1.1
Impella
®
System for Use During Cardiogenic Shock
INDICATIONS (UNITED STATES)
IMPELLA
®
2.5, IMPELLA CP
®
, IMPELLA
®
5.0, AND IMPELLA
®
LD
The Impella
®
2.5, Impella CP
®
, Impella
®
5.0, and Impella
®
LD Catheters, in conjunction with
the Automated Impella
®
Controller, are temporary ventricular support devices intended for
short term use (< 4 days for the Impella
®
2.5 and Impella CP
®
, and < 6 days for the Impella
®
5.0 and Impella
®
LD) and indicated for the treatment of ongoing cardiogenic shock that occurs
immediately (< 48 hours) following acute myocardial infarction or open heart surgery as a
result of isolated left ventricular failure that is not responsive to optimal medical management
and conventional treatment measures.* The intent of the Impella
®
System therapy is to reduce
ventricular work and to provide the circulatory support necessary to allow heart recovery and
early assessment of residual myocardial function.
*Optimal medical management and conventional treatment measures include volume loading
and use of pressors and inotropes, with or without IABP
CONTRAINDICATIONS (UNITED STATES)
Patients with aortic stenosis or other abnormal aortic valve performance may be
compromised by the use of the Impella
®
Catheter. Patients with aortic valve disease
should be observed for aortic insufficiency.
The Impella
®
System is contraindicated in patients with:
•
Mural thrombus in the left ventricle
•
Mechanical aortic valve or heart constrictive device
•
Aortic valve stenosis/calcification (equivalent to an orifice of 0.6 cm
2
or less)
•
Moderate to severe aortic insufficiency (echocardiographic assessment of aortic
insufficiency graded as ≥ +2)
•
Severe peripheral arterial disease that precludes the placement of the Impella
®
System
•
Significant right heart failure
•
Combined cardiorespiratory failure
•
Presence of an atrial or ventricular sepal defect (including post-infarct VSD)
•
Left ventricular rupture
•
Cardiac tamponade
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Summary of Contents for Impella 2.5
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