Blog - Western State Hospital Internship Program

Interviewing at WKPIC

Posted on November 23, 2016 by Susan Vaught

WKPIC’s staff has begun the process of reviewing applications for the 2017-2018 intern year. We’re excited!

Soon, letters will go out, and we hope that we will meet many of you who applied to our program. If you accept, you’re probably wondering what our interview will be like.

For basic info, check out our Interview Information section. Note the “wear comfortable shoes” bit, if you plan to participate in the tour of the 165+ year-old Western State Hospital.

No, you really don’t have to study or prepare. We trust you have done that in graduate school. Ours is not a cut-throat or competitive process. We want you to see if you could be happy here and learn from us, and we want to see if we can teach you, and if you would enjoy being in our area and having the experiences we can offer. Seriously, you can wear comfortable shoes. If you Match with us, you’ll definitely want to wear them to work, too!

Just brings yourselves, and what you’ve learned. That’s enough. We look forward to meeting you!

Susan R. Redmond-Vaught, Ph.D.
Director of Psychology, Western State Hospital
Director, WKPIC

Posted in Announcements, Application Tips, Blog, Dr. Vaught, Match | Leave a comment

Friday Factoids: Disruptive Mood Dysregulation Disorder

Posted on October 28, 2016 by Susan Vaught

Disruptive mood dysregulation disorder (DMDD) is a newer diagnosis in childhood that is depicted by extreme irritability, anger, and frequent outbursts (National Institute of Mental Health [NIMH], 2016). Irritability is a clinical symptom of both bipolar disorder and DMDD (Wiggins et al., 2016). Comparatively, irritability in DMDD is “severe and relatively invariant over time,” yet irritability experienced with bipolar disorder may occur while a child is euthymic and may increase during manic or depressive episodes (Wiggins et al., 2016, p. 722). Thus the inclusion of DMDD in part allows for appropriate diagnosis for children with “severe, nonepisodic irritability” that is distinct from bipolar disorder (Wiggins et al., 2016, p. 722).

With DMDD being a new diagnosis, treatment is often based on other disorders with shared symptomatology (e.g., attention-deficit/hyperactivity disorder, anxiety disorders, oppositional defiant disorder, and major depression; NIMH, 2016). Cognitive-behavior therapy (CBT), parent training, and computer-based training are recommended psychological interventions (NIMH, 2016) for DMDD, where as medications may also be considered. For instance, stimulants may help address irritability, antidepressants may mitigate irritability and mood problems, and atypical antipsychotics could be used to alleviate severe outbursts with physical aggression (NIMH, 2016).

The potential for adverse effects with some treatments limit their use in children, resulting in the necessity to explore noninvasive means for treatment (Wiggins et al., 2016). For instance, the use of a video game to reduce the misinterpretation of ambiguous faces in children with irritability has shown to help reduce anger-based reactions found in DMDD. The literature has shown that children with DMDD and bipolar disorder tend to rate neutral faces as angry (Wiggins et al., 2016). Research conducted by Wiggins et al. (2016) has demonstrated that a computer game helped to change the tendency to misinterpret ambiguous faces as angry in irritable children. After training, children were more likely to rate ambiguous faces as happy (Wiggins et al., 2016). Such an intervention may appear superficial, however this research has demonstrated that brain activation patterns when labeling emotional faces differs between DMDD and bipolar disorder (Wiggins et al., 2016). Specifically, amygdala activation related to irritability differed between children with DMDD and bipolar disorder; and temporo-occipital regions of the brain had “associations between irritability and activation in response to ambiguous angry faces” (Wiggins et al., 2016, p. 728).

Thus, differing brain activation patterns helped distinguish the clinical presentation of DMDD versus bipolar disorder (Wiggins et al., 2016). As a result, the authors conclude that though irritability is a common symptom of both DMDD and bipolar disorder, they are in fact distinct disorders and given the different neural correlates, treatments may also be different (Wiggins et al., 2016).

