McLeod Rima, Boyer Kenneth, Karrison Theodore, Kasza Kristen, Swisher Charles, Roizen Nancy, Jalbrzikowski Jessica, Remington Jack, Heydemann Peter, Noble A Gwendolyn, Mets Marilyn, Holfels Ellen, Withers Shawn, Latkany Paul, Meier Paul
Department of Ophthalmology and Visual Sciences, University of Chicago, Chicago, Illinois 60637, USA.
Clin Infect Dis. 2006 May 15;42(10):1383-94. doi: 10.1086/501360. Epub 2006 Apr 11.
Without treatment, congenital toxoplasmosis has recurrent, recrudescent, adverse outcomes. Long-term follow-up of infants with congenital toxoplasmosis treated throughout their first year of life with pyrimethamine and sulfadiazine has not been reported.
Between 1981 and 2004, one hundred twenty infants (current mean age +/- standard deviation, 10.5 +/- 4.8 years) with congenital toxoplasmosis were treated with 1 of 2 doses of pyrimethamine plus sulfadiazine; therapy was initiated shortly after birth and continued for 12 months. Children who received treatment were evaluated at birth and at predetermined intervals; the focus of the evaluations was on prespecified end points: motor abnormalities, cognitive outcome, vision impairment, formation of new eye lesions, and hearing loss.
Treatment of infants without substantial neurologic disease at birth with pyrimethamine and sulfadiazine for 1 year resulted in normal cognitive, neurologic, and auditory outcomes for all patients. Treatment of infants who had moderate or severe neurologic disease (as defined in this article in the Treatments subsection of Methods) at birth resulted in normal neurologic and/or cognitive outcomes for >72% of the patients, and none had sensorineural hearing loss. Ninety-one percent of children without substantial neurologic disease and 64% of those with moderate or severe neurologic disease at birth did not develop new eye lesions. Almost all of these outcomes are markedly better than outcomes reported for children who were untreated or treated for 1 month in earlier decades (P<.01 to P<.001). Sex and severity of disease were comparable in our 2 treatment groups, and no significant differences in efficacy or toxicity were noted between the 2 treatment groups (P > .05).
Although not all children did well with treatment, the favorable outcomes we noted indicate the importance of diagnosis and treatment of infants with congenital toxoplasmosis.
未经治疗的先天性弓形虫病会出现反复、复发的不良后果。关于在出生后第一年全程接受乙胺嘧啶和磺胺嘧啶治疗的先天性弓形虫病婴儿的长期随访情况尚未见报道。
1981年至2004年间,120名先天性弓形虫病婴儿(当前平均年龄±标准差为10.5±4.8岁)接受了两种剂量的乙胺嘧啶加磺胺嘧啶中的一种治疗;治疗在出生后不久开始,并持续12个月。接受治疗的儿童在出生时及预定的间隔时间接受评估;评估重点为预先设定的终点:运动异常、认知结局、视力损害、新眼病变的形成及听力丧失。
出生时无严重神经疾病的婴儿接受乙胺嘧啶和磺胺嘧啶治疗1年,所有患者的认知、神经和听觉结局均正常。出生时患有中度或重度神经疾病(如本文方法部分治疗小节所定义)的婴儿接受治疗后,超过72%的患者神经和/或认知结局正常,且无一例发生感音神经性听力丧失。出生时无严重神经疾病的儿童中有91%,出生时患有中度或重度神经疾病的儿童中有64%未出现新的眼病变。几乎所有这些结局都明显优于前几十年未治疗或仅治疗1个月的儿童所报告的结局(P<0.01至P<0.001)。我们的两个治疗组在性别和疾病严重程度方面具有可比性,两个治疗组在疗效或毒性方面未发现显著差异(P>0.05)。
虽然并非所有儿童治疗效果都良好,但我们所观察到的良好结局表明了对先天性弓形虫病婴儿进行诊断和治疗的重要性。