某三甲医院先天性心脏病合并唐氏综合征的临床表现及治疗效果

J. Ferdous, N. Begum, Md. Harun Or Rashid
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摘要

导言:患有先天性心脏缺陷的唐氏综合症儿童的治疗在孟加拉国尚未得到很好的报道。开展这项研究的目的是向从业人员通报达卡军事联合医院的病例调查结果。方法:对2018年1月至2020年12月在达卡CMH儿科心内科接受诊断和治疗的114例患者(男49例,女65例,年龄1个月至12岁)进行为期3年的回顾性观察研究(临床资料、住院过程和随访)。结果:114例患者中,婴儿64例(57%),大龄儿童50例(43%),充血性心力衰竭25例,甲状腺功能减退18例。研究表明:房室间隔缺损(AVSD)占33.3%,动脉导管未闭(PDA)占28.1%,法洛四联症(TOF)占8.75%,主动脉缩窄(COA)占5.25%,动脉导管未闭合并主动脉缩窄占3.5%,双出口右心室合并肺动脉狭窄占3.5%,室间隔缺损占7%,房间隔缺损合并室间隔缺损占5.3%,房间隔缺损占3.5%。大动脉转位合并多发室间隔缺损占1.8%。经皮介入治疗40例(35%)患者手术成功率100%,无死亡。45例患者行手术治疗,少数患者因严重肺动脉高压而未行手术治疗。结论:先天性心脏病在退行性痴呆患儿中发病率较高,预后较差。由于肺动脉高压的风险增加,DS患儿需要特别注意。延迟治疗是导致预后不良的重要危险因素。因此,需要在不可逆PAH发生前进行早期诊断,以便提供最佳的干预和手术。[J]孟加拉大学物理外科20123;41: 7 - 14
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Presentation and Outcome of Management of Congenital Heart Diseases Associated with Down Syndrome in a Tertiary Care Hospital
Introduction: Treatment of children with Down syndrome having congenital heart defects has not been reported well in Bangladesh. This study has been carried out to inform practitioners about findings from cases in Combined Military Hospital, Dhaka. Methods: Three years retrospective observational study (clinical data, hospital course and follow-up) was carried out on 114 patients (49 males and 65 females, age range 1 month to 12 years) who underwent diagnostic and therapeutic work up in the pediatric cardiology department CMH Dhaka between January 2018 and December 2020. Results: Among 114 patients ,64 were (57%) were infants and 50 were older children (43%) , twenty-five had congestive cardiac failure and eighteen had hypothyroidism. The study showed that 33.3% were atrioventricular septal defect (AVSD), 28.1% were patent ductus arteriosus (PDA),8.75% were tetralogy of Fallot (TOF) ,5.25% were coartation of aorta (COA) ,3.5% were patent ductus arteriosus with coarctation of aorta 3.5%, double outlet right ventricle with pulmonary stenosis were 3.5%, ventricular septal defect were 7% whereas atrial septal defect along with ventricular septal defect were 5.3% ,atrial septal defect were 3.5%, transposition of great arteries with multiple ventricular septal defect were 1.8%.Forty (35%) patients using per cutaneous intervention,had 100% procedural success and no mortality .45 patients underwent surgery,few of them were not operated due to severe pulmonary hypertension. Conclusion: Congenital heart disease was more frequent in DS children,having worse prognosis.Children with DS required special attention due to increased risk of pulmonary hypertension. Delayed treatment was an important risk factor for poor prognosis.So early diagnosis is needed in order to provide optimal intervention and surgery ,before occurrence of irreversible PAH. J Bangladesh Coll Phys Surg 2023; 41: 7-14
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