References
National Institute on Drug Abuse (NIDA). (2016). Disruptive Mood Dysregulation Disorder. Retrieved from http://www.nimh.nih.gov/health/topics/disruptive-mood-dysregulation-disorder-dmdd/disruptive-mood-dysregulation-disorder.shtml

Wiggins, J. L., Brotman, M. A., Adleman, N. E., Kin, K., Oakes, A. H. Reynolds, R. C.,…Leibenluft, E. (2016). Neural correlates of irritability in disruptive mood dysregulation and bipolar disorders. American Journal of Psychiatry, 173, 722-730.

Dannie S. Harris, MA
WKPIC Doctoral Intern

Posted in Blog, Continuing Education, Current Interns, Friday Factoids, Mental Health and Wellness | Tagged Disruptive Mood Dysregulation Disorder, DMDD, DMDD vs. Bipolar Disorder, treatment options for DMDD in children | Leave a comment

Friday Factoids: Methamphetamine Psychosis

Posted on October 21, 2016 by Susan Vaught

As reported by the National Institute on Drug Abuse (NIDA; 2013) methamphetamine use continues to be a significant problem, with over 12 million people or 4.7 percent of the population having tried methamphetamine at least one time. According to NIDA (2013), methamphetamine use can cause memory loss, aggression, psychotic behavior, damage to one’s cardiovascular system, malnutrition, and dental problems.

Chronic use may cause an individual to have difficulty feeling pleasure outside of use, as well as anxiety, confusion, insomnia, mood disturbance, and violent behavior. Psychotic features experienced include paranoia, delusions, and visual, auditory, and tactile hallucinations. Stress has also been related to spontaneous methamphetamine psychosis in individuals who have abused methamphetamine in the past (NIDA, 2013). With acute methamphetamine intoxication individuals may experience hallucinations (auditory, visual, tactile), persecutory, influence, and control delusions, as well as are prone to violence (Zarrabi, Khalkhali, Hamidi, Ahmadi, & Zavarmousavi, 2016).

Even after intoxication passes, psychosis may occur over a prolonged period of time (Zarrabi et al., 2016). Acute psychosis usually has a maximum period of four to five days (Zarrabi et al., 2016); yet, a differing course of psychosis has been documented in the literature. For instance, three clinical groups for stimulant-induced psychosis have been identified: the first group is characterized by transient psychosis, where the duration of symptoms is limited to four or five days and may be associated with withdrawal; with the second group, psychosis is typically resolved in less than one month; and in the third group, psychosis may last several months or years (Zarrabi et al., 2016). It has been estimated that between 5-10% of individuals with methamphetamine-induce psychosis may not fully recover (as cited in Zarrabi et al., 2016).

Risk factors for methamphetamine-induced psychosis are duration, frequency, and amount of use, history of sexual abuse, family history, other substance use, and co-occurring personality and mood disorders (Grant et al., 2012). Of note, substance intoxication is differentiated from a substance/medication-induced psychotic disorder if reality testing for altered perceptions remains intact (American Psychiatric Association, 2013).

Zarrabi, Khalkhali, Hamidi, Ahmadi, and Zavarmousavi (2016) indicate there are no structured treatment guidelines for methamphetamine-induced psychosis. In their study, risperidone and olazapine were most frequently used, as well as benzodiazepines to reduce restlessness. Antipsychotics were reportedly preferred due to better control of violent behaviors. Another study indicated that quetiapine could also be used as an antipsychotic treatment with comparable effects to haloperidol (Verachai et al., 2014). Electroconvulsive therapy (ECT) has been used to control severe aggression and violent behaviors, as well as thoughts of suicide and homicide in methamphetamine-induced psychosis (Zarrabi et al., 2016). Results indicated that after six to nine sessions of ECT, symptoms began to disappear. Though limited by constraints of a case study, Grelotti, Kanayama, and Harrison (2010) again demonstrated the positive effects of ECT on methamphetamine-induced psychosis.

