Use of fecal elastase-1 to classify pancreatic status in patients with cystic fibrosis

被引:86
|
作者
Borowitz, D [1 ]
Baker, SS [1 ]
Duffy, L [1 ]
Baker, RD [1 ]
Fitzpatrick, L [1 ]
Gyamfi, J [1 ]
Jarembek, K [1 ]
机构
[1] SUNY Buffalo, Womens & Childrens Hosp, Dept Pediat, Div Pediat Pulmonol, Buffalo, NY 14222 USA
来源
JOURNAL OF PEDIATRICS | 2004年 / 145卷 / 03期
关键词
D O I
10.1016/j.jpeds.2004.04.049
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objective To test the hypothesis that some patients with cystic fibrosis (CF) are misclassified as pancreatic insufficient, using fecal elastase-1 (FE-1) to define pancreatic status. Study design Subjects with CF at 33 CF centers filled out questionnaires and submitted a stool specimen that was analyzed for FE-1. Subjects taking pancreatic enzyme supplements (PES) were asked to discontinue them and perform a 3-day fecal fat balance study if their FE-1 was >200 mug/g stool and they had never had panereatitis. Results The median value for FE-1 in 1215 subjects was 0 mug/g stool (range, 0-867). There was a significant difference between patients who had been prescribed PES (n = 1131) and those who had FE-1 <200 mug/g stool (n = 1074; P < .0001). Sixty-seven subjects met criteria for discontinuation of PES. The mean coefficient of fat absorption for these subjects was 96.1%. Conclusions FE-1 is an accurate, easily obtained screening test to classify pancreatic status in patients with CF. This information is important for prognostication, treatment, and to avoid misclassification in clinical research. Measurement of FE-1 should become a standard of care for patients with CF.
引用
收藏
页码:322 / 326
页数:5
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