Effect and associated factors of a clinical pharmacy model in the incidence of medication errors (EACPharModel) in the Hospital Pablo Tobón Uribe: study protocol for a stepped wedge randomized controlled trial (NCT03338725) [documento electrónico] / Juan Pablo Botero Aguirre, ; Andrés Felipe Valencia Quintero, ; Natalia Andrea Ortíz Cano,  . - 2020.
Obra : Trials

Idioma : Inglés (eng)

Palabras clave :	Medication errors  Drug-related problems  Pharmacy service  Hospital (clinical pharmacy services)  Pharmacists
Resumen :	Background: According to WHO, medication error (ME) is a subject that requires attention at all levels of care to reduce severe and preventable damage related to medication use. Clinical pharmacy practice standards have been proposed around the world so that the pharmacist, as part of a multidisciplinary health team, can help improve patient safety; however, further evidence derived from adequate studies is needed to demonstrate this. This study aims to assess the effect of a clinical pharmacy practice model (CPPM) in preventing MEs associated with the medication use process. Methods: A prospective, stepped-wedge, cluster-randomized, controlled trial with a duration of 14 months will be performed to compare the effect of a CPPM along with the usual care process of patients in the Pablo Tobón Uribe Hospital (Medellin, Colombia). The study is designed as a cluster-randomized controlled trial, involving five hospital wards (clusters) and 720 patients. Medical wards are allocated to interventions using a stepped-wedge design. Clusters are initially assigned to the control group. After a 2-month observation period, hospital clusters were randomly allocated to the intervention group. Study outcomes will be assessed at baseline and at 2, 4, 6, 8, 10, and 12 months after randomization. The primary outcome will be to assess the effect of a CPPM on the incidence of medication errors associated with the medication use process. Drug-related problems and factors that contribute to the occurrence of MEs will be assessed as secondary outcomes. Statistical analyses will be performed using a mixed model, with the treatment group and time as fixed effects and the clustering structure as a random effect. Statistical analysis will be performed using Pearson chi-square tests and Student's t-tests, and a P value
Mención de responsabilidad :	J Granados, A Salazar-Ospina, J P Botero-Aguirre, A F Valencia-Quintero, N Ortiz, P Amariles
Referencia :	Trials. 2020;21(1):26.
DOI (Digital Object Identifier) :	10.1186/s13063-019-3945-8
PMID :	31907009
Derechos de uso :	CC BY
En línea :	https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-019-3945-8
Enlace permanente :	https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=5074