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CPR decision-making conversations in the UK: an integrative review
Charlie C Hall1, Jean Lugton2, Juliet Anne Spiller2
1St Columba's Hospice, Edinburgh, UK.
Patients and families prefer trusted individuals to initiate Do Not Attempt Cardio-Pulmonary Resuscitation (DNACPR) discussions earlier in illness, ideally within broader future care conversations. These patient-centered insights conflict with current healthcare pressures for early DNACPR discussions.
Area of Science:
- Medical Ethics
- Patient Experience
- Healthcare Communication
Background:
- Do Not Attempt Cardio-Pulmonary Resuscitation (DNACPR) discussions are ethically and legally complex.
- Existing guidelines lack patient, family, and caregiver perspectives.
- This review synthesizes experiences of advance cardiopulmonary resuscitation (CPR) decision-making discussions.
Purpose of the Study:
- To explore patient, family, and caregiver experiences with DNACPR discussions.
- To identify best practices for approaching these sensitive conversations from the patient's viewpoint.
- To inform future guidelines and clinical practice regarding DNACPR decision-making.
Main Methods:
- Integrative review of UK literature (2000-2016).
- Inclusion of qualitative and quantitative studies.
- Analysis of 20 UK papers from 773 identified abstracts.
Main Results:
- Patients and families prefer discussions initiated by trusted individuals.
- Family involvement preferences vary contextually; earlier discussions are often preferred.
- Acute care settings are suboptimal for these conversations; they should be part of wider future care planning.
- Effective communication skills training is crucial for healthcare professionals.
Conclusions:
- Patient narratives regarding DNACPR discussions are often at odds with current statutory frameworks.
- Healthcare professionals face challenges balancing service pressures with patient-centered care.
- Prioritizing patient and family experiences is essential for minimizing harm and advancing realistic medicine.
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