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Pharmacogenomics to Improve Supportive Care Symptoms. A Prospective Observational Study Protocol
Martyn Patel1,2, John McDermott3,4, William Newman3,4
1Norfolk and Norwich University Hospital NHS Foundation Trust, Norwich, England, UK.
Pharmacogenomic testing can personalize palliative care by predicting drug responses and side effects in patients with life-limiting conditions. This study explores its impact on prescribing practices and feasibility in an NHS hospital setting.
Area of Science:
- Pharmacogenomics and Palliative Care
Background:
- Life-limiting conditions often involve symptoms like pain and vomiting, impacting quality of life.
- Supportive and palliative care aims to manage these symptoms, especially near the end of life.
- Current medications may be ineffective or cause side effects, highlighting the need for personalized approaches.
Purpose of the Study:
- To investigate the impact of multi-gene pharmacogenetic testing on prescribing practices in palliative care.
- To assess the feasibility of incorporating pharmacogenomic testing in an acute NHS hospital setting for palliative care patients.
- To understand the acceptability of this research within the palliative care population.
Main Methods:
- A prospective observational study involving 50 adult patients with life-limiting conditions.
- Collection of a single blood sample for multi-gene pharmacogenetic testing.
- Monitoring prescribing patterns over 90 days post-recruitment to identify drug-gene interactions.
Main Results:
- The study will report on prescribing patterns and variations related to actionable drug-gene interactions.
- A drug-gene interaction ratio will indicate the prevalence of relevant medications in palliative care.
- Data will inform future clinical trial design regarding pharmacogenomic utility.
Conclusions:
- Pharmacogenomic testing holds potential for optimizing symptom management in palliative care.
- Preliminary data will guide the design of larger trials to establish clinical utility.
- The study assesses the feasibility and acceptability of pharmacogenomic research in this patient group.
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