Takase Z, Kohmoto Y, Shirafuji H, Shimizu T, Ishikawa M, Sakuraba M, Ichinohe K, Sugahara S, Hayashi H, Cho N
Jpn J Antibiot. 1984 Jun;37(6):991-1005.
Fundamental and clinical studies on latamoxef (LMOX) in the perinatal period were carried out, and following results were obtained. Concentration of LMOX was showed high peak levels in maternal serum, umbilical serum and amniotic fluid. LMOX seemed to be a very transferable compound to human tissues. LMOX was administered to 28 cases of various perinatal infections. Clinical responses were excellent in 13 cases, good in 15 cases and poor in none. And 140 cases of prophylactic use in the field of perinatal period were evaluated in good. No side effect was seen and an abnormal laboratory finding, the increase of GPT, was observed in only 1 case. LMOX was a highly useful antibiotic in perinatal infections, the safe dose range of LMOX into the perinatal mothers was estimated to be 2 g/day, with the maximum safe dose being 4 g/day.
开展了拉氧头孢(LMOX)围生期的基础及临床研究,获得以下结果。LMOX在母血、脐血和羊水中显示出高的峰值水平。LMOX似乎是一种极易转移至人体组织的化合物。对28例各种围生期感染患者给予LMOX治疗。临床反应13例为优,15例为良,无不良反应差的病例。对围生期领域140例预防性使用情况评估为良好。未观察到副作用,仅1例出现实验室异常发现,即谷丙转氨酶升高。LMOX是围生期感染中非常有用的抗生素,围生期母亲使用LMOX的安全剂量范围估计为2g/天,最大安全剂量为4g/天。