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Improving organisation to improve care: ERN ReCONNET organisational reference model for systemic sclerosis patients’ care pathway

  • Rosaria Talarico*
  • , Diana Marinello
  • , Ilaria Palla
  • , Sara Cannizzo
  • , Ilaria Galetti
  • , Sue Farrington
  • , Silvia Aguilera
  • , Jeanette Andersen
  • , Eva Ceccatelli
  • , Alain Cornet
  • , Gema Cutillas
  • , Marco Esteves
  • , Charissa Frank
  • , Catarina Leite
  • , Gabi Niehaus
  • , Elisabeth Perez Gomez
  • , Katleen Polfliet
  • , Silvia Sandulescu
  • , Rita Schriemer
  • , Simone Barsotti
  • Silvia Bellando-Randone, Lorenzo Beretta, Vera Bernardino, Goncalo Boleto, Stefano Bombardieri, Gerd Burmester, Ilaria Cavazzana, Veronica Codullo, Maurizio Cutolo, Virgil Dalm, Laura Damian, Alessandra Della Rossa, Andrea Doria, Meryem Maud Farhat, João Eurico Fonseca, Eric Hachulla, Frédéric Houssiau, Maria Grazia Lazzaroni, Maarten Limper, Valentina Lorenzoni, Carlomaurizio Montecucco, Marta Mosca, Luc Mouthon, Ulf Müeller-Ladner, Micheline Pha, Cristina Ponte, Julia Spierings, Alberto Sulli, Anna Viola Taulaigo, Simone Ticciati, Angela Tincani, Natasha Toplak, Leopoldo Trieste, P. M. van Hagen, Jacob van Laar, Marie Vanthuyne, Barbara Vigone, Jeska K. de Vries-Bouwstra, Margherita Zen, Giuseppe Turchetti, Vanessa Smith, Marco Matucci Cerinic
*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Objective: To optimise the organisation of care and encourage the adoption of good clinical practices, the RarERN Path© methodology was designed within ERN ReCONNET. The aim of our work was to report the application of RarERN Path© on systemic sclerosis within the ERN ReCONNET centres, providing a feasible and flexible organisational reference model for optimising the systemic sclerosis care pathway in different countries. Methods: RarERN Path© is a six-phase methodology which enables the creation of a reference organisational model co-designed on the basis of the expertise of different stakeholders. It foresees six phases, ranging from the map of existing patients’ care pathways and patients’ stories, to the consensus on a common organisational patient care pathways, and its key performance indicators definition. Results: The agreed reference model highlights the importance of having an organisational flow for referrals that foresees how patients may access directly the specialised unit from the different referrals. Specific specialised visits were considered as mandatory to be organised and they included cardiologist, pneumologist, gastroenterologist, psychologist, nephrologist, dermatologist, wound care specialist/nurses and other healthcare professionals (such as nurses, social workers and nutritional counselling). Moreover, specific services related to therapy were highlighted as strongly recommended to be organised, mainly represented by infusion therapy and wound care, as well as occupation therapy and physiotherapy. Conclusion: The organisational model emerged from our investigation emphasises that the organisation of specific services for systemic sclerosis treatment should be organised as a solid support for implementing the existing recommendations on systemic sclerosis management in real life.

Original languageEnglish
Pages (from-to)625-632
Number of pages8
JournalJournal of Scleroderma and Related Disorders
Volume10
Issue number3
Early online date7 Oct 2024
DOIs
Publication statusPublished - Oct 2025

Keywords

  • European Commission
  • European Reference Networks
  • organisation of care
  • organisational reference model
  • patients’ care pathways
  • RarERN Path
  • systemic sclerosis

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