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An audit of a patient-at-risk trigger scoring system for identifying seriously ill ward patients
Clair Sterling1, Casiano Barrera Groba
1Intensive Care Unit, University Hospital Lewisham, London. clair.sterling@uhl.nhs.uk
Insights
The Lewisham patient-at-risk trigger scoring system (PAR-T) effectively identifies adult patients at risk of critical illness. Further analysis is recommended to refine its sensitivity and specificity for broader trust-wide implementation.
Area of Science:
- Critical Care Medicine
- Health Services Research
Background:
- Early identification of patients at risk of critical illness is crucial for timely intervention.
- Existing early warning systems require validation for effectiveness and clinical utility.
Purpose of the Study:
- To evaluate the Lewisham patient-at-risk trigger scoring system (PAR-T) as an early identification tool for critical illness.
- To assess the benefit of the PAR-T flowchart protocol and patient outcomes.
- To explore illness severity, management of chronically ill patients, and organizational factors.
Main Methods:
- A prospective trial of the PAR-T system was conducted across five acute ward areas.
- Data collection focused on the scoring system's effectiveness, protocol adherence, and patient outcomes.
- An audit approach was used to explore various aspects of patient management and organizational issues.
Main Results:
- The PAR-T scoring system demonstrated sensitivity in identifying patients at risk of critical illness.
- The audit provided insights into illness severity and management strategies within different patient groups.
Conclusions:
- The PAR-T system is a sensitive tool for early identification of critical illness.
- Wider implementation is recommended to further analyze PAR-T's sensitivity and specificity.
- Further research should focus on identifying the most sensitive markers for critical illness.
Abstract:
The Lewisham patient-at-risk trigger scoring system (PAR-T) comprises an early warning 'trigger' system, designed to identify adult patients at risk of developing critical illness at an early stage, and a protocol to use for those patients identified. PAR-T was trialled on five acute ward areas in the trust. The aims were to evaluate the effectiveness of the scoring system as an early identification tool, the benefit of the flow chart protocol and the outcomes of those patients who were identified. Other issues explored during the audit were severity of illness amongst different groups of patients, management of chronically seriously ill patients and related organisational issues. The audit confirmed that PAR-T is a sensitive tool for identifying critical illness. Therefore, it was recommended that PAR-T be introduced on a wider scale in the trust, so that its sensitivity and specificity could be analysed further, particularly with regard to establishing the most sensitive markers of critical illness.
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