Role and effectiveness of cardiovascular magnetic resonance in the diagnosis, preoperative evaluation and follow-up of patients with congenital heart diseases

2007 ◽  
Vol 112 (5) ◽  
pp. 660-680 ◽  
Author(s):  
L. Lovato ◽  
A. Giardini ◽  
C. La Palombara ◽  
V. Russo ◽  
V. Gostoli ◽  
...  
2020 ◽  
Vol 16 ◽  
Author(s):  
Farhan Bajwa ◽  
Syed M Jafri ◽  
Karthik Ananthasubramaniam

: The advancement in corrective surgical procedures and anaesthesia technology has resulted in the increase survival of patients with Congenital Heart Diseases (CHD). Most of the surviving CHD patients have successfully reached adulthood and those surviving adults now outnumber the infants born with the CHD. Unfortunately, the surviving adults with CHD do not get proper care due to either inconsistent follow up or not getting care from a specialist in the field of CHD. It is imperative for general practicing clinicians to be aware of the congenital diseases as well as the current clinical recommendations. This manuscript reviews some of the common congenital diseases seen in adults such as cardiac shunts, left heat obstructive lesions and aortopathies.


2020 ◽  
Vol 7 (1) ◽  
Author(s):  
Ayumi Shishido ◽  
Naoya Morisada ◽  
Kenta Tominaga ◽  
Hiroyasu Uemura ◽  
Akiko Haruna ◽  
...  

AbstractNAA10-related syndrome is an extremely rare X-chromosomal disorder, the symptoms of which include intellectual disability (ID), ocular anomalies, or congenital heart diseases, such as hypertrophic cardiomyopathy (HCM). Here, we describe a 4-year-old Japanese male patient who exhibited mild ID, HCM, and specific facial features. A hemizygous mutation (NM_003491.3: c.455_458del, p. Thr152Argfs*6) in exon 7 of NAA10 was detected. We recommend that patients undergo precise medical follow-up considering the characteristics of NAA10-related syndrome.


Author(s):  
Tanjonirina Razafindrainibe ◽  
Sidonie Rakotonomenjanahary ◽  
Mamitiana Andrianirina ◽  
Nasolotsiry E. Ravel

Background: Congenital heart diseases are malformations formed during the first weeks of life. Thanks to advances in medicine, they could be cared properly and pregnancies on heart diseases could be continued and completed. These malformations are sources of morbidity even high maternal fetal mortality. Whence our motivation to carry out this study and improve its care.Methods: This is a retrospective observational study reporting clinical cases of congenital heart disease pregnancies, only seen at the UHC-GOB over a seven years period (01 February 2007 - 28 February 2014).Results: We have identified 10 cases of congenital heart diseases out of 56 320 deliveries, that is, an incidence of 0.12 per 1000 deliveries. Isolated arterial canal persistence is predominant. The average age is 26±1. Four cases of congenital heart diseases diagnosed and repaired during childhood, have been noted as well as 02 cases of fortuitous discovery during pregnancy. No joint obstetric and cardiac follow up was performed for our patients. Delivery by high way is recommended in 70% of cases which 57% under peridural anesthesia. Half of the patients had peri-gestational cardiac decompensation such as dyspnea, pre-eclampsia and vacuo-shock progressively decreasing in post-partum. On the fetal side, we recorded 01 intra-uterine delayed growths, 03 premature births and 02 deaths.Conclusions: Pregnancy prognosis on congenital heart disease is based on the type of malformation, close follow up and a multidisciplinary care (Gyneco-obstetrician, Cardiologist, Reanimator, Pediatrician and Geneticist.


1989 ◽  
pp. 324-329
Author(s):  
W. Kasper ◽  
A. Geibel ◽  
T. Hofmann ◽  
N. Tiede ◽  
G. Spillner ◽  
...  

2020 ◽  
Vol 22 (1) ◽  
Author(s):  
Saeed Karimi-Bidhendi ◽  
Arghavan Arafati ◽  
Andrew L. Cheng ◽  
Yilei Wu ◽  
Arash Kheradvar ◽  
...  

Abstract Background For the growing patient population with congenital heart disease (CHD), improving clinical workflow, accuracy of diagnosis, and efficiency of analyses are considered unmet clinical needs. Cardiovascular magnetic resonance (CMR) imaging offers non-invasive and non-ionizing assessment of CHD patients. However, although CMR data facilitates reliable analysis of cardiac function and anatomy, clinical workflow mostly relies on manual analysis of CMR images, which is time consuming. Thus, an automated and accurate segmentation platform exclusively dedicated to pediatric CMR images can significantly improve the clinical workflow, as the present work aims to establish. Methods Training artificial intelligence (AI) algorithms for CMR analysis requires large annotated datasets, which are not readily available for pediatric subjects and particularly in CHD patients. To mitigate this issue, we devised a novel method that uses a generative adversarial network (GAN) to synthetically augment the training dataset via generating synthetic CMR images and their corresponding chamber segmentations. In addition, we trained and validated a deep fully convolutional network (FCN) on a dataset, consisting of $$64$$ 64 pediatric subjects with complex CHD, which we made publicly available. Dice metric, Jaccard index and Hausdorff distance as well as clinically-relevant volumetric indices are reported to assess and compare our platform with other algorithms including U-Net and cvi42, which is used in clinics. Results For congenital CMR dataset, our FCN model yields an average Dice metric of $$91.0\mathrm{\%}$$ 91.0 % and $$86.8\mathrm{\%}$$ 86.8 % for LV at end-diastole and end-systole, respectively, and $$84.7\mathrm{\%}$$ 84.7 % and $$80.6\mathrm{\%}$$ 80.6 % for RV at end-diastole and end-systole, respectively. Using the same dataset, the cvi42, resulted in $$73.2\mathrm{\%}$$ 73.2 % , $$71.0\mathrm{\%}$$ 71.0 % , $$54.3\mathrm{\%}$$ 54.3 % and $$53.7\mathrm{\%}$$ 53.7 % for LV and RV at end-diastole and end-systole, and the U-Net architecture resulted in $$87.4\mathrm{\%}$$ 87.4 % , $$83.9\mathrm{\%}$$ 83.9 % , $$81.8\mathrm{\%}$$ 81.8 % and $$74.8\mathrm{\%}$$ 74.8 % for LV and RV at end-diastole and end-systole, respectively. Conclusions The chambers’ segmentation results from our fully-automated method showed strong agreement with manual segmentation and no significant statistical difference was found by two independent statistical analyses. Whereas cvi42 and U-Net segmentation results failed to pass the t-test. Relying on these outcomes, it can be inferred that by taking advantage of GANs, our method is clinically relevant and can be used for pediatric and congenital CMR segmentation and analysis.


Sign in / Sign up

Export Citation Format

Share Document