Neurodevelopmental outcome after intrauterine red cell transfusion for Parvovirus B19-induced fetal hydrops

被引:17
作者
Dembinski, J
Haverkamp, F
Maara, H
Hansmann, M
Eis-Hübinger, AM
Bartmann, P
机构
[1] Univ Bonn, Ctr Pediat, Dept Neonatol, D-53113 Bonn, Germany
[2] Univ Bonn, Div Prenatal Diag & Therapy, D-53113 Bonn, Germany
[3] Univ Bonn, Div Microbiol & Immunol, D-53113 Bonn, Germany
关键词
D O I
10.1046/j.1471-0528.2002.02118.x
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective To assess long term neurodevelopmental outcome of children after intrauterine intravascular red cell transfusion (IUT) for Parvovirus B19-induced fetal hydrops. Design Data of study children were investigated retrospectively. Neurodevelopmental evaluation was performed by appropriate standard tests (Griffiths, Snijders-Oomen, Kaufmann Assessment Battery for Children tests). Setting Tertiary care university teaching hospital. Sample Twenty children who had Parvovirus-induced fetal hydrops and intrauterine transfusion of packed red blood cells (JUT). Methods Retrospective chart analysis and standard neurodevelopmental testing. Main outcome measures Developmental quotient (DQ) and intelligence quotient (IQ) according to the age at testing. Results Twenty survivors of Parvovirus B19-induced fetal hydrops successfully treated by IUT were followed until 13 months to nine years of age. On clinical follow up, no neurologic sequelae were evident. Neurodevelopmental scores of all children ranged within two standard deviations of a normal population (median 101, range 86-116) and exceeded one standard deviation in three children. There was no significant neurodevelopmental delay. Conclusion Children having survived successful IUT for Parvovirus B19-induced fetal anaemia and hydrops have a good neurodevelopmental prognosis. Our results support the use of IUT for correction of Parvovirus B19-induced fetal anaemia and subsequent hydrops.
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页码:1232 / 1234
页数:3
相关论文
共 26 条
  • [1] Brandt I., 1983, GRIFFITHS ENTWICKLUN
  • [2] Haematological consequences of parvovirus B19 infection
    Brown, KE
    [J]. BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2000, 13 (02) : 245 - 259
  • [3] Human parvovirus B19 infection associated with hydrops fetalis
    Cameron, AD
    Swain, S
    Patrick, WJA
    [J]. AUSTRALIAN & NEW ZEALAND JOURNAL OF OBSTETRICS & GYNAECOLOGY, 1997, 37 (03) : 316 - 319
  • [4] Detection of parvovirus B19 infection in first and second trimester fetal loss
    de Krijger, RR
    van Elsacker-Niele, AMW
    Mulder-Stapel, A
    Salimans, MMM
    Dreef, E
    Weiland, HT
    van Krieken, JHJM
    Vermeij-Keers, C
    [J]. PEDIATRIC PATHOLOGY & LABORATORY MEDICINE, 1998, 18 (01): : 23 - 34
  • [5] Dong ZW, 2000, J REPROD MED, V45, P410
  • [6] DOYLE LW, 1993, OBSTET GYNECOL, V81, P931
  • [7] Haematological parameters of parvovirus B19 infection in 13 fetuses with hydrops foetalis
    Forestier, F
    Tissot, JD
    Vial, Y
    Daffos, F
    Hohlfeld, P
    [J]. BRITISH JOURNAL OF HAEMATOLOGY, 1999, 104 (04) : 925 - 927
  • [8] Gilbert G L, 2000, Commun Dis Intell, V24 Suppl, P69
  • [9] HANSMANN M, 1989, Fetal Therapy, V4, P29
  • [10] HANSMANN M, 1985, Archives of Gynecology, V238, P169, DOI 10.1007/BF02429951