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相似文献

1
[Pharmacokinetics and clinical efficacy of flomoxef in neonates].氟氧头孢在新生儿中的药代动力学及临床疗效
Jpn J Antibiot. 1991 Nov;44(11):1228-39.
2
[Flomoxef in neonates and young infants; clinical efficacy, pharmacokinetic evaluation and effect on the intestinal bacterial flora].
Jpn J Antibiot. 1991 Nov;44(11):1216-27.
3
[Pharmacokinetics and clinical studies of flomoxef in the pediatric field].
Jpn J Antibiot. 1987 Aug;40(8):1515-34.
4
[Pharmacokinetics and clinical studies on flomoxef in neonates and premature infants. A study of flomoxef in the perinatal collaboration research group].氟氧头孢在新生儿和早产儿中的药代动力学及临床研究。围产期协作研究组关于氟氧头孢的一项研究
Jpn J Antibiot. 1993 Jul;46(7):518-38.
5
[Laboratory and clinical evaluations of flomoxef sodium in neonates].
Jpn J Antibiot. 1991 Nov;44(11):1265-85.
6
[Pharmacokinetic and clinical studies on flomoxef in neonates and premature infants].氟氧头孢在新生儿及早产儿中的药代动力学与临床研究
Jpn J Antibiot. 1991 Nov;44(11):1240-9.
7
[Pharmacokinetic and clinical evaluations of flomoxef in neonates].氟氧头孢在新生儿中的药代动力学及临床评价
Jpn J Antibiot. 1991 Nov;44(11):1259-64.
8
[Laboratory and clinical studies on flomoxef in neonates and premature infants].氟氧头孢在新生儿及早产儿中的实验室与临床研究
Jpn J Antibiot. 1993 Jul;46(7):547-67.
9
[Studies of flomoxef in neonates].[氟氧头孢在新生儿中的研究]
Jpn J Antibiot. 1991 Nov;44(11):1250-8.
10
[Laboratory and clinical studies of flomoxef in the pediatric field].
Jpn J Antibiot. 1987 Aug;40(8):1426-38.

引用本文的文献

1
Flomoxef for neonates: extending options for treatment of neonatal sepsis caused by ESBL-producing Enterobacterales.氟莫头孢治疗新生儿:为产 ESBL 肠杆菌科导致的新生儿败血症治疗提供更多选择。
J Antimicrob Chemother. 2022 Feb 23;77(3):711-718. doi: 10.1093/jac/dkab468.
2
Potential Antibiotics for the Treatment of Neonatal Sepsis Caused by Multidrug-Resistant Bacteria.用于治疗多重耐药菌引起的新生儿败血症的潜在抗生素
Paediatr Drugs. 2021 Sep;23(5):465-484. doi: 10.1007/s40272-021-00465-z. Epub 2021 Aug 26.

氟氧头孢在新生儿中的药代动力学及临床疗效

[Pharmacokinetics and clinical efficacy of flomoxef in neonates].

作者信息

Azagami S, Isohata E, Takeda S, Kin Y, Oikawa T, Osano M, Shiro H

机构信息

Department of Pediatrics, School of Medicine, Keio University.

出版信息

Jpn J Antibiot. 1991 Nov;44(11):1228-39.

PMID:1784073
Abstract

Clinical pharmacology and efficacy of flomoxef (FMOX) in neonates were investigated. And the following results were obtained. 1. Mean serum concentrations of FMOX at 30 minutes after administration were 24.3 micrograms/ml, 47.6 micrograms/ml, and 85.8 micrograms/ml at doses of 10 mg/kg, 20 mg/kg, and 40 mg/kg administered, respectively. 2. Mean serum half-lives of FMOX were 3.4 hours in 0-3 day-old neonates, and 2.6 hours in 4 day-old or older subjects. 3. A dose response was evident among different dose groups given 10 mg/kg, 20 mg/kg, and 40 mg/kg. 4. Urinary recovery rates of FMOX in the first 6 hours after administration ranged between 12.8 and 51.1%. 5. FMOX was effective in 7 out of 8 cases in which causative pathogens were identified. 6. Diarrhea was observed in 1 case as a side effect of the drug, but the symptom was relieved soon after the completion of the treatment. There was no case in which any abnormal laboratory results were observed. 7. FMOX has a broad spectrum of activities against Gram-positive and Gram-negative aerobes and anaerobes. It is stable against most of beta-lactamases. It was demonstrated to be highly effective in our study, and yet without any serious side effects. FMOX is therefore considered to be one of the useful agents of the first choice for the treatment of bacterial infections such as sepsis and urinary tract infections in neonates and infants.

摘要

研究了氟氧头孢(FMOX)在新生儿中的临床药理学及疗效,结果如下:1. 给药后30分钟,给予10mg/kg、20mg/kg和40mg/kg剂量时,FMOX的平均血清浓度分别为24.3μg/ml、47.6μg/ml和85.8μg/ml。2. FMOX在0至3日龄新生儿中的平均血清半衰期为3.4小时,在4日龄及以上婴儿中为2.6小时。3. 在给予10mg/kg、20mg/kg和40mg/kg的不同剂量组之间,剂量反应明显。4. 给药后前6小时FMOX的尿回收率在12.8%至51.1%之间。5. 在8例鉴定出病原体的病例中,7例使用FMOX有效。6. 观察到1例腹泻为药物副作用,但治疗结束后症状很快缓解。未观察到任何实验室检查结果异常的病例。7. FMOX对革兰氏阳性需氧菌、革兰氏阴性需氧菌和厌氧菌均有广泛的抗菌活性。它对大多数β-内酰胺酶稳定。在我们的研究中已证明其高效且无任何严重副作用。因此,FMOX被认为是治疗新生儿和婴儿败血症及尿路感染等细菌感染的首选有效药物之一。