{"id":62742,"date":"2015-12-31T12:48:00","date_gmt":"2015-12-31T17:48:00","guid":{"rendered":"http:\/\/1boringoldman.com\/?p=62742"},"modified":"2015-12-31T14:07:48","modified_gmt":"2015-12-31T19:07:48","slug":"a-story-the-second-ending","status":"publish","type":"post","link":"https:\/\/1boringoldman.com\/index.php\/2015\/12\/31\/a-story-the-second-ending\/","title":{"rendered":"a story: the second ending&#8230;"},"content":{"rendered":"\n<ol><sup> <\/p>\n<div class=\"big\"><u><strong><font color=\"#200020\">December Tales<\/font><\/strong><\/u><\/div>\n<p>             <\/p>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/07\/creative-funding-i\/\">creative funding I&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/08\/creative-funding-ii\/\">creative funding II&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/09\/62027\/\">creative funding III &amp; some other things&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/11\/skepticism-unchanged\/\">skepticism unchanged&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/19\/the-extra-mile\/\">the extra mile&hellip; <\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/20\/follow-the-money-2\/\">a worksheet post&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/21\/extending-the-risk\/\">extending the risk&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/22\/a-postscript\/\">a postscript&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/25\/a-story-starting-in-the-middle\/\">a story: starting in the middle&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/26\/a-story-the-end-of-the-middle\/\">a story: the end of the middle&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/27\/a-story-the-beginning-of-the-end\/\">a story: the beginning of the end&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/28\/a-story-getting-near-the-endings\/\">a story: getting near the ending[s]&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/28\/a-story-the-first-ending\/\">a story: the first ending&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/31\/a-story-the-second-ending\/\" target=\"_blank\">a story: the second ending&hellip;<\/a><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><a href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/31\/a-story-the-epilogue\/\" target=\"_blank\">a story: the epilogue&hellip;<\/a><\/div>\n<\/li>\n<p> <\/sup><\/ol>\n<p align=\"justify\" class=\"small\">I am personally drawn to the mathematical\/statistical analyses employed in a properly conducted <font color=\"#200020\"><strong>R<\/strong>andomized Double Blind <strong>C<\/strong>linical <strong>T<\/strong>rial<\/font> [RCT], and would like to think that if we had access to the raw data from Clinical Trials [Data Transparency], we could generate an accurate efficacy and safety profile for our drugs based that data. That was the general gist of the first ending to this story. In that scenario, the carefully analyzed RCT would become the <font color=\"#200020\">gold standard<\/font> for evaluating medications. Certainly, the RCT is, by Congressional Decree, already the <font color=\"#200020\">gold standard<\/font> for the FDA&#8217;s Approval process. <\/p>\n<p align=\"justify\" class=\"small\">There are other ways to look at this [see <a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2013\/04\/01\/hearing-voices\/\">hearing voices&hellip;<\/a> and <a href=\"http:\/\/1boringoldman.com\/index.php\/2013\/04\/02\/something-essential-betrayed\/\">something essential betrayed&hellip;<\/a>]. While the RCT may be a reasonable way for the FDA to evaluate new drugs for approval, that doesn&#8217;t necessarily translate to a standard for clinical practice [see this <a href=\"http:\/\/1boringoldman.com\/index.php\/2013\/04\/01\/hearing-voices\/#comment-239818\" target=\"_blank\">comment by Dr. Bernard Carroll<\/a> and <a target=\"_blank\" href=\"http:\/\/www.amazon.com\/Pharmageddon-David-Healy\/dp\/0520275764\"><font color=\"#990000\">Pharmageddon<\/font><\/a> by Dr. David Healy]. Subjects are screened for exclusions. Subjects are recruited and often paid whereas Patients are help-seeking. The RCTs are short-term [6-8 weeks] while Patients are on medications much longer [these days, sometimes indefinitely]. Subjects are seen weekly for a while [metrics and questionnaires].