ST Elevation Myocardial Infarction Clinical Trial
Official title:
Early Discharge After Primary Percutaneous Coronary Intervention: A Prospective Randomized Multi-center Trial (the EDAP PCI Trial)
- When Primary percutaneous coronary intervention (PPCI) is performed expeditiously and
at a high-volume centre, it is the optimal approach for ST elevation myocardial
infarction (STEMI) . In contrast to the clarity of how to treat STEMI, there is no
clear definition for when to discharge and which patient to discharge.
- An early discharge strategy may be desired by all parties (financial health care
provider, treating physician, nurse, patient, patient's relatives)involved in STEMI.
- The main goal in our study is to test the hypothesis that an early discharge strategy
within 48-56 hours in patients with successful PPCI is as safe as in those patients who
stay longer (96-120 hours) as of a standard procedure.
- Primary percutaneous coronary intervention (PPCI) has become the optimal reperfusion
strategy for ST elevation myocardial infarction (STEMI) when the procedure is performed
expeditiously and at a high-volume centre.In contrast to the clarity of how to treat
STEMI, there is no clear definition for when to discharge and which patient to
discharge.
- It is conceivable to discharge patients with successful PPCI as early as possible,
because a hospital stay longer than needed may create undesirable outcomes in terms of
hospital infections, psychosocial reasons, adequate mobilization and patient comfort.
In many tertiary centres with a busy PPCI programme insufficient bed capacity is an
ongoing concern and threatens the continuous acceptance of new cases of acute
infarctions. In addition, it has been indicated that an early discharge policy may lead
to a substantial cost saving.
- Although much work has been done in developing and validating risk scores that identify
low risk patients, data on the implementation of early discharge strategies have been
quite limited There are 3 randomised trials investigating the possibility of early
discharge after PPCI. However, certain limitations of these studies are preventing to
implement an early discharge strategy in all-comers, particularly because of the
underrepresentation of older patients in clinical trials. The verification of this
policy is also needed in patients with multivessel disease. The first prospective
randomized trial, the PAMI II,7 is partly obsolete as major changes have been made in
PPCI with respect to devices and adjunctive medication. The other two randomized trials
were single-center pilot studies with small number of patients.
- Therefore, the above mentioned literature information warrants to test the
reproducibility of safety endpoints in a large scale multicenter trial, prior to
application of the early discharge strategy in clinical practice.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
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