Background: In 1998, a permanent registry of myocardial infarction was deve
loped in the Liege area (Belgium) to provide updated, exhaustive and valida
ted data on the morbidity and mortality from cardiovascular causes, to defi
ne the patients' profile, to identify myocardial infarction therapeutic str
ategies and to complete and make comparisons with data collected in other p
arts of the country through methodologically identical registers.
Methods: All acute coronary events lethal or non lethal among individuals f
rom both genders aged from 25 to 69 years and living in the area were regis
tered according to the methodology developed for the MONICA project (Multin
ational Monitoring of Trends and Determinants in Cardiovascular Diseases) o
f WHO. The three main selected data sources were: death certificates, gener
al practitioners and cardiologists, hospitals. The events were categorised
according to symptoms, cardiac enzymes, electrocardiogram, history of chron
ic ischaemic heart disease and necropsy findings.
Results: The coronary-event rates were 283/100,000 in men and 102/100,000 i
n women. The case fatality rate, 28 days after the onset of the symptoms, w
as 30.6% for men and 36.2% for women, and 77.5% of deaths occurred in the f
irst 24 hours after the onset of the symptoms.
Conclusion: The development of a myocardial infarction register at a region
al level requires the involvement of all health professionals dealing with
that pathology. Such register has valuable public health interests, providi
ng exhaustive and validated data on the pathology and its evolution as well
as useful information for improving therapeutic strategies and developing
adapted preventive measures.