Evidence map›Paper›PMID 41510449›Full record

ArticleCureus2025

Pregnancy and Delivery in a Woman With Achondroplasia: A Multidisciplinary Management Approach.

Falak Baloch, Liliana Grosu

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Falak BalochDepartment of Obstetrics and Gynaecology, Bedfordshire Hospitals NHS Foundation Trust, Bedford, GBR.
Liliana GrosuDepartment of Obstetrics and Gynaecology, Bedfordshire Hospitals NHS Foundation Trust, Bedford, GBR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Achondroplasia is the most common skeletal dysplasia, characterised by disproportionate short stature and associated with obstetric and anaesthetic challenges, with limited evidence on optimal pregnancy management. We report a 39-year-old Gravida 3 Para 2 woman with achondroplasia and two previous caesarean sections who received consultant-led, multidisciplinary antenatal care involving obstetrics, anesthesiology, cardiology, and neonatology teams. Her pregnancy was complicated by short stature, prior caesarean deliveries, and previous children affected by achondroplasia. She underwent an elective lower segment caesarean section and bilateral tubal ligation at 37 weeks under combined spinal-epidural anesthesia, delivering a live female infant weighing 2,760 grams (94.6th centile) with Apgar scores of 9 and 10. Postoperative maternal and neonatal recovery was uneventful, and the neonate showed no clinical, radiological, or genetic evidence of achondroplasia. A tailored multidisciplinary approach, early anesthetic assessment, careful delivery planning, prenatal counseling, and risk evaluation, including discussion of invasive prenatal testing, were crucial to minimize maternal and neonatal complications. Maternal postoperative care included monitoring for hypertensive episodes and adjustment of obstetric hemorrhage thresholds due to body habitus. This case highlights that pregnancy in women with achondroplasia requires individualized, multidisciplinary care to optimize maternal and neonatal outcomes, with early consultation, detailed anomaly scanning, anesthetic planning, and comprehensive risk assessment being key to successful management.

Indexed as

achondroplasiaachondroplasticcombined spinal epiduraldwarfismpregnancy

Identifiers

PMID41510449
PMCPMC12778887

What OpenQuestion holds

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LicenceCC BY
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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.