Retinopathy of prematurity in infants of birth weight >2000g after haemorrhagic shock at birth

被引:17
作者
Jandeck, C [1 ]
Kellner, U [1 ]
Kossel, H [1 ]
Bartsch, M [1 ]
Versmold, HT [1 ]
Foerster, MH [1 ]
机构
[1] FREE UNIV BERLIN,KLINIKUM BENJAMIN FRANKLIN,DEPT PAEDIAT,D-12200 BERLIN,GERMANY
关键词
D O I
10.1136/bjo.80.8.728
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Background - The risk of retinopathy of prematurity (ROP) is associated with low birth weight and low,gestational age. For ROP screening examination is recommended in infants weighing less than or equal to 1500 g or of less than 32 weeks' gestational age. Methods - From 1991 ROP screening was performed in 452 premature infants with either a birth weight less than or equal to 1500 g (n=303) or a birth weight >1500 g (n=149) and who required additional oxygen supplementation or underwent surgery with general anaesthesia before estimated term. Results - Unexpectedly, three infants with birth weights between 2080 and 2325 g and a gestational ape of 32 or 33 weeks developed stage 2 or 3 ROP. One of these underwent cryocoagulation, In three infants, preterm birth was induced by sudden placental abruption with severe prenatal blood loss followed by haemorrhagic shock. The umbilical cord packed cell volume was reduced to 0.14-0.19 (normal 0.43-0.63). All three infants underwent surgery with general anaesthesia within the first weeks of life. Of the remaining 449 infants none with a birth weight >1650 g developed any stage of ROP. Conclusion - Severe prenatal blood loss requiring blood transfusions and surgery with general anaesthesia may induce higher stages of ROP even in infants with birth weights exceeding the usual screening criteria.
引用
收藏
页码:728 / 731
页数:4
相关论文
共 47 条
[1]   ISOLATION OF A CANDIDATE GENE FOR NORRIE DISEASE BY POSITIONAL CLONING [J].
BERGER, W ;
MEINDL, A ;
VANDEPOL, TJR ;
CREMERS, FPM ;
ROPERS, HH ;
DOERNER, C ;
MONACO, A ;
BERGEN, AAB ;
LEBO, R ;
WARBURG, M ;
ZERGOLLERN, L ;
LORENZ, B ;
GAL, A ;
BLEEKERWAGEMAKERS, EM ;
MEITINGER, T .
NATURE GENETICS, 1992, 1 (03) :199-203
[2]  
BROCKHURST RJ, 1975, GRAEFES ARCH KLIN EX, V195, P113
[3]   A MUTATION IN THE NORRIE DISEASE GENE (NDP) ASSOCIATED WITH X-LINKED FAMILIAL EXUDATIVE VITREORETINOPATHY [J].
CHEN, ZY ;
BATTINELLI, EM ;
FIELDER, A ;
BUNDEY, S ;
SIMS, K ;
BREAKEFIELD, XO ;
CRAIG, IW .
NATURE GENETICS, 1993, 5 (02) :180-183
[4]   CHARACTERIZATION OF A MUTATION WITHIN THE NDP GENE IN A FAMILY WITH A MANIFESTING FEMALE CARRIER [J].
CHEN, ZY ;
BATTINELLI, EM ;
WOODRUFF, G ;
YOUNG, I ;
BREAKEFIELD, XO ;
CRAIG, IW .
HUMAN MOLECULAR GENETICS, 1993, 2 (10) :1727-1729
[5]   THE APPARENT ROLE OF BLOOD-TRANSFUSIONS IN THE DEVELOPMENT OF RETINOPATHY OF PREMATURITY [J].
COOKE, RWI ;
CLARK, D ;
HICKEYDWYER, M ;
WEINDLING, AM .
EUROPEAN JOURNAL OF PEDIATRICS, 1993, 152 (10) :833-836
[6]   FAMILIAL EXUDATIVE VITREORETINOPATHY [J].
CRISWICK, VG ;
SCHEPENS, CL .
AMERICAN JOURNAL OF OPHTHALMOLOGY, 1969, 68 (04) :578-&
[7]   NATURAL-HISTORY OF RETINOPATHY OF PREMATURITY - A PROSPECTIVE-STUDY [J].
FIELDER, AR ;
SHAW, DE ;
ROBINSON, J ;
NG, YK .
EYE, 1992, 6 :233-242
[8]   SCREENING FOR RETINOPATHY OF PREMATURITY [J].
FIELDER, AR ;
LEVENE, MI .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 1992, 67 (07) :860-867
[9]  
FLYNN JT, 1987, PEDIATR CLIN N AM, V34, P1487
[10]   MISSENSE MUTATION (ARG121TRP) IN THE NORRIE DISEASE GENE ASSOCIATED WITH X-LINKED EXUDATIVE VITREORETINOPATHY [J].
FUCHS, S ;
KELLNER, U ;
WEDEMANN, H ;
GAL, A .
HUMAN MUTATION, 1995, 6 (03) :257-259