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罗他霉素治疗小儿感染的疗效、安全性及剂量研究

[Studies on efficacy, safety and dosage of rokitamycin in the treatment of pediatric infections].

作者信息

Hirosawa H, Ishikawa Y, Takahashi S, Matsuda H, Ichihashi H

机构信息

Department of Pediatrics, School of Medicine, Kyorin University.

出版信息

Jpn J Antibiot. 1988 Jun;41(6):712-9.

PMID:3221435
Abstract

The usefulness of a new macrolide antibiotic rokitamycin (RKM, TMS-19-Q) was evaluated in the field of pediatrics. 1. Twenty seven patients were enrolled in the study. One patient was excluded from the study because the illness was due to a viral infection. They included 14 boys and 13 girls with ages 7 months to 9 years 11 months. 2. The patients were treated with RKM at daily doses ranging 19.2-41.1 mg/kg, divided into 3 equal portions. The administration was done orally at fasting, lasting 2-15 days, with total doses of 22.2-500.0 mg/kg. 3. The patients were diagnostically classified into the following categories: 9 with acute pharyngitis, 15 with acute bronchitis, and one each with pneumonia, purulent lymphadenitis and Campylobacter enteritis. 4. The clinical response to the treatment was good or excellent in 22 of the patients with an overall efficacy rate of 81.5%. An efficacy rate of 88.9% was achieved for the patients with acute pharyngitis, 80.0% for those with acute bronchitis, and 100% for the patient with purulent lymphadenitis and the patient with Campylobacter enteritis. From the patient with pneumonia whose response was evaluated "fair" was Haemophilus influenzae isolated by culturing pharyngeal material. This organism was found resistant to RKM by the disk method. 5. Bacteriological responses were as follows; of 26 isolates presumed to be pathogens, 9 were eradicated, 5 decreased, 7 unchanged and 5 unknown, with an eradication rate of 42.9%. 6. Neither adverse reactions nor abnormal changes in laboratory findings were observed with the medication in any patients during and after the end of the treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在儿科领域评估了一种新型大环内酯类抗生素罗他霉素(RKM,TMS-19-Q)的效用。1. 27名患者纳入本研究。1名患者因疾病由病毒感染引起而被排除。他们包括14名男孩和13名女孩,年龄从7个月至9岁11个月。2. 患者接受RKM治疗,日剂量范围为19.2 - 41.1mg/kg,分为3等份。空腹口服给药,持续2 - 15天,总剂量为22.2 - 500.0mg/kg。3. 患者诊断分类如下:9例急性咽炎,15例急性支气管炎,各1例肺炎、化脓性淋巴结炎和弯曲杆菌肠炎。4. 22例患者治疗的临床反应为良好或优秀,总有效率为81.5%。急性咽炎患者有效率为88.9%,急性支气管炎患者为80.0%,化脓性淋巴结炎患者和弯曲杆菌肠炎患者为100%。对反应评估为“一般”的肺炎患者,通过咽拭子培养分离出流感嗜血杆菌。通过纸片法发现该菌对RKM耐药。5. 细菌学反应如下:在26株推测为病原体的分离株中,9株被根除,5株减少,7株未变,5株情况不明,根除率为42.9%。6. 在治疗期间及结束后,未观察到任何患者用药出现不良反应或实验室检查结果异常变化。(摘要截断于250字)

相似文献

1
[Studies on efficacy, safety and dosage of rokitamycin in the treatment of pediatric infections].罗他霉素治疗小儿感染的疗效、安全性及剂量研究
Jpn J Antibiot. 1988 Jun;41(6):712-9.
2
[Clinical study of rokitamycin dry syrup in pediatrics].罗他霉素干糖浆在儿科的临床研究
Jpn J Antibiot. 1988 Jul;41(7):863-70.
3
[Microbiological, pharmacokinetic and clinical studies of rokitamycin dry syrup in the pediatric field].
Jpn J Antibiot. 1988 Jul;41(7):920-59.
4
[Laboratory and clinical studies of rokitamycin dry syrup in the field of pediatrics].
Jpn J Antibiot. 1988 Jul;41(7):875-84.
5
[Clinical studies of rokitamycin dry syrup in the field of pediatrics].罗他霉素干糖浆在儿科领域的临床研究
Jpn J Antibiot. 1988 Jul;41(7):914-9.
6
[Clinical results of a rokitamycin dry syrup in pediatric infections].[罗他霉素干糖浆治疗小儿感染的临床效果]
Jpn J Antibiot. 1988 Jun;41(6):673-85.
7
[A clinical study of rokitamycin in pediatrics].罗他霉素在儿科的临床研究
Jpn J Antibiot. 1988 Jun;41(6):745-54.
8
[Appraisal of rokitamycin in the pediatric field].[儿科领域中罗他霉素的评估]
Jpn J Antibiot. 1988 Jun;41(6):646-62.
9
[Studies of rokitamycin in pediatrics].[罗他霉素在儿科的研究]
Jpn J Antibiot. 1988 Jul;41(7):885-900.
10
[Evaluation of effectiveness of rokitamycin dry syrup in acute enteritis in pediatrics. A comparative study on rokitamycin and fosfomycin dry syrups].
Jpn J Antibiot. 1990 Feb;43(2):257-84.

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