Posted on Thursday 25 December 2014

I’m back from my tangent now. I wasn’t offering my objections to that legal study [An Institutionalization Effect…] as a proof in transinstitutionalization? III…, but more as an example of a place where having the numbers work out in some mathematical model is one thing, but it doesn’t necessarily prove the relationship in the conclusions. My own guess is that the shoddy implementation of deinstitutionalization, the rise in violent crimes from 1980 through 2000, and our becoming the biggest jailer on the planet are definitely related to each other, but that all three are parameters that relate to something else, something unmeasured that has something vital to say about our country’s as yet unwritten history of the second half of the 20th century. I expect that the way we’ve dealt with chronic mental illness in general belongs in that unwritten story too.
I don’t know anything much about incarceration except that it’s something societies do when they don’t know what else to do. The creation of a dual system [prisons and asylums] had an intent apparent in the very names we use to talk about them, and by the mid twentieth century, that distinction between institutions had lost its meaning. The coming of effective antipsychotic medications at the mid-century mark may have been the key that unlocked the door to the State Hospitals, but it was anything but a cure. Whether you think of psychotic illness as biological or psychological, a disease or a collection of conditions, or something else – the antipsychotics are symptomatic medications [nothing like penicillin that cures certain infections or insulin that replaces something that’s not working right]. They are often dramatically effective for the positive symptoms of acute psychosis but do nothing of note for the less dramatic negative symptoms [anhedonia, cognitive deficits, lack of motivation, etc.] nor for the often elaborate delusions seen in chronic paranoia.
One of he things I liked about the articles by Seth Prins was that he transcended all the rhetoric that often goes with this issue and seemed to be after the facts. What was not in his data that I wanted to see was the distinction between jails and prisons. I couldn’t find anything omnibus on jails for mental illness prevalence, but I did, at least, find some comparative total incarceration rates:
I’ll have to admit that I’m overwhelmed by these numbers. I had no idea that the incarceration rates were this high. I keep running across the phrase, "America’s experiment with mass incarceration," a label that seems apt [apparently it was an easier experiment to do than it has been to undo]. And it has hardly been cheap…
Speculations about the causes for our high rate of incarceration and the over-representation of the mentally ill in the prison and jail populations are met with divisive opinions about what to do about either situation. One pole, for example, supports the solutions proposed by the Treatment Advocacy Center advocatng community commitment including mandated medication. On the other pole, there is strong opposition to those methods from civil libertarians groups [see here-we-go-again?]. While the debates are often cached in terms of biomedicine and psychiatry versus other mental health disciplines and the civil liberties, or neuroscience versus humanism, my impression is that the mental health disciplines as a group [psychiatry, psychology, social work, etc.] have been otherwise preoccupied for the last quarter-century, and with the exception of those directly employed by public facilities or those involved in brain research, they have been monotonously saying the same things they said a long time ago. There is so much in this story to decry, and there’s certainly still a lot of decrying going on, but solutions or progress? not so much.
Commentary: Not Just Variation in Estimates: Deinstitutionalization of the Justice Systemby Jeffrey Draine and Miguel Muñoz-LaboyPsychiatric Services. 2014 65[7]:873-873.… In 2002, the first author and his colleagues questioned the presumption that the large number of incarcerated people with mental illness was attributable to failures in the assessment and treatment of mental illness and concluded that there is no reliable evidence that directing resources toward psychiatric treatment would have a significant impact on incarceration rates. In this commentary, we argue that this conclusion remains true. In the article by Prins, the implied logic is that there is interpretive value in examining variations in the rates of mental illnesses in jails and prisons to discern the impact of psychiatric interventions. Holding to the principle that the most parsimonious explanation is best, the factor that explains the variation in the proportions of prisoners with mental illness is variation in correctional policy and practice among jurisdictions and over time, rather than variation in access to treatment for mental illness or in how mental illness is assessed or counted in prisons and jails. The more recent variation in rates of mental illness is also likely enhanced by the beginning of a shift in correctional policy: the decline of incarceration in prisons.
Abramson laid the groundwork for examining connections between deinstitutionalization of psychiatric treatment and the rising number of incarcerated people with mental illnesses. Historically, institutions such as orphanages, poorhouses, and asylums have, each in their own time, experienced a profound increase in their populations, which was followed by a period of deinstitutionalization. Initially, the reasons given for deinstitutionalization are humane treatment, but eventually the most persuasive arguments center on cost and efficiency in state systems and the availability of plausible alternatives. In the United States, practice shifted from poorhouses to outdoor relief, charity movements, and social work; from orphanages to child welfare systems, foster care, and juvenile justice systems; from asylums to community mental health; and now from prisons to community corrections.
With the emergence of community corrections and the eventual downsizing of prisons and jails, many people with mental illness once incarcerated in conventional facilities will more often be involved in various forms of community corrections… Correctional health care policy focused on large prisons and jails has not caught up with the impact of deinstitutionalization in the provision of psychiatric care to vulnerable populations. As a result, a growing number of individuals with serious psychiatric disorders are left without reliable access to effective psychiatric treatment. This commentary seeks to refocus attention away from efforts to establish a standard for rates of incarcerated persons with mental illness in conventional facilities with the aim of informing mental health interventions. The action is not there. The place for action in innovation, change, and planning is in community settings. Our goal should be to document variations across place and time in how the differences and changes in corrections practices interrupt effective care and to develop creative ways to recognize as a reality in the justice system the ongoing changes in corrections environments and the broad variation in incarcerated populations.
Whereupon 1boringoldman goes off on a tangent
My problem is that transinstitutionalization as a concept both makes good sense and makes absolutely no sense at all. It was a huge happening, moving half a million people into the community, many of whom had chronic psychotic illnesses and a history of having been institutionalized. In my time [1970s], there was plenty of commerce among the jails, the police, the psychiatric emergency rooms, and the dwindling mental hospitals, but there was nothing that felt like it had to do with past history – even then. It felt like a today problem. The problem was with actively psychotic people with no place to stabilize them or chronic patients living on the streets with no place to go. And as brisk as the traffic between the hospitals and the jails, I don’t recall prison being in the mix. We had a model, but no way to adequately implement it. So I went back and started over. I began with this graph in transinstitutionalization? I…:
by Bernard E. HarcourtThe Journal of Legal Studies. 2011 40[1]:39-83.[full text on-line]
Previous research suggests that mass incarceration in the United States may have contributed to lower rates of violent crime since the 1990s but, surprisingly, finds no evidence of an effect of imprisonment on violent crime prior to 1991. This raises what Steven Levitt has called “a real puzzle.” This study offers the solution to the puzzle: the error in all prior studies is that they focus exclusively on rates of imprisonment, rather than using a measure that combines institutionalization in both prisons and mental hospitals. Using state-level panel-data re- gressions over the 68-year period from 1934 to 2001 and controlling for economic conditions, youth population rates, criminal justice enforcement, and demographic factors, this study finds a large, robust, and statistically significant relationship between aggregated institutionalization [in mental hospitals and prisons] and homicide rates, providing strong evidence of what should now be called an institutionalization effect — rather than, more simply but inaccurately, an imprisonment or incapacitation effect.
