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Article: Feasibility study comparing oral paracetamol and oral non-steroidal anti-inflammatory drugs for treating pain after musculoskeletal injury: A randomised, double blind, controlled trial

TitleFeasibility study comparing oral paracetamol and oral non-steroidal anti-inflammatory drugs for treating pain after musculoskeletal injury: A randomised, double blind, controlled trial
Authors
KeywordsNSAID
Indomethacin
Diclofenac
Wounds and injuries
Issue Date2004
Citation
Hong Kong Journal of Emergency Medicine, 2004, v. 11, n. 2, p. 78-84 How to Cite?
AbstractObjectives: To investigate the efficacy and safety of oral paracetamol compared with oral non-steroidal anti-inflammatory drugs (NSAIDs) or combination therapy in relieving pain after limb injury in an emergency department. Design: Double blind, randomised, controlled study. Setting: Emergency department of a university hospital in the New Territories of Hong Kong. Subjects: 50 adult patients with painful isolated limb injuries. Main outcome measures: Primary outcome measures were pain relief at rest and with limb movement, and adverse events. Results: There was no statistical difference in the mean reduction in pain score between oral paracetamol and oral NSAIDs in the first two hours of treatment or over three days. Patients' pain reduced significantly over three days but it was unclear whether this was due to natural healing rather than analgesic medication. There was no significant difference in pain relief between paracetamol and NSAIDs over three days treatment. All combinations appeared to be safe with no major adverse effects reported in the study. Conclusion: Oral paracetamol may be as effective and as safe as moderate dose of NSAIDs in the management of musculoskeletal pain. A larger study is required to confirm this hypothesis.
Persistent Identifierhttp://hdl.handle.net/10722/291740
ISSN
2023 Impact Factor: 0.8
2023 SCImago Journal Rankings: 0.297

 

DC FieldValueLanguage
dc.contributor.authorMan, Shin Yan-
dc.contributor.authorWoo, Wing Keung-
dc.contributor.authorLam, Peggo Kwok Wai-
dc.contributor.authorRainer, Timothy Hudson-
dc.date.accessioned2020-11-17T14:55:01Z-
dc.date.available2020-11-17T14:55:01Z-
dc.date.issued2004-
dc.identifier.citationHong Kong Journal of Emergency Medicine, 2004, v. 11, n. 2, p. 78-84-
dc.identifier.issn1024-9079-
dc.identifier.urihttp://hdl.handle.net/10722/291740-
dc.description.abstractObjectives: To investigate the efficacy and safety of oral paracetamol compared with oral non-steroidal anti-inflammatory drugs (NSAIDs) or combination therapy in relieving pain after limb injury in an emergency department. Design: Double blind, randomised, controlled study. Setting: Emergency department of a university hospital in the New Territories of Hong Kong. Subjects: 50 adult patients with painful isolated limb injuries. Main outcome measures: Primary outcome measures were pain relief at rest and with limb movement, and adverse events. Results: There was no statistical difference in the mean reduction in pain score between oral paracetamol and oral NSAIDs in the first two hours of treatment or over three days. Patients' pain reduced significantly over three days but it was unclear whether this was due to natural healing rather than analgesic medication. There was no significant difference in pain relief between paracetamol and NSAIDs over three days treatment. All combinations appeared to be safe with no major adverse effects reported in the study. Conclusion: Oral paracetamol may be as effective and as safe as moderate dose of NSAIDs in the management of musculoskeletal pain. A larger study is required to confirm this hypothesis.-
dc.languageeng-
dc.relation.ispartofHong Kong Journal of Emergency Medicine-
dc.subjectNSAID-
dc.subjectIndomethacin-
dc.subjectDiclofenac-
dc.subjectWounds and injuries-
dc.titleFeasibility study comparing oral paracetamol and oral non-steroidal anti-inflammatory drugs for treating pain after musculoskeletal injury: A randomised, double blind, controlled trial-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.1177/102490790401100203-
dc.identifier.scopuseid_2-s2.0-2342486780-
dc.identifier.volume11-
dc.identifier.issue2-
dc.identifier.spage78-
dc.identifier.epage84-
dc.identifier.issnl1024-9079-

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