Evidence map›Paper›PMID 41545997›Full record

ArticleOrphanet journal of rare diseases2026

Austrian Pompe Outcome Consensus (APOC): a national Delphi study.

Florian B Lagler, Thomas Scherer, Jörg Weber, Martina Huemer, Wolfgang Löscher

Abstract read
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Article in Orphanet journal of rare diseases, 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

5 authors.

Florian B LaglerInstitute for Inborn Errors of Metabolism and Department of Pediatrics, Paracelsus Medical University, Salzburg, Austria. f.lagler@salk.at.ORCID http://orcid.org/0000-0002-1439-6961
Thomas SchererDivision of Endocrinology and Metabolism, Department of Internal Medicine III, Medical University of Vienna, Währinger Gürtel 18-20, Vienna, 1090, Austria.
Jörg WeberDepartment of Neurology, Klinikum Klagenfurt, Feschnigstraße 11, Klagenfurt am Wörthsee, 9020, Austria.
Martina HuemerDepartment of Paediatrics, Landeskrankenhaus Bregenz, Bregenz, Austria.
Wolfgang LöscherDepartment of Neurology, Medical University Innsbruck, Anichstrasse 35, Innsbruck, 6020, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFollow-up assessments form the basis for the continuous optimization of therapy and supportive care on an individual level, for confirming treatment efficacy, and for detecting newly emerging or unexpectedly progressive symptoms early enough to permit timely therapeutic intervention. For Pompe disease, evidence based guidelines on which assessments should constitute the minimum standard and which are required in specific situations only, were missing. Therefore, we started the Austrian Pompe Outcome Consensus (APOC) Study.

methodsAPOC was a Delphi process with two classical online and a modified third round, implemented September 2023-May 2024, following the AWMF S2k guideline. A five-member interdisciplinary steering committee invited 23 clinical experts, achieving response rates of 69.6% and 100%. A questionnaire was developed via literature scoping and an expert workshop. The importance and recommended frequency of follow-up assessments were rated using AGREE II consensus thresholds, and the classification for recommendation strength of the German Association of the Scientific Medical Societies (AWMF;Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften e. V.).

results34 statements achieved consensus. Strong recommendations included the 6-minute walk test (6MWT), timed tests, Pompe PEDI and other age-appropriate functional tests in children, muscle tests, handheld dynamometry, Fatigue Severity Scale, patient-reported outcome measures (e.g. R-Pact), forced vital capacity (sitting/supine), morphologic muscle imaging studies, pain and quality of life assessment. Further recommendations included respiratory (MIP/MEP) and sleep studies (polysomnography), creatine kinase, antibody titers, swallowing studies, liver sonography, hearing tests and speech and speech/oromotor function, physical therapy and rehabilitation, bone density assessment, and caregiver psychosocial care.

conclusionsThe APOC Delphi consensus yields AGREE II-compliant, systematically weighted recommendations delineating essential and optional follow-up assessments for Pompe disease in the context of Austrian healthcare. The applied method enabled a structured and efficient consensus-building process and appears well suited for addressing comparable questions in other rare disease contexts. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Glycogen Storage Disease Type IIAustriaConsensusDelphi TechniqueHumansSurveys and QuestionnairesAustriaAWMF S2k guidelinesDelphi consensusEnzyme replacement therapyFollow-up assessmentsPompe disease

Identifiers

PMID41545997
PMCPMC12895735

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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.