{"id":27407,"date":"2012-09-15T15:44:41","date_gmt":"2012-09-15T19:44:41","guid":{"rendered":"http:\/\/1boringoldman.com\/?p=27407"},"modified":"2012-09-15T17:00:57","modified_gmt":"2012-09-15T21:00:57","slug":"hardly-justify","status":"publish","type":"post","link":"https:\/\/1boringoldman.com\/index.php\/2012\/09\/15\/hardly-justify\/","title":{"rendered":"hardly justify&#8230;"},"content":{"rendered":"<div align=\"justify\">Reading a discussion in the recent <a target=\"_blank\" href=\"http:\/\/1boringoldman.com\/index.php\/2012\/09\/14\/a-firm-line-in-the-sand\/#comment-229387\"><u><strong><font color=\"#200020\">comments<\/font><\/strong><\/u><\/a>, I ran across a reference I hadn&#8217;t seen. It was a report [<strong><font color=\"#200020\">ACNP Task Force Report on SSRIs and Suicidal Behavior in Youth<\/font><\/strong>] published in 2006 &#8211; yet another meta-analysis of the Clinical Trials of SSRIs in adolescents, and something of a critique of <a target=\"_blank\" href=\"http:\/\/archpsyc.jamanetwork.com\/article.aspx?articleid=209399\"><u><strong><font color=\"#200020\">Hammad&#8217;s FDA meta-analysis<\/font><\/strong><\/u><\/a> [<a target=\"_blank\" href=\"http:\/\/www.google.com\/url?sa=t&#038;rct=j&#038;q=&#038;esrc=s&#038;source=web&#038;cd=2&#038;sqi=2&#038;ved=0CCQQFjAB&#038;url=http%3A%2F%2Fwww.fda.gov%2Fohrms%2Fdockets%2Fac%2F04%2Fslides%2F2004-4065S1_08_FDA-Hammad.ppt&#038;ei=Y5VUUJb6OZTQ8wTK7IDICw&#038;usg=AFQjCNGlVIQWyGjKx48o7spifA3Hmq3Bmg&#038;sig2=527Ggeapy_-TCl5LWBq7pw\"><u><strong><font color=\"#200020\">PowerPoint<\/font><\/strong><\/u><\/a>]:<\/div>\n<blockquote>\n<div align=\"center\"><a target=\"_blank\" href=\"http:\/\/dx.doi.org\/10.1038\/sj.npp.1300958\"><u><strong><font color=\"#200020\">ACNP Task Force report on SSRIs and suicidal behavior in youth.<\/font><\/strong><\/u><\/a><br \/>             <sup>by Mann JJ, Emslie G, Baldessarini RJ, Beardslee W, Fawcett JA, Goodwin FK, Leon AC, Meltzer HY, Ryan ND, Shaffer D, and Wagner KD.<\/sup><br \/>             <strong><font color=\"#200020\">Neuropsychopharmacology<\/font><\/strong>. 2006 31[3]:473-492.<br \/>             [<a target=\"_blank\" href=\"http:\/\/dx.doi.org\/10.1038\/sj.npp.1300958\"><u><strong><font color=\"#200020\">Full Text On-Line<\/font><\/strong><\/u><\/a>]<\/div>\n<p>             <\/p>\n<div align=\"justify\"><sup><strong><font color=\"#200020\"><u>Abstract<\/u><\/font><\/strong>:<br \/>             This  Task Force report by the American College of Neuropsychopharmacology  evaluates the safety and efficacy of selective serotonin reuptake  inhibitor (SSRIs) antidepressants for depressed youth under 18 years.  The report was undertaken after regulatory agencies in the United States  and United Kingdom raised concerns in 2003 about the possibility that  treatment of depression in children and adolescents with SSRIs may  increase the risk of suicidal thinking or suicide attempts.<\/sup><\/div>\n<\/blockquote>\n<div align=\"justify\">The <a href=\"http:\/\/www.acnp.org\/\" target=\"_blank\"><u><strong><font color=\"#200020\">American College of Neuropsychopharmacology<\/font><\/strong><\/u><\/a> is a primo organization for neuroscientists and psychopharmacologists, publishing <a href=\"http:\/\/www.nature.com\/npp\/index.html\" target=\"_blank\"><u><strong><font color=\"#200020\">Neuropsychopharmacology<\/font><\/strong><\/u><\/a>.