{"id":47038,"date":"2014-06-11T12:29:17","date_gmt":"2014-06-11T16:29:17","guid":{"rendered":"http:\/\/1boringoldman.com\/?p=47038"},"modified":"2014-06-11T17:14:44","modified_gmt":"2014-06-11T21:14:44","slug":"spellbound-2","status":"publish","type":"post","link":"https:\/\/1boringoldman.com\/index.php\/2014\/06\/11\/spellbound-2\/","title":{"rendered":"spellbound&#8230;"},"content":{"rendered":"\n<p align=\"center\"><img decoding=\"async\" width=\"350\" border=\"0\" src=\"http:\/\/1boringoldman.com\/images\/1962.gif\" \/><\/p>\n<p align=\"justify\" class=\"small\">In 1962, I was in college and even though I was applying to medical school at the time, the <a target=\"_blank\" href=\"http:\/\/en.wikipedia.org\/wiki\/Kefauver_Harris_Amendment\">Kefauver&middot;Harris Amendment<\/a>&nbsp;<a target=\"_blank\" href=\"http:\/\/en.wikipedia.org\/wiki\/Kefauver_Harris_Amendment\"><\/a> to the Federal Food, Drug, and Cosmetic Act was hardly on a college guy&#8217;s radar. But I sure knew about Frances Kelsey PhD, the FDA Reviewer who refused to approve Thalidomide and became a national hero. We had all seen those pictures of the <em>Thalidomide Babies<\/em>. Kefauver was a Senator from the Great State of Tennessee, and we all knew him as the guy with the coon-skin cap, not as a medication reformer. I&#8217;m a Tennessean who met Estes Kefauver several times as a kid, but I first read about those Kefauver Hearings in the recent writings of Dr. David Healy [<a href=\"http:\/\/www.amazon.com\/Pharmageddon-David-Healy\/dp\/0520275764\" target=\"_blank\"><font color=\"#990000\">Pharmageddon<\/font><\/a>, <a href=\"http:\/\/davidhealy.org\/category\/the-lasagna-series\/\" target=\"_blank\">The Lasagna Series<\/a>, etc]. <\/p>\n<div align=\"justify\" class=\"small\">Although it was in the area of Adverse Events that Frances Kelsey became a hero, worrying if Thalidomide crossed the placental barrier and holding up its approval, the main change in the&nbsp; Kefauver&middot;Harris Amendment had to do with adding proof of efficacy &#8211; ultimately meaning the Randomized Clinical Trials, championed by Dr. Louis Lasagna [from the&nbsp;first ever Department of&nbsp;Clinical Pharmacology &#8211; Johns  Hopkins]. This is from a 50 year retrospective of the  Kefauver&ndash;Harris Amendment in 2012:       <\/div>\n<blockquote>\n<div align=\"center\" class=\"big\"><a href=\"http:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMp1210007\" target=\"_blank\">Reform, Regulation, and Pharmaceuticals &mdash; The Kefauver&ndash;Harris Amendments at 50<\/a><\/div>\n<div align=\"center\" class=\"small\">by Jeremy A. Greene, M.D., Ph.D., and Scott H. Podolsky, M.D.<\/div>\n<div align=\"center\" class=\"middle\"><span class=\"citation\"><strong><font color=\"#200020\">New England Journal of Medicine<\/font><\/strong>. 2012  367:1481-1483.<\/span><\/div>\n<div align=\"center\" class=\"middle\">[<a href=\"http:\/\/www.nejm.org\/doi\/full\/10.1056\/NEJMp1210007\" target=\"_blank\">full text on-line<\/a>]         <\/div>\n<p>        <\/p>\n<div align=\"center\"><img decoding=\"async\" height=\"12\" border=\"0\" src=\"http:\/\/1boringoldman.com\/images\/snip.gif\" \/><\/div>\n<div align=\"justify\">By the time Kefauver began his investigation into the pharmaceutical  industry in the late 1950s, the escalating expense of lifesaving  prescription drugs was illustrating that the free-market approach to  medical innovation had costs as well as benefits. From the development  of insulin in the 1920s, through the &ldquo;wonder drug&rdquo; revolutions of sulfa  drugs, steroids, antibiotics, tranquilizers, antipsychotics, and  cardiovascular drugs in the ensuing decades, the American pharmaceutical  industry had come to play a dominant role in the public understanding  of medical science, the economics of patient care, and the rising  politics of consumerism. For Kefauver, the &ldquo;captivity&rdquo; of the  prescription-drug consumer in the face of price gouging and dubious  claims of efficacy under-scored the need for the state to ensure that  innovative industries worked to the benefit of the average American.