Key result
The development of single-pin DF4 and IS4 lead connectors, along with new labeling guidelines, has simplified operative procedures and reduced errors during device implantation.
The evolution to single-pin DF4 and IS4 connectors has simplified CIED implantation procedures and reduced connection errors.
Answers are grounded in this paper and cite their sources.
May reduce CIED implantation errors with DF4/IS4 connectors; extends connector standardization literature but leaves open prospective validation.
Cardiac implantable electronic devices (CIEDs) play a vital role in the management of cardiac rhythm disturbances. The devices are comprised of two primary components: a generator and lead joined by a connector. Original pacemaker lead connectors were created de novo at the time of implantation or replacement and were very unreliable. With the development of new lead designs, creation of a standard connector configuration, the IS-1 connector became mandatory. Similar connector development also occurred with the advent of the implantable cardioverter defibrillator (ICD), resulting in creation of the high voltage standard: the DF-1 connector. Differing from a pacemaker lead, the ICD lead connector requires one IS-1 connector and one or two DF-1 connectors, resulting in a large cumbersome lead connector and generator header block. Recently, a revolutionary quad pole single plug connector standard has been approved for market release. These are the single-pin DF4 and IS4 lead connectors that carry low- and high-voltage poles or all low-voltage poles, respectively. These connectors, together with new labeling guidelines, have simplified operative procedures and reduced errors, when mating lead connectors into the generator's connector block.
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Mond et al. (2013) conducted a review in Cardiac rhythm disturbances. Cardiac implantable electronic device connectors (DF4 and IS4) was evaluated. The development of single-pin DF4 and IS4 lead connectors, along with new labeling guidelines, has simplified operative procedures and reduced errors during device implantation.
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