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This article discusses the experience of the Iowa Newborn Screening Program (INSP) in screening for hemoglobinopathies, particularly sickle cell disease and non-sickling hemoglobinopathies, over the past two decades. It highlights the increasing prevalence of these conditions due to changing migration patterns, the importance of newborn screening for healthcare equity, and the necessity for newborn screening programs to adapt to meet the healthcare needs of diverse populations.
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How to fill out iowa newborn screening program

01
Obtain the Iowa newborn screening collection form from the hospital or healthcare provider.
02
Ensure that the infant is at least 24 hours old before collecting the sample.
03
Use a heel lance to obtain a few drops of blood from the baby's heel.
04
Apply the blood spots onto the designated areas of the screening card following the provided guidelines.
05
Allow the blood spots to dry completely before handling the card.
06
Fill out the infant's demographic information on the form, including name, date of birth, and mother's details.
07
Send the completed screening card to the Iowa State Hygienic Laboratory as per the instructions provided.

Who needs iowa newborn screening program?

01
All newborns in Iowa are required to undergo the newborn screening program to detect certain genetic, metabolic, and endocrine disorders.
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The Iowa Newborn Screening Program is a public health initiative designed to screen newborns for various genetic, metabolic, and endocrine disorders that can affect their health and development.
All birthing hospitals and healthcare providers in Iowa are required to participate in the Iowa Newborn Screening Program by submitting blood samples and relevant information for every newborn.
To fill out the Iowa Newborn Screening Program, healthcare providers must complete a specific form that collects information about the newborn and the mother, ensuring accurate identification and follow-up for screening results.
The purpose of the Iowa Newborn Screening Program is to identify newborns at risk for serious health conditions, allowing for early intervention and treatment to improve health outcomes.
The information that must be reported includes the newborn's name, date of birth, mother's name, and medical record number, along with the results of the screening tests conducted.
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