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Need to improve end of life care. The Health Care Commission, 2007 (UK)~54% of complaints about hospital treatment were about communication and preparation for deathwww.healthcarecommission.org.uk/db/documents/spotlightoncokmplaints.pdf . NICE Supportive
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1. Advance Care Planning
2. Need to improve end of life care The Health Care Commission, 2007 (UK)
~54% of complaints about hospital treatment were about communication and preparation for death
www.healthcarecommission.org.uk/db/documents/spotlightoncokmplaints.pdf
3. NICE Supportive & Palliative Care Guidelines 24.03.04 Patients with palliative needs are identified and a management plan discussed with MDT.
Needs and preferences should be noted, planned for and addressed.
Preferred place of care and place of death are discussed, noted and measures taken to comply where possible.
Providers should ensure systems are in place to obtain rapid and safe discharge for those who wish to die at home.
Carers are educated, enabled and supported.
4. The Gold Standards Framework A framework to deliver a ‘gold standard of care’ for all people approaching the end of their lives
It is not disease specific
A systematic approach to optimising the care delivered by healthcare professionals
Developed from primary care for primary care
On National Agenda and GPs can claim QOF points
5. The Seven Cs 1 Communication
2 Co-ordination
3 Control of symptoms
4 Continuity out of hours
5 Continued learning
6 Carer support
7 Care of the dying
6. Undertaking the Principles of GSF Appoint coordinator and lead GP/DN
Formulate a palliative care register of patients
Arrange regular MDTs
Proactively address, record and communicate current and future needs including preferred place of care, end of life care planning, DNA CPR, pre-emptive prescribing etc
Address carer’s needs
Bereavement follow-up
Significant events analysis/education
7. End of life care strategy 2008 All people approaching the end of life need to have their needs assessed, their wishes and preferences discussed and an agreed set of actions reflecting the choices they make about their care, recorded in a care plan.
In some cases, people may want to make an advanced decision to refuse treatment should they lack capacity to make such a decision in the future.
Others may want to set out more general wishes and preferences about how they are cared for and where they would wish to die.
8. Advance Care Planning
Voluntary
It is a process of discussion between an individual and their care provider which may or may not include family and friends.
Makes clear a persons wishes if their condition deteriorates and they lose mental capacity or ability to communicate wishes to others
9. ACP can lead to:- Statement of wishes and preferences reflecting an individual’s preferences and wishes in relation to future treatment and care
Medical and non-medical issues
NOT legally binding
Used to determine a person’s best interest should they lose mental capacity
10. ACP can lead to:- Advanced Decisionto refuse treatment
Relates to refusal to specific treatment in specified circumstances
Comes into effect when individual has lost capacity to give or refuse consent to treatment
Assessment of the validity and applicability of an advanced decision is essential
Legally binding
11. When to do it Part of routine clinical practice
Initiated in patients with long term conditions or receiving end of life care
depending on prognosis and pattern of disease progression
Helps to avoid stress and anxiety regarding the future
12. Who Appropriate person who has rapport and can help facilitate an informed decision
Individual encouraged to choose who they want to include in the discussion
Does not necessarily need to be a health care professional
13. Summary
14. Lasting Power of Attorney Statutory form of power of attorney
Patient chooses a person to take decisions on their behalf if they lose capacity
Personal and financial welfare
Register with Office of Public Guardian
15. Benefits of lasting power of attorney Manage affairs while still able
Ensuring that wishes are met
Peace of mind
Decreasing burden on loved ones
Keeping peace within the family
16. Birth Plan Advance Care Plan Preferred Priorities for Care
17. Introduction The PPC is a tool to determine and record patient and carers’ wishes in relation to their care and ultimate place of death.
A nationally recognised tool for all palliative care patients.
PPC has been identified within the End of Life Care Programme as an example of an Advance Care Plan
18. Identifying and Recording Preferences The explicit recording of patients/carers wishes can form the basis of care planning in multi-disciplinary teams and other services, minimizing inappropriate admissions and interventions.
In relation to your health what has been happening to you?
What are your preferences and priorities for your future care?
Where would you like to be cared for in the future?
19. Potential triggers to introduce PPC Following life changing event
Following diagnosis of a life limiting illness
During assessment of a persons need
Following a significant shift in treatment
In conjunction with prognostic indicators
Multiple hospital admissions
Admission to a care home
20. PPC as an Advance Care Plan Enables initiation of End of Life Care decisions
Facilitates recording of Preferences and Priorities
May identify potential need for Advance Decisions to Refuse Treatment to be initiated
Accessible Version enables Best Interest Process to be followed
Under MCA preferences SHOULD be taken into account
21. Do Not Attempt Cardio Pulmonary Resuscitation
CPR is undertaken unless a DNA CPR order exists
For the vast majority of patients receiving care in hospital no advance decision is made unless CPR is thought to be futile
DNA CPR is a medical decision
There is now a Yorkshire and Humber generic transferable form to remain with the patient
22. When is DNA CPR appropriate? Where CPR is contrary to the competent patient’s wishes
Where attempting CPR will not restart the patient’s heart and breathing
Where there is no benefit in restarting the patient’s heart and breathing
Where the expected benefit is out weighed by the burdens
23. Should patients be involved in DNA CPR decisions? People have ethical and legal rights to be involved in decisions that relate to them
Where patients are at foreseeable risk of cardiopulmonary arrest, or have a terminal illness, there should be a sensitive exploration of their views regarding CPR
Discussion should be part of general discussions about that person’s care
24. References End of Life Care Strategy. Professor Mike Richards (Chair) Department of Health. July 2008
Improving Supportive and Palliative Care for Adults with Cancer. Nice, 2004
www.endoflifecareforadults.nhs.uk
www.resus.org.uk/pages/dnar.pdf
www.ncpc.org.uk/publications
www.dca.gov.uk/legal-policy/mental-capacity/publications.htm
www.publicguardian.gov.uk/mca/code-of-practice.htm
www.goldstandardsframework.nhs.uk
25. Case Scenario 55 year old man diagnosed with inoperable lung cancer April 2010.
Is widowed with two teenage children. His partner has taken on the parental role and their Grandmother remains involved.
Received palliative chemotherapy but discontinued July 2010 as disease progressing to bones and brain.
August 2010 Received palliative radiotherapy to ribs and brain and receiving monthly bone strengthening infusions .
On fentanyl patch, oral analgesia, aperients, anticonvulsants and steroids.
Oct 2010 Deteriorating, becoming drowsy and bedbound.
26. Considerations for Patient What do you think would be concerns/wishes for the patient throughout this journey?
How do you think the patient would wish professionals to respond to these concerns?
27. Considerations for Relatives What do you think would be concerns/wishes for the relatives along the patient journey?
How do you think they would want professionals to address concerns/wishes?
28. Considerations for Professionals What Advanced Care Planning should be considered by professionals?
How would you ensure seamless Advanced Care Planning?
How can Advanced Care Planning be addressed?