Evidence map›Paper›PMID 41545048›Full record

ArticleBMJ open2026

Protocol for the development of a global core outcome set for the surgical treatment of sacrococcygeal teratoma in children: a systematic review and international Delphi study.

Malou Cécile Dongen, Rick van Rijn, Shilpa Sharma, Martine F Raphael, Ralph de Vries, Amr A Abouzeid, Marianna Bugiani, Lohfa B Chirdan, Ernest L W van Heurn, Joep P M Derikx and 2 more

Abstract read
In one paragraph

Article in BMJ open, 2026. 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

12 authors.

Malou Cécile DongenDepartment of Paediatric Surgery, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands m.c.dongen@amsterdamumc.nl.ORCID http://orcid.org/0009-0000-5529-5414
Rick van RijnDepartment of Radiology and Nuclear Medicine, Amsterdam UMC, Amsterdam, The Netherlands.
Shilpa SharmaDepartment of Paediatric Surgery, All India Institute of Medical Sciences New Delhi, New Delhi, DL, India.
Martine F RaphaelDepartment of Paediatric Oncology, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Ralph de VriesMedical Library, Vrije Universiteit, Amsterdam, The Netherlands.ORCID http://orcid.org/0000-0002-2075-7495
Amr A AbouzeidDepartment of Paediatric Surgery, Ain Shams University, Cairo, Egypt.
Marianna BugianiDepartment of Pathology, Amsterdam UMC, Amsterdam, The Netherlands.
Lohfa B ChirdanDepartment of Surgery, Paediatric Surgery Unit, Jos University Teaching Hospital, Jos, Plateau, Nigeria.
Ernest L W van HeurnDepartment of Paediatric Surgery, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Joep P M DerikxDepartment of Paediatric Surgery, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Marijke E B KremerDepartment of Paediatric Surgery, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Sct-Cos Steering GroupDepartment of Paediatric Surgery, Emma Children's Hospital, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionOutcome reporting in studies on sacrococcygeal teratoma (SCT) is highly heterogeneous, which limits comparability across studies and thus hampers the development of international treatment guidelines.Variation in treatment and access to facilities contributes to differences in outcome reporting between centres and countries. Establishing a Core Outcome Set (COS) can improve consistency in outcome reporting and facilitate global collaboration and data comparison. We therefore aim to develop a Core Outcome Set for SCT (COS-SCT) using the Delphi method to achieve consensus on key outcomes. This will enhance the standardisation of outcome reporting and improve the quality of research and clinical care for SCT patients globally. METHODS AND ANALYSIS: The development of the COS-SCT will consist of three phases. First, a systematic review will be performed to identify outcomes reported in studies on the surgical treatment of SCT in children. Second, an international Delphi survey will be conducted among key stakeholders, including clinicians, researchers and patient representatives, to establish consensus on outcome prioritisation. Finally, a consensus meeting with representatives from all stakeholder groups will be held to ratify the final Core Outcome Set. The study will follow methodological guidance from the Core Outcome Measures in Effectiveness Trials (COMET) initiative and will be developed and reported in accordance with the Core Outcome Set Standards for Development (COS-STAD) and Core Outcome Set Standards for Reporting (COS-STAR). ETHICS AND DISSEMINATION: The medical research ethics committee of the Amsterdam University Medical Centre (Amsterdam UMC) confirmed that the Dutch Medical Research Involving Human Subjects Act (WMO) does not apply to this study, and therefore a full review by the ethics committee is not required. This study is registered in the COMET initiative database. Results will be disseminated in peer-reviewed academic journals and conference presentations.

Indexed as

Outcome Assessment, Health CareSacrococcygeal RegionTeratomaChildConsensusDelphi TechniqueHumansResearch DesignSystematic Reviews as TopicDelphi TechniquePaediatric oncologyPaediatric surgerySystematic Review

Identifiers

PMID41545048
PMCPMC12815119

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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.