Cystic Fibrosis Foundation Evidence-Based Guidelines for Management of Infants with Cystic Fibrosis

被引:302
作者
Borowitz, Drucy [1 ]
Robinson, Karen A. [2 ]
Rosenfeld, Margaret [4 ]
Davis, Stephanie D. [5 ]
Sabadosa, Kathryn A. [6 ]
Spear, Stephanie L. [7 ]
Michel, Suzanne H. [8 ]
Parad, Richard B. [9 ]
White, Terry B. [3 ]
Farrell, Philip M. [10 ]
Marshall, Bruce C. [3 ]
Accurso, Frank J. [11 ]
机构
[1] SUNY Buffalo, Womens & Childrens Hosp Buffalo, Buffalo, NY 14260 USA
[2] Johns Hopkins Sch Med, Baltimore, MD USA
[3] Cyst Fibrosis Fdn, Bethesda, MD 20814 USA
[4] Univ Washington, Seattle, WA 98195 USA
[5] Univ N Carolina, Chapel Hill, NC USA
[6] Dartmouth Coll, Hanover, NH 03755 USA
[7] Cincinnati Childrens Hosp Med Ctr, Cincinnati, OH USA
[8] Childrens Hosp Philadelphia, Philadelphia, PA 19104 USA
[9] Brigham & Womens Hosp, Boston, MA 02115 USA
[10] Univ Wisconsin, Sch Med & Publ Hlth, Madison, WI USA
[11] Childrens Hosp, Denver, CO 80218 USA
关键词
RESPIRATORY SYNCYTIAL VIRUS; PSEUDOMONAS-AERUGINOSA COLONIZATION; PANCREATIC-ENZYME SUPPLEMENTS; INHALED HYPERTONIC SALINE; SOLUBLE VITAMIN STATUS; YOUNG-CHILDREN; LUNG-FUNCTION; PULMONARY-FUNCTION; COMPUTED-TOMOGRAPHY; AIRWAY FUNCTION;
D O I
10.1016/j.jpeds.2009.09.001
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Newborn screening for cystic fibrosis (CF) offers the opportunity for early medical and nutritional intervention that can lead to improved outcomes. Management of the asymptomatic infant diagnosed with CF through newborn screening, prenatal diagnosis, or sibling screening is different from treatment of the symptomatically diagnosed individual. The focus of management is on maintaining health by preventing nutritional and respiratory complications. The CF Foundation convened a committee to develop recommendations based on a systematic review of the evidence and expert opinion. These guidelines encompass monitoring and treatment recommendations for infants diagnosed with CF and are intended to help guide families, primary care providers, and specialty care centers in the care of infants with CF. (J Pediatr 2009; 155:S73-93).
引用
收藏
页码:S73 / S93
页数:21
相关论文
共 150 条
[11]   METABOLIC ALKALOSIS AND SALT DEPLETION IN CYSTIC-FIBROSIS [J].
ARVANITAKIS, SN ;
LOBECK, CC .
JOURNAL OF PEDIATRICS, 1973, 82 (03) :535-536
[12]   PULMONARY-FUNCTION IN INFANTS WITH CYSTIC-FIBROSIS - THE EFFECT OF ANTIBIOTIC-TREATMENT [J].
BEARDSMORE, CS ;
THOMPSON, JR ;
WILLIAMS, A ;
MCARDLE, EK ;
GREGORY, GA ;
WEAVER, LT ;
SIMPSON, H .
ARCHIVES OF DISEASE IN CHILDHOOD, 1994, 71 (02) :133-137
[13]   LUNG-FUNCTION IN INFANTS WITH CYSTIC-FIBROSIS [J].
BEARDSMORE, CS ;
BARYISHAY, E ;
MAAYAN, C ;
YAHAV, Y ;
KATZNELSON, D ;
GODFREY, S .
THORAX, 1988, 43 (07) :545-551
[14]   How useful is fecal pancreatic elastase 1 as a marker of exocrine pancreatic disease? [J].
Beharry, S ;
Ellis, L ;
Corey, M ;
Marcon, M ;
Durie, P .
JOURNAL OF PEDIATRICS, 2002, 141 (01) :84-90
[15]   BT-PABA TEST IN THE DIAGNOSIS OF PANCREATIC EXOCRINE INSUFFICIENCY IN CYSTIC-FIBROSIS - URINARY AND SERUM DETERMINATIONS COMPARED [J].
BELLENTANI, S ;
GRISENDI, A ;
RINALDI, M ;
BERTOLANI, P ;
COSTA, G ;
AGOSTINI, M ;
MASTELLA, G ;
BALLI, F ;
MANENTI, F .
EUROPEAN JOURNAL OF PEDIATRICS, 1984, 143 (02) :145-148
[16]  
Berge Maartje Ten, 2003, J Cyst Fibros, V2, P183, DOI 10.1016/S1569-1993(03)00090-0
[17]   DEVELOPMENT OF FOOD ACCEPTANCE PATTERNS [J].
BIRCH, LL .
DEVELOPMENTAL PSYCHOLOGY, 1990, 26 (04) :515-519
[18]   Recommended Childhood and Adolescent Immunization Schedules-United States, 2009 [J].
Bocchini, Joseph A. ;
Bradley, John S. ;
Brady, Michael T. ;
Bernstein, Henry H. ;
Byington, Carrie L. ;
Dennehy, Penelope H. ;
Fisher, Margaret C. ;
Frenck, Robert W., Jr. ;
Glode, Mary P. ;
Keyserling, Harry L. ;
Kimberlin, David W. ;
Orenstein, Walter A. ;
Rubin, Lorry G. .
PEDIATRICS, 2009, 123 (01) :189-190
[19]   Monitoring growth, body composition, pubertal and bone status [J].
Borowitz, D ;
Baker, RD ;
Stallings, V .
JOURNAL OF PEDIATRIC GASTROENTEROLOGY AND NUTRITION, 2002, 35 (03) :246-259
[20]   Update on the evaluation of pancreatic exocrine status in cystic fibrosis [J].
Borowitz, D .
CURRENT OPINION IN PULMONARY MEDICINE, 2005, 11 (06) :524-527