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Efficacy and Safety of Inhalation Sedation during Office Probing for Congenital Nasolacrimal Duct Obstruction

机译:在办公室探究先天性鼻腔治梗阻期间吸入镇静的功效和安全性

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摘要

We compared the effectiveness of inhaled sevoflurane versus physical restraint during probing in children with congenital nasolacrimal duct obstruction (CNLDO). We performed a retrospective review of children with CNLDO who underwent office probing procedures by a single surgeon under sedation or restraint. Patients’ characteristics at the time of probing, including age, sex, laterality, previous non-surgical treatment, presence of dacryocystitis, outcomes of probing, and complications were compared between the sedation and restraint groups. A multivariable logistic regression analysis was performed to investigate the prognostic factors associated with the success of probing. A subgroup analysis by 12 months of age was also conducted. The overall success rate was 88.6% in 202 eyes of 180 consecutive children (mean age, 15.1 ± 7.7 months). The sedation group had a marginally higher success rates than the restraint group (93.8% vs. 85.1%, p = 0.056). The success rate was not significantly different between the two groups in children aged <12 months (90.9% vs. 93.1%, p = 0.739), but it was significantly higher in the sedation group (94.7% vs. 77.8%. p = 0.006) in children aged ≥12 months. Inhalation sedation was the most potent factor associated with success (adjusted odds ratio = 5.56, 95% confidence interval = 1.33–23.13, p = 0.018) in children aged ≥12 months. There were no surgical or sedation-related complications intra- and postoperatively. Inhaled sevoflurane sedation resulted in more successful, controlled, painless probing, particularly in children aged ≥12 months. It represents a safe, efficient alternative to general anesthesia.
机译:我们将吸入的七氟醚与物理约束的有效性与先天性鼻腔治疗(CNLDO)探测中的吸入七氟醚。我们对CNLDO的儿童进行了回顾性审查,他们在镇静或克制下由单个外科医生接受办公室探测程序。在镇静和约束群之间比较了探测时患者的特征,包括年龄,性别,横向,先前的非手术治疗,探测结果以及并发症的存在。进行多变量的逻辑回归分析以研究与探测成功相关的预后因素。还进行了12个月的亚组分析。总成功率为88.6%,为202只连续180名儿童(平均年龄,15.1±7.7个月)。镇静基团的成功率比约束群更高(93.8%,5.1%,P = 0.056)。在<12个月的儿童(90.9%对93.1%,P = 0.739)之间的两组之间的成功率没有显着差异,但在镇静组中显着较高(94.7%vs. 77.8%。P = 0.006 )在≥12个月的儿童中。吸入镇静是与成功相关的最有效因素(调整的赔率比= 5.56,95%,95%置信区间= 1.33-23.13,P = 0.018)。没有手术或镇静相关的并发症,术语和术后。吸入的七氟脲镇静导致更成功,控制,无痛的探测,特别是在≥12个月的儿童。它代表全身麻醉安全,有效的替代品。

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