Unstable Angina Clinical Trial
Official title:
Appropriateness of Coronary Angioplasty in PAtients With isCHEmic Heart Disease
An observational, retrospective, multicenter, blinded adjudication study to evaluate the
clinical appropriateness of Percutaneous Coronary Intervention (PCI) indication and
execution in patients with stable Coronary Artery Disease (CAD) and in patients with acute
coronary syndrome without ST-segment elevation (NSTE-ACS) (ratio 4:1). Half of the included
patients will be diabetic. Also the implementation of selected, key guideline
recommendations will be examined.
At least 400 patients will be retrospectively selected among 22 Catheterization Laboratories
in Italy in the region of Lombardia and Veneto.
This study will be conducted in compliance with Good Clinical Practices (GCP) including the
Declaration of Helsinki and all applicable regulatory requirements.
A strategy based on early invasive coronary angiography followed by revascularization is the
most effective treatment of patients with acute coronary syndrome, especially in those with
ST-segment elevation (STE-ACS). In patients with acute coronary syndrome without ST-segment
elevation (NSTE-ACS), an early invasive strategy is associated with a reduction in cardiac
death and myocardial infarction in patients at higher risk. In stable coronary artery
disease rather no data so convincing. The undeniable evolution of techniques of PCI has been
accompanied by a parallel progress of medical therapy and also from increased awareness,
both cardiologists and patients, the importance of the control of coronary risk factors.
European Society of Cardiology Guide give precise indications (but often ignored) on the use
of PCI or coronary artery bypass grafting according to the extent of coronary artery disease
and the site of injury . However, especially in patients with NSTE-ACS often we limit
ourselves to dilate the culprit stenosis, leaving untreated other injuries that underlie
large myocardial territory, that is, by configuring an incomplete revascularization
framework. The calculation of the SYNTAX score residual (that is, what remains after
percutaneous revascularization procedure) allows to objectively verify the incompleteness of
PCI treatment, which correlates with the outcome in the patient's distance . Moreover, in
case of equivocal stenosis, especially in patients with stable coronary disease, large
should be the use of a functional assessment using the calculation of the Fractional Flow
Reserve (FFR).
This could indicate that the increase of the number of invasive diagnostic tests does not
increase the number of patients with coronary artery disease extended, in which is usually
indicated a surgical revascularization. So to identify patients at higher risk, may be
enough specific investigations and conducted selectively.
The purpose of the pilot study APACHE is to assess the appropriateness of indication and
appropriateness of execution of a sample carried out PCI in patients with stable coronary
artery disease and in patients with NSTE-ACS (in the ratio 4: 1). As such, the APACHE be
considered a quality improvement initiative.
Retrospective observational study, multicenter. The study population will consist of 20
cases of PCI per center (then about 400 PCI in total) selected randomly within the center of
the case studies in the previous approval of the study. Of these 16 will be patients with
stable coronary artery disease (including 8 with diabetes mellitus in medical therapy) and 4
will be patients with NSTE-ACS (4: 1 ratio).
Patients with a history of coronary artery bypass are excluded. The series will consist of
patients in whom the procedure was carried out in the previous year to a declaration of
participation in the survey and in any case after the publication of the document. There
have been no previous analysis of this type in Italy and is therefore not known what is the
rate of inappropriateness for PCI procedures in stable patients. It is not possible
therefore to perform a calculation of sample size. However, the investigators believes that
for a pilot analysis, an initial sample of 400 PCI procedures, analytically considered, is
sufficient to verify the magnitude of the problem in the Italian Catheterization
Laboratories.
The investigators anticipate the participation of about 20 centers in total between
Lombardia and Veneto italian regions. The study will have an approximate duration of about 2
years.
The data to be collected will be different in patients with nSTE - ACS compared to patients
with stable coronary artery disease. As an initiative of quality improvement, and according
to extensive international literature on the subject, will not be requested individual
informed consent to selected patients but only the approval of the Ethics Committee of the
Center Coordinator. Patient data will be de-identified and used only in the aggregate and
all individual sensitive information (name, phone, address) will be erased.
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Observational Model: Cohort, Time Perspective: Retrospective
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