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            "title": "Advanced care planning in health service users",
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            "abstractNote": "Aims and objectives. To examine the use of advanced directives (ADs) in patients actively using health services in the USA. Background. Since 1991, USA law (PSDA 1991) has required hospitals, skilled nursing facilities (SNFs) and home health services to inquire, at admission, if patients have in place ADs, to provide patients with a written summary of their rights in regard to health-related decision-making and to provide education to staff and the community about ADs. Design. Via chart review and observation, the AD status of patients residing in three SNFs during a six-week period was ascertained ( n = 272). Those with ADs were further evaluated to examine the timing of the directive in regards to their health status. Methods. Patients residing at SNFs were selected for study because SNF patients are admitted from the hospital; therefore, there are at least two opportunities - at hospital admission and at SNF admission - to inquire and educate about advance directives. Results. Residents ranged in age from 35 to 100 years and included patients admitted for short-term rehabilitation after hospitalisation, as well as residents who were initially admitted after a hospitalisation but required long-term care. A full 90·44% ( n = 246) entered skilled care without an AD, and 69·11% ( n = 188) remained without an AD. The most likely reason for the development of an AD was lengthy decline in health status associated with multiple hospitalisations. Conclusions. Current law appears ineffective. A more appropriate approach is to encourage open dialogue about treatment options and quality of life. Relevance to clinical practice. Given the rapidity with which populations are ageing in countries worldwide, ADs would appear to be a phenomenon that should be embraced. However, experience in the USA has called into question their usefulness.",
            "publicationTitle": "Journal of Clinical Nursing",
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            "date": "November 2012",
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            "creatorSummary": "Durbin et al.",
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            "title": "Lost in translation: the unintended consequences of advance directive law on clinical care",
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                    "firstName": "Ls",
                    "lastName": "Castillo"
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                    "lastName": "Williams"
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                    "lastName": "Sabatino"
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                    "firstName": "Rl",
                    "lastName": "Sudore"
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            "abstractNote": "Background: Advance directive law may compromise the clinical effectiveness of advance directives. Purpose: To identify unintended legal consequences of advance directive law that may prevent patients from communicating end-of-life preferences. Data Sources: Advance directive legal statutes for all 50 U.S. states and the District of Columbia and English-language searches of LexisNexis, Westlaw, and MEDLINE from 1966 to August 2010. Study Selection: Two independent reviewers selected 51 advance directive statutes and 20 articles. Three independent legal reviewers selected 105 legal proceedings. Data Extraction: Two reviewers independently assessed data sources and used critical content analysis to determine legal barriers to the clinical effectiveness of advance directives. Disagreements were resolved by consensus. Data Synthesis: Legal and content-related barriers included poor readability (that is, laws in all states were written above a 12th-grade reading level), health care agent or surrogate restrictions (for example, 40 states did not include same-sex or domestic partners as default surrogates), and execution requirements needed to make forms legally valid (for example, 35 states did not allow oral advance directives, and 48 states required witness signatures, a notary public, or both). Vulnerable populations most likely to be affected by these barriers included patients with limited literacy, limited English proficiency, or both who cannot read or execute advance directives; same-sex or domestic partners who may be without legally valid and trusted surrogates; and unbefriended, institutionalized, or homeless patients who may be without witnesses and suitable surrogates. Limitation: Only appellate-level legal cases were available, which may have excluded relevant cases. Conclusion: Unintended negative consequences of advance directive legal restrictions may prevent all patients, and particularly vulnerable patients, from making and communicating their end-of-life wishes and having them honored. These restrictions have rendered advance directives less clinically useful. Recommendations include improving readability, allowing oral advance directives, and eliminating witness or notary requirements. Primary Funding Source: U.S. Department of Veterans Affairs and the Pfizer Foundation.",
            "publicationTitle": "Annals of Internal Medicine",
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            "date": "2011",
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