The Effect of Nonsteroidal Anti-Inflammatory Drug Administration on Acute Phase Fracture-Healing: A Review

被引:67
|
作者
Kurmis, Andrew P. [1 ]
Kurmis, Timothy P. [1 ]
O'Brien, Justin X. [1 ]
Dalen, Tore [1 ]
机构
[1] Repatriat Gen Hosp, Dept Orthopaed, Daw Pk, SA 5041, Australia
关键词
INGROWTH IN-VIVO; HETEROTOPIC OSSIFICATION; BONE-FORMATION; CYCLOOXYGENASE-2; INHIBITORS; PHARMACOLOGICAL AGENTS; CARDIOVASCULAR EVENTS; COX-2; SPINAL-FUSION; RATS; INDOMETHACIN;
D O I
10.2106/JBJS.J.01743
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Background: The analgesic efficacy of nonsteroidal anti-inflammatory drugs (NSAIDs) is well established, and these agents often form an integral part of posttraumatic pain management. However, potentially deleterious effects of resulting prostaglandin suppression on fracture-healing have been suggested. Methods: A systematic literature review involving searches of electronic databases and online sources was performed to identify articles exploring the influence of NSAIDs on fracture-healing. Results: A structured search approach identified 316 papers as potentially relevant to the topic, and these were manually reviewed. The majority described small-scale studies that were retrospective or observational in nature, with limited control of potentially confounding variables, or presented little key information that was not also present in other studies. Conclusions: Although increasing evidence from animal studies suggests that cyclooxygenase-2 (COX-2) inhibition suppresses early fracture-healing, in vivo studies involving human subjects have not provided convincing evidence to substantiate this concern. We found no robust evidence to attest to a significant and appreciable patient detriment resulting from the short-term use of NSAIDs following a fracture. The balance of evidence in the available literature appears to suggest that a short-duration NSAID regimen is a safe and effective supplement to other modes of post-fracture pain control, without a significantly increased risk of sequelae related to disrupted healing.
引用
收藏
页码:815 / 823
页数:9
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