By Kyle J. Norton
Cystic fibrosis (CF) is a genetic preposition that leads to diseases mostly in the lungs in children and young adults.
According to statistics provided by the Canadian Cystic Fibrosis Foundation, approximately 1 in every 3,600 children born in Canada has CF.
In age perspective,
* 60% of patients are diagnosed in the first year of life, and 90% by 10 years of age.
* Anti-inflammatory medications to protect the lung airways.
On finding a natural compound for the treatment of cystic fibrosis, researchers compared with identical capsules half filled with mini-tablets of a new high lipase preparation in a randomized double-blind crossover study in children with cystic fibrosis.
According to the results from the 18 children completed the study, pancreatic enzyme applied in the high lipase preparation showed fewer gastrointestinal symptoms compared to the low lipase group.
Compared to the baseline, pancreatic enzyme group showed a significant improvement in fat absorption and reduction in fecal fat output.
Fecal energy loss was also improved in the treatment group.
Based on the findings, researchers at the St James’s Hospital wrote, ” (The) half filled capsules of the new high lipase preparation are more effective than the standard preparation and it is likely that filled capsules would allow patients to use fewer than half the number of pancreatic enzyme capsules”.
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Kyle J. Norton (Scholar, Master of Nutrition, All right reserved)
Health article writer and researcher; Over 10.000 articles and research papers have been written and published online, including worldwide health, ezine articles, article base, health blogs, self-growth, best before it’s news, the karate GB daily, etc.,.
Named TOP 50 MEDICAL ESSAYS FOR ARTISTS & AUTHORS TO READ by Disilgold.com Named 50 of the best health Tweeters Canada – Huffington Post
Nominated for shorty award over last 4 years
Some articles have been used as references in medical research, such as international journal Pharma and Bioscience, ISSN 0975-6299.
(1) Gut inflammation in children with cystic fibrosis on high-dose enzyme supplements by Croft NM1, Marshall TG, Ferguson A. (PubMed)
(2) A double blind lipase for lipase comparison of a high lipase and standard pancreatic enzyme preparation in cystic fibrosis by Bowler IM1, Wolfe SP, Owens HM, Sheldon TA, Littlewood JM, Walters MP. (PubMed)