From the Guidelines
To estimate the risk factor weighted clinical likelihood, I recommend using a structured approach that combines patient-specific risk factors with clinical presentation, as this method has been shown to provide a more reliable and unbiased estimation of prognosis compared to clinical judgement alone 1. When estimating the risk factor weighted clinical likelihood, it is essential to consider the patient's characteristics, clinical signs, and laboratory tests.
- Identify established risk factors such as age, family history, comorbidities, and lifestyle factors, and assign each a weighted score based on validated clinical tools or guidelines.
- Assess clinical symptoms and findings, and assign appropriate weights.
- Combine these scores to calculate an overall risk probability that can guide clinical decision-making. For implementation, use condition-specific risk calculators when available, such as the ASCVD risk score for cardiovascular disease, as mentioned in the study by 1. However, it is crucial to note that the quality of evidence for the prediction of certain outcomes, such as foot ulcer-related outcomes, is weak, and the applicability of the accuracy of a classification system in predicting individual patient outcomes is poor 1. Therefore, it is recommended to use a structured approach with caution and consider the limitations of the available evidence, prioritizing the use of validated clinical tools and guidelines to estimate the risk factor weighted clinical likelihood. In the absence of formal tools, create a simple scoring system where major risk factors receive higher weights than minor factors, and document both the individual risk factors and the composite score in the patient record. This approach works because it systematically incorporates multiple variables that affect disease probability, reducing cognitive bias and improving diagnostic accuracy, as supported by the study 1.
From the Research
Estimating Risk Factor Weighted Clinical Likelihood
To estimate the risk factor weighted clinical likelihood, we need to consider the impact of various lipid-lowering therapies on cardiovascular outcomes. The following points summarize the key findings:
- The use of ezetimibe and PCSK9 inhibitors in addition to statin therapy can reduce the risk of non-fatal myocardial infarction (MI) and stroke in adults with very high or high cardiovascular risk 2.
- Among adults with very high cardiovascular risk, adding PCSK9 inhibitor to statins can reduce MI (16 per 1000) and stroke (21 per 1000) with moderate to high certainty 2.
- Adding ezetimibe to statins can reduce stroke (14 per 1000), but the reduction of MI (11 per 1000) may not reach the minimal important difference (MID) 2.
- In adults with high cardiovascular risk, adding PCSK9 inhibitor to statins can reduce MI (12 per 1000) and stroke (16 per 1000) with moderate certainty 2.
- The combination of ezetimibe, PCSK9 inhibitor, and statin may reduce stroke (11 per 1000) and MI (9 per 1000), but the reduction of MI may not reach MID 2.
Key Considerations
Some key considerations when estimating the risk factor weighted clinical likelihood include:
- The level of cardiovascular risk, with very high or high risk patients being more likely to benefit from additional lipid-lowering therapies 2, 3, 4, 5, 6.
- The use of statins as first-line therapy, with ezetimibe and PCSK9 inhibitors being considered as add-on therapies for patients who are not achieving treatment goals on statins alone 3, 4, 5, 6.
- The potential benefits and risks of each therapy, including the reduction of LDL-C levels and the risk of major adverse cardiovascular events (MACE) 2, 3, 4, 5, 6.
Lipid-Lowering Therapies
The following lipid-lowering therapies have been studied for their impact on cardiovascular outcomes:
- Statins: first-line therapy for reducing LDL-C levels and preventing MACE 3, 4, 5, 6.
- Ezetimibe: reduces intestinal absorption of cholesterol and can be used in combination with statins to further reduce LDL-C levels 2, 3, 4, 6.
- PCSK9 inhibitors: monoclonal antibodies that inactivate the liver proprotein convertase subtilisin kexin 9 (PCSK9) and can be used to reduce LDL-C levels in patients with very high or high cardiovascular risk 2, 3, 4, 5, 6.