Nice article on risk assessment

28 09 2007

A colleague pointed me to a nice article on suicide risk assessment written by David J. Muzina, MD in the September issue of Current Psychiatry Online.   The article is well-written and well-organized.  The stepwise approach described can be quite helpful.  I wish the article included more on documentation (there is only one sample note, and I’m not sure how helpful it is).   The article also pays scant attention to families.  But otherwise this is a really solid general reference on the subject.

Related Posts:

Where’s the Family?

At the crossroads of family therapy and suicide prevention





Reminder from the bridge: Suicidal individuals are full of ambivalence

28 09 2007

Sign on NYS BridgesToday Mike Hogan, Ph.D., the Commissioner of the New York State Office of Mental Health honored RNN-TV and the NYS Bridge authority for their work in suicide prevention. The bridge authority put up signs and installed lifeline phones with direct link to the National Suicide Prevention Lifeline.

For clinicians assessing and managing suicide risk, the fact that phones installed on a bridge have been used by individuals who went on to live is testimony to just how much ambivalence remains, even in people who have gone very far toward resolved plans and preparatory behavior.

Understanding that ambivalence is key to clinical work with suicidal individuals. When I train clinicians about assessment and response to suicide risk, I often get questions about whether it is useful or even right to assess suicide risk. I’m also asked, “What about people who have good reasons for killing themselves or who rationally decide they want to end their lives?” My answer goes something like this:

Thankfully, for health care professionals there is no practical dilemma here. If you find out about a person’s suicidal thinking, then there is some degree of ambivalence. Everyone knows that psychotherapy or primary care are about health…that is life. We’re not about suicide and death. So if someone is coming to us, at least some small part of them is aligned in that direction. And it’s our job to understand that ambivalence and work toward health and life until such time as the ambivalence is resolved in one direction or the other.

That line of thinking can apply to any person, really–not just healthcare professionals. Except in some rare circumstance that you’d have to work hard to construct, the fact that someone is still alive and letting someone know by words or action about suicidality reflects ambivalence.

The fact that people read signs and use phones on bridges also discourages a fatalistic stance on the part of clinicians. We can’t simplify the matter by saying “If someone really wants to kill themselves they will, so what’s the point of screening or assessing?” That question misses the point. We assess because people don’t want to kill themselves. Some just don’t see options for life and, under the wrong circumstances (like under the influence of substances or after a particularly deep emotional wound), they overcome their ambivalence just long enough to do the unthinkable. We need to have deep compassion for the amount of pain that must be, and nurture the life-embracing side of the ambivalence until the person can see options again.





I’m an intellectual stalker!

20 09 2007

One of the URMC colleagues with whom I previously talked about blogging, asked me about mindmapping today (see my mapping posts).  Because she has sequentially hit upon a couple of my key interests, she questioned whether she’s an “intellectual stalker”–a phrase I thought was just hilarious.  Part of what tickles me about the phrase and concept, is that “intellectual stalking” is what the blogosphere is all about!   RSS is the übertool of the intellectual stalker, allowing a person to obsessively track the thoughts and experiences of another.  Best of all–it’s anonymous and free!   Thank you to my colleague for this great phrase!





Conversation with Michelle Lang, Ph.D. of RFMH

18 09 2007

I had an interesting conversation a few weeks ago with Michelle Lang, PhD, a colleague with the New York State Research Foundation for Mental Hygiene. RFMH is essentially the research and program evaluation arm of the NYS Office of Mental Health. Dr. Lang has completed a pilot study on the feasibility of routine suicidality screening in community mental health, which she conducted in collaboration with the CSPS here at the University of Rochester.

Dr. Lang and her colleagues learned a great deal from their pilot. As someone developing clinician training in risk assessment, I was especially interested in what they discovered about the range of clinician reactions to the idea of screening for suicide risk:

  • Many clinicians shared the popular myth that asking about suicide might make it more likely.
  • There was more resistance to the screening than the implementation team anticipated.
  • Reactions, both positive and negative toward the program were strong.

