Motohiro T, Aramaki M, Oda K, Kawakami A, Tanaka K, Koga T, Shimada Y, Tomita S, Koga M, Sakata Y
Department of Pediatrics, School of Medicine, Kurume University.
Jpn J Antibiot. 1988 Oct;41(10):1493-502.
A dry syrup preparation for infants and children of a newly developed 16-membered macrolide antibiotic, rokitamycin, was administered to 5 neonates and low birth weight infants of 6 to 25 days after births at a dose level of 10 mg/kg on an empty stomach then plasma drug levels were determined. The dry syrup preparation was also given to a total of 19 Chlamydia trachomatis infection cases of 7 days to 8 months old neonates, low birth weight infants and infants including 12 cases of pneumonia, 2 cases of conjunctivitis and 5 non-symptomatic carriers at an average daily dose level of 48.1 mg/kg in 2 to 4 doses for an average of 19 days and its clinical effects, bacteriological effectiveness, side effects and effects on laboratory test values were examined. The obtained results are summarized as follows. 1. Because the test subjects were neonates and premature infants, obtainable amounts of blood samples were limited, thus it was not possible to determine time courses of plasma drug levels to reach their peaks. Peak plasma levels, however, were speculated to be similar to those in children. Plasma half-lives of the drug were also not determinable, but they seemed to be somewhat longer than those in children. 2. Clinical efficacies were determinable in the 2 cases of conjunctivitis and 10 of the 12 cases of pneumonia, with excellent or good results in both cases of the former and with excellent or good results in 9 of the 10 determinable cases of the latter. Thus, the overall efficacy rate was high, 91.7%. 3. Bacteriological efficacies were determinable in 18 cases including non-symptomatic carriers. C. trachomatis was eradicated in 16 of the cases with an overall efficacy rate of 88.9%. 4. Diarrhea was observed in 2 cases, which were suspected as side effects of the drug. 5. No abnormalities were observed in the laboratory test results. Judging from the above results, this drug appears to be useful for the treatment of C. trachomatis infections of neonates, low birth weight infants and infants.
给5名出生后6至25天的新生儿和低体重婴儿空腹服用了一种新开发的16元大环内酯类抗生素罗他霉素的婴幼儿干糖浆制剂,剂量为10mg/kg,然后测定血浆药物水平。还对总共19例7天至8个月大的新生儿、低体重婴儿和婴儿的沙眼衣原体感染病例给予了该干糖浆制剂,其中包括12例肺炎、2例结膜炎和5例无症状携带者,平均日剂量为48.1mg/kg,分2至4次给药,平均给药19天,并检查了其临床效果、细菌学疗效、副作用以及对实验室检查值的影响。所得结果总结如下。1. 由于受试对象为新生儿和早产儿,可获取的血样量有限,因此无法确定血浆药物水平达到峰值的时间过程。然而,推测血浆峰值水平与儿童相似。药物的血浆半衰期也无法确定,但似乎比儿童的半衰期略长。2. 在2例结膜炎和12例肺炎中的10例中可确定临床疗效,前者2例均为优或良,后者10例可确定疗效的病例中有9例为优或良。因此,总有效率较高,为91.7%。3. 在包括无症状携带者在内的18例中可确定细菌学疗效。16例沙眼衣原体被根除,总有效率为88.9%。4. 观察到2例腹泻,怀疑是药物的副作用。5. 实验室检查结果未发现异常。从上述结果判断,该药物似乎对治疗新生儿、低体重婴儿和婴儿的沙眼衣原体感染有用。