Search Results Search Sort by RelevanceMost Recent Letter to the Editor Oct 2019 Response to “Will We Code for Default ECMO?”: Clarifying the Scope of Do-Not-ECMO Orders Jacob A. Blythe, MA, Sarah E. Wieten, PhD, and Jason N. Batten, MD, MA The authors further consider the merits of preventing ECMO from becoming a default treatment. AMA J Ethics. 2019;21(10):E926-929. doi: 10.1001/amajethics.2019.926. Medicine and Society Oct 2010 The Personal, Social, and Economic Determinants of Cardiovascular Disease Jane S. Jue, MD, MSc Personal, social, economic, and environmental factors all contribute to the increased incidence of cardiovascular disease in the United States. Virtual Mentor. 2010;12(10):812-817. doi: 10.1001/virtualmentor.2010.12.10.msoc1-1010. Health Law Oct 2010 Testing Manufacturer Liability in FDA-Approved Device Malfunction Ryan Bailey and Kristin E. Schleiter, JD, LLM The Supreme Court’s ruling in Riegel v. Medtronic, Inc., may prevent consumers injured by medical devices that have FDA premarket approval from receiving compensation. Virtual Mentor. 2010;12(10):800-803. doi: 10.1001/virtualmentor.2010.12.10.hlaw1-1010.
Letter to the Editor Oct 2019 Response to “Will We Code for Default ECMO?”: Clarifying the Scope of Do-Not-ECMO Orders Jacob A. Blythe, MA, Sarah E. Wieten, PhD, and Jason N. Batten, MD, MA The authors further consider the merits of preventing ECMO from becoming a default treatment. AMA J Ethics. 2019;21(10):E926-929. doi: 10.1001/amajethics.2019.926.
Medicine and Society Oct 2010 The Personal, Social, and Economic Determinants of Cardiovascular Disease Jane S. Jue, MD, MSc Personal, social, economic, and environmental factors all contribute to the increased incidence of cardiovascular disease in the United States. Virtual Mentor. 2010;12(10):812-817. doi: 10.1001/virtualmentor.2010.12.10.msoc1-1010.
Health Law Oct 2010 Testing Manufacturer Liability in FDA-Approved Device Malfunction Ryan Bailey and Kristin E. Schleiter, JD, LLM The Supreme Court’s ruling in Riegel v. Medtronic, Inc., may prevent consumers injured by medical devices that have FDA premarket approval from receiving compensation. Virtual Mentor. 2010;12(10):800-803. doi: 10.1001/virtualmentor.2010.12.10.hlaw1-1010.