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阿奇霉素与托氟沙星甲苯磺酸盐治疗急性牙源性感染的比较临床研究

[Comparative clinical study of azithromycin with tosufloxacin tosilate in the treatment of acute odontogenic infection].

作者信息

Sasaki J, Kaneko A, Karakida K, Shiiki K, Sakamoto H, Naitoh H, Yamane N, Tomita F, Katoh H, Yoshida H

机构信息

Department of Oral Surgery, School of Medicine, Tokai University.

出版信息

Jpn J Antibiot. 1995 Sep;48(9):1093-118.

PMID:7474331
Abstract

To objectively assess azithromycin (AZM) for its clinical efficacy, safety and usefulness in the treatment of acute odontogenic infections (periodontitis, pericoronitis and osteitis of the jaw), a double-blind, randomized, multi-center trial was conducted in which tosufloxacin tosilate (TFLX) was used as the control drug. AZM was administered to 90 patients at a once-daily 500 mg dose for 3 days, while TFLX was given to 90 patients at a 150 mg t.i.d. dose for 7 days. 1. The clinical efficacy rates calculated according to evaluation at an endpoint set on the 3rd day of treatment by a committee of experts were 85.9% (73/85) in the AZM group and 78.9% (71/90) in the TFLX group. No statistically significant difference between the treatment groups was detected, and clinical equivalence was verified (p = 0.002). 2. The clinical efficacy rates according to evaluations made by investigators at the end-of-tail point was 87.1% (74/85) in the AZM group and 73.3% (66/90) in the TFLX group. The efficacy rate in the AZM group was higher than that in the TFLX group, and the difference was statistically significant (p = 0.006). 3. The bacteriological elimination rate in the AZM group was 97.5% (39/40) and that in the TFLX group was 85.7% (30/35), but the difference was deemed statistically not significant. 4. Adverse reactions were observed in 11 of 88 cases (12.5%) in the AZM group and 5 of 90 cases (5.6%) in the TFLX group. Six of 85 cases (7.1%) in the AZM group and 5 of 85 cases (5.9%) in the TFLX group showed laboratory abnormalities. However, neither adverse reactions nor laboratory abnormalities showed any differences in statistical significance between the treatment groups. 5. The safety rates, expressed as percentages of cases with no adverse events and no laboratory abnormalities, was 84.1% (74/88) in the AZM group and 90.0% (81/90) in the TFLX group. The difference between the two groups was found to be statistically insignificant. 6. The usefulness rates, the ratio of cases rated as either "Very useful" or "Useful", was 83.9% (73/87) in the AZM group, and it was statistically higher (p = 0.025) than 72.2% (65/90) obtained for TFLX group. Judging from the above results, it has been concluded that AZM is as useful as TFLX in the treatment of acute dental infections.

摘要

为客观评估阿奇霉素(AZM)治疗急性牙源性感染(牙周炎、冠周炎和颌骨骨髓炎)的临床疗效、安全性及实用性,开展了一项双盲、随机、多中心试验,其中以托氟沙星(TFLX)作为对照药物。90例患者接受AZM治疗,每日一次,剂量为500mg,疗程3天;90例患者接受TFLX治疗,每日3次,剂量为150mg,疗程7天。1. 根据专家委员会在治疗第3天设定的终点进行评估,AZM组的临床有效率为85.9%(73/85),TFLX组为78.9%(71/90)。两组间未检测到统计学显著差异,证实了临床等效性(p = 0.002)。2. 根据研究者在终点时的评估,AZM组的临床有效率为87.1%(74/85),TFLX组为73.3%(66/90)。AZM组的有效率高于TFLX组,差异具有统计学显著性(p = 0.006)。3. AZM组的细菌清除率为97.5%(39/40),TFLX组为85.7%(30/35),但差异被认为无统计学显著性。4. AZM组88例中有11例(12.5%)出现不良反应,TFLX组90例中有5例(5.6%)出现不良反应。AZM组85例中有6例(7.1%)出现实验室异常,TFLX组85例中有5例(5.9%)出现实验室异常。然而,两组间不良反应和实验室异常均未显示出统计学显著差异。5. 以无不良事件且无实验室异常的病例百分比表示的安全率,AZM组为84.1%(74/88),TFLX组为90.0%(81/90)。两组间差异无统计学显著性。6. 有用率,即被评为“非常有用”或“有用”的病例比例,AZM组为83.9%(73/87),在统计学上高于TFLX组的72.2%(65/90)(p = 0.025)。根据上述结果得出结论,AZM在治疗急性牙源性感染方面与TFLX同样有效。

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