prospective observational study conducted in the Department of Gynecology & Obstetrics,
Sadiq Abbassi Hospital / Quaid-e-Azam Medical College, Bahawalpur, from 21-Nov-2024 to 21-May-2025.
Methodology: Primigravida with singleton, cephalic, 37–42-week gestations, Bishop score >5, and reactive CTG were
enrolled; women with prior uterine surgery or other contraindications to vaginal birth were excluded. Misoprostol 200 µg
was dissolved in 200 mL of water; 20 mL (20 µg) was given orally every hour until adequate uterine activity or a maximum
of 10 doses. Oxytocin was started if contractions became inadequate after active labour onset.
Results: One hundred women were included (mean age 27.20 ± 3.62 y; mean gestation 38.65 ± 1.51 weeks; mean estimated
fetal weight 2511.05 ± 265.42 g). Mean pre-induction Bishop score 6.32 ± 0.98 improved to 7.43 ± 1.65 at 6 h. The mean
induction-to-delivery interval was 12.43 ± 3.21 h; the mean misoprostol doses were 5.52 ± 1.62. Vaginal birth within 24
h occurred in 79/100 (79%; 95% CI 71–87). Oxytocin augmentation was required in 28% and meconium-stained liquor
occurred in 18%.
Conclusion: Hourly 20 µg oral misoprostol solution achieved high 24-h vaginal-delivery rates with generally reassuring
short-term outcomes within recorded parameters in primigravid women at term in this tertiary-care Pakistani cohort. Larger
comparative studies are warranted 

References

1. Middleton P, Shepherd E, Morris J, Crowther CA, Gomersall

JC. Induction of labour at or beyond 37 weeks’ gestation.

Cochrane Database Syst Rev. 2020;7:CD004945. doi:10.1002/

14651858.CD004945.pub5

2. Banner H, D’Souza R. Towards an evidence-based approach

to optimize the success of labour induction. Best Pract Res

Clin Obstet Gynaecol. 2021;77:129–143. doi:10.1016/j.

bpobgyn.2021.08.006

3. Coates D, Makris A, Catling C, Henry A, Scarf V, Watts N,

et al. Clinical indications for induction of labour: a systematic

scoping review. PLoS One. 2020;15(1):e0228196.

doi:10.1371/journal.pone.0228196

4. Kumar N, Haas DM, Weeks AD. Misoprostol for labour

induction. Best Pract Res Clin Obstet Gynaecol. 2021;77:

53–63. doi:10.1016/j.bpobgyn.2021.09.003

5. ten Eikelder ML, Oude Rengerink K, Jozwiak M, de Leeuw

JW, de Graaf IM, van Pampus MG, et al. Induction of labour

at term with oral misoprostol versus a Foley catheter

(PROBAAT-II): multicentre randomised controlled noninferiority trial. Lancet. 2016;387(10028):1619–1628.

doi:10.1016/S0140-6736(16)00084-2

6. World Health Organization. WHO recommendations on

induction of labour at or beyond term. Geneva: World Health

Organization; 2022.

7. American College of Obstetricians and Gynecologists. Cervical

ripening in pregnancy: ACOG Clinical Practice Guideline

No. 9. Obstet Gynecol. 2025;146(1):148–160. doi:10.1097/

AOG.0000000000005951

8. International Federation of Gynecology and Obstetrics.

Misoprostol-only dosing chart: recommended regimens.

London: FIGO; 2023.

9. Deshmukh VL, Rajamanya AV, Yelikar KA. Oral misoprostol

solution for induction of labour. J Obstet Gynaecol India.

2017;67(2):98–103. doi:10.1007/s13224-016-0937-4

10. Rahimi M, Haghighi L, Baradaran HR, Azami M, Larijani

SS, Kazemzadeh P, et al. Oral versus vaginal misoprostol for

labour induction: updated systematic review and meta-analysis

of interventional studies. Eur J Med Res. 2023;28:51.

doi:10.1186/s40001-023-01007-8

11. Aduloju OP, Ipinnimo OM, Aduloju T. Oral misoprostol for

induction of labor at term: a randomized controlled trial of

hourly titrated and 2-hourly static oral misoprostol solution.

