Percutaneous coronary intervention with medical therapy does not reduce the risk of death, myocardial infarction or the need for unplanned revascularization procedures compared with medical therapy alone, a meta-analysis of five studies confirms.
A new meta-analysis of percutaneous coronary intervention (PCI) trials supports the current clinical practice guidelines recommending medical therapy, rather than immediate stenting, as the primary therapy choice for patients with stable obstructive coronary disease and myocardial ischemia.
The meta-analysis of five trials enrolling a total of 5,286 patients was led by Kathleen Stergiopoulos of the Stony Brook School of Medicine in Stony Brook, N.Y., and was published...
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Medtronic announced it received expanded MRI labeling for its DBS systems, which is critical, given that almost 70% of all DBS-eligible patients will likely need an MRI at some point in their care, says Ashwini Sharan, CMO for Medtronic Neuromodulation.
In this episode, Medtech Insight reporter Natasha Barrow speaks to LungLife AI CEO Paul Pagano. Lung Life AI is a US-based AIM-listed medical technology company that has developed a liquid biopsy test for the early detection of lung cancer called Lung LB. Pagano runs through the highlights of Lung Life AI journey to date and its future ambition for a strategic partnership. He also provides advice to similar diagnostic companies seeking reimbursement andcompliance with the US FDA Lab Developed Test ruling.
The US’ 90-day suspension of higher “reciprocal tariffs” will expire on 9 July, raising fears that the 31% tariff rate on Swiss medtech and other goods exported to the US might make a comeback. While the tariff situation changes on an almost daily basis, medtechs should forearm for any eventually, say local business organizations.
Guardant Health introduces a new germline panel test to help guide cancer treatment, assess the risk of secondary cancers in patients and identify family members at risk of cancer.
A Texas court's decision against US FDA regulation of lab-developed tests (LDTs) has introduced new uncertainties for clinical labs. Industry stakeholders are now worried about potential future regulations while also managing existing compliance requirements. Recent conference discussions underscored the complexities of FDA oversight.
