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May 5, 2018 by Sandra Steingard, MD

20-year Outcomes for First-episode Psychosis: Impact of Neuroleptic Drug Discontinuation

Standard treatment guidelines in psychiatry recommend that neuroleptic drugs are continued indefinitely after a person has experienced more than one psychotic episode. These recommendations are based on studies which have found a higher rate of recurrence of psychosis among those who stop as compared to those who remain on drug.

Anatomy of an Epidemic raised concerns about the long-term outcomes for those who remain on these drugs. Most psychiatrists, including me, assumed that by reducing risk of relapse one would be improving long-term outcome. However, there seems to be reasonable evidence that this assumption is not correct.

Not only does long-term use of drugs expose people to the risks of weight gain and tardive dyskinesia, the drugs may also impair functional outcome. My own view is that this is a discussion psychiatrists need to have with their patients. A person may choose to accept a higher (and not inevitable) risk of recurrence of psychosis as a way to minimize the long-term risks of negative outcomes associated with staying on drug.

While it appears that psychiatric authorities continue to favor long-term use of drugs for most people who have experienced multiple episodes of psychosis, there is less uniformity of opinion regarding recommendations following a single psychotic episode. Current guidelines recommend drug treatment for two to five years, the idea being that if a person remains well during that time, it might then be safe to stop the drug.

A recent study by Tiihonen and colleagues, “20-Year Nationwide Follow-Up Study on Discontinuation of Antipsychotic Treatment in First-Episode Schizophrenia,” published in The American Journal of Psychiatry, is an attempt to shed light on this issue. The authors’ conclusion stated in their abstract is that “contrary to general belief, the risk of treatment failure or relapse after discontinuation of antipsychotic use does not decrease as a function of time during the first 8 years of illness and that long-term antipsychotic treatment is associated with increased survival.” This is a sobering finding and the paper warrants careful review and reflection.

It is hard to study outcomes over extended periods of time. To address this problem, Tiihonen and colleagues have been using, as the basis of their research, the extensive databases available from registers in Finland that allowed them to determine diagnosis, hospitalizations, and death. From the national prescription register, they can determine reimbursed medication dispensations to all residents of Finland. Reimbursed medications is used as a proxy for medication adherence.

In this study, they were interested in the correlation between adherence to medication after a first hospitalization during which a person is diagnosed with schizophrenia with subsequent re-hospitalization and death. By determining who was adherent to medications and for how long, they could determine whether longer adherence would correlate with reduced rate of re-hospitalization.

The cohort under study included individuals who had been admitted to a psychiatric hospital between 1994 and 2014 and given a diagnosis of schizophrenia. To identify those who were experiencing a first episode, they excluded any individuals who had been prescribed an antipsychotic drug for the year prior to this index admission. From this group they excluded anyone who was re-hospitalized or died within 30 days of discharge from hospital. At that point (30 days post discharge from index hospitalization), they identified 4,217 users of antipsychotic drugs and 3,217 non-users. Of the 4,217 users, 1,714 were subsequently identified as discontinuers if during the follow-up period they stop having prescriptions issued to them. That group was further subdivided according to the time between discharge from first hospitalization and stopping of drug: <1 year (1,019), 1-<2 years (284),2-<5 years (274) and  greater than 5 years (137). They then analyzed these groups over time until they died, were re-hospitalized, stopped drug (for users), or started drug (for non-users).

The authors had thought that those who remain on drug for longer periods of time might have better outcomes when the drugs are stopped, but this is not what they found. While the continuous users did best with regard to re-hospitalization rate, the group that did second best were those who stopped immediately. The longer one remained on the drug, the greater the risk of re-hospitalization if the drug is stopped as compared to those who remain adherent. The group that fared worse were those who stopped after five years.

They also analyzed death rates and in this analysis, they compared three groups: continuous users, non-users and those who discontinued within one year (these were the groups with the highest numbers). The death rate was highest among non-users and best among those who had continuous use of drug although the deaths in all groups were low.

This paper supports a recommendation for long-term use of the drugs even among those who have only experienced one episode of psychosis.

This paper offers a bird’s eye view. This was naturalistic in the way that Harrow’s work was naturalistic; the numbers are much bigger but outcomes are cruder. Tiihonen uses re-hospitalization as a proxy for relapse whereas Harrow and colleagues met with each person and conducted extensive assessment. Harrow studied individuals for 20 years regardless of outcome. In this study, the follow up period ended when the person was hospitalized or died.

