Preferences for palliative care discussions in COPD

  • Research type

    Research Study

  • Full title

    Palliative care discussions in COPD - patients’ preferences and clinicians’ judgements

  • IRAS ID

    203444

  • Contact name

    Nuno C Tavares

  • Contact email

    nct1g14@soton.ac.uk

  • Sponsor organisation

    University of Southampton

  • Duration of Study in the UK

    1 years, 0 months, 1 days

  • Research summary

    COPD, or Chronic Obstructive Pulmonary Disease, is a chronic life-limiting disease which causes airflow obstruction and progressive breathlessness. In the UK, it’s estimated that 3 million people have COPD and it’s responsible for 30,000 deaths a year.
    During their disease trajectory, COPD patients experience several acute exacerbations which lead to hospital admissions, to prolonged mechanical ventilation and premature death. Therefore, COPD patients benefit from palliative care conversations because they require stand-by decisions as to how to proceed in the future. Currently, only a small proportion of patients discuss palliative care, despite more than half of patients wanting them. When these discussions do occur, most occur during an acute exacerbation, at very stressful times, and with a clinician who does not know the patient.
    Therefore, to improve the frequency and quality of discussions a research study to understand the preferences of COPD patients and to understand clinicians’ judgement when starting conversations was developed.
    The research study is divided into 3 phases:
    Phase 1 - Systematic literature review about palliative care conversations in COPD.
    Phase 2 – Interviews and case-note review of COPD patients in 3 different stages of disease severity: mild, moderate and severe. Each group will contain 7-15 patients and interviews will be stopped when data saturation has been achieved. Phase 2 aims to understand preferences of patients regarding time and nature of palliative care conversations with clinicians.
    Phase 3 – Interviews with healthcare professionals.
    Data gathered across all phases will be analysed using thematic analysis and simple descriptive statistics. This data will be used to answer the initial research question: How do COPD patients’ preferences and clinicians’ judgement shape the timing and nature of palliative care conversations?

  • REC name

    South Central - Hampshire B Research Ethics Committee

  • REC reference

    16/SC/0471

  • Date of REC Opinion

    12 Jan 2017

  • REC opinion

    Further Information Favourable Opinion