| Antipsychotics pose "Ominous long-term health implications" for children_JAMA |
| Wednesday, 28 October 2009 | |
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Prominent psychotropic drug investigators acknowledge that the rapid
onset of "cardiometabolic risks" is "alarming." They recommend that
consideration be given for lower-risk alternatives.
A study published in the current issue of The Journal of the American Medical Association [1], confirms that children and adolescents who are prescribed second generation neuroleptics are put at high risk of severe harm: prominent psychotropic drug investigators acknowledge that the rapid onset of "cardiometabolic risks" is "alarming." They recommend that consideration be given for lower-risk alternatives. This government-sponsored study is the largest ever conducted on first-time users of neuroleptics (a.k.a. antipsychotics). It sought to document the association of second-generation neuroleptics (antipsychotics) with body composition and metabolic parameters in patients not previously exposed to antipsychotic drugs. The four drugs in the study—Zyprexa (olanzapine), Risperdal (risperidone) Seroquel (quetiapine) and Abilify (aripiprazole)—are the most popular antipsychotic medications. They are industry blockbusters, with combined sales of $12.7 billion last year. Two hundred and fifty seven young children and adolescents, aged 4 to 19, in the New York study added 8% to 15% to their weight after taking one of four neuroleptics for only 11 weeks. All but Abilify showed rapid and significant increases in one or more metabolic markers, which can presage adult obesity, hypertension and Type 2 diabetes. The metabolic markers included glucose, insulin, triglycerides and cholesterol. "Adverse baseline-to-end-point changes reached statistical significance for olanzapine and quetiapine for total cholesterol, triglycerides, non-HDL cholesterol, and ratio of triglycerides to HDL cholesterol. [ sic] With risperidone, levels of triglycerides increased significantly. Metabolic baseline-to-end-point changes were not significant with aripiprazole or in the untreated comparison group. Patients receiving quetiapine had modestly higher incidence rates of hyperglycemia and the metabolic syndrome and patients receiving olanzapine experienced the highest incidence rates (eTable 3). Pubertal status was unrelated to metabolic changes in any antipsychotic medication group." In this short-term study of youth naïve to antipsychotic medications, aripiprazole, olanzapine, quetiapine, and risperidone were each associated with rapid and significant increases in body composition, whereas metabolic changes were less uniform. Effect sizes for body composition changes were large (eTable 2). Altogether, 10% to 36% of patients transitioned to overweight or obese status within 11 weeks. "The lack of significant changes in weight and metabolic parameters in psychiatric comparison patients and short inpatient stays (10-18 days is equal to 14%-25% of treatment time) indicates that the observed alterations are not likely due to a newly developing or worsening psychiatric disorder or hospitalization. "The results are concerning because they include fat mass and waist circumference, which are associated with the metabolic syndrome in adults treated with antipsychotic medications and heart disease in the general population. Moreover, abnormal childhood weight and metabolic status adversely affect adult cardiovascular outcomes."The findings, led Dr. Wayne K. Goodman, chairman of psychiatry at Mount Sinai School of Medicine and head of an FDA advisory panel that had been charged with assessing these drugs risk for children last summer, expressed shock. He told The New York Times: “The degree of weight gain is alarming. The magnitude is stunning.” And Dr. Judith Rapoport, chief of the child psychiatry branch at the National Institute of Mental Health, acknowledged in an interview with The New York Times, “It’s by far the best documentation of not just weight gain and metabolic changes…” In an editorial accompanying the study [2], child psychiatrists, Dr. Christopher K. Varley (Seattle Children’s Hospital) and Dr. Jon McClellan (University of Washington School of Medicine) wrote that “ominous long-term health implications” arise from weight gain and changes in blood fat levels early in life: "These data confirm prior findings that children and adolescents are highly vulnerable to antipsychotic medication–induced weight gain and metabolic adverse effects. The magnitude of weight gain is particularly concerning, as is the implication that metabolic adverse events may be underestimated in studies in which participants have had prior atypical antipsychotic medication exposure. Furthermore, the development of clinically significant hyperlipidemias and insulin resistance after only 12 weeks of treatment portends severe long-term metabolic and cardiovascular sequelae." "These results challenge the widespread use of atypical antipsychotic medications in youth."In view of these indisputable, confirmatory alarming findings, not only the authors of the study, but the authors of the JAMA editorial, the chief of child psychiatry at the NIMH, and even the chairman of the FDA advisory panel who in June 2009 voted to approve the use of three of the drugs for children--all acknowledge the need