&nbsp; And as long as I seem to be having a <em>link-fest<\/em>, let me just create us a little reference library for this post:<\/div>\n<ol><sup>            <\/p>\n<li>[The 1991 hearings on suicidality with Prozac]<br \/>        <strong><font color=\"#200020\">FDA PSYCHOPHARMACOLOGICAL DRUGS ADVISORY COMMITTEE<\/font><\/strong> <a target=\"_blank\" href=\"http:\/\/www.fda.gov\/ohrms\/dockets\/ac\/prozac\/2443T1.pdf\"><u>September 20, 1991<\/u><\/a><\/li>\n<li>[The 2004 FDA Hearings that approved the Black Box warning]<br \/>        <strong><font color=\"#200020\">FDA HEARING:<\/font><\/strong> <a target=\"_blank\" href=\"http:\/\/www.fda.gov\/ohrms\/dockets\/ac\/04\/transcripts\/2004-4065T1.htm\"><u>September 13, 2004                  Transcript<\/u><\/a> (<a href=\"http:\/\/www.fda.gov\/ohrms\/dockets\/ac\/04\/transcripts\/2004-4065T1.pdf\"><u>PDF<\/u><\/a>)                  (<a href=\"http:\/\/www.fda.gov\/ohrms\/dockets\/ac\/04\/transcripts\/2004-4065T1.DOC\"><u>Word<\/u><\/a>)<br \/>         <strong><font color=\"#200020\">FDA HEARING:<\/font><\/strong> <a target=\"_blank\" href=\"http:\/\/www.fda.gov\/ohrms\/dockets\/ac\/04\/transcripts\/2004-4065T2.htm\"><u>September 14, 2004                  Transcript<\/u><\/a> (<a href=\"http:\/\/www.fda.gov\/ohrms\/dockets\/ac\/04\/transcripts\/2004-4065T2.pdf\"><u>PDF<\/u><\/a>)                  (<a href=\"http:\/\/www.fda.gov\/ohrms\/dockets\/ac\/04\/transcripts\/2004-4065T2.DOC\"><u>Word<\/u><\/a>)<\/li>\n<li>[The FDA Meta-Analyses: Hammad and Kaizar]<br \/>        <a target=\"_blank\" href=\"http:\/\/archpsyc.jamanetwork.com\/article.aspx?articleid=209399\"><u><strong><font color=\"#200020\">Hammad&#8217;s FDA meta-analysis<\/font><\/strong><\/u><\/a> <br \/>        <a href=\"http:\/\/www.ncbi.nlm.nih.gov\/pubmed\/16773951\" target=\"_blank\"><u><strong><font color=\"#200020\">Do antidepressants cause suicidality in children? A Bayesian meta-analysis<\/font><\/strong><\/u><\/a><\/li>\n<li>[Bridge&#8217;s Meta-Analysis]<br \/>        <a href=\"http:\/\/jama.jamanetwork.com\/article.aspx?articleid=206656\" target=\"_blank\"><u><strong><font color=\"#200020\">Clinical Response and Risk for Reported Suicidal Ideation and Suicide Attempts in Pediatric Antidepressant Treatment<\/font><\/strong><\/u><\/a> <\/li>\n<li>[The Institute of Medicine Conference]<br \/>        <a href=\"http:\/\/www.nap.edu\/openbook.php?record_id=12829&#038;page=1\" target=\"_blank\"><u><strong><font color=\"#200020\">CNS CLINICAL TRIAL: SUICIDALITY AND DATA COLLECTION<\/font><\/strong><\/u><\/a> <\/li>\n<li>[ACNP Task Force]<br \/>        <a target=\"_blank\" href=\"http:\/\/dx.doi.org\/10.1038\/sj.npp.1300958\"><u><strong><font color=\"#200020\">ACNP Task Force report on SSRIs and suicidal behavior in youth<\/font><\/strong><\/u><\/a> <\/li>\n<p>            <\/sup><\/ol>\n<div align=\"justify\">So, back to the Task Force report by the <strong><font color=\"#200020\">American College of Neuropsychopharmacology<\/font><\/strong>, the list of Task Force Members certainly had some beyond remarkable choices: the senior author on all of Robert Gibbons papers on the subject [Mann]; three authors from Keller&#8217;s Study 329 paper [Ryan, Emslie, Wagner]; an author on the Zoloft, Paxil, Prozac, and Celexa adolescent trials [Wagner]; an author of two Prozac, one Paxil, and the TADS adolescent trials [Emslie]; and a heavy smattering of other industry affiliations:      <\/div>\n<ol><sup>   <\/p>\n<li>\n<div align=\"justify\"><strong>J John Mann, MD<\/strong><br \/>   <strong>Task Force Co-Chair<\/strong><br \/>   The  Paul Janssen Professor of Translational Neuroscience in Psychiatry and  Radiology, Columbia University College of Physicians and Surgeons<br \/>   Chief, Department of Neuroscience,<br \/>   New York State