&nbsp; Patients are seen for brief <em><font color=\"#200020\">med-checks<\/font><\/em> at infrequent intervals. Subjects are assessed using sensitive standardized scales. Patients are asked, &quot;How&#8217;s it going?&quot; Lots of differences.      <\/p>\n<p align=\"justify\" class=\"small\">Those are concrete differences between the RCTs that we read about in our journals and the actual practice of medicine. But there&#8217;s another glaring difference. The RCTs are done by the company that has the patent on the drug, and who obviously wants to sell it widely for a maximal price. This blog and many others are filled with examples where the RCT is selectively-analyzed\/reported to achieve that end. For example, all of the studies of <font color=\"#200020\"><em>Atypical Antipsychotic Augmentation of Treatment Resistant Depression<\/em><\/font> studies reported in this series were statistically significant, but the Strength of the Effect for the primary outcome variables wasn&#8217;t reported. Here are the values extracted in the Spielman et al meta-analysis for those outcomes and  the values I got using their same methodology [Cochrane Handbook] in the Geodon<font color=\"#200020\">&reg;<\/font> and Rexulti<font color=\"#200020\">&reg;<\/font> reports [also showing the IDS-SR Effect Sizes where available]:      <\/p>\n<table cellspacing=\"0\" cellpadding=\"0\" border=\"0\" align=\"center\" class=\"small\">\n<tr>\n<td align=\"center\"><strong><font color=\"#200020\">SOURCE<\/font><\/strong><\/td>\n<td align=\"center\"><strong><font color=\"#200020\">&nbsp;&nbsp;&nbsp;&nbsp;<\/font><\/strong><\/td>\n<td align=\"center\"><strong><font color=\"#200020\">MADRS\/HAM-D [d]<\/font><\/strong><\/td>\n<td align=\"center\"><strong><font color=\"#200020\">&nbsp;&nbsp;&nbsp;&nbsp;<\/font><\/strong><\/td>\n<td align=\"center\"><strong><font color=\"#200020\">IDS-SR [d]<\/font><\/strong><\/td>\n<\/tr>\n<tr>\n<td colspan=\"5\">\n<hr size=\"1\" \/><\/td>\n<\/tr>\n<tr>\n<td><strong><font color=\"#200020\">Spielmans et al<br \/>   <\/font><\/strong><\/td>\n<td>&nbsp;<\/td>\n<td align=\"center\">0.32<\/td>\n<td>&nbsp;<\/td>\n<td align=\"center\">0.14<\/td>\n<\/tr>\n<tr>\n<td><strong><font color=\"#200020\">Ziprasidone<br \/>   <\/font><\/strong><\/td>\n<td>&nbsp;<\/td>\n<td align=\"center\">0.25<\/td>\n<td>&nbsp;<\/td>\n<td align=\"center\">&#8211;<\/td>\n<\/tr>\n<tr>\n<td><strong><font color=\"#200020\">Brexpiprazole 1mg-3mg<br \/>   <\/font><\/strong><\/td>\n<td>&nbsp;<\/td>\n<td align=\"center\">0.29<\/td>\n<td>&nbsp;<\/td>\n<td align=\"center\">0.16<\/td>\n<\/tr>\n<tr>\n<td><strong><font color=\"#200020\">Brexpiprazole 2mg<br \/>   <\/font><\/strong><\/td>\n<td>&nbsp;<\/td>\n<td align=\"center\">0.29<\/td>\n<td>&nbsp;<\/td>\n<td align=\"center\">0.20<\/td>\n<\/tr>\n<\/table>\n<p align=\"justify\" class=\"small\">The observer rated MADRS\/HAM-D numbers are in the weak to moderate range, but the self-rated scales are dramatically <em><font color=\"#200020\">near-null<\/font><\/em> &#8211; Statistically Significant, but trivial Effect from the Subject&#8217;s perspective. So with Data Transparency, willing independent analysts, and cooperative journal editors we could correct a lot of the misbehavior and get all the information.<\/p>\n<p align=\"justify\" class=\"small\">But these short-term industry run &quot;Approval&quot; RCTs really are still nothing more than a starting place for understanding either efficacy or safety, even at their best.  