{"id":3295,"date":"2016-12-27T10:00:52","date_gmt":"2016-12-27T16:00:52","guid":{"rendered":"http:\/\/www.robertkreisman.com\/medical-malpractice-lawyer\/?p=3295"},"modified":"2016-12-26T08:11:01","modified_gmt":"2016-12-26T14:11:01","slug":"warning-use-transvaginal-mesh-u-s-food-drug-administration","status":"publish","type":"post","link":"https:\/\/www.robertkreisman.com\/medical-malpractice-lawyer\/warning-use-transvaginal-mesh-u-s-food-drug-administration\/","title":{"rendered":"Warning of Use of Transvaginal Mesh by U.S. Food and Drug Administration"},"content":{"rendered":"

In a recent Journal of the American Medical Association Surgery (JAMA Surgery)<\/a> article, the safety concerns of the use of the transvaginal mesh<\/a> in pelvic organ prolapse (POP) repair has been noted by the U.S. Food and Drug Administration (FDA)<\/a>.The recent article by two physicians was published in the Journal of the American Medical Association Surgery edition published online on Nov. 30, 2016. <\/p>\n

The article highlights studies that reveal the incidences and timing of complications related to the use of the transvaginal mesh organ prolapse repair, the amount of vaginal mesh used with mesh erosions and repeated surgery after pelvic organ prolapse repair and urinary incontinence surgery. The study is discussed expertly in the JAMA article by the authors, physicians Bhumy A. Dav\u00e9, M.D., a female pelvic medicine & reconstructive surgeon associated with Northwestern Medicine, and Anne-Marie Boller, M.A., M.D., FACRS, a colon and rectal surgeon also with the Northwestern Medical Group in Chicago. <\/p>\n

The article points out that the recent transvaginal mesh study focused on the clinically important mesh complications (those that require an intervention as opposed to asymptomatic erosions) and it references a statewide database, which minimizes under reporting that occurs when patients change doctors secondary to complications.
\n Continue reading<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"

In a recent Journal of the American Medical Association Surgery (JAMA Surgery) article, the safety concerns of the use of the transvaginal mesh in pelvic organ prolapse (POP) repair has been noted by the U.S. Food and Drug Administration (FDA).The recent article by two physicians was published in the Journal of the American Medical Association […]<\/p>\n","protected":false},"author":795,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"jetpack_post_was_ever_published":false,"footnotes":"","jetpack_publicize_message":"","jetpack_publicize_feature_enabled":true,"jetpack_social_post_already_shared":true,"jetpack_social_options":{"image_generator_settings":{"template":"highway","default_image_id":0,"enabled":false},"version":2}},"categories":[8,16,32],"tags":[],"class_list":["post-3295","post","type-post","status-publish","format-standard","hentry","category-medical-device-liability","category-product-liability","category-transvaginal-mesh-litigation"],"yoast_head":"\nWarning of Use of Transvaginal Mesh by U.S. Food and Drug Administration — Chicago Medical Malpractice Attorney Blog<\/title>\n<meta name=\"description\" content=\"In a recent Journal of the American Medical Association Surgery (JAMA Surgery) article, the safety concerns of the use of the 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