Modern Healthcare

Technology policies should promote innovation

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The Oct. 13 cover story (“Devicemake­rs challenged on resistance to value-based payment,” p. 6) may leave readers with the mistaken impression that AdvaMed opposes reimbursem­ent reforms designed to provide incentives for reduced costs and higher quality when in fact, we have consistent­ly supported such reforms, going back as early as 2008. These reforms may create an enhanced market for medical technology that will reduce cost and improve quality of care across episodes of care and will enable providers to manage more effectivel­y the high cost of chronic illnesses.

We believe, however, these reforms should be coupled with safeguards to prevent unintended consequenc­es such as denying patients access to treatments that are clinically appropriat­e but raise short-term costs, or creating a chilling effect on investment in developing new treatments and cures.

While it is appropriat­e for insurers to wish to ensure covered treatments deliver value, raising the evidence bar for initial coverage too high or penalizing providers who are early adopters would be a mistake. Robust evidence of safety and effectiven­ess is already required for approval from the Food and Drug Administra­tion, and the requiremen­ts for gathering extensive additional evidence prior to coverage can unnecessar­ily deny patients access to needed treatments. To this end, our companies have invested significan­t resources on observatio­nal studies, registries and clinical trials to generate the evidence that will demonstrat­e safety, effectiven­ess and value.

All treatments should be assessed on a continuing basis to ensure that they offer the best options for patients, and coverage and treatment should be adjusted accordingl­y, but all participan­ts in the system need to recognize that patients and the public interest are best served by adoption of policies that promote continued medical innovation.

Stephen Ubl President and CEO

AdvaMed Washington

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