<\/div>\n<div align=\"center\"><img decoding=\"async\" height=\"12\" border=\"0\" src=\"http:\/\/1boringoldman.com\/images\/snip.gif\" \/><\/div>\n<\/blockquote>\n<div align=\"justify\" class=\"small\">Sound familiar? How did it happen that this landmark reform legislation has us reading this description of the problem fifty years ago and thinking it could&#8217;ve been written yesterday? about today? I&#8217;m not going to quote this article as much as it deserves because I&#8217;m about a particular topic here, but this short retrospective, along with the <a href=\"http:\/\/en.wikipedia.org\/wiki\/Kefauver_Harris_Amendment\" target=\"_blank\">Wikipedia article<\/a> and Dr. Healy&#8217;s&nbsp; <a href=\"http:\/\/davidhealy.org\/category\/the-lasagna-series\/\" target=\"_blank\">The Lasagna Series<\/a>, all deserve a full reading by anyone interested in the topic of Randomized Clinical Trials, or for that matter, anything about Evidence-Based Medicine.       <\/div>\n<p align=\"justify\" class=\"small\">If you&#8217;re reading this, you&#8217;re likely already convinced that the last twenty years of Randomized Clinical Trials, Treatment Guidelines, and the cry of Evidence-Based Medicine have lead to some of the more egregious misadventures in the history of Medicine and Science itself. And you likely support one or another versions of Clinical Trial Data Transparency schemes currently fighting to be heard as a way of dealing with the widespread corruption. I&#8217;ve been vocal enough about my own take on the topic, most recently in  <a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2014\/06\/06\/in-the-details-2\/\">in the details&hellip;<\/a>, <a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2014\/06\/08\/achilles-heel-2\/\">achilles&rsquo; heel&hellip;<\/a>, <a href=\"http:\/\/1boringoldman.com\/index.php\/2014\/06\/09\/the-wrong-compromise\/\">the wrong compromise&hellip;<\/a>, and <a href=\"http:\/\/1boringoldman.com\/index.php\/2014\/06\/10\/repeal-the-proprietary-data-act\/\" target=\"_blank\">repeal the proprietary data act&hellip;<\/a>. I would be wearing out my welcome to say it yet again. <\/p>\n<p align=\"justify\" class=\"small\">But there&#8217;s another larger point that can and does get lost in the shuffle &#8211; a point made by Dr. Healy in the background to much of his writing [iincluding his current <a href=\"http:\/\/davidhealy.org\/sense-about-science-follow-the-rhetoric\/\" target=\"_blank\">four part series<\/a>]. <strong><font color=\"#200020\">There&#8217;s something else very wrong with the modern preoccupation with Randomized Clinical Trials, Standardized Treatment Guidelines, and the overall concept of Evidence-Based Medicine over and above being conduits for corruption<\/font><\/strong> [as if that weren&#8217;t enough] &#8211; something that&#8217;s apparently difficult to articulate. Many try to explain it in terms of the loss of the human relationship between doctor and patient:       <\/p>\n<ul>\n<div align=\"justify\" class=\"small\"><em><font color=\"#200020\">Originally conceived to help physicians make enlightened decisions, evidence-based medicine in North America and elsewhere has become a risk management method fostering the standardization of medical practice and the dehumanization of relations between doctors and patients.<\/font><\/em><\/div>\n<div align=\"right\" class=\"small\"><em><a href=\"http:\/\/www.booksandideas.net\/The-Human-Element-vs-the.html\" target=\"_blank\">The Human Element vs. the Standardization of Medical Care<\/a> by \u00c9lie Azria<\/em><\/div>\n<\/ul>\n<div align=\"justify\" class=\"small\">Of course that&#8217;s right, but it&#8217;s not a definitive scientific argument. For one thing, Randomized Clinical Trials, Standardized Treatment Guidelines, and Evidence-Based Medicine itself are based on the notion that all subjects are represented by the mean &#8211; that what is statistically favored for a group is good for its individuals as if they are all the same. They aren&#8217;t, so in a given patient, it&#8217;s only a <em>maybe<\/em>, often a <em>very weak maybe<\/em>. The statistical universe created by Randomized Clinical Trials and Evidence-Based Medicine is a simplified and homogenized virtual space devoid of reality&#8217;s confounds, or even the actual variance seen in the studies that defined it. The models created are to the cases seen in medical practice as model airplanes are to the modern airbus fleet. Likewise&#8230;    <\/div>\n<blockquote>\n<div align=\"center\"><img decoding=\"async\" height=\"12\" border=\"0\" src=\"http:\/\/1boringoldman.com\/images\/snip.gif\" \/><\/div>\n<div align=\"justify\">The amendments granted the FDA the power to demand proof of efficacy &mdash;  in the form of &ldquo;adequate and well-controlled investigations&rdquo; &mdash; before  approving a new drug for the U.S. market. They also led to a  retrospective review of all drugs approved between 1938 and 1962 [the  Drug Efficacy Study Implementation program], which by the early 1970s  had categorized approximately 600 medicines as &ldquo;ineffective&rdquo; and forced  their removal from the market.