Nyang Mariama, Makalo Lamin, Adegoke Samuel Ademola
Department of Paediatrics, Edward Francis Small Teaching Hospital, Banjul, The Gambia.
School of Medicine and Allied Health Sciences, University of The Gambia, Serrekunda, The Gambia.
BMC Cardiovasc Disord. 2025 Jul 23;25(1):539. doi: 10.1186/s12872-025-04948-6.
Congenital heart defects (CHDs) are the most common major congenital anomalies, accounting for approximately one-third of all birth defects. They significantly contribute to morbidity, mortality, and healthcare costs. This study provides insights into the prevalence, characteristics, and management challenges of CHDs in The Gambia, emphasizing the need for early diagnosis, risk factor identification, and improved cardiac care infrastructure.
To determine the prevalence, management strategies, and outcomes of CHDs in children at Edward Francis Small Teaching Hospital from January 2020 to December 2022.
This retrospective descriptive cross-sectional study reviewed medical records of pediatric patients admitted to Edward Francis Small Teaching Hospital, the main referral center in The Gambia and the teaching hospital for the University of The Gambia Medical School. Patient data from January 2020 to December 2022 were analyzed.
A total of 89 patients were included, with 57.3% (n = 51) females and 42.7% (n = 38) males. The median age was 1.4 years. The most common ethnic group was Mandinka, followed by Fula. Diagnosis was confirmed by using 2D trans-thoracic echocardiography, which was performed on most of the patients (84.3%) in addition to clinical features and chest X-ray. The most prevalent CHD was ventricular septal defect (VSD) (39.3%), followed by atrial septal defect (ASD) (20.2%), tetralogy of Fallot (TOF) (16.9%), and patent ductus arteriosus (PDA) (10.1%) were also not uncommon. 15.7% of cases were unclassified. The most commonly associated clinical condition among these children with congenital heart disease was Down syndrome (18.0%), predominantly observed in children born to mothers aged over 35 years. This finding underscores the known association between advanced maternal age and chromosomal abnormalities. Maternal diabetes (2.2%) and osteogenesis imperfecta (2.2%) were also noted as less frequent but relevant associated risk factors, highlighting the multifactorial nature of congenital heart disease. Two (2.2%) had a positive family history of congenital heart disease. However, in 65(73%) of cases, there were no associated conditions or family history of CHD. The most frequently used medication in the treatment of these children was furosemide, and heart failure was the most common complication. Surgical interventions were rare: only 2.2% of these children underwent defect closure and 2.2% had pulmonary artery banding, while 95.5% of them did not receive any form of surgical treatment. Seventy-three (82.0%) were discharged and followed up in the clinic, while 6 (6.7%) died.
VSD was the most common congenital heart disease observed in this study, with a median age at diagnosis of 1.4 years (95% Confidence Interval: within 12 to 60 months). Down syndrome with maternal age > 35 years was the most frequent associated condition, and heart failure was the leading complication and primary cause of death. While both pharmacological and surgical treatment mode were used, surgical intervention for treatment of these defects remains unavailable in The Gambia, highlighting the urgent need to develop local paediatric cardiac surgery services.
先天性心脏病(CHD)是最常见的主要先天性异常,约占所有出生缺陷的三分之一。它们对发病率、死亡率和医疗成本有显著影响。本研究深入探讨了冈比亚先天性心脏病的患病率、特征和管理挑战,强调了早期诊断、危险因素识别以及改善心脏护理基础设施的必要性。
确定2020年1月至2022年12月期间爱德华·弗朗西斯·斯莫尔教学医院儿童先天性心脏病的患病率、管理策略和结局。
这项回顾性描述性横断面研究回顾了冈比亚主要转诊中心及冈比亚大学医学院教学医院爱德华·弗朗西斯·斯莫尔教学医院收治的儿科患者的病历。分析了2020年1月至2022年12月的患者数据。
共纳入89例患者,其中女性占57.3%(n = 51),男性占42.7%(n = 38)。中位年龄为1.4岁。最常见的种族是曼丁卡族,其次是富拉族。除临床特征和胸部X光外,大多数患者(84.3%)通过二维经胸超声心动图确诊。最常见的先天性心脏病是室间隔缺损(VSD)(39.3%),其次是房间隔缺损(ASD)(20.2%),法洛四联症(TOF)(16.9%),动脉导管未闭(PDA)(10.1%)也较为常见。15.7%的病例未分类。这些先天性心脏病患儿中最常见的相关临床情况是唐氏综合征(18.0%),主要见于35岁以上母亲所生的孩子。这一发现强调了高龄产妇与染色体异常之间已知的关联。母亲糖尿病(2.2%)和成骨不全(2.2%)也被指出是不太常见但相关的危险因素,凸显了先天性心脏病的多因素性质。2例(2.2%)有先天性心脏病家族史阳性。然而,65例(73%)病例中没有相关疾病或先天性心脏病家族史。治疗这些患儿最常用的药物是呋塞米,心力衰竭是最常见的并发症。手术干预很少见:这些患儿中只有2.2%接受了缺损闭合手术,2.2%进行了肺动脉环扎术,而95.5%未接受任何形式的手术治疗。73例(82.0%)出院并在门诊随访,6例(6.7%)死亡。
室间隔缺损是本研究中观察到的最常见先天性心脏病,诊断时的中位年龄为1.4岁(95%置信区间:12至60个月内)。母亲年龄>35岁的唐氏综合征是最常见的相关情况,心力衰竭是主要并发症和主要死亡原因。虽然同时使用了药物和手术治疗方式,但冈比亚仍无法进行这些缺陷的手术干预,凸显了发展当地小儿心脏手术服务的迫切需求。