This is where we left off:
by Seth J. Prins, M.P.H.Psychiatric Services. 2014 65:862-872.Objective: People with mental illnesses are understood to be over-represented in the U.S. criminal justice system, and accurate prevalence estimates in corrections settings are crucial for planning and implementing preventive and diversionary policies and programs. Despite consistent scholarly attention to mental illness in corrections facilities, only two federal self-report surveys are typically cited, and they may not represent the extent of relevant data. This systematic review was conducted to develop a broader picture of mental illness prevalence in U.S. state prisons and to identify methodological challenges to obtaining accurate and consistent estimates.Methods: MEDLINE, PsycINFO, the National Criminal Justice Reference Service, Social Services Abstracts, Social Work Abstracts, and Sociological Abstracts were searched. Studies were included if they were published between 1989 and 2013, focused on U.S. state prisons, reported prevalence of diagnoses and symptoms of DSM axis I disorders, and identified screening and assessment strategies.Conclusions: Definitions of mental illnesses, sampling strategies, and case ascertainment strategies likely contributed to inconsistency in findings. Other reasons for study heterogeneity are discussed, and implications for public health are explored.
Methods: A systematic review of the scholarly literature was conducted to identify studies that presented prevalence estimates of mental illnesses in prisons. Articles were included if they were published in peer-reviewed, English-language journals between January 1989 and December 2013, focused on U.S. state prisons, reported prevalence estimates of diagnoses or symptoms of DSM axis I disorders, and clearly identified the denominator for prevalence proportions.Articles were excluded if they did not present original data; focused solely on axis II disorders, youths, jails, or foreign prisons; selected samples only of people with mental illnesses or substance use disorders; presented only combined jail and prison prevalence estimates; did not present prevalence estimates [for example, presented only mean scale scores or odds ratios for disorders]; or the denominator for prevalence estimates was not apparent. Samples selected on the basis of substance use were excluded given the high rates at which substance use disorders co-occur with mental illnesses among incarcerated individuals, which would therefore not provide good estimates of mental illnesses per se. A review of the prevalence of substance use disorders in prisons was beyond the scope of this report.MEDLINE, PsycINFO, the National Criminal Justice Reference Service, Social Services Abstracts, Social Work Abstracts, and Sociological Abstracts were searched. For MEDLINE and PsycINFO, combinations of the following medical subject headings [MeSH] were used: mental disorders, mental health, prevalence, incidence, epidemiology, psychotropic drugs, drug therapy, prisons, and prisoners. For the remaining databases, similar keyword combinations, including axis I disorder terms, were searched…The initial search yielded 3,670 non-duplicated articles. Based on titles and abstracts, 3,388 articles did not meet inclusion criteria and were excluded… Full texts of the 282 remaining articles were reviewed, and an additional 254 studies were rejected based on exclusion criteria outlined above… Twenty-eight articles were thus included in the review…
As such, accurately measuring the prevalence of mental illnesses “inside the walls” is essential for community corrections planning. Given the existence of brief, well-validated instruments that screen for mental illnesses, such as the Brief Jail Mental Health Screen, K6, and Correctional Mental Health Screen, reporting standards for routine assessments upon intake are clearly feasible. Even in the absence of such standards, prison administrators, working in collaboration with mental health policy makers and practitioners, can [at relatively low cost] calibrate such screening instruments to their populations and begin collecting valid and reliable prevalence estimates.
Severe mental illness in 33,588 prisoners worldwide: systematic review and meta-regression analysis.by Fazel S and Seewald KBritish Journal of Psychiatry. 2012 200[5]:364-373.
BACKGROUND: High levels of psychiatric morbidity in prisoners have been documented in many countries, but it is not known whether rates of mental illness have been increasing over time or whether the prevalence differs between low-middle-income countries compared with high-income ones.AIMS: To systematically review prevalence studies for psychotic illness and major depression in prisoners, provide summary estimates and investigate sources of heterogeneity between studies using meta-regression.METHOD: Studies from 1966 to 2010 were identified using ten bibliographic indexes and reference lists. Inclusion criteria were unselected prison samples and that clinical examination or semi-structured instruments were used to make DSM or ICD diagnoses of the relevant disorders.RESULTS: We identified 109 samples including 33 588 prisoners in 24 countries. Data were meta-analysed using random-effects models, and we found a pooled prevalence of psychosis of 3.6% [95% CI 3.1-4.2] in male prisoners and 3.9% [95% CI 2.7-5.0] in female prisoners. There were high levels of heterogeneity, some of which was explained by studies in low-middle-income countries reporting higher prevalences of psychosis [5.5%, 95% CI 4.2-6.8; P = 0.035 on meta-regression]. The pooled prevalence of major depression was 10.2% [95% CI 8.8-11.7] in male prisoners and 14.1% [95% CI 10.2-18.1] in female prisoners. The prevalence of these disorders did not appear to be increasing over time, apart from depression in the USA [P = 0.008].CONCLUSIONS: High levels of psychiatric morbidity are consistently reported in prisoners from many countries over four decades. Further research is needed to confirm whether higher rates of mental illness are found in low- and middle-income nations, and examine trends over time within nations with large prison populations.
Method: We identified publications estimating the prevalence of psychotic disorders [including psychosis, schizophrenia, schizophreniform disorders, manic episodes] and major depression among prisoners that were published between 1 January 1966 and 31 December 2010. For the period 1 January 1966 to 31 December 2000, methods are described in a previous systematic review conducted by one of the authors. For the update and expanded review, from 1 January 2001 to 31 December 2010, we used the following databases: PsycINFO, Global Health, MEDLINE, Web of Science, PubMed, National Criminal Justice Reference Service, EMBASE, OpenSIGLE, SCOPUS, Google Scholar, scanned references and corresponded with experts in the field. Key words used for the database search were the following: mental*, psych*, prevalence, disorder, prison*, inmate, jail, and also combinations of those. Non-English language articles were translated. We followed PRISMA criteria. Inclusion criteria were the: [a] study population was sampled from a general prison population; [b] diagnoses of the relevant disorders were made by clinical examination or by interviews using validated diagnostic instruments; [c] diagnoses met standardised diagnostic criteria for psychiatric disorders based on the ICD or the DSM; [d] prevalence rates were provided for the relevant disorders in the previous 6 months.![]()
There is so much divisiveness in discussions of matters that have to do with Mental Health and Mental Illness that it’s sometimes difficult to separate the wheat from the chaff. There’s a strong backlash to the medicalization of psychiatry, the heavy use of medications, the DSM-III etc. diagnostic system, and the claim/implication that all mental illness has some biological basis. On the other side there are claims that psychological counseling focusing on trauma and recovery will clear up most problems now called mental illness. It’s kind of hard to find much to read that doesn’t have some sort of rhetorical bias, visible in the first several paragraphs.
Back in my days on the wards as the de-Institutionalization of mental hospitals was winding down, it would’ve been pretty hard for anyone to maintain a belief that things were going very smoothly. Our admission units were full of people, many psychotic, and hospital beds were evaporating like a sno-cone dropped on hot pavement. At seminars and meetings, the topic was often punctuated by the Szasz meme of that day about the Myth of Mental Illness, and then back to work at the Grady Hospital Emergency room where things didn’t feel a bit mythical at all. Nobody I knew wanted to re-open any huge mental hospitals again. We just wanted short term beds to stabilize patients, and that didn’t mean just medicate, it meant trying to find a source of food and shelter that worked – a social placement, a life. The flow and the dwindling resources worked against that goal, resulting in the revolving door hospitalizations, very high rates of recidivism, and homeless people on the streets and sleeping under the bridges. The back-up promised by the Community Mental Health Movement seemed to be disappearing. The police that had to deal with these patients were fed up and vocal about it when they brought someone in for the second time in a week because the last hospitalization was so brief.
by Prins SJCommunity Mental Health Journal. 2011 47[6]:716-722.
