Evidence map›Paper›PMID 41031976›Full record

ArticleThe journal of obstetrics and gynaecology research2025

The initial report of prospective study for maternal and fetal outcomes to investigate the safety of multifetal pregnancy reduction in Japan.

Nao Wakui, Masayuki Endo, Ayaka Shima, Aiko Okada, Tatsuya Miyake, Shoko Sugao, Kazuya Mimura, Tadashi Kimura, Michiko Kodama

Abstract read
In one paragraph

Article in The journal of obstetrics and gynaecology research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

9 authors.

Nao WakuiObstetrics and Gynecology, Graduate School of Medicine, The University of Osaka, Suita, Japan.
Masayuki EndoObstetrics and Gynecology, Graduate School of Medicine, The University of Osaka, Suita, Japan.
Ayaka ShimaClinical Psychology, Graduate School of Human Sciences, The University of Osaka, Suita, Osaka, Japan.
Aiko OkadaObstetrics and Gynecology, Graduate School of Medicine, The University of Osaka, Suita, Japan.ORCID https://orcid.org/0000-0001-7030-8332
Tatsuya MiyakeObstetrics and Gynecology, Graduate School of Medicine, The University of Osaka, Suita, Japan.
Shoko SugaoClinical Psychology, Graduate School of Human Sciences, The University of Osaka, Suita, Osaka, Japan.
Kazuya MimuraObstetrics and Gynecology, Graduate School of Medicine, The University of Osaka, Suita, Japan.
Tadashi KimuraChildren's and Women's Health, Division of Health Science, Graduate School of Medicine, The University of Osaka, Suita, Osaka, Japan.
Michiko KodamaObstetrics and Gynecology, Graduate School of Medicine, The University of Osaka, Suita, Japan.ORCID https://orcid.org/0000-0003-4046-7572

Funding

Obstetrics and Gynecology, Graduate School of Medicine, Osaka University
6 · The paper itself

Abstract

aimThis study aimed to establish the safety of multifetal pregnancy reduction (MFPR) and examine its complications, patient background, and psychological impact.

methodsThis single-center, single-arm, prospective intervention study included 10 women who were treated at our institution between April and December 2024. The indications were triplet or higher-order multiple pregnancies, as well as twin pregnancies with serious maternal complications. Procedures were performed between 11 and 13 gestational weeks, and the patients were observed for up to 1 week postoperatively. The primary outcome was the completion ratio at hospital discharge, whereas the secondary outcomes were the survival rate of non-targeted fetuses, the number of adverse events, and the psychological evaluation of the patients at 1 week postoperatively.

resultsAmong the 10 patients, one carried twins, seven carried triplets, and two carried quadruplets; half had received ovulation-induction treatment. The procedure completion rate at discharge was 100%, although one patient required reoperation. The survival rate of non-targeted fetuses was 89.5% (17/19), and adverse events included vaginal bleeding and complete miscarriage. Maternal state-anxiety scores decreased significantly postprocedure, whereas depression scores remained elevated both before and after the procedure.

conclusionsThe completion rate of MFPR using echo-guided transabdominal potassium chloride infusion was high, ensuring short-term maternal safety. Although no serious adverse event other than one case of total miscarriage was observed, a long-term safety evaluation is warranted. Moreover, the emotional burden on patients is high before and after the procedure, necessitating the importance of long-term support.

Indexed as

Pregnancy, MultiplePregnancy Reduction, MultifetalAdultFemaleHumansJapanPregnancyPregnancy OutcomeProspective Studiesmultiple pregnancypatient safetypregnancy reductionprospective studypsychological safety

Identifiers

PMID41031976
PMCPMC12487742

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Registered trials

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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.