Psychiatric Institute<br \/>   ACNP<\/div>\n<div align=\"justify\">Industry Affiliations:  <\/div>\n<ul>\n<li>Consultant: GlaxoSmithKline, Pfizer, 2001 (expert trial witness)<\/li>\n<li>Grants\/Research Support: PET ligand development grant from Pfizer (2003), Beta-amyloid imaging grant from GlaxoSmithKline (2005)<\/li>\n<li>Attended a 2002 GlaxoSmithKline Advisory group meeting on lamotrigine<\/li>\n<\/ul>\n<\/li>\n<li>\n<div align=\"justify\"><strong>Graham Emslie, MD<\/strong><br \/>   <strong>Task Force Co-Chair<\/strong><br \/>   Chief, Division of Child and Adolescent Psychiatry and Professor of Psychiatry,<br \/>   The University of Texas Southwestern Medical Center at Dallas<br \/>   ACNP<\/div>\n<div align=\"justify\">Industry Affiliations:  <\/div>\n<ul>\n<li>Consultant\/Speaker&#8217;s Bureau: Bristol-Myers Squibb, Eli  Lilly, Forest Laboratories, GlaxoSmithKline, McNeil, Otsuka, Pfizer,  Inc. Wyeth-Ayerst<\/li>\n<li>Grants\/Research Support: Eli Lilly, Novartis, Organon<\/li>\n<\/ul>\n<\/li>\n<li>\n<div align=\"justify\"><strong>Ross J Baldessarini, MD<\/strong><br \/>   Professor of Psychiatry and Neuroscience, Harvard Medical School<br \/>   Director, Laboratories for Psychiatric Research, Mailman Research Center<br \/>   Director, Bipolar &amp; Psychiatric Disorders\/Director, Psychopharmacology, McLean Hospital<br \/>   <strong>ACNP<\/strong><\/div>\n<div align=\"justify\">Industry Affiliations:  <\/div>\n<ul>\n<li>Consultant\/Research Collaborator: Auritec Laboratories, Eli  Lilly Laboratories, IFI SpA, Janssen Pharmaceuticals, JDS Corporation,  NeuroHealing Pharmaceuticals<\/li>\n<li>Grants\/Research Support: Eli Lilly Laboratories (former grant recipient), Janssen Pharmaceuticals<\/li>\n<\/ul>\n<\/li>\n<li>\n<div align=\"justify\"><strong>William Beardslee, MD<\/strong><br \/>   Psychiatrist-in-Chief and Chair, Children&#8217;s Hospital Department of Psychiatry<br \/>   Professor of Child Psychiatry, Harvard Medical School<\/div>\n<div align=\"justify\"><em>No Industry Affiliations<\/em><\/div>\n<\/li>\n<li>\n<div align=\"justify\"><strong>Jan Fawcett, MD<\/strong><br \/>   Professor of Psychiatry, University of New Mexico<br \/>   ACNP<\/div>\n<div align=\"justify\">Industry Affiliations:  <\/div>\n<ul>\n<li>Consultant: Abbott Laboratories, Bristol-Myers Squibb, Eli  Lilly and Company, Forest Laboratories, Janssen Pharmaceutica,  GlaxoSmithKline, Merck &amp; Co. Inc., Pfizer, Inc., Pharmacia &amp;  Upjohn, Wyeth-Ayerst Laboratories<\/li>\n<li>Speaker&#8217;s Bureau: Abbott  Laboratories, Bristol-Myers Squibb, Eli Lilly and Company,  Pfizer\/Roerig, Pharmacia, GlaxoSmithKline, Solvay Pharmaceuticals, Inc.,  Wyeth-Ayerst Laboratories<\/li>\n<li>Grants\/Research Support: National  Institute of Mental Health, Abbott Laboratories, Astra Zeneca  Pharmaceuticals, Bristol-Myers Squibb, GlaxoSmithKline, Eli Lilly and  Company, Organon, Pfizer, Inc., Wyeth-Ayerst Laboratories<\/li>\n<\/ul>\n<\/li>\n<li>\n<div align=\"justify\"><strong>Fred Goodwin, MD<\/strong><br \/>   Research Professor of Psychiatry and Director, Psychopharmacology Research Center, George Washington University<br \/>   ACNP<\/div>\n<div align=\"justify\">Industry Affiliations:  <\/div>\n<ul>\n<li>Consultant: Glaxo, Lilly, Pfizer, Bristol Myers Squibb, Solvay. Elan, Novartis<\/li>\n<li>Speakers  Bureau: Bristol Myers Squibb, Solvay, Glaxo, Pfizer, Janssen, Lilly,  AstraZeneca, Grants\/Research Support: Abbott Laboratories, Glaxo,  Solvay, Janssen, Pfizer, Lilly, Forest, Sanofi,<\/li>\n<\/ul>\n<\/li>\n<li>\n<div align=\"justify\"><strong>Andrew C Leon, PhD<\/strong><br \/>   Professor of Biostatistics in Psychiatry and Professor of Public Health,<br \/>   Weill Medical College of Cornell University.