National profiling of elder abuse referrals
Marguerite Clancy1, Bridget McDaid, Desmond O'Neill
1Health Services Executive, Limerick, Ireland.
Age and Ageing
|March 19, 2011
Summary
Elder abuse reporting in Ireland, without mandatory reporting, revealed under-reporting and diverse abuse patterns. Specialist services offered therapeutic benefits, highlighting the need for data sharing across Europe.
Area of Science:
- Gerontology
- Public Health
- Social Work
Background:
- Limited consistent data exists on elder abuse reporting patterns across Europe.
- Ireland established dedicated elder abuse services (2002-2007) without mandatory reporting, focusing on prevention, detection, and management.
- A national database was developed to gain insights for coordinated European elder abuse responses.
Purpose of the Study:
- To document the referral rates for elder abuse.
- To analyze patterns of elder abuse and the outcomes of interventions.
- To evaluate a dedicated elder abuse service operating without mandatory reporting.
Main Methods:
- Data collected from a national network of Senior Case Workers on all elder abuse referrals.
- Follow-up assessments conducted at 6 months and/or case closure.
- A cross-sectional study design utilized a central database to track cases over two time points.
Main Results:
- 1,889 referrals received; 381 involved self-neglect. Of the remaining, 67% were women, and 40% experienced multiple forms of abuse.
- Over 80% of cases involved individuals living at home. Services were offered to 84%, with 74% accepting interventions like monitoring, home support, and counseling.
- 86% of cases were closed by review; 10% of clients who died had declined intervention. Substantiated cases were more likely to remain open longer than 6 months.
Conclusions:
- The number of reported elder abuse cases in Ireland suggests under-reporting.
- The high rate of inconclusive cases necessitates further analysis and refinement of classification and follow-up procedures.
- Specialist elder abuse services demonstrated therapeutic value, and a pooled European database could enhance research and service development.
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