Evidence map›Paper›PMID 42377852›Full record

ArticleMolecular and cellular pediatrics2026

Diagnostic value of basic and extended procedures in pediatric fever of unknown origin - results of a nation-wide surveillance study.

Mira Katarina Bienioschek, Alice Lejeune, Gonza Ngoumou, Michael S Urschitz, Stefanie Dollinger, Martina Hagenberg, Kai Lehmberg, Simone Schrauth, Johannes Wolf, Horst von Bernuth and 2 more

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Article in Molecular and cellular pediatrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Mira Katarina BienioschekDepartment of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité Universitätsmedizin Berlin, Augustenburger Platz, Berlin, 13353, Germany.
Alice LejeuneDepartment of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité Universitätsmedizin Berlin, Augustenburger Platz, Berlin, 13353, Germany.
Gonza NgoumouCharité Universitätsmedizin Berlin, Charité Competence Center for Traditional and Integrative Medicine (CCCTIM), Berlin, Germany.
Michael S UrschitzGerman Paediatric Surveillance Unit (GPSU), Division of Paediatric Epidemiology, Institute of Medical Biostatistics, Epidemiology and Informatics, University Medical Centre of the Johannes Gutenberg- University, Mainz, Germany.
Stefanie DollingerGerman Centre for Paediatric and Adolescent Rheumatology, Garmisch-Partenkirchen, Germany.
Martina HagenbergChildren's Hospital St. Elisabeth and St. Barbara, Halle (Saale), Germany.
Kai LehmbergDepartment of Pediatric Hematology and Oncology, University Medical Center Eppendorf, Hamburg, Germany.
Simone SchrauthDepartment of Paediatrics, Division of Paediatric Infectious Diseases, University Hospital of Würzburg, Würzburg, Germany.
Johannes WolfSt. Vincenz-Krankenhaus Paderborn, Klinik für Kinder- und Jugendmedizin, Paderborn, Germany.
Horst von BernuthDepartment of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité Universitätsmedizin Berlin, Augustenburger Platz, Berlin, 13353, Germany.
Dirk FoellDepartment of Pediatric Rheumatology and Immunology, University Hospital Münster, Münster, Germany.
Tilmann KallinichDepartment of Pediatric Respiratory Medicine, Immunology and Critical Care Medicine, Charité Universitätsmedizin Berlin, Augustenburger Platz, Berlin, 13353, Germany. tilmann.kallinich@charite.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPediatric fever of unknown origin (FUO) remains a major diagnostic challenge encompassing infectious, autoimmune and autoinflammatory as well as malignant diseases. Despite improved diagnostical procedures, no underlying disease can be identified in approximately one third of patients. Current guidelines recommend stepwise diagnostical approaches based on potential diagnostic clues (PDC+). This prospective nation-wide surveillance study aims to evaluate basic and advanced diagnostic procedures in the diagnostic of FUO. METHODS AND

resultsVia the German Pediatric Surveillance Unit, children were pseudonymized enrolled based on the following inclusion criteria: fever ≥ 38.5 °C for at least five out of ten consecutive days and no identifiable cause after standard diagnostic workup. The questionnaire collected patient data, symptoms, performed diagnostic workup, and the final diagnosis, if applicable. Among 113 included children, an underlying disease was identified in 72 cases (63.7%). 26 patients (23.1%) had infections, 31 children (27.4%) had systemic onset juvenile idiopathic arthritis/Still's disease (sJIA/SD), and 15 children (13.3%) were classified as "other diagnoses" including autoinflammatory diseases, vasculitides, and malignancies. Children with sJIA/SD presented with more clinical symptoms (mean = 4.6, SD = 2.17) compared to those with infections (mean = 2.7, SD = 1.40, p=.002). Basic diagnostic workup revealed at least one PDC + in every case (mean = 6.6). Most PDC+ (mean = 3.1, SD = 1.82) were identified by history taking and physical examination as well as by laboratory testing and blood count (mean = 2.5 PDC+, SD = 1.32). A total of 370 basic imaging investigations, e.g. abdominal ultrasound and echocardiography, provided in total 50 PDCs+ demonstrating their high diagnostical yield. Primarily in children with unclear clinical presentation advanced imaging revealed PDC+. Overall, the number of misleading PDCs (PDC-) was low (mean = 1.0, SD = 1.14) with autoantibody testing being the basic diagnostic procedure accounting for the majority of PDC-.

conclusionThe results of this nation-wide surveillance study highlight the value of basic and advanced diagnostical approaches in the management of pediatric FUO. Careful history taking, physical examination, and targeted basic diagnostic testing can identify multiple PDC+ with only few misleading PDC-, which may contribute to diagnostic accuracy and avoid unnecessary testing. The findings can be introduced into guidelines in order to standardize and improve the diagnostic approaches in children with FUO.

Indexed as

ChildrenDiagnosticFever of unknown originInfectiousInflammatoryNeoplastic

Identifiers

PMID42377852
PMCPMC13319292

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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.