Overall, the most common symptoms with methamphetamine-induced psychosis are paranoid delusions and auditory hallucinations, and such symptoms may prove resistant or refractory to antipsychotic medications (Grelotti, Kanayama, & Pope, 2010). As indicated in the literature, clinicians faced with refractory cases of methamphetamine-induced psychosis may consider ECT as a treatment option.

References
American Psychiatric Association. (2013). Diagnostic and statistical manual of mental disorders (5^th ed.). Washington, DC: Author.

Gerlotti, D., Kanayama, G., & Pope, H. G. (2010). Remission of persistent methamphetamine-induced psyhcosis after electroconvulsive therapy: Presentation of a case and review of literature. The American Journal of Psychiatry, 167(1), 17-23.

Grant, K. M., LeVan, T. D., Wells, S. M., Li, M., Stoltenberg, S. F., Gendelman, H. E.,…BEvins, R. A. (2012). Methamphetamine-associated psychosis. Journal of Neuroimmune Pharmacology, 7(1), 113-139.

National Institute on Drug Abuse (NIDA). (2013). Methamphetamine. Retrieved from https://www.drugabuse.gov/publications/research-reports/methamphetamine

Verachai, V., Rukngan, W., Chaswanakrasaesin, K., Nilaban, S., Suwanmajo, S., Thanateerabunjong, R.,…Kalayasiri, R. (2014). Treatment of methamphetamine-induced psychosis: a double-blind randomized controlled trial comparing haloperidol and quetiapine. Psychopharmacology, 231(16), 3099-3108.

Zarrabi, H., Khalkhali, M., Hamidi, A., Ahmadi, R., & Zavarmousavi, M. (2016). Clinical features, course and treatment of methpahetamine-induce psychosis in psychiatric inpatients. BMC Psychiatry, 16, 1-8.

Dannie S. Harris, MA
WKPIC Doctoral Intern

Posted in Blog, Continuing Education, Current Interns, Friday Factoids, Mental Health and Wellness, Resources for Interns | Tagged consequences of meth use, meth, methamphetamine, Methamphetamine Psychosis | Leave a comment

Friday Factoids: Motivational Interviewing as a Clinical Option for Generalized Anxiety Disorder

Posted on October 14, 2016 by Susan Vaught

Cognitive-behavior therapy (CBT) has shown to be efficacious for treating anxiety, yet some clients “either fail to respond, respond only partially, or relapse at follow-up” (Westra, Constantino, & Antony, 2016, p. 768). As reported by Hunot, Churchhill, Teixeria, and Silva de Lima (2007; as cited in Westra et al., 2016), only 46% of clients with Generalized Anxiety Disorder (GAD) demonstrated significant improvement after therapy. One factor that may contribute to poorer outcomes is ambivalence. Ambivalence in anxiety is holding positive beliefs about worry and being reluctant to change or let go of the worry (Westra & Arkowitz, 2010; as cited in Westra et al., 2016). Additionally, therapeutic directness or demands related to change might be met with resistance (Westra et al., 2016). Thus, additional components that work with ambivalence may boost treatment outcomes by working through resistance, all while remaining anchored in CBT.

Motivational Interviewing (MI) is a treatment with a focus on ambivalence (Miller & Rollnick, 2002). Here the therapist is not the advocate for change, rather therapists assist clients to be their own advocate for change (Westra et al., 2016). With specific strategies, MI helps reduce resistance and “increases intrinsic motivation” for change (Westra et al., 2016, p. 769). In their study, Westra, Constantino, and Antony (2016) investigated the effects of integrating MI and CBT for severe GAD. In the study, one group received 15 weekly session of CBT alone (CBT-alone) and another group had 4 sessions of MI followed by 11 sessions of CBT integrated with MI (MI-CBT). Initially, there were no posttreatment differences between groups; yet, at the 6- and 12-month follow-up, several group differences emerged. The MI-CBT group reported a continued improvement on self-reported worry and general distress after treatment ended. MI-CBT clients also had significantly higher rates of recovery and clinically significant change (five times as likely to not meet diagnostic criteria for GAD). Westra et al. (2016) indicated that similar sleeper-type effects are often reported with MI use in treating other disorders.

