{"id":49956,"date":"2012-07-22T16:20:48","date_gmt":"2012-07-22T16:20:48","guid":{"rendered":"http:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/uncategorized\/embargoed-news-from-annals-of-internal-medicine.php"},"modified":"2012-07-22T16:20:48","modified_gmt":"2012-07-22T16:20:48","slug":"embargoed-news-from-annals-of-internal-medicine","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/medicine\/embargoed-news-from-annals-of-internal-medicine.php","title":{"rendered":"Embargoed news from Annals of Internal Medicine"},"content":{"rendered":"<p><p>Public  release date: 22-Jul-2012  [ |   E-mail   |  Share    ]  <\/p>\n<p>    Contact: Abbey Anderson    <a href=\"mailto:aanderson@acponline.org\">aanderson@acponline.org<\/a>    215-351-2656    American College of    Physicians<\/p>\n<p>    1. FDA Panel Members Express Opposing Views on Truvanda    Approval  <\/p>\n<p>    In May, the FDA Antiviral Advisory Committee met to review    evidence for the approval of two antiretroviral drugs,    tenofovir and emtricitabine for pre-exposure prophylaxis (PrEP)    against HIV infection. Two members of the Committee explain why    they voted for or against the approval. Judith Feinberg, MD,    Professor of Medicine at the University of Cincinnati College    of Medicine and director of the University of Cincinnati AIDS    Clinical Trials Unit, serves as chairperson of the FDA    Antiviral Advisory Committee. She voted in favor of the    approval. She explains that while the observation period for    tenofovir-emtricitabine has been short, the outcomes and    tolerability have been very good. Dr. Feinberg writes that PrEP    is particularly important now that HIV is on the rise among    young men who have sex with men. Over the past 30 years, HIV    has killed 30 million people and infected 60 million. With    hundreds of millions of people still at risk, and no vaccine    available, PrEP may be the strategy that helps to turn the tide    on HIV. Lauren V. Wood, MD, Staff Clinician at the National    Cancer Institute and Assistant Professor at the Uniformed    Services University of the Health Sciences is also a member of    the FDA Antiviral Advisory Committee. Dr. Wood voted against    the approval for several reasons. First, Dr. Wood did not find    consistent evidence of the benefit of PrEP, especially in    women. Second, she expressed concern about low rate of    adherence to the tenofovir-emtricitabine regimen. Since    adherence is crucial to efficacy, she could not support    approval. And finally, Dr. Wood cited safety concerns about    PrEP dosing. And since no long-term studies have been done, the    potential for the emergence and spread of drug resistant virus    as a consequence of PrEP remains a concern.  <\/p>\n<p>    2. With Drug Approval Comes Added Responsibility for Primary    Care Docs  <\/p>\n<p>    Prescribing antiretrovirals to uninfected individuals who are    at high risk for HIV has shown promise at decreasing HIV    incidence in some populations. Last week, the FDA approved oral    tenofovir-emtricitabine for pre-exposure prophylaxis (PrEP) for    high-risk patients. According to HIV thought leaders, primary    care physicians are likely to care for many at-risk    individuals, and therefore must be fully informed about PrEP.    The experts reviewed available literature to outline key areas    of knowledge that can help physicians manage potential PrEP    patients. According to the experts, it is imperative for    primary care doctors to understand which patients would benefit    from PrEP. PrEP has been proven most effective in HIV    serodiscordant couples, men who have sex with men, and    heterosexual men and women in Africa. Patients on PrEP need    counseling to maximize adherence and minimize potential    increases in risky behavior. They also must be monitored for    potential drug toxicities, HIV acquisition, and antiretroviral    drug resistance. While PrEP therapy is safe and effective at    preventing HIV in some populations, it also has the potential    to be very expensive.  <\/p>\n<\/p>\n<p>        AAAS and EurekAlert! are not responsible for the accuracy    of news releases posted to EurekAlert! by contributing    institutions or for the use of any information through the    EurekAlert! system.  <\/p>\n<\/p>\n<p>Read this article: <\/p>\n<p><a target=\"_blank\" href=\"http:\/\/www.eurekalert.org\/pub_releases\/2012-07\/acop-enf071712.php\" title=\"Embargoed news from Annals of Internal Medicine\">Embargoed news from Annals of Internal Medicine<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> Public release date: 22-Jul-2012 [ | E-mail | Share ] Contact: Abbey Anderson <a href=\"mailto:aanderson@acponline.org\">aanderson@acponline.org<\/a> 215-351-2656 American College of Physicians 1. FDA Panel Members Express Opposing Views on Truvanda Approval In May, the FDA Antiviral Advisory Committee met to review evidence for the approval of two antiretroviral drugs, tenofovir and emtricitabine for pre-exposure prophylaxis (PrEP) against HIV infection. Two members of the Committee explain why they voted for or against the approval.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/medicine\/embargoed-news-from-annals-of-internal-medicine.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[35],"tags":[],"class_list":["post-49956","post","type-post","status-publish","format-standard","hentry","category-medicine"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/49956"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=49956"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/49956\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=49956"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=49956"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=49956"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}