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Division of Family and Community ServicesRHigh Risk Infant Followup (HRI) Program Manual AFForLocal Health Departments and Community Agencies January 1, 2017Table of Contents Purpose of Document A.
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How to fill out high risk infant follow-up

01
Start by gathering all necessary information about the infant's medical history, including any complications or high-risk factors identified during pregnancy or at birth.
02
Use a standardized high risk infant follow-up form or template, if available, to ensure consistency in data collection.
03
Record the infant's demographic details, including name, date of birth, gender, and contact information.
04
Assess the infant's growth parameters, such as weight, height, and head circumference, at regular intervals as recommended by the follow-up protocol.
05
Document any developmental milestones achieved by the infant, including motor skills, language development, and cognitive abilities.
06
Conduct a thorough physical examination, including evaluating the infant's organ systems, sensory functions, and reflexes.
07
Perform any necessary diagnostic tests or screenings based on the specific high-risk conditions associated with the infant.
08
Collaborate with other healthcare professionals involved in the infant's care, including pediatricians, specialists, and early intervention therapists if needed.
09
Provide parents or caregivers with detailed information about the purpose and importance of high risk infant follow-up, as well as any recommended interventions or services.
10
Maintain accurate and up-to-date records of all assessments, interventions, and referrals made during the follow-up process.
11
Regularly review and monitor the infant's progress, adjusting the follow-up plan as necessary to address any emerging needs or concerns.

Who needs high risk infant follow-up?

01
High risk infant follow-up is typically recommended for infants who have experienced complications during pregnancy, childbirth, or the neonatal period.
02
Infants with a low birth weight (less than 2,500 grams) or born prematurely (before 37 weeks gestation) are often considered high risk and may benefit from follow-up.
03
Medical conditions or genetic abnormalities identified in the infant, such as congenital heart defects, chromosomal disorders, or metabolic disorders, may warrant high risk follow-up.
04
Infants exposed to maternal risk factors during pregnancy, such as substance abuse, maternal infections, or inadequate prenatal care, may require closer monitoring.
05
Babies who have spent time in the neonatal intensive care unit (NICU) due to respiratory distress, sepsis, birth asphyxia, or other complications may also need follow-up care.
06
Children born to parents with a history of genetic disorders or a family history of developmental delays or intellectual disabilities should be considered for high risk follow-up.
07
Ultimately, the decision to recommend high risk infant follow-up is made by healthcare professionals based on individualized assessments and evaluation of risk factors.
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High risk infant follow-up is a program designed to monitor and support infants who are at risk for developmental delays or medical complications.
Healthcare providers, hospitals, and clinics are required to file high risk infant follow-up for infants identified as high risk.
High risk infant follow-up forms can be filled out online or submitted via mail, following the guidelines provided by the relevant health department.
The purpose of high risk infant follow-up is to ensure that high risk infants receive appropriate medical care, development monitoring, and support services.
Information such as the infant's medical history, developmental milestones, and any interventions or therapies received must be reported on high risk infant follow-up.
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