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美洛昔康对犬骨关节炎跛行严重程度及其他临床症状的影响。

Effects of meloxicam on severity of lameness and other clinical signs of osteoarthritis in dogs.

作者信息

Peterson Kurt D, Keefe Thomas J

机构信息

Boehringer Ingelheim Vetmedica Inc, 2621 N Belt Hwy, St Joseph, MO 64506, USA.

出版信息

J Am Vet Med Assoc. 2004 Oct 1;225(7):1056-60. doi: 10.2460/javma.2004.225.1056.

DOI:10.2460/javma.2004.225.1056
PMID:15515983
Abstract

OBJECTIVE

To evaluate effects of meloxicam on severity of lameness and other clinical signs in dogs with osteoarthritis (OA).

DESIGN

Randomized, controlled, multicenter clinical trial.

ANIMALS

217 client-owned dogs with clinical and radiographic signs of OA.

PROCEDURE

Dogs were randomly assigned to be treated with meloxicam (n = 105; 0.2 mg/kg [0.09 mg/lb], SC, once on day 1, then 0.1 mg/kg [0.045 mg/lb], PO, q 24 h, for 13 days) or a placebo (n = 112). A general clinical score was assigned by investigators on days 1 (ie, prior to initiation of treatment), 8, and 15 on the basis of severity of lameness, extent of weight bearing, and severity of signs during palpation of the affected joint. Owners and investigators provided overall evaluations on days 8 and 15.

RESULTS

Dogs treated with meloxicam had significantly greater improvements in general clinical scores, compared with baseline scores, on days 8 and 15 than did dogs treated with placebo. On days 8 and 15, percentages of dogs treated with meloxicam in which owners and investigators considered treatment to be successful were significantly higher than percentages of control dogs in which treatment was considered to be successful. No abnormalities in hematologic and serum biochemical test results were detected.

CONCLUSIONS AND CLINICAL RELEVANCE

Results suggest that compared with administration of a placebo, administration of meloxicam for 14 days significantly improved the clinical condition of dogs with OA without causing adverse effects.

摘要

目的

评估美洛昔康对患骨关节炎(OA)犬的跛行严重程度及其他临床症状的影响。

设计

随机、对照、多中心临床试验。

动物

217只临床和影像学检查有OA体征的宠物犬。

步骤

犬被随机分为两组,分别接受美洛昔康治疗(n = 105;0.2mg/kg[0.09mg/lb],皮下注射,第1天一次,然后0.1mg/kg[0.045mg/lb],口服,每24小时一次,共13天)或安慰剂治疗(n = 112)。研究人员在第1天(即治疗开始前)、第8天和第15天根据跛行严重程度、负重程度以及触诊患关节时的症状严重程度进行总体临床评分。主人和研究人员在第8天和第15天提供总体评估。

结果

与接受安慰剂治疗的犬相比,接受美洛昔康治疗的犬在第8天和第15天的总体临床评分较基线评分有显著改善。在第8天和第15天,主人和研究人员认为美洛昔康治疗成功的犬的百分比显著高于认为安慰剂治疗成功的对照犬的百分比。未检测到血液学和血清生化检测结果异常。

结论及临床意义

结果表明,与给予安慰剂相比,给予美洛昔康14天可显著改善患OA犬的临床状况,且无不良反应。

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