There were many other lessons, and I look forward to reading the process papers that will come out of the experience.

Reflections: Many of the experiences Dr. Lang shared point to how difficult and loaded the topic of suicide is for clinicians–even the most experienced ones. As a trainer, this highlights to me the need to find predictable and replicable ways to create a safe learning environments, where clinicians feel understood and where their current practice patterns are honored. This can be hard to do when you are suggesting a change in practice. Dr. Lang and her colleagues made huge efforts to support clinicians, yet still encountered challenges.

Making clinicians feel safe enough in a training that they’ll consider changing practice patterns involves the tone and stance, as well as the content of a training. In reviewing training curricula, I’ve discovered that tone, stance, and conceptual starting points are often not explicitly developed. Contrast this with the way people develop treatment interventions and manuals. For example, in the first chapters of Marsha Linehan‘s highly successful intervention manual, Linehan lays out an entire dialectical worldview that undergirds her intervention program. That kind of elaboration is rare in developing educational interventions. A recent conversation I had with DeQuincy Lezine, Ph.D. underscored this point for me–he advocated for using “logic models” to examine the assumptions and mechanisms behind any community or training program.

Here are a few ideas about tone, stance, and starting points that I’d like develop further:

  • Drawing on Marsha Linehan’s work again, clinician training in suicide assessment requires a balance in the “dialectic” between unconditional acceptance and push for change. Why is this balance so important (and difficult) when it comes to suicide? Perhaps Linehan’s concept of “invalidating environments” may apply more than we’d like here, as well. Many of the administrative and legal systems in which we work are invalidating and blaming! Furthermore, one’s work vis-à-vis suicide is so personal and fundamental that the suggestion of need for improvement can be hard to take in.
  • Another way of considering the stance and tone needed for effective clinical training in this area from a stages of change (transtheoretical) perspective, i.e. that training needs to have a motivational interviewing stance. The trainer must have an awareness of the ambivalence toward change, and present change tentatively and in a way that draws upon the internal motivation clinicians have to improve their practice in this regard. In my trainings, I’ve found that one way to do that is to talk about the unspoken dissatisfaction I carried for years about the experience of working with suicidal patients–I share with participants that I always found the experience unrewarding and that I had a vague pre-verbal sense that the way I approached suicide was probably not that helpful to the individuals I worked with. In addition to being genuine, that kind of stance may stoke clinician motivation in a way that the public health arguments do not.
  • In addition to these considerations regarding the pedagogical stance, there are also content emphases that might reduce clinician resistance. As I have noted in almost every post on teaching and training, I feel training in this area should begin with what and how clinicians think and that many efforts in clinician training have the wrong starting point-i.e. they begin with the question: “what do experts say clinicians know about suicide or suicide risk assessment” rather than “what do clinicians want to know.” In my experience, clinicians are most hungry for how to document their work and decisions so that they can feel less anxious and can focus on doing what is best for the patient. If that’s the case (and this remains an empirical question), then documentation should be a starting point…through which other content (including what experts would say clinicians should know) can be delivered.

Thanks again to Dr. Lang for an informative, stimulating, and enjoyable conversation. She is doing good and interesting work with the State. I look forward to reading the papers that come out of her most recent project, and about the next stages of it development.





Blogging out in the open: Response to post from Wynne Center Board

10 09 2007

Some of the members of the Wynne Center for Family Research board read my blog post from yesterday about my presentation to the Board.  When I saw them today their response was quite positive–lots of comments (and humor) about it.  This brings me back to some of my initial posts about blogging in a professional setting (see Blogging out in the open in a clinical setting and How clinicians learn: Web 2.0 Opportunities?).   I’m now at the point of being pretty open about it where I work, and I continue to see it as a useful way for developing ideas, connecting with others with similar interests, and disseminating information to and dialogue with front-line clinicians and trainees.





