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Posts tagged service user perspectives
Stigma and Difficulty Accessing Medical Care in a Sample of Adults with Serious Mental Illness

Lack of comprehensive medical care coverage and mental health symptoms were associated with increased odds of perceived difficulties in accessing medical care; personal empowerment was negatively associated with perceived difficulties attributed to stigma; education was positively associated. The findings highlight unmet need for medical care in this population and the need to recognize stigma as a barrier medical care. Interventions to empower patients and educate medical providers about wellness for people with serious mental illness could help to reduce barriers.

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Measurement of Perceived and Technical Quality of Care for Depression in Racially and Ethnically Diverse Groups

This study examined the relationship between the culturally determined beliefs and expectations of four ERD groups (African Americans, Latinos, Portuguese-speakers, and Haitians, total N = 160) and the technical quality of treatment for depression provided in four “culturally-specific” primary care clinics. Using data from the Experiences of Care and Health Outcomes survey, chart reviews and focus groups, the study addressed a set of questions related to the psychometric properties of perceived care measures and the technical quality of care. The groups differed in preferred cultural elements except all preferred inclusion of religion. They did not differ in overall perceived quality.

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What Happens When you Stop Taking Psychiatric Medication | Pacific Standard Magazine

"This is something people choose, and we don't know enough about it to help people," says Laysha Ostrow, chief executive officer of a mental-health consultancy in California and a public-health researcher who worked on the study. "I feel that it's important to bring those ideas into more of a mainstream conversation, given how many people decide to discontinue. It shouldn't be this subversive thing that we don't talk about in the health-care system or in research."

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Discontinuing Psychiatric Medications: A Survey of Long-Term Users

To enhance service user choice and prevent undesirable outcomes, this first U.S. survey of a large sample of longer-term users sought to increase knowledge about users’ experience of medication discontinuation. About half (54%) met their goal of completely discontinuing one or more medications; 46% reported another outcome (use was reduced, use increased, or use stayed the same). Of respondents who completely discontinued, 82% were satisfied with their decision.

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An exploratory analysis of the role of social supports in psychiatric medication discontinuation: results related to family involvement

Individuals in psychiatric treatment frequently choose to stop taking psychiatric medications, but little is known about the role of social supports in this process. Of all social support groups, only family was significantly associated with medication discontinuation. Respondents who rated family as helpful in the discontinuation process were less likely to completely discontinue than those who rated family as unhelpful or who reported no family involvement. Additionally, we observed a statistically significant but nonlinear relationship where respondents who rated their families as either “very supportive” or “very unsupportive” of the decision to discontinue were less likely to meet their original discontinuation goal than those with more neutral ratings. The results of this study suggest families have an important and complex role in medication decision-making.

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