Abstract: Although there is broad consensus that people with serious mental illnesses [SMI] are overrepresented in correctional settings, there is less agreement about the policy trends that may have created this situation. Some researchers and policymakers posit a direct link between deinstitutionalization and increased rates of SMI in jails and prisons, a phenomenon described as transinstitutionalization. Others offer evidence that challenges this hypothesis and suggest that it may be a reductionist explanation. This paper reviews claims from both sides of the debate, and concludes that merely increasing access to state psychiatric hospital beds would likely not reduce the number of people with SMI in jails and prisons. A more nuanced approach is recommended for explaining why people with SMI become involved in the criminal justice system and why developing effective strategies to divert them out of jails and prisons and into community-based treatment is needed to improve both their mental health and criminal justice outcomes.
Discussion In the debate summarized above, proponents of the transinstitutionalization hypothesis may be mistakenly drawing a causal connection between two merely correlated trends: the decline in availability of state psychiatric hospital beds and the rise in prevalence of SMI in jails and prisons. More specifically, they may [a] misinterpret deinstitutionalization as a flood of individuals who were released from state psychiatric hospitals only to be arrested and incarcerated, [b] conflate evidence that people released from psychiatric hospitals often require re-hospitalization with evidence that jails and prisons are serving that function [c] erroneously assume that people who require inpatient services are clinically and demographically similar to people with SMI who wind up in jails and prisons and [d] underestimate the effectiveness of high quality community-based treatment. The evidence against the transinstitutionalization hypothesis is compelling because [a] most people released from state psychiatric hospitals do not appear to end up incarcerated, [b] the characteristics of people with SMI in jails and prisons differ from both the characteristics of people who were deinstitutionalized and the past decades’ increasingly forensic state psychiatric hospital population, and [c] many agree that community-based treatment works for the majority of people with SMI.This is not to say, however, that conclusive evidence currently exists on either side of the debate. More rigorous analysis to clearly define the causal relationship between deinstitutionalization and the overrepresentation of people with SMI in jails and prisons is certainly warranted [for example, retrospectively matching archival inpatient, arrest, and incarceration records]. The arguments presented above should also not imply that the cases for and against increased access to inpatient services are irreconcilable. Indeed, the most important takeaway from this debate may be a fact that is often overlooked by policymakers working to address this issue: people with mental illnesses are not a homogenous population. Increased access to acute and intermediate psychiatric beds may, in fact, be necessary for a small but high-risk, high-cost group of people with severe mental illnesses who cycle through emergency rooms and the criminal justice system without obtaining the treatment they need [Pasic et al. 2005 ]. For these individuals, shortages of 24-hour hospital care [and for this group and others with SMI, affordable housing more broadly] are indeed a problem.
Nevertheless, increased access to inpatient services may not be an optimal focus for a multi-systemic criminal justice/mental health policy strategy. The ramifications of casting too wide an inpatient net would not only be expensive, but would move away from the goal of full community integration of people with mental illnesses that is the hallmark of the rights and recovery movement [New Freedom Commission on Mental Health 2003 ]. Pragmatically, it might be argued, that reinstitutionalizing people with SMI who become involved in the criminal justice system is the lesser of evils, since treatment conditions in psychiatric hospitals are bound to be better than those in jails and prisons. This reasoning, however, addresses one problem by creating a new [but familiar] one, and avoids tackling the issues at the heart of the matter.
Broadly speaking, the popular account of current mental health policy is correct: people with SMI are being ‘‘locked up’’ in jails and prisons as was the case 200 years ago. Understanding why this is happening, however, is important for developing strategies to appropriately divert people with SMI out of jails and prisons and into the treatment they need to become productive members of their communities. The history of deinstitutionalization provides an intuitive but reductionist narrative about the reasons why people with SMI are overrepresented in correctional settings. At the very least, policymakers and researchers should treat the transinstitutionalization hypothesis with caution and not as a presupposition. Failure to approach this issue with the nuance it requires may unwittingly imply expen- sive interventions that will benefit only a fraction of the population at issue. For the large remainder of people with SMI in jails and prisons, other causes of their involvement with the criminal justice system should not be ignored. In this regard, shifts in philosophy and ideology behind the concept of deinstitutionalization are still relevant. For the majority of this group, the key to staying out of hospitals, jails, and prisons may be a place to live, a job or some income support, a meaningful relationship or social network, quality healthcare, or linkage to treatment instead of frequent arrest for substance use disorders — fundamental needs that can best be redressed in the community, not psychiatric or correctional institutions.
by Seth J. Prins, M.P.H.Psychiatric Services. 2014 65:862-872.
Objective: People with mental illnesses are understood to be over-represented in the U.S. criminal justice system, and accurate prevalence estimates in corrections settings are crucial for planning and implementing preventive and diversionary policies and programs. Despite consistent scholarly attention to mental illness in corrections facilities, only two federal self-report surveys are typically cited, and they may not represent the extent of relevant data. This systematic review was conducted to develop a broader picture of mental illness prevalence in U.S. state prisons and to identify methodological challenges to obtaining accurate and consistent estimates.Methods: MEDLINE, PsycINFO, the National Criminal Justice Reference Service, Social Services Abstracts, Social Work Abstracts, and Sociological Abstracts were searched. Studies were included if they were published between 1989 and 2013, focused on U.S. state prisons, reported prevalence of diagnoses and symptoms of DSM axis I disorders, and identified screening and assessment strategies.Conclusions: Definitions of mental illnesses, sampling strategies, and case ascertainment strategies likely contributed to inconsistency in findings. Other reasons for study heterogeneity are discussed, and implications for public health are explored.
by Delbert G. Robinson, Nina R. Schooler, Majnu John, Christoph U. Correll, Patricia Marcy, Jean Addington, Mary F. Brunette, Sue E. Estroff, Kim T. Mueser, David Penn, James Robinson, Robert A. Rosenheck, Joanne Severe,Amy Goldstein, Susan Azrin, Robert Heinssen, and John M. KaneAmerican Journal of Psychiatry. 2014; AiA:1–12; doi: 10.1176/appi.ajp.2014.13101355.