<\/div>\n<div align=\"justify\">Industry Affiliations:  <\/div>\n<ul>\n<li>Consultant: Cyberonics, Inc., Cortex Pharmaceuticals, Pfizer.<\/li>\n<\/ul>\n<\/li>\n<li>\n<div align=\"justify\"><strong>Herb Meltzer, MD<\/strong><br \/>   Professor of Psychiatry &amp; Pharmacology, Director Division of Psychopharmacology<br \/>   President, Collegium Internationale Neuropsychopharmacologicum (CINP),<br \/>   Vanderbilt University Medical Center<br \/>   <em>ACNP<\/em><\/div>\n<div align=\"justify\">Idustry Affiliations:  <\/div>\n<ul>\n<li>Consultant, Speaker&#8217;s Bureau, Honorarium, Grant\/Research Support: Eli Lilly, Pfizer, GlaxoSmithKline, Janssen, AstraZeneca<\/li>\n<\/ul>\n<\/li>\n<li>\n<div align=\"justify\"><strong>Neal Ryan, MD<\/strong><br \/>   Professor of Psychiatry, Western Psychiatric Institute &amp; Clinic, University of Pittsburgh<br \/>   ACNP<\/div>\n<div align=\"justify\">Industry Affiliations:  <\/div>\n<ul>\n<li>Consultant: GlaxoSmithKline (designed study and a  performance site for the GSK study of paroxetine in adolescents and was  second author on the resulting publication as well as a co-author on  related letters to the editor including one letter related to  suicidality assessment in that study)<\/li>\n<li>Consultant: GlaxoSmithKline (examination of their data related to suicidality in their aggregate paroxetine data.)<\/li>\n<li>Consultant (design of studies of antidepressants in youth): Pfizer, GSK, and Wyeth<\/li>\n<li>Primary Investigator: Wyeth (Pittsburgh performance site for the study of Venlafaxine and children.)<\/li>\n<\/ul>\n<\/li>\n<li>\n<div align=\"justify\"><strong>David Shaffer, MD<\/strong><br \/>   Professor of Child Psychiatry, and Professor of Psychiatry and Pediatrics,<br \/>   Columbia University College of Physicians and Surgeons<br \/>   Director, Division of Child Psychiatry, New York State Psychiatric Institute<\/div>\n<div align=\"justify\">Industry Affiliations:  <\/div>\n<ul>\n<li>Consultant: Hoffman la Roche, Wyeth (expert trial witness)<\/li>\n<li>Consultant: GlaxoSmithKline (on the matter of paroxetine and adolescent suicide)<\/li>\n<\/ul>\n<\/li>\n<li>\n<div align=\"justify\"><strong>Karen Wagner, MD, PhD<\/strong><br \/>   Director, Division of Child and Adolescent Psychiatry,<br \/>   Professor and Vice Chair, Department of Psychiatry and Behavioral Sciences,<br \/>   University of Texas Medical Branch, Galveston<br \/>   <em>ACNP<\/em><\/div>\n<div align=\"justify\">Industry Affiliations:  <\/div>\n<ul>\n<li>Consultant: Abbott Laboratories, Bristol-Myers Squibb,  Cyberonics, Eli Lilly, Forest Laboratories, Glaxo-Smith Kline, Janssen,  Novartis, Otskua, Pfizer, UCB Pharma, Wyeth-Ayerst<\/li>\n<li>Speaker&#8217;s Bureau: Abbott Laboratories, Eli Lilly and Co., Forest Laboratories, Glaxo-Smith Kline, Janssen, Novartis, Pfizer Inc.<\/li>\n<li>Advisory  Board: Abbott Laboratories, Eli Lilly and Co., Forest Laboratories,  Glaxo-Smith Kline, Janssen, Novartis, Otsuka, Pfizer, UCB Pharma,  Wyeth-Ayerst<\/li>\n<li>Research Support: Abbott, Bristol-Myers Squibb, Eli  Lilly, Forest Laboratories, GlaxoSmithKline, Organon, Pfizer,  Wyeth-Ayerst, National Institute of Mental Health<\/li>\n<\/ul>\n<\/li>\n<p>   <\/sup><\/ol>\n<div>The Task Force said:<\/div>\n<blockquote>\n<div align=\"justify\"><sup><u><font color=\"#200020\">SUMMARY OF FINDINGS<\/font><\/u><\/p>\n<p>     Depression in youth is a  serious public health problem and the leading cause of suicide. Suicide  is the third leading cause of death among 15&ndash;24-year olds in the United  States and the leading cause of death in that age group in several other  countries. As suicide most commonly occurs in untreated depression,  diagnosis and treatment of juvenile depression require urgent attention.