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罗马尼亚(一个发展中国家)患有和未患有唐氏综合征的儿童房室间隔缺损手术治疗中的挑战

Challenges in the Surgical Treatment of Atrioventricular Septal Defect in Children With and Without Down Syndrome in Romania-A Developing Country.

作者信息

Olariu Ioana-Cristina, Popoiu Anca, Ardelean Andrada-Mara, Isac Raluca, Steflea Ruxandra Maria, Olariu Tudor, Chirita-Emandi Adela, Stroescu Ramona, Gafencu Mihai, Doros Gabriela

机构信息

Department of Pediatrics, "Victor Babeş" University of Medicine and Pharmacy, Timisoara, Romania.

Department of Pediatrics, "Louis Turcanu" Emergency Hospital for Children, Timisoara, Romania.

出版信息

Front Pediatr. 2021 Jul 7;9:612644. doi: 10.3389/fped.2021.612644. eCollection 2021.

Abstract

Atrioventricular septal defect (AVSD) is a cardiac malformation that accounts for up to 5% of total congenital heart disease, occurring with high frequency in people with Down Syndrome (DS). We aimed to establish the surgical challenges and outcome of medical care in different types of AVSD in children with DS compared to those without DS (WDS). The study included 62 children (31 with DS) with AVSD, evaluated over a 5 year period. Complete AVSD was observed in 49 (79%) children (27 with DS). Six children had partial AVSD (all WDS) and seven had intermediate types of AVSD (4 with DS). Eight children had unbalanced complete AVSD (1 DS). Median age at diagnosis and age at surgical intervention in complete AVSD was not significantly different in children with DS compared to those WDS (7.5 months vs. 8.6). Median age at surgical intervention for partial and transitional AVSDs was 10.5 months for DS and 17.8 months in those without DS. A large number of patients were not operated: 13/31 with DS and 8/31 WDS. The complete form of AVSD was more frequent in DS group, having worse prognosis, while unbalanced AVSD was observed predominantly in the group without DS. Children with DS required special attention due to increased risk of pulmonary hypertension. Late diagnosis was an important risk factor for poor prognosis, in the setting of suboptimal access to cardiac surgery for patients in Romania. Although post-surgery mortality was low, infant mortality before surgery remains high. Increased awareness is needed in order to provide early diagnosis of AVSD and enable optimal surgical treatment.

摘要

房室间隔缺损(AVSD)是一种心脏畸形,占先天性心脏病总数的5%,在唐氏综合征(DS)患者中高发。我们旨在确定与非唐氏综合征(WDS)儿童相比,唐氏综合征儿童不同类型AVSD的手术挑战和医疗结局。该研究纳入了62例患有AVSD的儿童(31例患有DS),在5年期间进行了评估。49例(79%)儿童观察到完全性AVSD(27例患有DS)。6例儿童患有部分性AVSD(均为WDS),7例患有中间型AVSD(4例患有DS)。8例儿童患有不平衡完全性AVSD(1例患有DS)。完全性AVSD的诊断中位年龄和手术干预年龄在患有DS的儿童与WDS儿童之间无显著差异(7.5个月对8.6个月)。部分性和过渡性AVSD的手术干预中位年龄在患有DS的儿童中为10.5个月,在非DS儿童中为17.8个月。大量患者未接受手术:31例患有DS的患者中有13例,31例WDS患者中有8例。AVSD的完全形式在DS组中更常见,预后较差,而不平衡AVSD主要在非DS组中观察到。由于肺动脉高压风险增加,患有DS的儿童需要特别关注。在罗马尼亚,由于患者获得心脏手术的机会不理想,晚期诊断是预后不良的重要危险因素。虽然术后死亡率较低,但术前婴儿死亡率仍然很高。需要提高认识,以便早期诊断AVSD并实现最佳手术治疗。

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