Objective: Treatment guidelines suggest distinctive medication strategies for first-episode and multiepisode patients with schizophrenia. To assess the extent to which community clinicians adjust their usual treatment regimens for first-episode patients, the authors examined prescription patterns and factors associated with prescription choice in a national cohort of early-phase patients.Method: Prescription data at study entry were obtained from 404 participants in the Recovery After an Initial Schizophrenia Episode Project’s Early Treatment Program [RAISE-ETP], a nationwide multisite effectiveness study for patients with first-episode schizophrenia spectrum disorders. Treatment with antipsychotics did not exceed 6 months at study entry.Results: The authors identified 159 patients [39.4% of the sample] who might benefit from changes in their psychotropic prescriptions. Of these, 8.8% received prescriptions for recommended antipsychotics at higher than recommended dosages; 32.1% received prescriptions for olanzapine [often at high dosages], 23.3% for more than one antipsychotic, 36.5% for an antipsychotic and also an antidepressant without a clear indication, 10.1% for psychotropic medications without an antipsychotic, and 1.2% for stimulants. Multivariate analysis showed evidence for sex, age, and insurance status effects on prescription practices. Racial and ethnic effects consistent with effects reported in previous studies of multiepisode patients were found in univariate analyses. Despite some regional variations in prescription practices, no region consistently had different practices from the others. Diagnosis had limited and inconsistent effects.Conclusions: Besides prescriber education, policy makers may need to consider not only patient factors but also service delivery factors in efforts to improve prescription practices for first-episode schizophrenia patients.
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Harvard Mental Health LetterJUN 2010The PORT recommendations, issued in 1998 and first updated in 2003, were funded by the Agency for Healthcare Research and Quality and the National Institute of Mental Health. Researchers at the University of Maryland wrote the latest update after consulting with leading schizophrenia experts. In contrast to efforts like the American Psychiatric Association practice guidelines for schizophrenia and the Texas Medication Algorithm Project, which attempt to address the full range of situations clinicians encounter, the PORT review is more conservative in scope. The PORT authors limit their recommendations to those interventions that have been tested in randomized controlled trials…
Since the last PORT review, two large clinical trials have compared efficacy of first- and second-generation antipsychotics: the Clinical Antipsychotic Trials of Intervention Effectiveness [CATIE] and the Cost Utility of the Latest Antipsychotic Drugs in Schizophrenia Study [CUtLASS]. Based on the findings of these studies, the PORT reviewers noted that in many cases, first- and second-generation antipsychotics are equally effective for treating schizophrenia.First-episode psychosis. The PORT review recommends using any antipsychotic except clozapine [Clozaril] and olanzapine [Zyprexa], because these drugs are most likely to cause significant weight gain and other metabolic side effects. Because patients experiencing psychosis for the first time are both more responsive to medications and more likely to have side effects, antipsychotics should be prescribed at doses that are lower — generally about half — compared with those recommended for patients with chronic schizophrenia.Relapse. Patients who initially responded to medication but suffer a relapse of symptoms have several options. The PORT team recommends any first- or second-generation antipsychotic other than clozapine, and stipulates that medication be prescribed at the lowest effective doses to reduce side effects. Choice of which antipsychotic to use depends on patient preference, past medication response, side effects, and medical history.Maintenance therapy. Studies that have followed patients with first-episode or chronic schizophrenia for one to two years have concluded that continuous maintenance antipsychotic treatment reduces risk of relapse. The PORT review recommends that intermittent maintenance therapy — a strategy of stopping antipsychotics until symptoms reappear or worsen — be reserved only for patients who refuse to continue taking an antipsychotic or for those who cannot tolerate the side effects. For patients with chronic schizophrenia, both first- and second-generation antipsychotics are equally effective at preventing relapse. During maintenance therapy, first-generation drugs may be used at lower doses than those required to treat the initial [acute] episode, while second-generation drugs can be prescribed at whatever dose was effective in the initial phase. Long-acting injectable antipsychotics provide another option in maintenance therapy, especially for patients who have trouble taking medication. The PORT review concluded that it is unclear whether injectable medications are any more effective than pills at preventing relapse, mainly because of a lack of randomized controlled studies….
"The guidelines linked on this page, excluding Major Depressive Disorder, are more than 5 years old and have not yet been updated to ensure that they reflect current knowledge and practice. In accordance with national standards, including those of the Agency for Healthcare Research and Quality’s National Guideline Clearinghouse, these guidelines can no longer be assumed to be current."
by Delbert G Robinson, Margaret G Woerner, Howard M Delman, and John M KaneSchizophrenia Bulletin. 2005 31[3]: 705-722.
Studies with first-episode populations offer the unique opportunity to examine the effectiveness and side effects of medications without the confounding effects of prior medication use. This review focuses upon studies of [1] treatment of the initial episode, [2] maintenance treatment issues, [3] recovery, and [4] side effects. Response rates for the initial episode are high with both conventional and new-generation antipsychotics. However, we lack data directly comparing the new-generation agents with one another for treatment of the initial episode, and data about options for patients with treatment resistance at illness onset are very limited. With the most commonly used pharmacological therapies, the course of early-phase schizophrenia is characterized by repeated relapses and a low rate of recovery. Medication treatment is also associated with a variety of side effects. Of particular concern for treatment of first-episode patients are the metabolic side effects with the new-generation antipsychotics because they occur rapidly, are very distressful to adolescents and young adults, and have long-term medical consequences. Available data support maintenance treatment to prevent relapse, but questions remain about the optimal duration of maintenance treatment, whether there are differences among the new-generation agents for maintenance treatment, and balancing the benefits of maintenance antipsychotics with their long-term side effects.
"The study found that about 40% of patients who’d been diagnosed with having psychotic experiences for the first time in their lives were being too heavily medicated right away."
First episode schizophrenia isn’t that hard to diagnose, so my assumption is that the patients enrolled in the RAISE study fit the bill for that diagnosis. Whether the medications they were on when they showed up are typical for the whole country or represent something else, it’s a bad showing. By my read, it’s worse than these authors say it is. 10% were on no psychoactive medication at all. The only reason I can think of that would explain that is that the clinicians knew they were going into the study and deferred treatment on that basis, but there’s nothing supporting that in the paper. Of the ones on antipsychotics, the big majority were on atypicals [SGAs] in spite of ample evidence that those drugs are no better than the older drugs [FGAs] and the side effects are really no less benign taken en masse. There’s no slightly reasonable explanation why so many were on Olanzapine, and in the higher dose range at that. It doesn’t take Guidelines to know that the weight gain/metabolic profile of that particular drug is a problem waiting to happen, particularly in first episode patients. You can see that in a waiting room. The author’s explanation for the too high dose being related to the treating chronic patients does make some sense relating to using Olanzapine and Haldol, the two drugs given in excess, but that doesn’t make it right. And a third of them taking antidepressants? That’s the kind of thing that happens when doctors equate the class nick-name "antidepressants" with what the drug actually does, and give them to anyone who says "I’m depressed." I know of no evidence that they help people with psychosis who say, "I’m depressed." That’s not who they’re for. We can do a hell of a lot better than what this study reveals. It’s tempting to see this result as a triumph of the "detail men" over science and good sense.
Gaebel et al. report results involving a subsample of first-episode patients participating in a 2-year randomized open treatment study comparing 3 medication strategies: continuous maintenance treatment, prodrome-based intervention, and crisis intervention. Prodrome-based intervention involved the reintroduction of antipsychotic medication as soon as prodromal symptoms [suspected predictors of impending relapse, e.g., restlessness, trouble sleeping, trouble concentrating, tension and nervousness, loss of interest or depression] occurred. Once restabilization was attained the antipsychotic drugs were again discontinued. Crisis intervention provided for the reintroduction of antipsychotic medication only in the case of a full relapse. Relapse rates during the 2-year period for first-episode subjects who completed the study were as follows: maintenance treatment, 38%; prodrome-based intervention, 42%; crisis intervention, 67%.
