Pediatric Provider Insight Into Newborn Screening for Glucose-6-Phosphate Dehydrogenase Deficiency.

Abstract:

OBJECTIVE:Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a major contributor to neonatal hyperbilirubinemia, yet newborn screening for this disorder in the United States is not standard practice. We surveyed pediatric providers regarding a novel newborn G6PD screening program successfully implemented in 2007 at a US urban women's hospital newborn nursery. STUDY DESIGN:An electronic survey was distributed to 472 pediatric providers addressing extent to which they were influenced by the screening program. RESULTS:Ninety-two (20%) providers responded, of whom 74 (80%) had taken care of G6PD-deficient patients diagnosed by the screening program. A majority found the diagnosis helpful for patient management and influential in their management. Most common changes in management included more counseling on jaundice and follow-up and avoidance of hemolytic crisis triggers. CONCLUSIONS:General pediatric providers support newborn G6PD screening and appreciate the current program. Knowing the G6PD deficiency status of newborns informed and influenced pediatric providers' care.

journal_name

Clin Pediatr (Phila)

journal_title

Clinical pediatrics

authors

Bernardo J,Nock M

doi

10.1177/0009922814557786

subject

Has Abstract

pub_date

2015-06-01 00:00:00

pages

575-8

issue

6

eissn

0009-9228

issn

1938-2707

pii

0009922814557786

journal_volume

54

pub_type

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