So, why did clients continue to improve after treatment? Westra et al. (2016) indicated that the opportunity to explore ambivalence and becoming more committed to change might help clients not respond to worry, thus reducing relapse rates. Additionally, the authors suggested that MI techniques fostered the development of personal agency, which may have led to the client’s belief that they are capable of change, resulting in internalization of this belief. By “rolling with resistance” and viewing the “client-as-expert” helped to “promote internal attributions for progress” (Westra et al., 2016, p. 777). With this model, the efficacy of CBT treatment for GAD is maintained, yet by integrating MI where clients can openly explore resistance may help clients become more receptive to traditional CBT techniques.

References
Miller, W. R., & Rollnick, S. (2002). Motivational interviewing: Preparing people for change (2nd ed.). New York, NY: Guilford Press.

Westra, H. A., Constantino, M. J., & Antony, M. M. (2016). Integrating motivational interviewing with cognitive-behavioral therapy for severe generalized anxiety disorder: An allegiance-controlled randomized clinical trial. Journal of Consulting and Clinical Psychology, 84(9), 768-782.

Dannie S. Harris, MA
WKPIC Doctoral Intern

Posted in Uncategorized | Tagged CBT and Motivational Interviewing, Generalized Anxiety Disorder, Motivational Interviewing | Leave a comment

Friday Factoids: Working With Children Who Have Early-Onset Schizophrenia

Posted on October 7, 2016 by Susan Vaught

Though diagnostic criteria for early-onset schizophrenia are the same for adults and children, the treatment approach may differ. For instance, discussing the symptoms of psychosis with children can be challenging. Often parental report is utilized when discussing symptoms; however, as noted by Caplan (2011), parents may be unaware of the experience of hallucinations by their child.

Children may not spontaneously talk about hallucinations due to others negating the experience (e.g., It’s nothing; It’s only your imagination), being scared to talk about it, feeling they will burden their parents with it, or believing that talking about the hallucination will make it happen (Caplan, 2011). Clinicians should use careful wording to ask about hallucinations. Delusions, like hallucinations, should be differentiated from normal developmental phenomena (e.g., fantasies, magical thinking; Caplan, 2011). Though morbid fantasies may be upsetting, they too are common (Caplan, 2011); however, if they are pervasive and acted upon they might be “precursors of delusions” (Caplan, 2011, p. 60). Disorganized speech and thought disorders are reflected in illogical thinking, loose associations, and impaired discourse skills (Caplan, 2011; Shatkin, 2015). This communication difficulty must be distinguished from language problems related to language disorders or intellectual disability (Caplan, 2011; Stentebjerg-Olesen et al., 2016); thus it may be beneficial to refer to speech or language therapist to help clarify diagnoses.

Compared to adults, negative symptoms are more prominent in children and adolescents (Harvey, James, & Shields, 2016). Additionally, negative symptoms are noted to be predictors of poorer clinical and functional outcomes (Harvey et al., 2016). Other symptoms related to early-onset schizophrenia are abnormalities of gait, posture, and muscle tone (Shatkin, 2015).

Given the trajectory and progressive course of schizophrenia, early identification and intervention should be emphasized, especially in light of the findings that longer duration of untreated psychosis and poorer premorbid adjustment are associated with poorer outcomes (Stentebjerg-Olesen, Pagsberg, Fink-Jensen, Correll, & Jeppesen, 2016). Furthermore, early-onset schizophrenia is often refractory to treatment. Recent research has indicated that clozapine demonstrated greater efficacy compared to other antipsychotics (Kasoff, Ahn, Gochman, Broadnax, & Rapoport, 2016), where as other research (Harvey et al., 2016) demonstrated that antipsychotics showed a trend of reduction of symptoms compared to placebos, but only olanzapine and risperidone demonstrated statistically significant improvements for positive symptoms, as well as general psychopathology as measured by the Positive and Negative Syndrome Scale (PANSS).

References
Caplan, R. (2011). Childhood schizophrenia: Diagnostic and treatment challenges. Cutting Edge Psychiatry in Practice, 3(1), 55-67.