New York TimesBy GARDINER HARRISOctober 3, 2008One of the nation’s most influential psychiatrists earned more than $2.8 million in consulting arrangements with drug makers from 2000 to 2007, failed to report at least $1.2 million of that income to his university and violated federal research rules, according to documents provided to Congressional investigators.
The psychiatrist, Dr. Charles B. Nemeroff of Emory University, is the most prominent figure to date in a series of disclosures that is shaking the world of academic medicine and seems likely to force broad changes in the relationships between doctors and drug makers. In one telling example, Dr. Nemeroff signed a letter dated July 15, 2004, promising Emory administrators that he would earn less than $10,000 a year from GlaxoSmithKline to comply with federal rules. But on that day, he was at the Four Seasons Resort in Jackson Hole, Wyo., earning $3,000 of what would become $170,000 in income that year from that company — 17 times the figure he had agreed on….
The British Medical JournalThe Carlat Psychiatry Blogby Danny CarlatNovember 6, 2014After substantial delays, the Open Payments website was launched on 30 September. The website was mandated by the Physician Payments Sunshine Act of 2010, and it is a comprehensive registry of payments made to physicians and teaching hospitals by drug and device companies…
Although the website is not complete, it still provides unprecedented insight into the extent and nature of financial relationships between physicians and industry. In total, companies paid $3.5bn [£2.2bn; €2.8bn] to 546 000 physicians [about 60% of all US doctors] and to 1360 teaching hospitals over the five months…
Breakdown of $3.5bn payments made to US doctors in last five months of 2013 Reason for payment Amount ($) Research 1.5bn Physician investors/owners 1bn General: 1bn Royalties and licences 302m Promotional speaking 203m Consulting 158m Food 93m Travel and lodging 74m Education 36m Gifts 19m …The Sunshine Act is only a transparency initiative and does not regulate what doctors can or cannot receive. However, the new website has been launched within a broader context of increasing pressure to reform industry payments…
For several years, many of the larger companies have published their own physician payment registries, most of which were required by settlements of lawsuits alleging illegal marketing practices. As these payments have been made public, several companies have decreased their spending for promotional talks, and one company, GlaxoSmithKline, is eliminating such payments altogether. Like industry, the medical profession is regulating itself. In 2008, the Association of American Medical Colleges published strict conflict of interest recommendations for academic medical centers, which have responded by strengthening their policies. From 2008 to 2014, the percentage of medical schools that ban their faculty from giving promotional talks has increased from 4% to 49%; the percentage of schools banning gifts and meals has also risen sharply. Since 2007, the American Medical Students Association has tracked such conflict of interest metrics in scorecards, which it publishes annually [www.amsascorecard.org]…
How will the Open Payments database be helpful in the future? Although the Sunshine Act was ostensibly passed to allow consumers to make more informed healthcare choices, it is likely that the site will have even more value to researchers and policy makers. The degree to which industry payments actually influence medical care has not been resolved because until now there were scant data with which to properly investigate the issue. But researchers will now be able to compare a trove of industry payment data with other databases recently released by CMS, such as detailed disclosures of physicians’ prescribing patterns.
Even before Open Payments, one research group merged the prescribing database with industry payment data aggregated by the investigative journalism organization ProPublica. They found that payments were strongly correlated with increased prescriptions of companies’ products. Such results, if replicated on a larger scale, may well lead to stricter government regulation of financial relations between companies and physicians. Such regulations, in turn, would hopefully lead to more evidence based healthcare and improved patient outcomes. If so, Open Payments will turn out to be an enterprise well worth the effort.
I am not referring to the companies that manufacture pharmaceuticals or medical equipment and supplies. Such businesses have sometimes been described at part of a "medical-industrial complex’ but I see nothing particularly worrisome about them. They have been around for a long time, and no one has seriously challenged their social usefulness. Furthermore, in a capitalistic society, there are no practical alternatives to the private manufacture of drugs and medical equipment.
I used to feel guilty for not seeing how corrupt things had become in the alliance between academic/organized psychiatry and the pharmaceutical industry – guilty for having dropped so far out of things. At the time, it honestly felt more like psychiatry left me than vice versa, but that’s neither here nor there at this point. Lately, I’m kind of glad to have been so isolated. It allowed me to practice in a way that I felt good about, retiring with a feeling that I’d been able to do what I set out to do. And the five years between retiring and the awakening that article brought were a good respit from a long career. Reading Danny’s post, and skimming through his older posts put me in a reflective mood, and had me thinking about medicine as a whole rather than just psychiatry. The same thing happened reading through Dr. Relman’s articles. Medicine has changed in my fifty years of being around, and I’m not talking about the scientific advances. I’m talking about its businessification, and about the resultant changes in the fabric of its morality.
Health care around the world is beset by rising costs, declining access, stagnant quality, and increasingly dissatisfied health care professionals. Discussions with physicians and other professionals revealed pervasive concerns that the core values of health care are under seige. Patients and physicians are caught in cross-fires between conflicting interests, and subject to perverse incentives. Free speech and academic freedom are threatened. Psuedo-science and anti-science are gaining ground. Causes include the increasing dominance of health care by large organizations, often lead by the ill-informed, the self-interested, and even the corrupt. However, such concentration and abuse of power in health care has rarely been discussed openly. This blog is dedicated to the open discussion of health care’s current dysfunction with the hopes of generating its cures.
by Relman AS.New England Journal of Medicine. 1980 303[17]:963-70.
The most important health-care development of the day is the recent, relatively unheralded rise of a huge new industry that supplies health-care services for profit. Proprietary hospitals and nursing homes, diagnostic laboratories, home-care and emergency-room services, hemodialysis, and a wide variety of other services produced a gross income to this industry last year of about $35 billion to +40 billion. This new "medical-industrial complex" may be more efficient than its nonprofit competition, but it creates the problems of overuse and fragmentation of services, overemphasis on technology, and "cream-skimming," and it may also exercise undue influence on national health policy. In this medical market, physicians must act as discerning purchasing agents for their patients and therefore should have no conflicting financial interests. Closer attention from the public and the profession, and careful study, are necessary to ensure that the "medical-industrial complex" puts the interest of the public before those of its stockholders.
Pharmalot: WSJby Ed SilvermanDec 4, 2014Walk into any physician’s office and promotional messages about medicines can be seen no matter where you look – brochures are typically displayed on a counter and advertorial messages are often playing on a flat-screen TV mounted on a wall. This type of patient outreach, which is called point-of-care marketing, is hardly new, but what is different is that the pharmaceutical industry and other companies selling health products are relying on this form of promotion more than ever before, according to a new study.
Since 2010, the amount of money spent on POC marketing in physician offices, hospitals and pharmacies grew 10% annually, reaching $400 million this year. Nearly 90% of that spending was done by drug makers, says Hensley Evans of ZS Associates, a consulting firm that conducted the study. Moreover, spending on POC is expected to exceed $500 million within the next two to four years. “This is clearly growing in importance,” says Evans, adding that POC communications are second only to television advertising in terms of reaching consumers.
Of course, patients waiting to see a doctor are the classic captive audience. ZS points to another study that found 89% percent of patients say they watch television in a waiting room, and 76% of patients recalled information they read or heard in a waiting room. Moreover, ZS notes that patients can wait 20 to 40 minutes to see a physician, and wait times are expected to rise over the next decade as the number of visits to primary care doctors reaches 565 million in 2025, up from 462 million in 2008. ZS also cites data indicating 65% of patients find POC materials credible because there is an implied endorsement from the doctor. This is a subtle but important distinction from DTC advertising on television, if only because the consumer receives the message at home or in some other surrounding.
