Naylor R J, Taylor A H, Knowles E J, Wilford S, Linnenkohl W, Mair T S, Johns I C
Equine Referral Hospital, Royal Veterinary College, Hatfield, Hertfordshire, UK.
Equine Vet J. 2014 Jul;46(4):427-34. doi: 10.1111/evj.12224. Epub 2014 Feb 18.
Ex vivo evidence suggests that cyclo-oxygenase (COX) 2-preferential inhibitor nonsteroidal anti-inflammatory drugs (NSAIDs), such as meloxicam, have a less detrimental effect on intestinal healing than flunixin meglumine (FM). Whether this translates to a beneficial effect in horses with naturally occurring strangulating small intestinal (SSI) lesions is unknown.
To compare the clinical outcome of horses with naturally occurring SSI lesions treated with meloxicam or FM.
Randomised prospective study.
Cases presenting to the Royal Veterinary College Equine Referral Hospital and Bell Equine Veterinary Clinic during 2010 and 2011 in which an SSI lesion was identified at exploratory laparotomy were eligible for inclusion. Horses received either 1.1 mg/kg bwt FM or 0.6 mg/kg bwt meloxicam i.v. q. 12 h. Clinical outcomes and clinical and laboratory parameters associated with endotoxaemia were compared between groups.
Sixty cases were enrolled, 32 horses received FM and 28 received meloxicam. There was no difference in signalment, physical examination or surgical factors between groups. The overall survival to discharge was 81%; there was no difference in survival (P = 0.14) or incidence of post operative ileus (P = 0.25) between groups. There was no significant difference between the plasma lipopolysaccharide (LPS) concentrations at 0 h (P = 0.18) or 48 h (P = 0.60); however, there was a significant difference between neutrophil count at 48 h (P<0.05) and at 96 h (P<0.01) with significantly greater cell numbers in horses receiving meloxicam compared with FM. Blinded pain score evaluation showed that more horses receiving meloxicam showed gross signs of pain than those treated with FM (P = 0.04).
Nonsteroidal anti-inflammatory drug choice did not affect major clinical outcomes in horses with SSI lesions but had some effects on signs of pain. This study provides no evidence to recommend one NSAID treatment above another based on survival or the incidence of ileus; however, evaluation of a larger number of cases is required.
体外实验证据表明,环氧化酶(COX)-2选择性抑制剂非甾体抗炎药(NSAIDs),如美洛昔康,对肠道愈合的不良影响小于氟尼辛葡甲胺(FM)。这是否能转化为对患有自然发生的绞窄性小肠(SSI)病变马匹的有益效果尚不清楚。
比较用美洛昔康或FM治疗的患有自然发生的SSI病变马匹的临床结局。
随机前瞻性研究。
2010年和2011年就诊于皇家兽医学院马转诊医院和贝尔马兽医诊所且在剖腹探查时确诊为SSI病变的病例符合纳入标准。马匹静脉注射1.1 mg/kg体重的FM或0.6 mg/kg体重的美洛昔康,每12小时一次。比较两组的临床结局以及与内毒素血症相关的临床和实验室参数。
共纳入60例病例,32匹马接受FM治疗,28匹马接受美洛昔康治疗。两组在品种、体格检查或手术因素方面无差异。出院时的总体生存率为81%;两组在生存率(P = 0.14)或术后肠梗阻发生率(P = 0.25)方面无差异。0小时(P = 0.18)或48小时(P = 0.60)时血浆脂多糖(LPS)浓度无显著差异;然而,48小时(P<0.05)和96小时(P<0.01)时中性粒细胞计数有显著差异,与接受FM治疗的马匹相比,接受美洛昔康治疗的马匹细胞数量显著更多。盲法疼痛评分评估显示,接受美洛昔康治疗的马匹出现明显疼痛体征的比接受FM治疗的更多(P = 0.04)。
非甾体抗炎药的选择对患有SSI病变的马匹的主要临床结局没有影响,但对疼痛体征有一些影响。本研究没有提供证据支持基于生存率或肠梗阻发生率推荐一种NSAID治疗优于另一种;然而,需要评估更多病例。