CardiologyOnline.net

Cardiology Xagena

Xagena Mappa
Medical Meeting
Xagena Salute
Dermabase.it

ESC 2019 - Aspirin should not be recommended for healthy people over 70


Low-dose Aspirin ( Acetylsalicylic acid ) does not prolong disability-free survival of healthy people over 70, even in those at the highest risk of cardiovascular disease.
The results of the ASPREE trial were presented at ESC Congress 2019 together with the World Congress of Cardiology.

European guidelines on the prevention of cardiovascular disease ( CVD ) do not recommend Aspirin for individuals free from CVD due to the increased risk of major bleeding.
This advice was subsequently supported by results in moderate risk patients ( ARRIVE ), diabetic patients ( ASCEND ), and in people over 70 ( ASPREE ) which has demonstrated that modest reductions in CVD risk were outweighed by the increased bleeding hazard.

The primary finding from the ASPREE randomised trial was that in people aged 70 years or over with no known cardiovascular disease, there was no effect of 100 mg of daily Aspirin on the composite primary endpoint of disability-free survival ( defined as those not reaching a primary endpoint of dementia or persistent physical disability or death ).
The primary endpoint was chosen to reflect the reasons for prescribing a preventive drug in an otherwise healthy elderly population.

This analysis has examined whether the results for the primary endpoint of disability-free survival might vary by the baseline level of CVD risk.
Analyses were also conducted for the secondary endpoints of all-cause mortality, major haemorrhage, and prevention of CVD ( defined as fatal coronary heart disease, nonfatal myocardial infarction, fatal or nonfatal stroke, or hospitalisation for heart failure ).

The researchers calculated ten-year CVD risk probabilities at baseline for the 19,114 ASPREE participants using the Framingham score ( up to 75 years ) and the atherosclerotic cardiovascular disease ( ASCVD ) pooled cohort risk equations ( up to 79 years ) and divided them into thirds.
As there are no CVD risk scores available beyond the age ranges specified in the equations, they also classified participants according to the presence of 0 to 1, 2 to 3, or more than 3 CVD risk factors.
Overall rates of disability-free survival, mortality, major bleeding and cardiovascular disease were examined for each risk group and outcomes were compared for those treated with Aspirin or placebo.

For participants in the lowest third of CVD risk, by both Framingham and ASCVD scores, there was no disability-free survival or cardiovascular benefit from Aspirin. This group also had the highest likelihood of bleeding.

In contrast, those in the highest third of CVD risk, by both Framingham and ASCVD scores, had significantly lower CVD event rates on Aspirin with similar rates of bleeding.
Hazard ratios for CVD reduction with Aspirin version placebo were 0.72 ( 95% confidence interval [ CI ] 0.54-0.95 ) for the group classified as high risk by the Framingham score and 0.75 ( 95% CI 0.58-0.97 ) for those defined as high risk by the ASCVD equations.

However, this reduction in CVD did not translate to a significantly improved disability-free survival.
Hazard ratios for disability-free survival with Aspirin versus placebo were 0.86 ( 95% CI 0.62-1.20 ) for the group designated high risk by the Framingham score and 0.89 ( 95% CI 0.62-1.28 ) for those considered high risk by the ASCVD equations.

In conclusion, the findings emphasise that the risk-benefit trade-off for Aspirin use in healthy older men and women varies across levels of cardiovascular risk. It also indicates that the reduction in CVD events in the highest risk groups using current stratification methods does not identify individuals in whom this advantage translates into longer disability-free survival.
Based on the results of the main ASPREE trial, daily low-dose Aspirin cannot be recommended in healthy people over 70 - even in those at the greatest CVD risk. ( Xagena )

Source: European Society of Cardiology - ESC Congress 2019

XagenaMedicine_2019



Indietro