Outcome of treatment for congenital toxoplasmosis, 1981-2004: The national collaborative Chicago-based, congenital toxoplasmosis study

被引:194
作者
McLeod, R
Boyer, K
Karrison, T
Kasza, K
Swisher, C
Roizen, N
Jalbrzikowski, J
Remington, J
Heydemann, P
Noble, AG
Mets, M
Holfels, E
Withers, S
Latkany, P
Meier, P
机构
[1] Univ Chicago, Dept Ophthalmol & Visual Sci, Chicago, IL 60637 USA
[2] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Pediat, Chicago, IL 60637 USA
[4] Univ Chicago, Dept Hlth Sci, Chicago, IL 60637 USA
[5] Univ Chicago, Div Infect Dis, Chicago, IL 60637 USA
[6] Univ Chicago, Dept Dev Pediat, Chicago, IL 60637 USA
[7] Rush Univ, Med Ctr, Dept Med, Chicago, IL 60612 USA
[8] Rush Univ, Med Ctr, Div Infect Dis, Chicago, IL 60612 USA
[9] Rush Univ, Med Ctr, Michael Reese Hosp & Med Ctr, Chicago, IL 60612 USA
[10] Rush Univ, Med Ctr, Dept Pediat, Chicago, IL 60612 USA
[11] Rush Univ, Med Ctr, Dept Neurol, Chicago, IL 60612 USA
[12] Rush Univ, Med Ctr, Div Pediat Infect Dis, Chicago, IL 60612 USA
[13] Northwestern Univ, Sch Med, Div Pediat Neurol, Evanston, IL 60208 USA
[14] Northwestern Univ, Sch Med, Dept Ophthalmol, Evanston, IL 60208 USA
[15] Cermak Hlth Serv Cook Cty, Chicago, IL USA
[16] Stanford Univ, Div Infect Dis, Dept Med, Stanford, CA 94305 USA
[17] Palo Alto Med Res Fdn, Palo Alto, CA USA
[18] NYU, Dept Retina Uveitis, New York Eye & Ear Infirm, New York, NY USA
[19] St Lukes Roosevelt Hosp, Dept Ophthalmol, New York, NY 10025 USA
[20] Columbia Univ, Dept Math & Stat, New York, NY USA
关键词
D O I
10.1086/501360
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. 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. Methods. 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. Results. 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 < 0.01 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). Conclusions. 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.
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收藏
页码:1383 / 1394
页数:12
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