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聚维酮碘灌洗治疗实验性诱导的马传染性关节炎

Povidone-iodine lavage treatment of experimentally induced equine infectious arthritis.

作者信息

Bertone A L, McIlwraith C W, Jones R L, Norrdin R W, Radin M J

出版信息

Am J Vet Res. 1987 Apr;48(4):712-5.

PMID:3592370
Abstract

Both tarsocrural joints of 4 horses were inoculated with 1.5 X 10(5) colony-forming units of Staphylococcus aureus. On days 1, 3, and 6, each horse had one tarsocrural joint lavaged with a balanced electrolyte solution and had the contralateral tarsocrural joint lavaged with 0.1% povidone-iodine solution. All horses were orally administered trimethoprim (5 mg/kg)/sufadiazine (25 mg/kg) combination twice daily and phenylbutazone (2 g) once daily for the duration of the study (21 days). On days 0, 1, 3, 6, 9, 14, and 21, synovial fluid specimens were collected and analyzed for color, clarity, total protein concentration, WBC count and differential, and mucin clot-forming ability. Synovial fluid specimens collected on days 1, 3, 6, 9, 14, and 21 were bacteriologically cultured. On day 21, all horses were euthanatized, the tarsocrural joints were opened and examined, synovial membrane specimens were collected, bacteriologically cultured, and histologically evaluated, and articular cartilage specimens were histochemically evaluated. Repeated measures analysis of variance were used to evaluate differences between lavage solutions and among days for objective measurements. A paired t test was used to evaluate differences between solutions for the indices of synovial membrane inflammation and articular cartilage staining intensity with safranin-O-fast green. To be considered significant, the probability of a type-I error was less than 0.05. Significant differences were not found between joints lavaged with electrolyte solution vs povidone-iodine solution for synovial total protein concentration, WBC count, results of synovial fluid and membrane bacteriologic culture, synovial membrane inflammation, or articular cartilage glycosaminoglycan concentration.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

给4匹马的两个跗关节接种1.5×10⁵个金黄色葡萄球菌菌落形成单位。在第1、3和6天,每匹马的一个跗关节用平衡电解质溶液灌洗,对侧跗关节用0.1%聚维酮碘溶液灌洗。在研究期间(21天),所有马匹每天口服两次甲氧苄啶(5毫克/千克)/磺胺嘧啶(25毫克/千克)合剂,每天口服一次保泰松(2克)。在第0、1、3、6、9、14和21天,采集滑膜液样本,分析其颜色、透明度、总蛋白浓度、白细胞计数及分类,以及黏蛋白凝块形成能力。在第1、3、6、9、14和21天采集的滑膜液样本进行细菌培养。在第21天,对所有马匹实施安乐死,打开跗关节进行检查,采集滑膜标本进行细菌培养和组织学评估,采集关节软骨标本进行组织化学评估。采用重复测量方差分析来评估灌洗溶液之间以及不同天数之间客观测量结果的差异。采用配对t检验来评估滑膜炎症指标和关节软骨番红O-固绿染色强度在不同溶液之间的差异。I型错误概率小于0.05时才被认为具有显著性差异。对于滑膜总蛋白浓度、白细胞计数、滑膜液和滑膜细菌培养结果、滑膜炎症或关节软骨糖胺聚糖浓度,用电解质溶液灌洗的关节与用聚维酮碘溶液灌洗的关节之间未发现显著差异。(摘要截短至250字)

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