Transcatheter closure of secundum atrial septal defect in a patient with dextrocardia using the Amplatzer septal occluder

Hakim, Fakhri; Madani, Awni; Samara, Yousef; Ata, Ibrahim Abu; Hiari, Aktham; Goussous, Yousef; Hijazi, Ziyad M.

doi:10.1002/(sici)1097-0304(199803)43:3<291::aid-ccd10>3.0.co;2-p

Cited by 7 publications

(2 citation statements)

References 10 publications

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“…Only a few cases have been reported of interventional closure of secundum ASD associated with situs inversus and dextrocardia. [2][3][4] Percutaneous device closure of multiple ASD associated with situs inversus and dextrocardia has also been reported. 4 In addition, device closure of a secundum ASD has been reported in a case of dextrocardia with a systemic venous anomaly in the form of interrupted inferior vena cava.…”

Section: Discussionmentioning

confidence: 99%

Percutaneous closure of atrial septal defect with situs solitus and dextrocardia

Galal

Khan

El-Segaier

2013

Asian Cardiovasc Thorac Ann

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Section: Discussionmentioning

confidence: 99%

Percutaneous closure of atrial septal defect with situs solitus and dextrocardia

Galal

Khan

El-Segaier

2013

Asian Cardiovasc Thorac Ann

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“…Subjects with simpler and single defects such as pulmonary valvar stenosis [ 30 ], atrial [ 31 , 32 , 33 , 34 , 35 ] or ventricular [ 36 , 37 ] septal defects and patent ductus arteriosus, though rare, should be addressed with either catheter-based [ 31 , 32 , 33 , 34 , 35 , 36 ] or surgical [ 37 ] procedures, as deemed appropriate.…”

Section: Management Of Cardiac Malpositionmentioning

confidence: 99%

Therapy of Patients with Cardiac Malposition

Rao

2023

Children

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Positional abnormalities per se do not require treatment, but in their place, the accompanying pulmonary pathology in dextroposition patients and pathophysiologic hemodynamic abnormalities resulting from multiple defects in patients with cardiac malposition should be the focus of treatment. At the time of the first presentation, treating the pathophysiologic aberrations caused by the defect complex, whether it is by improving the pulmonary blood flow or restricting it, is the first step. Some patients with simpler or single defects are amenable to surgical or transcatheter therapy and should be treated accordingly. Other associated defects should also be treated appropriately. Biventricular or univentricular repair dependent on the patient’s cardiac structure should be planned. Complications in-between Fontan stages and after conclusion of Fontan surgery may occur and should be promptly diagnosed and addressed accordingly. Several other cardiac abnormalities unrelated to the initially identified heart defects may manifest in adulthood, and they should also be treated.

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