1997
DOI: 10.1097/00006254-199708000-00004
|View full text |Cite
|
Sign up to set email alerts
|

Evaluation of Chemical Tests for Fetal Bleeding From Vasa Previa

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
7
0

Year Published

2006
2006
2015
2015

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 6 publications
(7 citation statements)
references
References 0 publications
0
7
0
Order By: Relevance
“…In the absence of prenatal diagnosis, a clinical diagnosis of vasa previa should be suspected in the setting of vaginal bleeding that occurs upon rupture of the membranes and is accompanied with fetal heart rate abnormalities, particularly a sinusoidal pattern or bradycardia [14,15,28].…”
Section: Introductionmentioning
confidence: 99%
“…In the absence of prenatal diagnosis, a clinical diagnosis of vasa previa should be suspected in the setting of vaginal bleeding that occurs upon rupture of the membranes and is accompanied with fetal heart rate abnormalities, particularly a sinusoidal pattern or bradycardia [14,15,28].…”
Section: Introductionmentioning
confidence: 99%
“…In order to exclude or confirm fetal bleeding, various tests are available for detection of fetal hemoglobin, such as alkali denaturation tests (Apt, Ogita, Loendersloot), hemoglobin electrophoresis, and the Kleihauer-Betke test [30]. The Kleihauer-Betke test and hemoglobin electrophoresis are both reliable and sensitive, i.e., they are able to identify the presence of HbF in concentrations down to a minimum of 0.01%.…”
Section: Intrapartum Diagnosis and Confirmation Of Hbfmentioning
confidence: 99%
“…The alkali denaturation tests (Ogita, Apt) are based on the principle that HbF is resistant to denaturation by alkali, unlike adult haemoglobin (HbA). These tests are reliable and fast but rather insensitive (Ogita needs 20% HbF, Apt 60%) and too complicated to perform routinely, certainly in an emergency situation [4]. Recently, a group from Sweden developed an 'easier-to-use' variation to detect HbF.…”
Section: Diagnosismentioning
confidence: 99%