to reassess the use of these drugs in children: “These results challenge the widespread use of atypical antipsychotic medications in youth.” But, will the evidence that these drugs pose “ominous long-term health implications” for children, provide the necessary political will to ban the use of antipsychotics for children??? These drugs’ hazardous effect on weight and metabolism—in adults and children—had been previously detected and reported. [3] Indeed, the principle investigator, Dr. Crisoph Correll, is a leading expert on the metabolic and cardiovascular ill effects of the second generation neuroleptics, whose critical scientific appraisals have been published widely. [4--9] However, the alarming speed and magnitude of the effects found in this pediatric study were greater than previously reported. The findings are all the more compelling because the children were new patients who had not previously been exposed to neuroleptics. Given the "ominous long-term health implications," we venture to say, the children's health would have been far better served without these drugs. Yet, psychiatrists' practice disregards the drugs' harmful effects: A 2008 study found that patients under 19 years old accounted for 15% of antipsychotic drug use in 2005, compared with 7% in 1996. Since 2005, that percentage has skyrocketed. Why are these toxic drugs so widely prescribed by US psychiatrists? Because prominent psychiatrists at prestigious universities who have served as paid consultants and speakers for drug manufacturers have promoted the off-label use of these drugs for children and teenagers, despite a body of knowledge documenting the severe adverse effects the drugs have on children’s physical health. Underscoring the abusive prescribing of these drugs for children is the fact that more than 70% of atypical antipsychotics prescribed for young children and teenagers have been for off-label—i.e., untested uses—mostly for misbehavior (e.g., attention deficit hyperactivity disorder). These drugs are being used as chemical restraints—the severity of their hazardous effects is not justified by any medical benefit. The drugs’ beneficiaries are not those who ingest them: antipsychotic drug sales have enriched not only drug manufacturers, but psychiatry’s leadership, leading medical institutions, the mental health provider industry, and so-called patient advocacy groups—all of who have sold their integrity, serving as industry’s partners in a despicable crime. The large number of industry-funded publications exalting the benefits of second generation neuroleptics, penned by the pillars of American psychiatry, should be discarded as fraudulent, mostly ghostwritten, industry propaganda. Commercially-crafted reports masquerading as evidence-based reports have undermined the integrity of the journals that published them and the profession whose practice was guided by them. Will the indisputable evidence of “ominous long-term health implications” from use of antipsychotics prompt the FDA to ban their use in children??? References: 1. See: http://jama.ama-assn.org/cgi/content/abstract/302/16/1765 Cardiometabolic Risk of Second-Generation Antipsychotic Medications During First-Time Use in Children and Adolescents Christoph U. Correll, MD; Peter Manu, MD; Vladimir Olshanskiy, MD; Barbara Napolitano, MA; John M. Kane, MD; Anil K. Malhotra, MD JAMA. 2009;302(16):1765-1773. 2. http://jama.ama-assn.org/cgi/content/full/302/16/1811 Christopher K. Varley; Jon McClellan Implications of Marked Weight Gain Associated With Atypical Antipsychotic Medications in Children and Adolescents JAMA. 2009;302(16):1811-1812 (doi:10.1001/jama.2009.1558) 3. Lieberman JA, Stroup TS, McEvoy JP, et al: Effectiveness of antipsychotic drugs in patients with chronic schizophrenia. New England Journal of Medicine 353:1209–1223,2005. The majority of patients in each medication group discontinued their assigned treatment mostly due to inefficacy or intolerable side effects. Zyprexa (olanzapine) had somewhat lower drop-out rate, but the drug was associated with greater weight gain and increases in measures of glucose and lipid metabolism. 4. Correll C and Carlson HE. Endocrine and Metabolic Adverse Effects of Psychotropic Medications in Children and Adolescents, J.Am Acad Child Adolesc.Psychiatry, 2006;45:771-791. 5. Correll CU, Penzner JB, Parikh UH, Mughal T, Javed T, Carbon M, Malhotra AK. Recognizing and monitoring adverse events of second-generation antipsychotics in children and adolescents. Child Adolesc Psychiatr Clin N Am. 2006 Jan;15(1):177-206. 6. Correll CU. Metabolic side effects of second-generation antipsychotics in children and adolescents: a different story? J Clin Psychiatry. 2005 Oct;66(10):1331-2. 7. Saito E, Correll CU, Gallelli K, McMeniman M, Parikh UH, Malhotra AK, Kafantaris V. A prospective study of hyperprolactinemia in children and adolescents treated with atypical antipsychotic agents. J Child Adolesc Psychopharmacol. 2004 Fall;14(3):350-8. Review. 8. Kane JM, Barrett EJ, Casey DE, Correll CU, Gelenberg AJ, Klein S, Newcomer JW. Metabolic effects of treatment with atypical antipsychotics. J Clin Psychiatry. 2004 Nov;65(11):1447-55. 9. Correll CU, Malhotra AK. Pharmacogenetics of antipsychotic-induced weight gain. Psychopharmacology (Berl). 2004 Aug;174(4):477-89. Posted by Vera Sharav THE NEW YORK TIMES |