Department of Clinical Sciences, Kansas State University, Manhattan, Kansas, USA.
Department of Diagnostic Medicine/Pathology, Kansas State University, Manhattan, Kansas, USA.
J Vet Intern Med. 2023 Jul-Aug;37(4):1561-1567. doi: 10.1111/jvim.16740. Epub 2023 May 26.
Prevention of spread of Streptococcus equi subspecies equi (S. equi) after an outbreak is best accomplished by endoscopic lavage of the guttural pouch, with samples tested by culture and real time, quantitative polymerase chain reaction (qPCR). Disinfection of endoscopes must eliminate bacteria and DNA to avoid false diagnosis of carrier horses of S. equi.
HYPOTHESIS/OBJECTIVES: Compare failure rates of disinfection of endoscopes contaminated with S. equi using 2 disinfectants (accelerated hydrogen peroxide [AHP] or ortho-phthalaldehyde [OPA]). The null hypothesis was that there would be no difference between the AHP and OPA products (based on culture and qPCR results) after disinfection.
Endoscopes contaminated with S. equi were disinfected using AHP, OPA or water (control). Samples were collected before and after disinfection and submitted for detection of S. equi by culture and qPCR. Using a multivariable logistic regression model-adjusted probability, with endoscope and day as controlled variables, the probability of an endoscope being qPCR-positive was determined.
After disinfection, all endoscopes were culture-negative (0%). However, the raw unadjusted qPCR data were positive for 33% AHP, 73% OPA, and 71% control samples. The model-adjusted probability of being qPCR-positive after AHP disinfection was lower (0.31; 95% confidence interval [CI], -0.03-0.64) compared to OPA (0.81; 95% CI, 0.55-1.06), and control (0.72; 95% CI, 0.41-1.04).
Disinfection using the AHP product resulted in significantly lower probability of endoscopes being qPCR-positive compared to the OPA product and control.
为了防止马流感嗜血杆菌(S. equi)爆发后的传播,最好通过对咽喉囊进行内镜冲洗,并通过培养和实时定量聚合酶链反应(qPCR)对样本进行检测。为了避免误诊 S. equi 带菌马,内窥镜的消毒必须消除细菌和 DNA。
假设/目的:比较两种消毒剂(加速过氧化氢[AHP]或邻苯二醛[OPA])对污染有 S. equi 的内窥镜的消毒失败率。零假设是,经过消毒后,AHP 和 OPA 产品(基于培养和 qPCR 结果)之间不会有差异。
使用 AHP、OPA 或水(对照)对污染有 S. equi 的内窥镜进行消毒。在消毒前后采集样本,并通过培养和 qPCR 检测 S. equi。使用多变量逻辑回归模型调整概率,以内窥镜和天数为控制变量,确定内窥镜 qPCR 阳性的概率。
消毒后,所有内窥镜的培养结果均为阴性(0%)。然而,未经调整的原始 qPCR 数据显示,AHP 组有 33%的样本为阳性,OPA 组有 73%的样本为阳性,对照组有 71%的样本为阳性。与 OPA(0.81;95%置信区间[CI],0.55-1.06)和对照组(0.72;95%CI,0.41-1.04)相比,AHP 消毒后 qPCR 阳性的模型调整概率较低(0.31;95%CI,-0.03-0.64)。
与 OPA 产品和对照组相比,AHP 产品的消毒效果显著降低了内窥镜 qPCR 阳性的概率。