Understanding the Treatment Preferences of People Living with Schizophrenia in Australia; A Patient Value Mapping Study
- PMID: 35898923
- PMCID: PMC9309312
- DOI: 10.2147/PPA.S366522
Understanding the Treatment Preferences of People Living with Schizophrenia in Australia; A Patient Value Mapping Study
Abstract
Purpose: To examine the treatment and long-term outcome preferences for people living with schizophrenia.
Patients and methods: Sixty-six Australian adults, living with schizophrenia completed a novel online survey with six sections: Demographic characteristics; Disease history; Quality-of-life; Patient support programmes; Discrete Choice Experiment, and Best-Worst Scaling exercise.
Results: Participants indicated that they preferred to be involved in treatment decision with their doctor. A minority of participants reported having been previously involved in a patient support programme (28.8%) and only one in six participants had a National Disability Insurance Scheme (NDIS) package (16.7%) with over a third of participants indicating that they were ineligible (37.9%). Participants' average quality-of-life score was 60%.
Conclusion: Recent hospitalisation influenced the relative importance of treatment attributes, with effectiveness on hearing voices being the most important treatment attribute. The most important long-term goals were having a stable place to live, being independent, and physical health. People with schizophrenia care about their long-term functional recovery outcomes, rating symptom control and independence as their highest priority. They want to be part of the treatment conversation with their doctors. Therefore, psychiatrists are encouraged to use shared decision-making to establish the treatment course that best aligns with individuals' long-term goals.
Keywords: discrete choice experiment; patient preference; patient value mapping; schizophrenia; shared decision-making; treatment goals.
© 2022 Fifer et al.
Conflict of interest statement
S Fifer and B Keen are employed by CaPPRe. CaPPRe has consulted to AbbVie, Amgen, AstraZeneca, Celgene, CSL Behring, Edwards, GSK, Ipsen, Janssen, Novo Nordisk, Roche, Sanofi, Shire and UCB, outside of the submitted work. A Puig and M McGeachie are employees of Janssen-Cilag Australia Pty Ltd. The authors report no other conflicts of interest in this work.
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