Ganciclovir therapy for congenital cytomegalovirus infection in six infants

被引:36
作者
Tanaka-Kitajima, N
Sugaya, N
Futatani, T
Kanegane, H
Suzuki, C
Oshiro, M
Hayakawa, M
Futamura, M
Morishima, T
Kimura, H
机构
[1] Nagoya Univ, Grad Sch Med, Dept Pediat, Showa Ku, Nagoya, Aichi 4668550, Japan
[2] Nagoya Mem Hosp, Dept Pediat, Nagoya, Aichi, Japan
[3] Japanese Red Cross Nagoya, Hosp 1, Dept Pediat, Nagoya, Aichi, Japan
[4] Nagoya Univ Hosp, Matern & Prenatal Care Ctr, Nagoya, Aichi, Japan
[5] Toyama Med & Pharmaceut Univ, Fac Med, Dept Pediat, Toyama, Japan
[6] Cent Hosp, Aichi Prefectural Colony, Dept Neonatol, Aichi, Japan
[7] Okayama Univ, Grad Sch Med & Dent, Dept Pediat, Okayama 7008530, Japan
关键词
congenital cytomegalovirus infection; real time polymerase chain reaction assay; ganciclovir;
D O I
10.1097/01.inf.0000177280.28694.00
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: Congenital cytomegalovirus (CMV) infection is common, and its morbidity rate is high. Ganciclovir (GCV) treatment has been used for congenital CMV infection, but there are few reports on viral loads associated with GCV therapy. Methods: A real-time PCR assay was used to monitor viral load in 6 cases of symptomatic CMV infection that received GCV therapy. Initially GCV was given at a dose of 5-12 mg/kg/d for 2-7 weeks. In 2 cases, additional doses were given as symptoms returned. Results: After GCV administration, active signs of chorioretinitis, thrombocytopenia and anemia disappeared or improved in all cases. During GCV therapy, viral loads decreased while patients improved clinically and increased again when GCV therapy was stopped. Although CMV DNA continued to be detectable for a long period, clinical findings did not always worsen. In 2 cases, an improvement of hearing loss was observed. Conclusion: GCV therapy transiently suppresses the CMV concentrations. Subsequent increases of viral titers do not appear to be correlated with the clinical course or neurologic outcome.
引用
收藏
页码:782 / 785
页数:4
相关论文
共 29 条
[1]   Quantitation of cytomegalovirus: Methodologic aspects and clinical applications [J].
Boeckh, M ;
Boivin, G .
CLINICAL MICROBIOLOGY REVIEWS, 1998, 11 (03) :533-+
[2]   INFECTIOUS-DISEASES SOCIETY OF AMERICA AND CENTERS FOR DISEASE-CONTROL - SUMMARY OF A WORKSHOP ON SURVEILLANCE FOR CONGENITAL CYTOMEGALOVIRUS DISEASE [J].
DEMMLER, GJ .
REVIEWS OF INFECTIOUS DISEASES, 1991, 13 (02) :315-329
[3]   GANCICLOVIR - A REVIEW OF PHARMACOLOGY, THERAPEUTIC EFFICACY AND POTENTIAL USE FOR TREATMENT OF CONGENITAL CYTOMEGALO-VIRUS INFECTIONS [J].
FANHAVARD, P ;
NAHATA, MC ;
BRADY, MT .
JOURNAL OF CLINICAL PHARMACY AND THERAPEUTICS, 1989, 14 (05) :329-340
[4]   Newborn hearing screening: Will children with hearing loss caused by congenital cytomegalovirus infection be missed? [J].
Fowler, KB ;
Dahle, AJ ;
Boppana, SB ;
Pass, RF .
JOURNAL OF PEDIATRICS, 1999, 135 (01) :60-64
[5]   THE OUTCOME OF CONGENITAL CYTOMEGALOVIRUS-INFECTION IN RELATION TO MATERNAL ANTIBODY STATUS [J].
FOWLER, KB ;
STAGNO, S ;
PASS, RF ;
BRITT, WJ ;
BOLL, TJ ;
ALFORD, CA .
NEW ENGLAND JOURNAL OF MEDICINE, 1992, 326 (10) :663-667
[6]  
Halwachs-Baumann G, 2002, J CLIN VIROL, V25, pS81
[7]   Flow cytometric analysis of cytomegalovirus-specific cell-mediated immunity in the congenital infection [J].
Hayashi, N ;
Kimura, H ;
Morishima, T ;
Tanaka, N ;
Tsurumi, T ;
Kuzushima, K .
JOURNAL OF MEDICAL VIROLOGY, 2003, 71 (02) :251-258
[8]  
Hebart H, 1996, BONE MARROW TRANSPL, V17, P861
[9]   Effect of ganciclovir therapy on hearing in symptomatic congenital cytomegalovirus disease involving the central nervous system:: A randomized, controlled trial [J].
Kimberlin, DW ;
Lin, CY ;
Sánchez, PJ ;
Demmler, GJ ;
Dankner, W ;
Shelton, M ;
Jacobs, RF ;
Vaudry, W ;
Pass, RF ;
Kiell, JM ;
Soong, SJ ;
Whitley, RJ .
JOURNAL OF PEDIATRICS, 2003, 143 (01) :16-25
[10]   Treatment of children with congenital cytomegalovirus infection with ganciclovir [J].
Michaels, MG ;
Greenberg, DP ;
Sabo, DL ;
Wald, ER .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2003, 22 (06) :504-508