Presentation to Board of Wynne Center for Family Research

9 09 2007

I presented at the Wynne Center for Family Research (WCFR) board meeting today. I presented about our clinical services and about my work in suicide risk assessment, including how it grew out of experiences with suicidal patients in couples and families. The Center board and the faculty of the WCFR were present.

The Board is unbelievable–a real dream team for family systems fans:

Barbara Fiese, Ph.D., Syracuse University
Nadine Kaslow, Ph.D., Emory University
William Pinsof, Ph.D., Northwestern University
Harry Reis, Ph.D., University of Rochester (Liaison)
Frederick S. Wamboldt, M.D., National Jewish Medical Center
Karen Weihs, M.D., University of Arizona

Given the stature and brilliance of this audience, I was both nervous and eager to get their feedback about our clinical service and about the work that has grown out of it. Here are my notes, and some reflections, from the discussion that followed my presentation:

— One board member shared an experience she had many years ago working with a prominent family therapist as her supervisor. She recounted the following experience:

She worked with the family of an adolescent who had attempted suicide. She wanted to do a suicide risk assessment as part of her session with the family. Her supervisor, at first, discouraged her because it wasn’t “systemic.” She persisted and ultimately prevailed by offering to do a suicide assessment for each person present (not just the child) and to invite others present to provide input on the others’ assessment! The supervisor allowed this as sufficiently systemic.

Reflection: This is a fascinating story that highlights the tension inherent in melding an activity that has traditionally been part of an individualistic medical model with a family systems view of people, their problems, and their strengths. I think few family therapy supervisors nowadays would advise against suicide risk assessment. Suicide risk assessment is taught (with a range of how much) in every family therapy training program. But I’m not sure if we’ve developed a lot further in terms of the actual how-to. My impression is that most of the time, there continues to be a one-dimensional linear approach to training suicide assessment that implicitly assumes individual therapy and interviewing.

– Other thoughts:  One key to resolving the potential tension is to think about suicide as residing in a family system. This view goes beyond thinking about family members a “collateral informants”, which is how family involvement is often described in the suicide literature. Instead, we need to develop conceptual AND CLINICAL models for assessing risk through the lens of interactions, relationships, roles, and family myths. For example, how does the hopeless that registers in the individual grow out of family roles and interactions…or from a strength-based approach how might shifts in the family give greater hope to the individual experiencing suicidality.  It is not that this is never talked about, it’s just that the focus on individual psychopathology and personality often overshadows this dimension–and perhaps more so than with other behaviors we assess and intervene with because the act of suicide is ultimately unilateral and done when alone.

– One member asked about me “sharing” what I’m working on. This is an important question to me on several levels:

  1. Blog. This blog is one mechanism I’m using to share thoughts and discoveries.
  2. Planned publications. I am on the cusp of conducting an evaluation of my risk assessment workshop and plan to publish the results. I am also working on another publication in which I’m collaborating with two faculty members of the Deaf-Wellness Center.
  3. Career Direction. If what I’m doing turns out to be helpful to clinicians and to families, I want to share it widely. That brings up interesting questions about how I spend my time professionally. Given the range of my interests (in terms of content (peds primary care, suicide) and professional activities (teaching, writing, clinical work), it is hard to know the right direction. A career in research is appealing in ways it hasn’t been in the past. This is probably a dilemma many of my readers (especially those in academia) are familiar with. I’ll be focusing on discerning this over the next year or so.

– After I talked about this blog, a board member recommended using it as a way of helping to disseminate science to general audience. I have done this a little (such as here), but could probably do more.

– A board member suggested that, in light of how heavy it is to focus on suicide (an adverse outcome), it would be advisable for our clinical service to also gather stories and data about positive outcomes of family therapy. This is a perceptive and appreciated comment because prevention of a bad outcome does have a peculiar emotional tone for an individual or group. I named this blog “Commitment to living” in part to cast this work in a positive direction. This comment is a good reminder to do that kind of thing in many ways also at a system level.

All of that in 30 minutes! I appreciated the opportunity to consult with such bright and experienced senior experts in our field.