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CARDIOVASCULAR JOURNAL OF AFRICA • Volume 32, No 1, January/February 2021

20

AFRICA

of pacemaker for SND should not be guided by the risk of

subsequent AF alone.

This study showed no difference in the rate of device infection

between the two groups (1.9% in the AAIR versus 1.6% in the

DDDR group,

p

= 1.00). These findings are similar to those

observed in the DANPACE trial, which showed no difference

in device infection between AAIR and DDDR pacing (0.4% in

both groups,

p

= 0.98).

6

This study also showed no difference

in the need for lead/s revision (7.4% in AAIR versus 3.2% in

DDDR group,

p

= 0.42). Similar findings were observed in

the DANPACE trial where no differences in the need for lead

revision were found between the two groups (5.2% in the AAIR

versus 4.2% in the DDDR groups,

p

= 0.42).

6

The DANPACE

trial reported that subsequent lead revision was associated with a

high complication rate. This study had only six lead revisions and

no complications were noted in any of these six patients.

Study limitations

This was a retrospective study from a single institution with a

relatively small number of patients. The conclusions are therefore

hypothesis generating. However, the results reflect real-world

practice in a contemporary South African population. Larger

randomised trials using AV nodal functional testing as required

need to be adopted. The interpretation of ECGs showing AF was

made by cardiac technologists who routinely perform pacemaker

device interrogations in the device clinic. It is possible that the

technologists may not have recognised AF and may have under-

reported episodes of AF. This study has all the limitations of a

retrospective study, including missing information. It is possible

that patients in the AAIR group who developed AV block may

have been lost to follow up or died. However, the numbers of

deaths between the two groups were similar.

Conclusion

In this typical elderly populationwho presentedwith symptomatic

SND, we found functional AV nodal testing with atrial pacing at

the time of pacemaker implantation to be a useful tool to help

guide the implanter about the choice of AAIR or DDDR pacing.

Patients who underwent AAIR pacing had a low subsequent risk

of AF, AV block or lead revision. In resource-limited settings,

AAIR pacing should be considered as an alternative to DDDR

pacing. Patients with AAIR pacemakers should be counselled

regarding future symptoms of AV block, and device follow up

may be required on a six-monthly basis to rule out the need for

ventricular pacing. Randomised trials are required to further

define the role of AV nodal functional testing.

We acknowledge the Department of Medicine, University of Cape Town

for their enormous support, as well as all the staff in the Medical Records

Department and Catheterisation Laboratory pacing unit at GSH for provid-

ing relevant documents, which were used for data collection.

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