肾上腺素减少阿卡因溶液(1:40万)在儿科牙科:一项多中心非介入性临床试验。

P W Kämmerer, N Krämer, J Esch, H Pfau, U Uhlemann, L Piehlmeier, M Daubländer
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引用次数: 18

摘要

目的:在儿科牙科,肾上腺素可能有助于全身和局部的副作用。另一方面,有必要提供良好和安全的局部镇痛。因此,降低肾上腺素浓度的阿替卡因溶液在临床环境中进行了测试。方法:采用非介入性临床研究方法,对4 ~ 17岁的儿童和青少年进行牙科治疗。局部镇痛采用阿替卡因4%加肾上腺素1:40万,方法由牙医选择。观察疗效、耐受性、软组织镇痛持续时间及副作用。结果:999例患者(男性50.5%,女性49.5%),平均年龄7.9岁(SD 2.34)。276例患者(27.6%)在治疗前接受镇静治疗。平均治疗时间15 min (SD 10)。在93.5%的病例中,最初的局部镇痛足以执行计划的治疗。99%的病例(n = 989)可以完成计划治疗。6.5%的病例需要第二次注射。软组织镇痛时间平均为2.19 h (SD 1.01)。3.1%的受试者出现轻微副作用。结论:阿替卡因4%降肾上腺素溶液(1:40万)具有较高的疗效、耐受性和安全性,是一种安全、适用于儿科常规治疗的药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Epinephrine-reduced articaine solution (1:400,000) in paediatric dentistry: a multicentre non-interventional clinical trial.

Epinephrine-reduced articaine solution (1:400,000) in paediatric dentistry: a multicentre non-interventional clinical trial.

Epinephrine-reduced articaine solution (1:400,000) in paediatric dentistry: a multicentre non-interventional clinical trial.

Epinephrine-reduced articaine solution (1:400,000) in paediatric dentistry: a multicentre non-interventional clinical trial.

Aim: In paediatric dentistry, epinephrine may contribute to systemic and local side-effects. On the other hand it is necessary to provide good and safe local analgesia. Therefore, an articaine solution with reduced epinephrine concentration was tested in a clinical setting.

Methods: In a non-interventional clinical study, dental treatment was performed in children and adolescents (4-17 years). For local analgesia, articaine 4 % plus epinephrine 1:400,000 was used in the technique chosen by the dentist. Efficacy and tolerance as well as duration of soft tissue analgesia and side-effects were evaluated.

Results: 999 patients (50.5 % male, 49.5 % female) with a mean age of 7.9 (SD 2.34) years were treated. Two hundred seventy six patients (27.6 %) received sedation prior to treatment. The mean treatment time was 15 min (SD 10). In 93.5 % of cases, initial local analgesia was sufficient to perform the planned treatment. In 99 % of cases (n = 989) the planned treatment could be completed. A second injection was necessary in 6.5 % of cases. A mean duration of soft tissue analgesia of 2.19 h (SD 1.01) was seen. Slight side-effects occurred in 3.1 % of subjects.

Conclusions: Due to high efficacy, tolerance and safety, the articaine 4 % solution with the reduced epinephrine concentration (1:400,000) was a safe and suitable drug for paediatric routine treatment.

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