Meanwhile, the growth in direct-to-consumer advertising for prescription drugs rose 1.3% on a compounded annual basis. As a result, ZS calculates that POC spending will have accounted for 10% of all DTC spending this year, up from slightly less than 7% in 2010. The shift reflects a few developments. For one, drug makers are increasingly trying to remind patients to take their medicine, since adherence boosts revenue. And ZS notes that a logical forum for delivering that message is in a location where diagnosis and treatment are discussed.
At the same time, drug makers are selling fewer blockbusters to the widest possible patient population and, instead, are increasingly marketing therapies targeted at specific patient groups. This shift calls for more customized marketing than what television commercials may allow, according to ZS. The marketing is apparently having the desired effect. ZS cites data indicating that 84% of patients who visited waiting rooms and were exposed to POC communications report that the messages made them interested in the product.
Nonetheless, Evans does not believe that POC marketing will overtake or supplant other forms of marketing. Rather, she believes that drug makers are simply increasing their POC spending in response to changing business models. “But we are seeing more consumers become more engaged,” says Evans. “They can have a more educated conversion with physicians and not just about a promoted brand [product], but also about broader information for treating a condition.”
If this sounds familiar it is because this is the same explanation that the pharmaceutical industry has used to explain why DTC advertising is beneficial. Some doctors, however, complained that patients were not given complete information or were unnecessarily prompted to ask for certain medicines. Now, though, the marketing is increasingly shifting to the physician office. In effect, the physician has become more of a marketing partner with the pharmaceutical industry.
In 1980, Dr. Relman saw what had already happened in the years after President Nixon opened Pandora’s Box in 1973 [see «parity?»…] with the Health Maintenance Organization Act, "which encouraged rapid growth of Health Maintenance Organizations [HMOs], the first form of managed care." While it may seem far-fetched to propose that things could change in so a short period, that’s certainly how it felt. 1980 was actually probably too late. Dr. Relman was the long-time editor of the New England Journal of Medicine [see Dr. Arnold Relman, 91, Journal Editor and Health System Critic, Dies] who continued the themes in this piece throughout the remainder of his career. I’m not aware of his mentioning psychiatry, but his wife, Marcia Angell, who later also became an editor of the NEJM herself, made up for that in her widely read review of the books of Irving Kirsch [The Emperor’s New Drugs: Exploding the Antidepressant Myth], Robert Whitaker [Anatomy of an Epidemic], and Danny Carlat [Unhinged: The Trouble with Psychiatry] [see in the name of ethics… and no leg to stand on…].
It’s such an old story – Pandora’s Box. She was given a box [actually, a jar] as a wedding present with the injunction to never open it. Pandora’s curiosity won out but in opening the box, she unwittingly unleashed all the evils stored inside to spread throughout the world. So the lesson of the story is that some things, once released, can be neither contained nor put back in the box.
While I would and did argue with the changes Drs. Sabshin and Spitzer brought to psychiatry with the DSM-III, that’s not my point this time. American psychiatry did everything possible to get with the Managed Care program including producing a code book that made things easy for them, gravitating to short sessions primarily focused on symptomatic drug treatments, abandoning traditional in depth evaluations, being empaneled in plans for the insured outpatients, abandoning hospital treatment for the severely disturbed, etc. In addition, Academic psychiatrists "signed on" as authors to papers written by medical writers that exaggerated drug efficacy and minimized adverse events. Many became traveling speakers for the pharmaceutical companies. But it all came for naught. Worse than that, it lead to the routine use of medications for almost anyone who showed up. And now the whole specialty is being appropriately discredited for these practices. Simply put, various industries increasingly controlled the psychiatry from 1980 forward. But psychiatry is just a loud and now very public example of a general trend felt throughout medicine – the one Dr. Relman warned us about in 1980.
In 2012, asked how his prediction had turned out, Dr. Relman said medical profiteering had become even worse than he could have imagined. His prescription was a single taxpayer-supported insurance system, like Medicare, to replace hundreds of private, high-overhead insurance companies, which he called “parasites.” To control costs, he advocated that doctors be paid a salary rather than a fee for each service performed.
Dr. Relman recognized that his recommendations for repairing the health care system might be politically impossible, but he insisted that it was imperative to keep trying. Though he said he was glad that the
signed by President Obama in 2010 enabled more people to get insurance, he saw the legislation as a partial reform at best. The health care system, he said, was in need of a more aggressive solution to fundamental problems, which he had discussed, somewhat philosophically, in an interview with Technology Review in 1989.
“Many people think that doctors make their recommendations from a basis of scientific certainty, that the facts are very clear and there’s only one way to diagnose or treat an illness,” he told the review. “In reality, that’s not always the case. Many things are a matter of conjecture, tradition, convenience, habit. In this gray area, where the facts are not clear and one has to make certain assumptions, it is unfortunately very easy to do things primarily because they are economically attractive.”
PsychiatricNewsby Paul SummergradPresident of the American Psychiatric AssociationDecember 2014Many laws can be difficult to enforce effectively, or in some cases, to enforce at all. That’s long been the case with environmental and human-rights laws, often because violations are committed by many and the government’s ability to inspect and monitor is limited. As psychiatrists, we are already keenly aware of the challenges in enforcing the Mental Health Parity and Addiction Equity Act [MHPAEA]. Yet the violations are all too real and are ones our patients and we experience frequently. APA remains committed to ensuring that parity is much more than a symbolic law. President George W. Bush signed parity into law in October 2008. And it was only last year, in November 2013, that the departments of Health and Human Services, Labor, and Treasury jointly issued the final rule implementing parity. Together the law and the regulations make it clear that patients with a mental illness, including a substance use disorder, should no longer be discriminated against by insurers. But how many patients know specifically what a parity violation looks like? How many of us? We know what it feels like. But it takes education and awareness to help patients be able to identify practices that make coverage for mental health treatment more restrictive than for other medical care. Patients who know their rights are better equipped to protect their rights.
That’s why I am pleased to provide you with a new tool to support parity enforcement. It’s a poster, developed by APA, titled “Fair Insurance Coverage: It’s the Law” and can be downloaded here…
No, this post isn’t about insurance. I don’t know anything about that, having practiced "off the grid." If my patients used insurance, I was an "out of network provider" and they did their own filing and collecting. This post is about something else…
When I was a medical house officer in the 1960s, there was a widely used term, "supratentorial". The Tentorium is membrane that supports the Occipital Lobe, separating the Cerebum from the Cerebellum [the Cerebrum being the "thinking" part of the brain]. It was a slang, a code word that patients didn’t understand that sounded medical. So in a bedside presentation, the presenter might say, "or this could be a supratentorial problem" – meaning, "it’s in his head" – meaning, a psychological rather than a physical problem – meaning, "there’s nothing really wrong". There were a lot of dismissive terms around like that for people who had what were then called "neurotic" symptoms. And that’s where things usually stopped. We were heroically occupying the front lines, locked in holy battle with "real" life-threatening physical illnesses and had little time or patience for "neurotic" problems. Patients with the major psychiatric illnesses like Schizophrenia or Melancholia who showed up un the medical wards were different – more like "hot potatoes." Psychiatrists were called and speedy transfer was the name of the game.
