Fetal MRI in experimental tracheal occlusion.

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Fetal MRI in experimental tracheal occlusion. / Wedegärtner, Ulrike; Schröder, Prof. Dr.; Adam, Gerhard.

In: EUR J RADIOL, Vol. 57, No. 2, 2, 2006, p. 271-277.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Wedegärtner, U, Schröder, PD & Adam, G 2006, 'Fetal MRI in experimental tracheal occlusion.', EUR J RADIOL, vol. 57, no. 2, 2, pp. 271-277. <http://www.ncbi.nlm.nih.gov/pubmed/16406439?dopt=Citation>

APA

Wedegärtner, U., Schröder, P. D., & Adam, G. (2006). Fetal MRI in experimental tracheal occlusion. EUR J RADIOL, 57(2), 271-277. [2]. http://www.ncbi.nlm.nih.gov/pubmed/16406439?dopt=Citation

Vancouver

Wedegärtner U, Schröder PD, Adam G. Fetal MRI in experimental tracheal occlusion. EUR J RADIOL. 2006;57(2):271-277. 2.

Bibtex

@article{80def5f01a0744dbb2e7eca9a6240ad5,
title = "Fetal MRI in experimental tracheal occlusion.",
abstract = "Congenital diaphragmatic hernia (CDH) is associated with a high mortality, which is mainly due to pulmonary hypoplasia and secondary pulmonary hypertension. In severely affected fetuses, tracheal occlusion (TO) is performed prenatally to reverse pulmonary hypoplasia, because TO leads to accelerated lung growth. Prenatal imaging is important to identify fetuses with pulmonary hypoplasia, to diagnose high-risk fetuses who would benefit from TO, and to monitor the effect of TO after surgery. In fetal imaging, ultrasound (US) is the method of choice, because it is widely available, less expensive, and less time-consuming to perform than magnetic resonance imaging (MRI). However, there are some limitations for US in the evaluation of CDH fetuses. In those cases, MRI is helpful because of a better tissue contrast between liver and lung, which enables evaluation of liver herniation for the diagnosis of a high-risk fetus. MRI provides the ability to determine absolute lung volumes to detect lung hypoplasia. In fetal sheep with normal and hyperplastic lungs after TO, lung growth was assessed on the basis of cross-sectional US measurements, after initial lung volume determination by MRI. To monitor fetal lung growth after prenatal TO, both MRI and US seem to be useful methods.",
author = "Ulrike Wedeg{\"a}rtner and Schr{\"o}der, {Prof. Dr.} and Gerhard Adam",
year = "2006",
language = "Deutsch",
volume = "57",
pages = "271--277",
journal = "EUR J RADIOL",
issn = "0720-048X",
publisher = "Elsevier",
number = "2",

}

RIS

TY - JOUR

T1 - Fetal MRI in experimental tracheal occlusion.

AU - Wedegärtner, Ulrike

AU - Schröder, Prof. Dr.

AU - Adam, Gerhard

PY - 2006

Y1 - 2006

N2 - Congenital diaphragmatic hernia (CDH) is associated with a high mortality, which is mainly due to pulmonary hypoplasia and secondary pulmonary hypertension. In severely affected fetuses, tracheal occlusion (TO) is performed prenatally to reverse pulmonary hypoplasia, because TO leads to accelerated lung growth. Prenatal imaging is important to identify fetuses with pulmonary hypoplasia, to diagnose high-risk fetuses who would benefit from TO, and to monitor the effect of TO after surgery. In fetal imaging, ultrasound (US) is the method of choice, because it is widely available, less expensive, and less time-consuming to perform than magnetic resonance imaging (MRI). However, there are some limitations for US in the evaluation of CDH fetuses. In those cases, MRI is helpful because of a better tissue contrast between liver and lung, which enables evaluation of liver herniation for the diagnosis of a high-risk fetus. MRI provides the ability to determine absolute lung volumes to detect lung hypoplasia. In fetal sheep with normal and hyperplastic lungs after TO, lung growth was assessed on the basis of cross-sectional US measurements, after initial lung volume determination by MRI. To monitor fetal lung growth after prenatal TO, both MRI and US seem to be useful methods.

AB - Congenital diaphragmatic hernia (CDH) is associated with a high mortality, which is mainly due to pulmonary hypoplasia and secondary pulmonary hypertension. In severely affected fetuses, tracheal occlusion (TO) is performed prenatally to reverse pulmonary hypoplasia, because TO leads to accelerated lung growth. Prenatal imaging is important to identify fetuses with pulmonary hypoplasia, to diagnose high-risk fetuses who would benefit from TO, and to monitor the effect of TO after surgery. In fetal imaging, ultrasound (US) is the method of choice, because it is widely available, less expensive, and less time-consuming to perform than magnetic resonance imaging (MRI). However, there are some limitations for US in the evaluation of CDH fetuses. In those cases, MRI is helpful because of a better tissue contrast between liver and lung, which enables evaluation of liver herniation for the diagnosis of a high-risk fetus. MRI provides the ability to determine absolute lung volumes to detect lung hypoplasia. In fetal sheep with normal and hyperplastic lungs after TO, lung growth was assessed on the basis of cross-sectional US measurements, after initial lung volume determination by MRI. To monitor fetal lung growth after prenatal TO, both MRI and US seem to be useful methods.

M3 - SCORING: Zeitschriftenaufsatz

VL - 57

SP - 271

EP - 277

JO - EUR J RADIOL

JF - EUR J RADIOL

SN - 0720-048X

IS - 2

M1 - 2

ER -