User's Manual

US-ENGLISH 15
Two of the 38 Defender IV DR 612 patients in Europe (37 patients
followed for a minimum of 3 months) experienced a total of three
complications, including device failures and replacements. Fourteen
of the 38 Defender IV DR 612 patients experienced a total of 18
observations. Complications and observations are reported in Tables
1 and 2. It should be noted that a patient can have more than one
observation or complication. There were no observations or
complications in the U.S.
5.2. TABLE 1: SUMMARY OF EUROPEAN
CLINICAL COMPLICATIONS
(Including Device Failures and Replacements)
All complications, 2 of 38 Defender IV DR 612 patients in Europe
Event
# of
Patients
% of
Patients
# of
Events
Events/100
Device-
Years*
Hematoma
1
2.6
1
5.2
Ventricular lead
migration/dislodgment
2
5.3
2
10.5
* There were 228.7 device months in this study.