Here is the PICO analysis for the third uploaded article:


✅ PICO Analysis

Full Article Title:

Normalising and planning for death in residential care: findings from a qualitative focus group study of a specialist palliative care intervention

Type of Study:

Qualitative focus group study (nested within a quasi-experimental design)

Journal and Year:

BMJ Supportive & Palliative Care (2019); 9:e12

DOI: 10.1136/bmjspcare-2016-001127


P – Population

  • Setting: Residential aged care facilities (nursing homes) in an Australian city
  • Participants:
    • Staff: 40 participants including carers, registered nurses, team leaders, managers, and one geriatrician
    • Relatives: 17 participants (mainly adult children of deceased residents)
  • Residents: Older adults receiving care in four facilities (360 total beds; 104 residents received the intervention)
  • Residents were generally in the final stages of life; inclusion for family focus groups required the resident to have died at least 3 months prior

I – Intervention

  • Type: Specialist palliative care service delivered by a Palliative Care Nurse Practitioner (PCNP)
  • Components:
    • Direct clinical care: symptom assessment, prescribing, case conferencing, family support
    • Indirect care: triage meetings, staff education, mentoring, needs rounds
    • Education included recognising dying, pain and symptom management, and communication strategies
    • Needs rounds (triage meetings) used to identify residents likely to die within 6 months and initiate planning
    • Total intervention time: ~2 days/week over 6 months

C – Comparison

  • No formal control group in this qualitative focus group study. However, this analysis was embedded in a wider quasi-experimental design where the facilities receiving the PCNP-led intervention were contrasted with usual care in other facilities (not analysed here).
  • Historical comparison (prior care practices before intervention) is implied in the staff and relative comments

O – Outcomes

Primary Outcomes (qualitatively derived):

  1. Normalisation of death and dying
    • Staff became more confident discussing end-of-life issues
    • Death recognised as a routine part of residential aged care
    • Earlier conversations with families about end-of-life planning
  2. Timely access to specialist palliative care
    • Improved symptom control and pain management
    • Faster and more appropriate prescribing through the nurse practitioner
    • Reduced reliance on GPs and improved interprofessional communication
    • Avoidance of unnecessary hospitalisations
  3. Improved advance care planning and decision-making
    • Families felt more prepared for the dying process
    • Staff reported greater confidence in recognising deterioration and initiating palliative care earlier
    • Use of anticipatory prescribing and structured case review supported better end-of-life experiences

Outcome Classification:

  • Person-centred outcomes: Family satisfaction, preparedness for death, comfort of residents
  • Process outcomes: Staff education, earlier ACP conversations, timely symptom management
  • Health system outcomes: Avoided hospitalisations, better coordination with GPs, reduced time to symptom relief

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