American Heart Association calls for treating women with coronary heart disease with interventional procedures commonly used with men
Physicians need to diagnose women with coronary
heart disease at an earlier stage and provide the same interventional
procedures that are commonly used for male patients, according to
a statement issued by the American Heart Association (AHA) and published
in the February 1st issue of Circulation.
The AHA addressed issues affecting care of
women with cardiovascular disease at an event called “Go red for
women,” held in New York City with a panel of experts. The scientific
statement released at the meeting calls for the need to improve
treatment by obtaining earlier diagnosis and referring women for
currently available interventional cardiovascular therapies.
The AHA statement addresses the rising rate
of mortality in women with cardiovascular disease, which is actually
higher than the death rate for men with the disease. Currently,
33 million American women suffer from cardiovascular disease, claiming
489,000 lives every year, compared with 31 million men with 432,245
deaths. More specifically, 5.9 million US women will have an adverse
coronary event this year, resulting in approximately 250,000 deaths.
Despite these statistics, and the known benefits of interventional
procedures such as angioplasty and stenting in reducing myocardial
infarctions, only one third of all patients treated with interventional
procedures are female.
“As proven in clinical trials time after time, interventional procedures
such as percutaneous coronary interventions are safe and effective
treatments for cardiovascular disease,” said Alexandra Lansky, MD,
lead author of the statement, Director of the Women’s Cardiovascular
Health Initiative at the Cardiovascular Research Foundation, and
director of clinical services for Interventional Cardiology at New
York-Presbyterian Hospital/Columbia. “In fact, the outcomes in women
and men continue to improve and it is now time to translate our
findings into real-world practice and start referring more women
to these life-saving procedures.”
“It used to be thought that the outcomes for women undergoing percutaneous
interventions were not favorable, but that is no longer true,” said
Lansky. “The current data clearly show that these minimally invasive
procedures are safe and effective, and in high risk patients, can
reduce subsequent heart attacks and save lives.”
Female cardiovascular patients tend to have a higher risk profile
compared to men when they seek medical attention. They have smaller
coronary arteries, higher prevalence of diabetes, are generally
older, and have more hypertension.
“It is also important to point out that women suffering from heart
attacks typically delay seeking emergency medical attention. These
delays lead to deaths or other lasting complications,” said Lansky.
“When interpreting any clinical trial data it is always important
to examine all risk factors and attributes of a certain patient
population. A closer look at known clinical data reveals that it
is these risk factors, and not gender per se, that is responsible
for the poorer results in women.”
In the new statement, the panel identified three areas of improvement
for outcomes in female cardiovascular patients. First, referral
for earlier treatment upon diagnosis needs to be improved. Second,
further research needs to be conducted to optimize therapy for patients
with diabetes and small vessel coronary disease − two conditions
extremely prevalent in the female population. Finally, the panel
called for more refined treatment pathways and strategies for women
who have ST-elevation myocardial infarction, a type of heart attack
where mortality rates and bleeding risk remain significantly higher
than in men.
“Our statement however is based on the gender-specific evidence
currently available to us as healthcare professionals,” said Lansky.
“To truly improve outcomes in women we need to recruit more female
patients into future clinical trials, as female representation in
previous percutaneous intervention trials has been 38 percent at
best, and often closer to just one quarter of the studied populations.”
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