Mostrar el registro sencillo del ítem
dc.contributor.author
Burch, Jane
dc.contributor.author
Ciapponi, Agustín
![Se ha confirmado la validez de este valor de autoridad por un usuario](/themes/CONICETDigital/images/authority_control/invisible.gif)
dc.date.available
2023-01-24T17:47:14Z
dc.date.issued
2018-10
dc.identifier.citation
Burch, Jane; Ciapponi, Agustín; What proportion of people with postoperative pain experience adverse events with single‐dose oral analgesics?; Wiley; Cochrane Clinical Answers; 10-2018; 1-9
dc.identifier.issn
2050-4217
dc.identifier.uri
http://hdl.handle.net/11336/185443
dc.description.abstract
Compared with placebo in adults with at least moderate‐intensity postoperative pain, people taking one of these analgesics at a single dose had greater rates of adverse events: aspirin 600/650 mg or 920/1000 mg, diflunisal 1000 mg, ibuprofen 200 mg plus caffeine 100 mg, dihydrocodeine 30 mg, paracetamol (any dose) + codeine 30 or 60 mg, and paracetamol 325 to 1000 mg plus oxycodone 5 to 10 mg. However, four analgesics led to lower rates of adverse events than placebo: ibuprofen 200 or 400 mg and ibuprofen 200 to 400 mg plus paracetamol 500 to 1000 mg, respectively. Trial authors typically reported serious adverse events as absent; such events were too few for statistical evaluation. Reviewers stated that trial results should be treated with caution, as the method used to collect adverse event data influences adverse event reporting rates; patient diaries yield significantly more adverse events when compared with other forms of assessment.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Wiley
![Se ha confirmado la validez de este valor de autoridad por un usuario](/themes/CONICETDigital/images/authority_control/invisible.gif)
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
SALUD
dc.subject.classification
Otras Ciencias de la Salud
![Se ha confirmado la validez de este valor de autoridad por un usuario](/themes/CONICETDigital/images/authority_control/invisible.gif)
dc.subject.classification
Ciencias de la Salud
![Se ha confirmado la validez de este valor de autoridad por un usuario](/themes/CONICETDigital/images/authority_control/invisible.gif)
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD
![Se ha confirmado la validez de este valor de autoridad por un usuario](/themes/CONICETDigital/images/authority_control/invisible.gif)
dc.title
What proportion of people with postoperative pain experience adverse events with single‐dose oral analgesics?
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2023-01-24T10:27:01Z
dc.journal.pagination
1-9
dc.journal.pais
Reino Unido
![Se ha confirmado la validez de este valor de autoridad por un usuario](/themes/CONICETDigital/images/authority_control/invisible.gif)
dc.description.fil
Fil: Burch, Jane. No especifíca;
dc.description.fil
Fil: Ciapponi, Agustín. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Centro de Investigaciones en Epidemiología y Salud Pública. Instituto de Efectividad Clínica y Sanitaria. Centro de Investigaciones en Epidemiología y Salud Pública; Argentina
dc.journal.title
Cochrane Clinical Answers
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://www.cochranelibrary.com/cca/doi/10.1002/cca.2334/full
Archivos asociados