Harvey, R. C., James, A. C., & Shields, G. E. (2016). Assess the relative efficacy of antipsychotics for the treatment of positive and negative symptoms in early-onset schizophrenia. CNS Drugs, 30(1), 27-39.

Kasoff, L. I., Ahn, K., Gochman, P., Broadnax, D. D., & Rapoport, J. L. (2016). Strong treatment response and high maintenance rates of clozapine in childhood-onset schizophrenia. Journal of Child and Adolescent Psychopharmacology, 26(5), 428-435.

Shatkin, J. P. (2015). Child & adolescent mental health: A practical, all-in-one guide. New York: W. W. Norton & Company.

Stentebjerg-Olesen, M., Pagsberg, A. K., Fink-Jensen, A., Correll, C. U., & Jeppesen, P. (2016). Clinical characteristics and predictors of outcome of schizophrenia-spectrum psychosis in children and adolescents: A systematic review. Journal of Child and Adolescent Psychopharmacology, 26(5), 410-427.

Dannie S. Harris
WKPIC Doctoral Intern

Posted in Blog, Continuing Education, Current Interns, Friday Factoids, Mental Health and Wellness, Resources for Interns | Tagged early onset schizophrenia, schizophrenic symptoms in children, symptoms of psychosis in children | Leave a comment

Friday Factoids: Effective Parenting

Posted on September 30, 2016 by Susan Vaught

In a press release for the American Psychological Association, Hamilton (2015) reviewed Larzelere’s presentation on effective parenting. Larzelere and his research team interviewed 102 mothers who described five times they disciplined their toddlers (ages 17 months to 3 years) for hitting, whining, defiance, negotiating, or not listening. The findings indicated that regardless of the type of behavior, compromising was the most effective for immediate behavioral improvement. For mildly annoying behaviors, reasoning was the next most effective. Punishments (e.g., timeout or taking away something) were more effective than reasoning for defiance or hitting; yet punishments were least effective for negotiating or whining. Additionally, reasoning was not effective for defiance or hitting.

When interviewed two months later, a different pattern emerged. Children were reportedly acting worse when mothers too frequently used compromising for hitting or defiance. Reasoning was reportedly the most effective over time, even though it was noted to be the least effective for these behaviors when used immediately. For defiant children, a moderate use of timeouts and other punishments resulted in improved behavior.

Hamilton (2015) also discussed Cipani’s research on punishment. Capani indicated that often timeouts do not work because they are not used properly. For example, spur of the moment timeouts are noted to not be effective. Capani indicated that children should know ahead of time what behaviors result in timeout and that consistent use of time out for specified behaviors has shown to significantly reduce problem behaviors.

Consequences of parental discipline style has been linked to both internalizing (e.g., withdrawal, anxiety, depression) and externalizing (e.g., aggression, delinquency, hyperactivity) behaviors in youth (Parent, McKee, & Forehand, 2016). Harsh discipline (e.g., physical or corporal punishment [hitting or spanking when angry]) often reinforces oppositional behavior (Granic & Patterson, 2006, as cited in Parent et al., 2016) and models hostile interaction patterns (Pettit et al., 1993, as cited in Parent et al., 2016). With regard to lax discipline (permissiveness and inconsistency), permissiveness often results in both internalizing and externalizing behaviors in children, where as inconsistency is associated with the development of more externalizing behavior than internalizing behavior (Parent et al., 2016).

Seesaw discipline, which is considered both harsh and lax, has been linked to high levels of internalizing problems in youth (Parent et al., 2016). Though parental education often focuses on the consequences of harsh and permissive discipline, it may be beneficial to discuss seesaw discipline as well, and paying close attention to the consequences of youth internalizing behaviors (Parent et al., 2016).

Further consideration related to parents suffering from psychopathology may also need to be discussed. Research has indicated that parents with psychopathology tend to create chaotic and unpredictable home environments, which may be aligned with inconsistent parental discipline (Parent et al., 2016); thus, psychoeducation and training for this population may be beneficial.

