Uludağ Alkaya Dilek, Öztürk Birol, Yüksel Ülker Aylin, Bozlak Serdar, Öztürk Esra, Dedeoğlu Reyhan, Eroğlu Ayşe Güler, Öztunç Funda, Tüysüz Beyhan
Department of Pediatric Genetics, İstanbul University-Cerrahpaşa, Cerrahpaşa Faculty of Medicine, İstanbul, Turkey.
Department of Pediatric Genetics, İstanbul University-Cerrahpaşa, Cerrahpaşa Faculty of Medicine, İstanbul, Turkey; Department of Pediatric Gastroenterology, Health Sciences University, Okmeydani Research and Training Hospital, İstanbul, Turkey.
Turk Arch Pediatr. 2023 Sep;58(5):473-479. doi: 10.5152/TurkArchPediatr.2023.23041.
Congenital heart defects occur in approximately 50% of children with Down syndrome and they contribute considerably to morbidity and mortality. The aim of this study is to investigate the prevalence, classification, and survival of congenital heart defects in Down syndrome.
About 1731 Down syndrome patients who underwent echocardiography between 1986 and 2022 were evaluated. The median follow-up duration was 8.7 years (range 1-35.8 years). Congenital heart defect was grouped as cyanotic and acyanotic.
Among the 1731 patients, 52.1% had congenital heart defects. Congenital heart defect was significantly more common in females than males. The most common cardiac defect was ventricular septal defect (35%), followed by atrial septal defect (31.8%), atrioventricular septal defect (23.4%), tetralogy of Fallot (5%), and patent ductus arteriosus (3.6%). In the follow-up, 43.2% of atrial septal defect, 17.8% of ventricular septal defect, and a total of 20% of congenital heart defects were closed spontaneously. About 34.4% of congenital heart defect was corrected by cardiac surgery/intervention. Five-year survival rate was 97.4% in patients without congenital heart defects, whereas it was 95.6% in mild congenital heart defects and 86.1% in moderate to severe congenital heart defects. There was no relationship between consanguinity, parental age, maternal disease, folic acid supplementation before/during pregnancy, gestational age, birth weight, and congenital heart defects. Neuromotor development was similar in patients with and without congenital heart defects.
We demonstrated that almost half of the patients had congenital heart defects; ventricular septal defect was the most common congenital heart defect type. This study is valuable in terms of the largest single-center study describing the classification, prognostic factors, and survival of Down syndrome patients with congenital heart defect from Turkey.
先天性心脏病发生于约50%的唐氏综合征患儿中,对其发病率和死亡率有相当大的影响。本研究旨在调查唐氏综合征患儿先天性心脏病的患病率、分类及生存率。
对1986年至2022年间接受超声心动图检查的约1731例唐氏综合征患者进行评估。中位随访时间为8.7年(范围1 - 35.8年)。先天性心脏病分为青紫型和非青紫型。
1731例患者中,52.1%患有先天性心脏病。先天性心脏病在女性中比男性更常见。最常见的心脏缺陷是室间隔缺损(35%),其次是房间隔缺损(31.8%)、房室间隔缺损(23.4%)、法洛四联症(5%)和动脉导管未闭(3.6%)。在随访中,43.2%的房间隔缺损、17.8%的室间隔缺损以及总共20%的先天性心脏病自发闭合。约34.4%的先天性心脏病通过心脏手术/介入治疗得到纠正。无先天性心脏病患者的五年生存率为97.4%,轻度先天性心脏病患者为95.6%,中重度先天性心脏病患者为86.1%。近亲结婚、父母年龄、母亲疾病、孕期前后叶酸补充、孕周、出生体重与先天性心脏病之间无关联。有无先天性心脏病患者的神经运动发育相似。
我们证明了几乎一半的患者患有先天性心脏病;室间隔缺损是最常见的先天性心脏病类型。本研究作为来自土耳其的描述唐氏综合征合并先天性心脏病患者分类、预后因素及生存率的最大规模单中心研究,具有重要价值。