Evidence map›Paper›PMID 39074461›Full record

ArticleHormone research in paediatrics2025

Development of Quality Indicators to Evaluate the Quality of Care for People with Differences of Sex Development.

Martina Jürgensen, Martina Jürgensen, Marion Rapp, Maike Schnoor, Andreas Heidenreich, Ulla Döhnert, Jannick Scherf, Olaf Hiort, Alexander Katalinic, DSDCare Study Group

Abstract read
In one paragraph

Article in Hormone research in paediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

10 authors.

Martina Jürgensen
Martina JürgensenDepartment of Pediatrics and Adolescent Medicine, Section for Pediatric Endocrinology and Diabetology, University Hospital Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Marion RappDepartment of Pediatrics and Adolescent Medicine, Section for Pediatric Endocrinology and Diabetology, University Hospital Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Maike SchnoorInstitute for Social Medicine and Epidemiology, University of Lübeck, Lübeck, Germany.
Andreas HeidenreichInstitute for Social Medicine and Epidemiology, University of Lübeck, Lübeck, Germany.
Ulla DöhnertDepartment of Pediatrics and Adolescent Medicine, Section for Pediatric Endocrinology and Diabetology, University Hospital Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Jannick ScherfInstitute for Social Medicine and Epidemiology, University of Lübeck, Lübeck, Germany.
Olaf HiortDepartment of Pediatrics and Adolescent Medicine, Section for Pediatric Endocrinology and Diabetology, University Hospital Schleswig-Holstein, Campus Lübeck, Lübeck, Germany.
Alexander KatalinicInstitute for Social Medicine and Epidemiology, University of Lübeck, Lübeck, Germany.
DSDCare Study Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAchieving evidence-based, high-quality medical care is the overarching goal of healthcare quality management. Quality indicators (QIs) serve as proxies to show whether good quality is reached or not. This article describes the development of QI for the evaluation of healthcare quality in the area of differences of sex development (DSD).

methodsFollowing the model of Donabedian, the aim was to develop QI to assess defined relevant aspects of the quality of structures, processes, and outcomes of care in DSD. Ten DSD clinical centres and two self-advocacy groups in Germany included in the DSDCare project were involved in the development of the QI and a benchmarking system. The development of the QI involved several structured steps: analysis of guidelines and recommendations, literature review, qualitative interviews with key stakeholders in the field of DSD, and patients or their carers. QIs were discussed in a multi-stage systematic consensus process and assessed in terms of their relevance, feasibility, and practicability.

resultsIn a multi-stage systematic consensus process involving medical and psychological experts from a range of disciplines, people with DSD and their families, and representatives of self-advocacy groups, we have developed a set of 37 QIs (22 structure, seven process, and eight outcome quality). The QIs serve to evaluate care in the field of DSD and may add to the German criteria for certification of Centres for Rare Conditions formulated by the National Action League for People with Rare Diseases (NAMSE) in this area of expertise.

conclusionWe have succeeded in developing and jointly adopting a set of QIs that consider a wide range of perspectives on the quality of care for people with DSD and their families. These QIs have been found to be relevant, feasible, and practicable, and they are now used for a yearly quality benchmarking in the participating DSD centres.

Indexed as

Disorders of Sex DevelopmentQuality Indicators, Health CareQuality of Health CareFemaleGermanyHumansMaleBenchmarkDifferences of sex developmentHealthcare quality managementQuality indicatorQuality of care

Identifiers

PMID39074461
PMCPMC12668713

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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.