Can newborn screening be cost benefit procedure if preventing serious complications of cystic fibrosis?
<p>Cystic Fibrosis (CF) is a common inherited disease with reported mean prevalence of 0.737/10,000 in 27 EU countries (Farrell J Cyst Fibros. 2008). Still, many EU countries have not implemented CF in the Newborn Screening (NBS) programme, including our country. We report the case of a 7-mon...
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| Main Authors: | , , , , , |
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| Format: | Book |
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Archives of Nursing Practice and Care - Peertechz Publications,
2021-12-03.
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| Online Access: | Connect to this object online. |
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| Summary: | <p>Cystic Fibrosis (CF) is a common inherited disease with reported mean prevalence of 0.737/10,000 in 27 EU countries (Farrell J Cyst Fibros. 2008). Still, many EU countries have not implemented CF in the Newborn Screening (NBS) programme, including our country. We report the case of a 7-month-old boy whose presenting signs of CF were life-threatening neurological symptoms caused by severe metabolic alkalosis and hypoelectrolytemia. By presenting this case, we argue hoping to persuade the authorities in any country that the available newborn screening for CF is the cost benefit procedure in preventing life treating consequences with the obvious impact on the long-term prognosis of this chronic disease. </p> |
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| DOI: | 10.17352/2581-4265.000056 |