Software Downloaded During Office Visits Could Cut Risk of ICD Shocks

Study highlights:

-- In a study of patients with implantable cardioverter defibrillators (ICD), downloadable software updates cut the risk of unnecessary shocks in half.

-- In the future, software upgrades may offer patients other ICD improvements without implanting new devices.

DALLAS, Sept. 27 /PRNewswire-USNewswire/ -- Software downloaded during a routine office visit cuts the risk of inappropriate shocks by 50 percent for patients with implantable cardioverter defibrillators (ICD), according to research reported in Circulation: Journal of the American Heart Association.

(Logo: http://www.newscom.com/cgi-bin/prnh/20100222/AHSALOGO)

(Logo: http://photos.prnewswire.com/prnh/20100222/AHSALOGO)

"Hundreds of patients have been saved from unnecessary shocks by software that is safe and can be painlessly downloaded in one minute during a standard defibrillator check," said Charles D. Swerdlow, M.D., lead author of the study and a cardiac electrophysiologist at the Cedars Sinai Heart Institute in Los Angeles and Clinical Professor of Medicine at the University of California, Los Angeles.

Implanted defibrillators monitor the heart's electrical activity and deliver a shock to reset the heart to a normal rhythm if the pulse becomes too rapid and unable to sustain life. But if the lead wires that connect the device to the heart muscle break, the defibrillator may interpret rapid electrical signals caused by the fracture as coming from the heart — delivering one or more unnecessary and often painful shocks, Swerdlow said.

Although all leads can fracture, the most widely sold model — the Sprint Fidelis®, used with many different defibrillator designs and removed from the market in October 2007 — had a much higher rate of breaks and inappropriate shocks. Downloadable Lead Integrity Alert (LIA) software monitors Fidelis leads for evidence of suspicious electrical signals, alerting the patient and recalibrating the device to make a shock less likely if a fracture is suspected, Swerdlow said.

"You don't wait to upgrade your operating system until you buy a new home computer, but prior to this people only got new software for defibrillators when the batteries ran low and they underwent surgery to implant a new device," Swerdlow said.

In the prospective study, researchers compared the experience of patients prior to their undergoing surgery to replace fractured leads, including 213 who had received standard daily monitoring and 213 monitored with the addition of the downloadable LIA.

The researchers found:

• One or more inappropriate shocks were delivered to 70 percent of the patients who received standard monitoring, but only 38 percent of the patients with LIA (a 46 percent reduction in risk).
• Five or more inappropriate shocks were delivered to 50 percent of the patients who received standard monitoring, but only 25 percent of patients with LIA (a 50 percent reduction in risk).
• 72 percent of patients with LIA had no inappropriate shock, or had at least three days warning prior to an inappropriate shock, whereas this was observed in only 50 percent of those who received standard monitoring.

"One year after LIA was released for download by physicians into patients' ICDs, 30 percent of patients undergoing remote monitoring had not had the software downloaded," Swerdlow said. "If your doctor hasn't done it yet, it can still be downloaded safely and painlessly."

The study is the first to demonstrate that the downloadable LIA software dramatically decreases the chance of unnecessary shocks in real patients. The results reveal the possibility of making other improvements to devices while they're implanted, researchers said.

About 114,000 inpatient implantable defibrillators procedures were performed in 2006 in the United States, according to the American Heart Association.

Co-authors are: Bruce D. Gunderson, M.S.; Kevin T. Ousdigian, M.S.; Athula Abeyratne, Ph.D.; Haresh Sachanandani, M.S.; and Kenneth A. Ellenbogen, M.D. Author disclosures are on the manuscript.

Medtronic, Inc., an ICD manufacturer, funded the study.

Statements and conclusions of study authors published in American Heart Association scientific journals are solely those of the study authors and do not necessarily reflect the association's policy or position.  The association makes no representation or guarantee as to their accuracy or reliability.  The association receives funding primarily from individuals; foundations and corporations (including pharmaceutical, device manufacturers and other companies) also make donations and fund specific association programs and events.  The association has strict policies to prevent these relationships from influencing the science content.  Revenues from pharmaceutical and device corporations are available at www.americanheart.org/corporatefunding.

NR10 – 1124 (Circ/Swerdlow)

Additional resources:

• Implantable Cardioverter Defibrillator (ICD) Animation
• Downloadable stock footage, animation, and our image gallery are located at www.heart.org/news under Multimedia.
• Stay up to date on the latest news from American Heart Association scientific meetings, including Scientific Sessions 2010, by following us at www.twitter.com/heartnews. We will be tweeting from the conference using hashtag #AHA10News.

SOURCE American Heart Association