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无症状先天性梅毒的治疗:苄星青霉素与普鲁卡因青霉素G疗法对比

Treatment of asymptomatic congenital syphilis: benzathine versus procaine penicillin G therapy.

作者信息

Paryani S G, Vaughn A J, Crosby M, Lawrence S

机构信息

Department of Pediatrics, University of Florida Health Science Center, Jacksonville 32209.

出版信息

J Pediatr. 1994 Sep;125(3):471-5. doi: 10.1016/s0022-3476(05)83300-1.

Abstract

We compared the efficacy of two treatment regimens for asymptomatic congenital syphilis. Between June 1989 and July 1991, we prospectively and randomly assigned 169 patients to receive either one dose of benzathine penicillin G or procaine penicillin G for 10 days. There were no significant differences between the treatment groups in regard to birth weight, sex, race, gestational age, Apgar scores, infant or maternal rapid plasma reagin (RPR) titers, fluorescent treponemal IgM antibody, or maternal treatment. Patients were examined at 2 to 3, 6, and 12 months after treatment; treatment failure was defined as clinical signs or persistent laboratory evidence of congenital syphilis. Nine patients were removed from the study during the neonatal period, eight were lost to follow-up, and 152 patients were examined 2 to 3 months or more after treatment. Among these 152 patients, none had clinical evidence of congenital syphilis at follow-up, and all the patients tested at 2 to 3 months after treatment (68 in the benzathine penicillin G group and 61 in the procaine penicillin G group) had at least a fourfold decrease in RPR titers. The RPR became nonreactive in all but three of the infants (two in the procaine penicillin G group and one in the benzathine penicillin G group; all three were 2 to 3 months of age when last tested). We conclude that treatment failure did not occur with either regimen and that there was no significant difference in outcome between the two groups.

摘要

我们比较了两种治疗方案对无症状先天性梅毒的疗效。在1989年6月至1991年7月期间,我们前瞻性地随机分配了169例患者,分别接受一剂苄星青霉素G或普鲁卡因青霉素G治疗10天。治疗组在出生体重、性别、种族、胎龄、阿氏评分、婴儿或母亲快速血浆反应素(RPR)滴度、荧光密螺旋体IgM抗体或母亲治疗方面无显著差异。在治疗后2至3个月、6个月和12个月对患者进行检查;治疗失败定义为先天性梅毒的临床体征或持续的实验室证据。9例患者在新生儿期退出研究,8例失访,152例患者在治疗后2至3个月或更长时间接受检查。在这152例患者中,随访时均无先天性梅毒的临床证据,且所有在治疗后2至3个月接受检测的患者(苄星青霉素G组68例,普鲁卡因青霉素G组61例)RPR滴度至少下降了四倍。除3例婴儿(普鲁卡因青霉素G组2例和苄星青霉素G组1例;最后一次检测时均为2至3个月大)外,所有婴儿的RPR均变为阴性。我们得出结论,两种方案均未出现治疗失败,且两组的治疗结果无显著差异。

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