Perhaps the analogy of a model airplane to a Jumbo Jet might be a more reasonable way to conceptualize their place. The real test is when the drugs are put into general use by Clinicians and Patients. And we often don&#8217;t hear about those results until well down the line when the side effects and harms start showing up in court-rooms. Patients have plenty of time in waiting rooms getting &quot;<em><font color=\"#200020\">screened<\/font><\/em>&quot; or watching tv getting &quot;<em><font color=\"#200020\">detailed<\/font><\/em>&quot; by DTC ads, but very little time in the med-check world of Managed Care getting carefully evaluated before or after prescriptions are written. And the time allotted for reporting is&#8230; well it just isn&#8217;t in the program. That clown at <font color=\"#200020\">the<\/font> <a target=\"_blank\" href=\"http:\/\/worldofdtcmarketing.com\/\">World of DTC Marketing<\/a> in the last post [<a href=\"http:\/\/1boringoldman.com\/index.php\/2015\/12\/30\/when-pigs-can-fly\/\" target=\"_blank\">when pigs can fly&hellip;<\/a>] has plenty of suggestions about how we can talk to our patients about the provocative questions raised by his silly ads when they &quot;<em><font color=\"#200020\">ask the doctor<\/font><\/em>&quot;, but apparently doesn&#8217;t know that we already don&#8217;t even have time to do an adequate medical interview much less what he suggests.<\/p>\n<div align=\"justify\" class=\"small\">These papers on <font color=\"#200020\"><em>Atypical Antipsychotic Augmentation of Treatment Resistant Depression<\/em><\/font> offer us a good lesson in the problems of the day. The RCTs are all deceptively presented, accentuating the positive and eliminating the negative. The actual felt impact of the intervention is in the slim to none range and these short term RCTs don&#8217;t show the grave potential harms of the Metabolic Syndrome or the potential for Tardive Dyskinesia which occur later. What they do tell us is that cleaning up RCTs won&#8217;t be enough. We need longitudinal information &#8211; not just the rough and inadequate start-up data. We need to have some way for physicians to learn and execute in an ongoing way the kind of clinical skills it takes to practice decent medicine, to prescribe with informed therapeutic intent. We need to grow an <a href=\"http:\/\/rxisk.org\/\" target=\"_blank\"><font color=\"#990000\">Rx<\/font><font color=\"#000001\">ISK<\/font><\/a> system that doesn&#8217;t just live on a Server in the UK, but is used responsibly and universally by patients and practitioners. If Amazon.com can do it, surely we can build a system that tells us how medications are playing in the field once&nbsp; they&#8217;re approved. By the&nbsp; way, that system used to be called <em><font color=\"#200020\">Academic Medicine<\/font><\/em>, but maybe we need a replacement. And, by the way, we don&#8217;t need to give Atypical Antipsychotics to people with life&#8217;s depressions except in dire circumstances, and then for a limited time only [if at all]&#8230;  <\/div>\n","protected":false},"excerpt":{"rendered":"<p>December Tales creative funding I&hellip; creative funding II&hellip; creative funding III &amp; some other things&hellip; skepticism unchanged&hellip; the extra mile&hellip; a worksheet post&hellip; extending the risk&hellip; a postscript&hellip; a story: starting in the middle&hellip; a story: the end of the middle&hellip; a story: the beginning of the end&hellip; a story: getting near the ending[s]&hellip; 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_forum_subforum_count":0,"footnotes":""},"categories":[5],"tags":[],"class_list":["post-62742","post","type-post","status-publish","format-standard","hentry","category-opinion"],"_links":{"self":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/62742","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=62742"}],"version-history":[{"count":26,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/62742\/revisions"}],"predecessor-version":[{"id":62811,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/62742\/revisions\/62811"}],"wp:attachment":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/media?parent=62742"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/categories?post=62742"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/tags?post=62742"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}