Literature DB >> 27013702

Multimodality imaging in congenital heart disease-related pulmonary arterial hypertension.

Michele D'Alto1, Konstantinos Dimopoulos2, Werner Budts3, Gerhard-Paul Diller4, Giovanni Di Salvo5, Santo Dellegrottaglie6, Pierluigi Festa7, Giancarlo Scognamiglio1, Gaetano Rea8, Lamia Ait Ali9, Wei Li2, Michael A Gatzoulis2.   

Abstract

Pulmonary arterial hypertension (PAH) in adult patients with congenital heart disease (CHD) is associated with increased morbidity and mortality. The present review aims to discuss the clinical applications of invasive and non-invasive diagnostic modalities and to describe the strengths and weaknesses of each technique. Chest radiograph is an inexpensive investigation providing information on pulmonary arterial and hilar dilatation, pruning of peripheral pulmonary arteries and cardiomegaly. Transthoracic two-dimensional and Doppler echocardiography is the most widely used imaging tool. It provides information on cardiac anatomy and an estimate of haemodynamics and biventricular remodelling and function. In addition, echocardiography is valuable in assessing prognosis and monitoring the efficacy of therapy. Structural and functional changes associated with CHD-PAH, mainly affecting the right ventricle and pulmonary circulation, may represent an ideal target for evaluation with cardiac magnetic resonance. This non-invasive imaging modality has a low biological impact. CT plays an important role for patients with limited echocardiographic windows and those who are unable to undergo MRI (claustrophobia, poor compliance, presence of a pacemaker/implantable cardioverter defibrillator). It is the modality of choice for detailed assessment of pulmonary vessel obstruction or thrombosis. Finally, heart catheterisation remains the gold standard for diagnosing and confirming PAH in patients with CHD and for shunt evaluation. The diagnostic assessment of CHD-PAH requires great expertise and a deep knowledge of both CHD and PAH pathophysiology and should take place in a tertiary centre, where multiple data can be appropriately integrated and applied clinically. Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/

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Year:  2016        PMID: 27013702     DOI: 10.1136/heartjnl-2015-308903

Source DB:  PubMed          Journal:  Heart        ISSN: 1355-6037            Impact factor:   5.994


  5 in total

1.  Unexpected transesophageal echocardiography tee finding: mediastinal lipomatosis fakes an aortic intramural haematoma.

Authors:  Gemma Salerno; Andreina Carbone; Gaetano Rea; Tullio Valente; Antonello D'Andrea; Marco Di Maio; Giuseppe Limongelli; Maurizio Muto; Giuseppe Pacileo
Journal:  Quant Imaging Med Surg       Date:  2017-02

Review 2.  Pulmonary hypertension in congenital heart disease.

Authors:  Emma Pascall; Robert Mr Tulloh
Journal:  Future Cardiol       Date:  2018-05-24

Review 3.  EDUCATIONAL SERIES IN CONGENITAL HEART DISEASE: Cardiovascular MRI and CT in congenital heart disease.

Authors:  Kuberan Pushparajah; Phuoc Duong; Sujeev Mathur; Sonya Babu-Narayan
Journal:  Echo Res Pract       Date:  2019-10-01

4.  Main pulmonary artery-to-descending aorta ratio in computed tomography: cut-off value to diagnose pulmonary hypertension in children.

Authors:  Muankwan Saetung; Supika Kritsaneepaiboon; Jirayut Jarutach
Journal:  Pol J Radiol       Date:  2021-02-02

5.  Initial ultrasound evaluation of an anterior mediastinal mass ultimately diagnosed as T-cell acute lymphoblastic leukemia: a report of three cases in children.

Authors:  Takahiro Hosokawa; Mamoru Honda; Yuki Arakawa
Journal:  Radiol Case Rep       Date:  2022-07-30
  5 in total

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