<\/div>\n<div align=\"center\"><img decoding=\"async\" height=\"12\" border=\"0\" src=\"http:\/\/1boringoldman.com\/images\/snip.gif\" \/><\/div>\n<\/blockquote>\n<div align=\"justify\" class=\"small\">&#8230;the major intent of the  <a target=\"_blank\" href=\"http:\/\/en.wikipedia.org\/wiki\/Kefauver_Harris_Amendment\">Kefauver&middot;Harris Amendment<\/a> was to remove inert medications from the pharmacopeia, not to certify drugs as effective for clinical use. At the time&#8230;  <\/div>\n<blockquote>\n<div align=\"center\"><img decoding=\"async\" height=\"12\" border=\"0\" src=\"http:\/\/1boringoldman.com\/images\/snip.gif\" \/><\/div>\n<p>The American Medical Association firmly opposed the regulation of  efficacy by a government agency, arguing that &ldquo;the only possible final  determination as to the efficacy and ultimate use of a drug is the  extensive clinical use of that drug by large numbers of the medical  profession over a long period of time.&quot;<\/p>\n<div align=\"center\"><img decoding=\"async\" height=\"12\" border=\"0\" src=\"http:\/\/1boringoldman.com\/images\/snip.gif\" \/><\/div>\n<\/blockquote>\n<div align=\"justify\" class=\"small\">&#8230;which is as true today as it was in 1962. One would&#8217;ve never set out fifty years ago by saying that short-term Randomized Clinical Trials conducted by the company that manufactures and sells the drug should become the benchmarks for clinical medicine, incorporated as dogma into practice guidelines [not only for treatment but for reimbursed patient contacts]. You wouldn&#8217;t have said that even if the RTCs were guaranteed to be reported with pristine accuracy [which they decidedly aren&#8217;t]. The minimal standards of the FDA were created to minimize fraudulent medications being approved. Over time, they&#8217;ve been declared the paradigm for Evidence-Based Medicine carrying a federal government seal of approval. What began as a firewall against fraudulent claims has become their principle conduit. The current version of Evidence-Based Medicine is a Svengali casting a spell over much of medical practice. We&#8217;re losing more than the human relationship between doctor and patient, we&#8217;re losing the doctor as a thinking scientist as well&#8230; <\/div>\n","protected":false},"excerpt":{"rendered":"<p>In 1962, I was in college and even though I was applying to medical school at the time, the Kefauver&middot;Harris Amendment&nbsp; to the Federal Food, Drug, and Cosmetic Act was hardly on a college guy&#8217;s radar. But I sure knew about Frances Kelsey PhD, the FDA Reviewer who refused to approve Thalidomide and became a [&hellip;]<\/p>\n","protected":false},"author":2,"featured_media":0,"comment_status":"open","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_bbp_topic_count":0,"_bbp_reply_count":0,"_bbp_total_topic_count":0,"_bbp_total_reply_count":0,"_bbp_voice_count":0,"_bbp_anonymous_reply_count":0,"_bbp_topic_count_hidden":0,"_bbp_reply_count_hidden":0,"_bbp_forum_subforum_count":0,"footnotes":""},"categories":[2],"tags":[],"class_list":["post-47038","post","type-post","status-publish","format-standard","hentry","category-politics"],"_links":{"self":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/47038","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/comments?post=47038"}],"version-history":[{"count":53,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/47038\/revisions"}],"predecessor-version":[{"id":47136,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/47038\/revisions\/47136"}],"wp:attachment":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/media?parent=47038"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/categories?post=47038"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/tags?post=47038"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}