Vall d'Hebron Risk Score II for myocardial infarction and cardiac death
Guillermo Romero-Farina1,2,3,4,5, Santiago Aguadé-Bruix6,2,3, Ignacio Ferreira González5,7
1Nuclear Cardiology, Department, Hospital Universitari Vall d'Hebron, Vall d'Hebron Research Institute (VHIR), Universitat Autònoma de Barcelona, Barcelona, Spain guiromfar@gmail.com.
Insights
A new Vall d'Hebron Risk Score-II (VH-RS-II) effectively stratifies risk for myocardial infarction (MI) and cardiac death (CD). This score uses gated SPECT variables for patients with or without prior MI or coronary revascularisation.
Area of Science:
- Cardiology
- Nuclear Cardiology
- Medical Imaging
Background:
- Accurate risk stratification for cardiac events is crucial in cardiovascular medicine.
- Existing risk scores may not fully capture risk in patients with or without prior myocardial infarction (MI) or coronary revascularisation (CR).
- Gated single-photon emission CT (SPECT) provides valuable functional and anatomical information for risk assessment.
Purpose of the Study:
- To develop and validate a novel risk score, the Vall d'Hebron Risk Score-II (VH-RS-II).
- To predict the risk of non-fatal myocardial infarction (MI) and/or cardiac death (CD) in patients undergoing gated SPECT.
- To exclude patients who undergo coronary revascularisation (CR) during follow-up from the analysis.
Main Methods:
- Analysis of 5215 consecutive patients undergoing gated SPECT.
- Stratification into two groups: no previous MI and/or CR (2960 patients) and previous MI and/or CR (2255 patients).
- Multivariate Cox and logistic regression analyses to identify independent predictors of cardiac events (CE), followed by validation in 679 patients.
Main Results:
- In patients without prior MI/CR, predictors of CE included age, diabetes, metabolic equivalent (METs), ST segment depression, ejection fraction (EF), and summed stress score (C-statistic: 0.8).
- In patients with prior MI/CR, predictors of CE included age, male sex, smoking status, METs, ST segment depression, EF, and summed difference score (C-statistic: 0.8).
- The VH-RS-II demonstrated good predictive accuracy in both patient cohorts.
Conclusions:
- The VH-RS-II, derived from clinical exercise and gated SPECT variables, enables effective risk stratification for MI and CD.
- The score is applicable to patients with or without a history of MI or CR.
- VH-RS-II provides a valuable tool for personalized risk assessment in cardiology.
Objectives:
The aim of this study was to create a new Vall d'Hebron Risk Score-II (VH-RS-II) for non-fatal myocardial infarction (MI) and/or cardiac death (CD), excluding patients with coronary revascularisation (CR) during the follow-up.
Methods:
We analysed 5215 consecutive patients underwent gated single photon emission CT (SPECT); 2960 patients (age 64.2±11, male 58.1%) had no previous MI and/or CR, and 2255 patients (age 63.3±11, male 81.9%) had previous MI and/or CR. During a follow-up of 4.3±2.6 years, the cardiac event (MI and CD) was evaluated. This study was reviewed and approved by the ethics committee of our institution (number form trial register, PR(AG)168.2012). To obtain the predictor model, multivariate Cox regression analysis and multivariate logistic regression analysis were used. RS-VH-II was validated with 679 patients.
Results:
In patients without previous MI and/or CR, age (HR: 1.01; p<0.001), diabetes (HR: 2.1, p=0.001), metabolic equivalent (METs) (HR: 0.89, p=0.038), ST segment depression (HR: 1.4, p=0.011), ejection fraction (EF) (HR: 0.97, p<0.001) and summed stress score (HR: 1.2, p<0.001) were the independent predictors of CE (C-statistic: 0.8). In patients with previous MI and/or CR, age (HR: 1.06, p<0.001), male (HR: 1.9, p=0.047), smoker (HR: 1.5, p=0.047), METs (HR: 0.8, p<0.001), ST segment depression (HR: 1.4, p=0.002), EF (HR: 0.96; p<0.001) and summed difference score (HR: 1.03, p=0.06) were the independent predictors of CE (C-statistic:0.8).
Conclusion:
The VH-RS-II obtained from different clinical exercise and gated SPECT variables allow the risk stratification for MI and CD in patients with or without previous MI and/or CR in due form.
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