Screening Test for Neonatal
Screening test is a test conducted on the most vulnerable populations against disease, but they do not have symptoms of the disease. The first examination in neonatal EEG is a screening test and its value in detecting abnormality couldn’t be too predicted. In order to be accepted, a screening test must be sufficiently sensitive to detect all cases of illness and had to be economical. The disease being detected must be a significant health issues and treatments must be available. Therefore, only certain diseases are known fromthe screening test neonatal EEG — in the United Kingdom, the subject of a screening program is a common type of phenylketonuria, congenital hypothyroid, sickle cell disease, and cystic fibrosis.
Midwives responsible for neonatal screening test

Feet must be held downward then gently pressed and released, the blood will flow out. The blood is then collected in a capillary tube or on a sheet of paper “absorber” that was designed for the purpose of this examination, depending on the purpose of the test lab. The procedure is repeated until sufficient blood is obtained. The heel is cleaned, the plaster and the baby were tacked on to his mother in order to feel comfortable. Identification of thoroughly equipped and specimen immediately sent.
The sample is usually necessary because the number of the first specimens were not adequate. It is important for midwives to be wary of anxiety incurred in the elderly due to the need to repeat the test and midwives need to appease these concerns with giving an explanation.
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