<\/p>\n<p>     The  ACNP Task Force reviewed published and unpublished data to evaluate the  benefits and risks of SSRIs and other new generation antidepressants  for adults and youth under 18 years of age. The Task  Force found that only fluoxetine showed strong statistical evidence of  efficacy in treating depression in youth in RCTs. No other SSRI and  nonSSRI new antidepressant has two controlled trials that demonstrate  efficacy. Differences in drug effectiveness across clinical trials may  result from real differences in efficacy or from differences in  methodology. We recommend an additional study of potential  antidepressants in children and adolescents by RCTs that include  fluoxetine as the only established reference compound. The  Task Force also found that the category of antidepressants known as  tricyclics have not been proven to be effective antidepressants in  youth. Other forms of treatment, including psychotherapies, were found  to be not widely available to youth, and have insufficient data [such as  effective in two controlled studies] to support their routine use in  pediatric depression.<\/p>\n<p>     The Task Force concluded that  SSRIs and other new generation antidepressant drugs, in aggregate, are  associated with a small increase in the risk of AE reports of suicidal  thinking or suicide attempts in youth. The evidence for this comes from  the FDA meta-analyses of all pediatric RCTs of antidepressants. This  effect is quite variable across SSRIs and it is not clear if that  variance is a measurement error or represents a real difference between  medications. Systematic questionnaire data do not identify a risk for  more suicidal ideation on SSRIs, raising concerns over ascertainment  artifacts in the AE report method. Three other lines of evidence in  youth, epidemiology, and autopsy studies, and recent cohort surveys [<strong><a href=\"http:\/\/www.nature.com\/npp\/journal\/v31\/n3\/full\/1300958a.html#bib65\" target=\"_blank\"><u>Valuck <em>et al<\/em>, 2004<\/u><\/a><\/strong>; <strong><a href=\"http:\/\/www.nature.com\/npp\/journal\/v31\/n3\/full\/1300958a.html#bib60\" target=\"_blank\"><u>Simon <em>et al<\/em>, 2005<\/u><\/a><\/strong>],  do not support the hypothesis that SSRIs induce suicidal acts and  suicide, instead indicating a possible beneficial effect, and that a  negligible number of youth suicides are taking antidepressants at the  time of death.<\/sup><\/div>\n<\/blockquote>\n<div align=\"justify\">I&#8217;ll spare you the rant about conflicts of interest &#8211; you can fill it in without any help from me. Their SUMMARY, and the RECOMMENDATIONS at the end of the report are consistent with the findings. I have two complaints other than to say that the make-up of the Task Force itself is an insult to any principle of medical ethics that I have ever known. First, they minimize the suicidal thinking. And second, they say:  <\/div>\n<blockquote>\n<div align=\"justify\"><sup>The Task Force recommends continued use of fluoxetine as an effective  and readily available treatment for major depression in youth. We  believe other SSRIs need further testing to establish efficacy by use of  RCTs preferably including fluoxetine as a reference compound. We urge  clinicians treating depressed youth to ask about suicide, suicidal  thinking, and plans for suicide. Ongoing monitoring of suicidal thoughts  in patients treated with antidepressants is necessary. To facilitate  that process, the FDA has issued a <em>Proposed Medication Guide: About Using Antidepressants in Children or Teenagers<\/em>, which should be made available to patients and parents alike.  