糖皮质激素或非甾体抗炎药对特发性猫尿路疾病症状比不治疗或安慰剂有效吗?

L. Sofyan
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引用次数: 1

摘要

在患有特发性猫尿路疾病(FLUTD)的猫中,糖皮质激素或非甾体类抗炎药在减少膀胱炎的临床症状方面是否比安慰剂或无治疗更有效?临床结论研究问题类别治疗研究设计的数量和类型回顾了三个随机对照试验,与安慰剂相比,研究了强的松龙或非甾体抗炎药(NSAIDs)在减少猫下尿路疾病临床症状方面的疗效,而一项回顾性队列研究比较了使用美洛昔康和不使用美洛昔康治疗的猫flud的复发率一项小型对照试验比较了强的松龙和安慰剂,发现对于诊断为特发性非阻塞性猫下尿路疾病(flud)的猫,住院10天在排尿困难、显微镜下血尿和隐血方面没有临床差异。然而,这项研究的样本量非常小。此外,该研究对出院回家的类似患者的外部效度尚不清楚。第二项小型对照试验比较了美洛昔康和安慰剂对诊断为阻塞性FLUTD的猫的疗效。采用统计分析来确定住院期间负责兽医和出院时主人评估的排尿行为、一般举止、血尿、食物摄入和腹痛是否存在显著差异。根据饲主问卷和兽医评估,两个治疗组之间没有统计学差异(P>0.05),但每个治疗组的样本都很小,可能限制了统计能力。第三项小型对照试验比较了在使用phenoxybenzamine和alprazolam,或不添加美洛昔康的情况下,猫在出院后10天、1、2和6个月的猫特发性膀胱炎(FIC)的复发率、相关临床症状和复发性尿路阻塞。在接受美洛昔康治疗或不接受美洛昔康治疗的猫中,梗阻性或非梗阻性FIC的复发率没有统计学上的显著差异。然而,每个干预组的全部细节不足以评估预后因素的平衡,临床体征的主观评分也不详细,研究对实际梗阻率的报道力度不足。第四篇论文是一项回顾性队列研究,研究了不同治疗因素与30天再梗阻的关系。3项小型随机对照试验和1项回顾性队列研究未能发现糖皮质激素或非甾体抗炎药的使用与FLUTD临床症状的严重程度或再梗阻风险之间存在显著关联。临床结果测量是异质的,研究明显不足和/或存在偏倚和/或混淆的风险。在特发性FLUTD或FIC病例中,没有足够的证据推荐使用任何一种药物类别来减少临床症状缓解或严重程度的时间。如何在实践中应用这一证据在实践中的应用应考虑多种因素,不限于:个人的临床专业知识,病人的情况和业主的价值观,你工作的国家,地点或诊所,你面前的个案,治疗和资源的可用性。知识摘要是帮助加强或告知决策的资源。他们不会凌驾于从业者的责任或判断之上,去做对他们照顾的动物最好的事情。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Are glucocorticoids or NSAIDs effective in idiopathic feline urinary tract disease signs than no treatment or placebo?
PICO question In cats with idiopathic feline urinary tract disease (FLUTD), are glucocorticoid or non-steroidal anti-inflammatory drugs more effective than placebo or no treatment in reducing clinical signs attributable to cystitis?   Clinical bottom line Category of research question Treatment The number and type of study designs reviewed Three randomised controlled trials have examined the efficacy of prednisolone or non-steroidal anti-inflammatory drugs (NSAIDs) in reducing the clinical signs of feline lower urinary tract disease compared to a placebo whilst one retrospective cohort study compared the reoccurrence of FLUTD in cats treated with meloxicam and without meloxicam Strength of evidence Weak Outcomes reported One small controlled trial compared prednisolone to a placebo and found no clinical differences in dysuria, microscopic haematuria, and occult blood for cats diagnosed with idiopathic non-obstructive feline lower urinary tract disease (FLUTD) hospitalised for 10 days. The study however had a very small sample size. Furthermore, the external validity of the study to similar patients discharged to their home environment is unclear. The second small controlled trial compared meloxicam to a placebo in cats diagnosed with obstructive FLUTD. Statistical analysis was applied to determine if there were significant differences in voiding behaviour, general demeanour, haematuria, food intake and abdominal pain as assessed by the veterinarians in charge during hospitalisation and owners at discharge. No statistically significant differences (P>0.05) were calculated between the two treatment groups based on the owner questionnaire and veterinarian assessment but small samples in each treatment probably limited statistical power. The third small controlled trial compared the reoccurrence of feline idiopathic cystitis (FIC), related clinical signs and recurrent urinary obstruction in cats at 10 days, 1, 2 and 6 months after discharge when treated with phenoxybenzamine and alprazolam, with or without the addition of meloxicam. No statistically significant differences were found in the reoccurrence of obstructed or non-obstructed FIC for cats treated with either meloxicam or no meloxicam. However, full details of each intervention group were not sufficient to assess for balance of prognostic factors, subjective scoring of clinical signs was not detailed, and the study was underpowered for the actual obstruction rates reported. The fourth paper was a retrospective cohort study that examined the association of different treatment factors with 30 days reobstruction. The study found no significant association between the use of meloxicam and the rate of reobstruction but a number of confounders were present Conclusion Three small randomised controlled trials and a single retrospective cohort study failed to find a significant association between the use of glucocorticoids or NSAIDs with severity of FLUTD clinical signs or risk of reobstruction. Clinical outcome measures were heterogeneous and studies were significantly underpowered and/or at risk for bias and/or confounding. There is insufficient evidence to recommend the use of either drug category in decreasing time to resolution or severity of clinical signs in cases of idiopathic FLUTD or FIC   How to apply this evidence in practice The application of evidence into practice should take into account multiple factors, not limited to: individual clinical expertise, patient’s circumstances and owners’ values, country, location or clinic where you work, the individual case in front of you, the availability of therapies and resources. Knowledge Summaries are a resource to help reinforce or inform decision making. They do not override the responsibility or judgement of the practitioner to do what is best for the animal in their care.  
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