Lurasidone for Adolescents With Complex Mental Disorders: A Case Series

Author:

Mole Tom B.1,Furlong Yulia2,Clarke Richard J.2ORCID,Rao Pradeep234,Moore Julia K.2,Pace Giulia2,Van Odyck Hugo2,Chen Wai56789

Affiliation:

1. Ramsay Health Care, Perth, Western Australia, Australia

2. Child and Adolescent Mental Health Service, Child and Adolescent Health Service, Perth, Western Australia, Australia

3. The University of Western Australia, Faculty of Health and Medical Sciences Perth, Western Australia, Australia

4. Telethon Kids Institute, Perth, Western Australia, Australia

5. Mental Health Service, Fiona Stanley Hospital, Perth, Australia

6. Child and Adolescent Mental Health Service, West Pilbara Mental Health Service, Australia

7. Graduate School of Education, University of Western Australia, Western Australia, Australia

8. Department of psychology, Murdoch University, Perth, Australia

9. School of Medicine, University of Notre Dame Australia, Fremantle, Australia

Abstract

Objectives: Lurasidone is a new second generation (atypical) antipsychotic agent with unique receptor affinity and side-effect profiles, but limited literature is available on its use in adolescent populations. Contrasting with research treatment trials which typically recruit patients by stringent selection criteria, this case series examined the effects and tolerability of using lurasidone in adolescents within real-life clinical settings in treating complex cases who had not responded to other therapy options. Methods: We conducted a retrospective case-note audit of 6 adolescents aged 14 to 17 years old attending community child and adolescent mental health services (CAMHS) who were prescribed lurasidone. Results: Lurasidone had been prescribed for a range of “hard-to-manage” conditions with complex comorbidities, in adolescents in relation to specific use of lurasidone on the basis of clinical and pharmacological indications after exhausting more conventional treatment options. Case-note review suggested response to lurasidone was clinically positive in 3 cases, equivocal/marginal in 2 cases, and ineffective in 1 case. There were no cases of poor tolerance or adverse effects. Notably, positive responses for depressive and irritable mood symptoms were specifically recorded by prescribing clinicians, indicative of benefits on symptom improvement. No lurasidone attributed weight gain, galactorrhoea, metabolic abnormalities, sexual dysfunction or intolerance were reported. Pro-cognitive effects were not detected; but our findings were constrained by the non-systematic and incomplete information ascertainment, typical in retrospective case-note review. Conclusion: This case series provides preliminary data supporting lurasidone’s potential use in adolescents of complex clinical needs (but without a clinical diagnosis of bipolar disorder) within real-life clinical settings. Lurasidone appears to show a weight-sparing effect, in addition to improving mood symptoms in some cases. Lurasidone deserves further study for its use in the adolescent population (outside the remit of FDA) given its potential more favorable risk-benefit profile in young people. The favorable tolerability appear to be borne out by the pharmacodynamic predictions in our complex patients who would be excluded in formal clinical trial studies.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

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