In that regard, this study privileges relapse in the way that so many other studies have done over the years. We do not know anything about quality of life. Implicit in the treatment recommendations that may come from this study is that it is never safe to stop an antipsychotic. While that may be true if “safe” is synonymous with reducing one’s chance of re-hospitalization, it may not be true if we were able to evaluate different kinds of outcome measures.

There is other valuable information in this data. Over 43% of individuals never start the drug and by one year, almost 57% have stopped. By the end of the study, 33.6% of the total cohort of 7,434 are still on drug. People do not want to take these drugs and regardless of this data, we still need to figure out how to engage with them in ways that might help them navigate the world with less risk to their well-being and safety.

It is also interesting that while treatment failure was higher among the discontinuers (38%), it was not exactly low in the adherent group who was used as a match sample (29.3%). Obviously, this means that the rate of remaining out of hospital is 62% for those who stop and 71% for those who remain on drug. A reasonable person might chose those odds and decide to stop especially if there is a plan in place to try to intervene if problems arise.

In this study, we know nothing about treatment, the way the drug was stopped, or overall quality of life. We also do not know what happens to those who do have a second hospitalization. It is assumed that one relapse indicates that long-term treatment is advised but I no longer believe that.

That is where other sources of data have relevance for me but these are the kinds of data that tend to be discounted. This is first person experience, qualitative analysis, self-report.  I have met too many individuals in the survivor community who took some time to sort out their troubles but eventually found some peace without the drugs. Eventually some chose to take some medications but not everyone did. For those who found their way through, it seemed to take years. That is what is suggested in the Harrow data. At two years, those who are not on drug are still experiencing a high degree of psychosis. Their improvement is only observed after 4 years. In contrast, those on drug continue to experience a fairly high rate of symptoms.

I listened recently to a short story written by a former girlfriend of Will Hall. Will is a brilliant man who has written about his own experiences with psychosis and has literally written the book on ways to stop psychiatric drugs. The story, by Susie Meserve, is part of an anthology, Show Me All Your Scars: True Stories of Overcoming Mental Illness. This funny and touching story chronicles their life together for a brief time. I confess to harboring private wonderings, having met Will, heard him speak, read his writing, that perhaps he was not “truly” psychotic. This is not an uncommon reaction from psychiatrists who meet a person who appears to have recovered from psychosis.

Something in this story helped me to understand that if I had met Will during his tougher times, I would likely have concurred with the diagnosis, schizophrenia, which was bestowed on him. And in that era, I would likely have predicted dire consequences when he chose to ignore the medical advice that he remain on the drugs. I would have been worried when he struggled and I would have suggested he resume the drugs. His story helps me understand that there are other paths and this is a message I can share with the people I see as well as with worried families.

On the other hand, I have known people who are so tortured by their experiences that there seems to be little room to engage. They are overcome by their world that can be distorted to the point that there is no safety for them even with those who are eager to just make a connection. For them the drugs can be enormously helpful.

I know others who are horrified by their psychosis and want to do everything they can to prevent a recurrence. Even if the drug only confers a slight advantage, they chose to take them.

And I do not discount those worried families. They are often experiencing their own trauma. Psychosis can be very scary for those who are trying to care for the person at the center of concern. I understand their wish to prevent it. I just want them to have a full understanding of what the drugs can and cannot do.

This paper offers some comfort to those who chose to stay on the drugs. It suggests that we must always be cautious when stopping them. But I would still assert that it does not tell us that staying on the drugs is the best path for everyone.


s-steingardNamed to “Best Doctors in America,” Dr. Sandra Steingard is Medical Director at HowardCenter, a community mental health center where she has worked for the past 21 years. She is also clinical Associate Professor of Psychiatry at the College of Medicine of the University of Vermont. For more than 25 years, her clinical practice has primarily included patients who have experienced psychotic states. Dr. Steingard serves as Board Chair of the Foundation for Excellence in Mental Health Care.

 

First published at MadInAmerica.com/2018/05/20-year-outcomes-for-first-episode-psychosis-impact-of-neuroleptic-drug-discontinuation/

3 thoughts on “20-year Outcomes for First-episode Psychosis: Impact of Neuroleptic Drug Discontinuation

  1. Chris Gordon says:

    What a thoughtful and measured analysis! I think this is very wise. Thank you, Sandy. Chris Gordon

  2. Jon Delman says:

    Very thoughtful!
    I work with this group on employment/education/careers now… I’ve always believed that a job/career or other meaningful activities and relationships will improve outcomes. Lots still to be learned.

  3. Pablo says:

    Excellent analysis Sandy.
    Thanks much for your in depth review of the paper and pragmatic approach.

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