Results 201 to 210 of about 121,138 (267)
Some of the next articles are maybe not open access.

Fetal double outlet right ventricle without heterotaxy syndrome: Diagnostic spectrum, associated extracardiac pathology and clinical outcomes

Prenatal Diagnosis, 2021
To document the clinical spectrum and outcomes of fetal double outlet right ventricle (DORV) without heterotaxy in a recent diagnostic era.
A. Young   +6 more
semanticscholar   +1 more source

Double-Outlet Right Ventricle [PDF]

open access: possible, 1987
There are eight fundamental types of double-outlet right ventricle based on the ventriculoarterial relationship, deviation of the great artery, and atrioventricular relationship. Combination of the dextroposition of the posterior great artery and levoposition of the anterior great artery provides conotruncal criss-cross.
Hiromi Kurosawa, Anton E. Becker
openaire   +2 more sources

Double-Outlet Right Ventricle [PDF]

open access: possible, 2014
The definition of double-outlet right ventricle (DORV) remains controversial. The consensus is that it is a type of ventriculoarterial connection in which both great vessels arise either or predominantly from the RV. Strictly speaking, the standard is either a semilunar valve that was separated by the cone muscle but is not a fibrous connection or some
Anita Sadeghpour, Azin Alizadehasl
openaire   +3 more sources

Double Outlet Right Ventricle

2018
Double outlet right ventricle (DORV) is a rare malformation that accounts for about 1–3% of all congenital heart disease. The reported incidence ranges from 3 to 14 per 100,000 live births [1]. For historical background, see Table 22.1.
Shi-Joon Yoo, Willem A Helbing
  +8 more sources

Double-Outlet Right Ventricle [PDF]

open access: possible, 1992
Double-outlet ventricle refers to a heterogeneous group of cardiac lesions unified by an abnormal ventriculoarterial connection. This is not a diagnosis made on clinical grounds alone. Rather it is made by contemporary imaging techniques including cross-sectional echocardiography and angiocardiography.
R. M. Freedom, J. F. Smallhorn
openaire   +1 more source

Double outlet right ventricle

2004
Double outlet right ventricle is the 12th most common congenital heart defect (1.5–2.0% of all congenital heart defects). Occurs in 0.03–0.1/1,000 live births. No sex prevalence is reported.
Audrey Smith, Roxane McKay
openaire   +4 more sources

Prenatal diagnosis of double‐outlet right ventricle with tricuspid valve atresia, anomalous pulmonary vein connection, persistent left superior vena cava, and right atrial isomerism

Journal of Clinical Ultrasound, 2020
Double‐outlet right ventricle is a conotruncal cardiac disease in which both the aorta and the pulmonary artery predominantly or completely originate from the right ventricle.
O. Yılmaz, O. Celik
semanticscholar   +1 more source

Successful pregnancy in a patient with double outlet right ventricle

Cardiology in the Young, 2020
Background: The double outlet right ventricle is uncommon and usually makes patients have haemodynamic and structural complications. Having a hyperdynamic state, such as pregnancy, with volume overload is very risky for a patient with complex CHD (CCHD).
Daniel Salame-Waxman   +2 more
semanticscholar   +1 more source

Double-Outlet Right Ventricle

2017
Anesthetizing a patient with double-outlet right ventricle (DORV) requires an understanding of a large spectrum of anatomic and physiologic variants. Caring for these patients may include preparing for a patient with dynamic right ventricular outflow obstruction similar to tetralogy of Fallot (TOF) or preparing for one with unrestricted pulmonary ...
Thomas Rupprecht   +2 more
openaire   +4 more sources

Double Outlet Right Ventricle

1985
Double outlet right ventricle is a rare congenital cardiac malformation that appears to result from lack of conotruncal inversion, failure of leftward conoventricular shift and persistance of a subaortic conus [1, 2]. The anomaly is classified into two categories: those hearts with and those without pulmonary stenosis [3, 4].
Arthur D. Hagan, Thomas G. DiSessa
openaire   +2 more sources

Home - About - Disclaimer - Privacy