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dc.contributor.author
Molina, Luis  
dc.contributor.author
Recinos, Byron  
dc.contributor.author
Paz, Bezner  
dc.contributor.author
Rovelo, Mauricio  
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Elias Rodriguez, Fanny Elizabeth  
dc.contributor.author
Calderón, José  
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Arellano, Arturo  
dc.contributor.author
Pomata, Santiago  
dc.contributor.author
Rey, María Verónica  
dc.contributor.author
Pérez Lloret, Santiago  
dc.date.available
2018-04-11T21:10:48Z  
dc.date.issued
2016-03  
dc.identifier.citation
Molina, 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.identifier.issn
1173-2563  
dc.identifier.uri
http://hdl.handle.net/11336/41808  
dc.description.abstract
Background 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.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Springer  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Ezquisofrenia  
dc.subject
Depresion  
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Quetipina  
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Efectos Tempranos  
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Medicina Critica y de Emergencia  
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Medicina Clínica  
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CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Factors Related to Early Clinical Effects of Quetiapine Extended-Release: A Multinational, Prospective, Observational Study  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2018-04-10T20:29:08Z  
dc.journal.volume
36  
dc.journal.number
6  
dc.journal.pagination
491-497  
dc.journal.pais
Alemania  
dc.journal.ciudad
Berlín  
dc.description.fil
Fil: Molina, Luis. Clínica de Especialidades Altamira; Nicaragua  
dc.description.fil
Fil: Recinos, Byron. Universidad San Carlos de Guatemala; Guatemala  
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Fil: Paz, Bezner. Hospital Juan de Dios de San Pedro; Honduras  
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Fil: Rovelo, Mauricio. Instituto de Salud Mental; Honduras  
dc.description.fil
Fil: Elias Rodriguez, Fanny Elizabeth. Colonia Médica; El Salvador  
dc.description.fil
Fil: Calderón, José. Clínica de la Conducta; Panamá  
dc.description.fil
Fil: Arellano, Arturo. Corporación Farmacéutica Recalcine; Costa Rica  
dc.description.fil
Fil: Pomata, Santiago. Corporación Farmacéutica Recalcine; Costa Rica  
dc.description.fil
Fil: Rey, María Verónica. Etymos Consulting Group; Argentina  
dc.description.fil
Fil: Pérez Lloret, Santiago. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Investigaciones Cardiológicas. Universidad de Buenos Aires. Facultad de Medicina. Instituto de Investigaciones Cardiológicas; Argentina  
dc.journal.title
Clinical Drug Investigation  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://link.springer.com/article/10.1007%2Fs40261-016-0395-x  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1007/s40261-016-0395-x