Evidence map›Paper›PMID 12920470›Full record

Trial reportSao Paulo medical journal = Revista paulista de medicina2003

Misoprostol versus oxytocin for labor induction in term and post-term pregnancy: randomized controlled trial.

Márcia Maria Auxiliadora de Aquino, José Guilherme Cecatti

Open access · diamondAbstract readClinical TrialComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Sao Paulo medical journal = Revista paulista de medicina, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 5 pooled it
4.2field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 5 syntheses or guidelines pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Induction of labour at or beyond 37 weeks' gestation.The Cochrane database of systematic reviews · 2020
    Pooled it
  3. Pooled it
  4. Pooled it
  5. Vaginal misoprostol for cervical ripening and induction of labour.The Cochrane database of systematic reviews · 2010
    Pooled it
  6. Trial
  7. Trial
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Márcia Maria Auxiliadora de AquinoMaternity Hospital Leonor Mendes de Barros, São Paulo, Brazil. mmaa@visualbyte.com.br
José Guilherme Cecatti
Universidade Estadual de Campinas (UNICAMP) · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextMisoprostol, a synthetic E1 methyl analog prostaglandin, is at present receiving attention as a cervical modifier and labor induction agent. However, there is still a need for better determination of its safety and effectiveness.

objectiveTo compare intravaginal misoprostol versus intravenous oxytocin for cervical ripening and labor induction in pregnant women with unripe cervices.

designRandomized controlled trial.

settingThe study was performed at the Leonor Mendes de Barros Maternity Hospital between November 1998 and December 2000.

participants210 pregnant women with intact membranes and indication for labor induction were selected. PROCEDURES: The women randomly received 25 g of vaginal misoprostol every 4 hours, not exceeding 8 doses (105 women), or oxytocin in a continuous infusion (105 women). MAIN MEASUREMENTS: The main parameters measured were: latent period, time from induction to vaginal delivery, delivery route, occurrence of vaginal delivery with time, occurrence of uterine tonus alterations, hypoxia and neonatal morbidity. To verify the statistical significance of the differences between the groups, the chi-squared, Student t and log-rank tests were used.

resultsThere were no significant differences between the groups concerning conditions for labor induction, age, parity, race, marital status, family income, initial Bishop Index and number of prenatal visits. The cesarean section rate, latent period and period from induction to vaginal delivery were significantly lower for the misoprostol group. With regard to uterine tonus alterations, tachysystole was significantly more common in the misoprostol group. However, there was no difference in hypoxia and neonatal morbidity between the groups.

conclusion25 g of misoprostol used vaginally every 4 hours is safer and more efficient for cervical ripening and labor induction than oxytocin.

Indexed as

Labor, InducedAbortifacient Agents, NonsteroidalAdultCervical RipeningFemaleHumansMisoprostolOxytocinPregnancyPregnancy, ProlongedReaction TimeTreatment OutcomeAbortifacient Agents, NonsteroidalMisoprostolOxytocin

Identifiers

PMID12920470
PMCPMC11108614
OpenAlexW2137878247

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.