Glucose-6-phosphate dehydrogenase deficiency screening: Difference between revisions

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==Overview==
==Overview==
G6PD defeciency screening in [[neonates]] is done routinly in some regions with high [[incidence]].


There is insufficient evidence to recommend routine screening for [disease/malignancy].
OR
According to the [guideline name], screening for [disease name] is not recommended.
OR
According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with [condition 1], [condition 2], and [condition 3].
==Screening==
==Screening==
r
*G6PD defeciency screening in neonates is done routinly in some regions with high [[incidence]]. <ref name="pmid19177059">{{cite journal |vauthors=Kaplan M, Hammerman C |title=The need for neonatal glucose-6-phosphate dehydrogenase screening: a global perspective |journal=J Perinatol |volume=29 Suppl 1 |issue= |pages=S46–52 |date=February 2009 |pmid=19177059 |doi=10.1038/jp.2008.216 |url=}}</ref>
 
*Screening test is quantitative laboratory assay for G6PD enzyme activity.
There is insufficient evidence to recommend routine screening for [disease/malignancy].<ref name="pmid19177059">{{cite journal |vauthors=Kaplan M, Hammerman C |title=The need for neonatal glucose-6-phosphate dehydrogenase screening: a global perspective |journal=J Perinatol |volume=29 Suppl 1 |issue= |pages=S46–52 |date=February 2009 |pmid=19177059 |doi=10.1038/jp.2008.216 |url=}}</ref>
*Screening is done before giving [[oxidant]] medication to high risk patients.  
 
*There is insufficient evidence to recommend routine screening for G6PD deficiency.
The question of whether testing for G6PD deficiency should be included in newborn screening programs worldwide has been raised [91]. This screening has not been widely implemented; however, routine newborn screening is done in some populations with a high incidence of G6PD deficiency.
 
OR
 
According to the [guideline name], screening for [disease name] is not recommended.
 
OR
 
According to the [guideline name], screening for [disease name] by [test 1] is recommended every [duration] among patients with:
*[Condition 1]
*[Condition 2]
*[Condition 3]


==References==
==References==
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{{Glucose-6-phosphate dehydrogenase deficiency}}
{{CMG}}; '''Associate Editor(s)-In-Chief:''' [[Priyamvada Singh|Priyamvada Singh, M.D.]] [mailto:psingh13579@gmail.com]
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==Overview==
==References==
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Latest revision as of 18:41, 25 October 2018

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mahda Alihashemi M.D. [2]

Overview

G6PD defeciency screening in neonates is done routinly in some regions with high incidence.

Screening

  • G6PD defeciency screening in neonates is done routinly in some regions with high incidence. [1]
  • Screening test is quantitative laboratory assay for G6PD enzyme activity.
  • Screening is done before giving oxidant medication to high risk patients.
  • There is insufficient evidence to recommend routine screening for G6PD deficiency.

References

  1. Kaplan M, Hammerman C (February 2009). "The need for neonatal glucose-6-phosphate dehydrogenase screening: a global perspective". J Perinatol. 29 Suppl 1: S46–52. doi:10.1038/jp.2008.216. PMID 19177059.

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