This is the post-test and evaluation for End Stage Renal Disease (ESRD): Coding and Documentation, presented by Cigna.

Credit Expiration 10.31.2021.

Accreditation:

This activity has been planned and implemented in accordance with the accreditation requirements and policies of the Accreditation Council for Continuing Medical Education (ACCME) through the joint providership of the Illinois Academy of Family Physicians and Cigna Health Spring. The Illinois Academy of Family Physician is accredited by the ACCME to provide continuing medical education for physicians.

Credit Designation:

AMA PRA Category 1 - The Illinois Academy of Family Physicians designates this web based enduring material, “ESRD: Coding and Documentation ,” for a maximum of 0.25 AMA PRA Category 1 credit™. 

Faculty Disclosure Statement

The Illinois Academy of Family Physicians adheres to the conflict of interest policy of the ACCME and the AMA. It is the policy of Illinois AFP to ensure balance, independence, objectivity, and scientific rigor in all its educational activities. All individuals in a position to control the content in our programs are expected to disclose any relationships they may have with  commercial companies whose products or Services may be mentioned so that participants may evaluate the objectivity of  the  presentations. In addition, any discussion of off-label, experimental, or investigational use of drugs or devices will be disclosed by the faculty. Only those participants who have no conflict of interest or who agree to an identified resolution process prior to their participation were involved in the CME activity.

Speaker & Faculty Disclosures

Nancy Gray, Michael Fessenden, MD, Donna “Michele” Prichard, RN, ANP-BC, MS, Linda Small RHIA, CDIP, CCS, and Sara Ortega (IAFP Staff) disclosed no relevant financial relationship or interest with a proprietary entity producing, marketing, reselling or distributing health care goods or services.

This program does not include any discussion or demonstration of any pharmaceuticals or medical devices that are not approved by the Food and Drug Administration (FDA) or that are considered “off-label.”