PLoS ONE (Jan 2022)

The Abdominal Pain Unit (APU). Study protocol of a standardized and structured care pathway for patients with atraumatic abdominal pain in the emergency department: A stepped wedged cluster randomized controlled trial.

  • Maria B Altendorf,
  • Martin Möckel,
  • Liane Schenk,
  • Antje Fischer-Rosinsky,
  • Johann Frick,
  • Lukas Helbig,
  • Dirk Horenkamp-Sonntag,
  • Dörte Huscher,
  • Luisa Lichtenberg,
  • Thomas Reinhold,
  • Daniel Schindel,
  • Britta Stier,
  • Hanna Sydow,
  • Yves-Noel Wu,
  • Grit Zimmermann,
  • Anna Slagman

DOI
https://doi.org/10.1371/journal.pone.0273115
Journal volume & issue
Vol. 17, no. 8
p. e0273115

Abstract

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This study aims to improve emergency department (ED) care for patients suffering from atraumatic abdominal pain. An application-supported pathway for the ED will be implemented, which supports quick, evidence-based, and standardized diagnosis and treatment steps for patients with atraumatic abdominal pain at the ED. A mixed-methods multicentre cluster randomized controlled stepped wedge trial design will be applied. A total of 10 hospitals with EDs (expected n = 2.000 atraumatic abdominal pain patients) will consecutively (every 4 months) be randomized to apply the intervention. Inclusion criteria for patients are a minimum age of 18 years, suffering from atraumatic abdominal pain and being insured with a German statutory health insurance. Primary outcomes: acute pain score at time of discharge from ED, duration of treatment at the ED, patient-reported satisfaction. Secondary endpoints include patient safety and quality of care parameters, process evaluation parameters, and costs and cost-effectiveness parameters. Quantitative data will be gathered from patient-surveys, clinical records, and routine data from hospital information systems as well as from a participating German statutory health insurance. Descriptive and analytic statistical analysis will be performed to provide summaries and associations for primary patient-reported outcomes, process measures, quality measures, and costs. Qualitative data collection consists of participatory patient observations and semi-structured expert interviews, which will be inductively analysed. Findings will be disseminated in publications in peer-reviewed journals, on conferences, as well as via a project website. To ensure data protection, appropriate technical and organisational measures will be taken. Trial registration: DRKS00021052.