Survey of national guidelines for the treatment of phenylketonuria

被引:34
作者
Schweitzer-Krantz, S
Burgard, P
机构
[1] Evangel Krankenhaus Dusseldorf, Childrens Hosp, D-40217 Dusseldorf, Germany
[2] Univ Heidelberg, Dept Gen Paediat, Heidelberg, Germany
关键词
phenylketonuria; dietary treatment; guidelines; recommendations;
D O I
10.1007/PL00014385
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Phenylketonuria treatment policies vary not only between different countries worldwide. but also within one country. Recommendations and guidelines for phenylketonuria should deal with the following subjects: 1. What is the target age to start dietary phenylalanine restriction under newborn-screening conditions? 2. At which plasma phenylalanine concentration should phenylalanine restriction be initiated? 3. Which are the recommended plasma phenylalanine concentrations at different ages? 4. What is the recommended frequency of monitoring phenylalanine in plasma? Statements from the following countries are presented: Czech Republic, Denmark, France, Germany, Great Britain, Hungary, Ireland, Poland, Slovakia and the United States. Conclusion Due to the lack of internationally accepted guidelines, management of phenylketonuria still varies between different countries. Our efforts should focus on the formulation of internationally acceptable and accepted recommendations for the treatment of patients with phenylketonuria at different ages.
引用
收藏
页码:S70 / S73
页数:4
相关论文
共 20 条
[1]   Summary of findings from the United States Collaborative Study of children treated for phenylketonuria [J].
Azen, C ;
Koch, R ;
Friedman, E ;
Wenz, E ;
Fishler, K .
EUROPEAN JOURNAL OF PEDIATRICS, 1996, 155 :S29-S32
[2]   INTELLECTUAL-DEVELOPMENT IN 12-YEAR-OLD CHILDREN TREATED FOR PHENYLKETONURIA [J].
AZEN, CG ;
KOCH, R ;
FRIEDMAN, EG ;
BERLOW, S ;
COLDWELL, J ;
KRAUSE, W ;
MATALON, R ;
MCCABE, E ;
OFLYNN, M ;
PETERSON, R ;
ROUSE, B ;
SCOTT, CR ;
SIGMAN, B ;
VALLE, D ;
WARNER, R .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1991, 145 (01) :35-39
[3]  
Bremer HJ, 1997, MONATSSCHR KINDERH, V145, P961
[4]   Phenylketonuria: Treatment in adolescence and adult life [J].
Brenton, DP ;
Tarn, AC ;
CabreraAbreu, JC ;
Lilburn, M .
EUROPEAN JOURNAL OF PEDIATRICS, 1996, 155 :S93-S96
[5]   Rationale for the German recommendations for phenylalanine level control in phenylketonuria 1997 [J].
Burgard, P ;
Bremer, HJ ;
Bührdel, P ;
Clemens, PC ;
Mönch, E ;
Przyrembel, H ;
Trefz, FK ;
Ullrich, K .
EUROPEAN JOURNAL OF PEDIATRICS, 1999, 158 (01) :46-54
[6]   Intellectual development of the patients of the German Collaborative Study of children treated for phenylketonuria [J].
Burgard, P ;
Schmidt, E ;
Rupp, A ;
Schneider, W ;
Bremer, HJ .
EUROPEAN JOURNAL OF PEDIATRICS, 1996, 155 :S33-S38
[7]  
BURGARD P, 1999, EUR PKU NEWS, V2, P4
[8]   Longitudinal study on early diagnosis and treatment of phenylketonuria in Poland [J].
Cabalska, MB ;
Nowaczewska, I ;
Sendecka, E ;
Zorska, K .
EUROPEAN JOURNAL OF PEDIATRICS, 1996, 155 :S53-S55
[9]   Long-term follow-up of patients treated for phenylketonuria (PKU) - Results from the Prague PKU Center [J].
Cechak, P ;
Hejcmanova, L ;
Rupp, A .
EUROPEAN JOURNAL OF PEDIATRICS, 1996, 155 :S59-S63
[10]  
COCKBURN F, 1993, BRIT MED J, V306, P115