Leadless Pacemaker Patients Less Likely to Experience Complications, Major U.S. Study Shows


Pacemakers that don’t use wires to connect the device to the heart are successfully reducing the number of short-term and mid-term complications patients experience, a study in the United States has found.

The findings of the research, led by Ohio-based Cleveland Clinic,appeared in the journal Heart Rhythm. The study compared patient outcomes for those fitted with new ‘leadless’ pacemakers compared with more conventional ‘transvenous’ designs.

Lead author Dr. Daniel Cantillon, M.D., research director for Cardiac Electrophysiology and Pacing at Cleveland Clinic, and a consultant for Abbott and Boston Scientific, said: “The data from this study is encouraging, and we expect complications from leadless pacemakers to continue to decline as the technology improves and physicians gain experience implanting these devices.

“While this research shows benefit for leadless pacing, we must keep in mind that the field is still too young to compare the long-term results of this technology, the implications of which will not be fully understood for at least another decade.”

More than one million pacemakers are implanted annually worldwide, providing electrical stimulation to regulate a patient’s heartbeat.Conventional models are surgically placed under the skin of the chest, and connected to the heart via a wire that stretches from the shoulder vein to the heart. These leads – and their surgical implantation – are the most common source of complications among pacemaker recipients as a whole, occurring in up to 12 percent of this group, according to previous research.

Leadless pacemakers, by contrast, do not need wires. These small, self-contained devices – about one-tenth of the size of a traditional pacemaker – are placed directly into the heart using a catheter that is carried from the leg to the heart via the thigh’s femoral vein.The first leadless pacemaker was introduced in 2014 and approved by the U.S. Food & Drug Administration (FDA) two years later.

The new multicenter study compared short- and mid-term complications between 718 patients receiving the Nanostim leadless pacemaker and 1,436 patients with conventional (transvenous) pacemakers. Leadless pacemaker patient data was taken from the LEADLESS II trial, a prospective, nonrandomized, multicenter clinical trial.

Transvenous patient data were obtained from Truven Health MarketScan claims databases for patients implanted with single-chamber pacemakers between April 2010 and March 2014 and more than one year of pre-implant enrollment data. Statistical methods were used to match patients between the two groups to compare the outcomes of a leadless versus traditional pacemaker with other key clinical variables being equal.

At one month, the study found that patients receiving one type of leadless pacemaker (Nanostim) overall had fewer complications (5.8 percent versus 9.4 percent). Leadless pacemakers eliminated lead and pocket complications, including infection. By comparison, complications among traditional pacemaker recipients included lead complications (3.62 percent), pocket complications (0.42 percent) and infection (1.74 percent).

There were no significant differences between the groups in regard to rates of vascular complications, electrode dislodgement,or generator complications.However, the study did find that those receiving leadless pacemakers had an increased risk of developing pericardial effusion – bleeding between the heart and the sac that surrounds it – of 1.53 percent versus 0.35 percent. These complications were uncommon but serious, and sometimes required surgery.

Beyond one month and up to 18 months of follow-up, leadless patients continued to experience overall fewer complications than transvenous patients (0.56 percent versus 4.94 percent). In the conventional pacemaker group, a number of complications were wholly absent from the leadless group, including lead-related complications, electrode dislodgement, infection, and pocket complications.

Company: Cleveland Clinic

Cleveland Clinic is a nonprofit multispecialty academic medical center that integrates clinical and hospital care with research and education. Located in Cleveland, Ohio, it was founded in 1921 by four renowned physicians with a vision of providing outstanding patient care based upon the principles of cooperation, compassion and innovation. Cleveland Clinic has pioneered many medical breakthroughs, including coronary artery bypass surgery and the first face transplant in the United States. U.S. News & World Report consistently names Cleveland Clinic as one of the nation’s best hospitals in its annual “America’s Best Hospitals” survey.

Among Cleveland Clinic’s 51,000 employees are more than 3,500 full-time salaried physicians and researchers and 14,000 nurses, representing 140 medical specialties and subspecialties. Cleveland Clinic’s health system includes a 165-acre main campus near downtown Cleveland, 10 regional hospitals, more than 150 northern Ohio outpatient locations – including 18 full-service family health centers and three health and wellness centers – and locations in Weston, Fla.; Las Vegas, Nev.; Toronto, Canada; Abu Dhabi, UAE; and London, England. In 2016, there were 7.1 million outpatient visits, 161,674 hospital admissions and 207,610 surgical cases throughout Cleveland Clinic’s health system. Patients came for treatment from every state and 185 countries.

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