Cohen David B, Kawamura Sumito, Ehteshami John R, Rodeo Scott A
Connecticut Orthopaedic Specialists, 2408 Whitney Avenue, Hamden, CT 06518, USA.
Am J Sports Med. 2006 Mar;34(3):362-9. doi: 10.1177/0363546505280428. Epub 2005 Oct 6.
Nonsteroidal anti-inflammatory drugs are commonly prescribed after rotator cuff repair. These agents can impair bone formation, but no studies have evaluated their impact on tendon-to-bone healing.
Traditional nonselective nonsteroidal anti-inflammatory drugs and cyclooxygenase-2-specific nonsteroidal anti-inflammatory drugs interfere with tendon-to-bone healing.
Controlled laboratory study.
One hundred eighty Sprague-Dawley rats underwent acute rotator cuff repairs. Postoperatively, 60 rats received 14 days of celecoxib, a cyclooxygenase-2-specific nonsteroidal anti-inflammatory drug; 60 received indomethacin, a traditional nonselective nonsteroidal anti-inflammatory drug; and 60 received standard rat chow. Animals were sacrificed at 2, 4, and 8 weeks and evaluated by gross inspection, biomechanical testing, histologic analysis, and polarized light microscopy to quantify collagen formation and maturation.
Five tendons completely failed to heal (4 celecoxib, 1 indomethacin). There were significantly lower failure loads in the celecoxib and indomethacin groups compared with the control groups at 2, 4, and 8 weeks (P < .001), with no significant difference between nonsteroidal anti-inflammatory drug groups. There were significant differences in collagen organization and maturation between the controls and both nonsteroidal anti-inflammatory drug groups at 4 and 8 weeks (P < .001). Controls demonstrated progressively increasing collagen organization during the course of the study (P < .001), whereas the nonsteroidal anti-inflammatory drug groups did not.
Traditional and cyclooxygenase-2-specific nonsteroidal anti-inflammatory drugs significantly inhibited tendon-to-bone healing. This inhibition appears linked to cyclooxygenase-2.
If the results of this study are verified in a larger animal model, the common practice of administering non-steroidal anti-inflammatory drugs after rotator cuff repair should be reconsidered.
非甾体类抗炎药常用于肩袖修复术后。这些药物会损害骨形成,但尚无研究评估其对肌腱与骨愈合的影响。
传统非选择性非甾体类抗炎药和环氧化酶-2特异性非甾体类抗炎药会干扰肌腱与骨的愈合。
对照实验室研究。
180只Sprague-Dawley大鼠接受急性肩袖修复术。术后,60只大鼠接受14天的塞来昔布(一种环氧化酶-2特异性非甾体类抗炎药)治疗;60只接受吲哚美辛(一种传统非选择性非甾体类抗炎药)治疗;60只接受标准大鼠饲料喂养。在2周、4周和8周时处死动物,通过大体检查、生物力学测试、组织学分析和偏振光显微镜检查来量化胶原蛋白的形成和成熟情况。
5条肌腱完全未愈合(4条使用塞来昔布,1条使用吲哚美辛)。在2周、4周和8周时,塞来昔布组和吲哚美辛组的失效负荷显著低于对照组(P <.001),非甾体类抗炎药组之间无显著差异。在4周和8周时,对照组与两个非甾体类抗炎药组之间在胶原蛋白的组织和成熟方面存在显著差异(P <.001)。在研究过程中,对照组的胶原蛋白组织逐渐增加(P <.001),而非甾体类抗炎药组则没有。
传统的和环氧化酶-2特异性非甾体类抗炎药显著抑制肌腱与骨的愈合。这种抑制作用似乎与环氧化酶-2有关。
如果本研究结果在更大的动物模型中得到验证,那么肩袖修复术后使用非甾体类抗炎药的常见做法应重新考虑。