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By
John F. Clarkin, Clinical Professor of Clinical Psychology in Psychiatry Co-Director, Personality Disorders Institute, Weill Medical College of Cornell University, New York, NY USA
Two dominant methods can be utilized today for matching the individual patient with the most optimal treatment. The method receiving extensive attention at this time is the empirically supported treatment movement (Chambless and Hollon, 1998). In this methodology, the patient who presents with a particular DSM disorder is matched with a therapist who is armed with a specific treatment, usually cognitive-behavioral, that will focus on and alleviate the symptom in a brief period of time. The suggestion that it is unethical to do otherwise implies that our training programs for clinicians should be focused on this match of patient symptoms with cognitive-behavioral technology.
However, a number of issues make one pause and resist joining the band-wagon of the empirically supported psychotherapy movement:
Most patients present with more than one, clearly defined, DSM disorder. This is especially true of those individuals with severe personality disorders.
Focused cognitive-behavioral treatments are limited in their effectiveness in the short-run, and often seem inadequate in the long-run. At termination from short-term treatment, a majority but not all patients has been helped with his/her symptoms. Upon follow-up, a much smaller group of patients has maintained their gains (Westen and Morrison, 2001).
The emphasis on therapy as a set of technical interventions tends to ignore the attributes of the therapist beyond just his/her skill in delivering specific techniques. This metaphor of a therapist as a dispenser of techniques leads logically to a computer providing programmed direction.
If a treatment fails and the patient drops out prematurely, it is often assumed that the patient's characteristics are the major contributor to the disruption. We have examined data describing such patients, including but not limited to diagnosis (Clarkin and Levy, 2004). The therapist's contribution to the failure has been less frequently examined.
Family members of patients with schizophrenia frequently report burdens associated with caring for their relatives.
Aims
We evaluate the impact of illness beliefs on the burden reported by family care-givers of people with bipolar illness.
Method
The multivariate relationships between patient symptomatology and family illness beliefs and report of burden were examined at baseline among care-givers of 266 patients with Research Diagnostic Criteria-diagnosed bipolar illness who were subsequently followed for 15 months.
Results
At baseline, 93% of care-givers reported moderate or greater distress in at least one burden domain. As a group, care-giver illness beliefs (illness awareness, perception of patient and family control) explained an additional 18–28% of variance in burden experienced beyond the effects of the patients clinical state and history.
Conclusions
Care-givers of patients with bipolar illness report widespread burden that is influenced by beliefs about the illness.
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