Evidence map›Paper›PMID 32066461›Full record

GuidelinePediatric rheumatology online journal2020

Consensus protocols for the diagnosis and management of the hereditary autoinflammatory syndromes CAPS, TRAPS and MKD/HIDS: a German PRO-KIND initiative.

Sandra Hansmann, Elke Lainka, Gerd Horneff, Dirk Holzinger, Nikolaus Rieber, Annette F Jansson, Angela Rösen-Wolff, Gabi Erbis, Martina Prelog, Juergen Brunner and 2 more

Open access · goldAbstract readConsensus StatementPractice Guideline
In one paragraph

Guideline in Pediatric rheumatology online journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 7% 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

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 63 citations in OpenAlex.

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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 10 institutions in 3 countries.

Sandra HansmannDepartment of Pediatric Rheumatology, autoinflammation reference centre Tuebingen (arcT), University Children's Hospital Tuebingen, Tuebingen, Germany.
Elke LainkaDepartment of Pediatric Rheumatology, University Children's Hospital Essen, Essen, Germany.
Gerd HorneffDepartment of Pediatrics, Asklepios Clinic Sankt Augustin GmbH, Sankt Augustin, Germany.
Dirk HolzingerDepartment of Pediatric Hematology-Oncology, University of Duisburg-Essen, Essen, Germany.
Nikolaus RieberDepartment of Pediatrics, Kinderklinik Muenchen Schwabing, Klinikum Schwabing, StKM GmbH und Klinikum rechts der Isar, Technical University of Munich, Munich, Germany.
Annette F JanssonDivision of Pediatric Rheumatology and Immunology, Dr. von Hauner Children's Hospital, University Hospital Munich, Munich, Germany.
Angela Rösen-WolffDepartment of Pediatrics, University Hospital Carl Gustav Carus, TU Dresden, Dresden, Germany.
Gabi ErbisDepartment of Pediatric Rheumatology, autoinflammation reference centre Tuebingen (arcT), University Children's Hospital Tuebingen, Tuebingen, Germany.
Martina PrelogDepartment of Pediatrics, Pediatric Rheumatology and Special Immunology, University Hospital Wuerzburg, Wuerzburg, Germany.
Juergen BrunnerDepartment of Pediatrics, Medical University Innsbruck, Innsbruck, Austria.
Susanne M BenselerDepartment of Pediatric Rheumatology, autoinflammation reference centre Tuebingen (arcT), University Children's Hospital Tuebingen, Tuebingen, Germany.
Jasmin B Kuemmerle-DeschnerDepartment of Pediatric Rheumatology, autoinflammation reference centre Tuebingen (arcT), University Children's Hospital Tuebingen, Tuebingen, Germany. Jasmin.kuemmerle-deschner@med.uni-tuebingen.de.ORCID http://orcid.org/0000-0002-6365-6598
University Children's Hospital Tübingen · DEAsklepios Klinik Sankt Augustin · DEEssen University Hospital · DEInnsbruck Medical University · ATMünchen Klinik · DETUM Klinikum · DEUniversitätsklinikum Würzburg · DEUniversity Hospital Carl Gustav Carus · DEUniversity of Calgary · CAUniversity of Duisburg-Essen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRare autoinflammatory diseases (AIDs) including Cryopyrin-Associated Periodic Syndrome (CAPS), Tumor Necrosis Receptor-Associated Periodic Syndrome (TRAPS) and Mevalonate Kinase Deficiency Syndrome (MKD)/ Hyper-IgD Syndrome (HIDS) are genetically defined and characterized by recurrent fever episodes and inflammatory organ manifestations. Early diagnosis and early start of effective therapies control the inflammation and prevent organ damage. The PRO-KIND initiative of the German Society of Pediatric Rheumatology (GKJR) aims to harmonize the diagnosis and management of children with rheumatic diseases nationally. The task of the PRO-KIND CAPS/TRAPS/MKD/HIDS working group was to develop evidence-based, consensus diagnosis and management protocols including the first AID treat-to-target strategies.

methodsThe national CAPS/TRAPS/MKD/HIDS expert working group was established, defined its aims and conducted a comprehensive literature review synthesising the recent (2013 to 2018) published evidence including all available recommendations for diagnosis and management. General and disease-specific statements were anchored in the 2015 SHARE recommendations. An iterative expert review process discussed, adapted and refined these statements. Ultimately the GKJR membership vetted the proposed consensus statements, agreement of 80% was mandatory for inclusion. The approved statements were integrated into three disease specific consensus treatment plans (CTPs). These were developed to enable the implementation of evidence-based, standardized care into clinical practice.

resultsThe CAPS/TRAPS/MKD/HIDS expert working group of 12 German and Austrian paediatric rheumatologists completed the evidence synthesis and modified a total of 38 statements based on the SHARE recommendation framework. In iterative reviews 36 reached the mandatory agreement threshold of 80% in the final GKJR member survey. These included 9 overarching principles and 27 disease-specific statements (7 for CAPS, 11 TRAPS, 9 MKD/HIDS). A diagnostic algorithm was established based on the synthesized evidence. Statements were integrated into diagnosis- and disease activity specific treat-to-target CTPs for CAPS, TRAPS and MKD/HIDS.

conclusionsThe PRO-KIND CAPS/TRAPS/MKD/HIDS working group established the first evidence-based, actionable treat-to-target consensus treatment plans for three rare hereditary autoinflammatory diseases. These provide a path to a rapid evaluation, effective control of disease activity and tailored adjustment of therapies. Their implementation will decrease variation in care and optimize health outcomes for children with AID.

Indexed as

Patient Care PlanningAntibodies, Monoclonal, HumanizedAntirheumatic AgentsCryopyrin-Associated Periodic SyndromesEtanerceptEvidence-Based MedicineGermanyHereditary Autoinflammatory DiseasesHumansInterleukin 1 Receptor Antagonist ProteinMevalonate Kinase DeficiencyRheumatologyAntibodies, Monoclonal, HumanizedAntirheumatic AgentscanakinumabEtanerceptInterleukin 1 Receptor Antagonist ProteinAutoinflammatory diseasesComparative effectivenessConsensus treatment plansManagementTreat-to-target

Identifiers

PMID32066461
PMCPMC7027082
OpenAlexW3007461053

What OpenQuestion holds

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Registered trials

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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.