Dannie S. Harris
WKPIC Doctoral Intern

References

Hamilton, A. (2015). Punishing a child is effective if done correctly. Retrieved from http://www.apa.org/news/press/releases/2015/08/punishing-child.aspx

Parent, J., McKee, L. G., & Forehand, R. J. (2016). Seesaw discipline: The interactive effect of harsh and lax discipline on youth psychological adjustment. Journal of Child and Family Studies, 25, 396-406.

Posted in Blog, Continuing Education, Current Interns, Friday Factoids, Mental Health and Wellness, Resources for Interns | Tagged defiant children, effective parenting, seesaw discipline | Leave a comment

Article Review: Cannon, T. D., Yu, C., Addington, J., Bearden, C. E., Cadenhead, K. S., Cornblatt, B. A.,…Kattan, M. W. (2016). An individualized risk calculator for research in prodromal psychosis.

Posted on September 21, 2016 by Susan Vaught

Psychosis has been described as a terrifying experience that has been associated with shame, guilt, and humiliation (National Alliance on Mental Illness [NAMI], 2011). As indicated by NAMI (2011) delay in assessment, identification, diagnosis, and treatment for psychosis is a public health crisis, for which efforts of prevention and early intervention are now being emphasized throughout communities. Therefore, understanding the onset of psychosis is necessary.

For the majority of individuals there is a period prior to the onset of psychosis during which individuals begin to exhibit changes in beliefs, thoughts, and perceptions (Cannon et al., 2016). Though not a diagnosis, according to the Center for the Assessment and Prevention of Prodromal States (CAPPS; 2011) this period of time is the prodromal period and could last from a couple of days to years. It is during this time that the subtle changes are said to represent “attenuated forms of delusions, formal thought disorder and hallucinations” (Cannon et al., 2016, p. 1). Individuals with such an onset or prodromal psychosis are designated high-risk and over a 2-year period, about 20% to 35% of these individuals go on to develop full psychotic symptoms (Cannon et al., 2016, pg. 1). As a result, Cannon et al. (2016) created a risk calculator to calculate the probability of conversion to psychosis among individuals identified with prodromal psychosis.

Cannon et al. (2016) emphasized that past research has investigated risk factors for conversion (e.g., demographic factors, symptoms), yielding high predictability and specificity, yet low sensitivity for the identification of conversion. Their current research focused on the ability to scale risk during initial patient contact by using easily accessible clinical, cognitive, and demographic variables. The study utilized data from the second phase of the North American Prodrome Longitudinal Study from 2008 to 2013. Participants in this study participated in the Structured Interview for Prodromal Syndromes (SIPS) and the Structured Clinical Interview (Diagnostic and Statistical Manual- [DSM] IV). Individuals with substance dependence, neurological disorders, an estimated IQ below 70, or past diagnosis of a psychotic disorder were excluded from the study. Follow-up evaluations were schedule for every 6-months for 2 years. Participants were identified as having high-risk syndromes (attenuated psychotic symptoms syndrome, brief intermittent psychotic symptom syndrome, and familial risk and deterioration syndrome). The final cohort consisted of 596 participants, who were followed up to the point of conversion to psychosis or up to 2 years.

By assessing the importance of each predictor variable, Cannon et al. (2016) created a risk calculator by “using time-to-event proportional hazards regression” (p. 2). The authors identified eight predictor variables apriori: age; SIPS items P1 and P2; Brief Assessment of Cognition in Schizophrenia (BACS), symbol coding raw score; Hopkins Verbal Learning Test-Revised, scores summed; stressful life events; family history of psychosis; a decline in functioning as shown on the Global Functioning Social Scale; and trauma history. More specifically, the SIPS items P1 and P2 assess unusual thought content and suspiciousness, which, per Cannon et al. (2016), for high-risk individuals have shown to be strongly predictive of psychosis. Additionally, the literature has demonstrated that slower processing speed, lower verbal learning, and memory functioning are predictive of conversion (Cannon et al., 2016). A decline in social functioning prior to conversion, childhood traumas, and stressful life events have also been shown to be predictive of psychosis in high-risk individuals. The Research Interview Life Events Scale and the Childhood Trauma and Abuse Scale were used to assess traumatic experiences. Finally, family history of psychosis was included though the authors indicated the literature does not support this factor as a “robust predictor” of conversion (p. 3). Regardless it was included due to the elevated risk compared to individuals with no familial history.