Given that the FDA is not empowered to make treatment recommendations,  professional organizations must issue comprehensive treatment guidelines  so that patients will continue to receive appropriate medications when  indicated. <\/sup><\/div>\n<\/blockquote>\n<div align=\"justify\">If there were a statistically significant association between SSRIs and suicide attempts or completed suicides, the drugs would have more than a Black Box warning. They would be banned for children. The warning is based on  well documented case reports and on the experience of clinicians who follow depressed adolescent patients, not statistical population data. The contrast between this injunction, &quot;<em>professional organizations must issue comprehensive treatment  guidelines  so that patients will continue to receive appropriate  medications when  indicated<\/em>&quot; and the failure of these same &quot;<em>professional organizations<\/em>&quot; to either censure or punish members who participate in ghost-written, deceitful publications of drug studies claiming unproven efficacy is striking. Do they not notice that there are three such people on their Task Force? Their point &quot;<em>the FDA is not empowered to make treatment recommendations<\/em>&quot; is true, but it doesn&#8217;t necessarily follow that &quot;<em>professional organizations must issue comprehensive treatment  guidelines  so that patients will continue to receive appropriate  medications when  indicated.<\/em>&quot; Treatment Guidelines have been a major portal for the inappropriate intrusion of the pharmaceutical industry into the practice of psychiatry. The TMAP\/CMAP scandal is a classic example. It would be hard to convince me that this ACNP recommendation isn&#8217;t also an example. The increments of efficacy shown for SSRIs in adolescents, when present at all, are clinically microscopic and hardly justify these comments&#8230;<\/div>\n","protected":false},"excerpt":{"rendered":"<p>Reading a discussion in the recent comments, I ran across a reference I hadn&#8217;t seen. It was a report [ACNP Task Force Report on SSRIs and Suicidal Behavior in Youth] published in 2006 &#8211; yet another meta-analysis of the Clinical Trials of SSRIs in adolescents, and something of a critique of Hammad&#8217;s FDA meta-analysis [PowerPoint]: [&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":[2],"tags":[],"class_list":["post-27407","post","type-post","status-publish","format-standard","hentry","category-politics"],"_links":{"self":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/27407","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=27407"}],"version-history":[{"count":35,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/27407\/revisions"}],"predecessor-version":[{"id":45509,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/posts\/27407\/revisions\/45509"}],"wp:attachment":[{"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/media?parent=27407"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/categories?post=27407"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/1boringoldman.com\/index.php\/wp-json\/wp\/v2\/tags?post=27407"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}