dc.creatorMolina, Luis
dc.creatorRecinos, Byron
dc.creatorPaz, Bezner
dc.creatorRovelo, Mauricio
dc.creatorElias Rodriguez, Fanny Elizabeth
dc.creatorCalderón, José
dc.creatorArellano, Arturo
dc.creatorPomata, Santiago
dc.creatorRey, María Verónica
dc.creatorPérez Lloret, Santiago
dc.date.accessioned2018-04-11T21:10:48Z
dc.date.accessioned2018-11-06T11:42:13Z
dc.date.available2018-04-11T21:10:48Z
dc.date.available2018-11-06T11:42:13Z
dc.date.created2018-04-11T21:10:48Z
dc.date.issued2016-03
dc.identifierMolina, Luis; Recinos, Byron; Paz, Bezner; Rovelo, Mauricio; Elias Rodriguez, Fanny Elizabeth; et al.; Factors Related to Early Clinical Effects of Quetiapine Extended-Release: A Multinational, Prospective, Observational Study; Springer; Clinical Drug Investigation; 36; 6; 3-2016; 491-497
dc.identifier1173-2563
dc.identifierhttp://hdl.handle.net/11336/41808
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1858059
dc.description.abstractBackground and Objectives The first weeks of treatment with antipsychotics are important for the development of their long-term efficacy. The objective of this study was to identify factors related to early clinical effects and quality of life (QoL) improvements with quetiapine extended-release (XR). Methods Six hundred and sixty-five patients starting with quetiapine XR were followed up for 8 weeks (schizophrenia = 153, major depression = 200, bipolar depression = 252, other psychiatric conditions = 60). Clinical effects were assessed by the Clinical Global Impression of Change scale (CGI-C), QoL by the visual analog scale (VAS) of the EQ-5D (QoL-VAS), and adherence by the Moriksy scale. Adverse events were explored: movement disorders by the UKU and Simpson-Angus scales, weight gain by calibrated balances, and diurnal somnolence by the Epworth Somnolence Scale (ESS). Results The mean dose of quetiapine XR during follow-up was 195.6 ± 154.8 mg/day. CGI and QoL-VAS scores improved significantly at week 8 by 2.7 ± 0.1 points and 25.1 ± 0.9 points. Adverse events were observed in 34 and 26 % of patients at weeks 4 and 8, respectively. A significant reduction in ESS score was also observed at week 8. Factors independently associated with change in QoL-VAS ≥20 points (n = 292, 43 %) were female gender, more severe disease at baseline, higher antipsychotic dose during follow-up, and improvements in somnolence. Factors independently associated with clinically significant improvement (CGI-C ≥5, n = 610, 93 %) were greater change in QoL-VAS, less frequent movement disorders at baseline, and lack of adverse events during follow-up, especially somnolence. Conclusions Results from this real-setting, large observational study in Central America suggest that disease severity at baseline, gender, antipsychotic dose, and occurrence of adverse reactions has a significant impact on the early clinical effects of quetiapine XR.
dc.languageeng
dc.publisherSpringer
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007%2Fs40261-016-0395-x
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1007/s40261-016-0395-x
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectEzquisofrenia
dc.subjectDepresion
dc.subjectQuetipina
dc.subjectEfectos tempranos
dc.titleFactors Related to Early Clinical Effects of Quetiapine Extended-Release: A Multinational, Prospective, Observational Study
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


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