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Integrating Patients Into Programmes to Address the Allergy Knowledge Practice Gap.

John O Warner1, Sophie Jacoba Irma Maria Spitters1,2

  • 1National Health and Lung Institute, Imperial College, London, UK.

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|September 24, 2024
PubMed
Summary
This summary is machine-generated.

Bridging the knowledge-practice gap in allergic diseases requires patient and carer involvement. Implementing integrated care pathways (ICPs) with stakeholder collaboration can improve patient outcomes.

Keywords:
allergic diseaseevidence translationguidelinesimprovement scienceintegrated care pathwaysknowledge/practice gappatient/public involvement

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Area of Science:

  • Health Services Research
  • Implementation Science
  • Patient Engagement

Background:

  • A significant gap exists between the availability of effective treatments and their clinical application, particularly in managing allergic diseases.
  • Traditional methods like systematic reviews and guidelines have not fully closed this knowledge-practice gap.
  • Lack of patient and carer involvement in research, evidence review, and guideline development is a key barrier.

Purpose of the Study:

  • To review the process of knowledge implementation into practice for improving patient experience and outcomes.
  • To argue for the benefits of involving patients and their carers as equal partners in healthcare delivery.
  • To discuss initiatives involving patients with allergic diseases and identify evidence gaps.

Main Methods:

  • Review of the step-wise and iterative process of knowledge implementation.
  • Discussion of integrated care pathways (ICPs) and quality improvement methodology.
  • Examination of stakeholder involvement at all stages of care planning and implementation.

Main Results:

  • Integrated care pathways (ICPs) show promise for improving outcomes, especially with diverse agency involvement in long-term conditions.
  • Stakeholder representation, including patients, families, and various professional groups, is crucial for successful implementation.
  • A current evidence gap exists linking direct patient involvement to improved health outcomes.

Conclusions:

  • Consistent adherence to evidence-based guidelines necessitates integrated care with clear patient navigation pathways.
  • Patient and carer involvement as equal partners can enhance the implementation process and improve outcomes.
  • Utilizing Core Outcome Sets (COS) and Patient Reported Experience Measures (PREMS) is recommended to monitor implementation research and patient involvement impact.