The results indicated that within the 2-year period, 84 individuals in the sample converted to psychosis. The mean time to conversion was 7.3 months. A 16% probability of conversion was reported. The overall model’s C-index was 0.71. Overall, the authors concluded that high levels of suspiciousness and unusual thought, decline in social functioning, lower verbal learning and memory performance, slower speeds of processing, and a younger age at baseline created a higher risk for conversion to psychosis. The variables of stressful life events, trauma, and family history were not predictive of conversion.

Given that this study used an established database, generalizability could be a concern. The authors argue for “predictive inference” (p. 4), due to the community based service centers used in the establishment of the database. Still, for clinical utility, each respective client should be assessed regarding relative fit to the sample. Additionally, the authors report that the output for the risk calculator is without a confidence interval. Thus, individuals are provided a percentage for conversion risk, which is taken without consideration of error or a range of values. As such, there is concern of patient distress if the risk calculator yields a relatively high conversion probability. The authors note the benefit of utilizing the risk calculator for identifying research participants (e.g., meeting a particular threshold), utilizing this risk calculator to communicate risk relative to treatment, and to identify the cost-benefit ratio related to treatment options. The risk-calculator did not include biological factors, and with future research may need to be amended to accommodate other factors that are predictive of conversion.

Overall this tool is related to early identification of risk, yet it appears to be more so applicable to research studies. The authors further note that a decision tree has been installed to ensure that individuals who use the risk calculator are in fact professionals that have conducted a SIPS interview and the client has a diagnosis of a prodromal risk syndrome. This risk calculator appears to be a practical tool, but clinical utility may be equivocal due to concerns of reporting risk of conversion to clients and not providing a probability of remission. The risk calculator is aligned with early intervention. Knowing the probability of conversion may help encourage clients to engage in treatment and help clinicians or researchers recommend treatment options best aligned to meet the client’s needs.

Dannie S. Harris
WKPIC Doctoral Intern

References
Cannon, T. D., Yu, C., Addington, J., Bearden, C. E., Cadenhead, K. S., Cornblatt, B. A.,…Kattan, M. W. (2016). An individualized risk calculator for research in prodromal psychosis. American Journal of Psychiatry. Advance online publication. http://dx.doi.org/10.1176/appi.ajp.2016.15070890

Center for the Assessment and Prevention of Prodromal States. (2011). What is the Prodrome? Retrieved from https://www.semel.ucla.edu/capps/what-prodrome

National Alliance on Mental Illness. (2011). First episode: Psychosis, results from a 2011 NAMI survey. Retrieved from http://www.nami.org/psychosis/report

Posted in Blog, Continuing Education, Current Interns, Mental Health and Wellness | Tagged early identification of psychosis, prodromal psychosis, risk of psychosis | Leave a comment

Friday Factoids: Diagnosing Early-Onset Schizophrenia

Posted on September 16, 2016 by Susan Vaught

Early-onset Schizophrenia is defined by an onset prior to adulthood, with an onset prior to 12 years of age being rare (Vyas et al., 2011). The Diagnostic and Statistical Manual of Mental Disorders (5^th ed.; DSM-5; American Psychiatric Association, 2013) identifies early onset as being associated with a worse prognosis. The DSM-5 further emphasizes that childhood schizophrenia is more difficult to diagnosis, where as compared to adults, “childhood delusions and hallucinations may be less elaborate” (p. 102), and visual hallucinations should be “distinguished from normal fantasy play” (p. 102). Furthermore, hallucinations are not uncommon in both healthy children and children with a psychiatric illness, yet often with childhood schizophrenia, hallucinations are multimodal (Driver, Gogtay, & Rapoport, 2013). Diagnostic criteria for schizophrenia are “age independent” (Stentebjerg-Olesen, Pagsberg, Fink-Jensen, Correll, & Jeppesen, 2016), which is supported by diagnostic stability throughout the lifespan.

