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Glasgow prognostic score as an outcome predictor for patients initiating hemodialysis
Gabriel Ștefan1,2, Adrian Zugravu1,2, Simona Stancu1,2
1Nephrology Department, University of Medicine and Pharmacy "Carol Davila", Bucharest, Romania.
Insights
The Glasgow Prognostic Score (GPS) at hemodialysis (HD) initiation is linked to patient mortality. Higher GPS scores indicate increased mortality risk, suggesting its use as a prognostic tool for high-risk hemodialysis patients.
Area of Science:
- Nephrology
- Clinical Medicine
- Prognostics
Background:
- The Glasgow Prognostic Score (GPS) is a marker of systemic inflammation.
- Its utility in predicting outcomes for patients initiating hemodialysis (HD) requires further investigation.
Purpose of the Study:
- To examine the association between the Glasgow Prognostic Score (GPS) at hemodialysis (HD) initiation and overall and cardiovascular mortality.
- To evaluate GPS as a prognostic indicator in patients commencing HD therapy.
Main Methods:
- Retrospective analysis of 264 patients initiating HD between 2014-2015.
- Follow-up until December 31, 2021, with a median duration of 6.8 years.
- Utilized Cox proportional hazard models to assess mortality risk.
Main Results:
- Higher GPS scores were associated with emergent HD initiation and increased eGFR at initiation.
- 60% of patients experienced mortality during follow-up, with cardiovascular disease as the primary cause.
- Significant differences in median survival time were observed across GPS classes, confirming GPS as a predictor of mortality.
Conclusions:
- A significant association exists between GPS at HD initiation and patient mortality.
- GPS demonstrates potential as a prognostic tool for identifying high-risk hemodialysis patients.
- Further research is warranted to validate these findings and explore GPS-based interventions.
Introduction:
This retrospective study examined the relationship between the Glasgow Prognostic Score (GPS) at hemodialysis (HD) initiation and overall/cardiovascular mortality.
Methods:
A total of 264 patients starting HD between 2014 and 2015 at a single center were studied. Follow-up persisted until therapy change, death, or study end (December 31, 2021), with a median of 6.8 years.
Results:
Patients with a higher GPS more frequently had emergent HD initiation and showed increased eGFR at initiation. During follow-up, 60% of patients died, with cardiovascular disease being the leading cause. Univariate analysis revealed a significant difference in median survival time across GPS classes. Cox proportional hazard models confirmed a significant association between GPS and mortality.
Conclusions:
We report a significant association between GPS at HD initiation and mortality. GPS may prove useful as a prognostic tool for identifying high-risk patients, underscoring the need for future research to validate these findings and explore the potential of GPS-based interventions.
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