Newborn screening for cystic fibrosis

被引:12
作者
Parad, RB
Comeau, AM
机构
[1] Univ Massachusetts, Sch Med, Massachusetts Cyst Fibrosis Newborn Screening, Amherst, MA 01003 USA
[2] Harvard Univ, Brigham & Womens Hosp, Dept Pediat, Boston, MA 02115 USA
[3] Childrens Hosp, Boston, MA 02115 USA
[4] Univ Massachusetts, New England Newborn Screening Program, Sch Med, Amherst, MA 01003 USA
[5] Univ Massachusetts, Dept Pediat, Sch Med, Amherst, MA 01003 USA
来源
PEDIATRIC ANNALS | 2003年 / 32卷 / 08期
关键词
D O I
10.3928/0090-4481-20030801-10
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
CF newborn screening benefits growth and prevents malnutrition in children with CF. Increasing evidence suggests long-term pulmonary benefits, but these data are still accumulating. With a standardized approach to clinical care for these pre-symptomatic patients, we should be able to ask questions about the optimal treatment strategy for therapies that are currently available, perhaps through randomized clinical trials in this group. For developing therapies, Massachusetts will have identified its CF patients before they have sustained significant malnutrition and lung injury, and it may be these patients who will benefit most from therapies still on the horizon.
引用
收藏
页码:528 / 535
页数:8
相关论文
共 45 条
[1]   ROLE OF RESPIRATORY SYNCYTIAL VIRUS IN EARLY HOSPITALIZATIONS FOR RESPIRATORY-DISTRESS OF YOUNG INFANTS WITH CYSTIC-FIBROSIS [J].
ABMAN, SH ;
OGLE, JW ;
BUTLERSIMON, N ;
RUMACK, CM ;
ACCURSO, FJ .
JOURNAL OF PEDIATRICS, 1988, 113 (05) :826-830
[2]   EARLY BACTERIOLOGICAL, IMMUNOLOGICAL, AND CLINICAL COURSES OF YOUNG INFANTS WITH CYSTIC-FIBROSIS IDENTIFIED BY NEONATAL SCREENING [J].
ABMAN, SH ;
OGLE, JW ;
HARBECK, RJ ;
BUTLERSIMON, N ;
HAMMOND, KB ;
ACCURSO, FJ .
JOURNAL OF PEDIATRICS, 1991, 119 (02) :211-217
[3]  
ALJADER LN, 1991, ADV EXP MED BIOL, V290, P347
[4]  
ALJADER LN, 1990, CLIN GENET, V38, P460
[5]   Epidemiology and survival analysis of cystic fibrosis in an area of intense neonatal screening over 30 years [J].
Assael, BM ;
Castellani, C ;
Ocampo, MB ;
Iansa, P ;
Callegaro, A ;
Valsecchi, MG .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 2002, 156 (05) :397-401
[6]   EFFECTS OF NEWBORN SCREENING OF CYSTIC-FIBROSIS ON REPORTED MATERNAL-BEHAVIOR [J].
BOLAND, C ;
THOMPSON, NL .
ARCHIVES OF DISEASE IN CHILDHOOD, 1990, 65 (11) :1240-1244
[7]   NEONATAL SCREENING FOR CYSTIC-FIBROSIS [J].
BOWLING, F ;
CLEGHORN, G ;
CHESTER, A ;
CURRAN, J ;
GRIFFIN, B ;
PRADO, J ;
FRANCIS, P ;
SHEPHERD, R .
ARCHIVES OF DISEASE IN CHILDHOOD, 1988, 63 (02) :196-198
[8]   PANCREATIC INSUFFICIENCY, GROWTH, AND NUTRITION IN INFANTS IDENTIFIED BY NEWBORN SCREENING AS HAVING CYSTIC-FIBROSIS [J].
BRONSTEIN, MN ;
SOKOL, RJ ;
ABMAN, SH ;
CHATFIELD, BA ;
HAMMOND, KB ;
HAMBIDGE, KM ;
STALL, CD ;
ACCURSO, FJ .
JOURNAL OF PEDIATRICS, 1992, 120 (04) :533-540
[9]   CFTR mutations and IVS8-5T variant in newborns with hypertrypsinaemia and normal sweat test [J].
Castellani, C ;
Bonizzato, A ;
Mastella, G .
JOURNAL OF MEDICAL GENETICS, 1997, 34 (04) :297-301
[10]   Protracted neonatal hypertrypsinogenaemia, normal sweat chloride, and cystic fibrosis [J].
Castellani, C ;
Tamanini, A ;
Mastella, G .
ARCHIVES OF DISEASE IN CHILDHOOD, 2000, 82 (06) :481-482