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Vol 41 # 3 September 2009 - Kma.org.kw

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<strong>September</strong> <strong>2009</strong><br />

KUWAIT MEDICAL JOURNAL 211<br />

Table 1: Baseline clinical characteristics of patients with ICD lead failure<br />

Pt. No.<br />

Age<br />

Sex<br />

Diagnosis<br />

LVEF %<br />

Indication<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

7<br />

8<br />

27<br />

62<br />

62<br />

42<br />

14<br />

55<br />

58<br />

66<br />

M<br />

F<br />

M<br />

M<br />

F<br />

M<br />

F<br />

M<br />

Idiopathic VT/VF, SCD<br />

DCM , HF<br />

Ischemic CMP, S/P CABG<br />

Ischemic CMP, S/P CABG<br />

Long QT<br />

Ischemic CMP<br />

DCM<br />

Ischemic CMP<br />

65<br />

25<br />

30<br />

25<br />

65<br />

35<br />

23<br />

20<br />

Idiopathic VT/VF Survivor of SCD<br />

Primary prevention<br />

Syncope and inducible VT<br />

Primary prevention<br />

Primary prevention<br />

Spontaneous VT<br />

Primary prevention<br />

Primary prevention<br />

M = Male, F = Female, VT= Ventricular tachycardia, VF= Ventricular fibrillation, Pt. = Patient, SCD- Sudden Cardiac Death, DCM<br />

= Dilated cardiomyopathy, HF = Heart Failure, CABG = Coronary Artery Bypass Graft, LVEF = Left Ventricular Ejection Fraction,<br />

CMP = Cardiomyopathy<br />

warn physicians. Lead malfunction is defined as<br />

lead failure that requires lead replacement. Lead<br />

failure is diagnosed if noise oversensing is present<br />

that is not related to cardiac cycle, lead impedance<br />

is out of normal range and/or sensing failure<br />

evidenced a drop in ventricular sensing signal less<br />

than two millivolt or lead fracture is seen on X-ray.<br />

Eight patients were included after having signed an<br />

informed consent form. This study was approved<br />

by the local ethical committee.<br />

RESULTS<br />

A total of eight defibrillator leads failed during<br />

follow-up. Lead failure was diagnosed at a mean time<br />

of 47.1 ± 29.1 months (range: 16 - 60.1 months) after<br />

ICD implantation. Six patients had a defibrillator<br />

device and two patients had bivent-ICD. Baseline<br />

clinical characteristics of patients with lead failure<br />

are listed in Table 1. There were five male and three<br />

female patients with a mean age of 48.3 ± 18.9 years<br />

(range: 14 - 66 years) at the time of diagnosis of lead<br />

failure. Four patients had the device implanted as<br />

primary prevention of sudden cardiac death due<br />

to ischemic cardiomyopathy and one for long QT<br />

syndrome. One patient had the device implanted for<br />

syncope and inducible ventricular tachycardia on<br />

electrophysiological study. The other two patients<br />

had the device implanted after resuscitation from<br />

spontaneous ventricular tachycardia / ventricular<br />

fibrillation. The affected lead models are listed<br />

in Table 2. All patients except one had the leads<br />

implanted through left subclavian venous access.<br />

Diagnosis of lead failure was made by clinical<br />

presentation as inappropriate shocks in four<br />

patients due to noise oversensing on a ventricular<br />

electrogram during sinus rhythm (Fig. 1A and 1B)<br />

and was discovered during routine follow-up in the<br />

remaining four patients who were asymptomatic.<br />

Routine device testing revealed high lead impedance<br />

out of normal range (Fig. 2A), noise registration on<br />

stored electrogram and drop in ventricular sensing<br />

signals in two patients (Fig. 2B). In other two patients<br />

routine testing revealed increased lead pacing<br />

threshold and sudden increase in lead impedance<br />

out of normal range without noise oversensing (Fig.<br />

2C). None of the patients had radiographic signs<br />

of lead fracture except patient no. 8 in whom the<br />

lead failure was due to Twiddler’s syndrome. All<br />

patients underwent new lead implantation without<br />

complications.<br />

DISCUSSION<br />

The annual rate of ICD lead failure requiring<br />

intervention increases with time and reaches<br />

Table 2: Clinical presentation and follow-up of patients with ICD lead failure<br />

Pt. No. Venous Site Lead Model ICD Implant Implant<br />

to fracture<br />

(Months)<br />

1<br />

2<br />

3<br />

4<br />

5<br />

6<br />

7<br />

8<br />

Left subclavian<br />

Left subclavian<br />

Left subclavian<br />

Left subclavian<br />

Left subclavian<br />

Left subclavian<br />

Right subclavian<br />

Left subclavian<br />

Medtronic 6947<br />

Medtronic 6949<br />

Medtronic 6945<br />

Medtronic 6949<br />

Medtronic 6943<br />

Medtronic 6944<br />

Medtronic 6948<br />

Guidant 0185<br />

Single Chamber Device<br />

Biventricular device<br />

Single Chamber Device<br />

Dual chamber device<br />

Single Chamber Device<br />

Dual chamber device<br />

Biventricular Device<br />

Single Chamber Device<br />

89<br />

16<br />

85<br />

20<br />

49<br />

54<br />

48<br />

16<br />

Clinical presentation<br />

at follow-up<br />

High impedance sensing failure, noise<br />

over sensing<br />

Inappropriate shocks<br />

Inappropriate shocks<br />

High impedance<br />

Inappropriate shocks<br />

High impedance<br />

Inappropriate shocks<br />

High impedance and loss of capture<br />

(Twiddler’s Syndrome)<br />

Pt. = Patient, ICD = Implantable cardioverter-defibrillator

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