Magnetic Resonance Imaging as a Decision-Making Tool in Congenital Heart Disease Surgery

Yoo, Shi Joon; Rito, Mauro Lo; Seed, Mike; Grosse-Wortmann, Lars

doi:10.1053/j.optechstcvs.2014.06.002

Cited by 6 publications

(3 citation statements)

References 23 publications

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“…left ventricle and aorta). Regarding the use of colours, patients suggested that using multiple colours might be helpful for highlighting different structures and the defect(s) being discussed, which would be feasible from a technical point of view (Yoo et al 2014).…”

Section: Discussionmentioning

confidence: 99%

Involving patients, families and medical staff in the evaluation of 3D printing models of congenital heart disease

Biglino

Capelli

Leaver

et al. 2016

Communication & Medicine

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Section: Discussionmentioning

confidence: 99%

Involving patients, families and medical staff in the evaluation of 3D printing models of congenital heart disease

Biglino

Capelli

Leaver

et al. 2016

Communication & Medicine

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“…(7)(8)(9) The prognosis of situs inversus with levocardia is poor, and only 5%-13% of patients survive for more than five years, mainly due to the severity of an associated cardiac abnormality. (6) It is important for clinicians to be aware of the fact that discordant ABSTRACT Levocardia (left-sided cardiac apex) with abdominal situs inversus is extremely rare.…”

Section: A 5bmentioning

confidence: 99%

Clinics in diagnostic imaging (160)

Abdullah¹,

Quek²,

Seto³

et al. 2015

smedj

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A 13-year-old male patient on long-term follow-up for complex congenital heart disease at the paediatric cardiology unit presented with shortness of breath. He was born via elective lower section Caesarian section (LSCS) at 38 weeks due to the mother's two previous LSCSs. He had normal body weight and Apgar scores at birth. He was apparently well until Day 3 of life, where he was found to have a cardiac murmur prior to discharge. Echocardiography then showed complex congenital heart disease with a single ventricle, left-sided major aortopulmonary collaterals and pulmonary atresia. At two months of life, he was admitted for an elective right Blalock-Taussig (BT) shunt. A subsequent left BT shunt was performed at 20 months of age. Chest radiography was performed for the patient (Fig. 1). What does the radiograph show?

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“…MRI has also been used for demonstrating double inlet ventricle (Yoo et al 1999), straddling atrioventricular valve (Fig. 5), tricuspid atresia, and mitral atresia.…”

Section: Atrioventricular Connectionsmentioning

confidence: 99%