Routine cervical cytology cancer screening should be delayed until age 21, according to guidelines released Nov. 20 by the American College of Obstetricians and Gynecologists. ACOG previously recommended that screening begin three years after first sexual intercourse or by age 21. The updated guidelines also call for women 21-30 to be screened less often - every two years instead of annually, using either the standard Pap test or liquid-based cytology. In a Practice Bulletin to be published in the December issue of Obstetrics & Gynecology, AGOG explains that "the recommendation to start screening at 21 years regardless of the age of onset of sexual intercourse is based in part on the very low incidence of cancer in younger women," as well as the potential for adverse effects associated with follow-up of young women with abnormal cytology screening results. Screening can jump to every three years in women 30 and older who have had three consecutive cervical cytology test results that are negative for intraepithelial lesions and malignancy, ACOG notes. Women with defined risk factors may benefit from more frequent screening, the guidelines state
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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.
AdvaMed has praised CMS’ Rural Health Transformation Program, which will allocate $50 billion over five years to enhance rural healthcare. States can apply for grants by Nov. 5 to develop sustainable healthcare systems and improve patient outcomes.
The US FDA will hold a public meeting of its Digital Health Advisory Committee in November to focus on generative AI-enabled medical devices to treat mental health.
The company is undergoing major leadership changes, having appointed 30-year medtech veteran Jane Wright as chief financial officer on Sept. 12. Wright’s appointment follows Gutteridge’s own transition to CEO earlier this year.
