Abstract | OBJECTIVE: METHODS: Analysis of clinical trials submitted to the U.S. Food and Drug Administration (FDA) for approval of PERT that enrolled 123 cystic fibrosis adult and pediatric patients treated with Creon, Pertzye, Ultresa, and Zenpep. RESULTS CONCLUSIONS: The CFA% defines lipase activity as a percentage of converting substrate of "Total Daily Dietary Fat Intake." PERT trials performed to date have modified the definition to converting the "Shared Daily Fat Intake," generating "Partial CFA" for the exogenous lipase: the higher the activity of coexisting endogenous lipase, the lower the "Partial CFA" of exogenous measured. This review shows that "Partial CFA" is not CFA. Enrollment of patients with low HPLA during treatment may improve the interpretability of "Partial CFA" measured by PERT trials.
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Authors | Wen-Yi Gao, Andrew E Mulberg |
Journal | Pancreas
(Pancreas)
Vol. 43
Issue 8
Pg. 1232-8
(Nov 2014)
ISSN: 1536-4828 [Electronic] United States |
PMID | 25102439
(Publication Type: Journal Article, Review)
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Chemical References |
- Dietary Fats
- Lipids
- Pancrelipase
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Topics |
- Adolescent
- Adult
- Child
- Child, Preschool
- Clinical Trials as Topic
(statistics & numerical data)
- Cystic Fibrosis
(complications)
- Dietary Fats
(pharmacokinetics)
- Drug Hypersensitivity
(etiology)
- Drug Monitoring
- Enzyme Replacement Therapy
(adverse effects)
- Exocrine Pancreatic Insufficiency
(drug therapy, genetics, metabolism)
- Feces
(chemistry)
- Gastrointestinal Diseases
(chemically induced)
- Humans
- Intestinal Absorption
(drug effects)
- Lipids
(analysis)
- Middle Aged
- Pancrelipase
(adverse effects, therapeutic use)
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