Evidence map›Paper›PMID 41446576›Full record

ArticleFrontiers in molecular biosciences2025

Limitations of PICADAR as a diagnostic predictive tool for primary ciliary dyskinesia.

Andre Schramm, Johanna Raidt, Sarah Riepenhausen, Caroline Marie Torp Nygaard, Retno Tenardi-Wenge, Tavs Qvist, Pernille Witt, Michael Storck, Heike Olbrich, Kim Gjerum Nielsen and 1 more

Abstract read
In one paragraph

Article in Frontiers in molecular biosciences, 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

11 authors.

Andre SchrammDepartment of General Pediatrics, University Hospital Münster, Münster, Germany.
Johanna RaidtDepartment of General Pediatrics, University Hospital Münster, Münster, Germany.
Sarah RiepenhausenInstitute of Medical Informatics, University of Münster, Münster, Germany.
Caroline Marie Torp NygaardDanish Primary Ciliary Dyskinesia Centre, Pediatric Pulmonary Service, Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Retno Tenardi-WengeDepartment of General Pediatrics, University Hospital Münster, Münster, Germany.
Tavs QvistDanish PCD Centre Copenhagen, Department of Infectious Diseases, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Pernille WittDanish Primary Ciliary Dyskinesia Centre, Pediatric Pulmonary Service, Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Michael StorckInstitute of Medical Informatics, University of Münster, Münster, Germany.
Heike OlbrichDepartment of General Pediatrics, University Hospital Münster, Münster, Germany.
Kim Gjerum NielsenDanish Primary Ciliary Dyskinesia Centre, Pediatric Pulmonary Service, Department of Pediatrics and Adolescent Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Heymut OmranDepartment of General Pediatrics, University Hospital Münster, Münster, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The Primary Ciliary Dyskinesia Rule (PICADAR) is a diagnostic predictive tool currently recommended by the European Respiratory Society (ERS) to assess the likelihood of a primary ciliary dyskinesia (PCD) diagnosis. Despite its recommendation according to the current ERS PCD diagnostic guideline, the performance of the PICADAR remains insufficiently studied. Methods: We evaluated the sensitivity of PICADAR in 269 individuals with genetically confirmed PCD. Using an initial question, PICADAR rates all individuals without daily wet cough negative for PCD. PICADAR evaluates seven questions in the daily wet cough group. We here calculated test sensitivity based on the proportion of individuals scoring ≥5 points as recommended. Subgroup analyses examined the impact of laterality defects and predicted hallmark ultrastructural defects. Results: 18 individuals (7%) reported no daily wet cough ruling out PCD according to PICADAR. The median PICADAR score was 7 (IQR: 5-9), with an overall sensitivity of 75% (202/269). Sensitivity was higher in individuals with laterality defects (95%; median score: 10; IQR 8-11) compared to those with situs solitus (61%, median score: 6; IQR 4-8; p*<0.0001). Further stratification by associated ciliary ultrastructure showed higher sensitivity in individuals with hallmark defects (83%) versus those without (59%, p*<0.0001). Conclusion: The PICADAR has limited sensitivity, particularly in individuals without laterality defects (61%) or absent hallmark ultrastructural defects (59%). Therefore, PICADAR should not be the only factor to initiate diagnostic work-up for PCD. Alternative predictive tools are needed, particularly for PCD individuals with normal body composition and normal ultrastructure.

Indexed as

ciliary ultrastructuremotile ciliopathyPCDPICADARpredictive toolscoresitus inversustest sensitivity

Identifiers

PMID41446576
PMCPMC12722925

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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.