Launch Date
06/22/2021
Credit Amount
0.00 Expired
Credit Expires
06/22/2022
Hepatitis B virus (HBV) poses a significant burden, as it is associated with an increased risk of morbidity and mortality in conjunction with a reduced quality of life (QoL). It is imperative that clinicians take the long view when considering medical comorbidities that may shift treatment decision-making, including recognizing that patients with chronic hepatitis B (CHB) are at-risk for bone loss independent of their antiviral treatment and aligning treatment initiation and switching decisions to AASLD guideline recommendations in the presence of renal impairment and/or bone loss.
This CME Outfitters BriefCase introduces Khadi, a 58-year-old woman who recently immigrated to the United States from Ghana and presents to her primary care provider for a new patient examination. This case will show how to optimize efficacy and safety profiles of current agents when initiating or switching treatment in patients with HBV.
At the end of this CME/CE activity, participants should be able to optimize efficacy and safety profiles of current agents when initiating or switching treatment in patients with HBV.
The following learning objectives pertain only to those requesting CNE or CPE credit: Describe efficacy and safety profiles of current agents for treatment in patients with HBV.
Supported by an educational grant from Gilead Sciences, Inc.
Primary care physicians, PAs, nurse practitioners, nurses, and pharmacists.
It is the policy of CME Outfitters, LLC, to ensure independence, balance, objectivity, and scientific rigor and integrity in all of their CE activities. Faculty must disclose to the participants any relationships with commercial companies whose products or devices may be mentioned in faculty presentations, or with the commercial supporter of this CE activity. CME Outfitters, LLC, has evaluated, identified, and attempted to resolve any potential conflicts of interest through a rigorous content validation procedure, use of evidence-based data/research, and a multidisciplinary peer review process. The following information is for participant information only. It is not assumed that these relationships will have a negative impact on the presentations.
Dr. Kumar reports that she receives grants from Gilead Sciences, Inc.; GlaxoSmithKline; and Merck & Co, Inc. She is a consultant for Amgen Inc.; GlaxoSmithKline; and Merck & Co., Inc. She is a stock shareholder (directly purchased) of Gilead Sciences, Inc.; Johnson & Johnson; Merck & Co., Inc.; and Pfizer Inc.
Maria Glukhovsky, PharmD (planning committee) has no disclosures to report.
Jan Perez (planning committee) has no disclosures to report.
Sharon Tordoff (planning committee) has no disclosures to report.
Disclosures were obtained from the CME Outfitters, LLC staff: No disclosures to report.
Faculty of this CE activity may include discussions of products or devices that are not currently labeled for use by the FDA. The faculty have been informed of their responsibility to disclose to the audience if they will be discussing off-label or investigational uses (any uses not approved by the FDA) of products or devices.
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