Prospective Multi-Center Longitudinal Study to Validate Accuracy of the Global Anatomic Staging System (GLASS) Score in Predicting Major Acute Limb Events in Patients With Chronic Limb Threatening Ischemia Undergoing Endovascular Intervention: The PROMOTE-GLASS Study Protocol
- Maram Darwish 1,2, Mario D'Oria 3,4, Alexander Croo 5, Ryan Gouveia Melo 6,7, Lewis Meecham 1,
- Maram Darwish 1,2, Mario D'Oria 3,4, Alexander Croo 5
- 1Southeast Wales Vascular Network, University Hospital of Wales, Cardiff, UK.
- 2The East Midlands Deanery, Health Education England, Leicester, UK.
- 3Department of Vascular and Endovascular Surgery, University Hospital of Trieste, Trieste, Italy.
- 4Medical School, University of Trieste, Trieste, Italy.
- 5Department of Thoracic and Vascular Surgery, Ghent University Hospital, Ghent, Belgium.
- 6Department of Angiology and Vascular Surgery, Centro Hospitalar Lisboa Norte, Lisboa, Portugal.
- 7Department of Angiology and Vascular Surgery, Hospital da Luz Torres de Lisboa, Lisboa, Portugal.
- 0Southeast Wales Vascular Network, University Hospital of Wales, Cardiff, UK.
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View abstract on PubMed
Summary
This summary is machine-generated.The Global Limb Anatomic Staging System (GLASS) shows promise in predicting outcomes for chronic limb-threatening ischemia (CLTI) patients undergoing endovascular treatment (EVT). This study validates GLASS for improved patient selection and treatment planning in CLTI cases.
Area Of Science
- Vascular Surgery
- Interventional Cardiology
- Health Services Research
Background
- The Global Limb Anatomic Staging System (GLASS) is an angiographic scoring system for infrainguinal disease extent in endovascular treatment (EVT).
- No current risk prediction model exists for chronic limb-threatening ischemia (CLTI) patients undergoing EVT.
- GLASS validation and adoption for research outside academic institutions are limited.
Purpose Of The Study
- To examine the validity and reliability of the GLASS score in predicting major acute limb events and overall survival (OS).
- To assess GLASS's utility in patients with CLTI undergoing EVT.
- To improve clinical decision-making and patient outcomes for CLTI.
Main Methods
- A prospective, international, multicenter, observational study (PROMOTE-GLASS).
- Inclusion of patients with CLTI referred for EVT.
- Assessment of primary outcomes (technical success/failure, 1-year limb patency) and secondary outcomes (adverse limb events, amputation, OS) up to 1 year post-procedure.
Main Results
- Data collection and analysis are ongoing as part of the PROMOTE-GLASS study.
- Validation of risk prediction through clinical and imaging data analysis at follow-up.
- The study aims to provide robust evidence for GLASS's predictive capabilities.
Conclusions
- PROMOTE-GLASS has the potential to revolutionize clinical decision-making for EVT in CLTI patients.
- The study findings may help identify patients likely to benefit from EVT, reducing the need for invasive procedures.
- Results will inform patient selection for future randomized controlled trials (RCTs) investigating EVT for CLTI.
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