What are the 5 newborn screening Program in Philippines?

Newborn screening program in the Philippines currently includes screening of six disorders: Congenital Hypothyroidism (CH), Congenital Adrenal Hyperplasia (CAH), Phenylketonuria (PKU), Galactosemia (GAL), Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency and Maple Syrup Urine Disease (MSUD).

What is newborn screening Philippines?

DESCRIPTION: Newborn screening (NBS) is an essential public health strategy that enables the early detection and management of several congenital disorders, which if left untreated, may lead to mental retardation and/or death.

Is newborn screening mandatory in the Philippines?

– Newborn screening shall be performed after twenty-four (24) hours of life but not later than three (3) days from complete delivery of the newborn. A newborn that must be placed in intensive care in order to ensure survival may be exempted from the 3-day requirement but must be tested by seven (7) days of age.

What is newborn screening Act 2004 under Doh?

Republic Act 9288, otherwise known as the Newborn Screening Act of 2004, illustrates a procedure to detect a genetic and metabolic disorder in newborns that may lead to mental retardation and even death if left untreated. In many countries, newborn screening has been a mechanism that protects babies from health risks.

Is newborn screening covered by PhilHealth?

Newborn Care Package (NCP) is a PhilHealth benefit package for essential health services of the newborn during the first few days of life. It covers essential newborn care, newborn screening and hearing screening tests.

What can be seen in newborn screening?

Newborn screening tests may include:

• Phenylketonuria (PKU). PKU is an inherited disease in which the body cannot metabolize a protein called phenylalanine.
• Congenital hypothyroidism.
• Galactosemia.
• Sickle cell disease.
• Maple syrup urine disease.
• Homocystinuria.
• Biotinidase deficiency.
• Congenital adrenal hyperplasia.

When did newborn screening start in the Philippines?

The Newborn Screening Study Group first introduced newborn screening in the Philippines in 1996.

When is newborn screening done in the Philippines?

The Newborn Screening test is done by collecting a few drops of blood from the baby’s heel. Ideally, newborn screening should be done two days after birth or before discharge from the hospital. The blood sample is placed on a special filter paper card.

How late can newborn be tested?

The blood test is generally performed when a baby is 24 to 48 hours old. This timing is important because certain conditions may go undetected if the blood sample is drawn before 24 hours of age. Newborn screening does not confirm a baby has a condition.

What are the three newborn screening tests?

It includes blood, hearing and heart screening. Your baby can be born with a health condition but may not show any signs of the problem at first. If a health condition is found early with newborn screening, it often can be treated.

How accurate is newborn screening?

The PPVs, however, range from 0.5% to 6.0%. Consequently, on average, there are more than 50 false-positive results for every true-positive result identified through newborn screening in the United States.