Yet there is still ambiguity with differential diagnosis for early-onset schizophrenia. As noted by Stentebjerg-Olesen, Pagsberg, Fink-Jensen, Correll, and Jeppesen (2016) there is “considerable overlap in phenomenology between schizophrenia and affective symptomatology in children and adolescents with psychosis” (p. 411). As cited in Stentebjerg-Olesen et al. (2016), Weary (1992) and Masi et al. (2006) the most common diagnostic mistake is a “misclassification of a mood disorder as schizophrenia” (p. 411). Other diagnostic considerations extend to pervasive developmental disorders, severe personality disorders or traits, posttraumatic stress disorder (PTSD), generalized anxiety disorder, and obsessive-compulsive disorder (Driver et al., 2013). As such understanding the “developmentally sensitive descriptions of symptomatology, clinical characteristics, and outcome” may offer a clearer diagnostic picture for early-onset schizophrenia (Stentebjerg-Olesen et al., 2016, p. 411).

In a systematic review of studies from 1990 to 2014 of early-onset psychosis, Stentebjerg-Olesen et al. (2016) found that hallucinations were mainly auditory (81.9%) and delusions were mostly persecutory and of reference (77.5%). Formal thought disorder was found in 65% of the patients and 36% had disorganized speech or pressured speech. Negative symptoms were found in about half of the patients, and half of the group with negative symptoms experienced positive symptoms as well. Comorbidity was high at 32% for substance abuse and 33.5% for ADHD and disruptive behavioral disorders. Trauma is also thought to play a significant role in early-onset schizophrenia, with Stentebjerg-Olesen et al. (2016) finding a high level of comorbid PTSD (34%).

Stentebjerg-Olesen et al. (2016) found that “severity of positive symptoms at baseline, the severity and the persistence of negative symptoms, longer [duration of untreated psychosis], and poorer premorbid adjustment each predicted a worse outcome of illness” (p. 423). Longer duration of untreated psychosis and poorer premorbid adjustment were also associated with poorer outcomes. In short, patients with early-onset schizophrenia were found to have substantial impairment from positive and negative symptoms, disorganized behavior, and pre- and comorbid conditions and diagnoses. The authors note that the “high prevalence of negative and disorganized” symptoms “may mask the emergence of psychosis” and delay identification and treatment (p. 424).

Dannie S. Harris
WKPIC Doctoral Intern

References
American Psychiatric Association. (2013). Diagnostic and statistical manual of mental disorders (5^th ed.). Washington, DC: Author.

Driver, D. I., Gogtay, N., & Rapoport, J. L. (2013). Childhood onset schizophrenia and early onset schizophrenia spectrum disorders. Child and Adolescent Psychiatric Clinics of North America, 22(4), 539-555.

Vyas, N. S., Patel, N. H., & Puri, B. K. (2011). Neurobiology and phenotypic expression in early onset schizophrenia. Early Intervention in Psychiatry, 5, 3-14.

Posted in Uncategorized | Tagged childhood mental illness, early onset schizophrenia, Schizophrenia, schizophrenia spectrum | Leave a comment

Interviewing at WKPIC

Friday Factoids: Disruptive Mood Dysregulation Disorder

Friday Factoids: Methamphetamine Psychosis

Friday Factoids: Motivational Interviewing as a Clinical Option for Generalized Anxiety Disorder

Friday Factoids: Working With Children Who Have Early-Onset Schizophrenia

Friday Factoids: Effective Parenting

Article Review: Cannon, T. D., Yu, C., Addington, J., Bearden, C. E., Cadenhead, K. S., Cornblatt, B. A.,…Kattan, M. W. (2016). An individualized risk calculator for research in prodromal psychosis.

Friday Factoids: Diagnosing Early-Onset Schizophrenia

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