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头孢泊肟酯治疗小儿感染的疗效、安全性及剂量研究

[Study of efficacy, safety and dosage on cefpodoxime proxetil in 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, Kyourin University.

出版信息

Jpn J Antibiot. 1989 Jul;42(7):1498-504.

PMID:2810726
Abstract

Cefpodoxime proxetil (CS-807, CPDX-PR), a new cephalosporin antibiotic, was investigated for its usefulness in pediatrics. 1. The total number of patients treated were 21 with their ages ranging from 3 months to 9 years and 1 month, consisting of 5 male and 16 female infants. 2. Single dosages of the drug ranged between 4.4 mg and 5.8 mg/kg with oral administration for 3 times daily in fasting. A total aggregated dosage was between 46.4 mg/kg and 200.0 mg/kg. The length of administration was 3 to 12 days. 3. The breakdown of symptoms were 9 cases of acute pharyngitis, 5 cases of acute tonsillitis, 3 cases of acute bronchitis, and 1 case each of impetigo + purulent rhinitis, cervical lymphadenitis, scarlet fever, and urinary tract infection. 4. The clinical efficacy rate was 100% with 18 excellent responses and 3 good responses. 5. The bacteriological efficacy rate was 90.9% in eradication rate, based on results on 17 strains of suspected causative microorganism among which 10 strains were eradicated, 1 strain was decreased, and 6 strains were unknown. 6. There was no side effect during the treatment and after the discontinuation, while, in clinical laboratory tests, GOT and GPT were elevated in 1 case which was judged as abnormal. No patient refused the drug. CPDX-PR was considered to be very useful drug because of its excellent efficacy and safety in pediatrics in treating infectious diseases.

摘要

头孢泊肟酯(CS - 807,CPDX - PR)是一种新型头孢菌素类抗生素,对其在儿科的应用价值进行了研究。1. 共治疗21例患者,年龄范围为3个月至9岁1个月,其中男童5例,女童16例。2. 药物单次剂量为4.4mg至5.8mg/kg,空腹口服,每日3次。总累积剂量在46.4mg/kg至200.0mg/kg之间。给药疗程为3至12天。3. 症状分类如下:急性咽炎9例,急性扁桃体炎5例,急性支气管炎3例,脓疱疮 + 脓性鼻炎、颈淋巴结炎、猩红热及尿路感染各1例。4. 临床有效率为100%,其中显效18例,有效3例。5. 根据17株疑似致病微生物的检测结果,细菌学根除率为90.9%,其中10株被根除,1株菌量减少,6株情况不明。6. 治疗期间及停药后均未出现副作用,不过在临床实验室检查中,有1例谷草转氨酶(GOT)和谷丙转氨酶(GPT)升高,判定为异常。无患者拒绝用药。鉴于CPDX - PR在儿科治疗感染性疾病方面疗效卓越且安全性高,故被认为是一种非常有用的药物。

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