Matches in SemOpenAlex for { <https://semopenalex.org/work/W2810702984> ?p ?o ?g. }
- W2810702984 endingPage "e021284" @default.
- W2810702984 startingPage "e021284" @default.
- W2810702984 abstract "The Drug-Associated Risk Tool (DART) has been developed as a self-administered questionnaire for patients with the aim of stratifying patients according to their risk of drug-related problems (DRPs). We aimed to validate the ability of the questionnaire to distinguish between hospitalised patients showing lower and higher numbers of DRPs.Cross-sectional study assessing the questionnaire's concurrent criterion validity.Five geriatric and the associated physical and neurological rehabilitation wards of a Swiss regional secondary care hospital with 617 beds.We recruited 110 patients from a total of 437 admissions. Exclusion criteria were insufficient knowledge in spoken or written German, medical conditions preventing meaningful conversations and already receiving pharmacy services.Comprehensive pharmacist-led clinical medication reviews were performed, including patient interviews, to identify potential and manifest DRPs. A cluster analysis was conducted to assess the discriminatory potential of the DART to group patients according to number (low and high) of identified DRPs. A subsequent discriminatory function analysis was performed to reduce the number of items. We determined which DART items may be used to trigger what type of medication review.Recruited patients had a median age of 79 years and were prescribed a median of 11 drugs. Patients with a median DART score of 10 and a median of 3 DRPs represented one cluster, whereas patients with a median DART score of 15 and a median of 8 DRPs represented another cluster. Discriminatory function analysis reduced the questionnaire to five items with a moderate to strong correlation with the number of DRPs per patient (Spearman's rank correlation ρ=0.44). Additional items were associated with patients benefiting from interviews.As a self-administered questionnaire for patients, the DART may be used to stratify hospitalised non-acute older patients in groups of having low and high likelihood of DRPs. The analyses showed that a short form of the DART can be used instead of the full tool to identify older inpatients at risk for DRPs. Additional eight items from the DART may be used to initiate additional clinical pharmacy services. The linkage between certain DART questions and type of medication review enables pharmacist resource allocation." @default.
- W2810702984 created "2018-07-10" @default.
- W2810702984 creator A5001806840 @default.
- W2810702984 creator A5007866223 @default.
- W2810702984 creator A5008639034 @default.
- W2810702984 creator A5012672681 @default.
- W2810702984 creator A5016984050 @default.
- W2810702984 creator A5029240041 @default.
- W2810702984 creator A5033369205 @default.
- W2810702984 date "2018-06-01" @default.
- W2810702984 modified "2023-09-27" @default.
- W2810702984 title "Assessing the ability of the Drug-Associated Risk Tool (DART) questionnaire to stratify hospitalised older patients according to their risk of drug-related problems: a cross-sectional validation study" @default.
- W2810702984 cites W1124723431 @default.
- W2810702984 cites W1607736619 @default.
- W2810702984 cites W1772070026 @default.
- W2810702984 cites W1965022993 @default.
- W2810702984 cites W2013462584 @default.
- W2810702984 cites W2013949127 @default.
- W2810702984 cites W2015757077 @default.
- W2810702984 cites W2025581287 @default.
- W2810702984 cites W2030775318 @default.
- W2810702984 cites W2037447951 @default.
- W2810702984 cites W2037557484 @default.
- W2810702984 cites W2064470295 @default.
- W2810702984 cites W2085074082 @default.
- W2810702984 cites W2102821201 @default.
- W2810702984 cites W2103801639 @default.
- W2810702984 cites W2104656228 @default.
- W2810702984 cites W2107505481 @default.
- W2810702984 cites W2108701948 @default.
- W2810702984 cites W2109271443 @default.
- W2810702984 cites W2112160339 @default.
- W2810702984 cites W2116620555 @default.
- W2810702984 cites W2117340419 @default.
- W2810702984 cites W2130510785 @default.
- W2810702984 cites W2138653626 @default.
- W2810702984 cites W2140920443 @default.
- W2810702984 cites W2149863648 @default.
- W2810702984 cites W2156108549 @default.
- W2810702984 cites W2274276369 @default.
- W2810702984 cites W2280359362 @default.
- W2810702984 cites W2288809946 @default.
- W2810702984 cites W2338651455 @default.
- W2810702984 cites W2588327698 @default.
- W2810702984 cites W2782601068 @default.
- W2810702984 cites W2794103508 @default.
- W2810702984 cites W4243177274 @default.
- W2810702984 cites W2156024703 @default.
- W2810702984 doi "https://doi.org/10.1136/bmjopen-2017-021284" @default.
- W2810702984 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6042600" @default.
- W2810702984 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/29950469" @default.
- W2810702984 hasPublicationYear "2018" @default.
- W2810702984 type Work @default.
- W2810702984 sameAs 2810702984 @default.
- W2810702984 citedByCount "9" @default.
- W2810702984 countsByYear W28107029842020 @default.
- W2810702984 countsByYear W28107029842021 @default.
- W2810702984 countsByYear W28107029842022 @default.
- W2810702984 countsByYear W28107029842023 @default.
- W2810702984 crossrefType "journal-article" @default.
- W2810702984 hasAuthorship W2810702984A5001806840 @default.
- W2810702984 hasAuthorship W2810702984A5007866223 @default.
- W2810702984 hasAuthorship W2810702984A5008639034 @default.
- W2810702984 hasAuthorship W2810702984A5012672681 @default.
- W2810702984 hasAuthorship W2810702984A5016984050 @default.
- W2810702984 hasAuthorship W2810702984A5029240041 @default.
- W2810702984 hasAuthorship W2810702984A5033369205 @default.
- W2810702984 hasBestOaLocation W28107029841 @default.
- W2810702984 hasConcept C104863432 @default.
- W2810702984 hasConcept C107130276 @default.
- W2810702984 hasConcept C126322002 @default.
- W2810702984 hasConcept C142052008 @default.
- W2810702984 hasConcept C142724271 @default.
- W2810702984 hasConcept C159110408 @default.
- W2810702984 hasConcept C1862650 @default.
- W2810702984 hasConcept C2426938 @default.
- W2810702984 hasConcept C2779457091 @default.
- W2810702984 hasConcept C512399662 @default.
- W2810702984 hasConcept C71924100 @default.
- W2810702984 hasConceptScore W2810702984C104863432 @default.
- W2810702984 hasConceptScore W2810702984C107130276 @default.
- W2810702984 hasConceptScore W2810702984C126322002 @default.
- W2810702984 hasConceptScore W2810702984C142052008 @default.
- W2810702984 hasConceptScore W2810702984C142724271 @default.
- W2810702984 hasConceptScore W2810702984C159110408 @default.
- W2810702984 hasConceptScore W2810702984C1862650 @default.
- W2810702984 hasConceptScore W2810702984C2426938 @default.
- W2810702984 hasConceptScore W2810702984C2779457091 @default.
- W2810702984 hasConceptScore W2810702984C512399662 @default.
- W2810702984 hasConceptScore W2810702984C71924100 @default.
- W2810702984 hasIssue "6" @default.
- W2810702984 hasLocation W28107029841 @default.
- W2810702984 hasLocation W28107029842 @default.
- W2810702984 hasLocation W28107029843 @default.
- W2810702984 hasLocation W28107029844 @default.
- W2810702984 hasOpenAccess W2810702984 @default.
- W2810702984 hasPrimaryLocation W28107029841 @default.
- W2810702984 hasRelatedWork W1784093982 @default.