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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 26, No 4, July/August 2015

186

AFRICA

more infections were found in the new pacemaker group (7%)

than in the re-used pacemaker group (2%). Kantharia

et al

.

25

found no significant complications in an Indian study cohort

of 53 patients who received cadaveric donated resterilised

pacemakers over a mean follow up of 661 days.

Panja

et al

.

26

found no difference in infection rates between the

new pacemaker group and cadaver-donated re-used pacemakers.

However, higher rates of infection were found on infected

re-sterilised devices that were implanted in the same patient,

which were taken out and implanted on the opposite side.

They attributed this higher infection rate to haematogenous

or lymphatic spread from the previously infected pocket.

26

Rosengarten

et al

.

27

also found no significant difference in major

pacemaker-related complications and reported that re-use of

devices is cost effective.

Pavri

et al

.,

24

in a retrospective, single-centre cohort study of

re-sterilised ICDs found no device-related infections, and 60.4%

re-used ICDs delivered life-saving shocks. Baman

et al

.,

28

in a

meta-analysis of 18 studies, found no significant difference in

infection rates between the new device group and the re-used

device group, but much higher device malfunction was associated

with re-used devices compared to new devices. This malfunction

was attributed to abnormality in the set screws.

28

In a recent study, Nava

et al

.

23

found no significant difference

in infection rates between re-used and new devices, although

more infections were found in the new device group. They also

found more device malfunction in the re-use device group, which

was similar to the above studies, and the fault was also attributed

to faulty pacemaker screws.

23

Device infection is thought to be associated with mortality

rates between 2.6 and 18%.

12-14

However studies that examined

this issue showed no significant difference in infection or

mortality rates between re-used and new device implantation.

14-22

In our study we did not compare mortality rates between the

two groups because of the selection bias of those who received

a re-used pacemaker.

From the findings of this study and also acknowledging its

limitations, pacemaker and ICD re-use is feasible and safe. It is

a reasonable option for those who cannot afford new devices,

provided that proper selection and sterilisation measures of

re-used devices are followed. In the developing world, where

there are major resource constraints, this option should be

explored for the benefit of those suffering from symptomatic

bradyarrhythmias and life-threatening tachyarrhythmias.

We acknowledge several limitations of our study. First, this

was a retrospective study with a small sample size of cases with

re-used pacemakers and ICDs. Second, the follow-up period of

patients with re-used devices was relatively short, with a median

period of 15 months, with a significant number of patients who

died within three months of device insertion. Finally, the patients

who were selected for re-used pacemakers had significant

co-morbidities, which were associated with a shortened life-span.

These factors may limit the generalisability of the study, and call

for appropriate prospective studies to answer this question.

Conclusion

Pacemaker and ICD re-use is feasible and safe in the short term

(i.e. over months) provided that the devices for re-use are selected

carefully and proper sterilisation methods are followed. Re-used

pacemakers and ICDs are a realistic option for patients with

co-morbidities who live in developing countries where there is

limited access to pacemakers and ICDs.

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