Current follow-up results of Cyanotic Congenital Heart Diseases detected during Pregnancy in a specific Region

D. Duman, D. Karpuz
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Abstract

Background/Aims: Congenital heart disease (CHD) is the main cause of death in infants among congenital anomalies. Fetal echocardiography is important for the diagnosis and treatment plan of congenital heart diseases in the prenatal period. This study aimed to retrospectively screen the follow-up and treatment results of cyanotic CHD patients detected on fetal echocardiography. Methods: Fetal echocardiography results were scanned from the hospital record system. Data of fetuses with major cardiac anomalies and cyanotic CHD were examined retrospectively. Results: Fetal echocardiography was performed on 420 pregnant women between July 2020 and April 2023. Major cardiac anomalies and cyanotic heart disease were detected in the fetuses of 40 pregnant women (9.5%) out of 420. The median age of the pregnant women was 29 (19-41 years). The median gestational age at check-up was 23 weeks (22-28 weeks). 9/40 pregnant women (22.5%) had risk factors. The most common cyanotic congenital heart diseases were hypoplastic left heart syndrome (HLHS) and unbalanced complete atrioventricular septal defects (AVSDs) with obstructive lesions of the right or left ventricle. Three fetuses (7.5%) with heart failure findings died intrauterine. Two fetuses with HLHS and critical aortic stenosis (AS) died before being operated on. A patient with complete AVSD, hypoplasia of the left heart chambers, AS, and severe aortic coarctation died due to sepsis during the post-operative follow-up period. Chromosome analysis was performed in 8 patients. Down syndrome was detected in 3 of the patients with complete AVSD. 22q11 deletion and DiGeorge Syndrome were detected in 2 patients with tetralogy of Fallot. Conclusions: Congenital heart diseases and rhythm problems can be safely detected with fetal echocardiography. It is beneficial to perform a fetal echo scan at the appropriate gestational week, especially in fetuses with risk factors and in whom the four chambers view cannot be seen.
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特定地区妊娠期发现的青紫型先天性心脏病的当前随访结果
背景/目的:先天性心脏病(CHD)是先天性畸形中导致婴儿死亡的主要原因。胎儿超声心动图对于产前先天性心脏病的诊断和治疗方案非常重要。本研究旨在回顾性筛查通过胎儿超声心动图发现的紫绀型先天性心脏病患者的随访和治疗结果:方法:从医院记录系统中扫描胎儿超声心动图结果。方法:从医院记录系统中扫描胎儿超声心动图检查结果,回顾性检查患有重大心脏畸形和紫绀型先天性心脏病的胎儿数据:2020年7月至2023年4月期间,为420名孕妇进行了胎儿超声心动图检查。结果:2020 年 7 月至 2023 年 4 月期间,对 420 名孕妇进行了胎儿超声心动图检查。在 420 名孕妇中,有 40 名孕妇(9.5%)的胎儿被检测出患有重大心脏畸形和紫绀型心脏病。孕妇的中位年龄为 29 岁(19-41 岁)。检查时的胎龄中位数为 23 周(22-28 周)。每 40 名孕妇中有 9 名(22.5%)存在风险因素。最常见的紫绀型先天性心脏病是左心发育不全综合征(HLHS)和右心室或左心室阻塞性病变的不平衡完全性房室间隔缺损(AVSD)。有三个胎儿(7.5%)发现心衰,死于宫内。两个患有 HLHS 和重度主动脉瓣狭窄(AS)的胎儿在手术前死亡。一名患有完全性 AVSD、左心房发育不良、AS 和严重主动脉瓣狭窄的患者在术后随访期间死于败血症。对 8 名患者进行了染色体分析。在 3 名完全性 AVSD 患者中检测到唐氏综合征。在 2 名法洛氏四联症患者中检测出 22q11 缺失和迪乔治综合征:结论:胎儿超声心动图可安全地检测出先天性心脏病和心律问题。结论:胎儿超声心动图可安全地检测出先天性心脏病和心律问题。在适当的孕周进行胎儿超声扫描是有益的,尤其是对有危险因素和无法看到四腔的胎儿。
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