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Vitamin A supplementation for cystic fibrosis (Review)

O'Neil, Catherine M., Shevill, Elizabeth and Chang, Anne B. (2008). Vitamin A supplementation for cystic fibrosis (Review)<br />. Cochrane Database of Systematic Reviews,2008(1 - Article No. CD006751).

Document type: Journal Article
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Title Vitamin A supplementation for cystic fibrosis (Review)
Author O'Neil, Catherine M.
Shevill, Elizabeth
Chang, Anne B.
Journal Name Cochrane Database of Systematic Reviews
Publication Date 2008
Volume Number 2008
Issue Number 1 - Article No. CD006751
ISSN 1469-493X   (check CDU catalogue  open catalogue search in new window)
Total Pages 12
Place of Publication United Kingdom
Publisher John Wiley & Sons Ltd.
Field of Research 1115 - Pharmacology and Pharmaceutical Sciences
HERDC Category C1 - Journal Article (DEST)
Abstract Background
People with cystic fibrosis and pancreatic insufficiency are at risk of fat soluble vitamin deficiency as these vitamins (A, D, E and K) are co-absorbed with fat. Thus, some cystic fibrosis centres routinely administer these vitamins as supplements but the centres vary in their approach of addressing the possible development of deficiencies in these vitamins. Vitamin A deficiency causes predominantly eye and skin problems while supplementation of vitamin A to excessive levels may cause harm to the respiratory and skeletal systems in children. Thus a systematic review on vitamin A supplementation in people with cystic fibrosis would help guide clinical practice.

Objectives

To determine if vitamin A supplementation in children and adults with CF:
1. reduces the frequency of vitamin A deficiency disorders;
2. improves general and respiratory health;
3. increases the frequency of vitamin A toxicity.

Search methods

We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Trials Register which comprises of references identified from comprehensive electronic database searches and handsearches of relevant journals and abstract books of conference proceedings.
Date of the most recent search of the Group's Cystic Fibrosis Trials Register: 26 November 2009.

Selection criteria

All randomised or quasi-randomised controlled trials comparing all preparations of oral vitamin A used as a supplement compared to either no supplementation (or placebo) at any dose and for any duration, in children or adults with cystic fibrosis (defined by sweat tests or genetic testing) with and without pancreatic insufficiency.

Data collection and analysis

No relevant studies for inclusion were identified in the search.

Main results

No studies were included in this review.

Authors' conclusions

As there were no randomised or quasi-randomised controlled trials identified, we cannot draw any conclusions on the benefits (or otherwise) of regular administration of vitamin A in people with cystic fibrosis. Until further data are available, country or region specific guidelines on the use of vitamin A in people with cystic fibrosis should be followed.
DOI http://dx.doi.org/10.1002/14651858.CD006751.pub2   (check subscription with CDU E-Gateway service for CDU Staff and Students  check subscription with CDU E-Gateway in new window)


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