Evidence map›Paper›PMID 35093254›Full record

ArticleJournal of pediatric surgery2022

Early investigations into improving bowel and bladder function in fetal ovine myelomeningocele repair.

Christina M Theodorou, Jordan E Jackson, Sarah C Stokes, Christopher D Pivetti, Priyadarsini Kumar, Zachary J Paxton, Karen E Matsukuma, Kaeli J Yamashiro, Lizette Reynaga, Alicia A Hyllen and 5 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of pediatric surgery, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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

15 authors at 2 institutions in 1 country.

Christina M TheodorouDepartment of Surgery, Division of Pediatric General, Thoracic, and Fetal Surgery. University of California Davis Medical Center. Sacramento, CA, United States. Electronic address: ctheodorou@ucdavis.edu.
Jordan E JacksonDepartment of Surgery, Division of Pediatric General, Thoracic, and Fetal Surgery. University of California Davis Medical Center. Sacramento, CA, United States.
Sarah C StokesDepartment of Surgery, Division of Pediatric General, Thoracic, and Fetal Surgery. University of California Davis Medical Center. Sacramento, CA, United States.
Christopher D PivettiSurgical Bioengineering Laboratory, University of California Davis Medical Center. Sacramento, CA, United States.
Priyadarsini KumarSurgical Bioengineering Laboratory, University of California Davis Medical Center. Sacramento, CA, United States.
Zachary J PaxtonSurgical Bioengineering Laboratory, University of California Davis Medical Center. Sacramento, CA, United States.
Karen E MatsukumaDepartment of Pathology and Laboratory Medicine, University of California Davis, Sacramento, CA, United States.
Kaeli J YamashiroDepartment of Surgery, Division of Pediatric General, Thoracic, and Fetal Surgery. University of California Davis Medical Center. Sacramento, CA, United States.
Lizette ReynagaSurgical Bioengineering Laboratory, University of California Davis Medical Center. Sacramento, CA, United States.
Alicia A HyllenSurgical Bioengineering Laboratory, University of California Davis Medical Center. Sacramento, CA, United States.
Arthur J de LorimierDepartment of Pediatrics, Division of Gastroenterology. University of California Davis Medical Center. Sacramento, CA, United States.
Maheen HassanDepartment of Pediatrics, Division of Gastroenterology. University of California Davis Medical Center. Sacramento, CA, United States.
Aijun WangSurgical Bioengineering Laboratory, University of California Davis Medical Center. Sacramento, CA, United States.
Diana L FarmerDepartment of Surgery, Division of Pediatric General, Thoracic, and Fetal Surgery. University of California Davis Medical Center. Sacramento, CA, United States.
Payam SaadaiDepartment of Surgery, Division of Pediatric General, Thoracic, and Fetal Surgery. University of California Davis Medical Center. Sacramento, CA, United States.
University of California Davis Medical Center · USUniversity of California, Davis · US

Funding

UC Davis Clinical and Translational Science CenterUL1TR001860 · NCATS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI KENYON, NICHOLAS J., LYLES, COURTNEY REES · 2016 to 2025
$47.3M
Engineered Neuroprotective Stem-Cell Exosomes for In Utero Spina Bifida TherapyR01NS115860 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI FARMER, DIANA LEE, WANG, AIJUN · 2020 to 2024
$2.5M
Fetal Tissue Engineering to Treat Spina Bifida Before BirthR01NS100761 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI WANG, AIJUN · 2017 to 2021
$1.7M
NCATS NIH HHS UL1 TR001860NINDS NIH HHS R01 NS100761NINDS NIH HHS R01 NS115860
6 · The paper itself

Abstract

introductionFetal myelomeningocele (MMC) repair improves lower extremity motor function. We have previously demonstrated that augmentation of fetal MMC repair with placental mesenchymal stromal cells (PMSCs) seeded on extracellular matrix (PMSC-ECM) further improves motor function in the ovine model. However, little progress has been made in improving bowel and bladder function, with many patients suffering from neurogenic bowel and bladder. We hypothesized that fetal MMC repair with PMSC-ECM would also improve bowel and bladder function.

methodsMMC defects were surgically created in twelve ovine fetuses at median gestational age (GA) 73 days, followed by defect repair at GA101 with PMSC-ECM. Fetuses were delivered at GA141. Primary bladder function outcomes were voiding posture and void volumes. Primary bowel function outcome was anorectal manometry findings including resting anal pressure and presence of rectoanal inhibitory reflex (RAIR). Secondary outcomes were anorectal and bladder detrusor muscle thickness. PMSC-ECM lambs were compared to normal lambs (n = 3).

resultsEighty percent of PMSC-ECM lambs displayed normal voiding posture compared to 100% of normal lambs (p = 1). Void volumes were similar (PMSC-ECM 6.1 ml/kg vs. normal 8.8 ml/kg, p = 0.4). Resting mean anal pressures were similar between cohorts (27.0 mmHg PMSC-ECM vs. normal 23.5 mmHg, p = 0.57). RAIR was present in 3/5 PMSC-ECM lambs that underwent anorectal manometry and all normal lambs (p = 0.46). Thicknesses of anal sphincter complex, rectal wall muscles, and bladder detrusor muscles were similar between cohorts.

conclusionOvine fetal MMC repair augmented with PMSC-ECM results in near-normal bowel and bladder function. Further work is needed to evaluate these outcomes in human patients.

Indexed as

MeningomyeloceleMesenchymal Stem CellsAnimalsFemaleFetusHumansPlacentaPregnancySheepSheep, DomesticUrinary BladderBladder functionBowel functionCellular therapyFetal surgeryMyelomeningoceleSpina bifida

Identifiers

PMID35093254
PMCPMC10372624
OpenAlexW4206820366

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.