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Module 3 – Case Study 1: First Episode Psychosis Mark's Pharmaceutical Care Plan Mark is a 24-year-old European man who has been admitted to an acute psychiatric unit for assessment after his family reported that they were concerned about his attempts to harm himself. History at presentation: Mark presents with a psychotic episode of acute onset. He is a young male aged 24 years (peak incidence for schizophrenia). Important symptoms at presentation include: Withdrawn behaviour (social/work), agitation, incoherence, and self-harm behaviour (slashed wrists). On interview he showed: Speech latency, auditory hallucinations, lack of self-esteem, quiet, euthymic mood, guarded, fearful. Although psychotic symptoms (auditory hallucinations) appear to have developed in the past month or two, social withdrawal (described as depression) and concentration problems have been present for over two years. His DSM-IV diagnosis using the multi-axial classification is summarized below: Axis I – First episode psychosis Axis II – No reported personality disorders or mental retardation Axis III – No known or history of concomitant medical condition Axis IV – Currently in an apprenticeship program as a plumber Axis V – Global Assessment of Functioning (GAF) score is unavailable. Based on current presentation, estimated GAF score = 50 (patient at 50% his normal functional state). Possible diagnosis: First episode psychosis. Patient needs to be monitored closely and frequently for subsequent episodes. Subsequent episodes may require a review and change of the initial diagnosis. Mark is at an increased risk for schizophrenia. Other psychiatric disorders may be considered in the differential diagnosis (eg. Psychotic depression). Management: The most immediate management goal for Mark is to minimize the risk for another selfharm episode, which can be achieved by decreasing the causative symptoms (hearing a male voice calling his name, telling him he is bad and that he deserves to die). Achieving this first goal will likely lead to a decrease in the acute distress associated with his psychotic symptoms, all of which will likely improve his quality of life and functionality. Mark was consequently prescribed Olanzapine 15mg nocte. This is a suitable choice, as atypical antipsychotics are the medications of first choice for the management of first episode psychosis. Other alternative agents include risperidone, quetiapine, ziprasidone and aripiprazole. However, funding issues may need to be considered and discussed with Mark. Monitoring Plan: Upon initiation of an atypical antipsychotic patients need to have a series of initial (or baseline) monitoring parameters, including those needed to monitor for the metabolic syndrome (e.g. weight, blood lipids, fasting glucose, and blood pressure). Some also advocate that a baseline electrocardiogram (ECG) should be done. Other monitoring parameters that may be required include renal function, liver function tests, and a full blood count (FBC). Serum prolactin is particularly important for risperidone and for typical antipsychotics, but may not be as crucial for olanzapine or other atypical agents. On admission, Mark’s physical examination and all blood tests were normal; thus, Mark will not require a repeat of these monitoring parameters if they were initially investigated on admission. According to monitoring guidelines for the metabolic syndrome, it is recommended to monitor these parameters again at 6 months of treatment, and up to 2 years after treatment initiation. Taking these opportunities to monitor treatment adherence is also of particular importance, especially in first episode psychosis. Monitoring for medication efficacy will require interviewing Mark and enquire for any changes in his initial presenting symptoms, such as his initial negative symptoms and mood (ex: improved social interaction, no suicide ideation/attempts, increased work function, improved concentration) and thought content ( ex: not hearing voices, improved speech and cognition, less guarded or fearful, not responding to auditory hallucinations or delusions). Adherence can be monitored by recording the number of tablets left on his vials, asking the patient, asking about adverse events, by checking his residual symptoms and identifying overall improved parameters. It is important to remember that there are a number of contributing factors to non-compliance with medications, including: attitudes of family, unmanageable or uncomfortable side effects, perceived stigma, and the fact that most patients are not involved initially in the choice of treatment. Follow up: Mark reports feeling tired all the time. This medication related problem has affected both, his work performance and his social life (he has slept in twice in the last week and has been getting to work late. His girlfriend has also complained that he doesn’t seem interested in going out anywhere). It is obvious that Mark is experiencing significant sedation associated with the high sedating properties of olanzapine. Of all the atypical antipsychotics, olanzapine and clozapine show the highest incidence of sedation. It is this property which leads to the usual recommendation of dosing them at night (as prescribed for Mark); however, many patients do have carry-over effects until the next morning, making it difficult for them to be active during the first hours of the day. Management strategies for this side effect may include: Decreasing the dose to lowest effective dose: Mark has responded quite well to 15 mg, he may remain well at a night time dose of 10 mg. Monitor for recurrent psychotic symptoms closely and ask for regular and continuous feedback from family (girlfriend). If it is considered that 15 mg is actually the lowest effective dose for Mark, the following management strategies may be tried: • Change the administration time to early evening (right after 6 PM supper) rather than leaving it for late night. • Split the dose, leaving the largest dose for the evening. New dosing regimen could be 5 mg AM and 10 mg in early evening as suggested above).