Evidence map›Paper›PMID 32825852›Full record

ArticleTrials2020

Development of a Core outcome set for fetal Myelomeningocele (COSMiC): study protocol.

Samar Altoukhi, Clare L Whitehead, Greg Ryan, Jan Deprest, Luc Joyeux, Katie Gallagher, James Drake, Paige Church, Daphne Horn, Yenge Diambomba and 2 more

Open access · goldAbstract read
In one paragraph

Article in Trials, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 9% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
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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

12 authors at 5 institutions in 5 countries.

Samar AltoukhiDepartment of Obstetrics and Gynaecology, Mount Sinai Hospital and University of Toronto, 600 University Avenue, Toronto, Canada.
Clare L WhiteheadDepartment of Obstetrics and Gynaecology, Mount Sinai Hospital and University of Toronto, 600 University Avenue, Toronto, Canada.
Greg RyanDepartment of Obstetrics and Gynaecology, Mount Sinai Hospital and University of Toronto, 600 University Avenue, Toronto, Canada.
Jan DeprestDepartment of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium.ORCID https://orcid.org/0000-0002-4920-945X
Luc JoyeuxDepartment of Obstetrics and Gynaecology, University Hospitals Leuven, Leuven, Belgium.
Katie GallagherInstitute of Child Health, University College London, London, UK.
James DrakeOntario Fetal Centre, Mount Sinai Hospital, Toronto, Canada.
Paige ChurchDepartment of Neonatology, Holland-Bloorview, Sunnybrook Health Centre and University of Toronto, Toronto, Canada.
Daphne HornDepartment of Medical Informatics, Mount Sinai Hospital and University of Toronto, Toronto, Canada.
Yenge DiambombaOntario Fetal Centre, Mount Sinai Hospital, Toronto, Canada.
Jose C A CarvalhoOntario Fetal Centre, Mount Sinai Hospital, Toronto, Canada.
Tim Van MieghemDepartment of Obstetrics and Gynaecology, Mount Sinai Hospital and University of Toronto, 600 University Avenue, Toronto, Canada. tim.vanmieghem@sinaihealthsystem.ca.ORCID http://orcid.org/0000-0002-3034-6905
Mount Sinai Hospital · CAKU Leuven · BELondon Women's Clinic · GBSunnybrook Health Science Centre · CAUniversity College London · GB

Funding

Belgian FWO TBM T002618NEngineering and Physical Sciences Research Council EPSRC; NS/A000027/1Great Ormond Street Hospital Charity NANational Health and Medical Research Council 1142380University of Toronto Dept ObstetricsWellcome TrustWellcome Trust WT101957
6 · The paper itself

Abstract

backgroundOpen spina bifida (OSB) is one of the most common congenital central nervous system defects and leads to long-term physical and cognitive disabilities. Open fetal surgery for OSB improves neurological outcomes and reduces the need for ventriculoperitoneal shunting, compared to postnatal surgery, but is associated with a significant risk of prematurity and maternal morbidity. Fetoscopic surgery comes with less maternal morbidity, yet the question remains whether the procedure is neuroprotective and reduces prematurity. Comparison of outcomes between different treatment options is challenging due to inconsistent outcome reporting. We aim to develop and disseminate a core outcome set (COS) for fetal OSB, to ensure that outcomes relevant to all stakeholders are collected and reported in a standardised fashion in future studies.

methodsThe COS will be developed using a validated Delphi methodology. A systematic literature review will be performed to identify outcomes previously reported for prenatally diagnosed OSB. We will assess maternal (primary and subsequent pregnancies), fetal, neonatal and childhood outcomes until adolescence. In a second phase, we will conduct semi-structured interviews with stakeholders, to ensure representation of additional relevant outcomes that may not have been reported in the literature. We will include patients and parents, as well as health professionals involved in the care of these pregnancies and children (fetal medicine specialists, fetal surgeons, neonatologists/paediatricians and allied health). Subsequently, an international group of key stakeholders will rate the importance of the identified outcomes using three sequential online rounds of a modified Delphi Survey. Final agreement on outcomes to be included in the COS, their definition and measurement will be achieved through a face-to-face consensus meeting with all stakeholder groups. Dissemination of the final COS will be ensured through different media and relevant societies. DISCUSSION: Development and implementation of a COS for fetal OSB will ensure consistent outcome reporting in future clinical trials, systematic reviews and clinical practice guidelines. This will lead to higher quality research, better evidence-based clinical practice and ultimately improved maternal, fetal and long-term childhood outcomes.

trial registrationInternational Prospective Register of Systematic Reviews (PROSPERO) CRD42018104880 . Registered on December 5, 2018. Core Outcome Measures in Effectiveness Trials (COMET): 1187.

Indexed as

MeningomyeloceleOutcome Assessment, Health CareAdolescentChildConsensusDelphi TechniqueFemaleHumansInfant, NewbornPregnancyResearch DesignSpina Bifida CysticaSystematic Reviews as TopicTreatment OutcomeCore outcome setDelphi studyFetal surgeryFetoscopic surgeryMyelomeningoceleMyeloschisisOpen spina bifidaSpina bifida

Identifiers

PMID32825852
PMCPMC7441650
OpenAlexW3080751662

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.