NUTRITIONAL REHABILITATION IN CYSTIC-FIBROSIS - A 5 YEAR FOLLOW-UP-STUDY

被引:67
作者
DALZELL, AM
SHEPHERD, RW
DEAN, B
CLEGHORN, GJ
HOLT, TL
FRANCIS, PJ
机构
[1] UNIV QUEENSLAND,BRISBANE,QLD 4000,AUSTRALIA
[2] ROYAL CHILDRENS HOSP,CHILDRENS NUTR RES CTR,BRISBANE,AUSTRALIA
[3] ROYAL CHILDRENS HOSP,CYST FIBROSIS CLIN,BRISBANE,AUSTRALIA
关键词
CYSTIC FIBROSIS; NUTRITION REHABILITATION; LUNG FUNCTION;
D O I
10.1097/00005176-199208000-00007
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Previously, we reported catch-up weight gain, growth, and improved lung function in a group of malnourished cystic fibrosis (CF) children receiving aggressive nutritional supplementation for 1 year compared with a forced expiratory volume in 1 s (FEV1)-, height-, and sex-matched comparison group receiving standard therapy. To evaluate long-term effects, the clinical progress of both groups has been studied over a 5 year period. The supplemented group (n = 10) received supplements for a median of 1.35 years to achieve nutritional rehabilitation. Compared with the nonsupplemented group (n = 14), the previously supplemented group had lower mortality (2 vs. 4. N.S.) and significantly greater weight and height z scores at 4 and 5 years. The progression of pulmonary function abnormalities as measured by FEV, and forced vital capacity (FVC) slopes was greater at 3 years in the nonsupplemented group (FEV1, p < 0.05) but no significant differences in rates of deterioration of pulmonary function were seen after 5 years in the two groups of survivors. We conclude that intensive nutritional support for 1 year has both short- and long-term effects on nutrition and growth, still evident some years after the cessation of this therapeutic modality. Supplementation for periods of longer than 1 year may produce greater gains and possibly prolong the improvement in pulmonary function observed in the earlier study.
引用
收藏
页码:141 / 145
页数:5
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