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Implantable cardioverter-defibrillator

Learn about heart disease symptoms.Get more information on heart disease treatment for your health!What can you do to prevent heart disease? Prevention details here.

The ICD generator is metal and will be detected by metal detectors such as those in airports or public places with safety checks. For air travel, public events, and admission to certain areas you will need to show your wallet card to the security personnel to prevent setting off any alarms.

People with ICDs still need to follow their doctor's advice about medication, diet, and exercise.

Benefits of the ICD

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Among patients considered good candidates for an ICD, the ICD has shown to prolong life by preventing sudden death. The device provides peace of mind, relieving concerns about fainting spells and risks of death. Most patients adapt to the uncertainty of the shocks. Most patients also can resume driving.

Potential risks of the ICD

The ICD is implanted through a surgical procedure which in itself might result in death, but this is very rare.

The most common problem with the ICD is that it sometimes delivers shocks when you do not need them. Even though a shock lasts a very short time, you can usually feel it. Every shock you feel should be notified to your doctor.

Potential ICD malfunctioning can be prevented by the incorporation of audible alerts that can be programmed by your electrophysiologist. If your ICD alert goes off, you should promptly contact your doctor.

WARNING: In June 2005, certain ICD models and biventricular pacemaker-defibrillators were recalled by the manufacturer because of a circuitry flaw that prevent the devices from delivering therapeutic electrical shocks when needed. The problem may result in patient death. Two deaths are believed to be associated with the malfunction.  Although the U.S. Food and Drug Administration did not make any specific recommendations, the agency encourages patients who may have such a device to ask their health care doctor if they should have it removed or replaced. The devices affected by this recall are:

  • PRIZM 2 DR, Model 1861, manufactured on or before April 16, 2002
  • CONTAK RENEWAL, Model H135, manufactured on or before August 26, 2004
  • CONTAK RENEWAL 2, Model H155, manufactured on or before August 26, 2004

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