(精选)Patient Involvement in Pain Guidelines教学课件.pptVIP

Patient Involvement in Pain Guidelines Judy Birch Pain Alliance Europe NHS Evidence Accreditation Advisory Committee  Disclosure Statement of Financial Interest I, Judy Birch, DO NOT have a financial interest/arrangement or affiliation with one or more organizations that could be perceived as a real or apparent conflict of interest in the context of the subject of this presentation. Background to patient involvement in policy Active Citizenship Network (ACN): “Charter of Patients Rights”: Right to participate in policy-making in the area of health International Alliance of Patients Organizations (IAPO) policy statement and guidelines on patient involvement Health and Social Care Act 2008, 2012 IAPO Policy statement: Patient involvement should occur whenever decisions are being discussed which will affect patients’ healthcare or lives including, but not restricted to, the following areas: Education and training programmes design ( for health professionals ) Research priorities and development Care and treatment guidelines  Guideline case study Guidelines case study: PPSN/WFIP Guideline development bodies Referred to the AGREE Instrument and IAPO policy statement and guidelines on patient involvement ( add link/wording) Ongoing involvement, patients are EQUAL participants,record results and act upon them to implement changes. Pain Policy Paul Burstow MP, Minister of State for Care Services announced the following statement: “ The Department recognizes chronic pain as a long term condition, either in its own right or as a component of other long-term conditions. Everyone who suffers persistent pain should have a timely assessment in order to determine the cause of pain- if a cause can be determined- and to advise on options for treatment, including self-help. Patients with refractory chronic pain will benefit from the care-planning approach, but decisions should be taken on an individual basis depending on the se