Thais Teles de Souza
Federal University of Paraná
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Featured researches published by Thais Teles de Souza.
Annals of Pharmacotherapy | 2013
Cassyano Januário Correr; Ana Carolina Melchiors; Thais Teles de Souza; Inajara Rotta; Teresa M. Salgado; Fernando Fernandez-Llimos
BACKGROUND The complexity of clinical pharmacy services usually leads to an inconsistent or even poor description of their interventions in scientific reports. To ensure comparability and reproducibility of the evidence, an in-depth description of pharmacist interventions is required. OBJECTIVE To validate a new tool called DEPICT (Descriptive Elements of Pharmacist Intervention Characterization Tool) to characterize clinical pharmacy services. METHODS We developed a 3-phase study. First, to create a theoretical framework, an overview of systematic reviews was performed in PubMed between 2000 and 2010. Then, an in-depth analysis of the included studies was carried out to identify a list of components in order to create the instrument. Finally, 2 independent raters separately applied the tool to a random sample of 28 randomized clinical trials extracted from the systematic reviews. Interrater agreement was evaluated using PABAK (prevalence-adjusted bias-adjusted κ) coefficient or intraclass correlation coefficient (ICC). RESULTS We included 49 systematic reviews in our overview. Analysis of these studies resulted in 58 intervention components, with 57 dichotomous variables and 1 discrete variable. These items resulted in a preliminary version of the instrument. The reliability analysis showed that 8 binary items of this version had a PABAK less than or equal to 0.60. These items were then excluded or modified, resulting in a final version of the tool, with 54 items organized into 12 domains. DEPICT showed an average PABAK of 0.85 (95% CI 0.81 to 0.88) and an ICC of 1.0. Twenty items presented a PABAK value between 0.61 and 0.80 (substantial agreement) and 33 had a value between 0.81 and 1.0 (almost perfect agreement). CONCLUSIONS DEPICT is a reproducible instrument for describing the components of pharmacist interventions performed as part of clinical pharmacy services. It allows retrospective analysis of published studies and can be used as a reference guide to report pharmacist interventions in future studies.
Journal of Evaluation in Clinical Practice | 2015
Inajara Rotta; Teresa M. Salgado; Daniel C. Felix; Thais Teles de Souza; Cassyano Januário Correr; Fernando Fernandez-Llimos
RATIONALE, AIMS AND OBJECTIVES DEPICT (Descriptive Elements of Pharmacist Intervention Characterization Tool) was created in response to the frequently reported issue of poor intervention description across studies assessing the impact of clinical pharmacy activities. The aim of this study was to create an improved version of DEPICT (i.e. DEPICT 2) to better characterize clinical pharmacy services in order to ensure consistent reporting, therefore enhancing reproducibility of interventions in practice. METHOD A qualitative approach through a thematic content analysis was performed to identify components of pharmacist interventions described in 269 randomized controlled trials. A preliminary version of DEPICT 2 was applied independently by two authors to a random sample of 85 of the 269 RCTs and reliability determined by the prevalence-adjusted bias-adjusted kappa (PABAK) or the intraclass correlation coefficient (ICC). The final version of DEPICT 2 was compared against DEPICT 1. RESULTS The final version of DEPICT 2 comprised 146 items and 11 domains. The inter-rater agreement analysis showed that DEPICT presented good to optimal reproducibility, with a mean PABAK value of 0.87 (95% CI 0.85-0.89) and a mean ICC value of 0.88 (95% CI 0.62-1.14). The mean difference between items checked in the two versions (DEPICT 2 - DEPICT 1) was 10.58 (95% CI 9.55-11.61), meaning that approximately 11 more components were identified in the new version of DEPICT. CONCLUSIONS DEPICT 2 is a reliable tool to characterize components of clinical pharmacy services, which should be used to ensure consistent reporting of interventions to allow their reproducibility in practice.
Pharmacy Practice (granada) | 2017
Wálleri C. Reis; Aline F. Bonetti; Wallace E. Bottacin; Alcindo S. Reis; Thais Teles de Souza; Roberto Pontarolo; Cassyano Januário Correr; Fernando Fernandez-Llimos
Objective: The purpose of this overview (systematic review of systematic reviews) is to evaluate the impact of clinical decision support systems (CDSS) applied to medication use in the care process. Methods: A search for systematic reviews that address CDSS was performed on Medline following Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) and Cochrane recommendations. Terms related to CDSS and systematic reviews were used in combination with Boolean operators and search field tags to build the electronic search strategy. There was no limitation of date or language for inclusion. We included revisions that investigated, as a main or secondary objective, changes in process outcomes. The Revised Assessment of Multiple Systematic Reviews (R-AMSTAR) score was used to evaluate the quality of the studies. Results: The search retrieved 954 articles. Five articles were added through manual search, totaling an initial sample of 959 articles. After screening and reading in full, 44 systematic reviews met the inclusion criteria. In the medication-use processes where CDSS was used, the most common stages were prescribing (n=38 (86.36%) and administering (n=12 (27.27%)). Most of the systematic reviews demonstrated improvement in the health care process (30/44 – 68.2%). The main positive results were related to improvement of the quality of prescription by the physicians (14/30 – 46.6%) and reduction of errors in prescribing (5/30 - 16.6%). However, the quality of the studies was poor, according to the score used. Conclusion: CDSSs represent a promising technology to optimize the medication-use process, especially related to improvement in the quality of prescriptions and reduction of prescribing errors, although higher quality studies are needed to establish the predictors of success in these systems.
BioDrugs | 2014
Hh Borba; Astrid Wiens; Thais Teles de Souza; Cassyano Januário Correr; Roberto Pontarolo
African Journal of Biotechnology | 2011
Bárbara L.S. Leite; Thais Teles de Souza; Angelo R. Antoniolli; Adriana G. Guimarães; Jullyana de Souza Siqueira Quintans; Leonardo Rigoldi Bonjardim; Péricles Barreto Alves; Marco Antonio Botelho; Jackson Roberto Guedes da Silva Almeida; Julianeli Tolentino de Lima; Lucindo J. Quintans-Júnior
Research in Social & Administrative Pharmacy | 2017
Inajara Rotta; Thais Teles de Souza; Teresa M. Salgado; Cassyano Januário Correr; Fernando Fernandez-Llimos
International Journal of Clinical Pharmacy | 2016
Patrícia Carvalho Baruel Okumura; Lucas Miyake Okumura; Wálleri Christini Torelli Reis; Rangel Ray Godoy; Bianca de Oliveira Cata-Preta; Thais Teles de Souza; Maria Luiza Drechsel Fávero; Cassyano Januário Correr
British Journal of Clinical Pharmacology | 2014
Thais Teles de Souza; Loreto Sáez-Benito; Cassyano Januário Correr; Fernando Fernandez-Llimos
Visão Acadêmica | 2013
Thais Teles de Souza; Rangel Ray Godoy; Roberto Pontarolo; Michel Fleith Otuki; Cassyano Januário Correr
Revista Portuguesa de Saúde Pública | 2012
Thais Teles de Souza; Wellington Barros da Silva; Jullyana de Souza Siqueira Quintans; Alexandre Sherlley Casimiro Onofre; Fabiana Botelho de Miranda Onofre; Lucindo J. Quintans-Júnior