Clinical Care Options, LLC (CCO) requires instructors, planners, managers, and other individuals who are in a position to control the content of this activity to disclose any relevant conflict of interest (COI) they may have as related to the content of this activity. All identified COI are thoroughly vetted and resolved according to CCO policy. CCO is committed to providing its learners with high-quality CME/CE activities and related materials that promote improvements or quality in healthcare and not a specific proprietary business interest of a commercial interest.
The faculty reported the following financial relationships or relationships to products or devices they or their spouse/life partner have with commercial interests related to the content of this CME/CE activity:
Irini Sereti, MD, MHS, has no real or apparent conflicts of interest to report.
Philip Grant, MD, has no real or apparent conflicts of interest to report.
Daniel R. Kuritzkes, MD, has disclosed that he has received consulting fees from Gilead Sciences, GlaxoSmithKline, Merck, and ViiV and funds for research support from Gilead Sciences, GlaxoSmithKline, Janssen, Merck, and ViiV. Dr. Kuritzkes disclosed in previous editions that he had received consulting fees from Bionor, Bristol-Myers Squibb, Celera, InnaVirVax, Janssen, Oncolys, Teva, Tobira, and ViroStatics and fees for non-CME/CE services from Merck and ViiV.
Joseph J. Eron, Jr., MD, has disclosed that he has received consulting fees from Gilead Sciences, Janssen, Merck, TRIO Health, and ViiV and funds for research support from Gilead Sciences, Janssen, and ViiV. Dr. Eron disclosed in previous editions that he had received consulting fees from AbbVie, Avexa, Bristol-Myers Squibb, Chimerix, EMD Serono, Inhibitex, Kainos, Koronis, Myriad, Pfizer, Roche Molecular Systems, Tobira, Tibotec/Janssen, and Virco; had received funds for research support from AbbVie, Bristol-Myers Squibb, Merck, Panacos, TaiMed, and Tobira; had served on speaker bureaus for Bristol-Myers Squibb, Gilead Sciences, Roche, Tibotec, and Virco; and had served on data and safety monitoring boards for TaiMed and Vertex.
Edward King, MA, has no real or apparent conflicts of interest to report.
Heather Stieglitz, PhD, has no real or apparent conflicts of interest to report.
Jennifer M. Blanchette, PhD, has no real or apparent conflicts of interest to report.
Jenny Schulz, PhD, has no real or apparent conflicts of interest to report.
Sheralee Connors, MA, has no real or apparent conflicts of interest to report.
The following staff have previously contributed to the content of this module and disclosed the following potential conflicts of interest:
Kathleen E. Squires, MD, disclosed that she had served on advisory boards for scientific purposes for Bristol-Myers Squibb, Gilead Sciences, Janssen, Merck, and ViiV; had served on advisory boards for marketing purposes for Gilead Sciences and Janssen; had served on advisory boards for Boehringer Ingelheim, GlaxoSmithKline, Koronis, Pfizer, Schering-Plough, Tibotec, and Tobira; had received funds for research support from BioCryst, Boehringer Ingelheim, Bristol-Myers Squibb, Gilead Sciences, GlaxoSmithKline, Koronis, Merck, Schering-Plough, Tibotec, and Vertex; and had received consulting fees from GlaxoSmithKline and Merck at the time she contributed to this module.
Paul E. Sax, MD, disclosed that he had received consulting fees from Abbott, Aileron, Bristol-Myers Squibb, Gilead Sciences, GlaxoSmithKline, Janssen, Merck, Pfizer, and ViiV and funds for research support from Bristol-Myers Squibb, Gilead Sciences, GlaxoSmithKline, and Tibotec/Janssen at the time he contributed to this module.
Steve McGuire, Anna Poppa, and Elaine P. Seeskin had no real or apparent conflicts of interest to report at the time they contributed to this module.
Kimberly Y. Smith, MD, MPH, disclosed that she had served on advisory boards and as a consultant for Bristol-Myers Squibb, Gilead Sciences, GlaxoSmithKline, Merck, Tibotec, and ViiV and had participated in speaker bureaus for GlaxoSmithKline and Merck at the time she contributed to this module.
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inPractice Hepatology current certification periodThis program is intended for physicians and other healthcare professionals involved in the medical management of patients with or at risk of viral hepatitis.
Goal:The goal of this activity is to improve learners’ knowledge and competence regarding the clinical management of patients with viral hepatitis.
Learning Objectives:At the conclusion of this activity, participants should be able to:
Commercial Support
This program is supported by educational grants from AbbVie.
This activity is intended for physicians and other healthcare professionals involved in the management of patients with HIV.
Goal:The goal of this activity is to provide a comprehensive clinical reference resource on the prevention, diagnosis, and treatment of HIV disease.
Learning Objectives:At the conclusion of this activity, participants should be able to:
This program is supported by educational grants from Gilead Sciences, Inc., Merck Sharp & Dohme Corp. and ViiV Healthcare.
For inPractice Hepatology and HIV
Physician Continuing Medical Education (for Point of Care CME activities)
inPractice offers physicians AMA PRA Category 1 CreditTM for participation in this individual Internet point-of-care activity. Physicians may claim 0.5 credits per search. To claim point-of-care (PoC) CME credit through inPractice, eligible physicians must complete the following steps:
After submitting the evaluation, you will be presented with your online CME certificate as a pdf file. Records of all CME activities completed can be found on the "My CME" page.