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[Best practice agreement: implementation of best practice guidelines in HCL hospitals in Lyon, France]

S Hédoux1, X Armoiry, X Dode

  • 1Service pharmaceutique, groupement hospitalier Edouard-Herriot, hospices civils de Lyon, 5, place d'Arsonval, 69437 Lyon cedex 03, France. stephanie.hedoux@chu-lyon.fr

Insights

Hospices Civils de Lyon (HCL) developed local best practice guidelines for healthcare products, adapting national standards and incorporating physician-validated emerging indications for improved drug management and patient care.

Area of Science:

  • Healthcare Management
  • Clinical Pharmacy
  • Health Economics

Context:

  • Hospices Civils de Lyon (HCL) implemented best practice guidelines for healthcare products reimbursed beyond diagnosis-related groups (DRGs) tariffs in France since 2004.
  • National guidelines required adaptation for practical, everyday clinical application within the HCL hospital system.
  • A dedicated working group, COPIL RBU, was established to manage and localize these best practice guidelines.

Purpose:

  • To adapt and implement national best practice guidelines for drug reimbursement within the Hospices Civils de Lyon (HCL).
  • To create a localized system for managing drug indications, including approved, assessed, and contraindicated uses.
  • To integrate emerging drug indications, validated by prescribing physicians, into clinical practice.

Summary:

  • The COPIL RBU group at HCL conducts scientific and regulatory monitoring and tracks emerging drug indications.
  • Best practice guidelines categorize indications into approved, assessed, and contraindicated, incorporating physician-validated emerging uses with scientific evidence.
  • Practical application involves a best practice prescription system for drug traceability from prescription to administration, supported by professional groups.

Impact:

  • Enhanced traceability of drug use from prescription to patient administration.
  • Improved adherence to best practices through physician validation and scientific argumentation for emerging indications.
  • Facilitation of future audits to assess guideline conformity and understand current medical practices.

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