Electrophysiology Devices Market Rising in United States | Fortune Business Insights

The global electrophysiology devices market size is projected to reach USD 9.71 billion by 2027, exhibiting a CAGR of 10.8% during the forecast period. The COVID-19 pandemic is expected to stoke the adoption of these devices owing to its close linkage with heart conditions, postulates Fortune Business Insights™ in its report, titled “Electrophysiology Devices Market Size, Share & COVID-19 Impact Analysis, Type (Ablation Catheters, Diagnostic Catheters, Mapping Systems, Accessories, and Others), By Application (Atrial Fibrillation, Supraventricular Tachycardia (SVT), Ventricular Tachycardia, and Others), By End User (Hospitals & ASCs, and Specialty Clinics & Diagnostic Centers), and Regional Forecast, 2020-2027”.

According to a research study published by the American Heart Association (AHA), in Wuhan, the epicenter of the coronavirus pandemic, 16.7% of the hospitalized COVID patients and 44.4% in the intensive care unit were suffering from arrhythmias. The report from Wuhan also revealed that patients in recovery experienced ventricular fibrillation and late myocardial dysfunction. In July 2020, the University of Edinburgh’s survey of heart scans of over 1,000 COVID patients from 69 countries showed that 55% of them displayed varying degrees of heart damage and nearly 13% with no previous heart condition developed severe cardiac disease. With heart disease being a high risk factor for COVID-19, the demand for electrophysiology devices is set to skyrocket during 2020.

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North America

United States, Canada and Mexico

Europe

Germany, UK, France, Italy, Russia and Turkey etc.

Asia-Pacific

China, Japan, Korea, India, Australia, Indonesia, Thailand, Philippines, Malaysia and Vietnam etc.

South America

Brazil, Argentina, Columbia etc.

Middle East & Africa

Saudi Arabia, UAE, Egypt, Nigeria and South Africa

 Boston Scientific Introduces Novel DIRECTSENSE™ Technology

Boston Scientific, the leading American medical devices manufacturer, launched a first-of-its-kind tool for monitoring the effect of radiofrequency energy delivered during cardiac ablation procedures called DIRECTSENSE™ Technology in June 2020. Cleared by the US Food and Drug Administration (FDA) in April, the next-gen technology is currently the only device that can detect and monitor changes in local electrical resistance occurring upon the application of the INTELLANAV™ ablation catheter. This will enable physicians and health workers to accurately measure the effect of therapy during an ablation, a delicate procedure which is conducted on the heart to eliminate heart tissue that is causing abnormal rhythms in the heart.

Rising Instances of Product Recalls to Impede Market Growth

Electrophysiology devices such as pacemakers and ablation catheters are designed to prevent adverse events in heart patients. Some of these products, however, have either been unable to deliver the desired results or have not conformed to regulatory norms or both, forcing companies to recall them from the market. The worrying part is the increasing frequency of such recalls. For example, in July 2017, the US FDA directed Sterilmed to recall its unexpired EP Ablation Cables as they did not adhere to FDA’s premarket review and approval norms. In February 2019, Stryker voluntarily called back some of the Lifepak defibrillators in response to reports of an issue in the devices which was causing them to malfunction and not deliver the required therapy. A more recent incident involved Medtronic, whose pacemaker had battery and wire defects that led to serious side effects in patients, compelling the FDA to order the company to recall its product in February 2020. These instances are expected to hamper the growth of this market.

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