My own interest came later – in practice. At first, I was awed at how many of the patients who were referred to me as an Internist who turned out to have "neurotic" or "psychosomatic" symptoms [75% – I counted]. Then I started asking them some questions and doing some exploring, and I discovered a whole new world of things were just too interesting not to pursue. But the point here is about legitimacy. In training, physical diseases were the legitimate domain of Medicine proper. And many patients feel the exact same way, feeling discounted by suggestions that their symptoms might not have some physical basis. And if physicians and their patients tend to see a biological basis as the sine qua non of legitimate medical illnesses, the insurance companies paying for medical care are absolutely adamant on that point. It’s not at all hard to see why that is.
A century ago, these matters were less clear. Many of the patients of the day presented much more dramatic symptoms that those seen now – paralyses, anesthesias, blindess. In fact, the term "neurotic" originally meant something akin to "neurology-like," psychologically derived symptoms that looked like brain or nerve problems. Much of what the early psychoanalysts had to say about such cases has been assimilated by our culture, and those "neurology-like" syndromes are rarely seen. The psychoanalysts and other psychotherapists turned their attention in a different direction – personality problems, post-traumatic syndromes, etc. And so about the insurance companies of the 1970s. Since most of us have our glitches or "baggage" from the past, the boundaries between normal and abnormal begin to fade, then disappear. So any given person and any given psychiatrist or psychotherapist could decide on any given day that a long course of psychotherapy was indicated [and frequently did] – aided and abetted by the DSM-II [1968-1980] that legitimized its vaguely psychoanalytic criteria for the "Neuroses."
And then, in what seemed like the twinkling of an eye, the businessification of Medicine [Managed Care, HMOs, PPOs, Hospital Corporations] and the [re]medicalization of Psychiatry [DSM-III, biological treatment, PHARMA] turned everything upside-down. The DSM-III couldn’t achieve legitimacy in the usual medical way [biological markers, etiology], but it did produce a syndromatic symptom-oriented medicalesque classification that made no mention of matters psychological [etiologically neutral]. We all know the rest of that story. The DSM-III legitimized a biologically oriented psychiatry. The DSM-III legitimized the non-psychiatric mental health specialties’ access to medical insurance, albeit in a tightly managed way. It even legitimized the patients’ illnesses – having a named and numbered Disorder, "I have been diagnosed with Bipolar Disorder." It wasn’t "in your head" anymore, it was "in your brain". In practice, most psychiatrists did medication management using the new drugs that flowed steadily from the PHARMA pipeline. Our journals filled with Clinical Trials of those drugs and reports of the advances in biological brain science – genomics, proteinomics, neuroimaging, cognitive sciences, and the like. The mental-illness-as-manifestation-of-brain-disease meme increasingly crept into the discourse, and by 2002, the fledgling DSM-5 Task Force announced that the biology would be added to the next revision of the diagnostic manual.
Apparently, the medication management/therapist split with its managed care reimbursement was an adequate enough compromise, because things settled down and the wars of the 1970s abated. As I said in the last post, it became something of a "therapist"/"psychiatrist" symbiosis. And this was an outpatient oriented solution aimed at treating what the psychologist next door called the walking wounded – the not so very ill. Hospital Care for the more profoundly afflicted was radically trimmed – almost to zero. People were only hospitalized in the direst of circumstances based not so much on treatment needs or treatment plans, but because there were no alternatives [and discharge planning started in the admission office] – very short stays. Patients with psychotic illnesses like Schizophrenia or Mania were mainly treated in the dwindling public sector with service availability varying widely from place to place. If you saw a severely ill patient, getting them adequate treatment was a nightmare with or without their being insured.
This system may have been an adequate compromise for the reimbursement needs of mental health clinicians, but it wasn’t so hot for the patients who felt the constraints of its limitations – a feeling shared by many of the "providers" who felt as if they were doing First Aid rather that medical care. Patients referred to psychiatrists rarely left without a medication prescription. "Counseling" was often time limited or catch-as-catch-can. Over the years, there has been an increasing disillusionment with the efficacy [and/or safety] of the ubiquitous psychiatric medications. While it’s true that all medical care has suffered under the system of Managed Care, mental health care has been the most closely watched, the most severely cut, the most vulnerable to being shaped by its control. We may have been declared legitimate, but apparently not all that legitimate. It feels like the whole medical system is run on cutting out everything they can get away with cutting, and in mental health, they can get away with cutting a whole lot. The disparity between medical coverage and mental health coverage was obvious to anyone that looked, and ultimately lead to the Mental Health Parity and Addiction Equity Act, signed in 2008. But, as Dr. Summergrad points out, it hasn’t really even been implemented – thus, this pdf APA poster. I guess it’s supposed to be stuck up on the office wall.
I started with the remembered attitudes towards matters mental from my medical house officer days – those "supratentorial" problems – because I actually think that attitude has controlled our fate [and by "our" I mean all of us – psychiatrists, psychologists, social workers, etc. and our patients with mental health problems]. The late-coming Mental Health Parity and Addiction Equity Act is an attempt to fix something that has largely shaped and contorted our specialties for forty years – another piece of legislation [see Managed Care]:
…and vice versa. Psychiatry did everything in its power to fit into the new Managed Care system – "a for-profit model that would be driven by the insurance industry." It created a medical diagnostic system [DSM-III] and adopted the principles of evidence-based medicine. Out came the white coats, and our journals followed suit with the graphs and tables more familiar from the medical journals. Psychiatry accepted the abbreviated sessions of medical consultations and the closing of our non-cost-effective hospitals. The psychologists, social workers, counselors jumped on board and agreed to accept the mandates and control of managed care – happy to be included. PHARMA didn’t just jump into the mix, they dove in with wild abandon, passing out some of the fortune they reaped from the windfall along the way. Researchers began to search for the missing links, the biomarkers that would concretize full membership in the medical fraternity.
But try as we might, psychiatry and the other mental health disciplines never had the bargaining power of the rest of medicine. We just didn’t really fit, in spite of our claims and an inordinate amount of chest-beating. So we’ve been clay in the hands of the bean counters, and had to follow their lead rather than leading – all of us. Worse than that, our patients most in need were left out of the loop. It goes without saying that "a for-profit model that would be driven by the insurance industry" would hardly be expected to focus on a chronic, psychotic [largely uninsured] population – people who need ongoing care and where the goal is often to prevent deterioration rather than effect some measurable cure. So parity? legitimacy? not even close.
Mad in Americaby Allen Frances, M.D. and Robert WhitakerDecember 4, 2014
It’s there for all to read so I won’t try to summarize it here. I’d suggest reading it, actually reading it several times. Because it’s so familiar, I tended to skim it the first time through. And it deserves a more thorough reading. The other thing I would suggest is to pretend you are a psychiatrist if you’re not. And pretend you’re not a psychiatrist if you are. We’re in such a rut with all of this, that about all you’ll come away with is having rooted for your home team if you don’t do something to break the frame of your well-worn ideas or ideology.