J Matern Fetal Neonatal Med. 2021;34(4):493–499.

doi:10.1080/14767058.2019.1610378

12. Kerr RS, Kumar N, Williams MJ, Cuthbert A, Aflaifel N,

Haas DM, et al. Low-dose oral misoprostol for induction of

labour. Cochrane Database Syst Rev. 2021;6:CD014484.

doi:10.1002/14651858.CD014484

13. Young DC, Delaney T, Armson BA, Fanning C. Oral

misoprostol, low-dose vaginal misoprostol, and vaginal

dinoprostone for labour induction: randomized controlled

trial. PLoS One. 2020;15(1):e0227245. doi:10.1371/journal.

pone.0227245

14. Khairnar PV, Khairnar VS, Chavan RB, Bobade PS. Efficacy

of oral and vaginal misoprostol for pre-induction cervical

ripening in term primigravida undergoing induction of labor:

a prospective study. Int J Reprod Contracept Obstet Gynecol.

2024;13(9):2436–2441. doi:10.18203/2320-1770.ijrcog

20242496

15. Antil S, Gupta U. Titrated low-dose oral misoprostol solution

in induction of labour. Int J Reprod Contracept Obstet Gynecol.

2016;5(3):775–782.

16. Asokan KM, Santhosh S. Titrated oral misoprostol solution

versus oxytocin for induction of labour: a comparative study

at Kannur Medical College. Int J Sci Study. 2016;3:255–258.

17. Pambet M, Delabaere A, Figuier C, Lambert C, Comptour A,

Rouzaire M, et al. Factors of non-compliance with a protocol

for oral administration of misoprostol (Angusta®) 25

micrograms to induce labor: an observational study. J Clin

Med. 2023;12(4):1521. doi:10.3390/jcm12041521

18. Yenuberi H, Abraham A, Sebastian A, Benjamin SJ, Jeyaseelan

V, Mathews JE. Stepwise oral misoprostol vs vaginal

misoprostol for induction of labour: randomized double-blind

placebo-controlled trial. Trop Doct. 2016;46(4):198–205.

doi:10.1177/0049475515624856

19. Aalami-Harandi R, Karamali M, Moeini A. Induction of

labour with titrated oral misoprostol solution versus oxytocin

in term pregnancy: randomized controlled trial. Rev Bras

Ginecol Obstet. 2013;35(2):60–65. doi:10.1590/S0100-

72032013000200004

20. Bendix JM, Friis Petersen J, Andersen BR, Bødker B,

Løkkegaard EC. High- vs low-dosage oral misoprostol for

induction of labour: Danish descriptive retrospective cohort

2015–16. Acta Obstet Gynecol Scand. 2020;99(2):222–230.

doi:10.1111/aogs.13739

21. Wasim AU, Khan MM, Aneela F, Khan H, Solís MDD, Shabir

I, et al. A comparative study of the efficacy and safety of oral

misoprostol, intravenous oxytocin, and intravaginal

dinoprostone for labor induction in Pakistani women. Cureus.

2023;15(5):e39768. doi:10.7759/cureus.39768

22. Das T, Thapa M. Induction of labour with oral misoprostol

vs oxytocin: comparative study. J South Asian Feder Obstet

Gynaecol. 2023;31(6):710–713. doi:10.5005/jp-journals-

10006-2147

23. Antonazzo P, Laoreti A, Personeni C, Grossi E, Martinelli A,

Cetin I. Vaginal dinoprostone vs intravenous oxytocin for

labour induction in women not responsive to first-dose

dinoprostone: randomized prospective study. Reprod Sci.

2016;23(6):779–784. doi:10.1177/1933719115618272

24. Bolnga JW, Morris M, Aipit J, Laman M. Trends in maternal

and perinatal mortality in a provincial hospital in Papua New

Guinea: six-year review. PNG Med J. 2016;59(1–2):34–37.

25. Iser R, Verave O, Bolnga JW, Hamura N. Decision-to-incision

time for emergency caesarean section: prospective

observational study from a regional referral hospital in Papua

New Guinea. BJOG. 2015;122(Suppl 2):107.

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Published

2026-01-14

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