Newborn screening involves testing every newborn for harmful or potentially fatal disorders through a simple blood test. The screening tests for congenital and heritable disorders that could cause severe issues if not treated early, such as intellectual disabilities, illness, or death. However, if treated, infants may live normal lives. The screening process involves pricking the baby's heel to collect a blood sample, which is placed on a special card and sent to a screening center where tests are performed. Abnormal results are reported quickly for case management, while normal results are sent to the submitter when all tests are finalized. The overall goal is to identify disorders that require early treatment and intervention to prevent long-term health problems in children.
Newborn screening involves testing every newborn for harmful or potentially fatal disorders through a simple blood test. The screening tests for congenital and heritable disorders that could cause severe issues if not treated early, such as intellectual disabilities, illness, or death. However, if treated, infants may live normal lives. The screening process involves pricking the baby's heel to collect a blood sample, which is placed on a special card and sent to a screening center where tests are performed. Abnormal results are reported quickly for case management, while normal results are sent to the submitter when all tests are finalized. The overall goal is to identify disorders that require early treatment and intervention to prevent long-term health problems in children.
Newborn screening involves testing every newborn for harmful or potentially fatal disorders through a simple blood test. The screening tests for congenital and heritable disorders that could cause severe issues if not treated early, such as intellectual disabilities, illness, or death. However, if treated, infants may live normal lives. The screening process involves pricking the baby's heel to collect a blood sample, which is placed on a special card and sent to a screening center where tests are performed. Abnormal results are reported quickly for case management, while normal results are sent to the submitter when all tests are finalized. The overall goal is to identify disorders that require early treatment and intervention to prevent long-term health problems in children.
Newborn screening involves testing every newborn for harmful or potentially fatal disorders through a simple blood test. The screening tests for congenital and heritable disorders that could cause severe issues if not treated early, such as intellectual disabilities, illness, or death. However, if treated, infants may live normal lives. The screening process involves pricking the baby's heel to collect a blood sample, which is placed on a special card and sent to a screening center where tests are performed. Abnormal results are reported quickly for case management, while normal results are sent to the submitter when all tests are finalized. The overall goal is to identify disorders that require early treatment and intervention to prevent long-term health problems in children.
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NEWBORN SCREENING
WHAT IS NEWBORN SCREENING ?
• Newborn screening is the practice of testing every newborn for certain harmful or potentially fetal disorder that aren’t otherwise apparent birth with a simple blood test, doctors often can tell whether newborns have certain conditions that eventually could cause problems. PURPOSE OF NEWBORN SCREENING • Program to screen for congenital and heritable disorder. • These disorder may cause severe mental retardation, illness or death if not treated early in life. • If treated, infants may live relatively normal lives. • Result in savings in medical costs over time. IF UNTREATED, DISORDER • CAN RESULT IN: • Growth problems • development/emotional problems • Blindness • Retardation • Seizures • Coma, sometimes leading of death RESULT FROM LAB NORMAL SCREEN RESULT • Result are sent to submitter when all test are final.
ABNORMAL SCREEN RESULT
• Result are reported to Case management as soon as available for that order. WHEN NEWBORN SCREENING DONE ? • NBS is ideally done immediately after 24 hours from birth.
HOW NEWBORN SCREENING DONE ?
• A few drops of blood are taken from the baby’s heel, bottled on a special absorbent filter card and then sent to NEWBORN SCREENING CENTER (NSC) NEWBORN SCREENING FLOW OF OPERATION • STEP 1: MOTIVATING PARENTS • STEP 2: COLLECTING SAMPLES • STEP 3: HANDLING AND SENDING SAMPLE TO THE LABORATORY • STEP 4: PERFORMING THE TESTS • STEP 5: RELAYING/RELEASING RESULT • STEP 6: RECALLING PATIENTS • STEP 7: MNAGING/REFERRING/MONITORING OF POSITIVE CASES STEP 1