I have a lot of respect for these men. Both have done something creative and courageous by running against the tide of the times. They’ve inserted themselves into the center of important debates that had grown monotonous, moved things into a much more productive though certainly no less divisive trajectory. I’ve read their writings with interest, and like most, I feel the better informed for having done it. But after reading this debate several times, I was surprised to find that I didn’t really think that either one of them had it quite right – too many straw men [heroes and villains]. But after writing multiple versions of this post, and then erasing them, I decided that I’m not really capable of transcending my own experience of the major issues covered in this debate and would start by talking about that experience.
Even in its inadequately funded days, the Community Mental Health Movement was partially successful. The Asylums disappeared and the patients were, indeed, back in the community. As a psychiatry resident in the first year, I spent my days with the patients who didn’t fit, who were too ill to manage being in open society and were brought or came to the "Emergency Receiving Unit" where I was assigned. In those days, I encountered the writings of Thomas Szasz early from a fellow resident [see Szasz by proxy…]. The model of the times was focused on relapses, episodes of intense psychosis, and the idea was to treat them with medications and return the patients to the community as quickly as possible. It was a laudable goal, but only when it worked. Unfortunately, chronic psychosis doesn’t respond to the medication like the acute illness does, and the patients don’t like to take it for reasons easily discovered if you take only one pill yourself. And so there was a subset of "revolving door" patients who came or were brought back to the hospital regularly. And there was the specter of Tardive Dyskinesia, a potential neurologic consequence of long term medication that you only have to see once to live in terror of causing.
I had not come to psychiatry to be in charge of keeping the streets of Atlanta safe nor to involuntarily treat anyone. I had discovered that many of the patients who came to my office as an Internist were there because of emotional tangles. I could see what was wrong, but I had no idea what to do, so I came to a psychiatry residency to find out. I knew nothing of psychosis – meeting it for the first time in my early thirties in a big city charity hospital in a difficult historical epoch. And that part was, indeed, difficult. I struggled with the same issues I now read about on Mad-in-America. Besides the fellow resident who was Szaszian, I was fortunate to have an advisor, Dr. Jonas Robitscher, a psychiatrist, psychoanalyst, lawyer who had famously written The Power of Psychiatry. While his conclusions were similar to those of Szasz, he was not a "blamer." He was a Civil Libertatian who believed that the right to due process belonged in our courts, not our doctors. As he related it, the historical addition of psychiatrists to the commitment process antedated the coming of medication, and was originally conceived as a reform movement to keep small town judges from "sending away" undesirables to mental hospitals.
Some years later, I had the opportunity to work with a lawyer friend tasked with drafting a new version of our State’s commitment law for the legislature. We changed it to make judicial review mandatory rather than voluntary. On the next iteration, he was able to change it further to take "psychiatrist" out of the mix altogether [see a clarification…]. That was years ago. I believe that’s now a general trend among the States. But what I’m arguing with is not the details. It’s the implication in Whitaker’s debate piece and among those who write on his site that psychiatrists want that power, or hang on to it [the power to commit] as a tool to retain some kind of hegemony among the mental health disciplines or power over patients. I’ve not seen that to be true. My own complaint is the opposite – that psychiatry proper has ignored the care of the chronic mental patients during the last quarter century just like everyone else – including the other mental health disciplines and governmental agencies. From my perspective, there are no heroes in this story.
While I am much more on the side of Bob Whitaker in looking at what happened in 1980 in terms of the APA and academic psychiatry, I see the forces at work and the motives in a very different way. Both Allen Frances and Bob Whitaker leave out too much of that story for my tastes, and neither addresses what I consider to be the central player in the piece – money. In the 1970s, the major third party payouts by medical insurance in mental health were for inpatient hospitalizations and long psychotherapies. That was not going to continue, and mental health coverage was under attack. That was a major factor in the medicalization of psychiatric diagnosis in 1980 – legitimizing access to third party payments. In that regard, it was successful for psychiatrists and the other mental health disciplines. I doubt it would’ve happened otherwise. What then happened was unexpected, at least by me. The insurance carriers took charge and split up mental health care. The [more expensive] psychiatrists were paid for medical things like medication management. The psychotherapy/counselling was partitioned to other disciplines in carefully controlled and monitored contracts. In-patient reimbursement essentially disappeared. The non-psychiatrists were happy to get access to covered care. Many psychiatrists migrated to medication management. And voila` – that was that. Most referrals to participating psychiatrists came from the now covered psychologists, counsellors, and social workers. It was a symbiosis and many patients/clients spoke of "my psychiatrist" and "my therapist" as an inter-related pair. Psychiatry and the other mental health disciplines needed to change in those days, but the changes that came were driven by economics, and that trend escalated when PHARMA jumped onboard. The chronic psychotic patients were marginalized in the process and the criminal justice system did the only thing it knows how to do – put many of them in jail.
I left those years being involved with the treatment of the psychotic patients feeling much the same way about psychotic illness as that advocated by Dr. Sandra Steingard in the current Mad-in-America CME – antipsychotics for acute psychosis with a constant drive towards as little as possible or none thereafter. I followed some patients with those diagnoses long term and was impressed that a practical psychotherapy tailored to fit the illness was more effective than I might have imagined [see 1. from n equals one… and the posts that follow]. But I was less successful in sustaining zero medication than I would’ve hoped, but I still never stopped trying.
I agree with Robert Whitaker about what happened when Managed Care, PHARMA, academic psychiatry, and the APA got together – it was a perfect storm of the worst kind. Pick any post on this blog to confirm that, though most of mine focus on the corruption involved in the clinical trials and promotion of drug treatments. But I don’t at all agree with his blanket indictment of psychiatry in the plight of our chronic mental patients. Psychiatry was just one of many who ignored them, including the other mental health disciplines, our governments, and our culture. I have nothing but respect for those psychiatrists, psychologists, and social workers who stuck with these patients on the front lines in the face of so little support. But I likewise have little positive to say about the KOLs who pontificated about their care from afar and generated guidelines of questionable scientific validity.
Nothing in life prepared me for the complexity of the schizophrenias – the acute psychoses, the chronic forms, the residual or negative symptoms, or even the miraculous recovery seen in some. It took years to get a feel for the many different ways they affect the lives of those afflicted, and there are surprises aplenty – good and bad for even the most experienced clinicians. Looking back over the history of the our various approaches, a clear pattern emerges. Each new reform movement has been built on the failures of what came before and ultimately replaced it – accompanied by great expectations bolstered by small samples of evidence. Over time, the refuges of the Quakers became the asylums of Dorthea Dix became the snake pits of the 1950s. The liberation of de-Institutionalization lead to a lot of desperate homelessness with people living under bridges. Szasz’s Myth of Mental Illness was a factor in inappropriately filling our prisons – just another kind of Institutionalism. The miracle of Thorazine became the cause of Tardive Dyskinesia and Chemical Restraint. I like the current Recovery meme, and the Open Dialog approaches of Northern Finland Whitaker mentions. They are hopeful hypotheses awaiting pilot projects and careful study with an eye to what kind of support is needed to see if they can work in an urban America. And while I am personally an advocate of minimizing the use of antipsychotics, I wasn’t nearly as successful as I wished to be. Medications overused? oh yes. Medications essential? more often than I thought. Likewise, I am a lifelong Civil Libertarian, but have seen many psychotic people who can’t manage with no restraint and end up losing all freedom when they would fare much better with much less restriction.