Drug-Associated Risk Tool: development and validation of a self-assessment questionnaire to screen for hospitalised patients at risk for drug-related problems

被引:12
|
作者
Kaufmann, Carole P. [1 ]
Stampfli, Dominik [1 ]
Mory, Nadine [1 ]
Hersberger, Kurt E. [1 ]
Lampert, Markus L. [1 ,2 ]
机构
[1] Univ Basel, Dept Pharmaceut Sci, Pharmaceut Care Res Grp, Basel, Switzerland
[2] Solothurner Spitaler, Inst Hosp Pharm, Olten, Switzerland
来源
BMJ OPEN | 2018年 / 8卷 / 03期
关键词
MEDICATION-RELATED PROBLEMS; CHRONIC KIDNEY-DISEASE; HEALTH LITERACY; OLDER-PEOPLE; CARE; PHARMACISTS; ADMISSION; IDENTIFICATION; PREVALENCE; PREDICTORS;
D O I
10.1136/bmjopen-2017-016610
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction Identifying patients with a high risk for drug related problems (DRPs) might optimise the allocation of targeted pharmaceutical care during the hospital stay and on discharge. Objective To develop a self-assessment screening tool to identify patients at risk for DRPs arid validate the tool regarding feasibility, acceptability and the reliability of the patients' answers. Design Prospective validation study. Setting Two mid-sized hospitals (300-400 beds). Participants 195 patients, exclusion criteria: under 18 years old, patients with a health status not allowing a meaningful communication (eg, delirium, acute psychosis, advanced dementia, aphasia, clouded consciousness state), palliative or terminally ill patients. Methods Twenty-seven risk factors for the development of DRPs, identified in a previous study, provided the basis of the self-assessment questionnaire, the Drug-Associated Risk Tool (DART). Consenting patients filled in DART, and we compared their answers with objective patient data from medical records and laboratory data. Results One hundred and sixty-four patients filled in DART V.1.0 in an average time of 7min. After a first validation, we identified statements with a low sensitivity and revised the wording of the questions related to heart insufficiency, renal impairment or liver impairment. The revised DART (V.2.0) was validated in 31 patients presenting heart insufficiency, renal impairment or liver impairment as comorbidity and reached an average specificity of 88% (range 27-100) and an average sensitivity of 67% (range 21-100). Conclusions DART showed a satisfying feasibility arid reliability. The specificity of the statements was mostly high. The sensitivity varied and was higher in statements concerning diseases that require regular disease control and attention to self-care and drug management. Asking patients about their conditions, medications and related problems can facilitate getting a first, broad picture of the risk for DRPs and possible pharmaceutical needs.
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页数:9
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