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Clinical Laboratory Tests to Assess Fetal and Neonatal Status
Live Event: Wednesday, April 15, 2020
PACE®
Credit available until October 15, 2020 | Florida Lab
Credit available |
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The neonatal period is the most
vulnerable time for a child. If the child is born prematurely,
there are additional risks during the neonatal period. In the
United States, about 380,000 babies are born prematurely (before
37 weeks) each year. The preterm birth rate is 9.8%, meaning 1
in 10 babies is born too soon1.
The accurate and timely identification of clinical parameters
related to rupture of membranes (ROM), intrapartum fetal health
as well as neonatal health is paramount to reduce neonatal
morbidity and mortality.
• Rupture of membranes and its associated complications
are leading causes of neonatal morbidity and mortality.
• Fetal scalp lactate measurement has been used as an
adjunct to electronic fetal monitoring to assess fetal
well-being intrapartum.
• Although there is ongoing debate regarding the
relationship between neonatal hypoglycemia and negative
neurodevelopmental outcomes, the measurement and interpretation
of time-dependent blood glucose levels are embedded into
standard clinical practice to assess neonatal health.
The overall goal of this webinar is to review the performance of
selective clinical laboratory tests to assess the risk of
preterm delivery, intrapartum fetal as well as neonatal health.
References:
1
“Fighting premature birth: the prematurity campaign.” March of
Dimes. Accessed March 10, 2020.
https://www.marchofdimes.org/mission/prematurity-campaign.aspx
This session will:
- Discuss the clinical utility of, placental alpha
microglobulin-1 and insulin like growth factor
binding protein-1 to detect premature rupture of
membranes
- Describe the clinical utility of measuring fetal
scalp lactate to detect intrapartum hypoxia and
describe the impact of analytical error in lactate
measurement on the misclassification of patients
- Examine the clinical utility of measuring
glucose to detect neonatal hypoglycemia and to
describe the impact of analytical error on the
misclassification of patients.
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Presenter:
Martha Lyon, PhD
Clinical Biochemist, Royal University Hospital
Saskatoon, Saskatchewan, Canada
Dr. Martha Lyon is a clinical biochemist at Royal University
Hospital in Saskatoon, Saskatchewan, Canada. Her primary
clinical duties encompass Pediatric and Neonatal Clinical
Biochemistry and Point of Care Testing. She has also served on
provincial and international committees related to Pediatrics
and Point of Care Testing.
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Whitehat Communications is approved as a provider of continuing
education programs in the clinical laboratory sciences by the
ASCLS P.A.C.E.® Program. |
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Additional Educational
Resources Sponsored by Qiagen |
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Qiagen's commitment to
education extends to our sponsorship of the long-running point of care
group webinars, which are produced by Whitehat Communications and free
to the point of care and laboratory community. You can register for the
2020 sessions a by visiting: 2020 Point of Care Group Webinars
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Communications, a division of Martek Inc. |
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