Massoure Pierre-Laurent, Roche Nicolas-Charles, Lamblin Gatien, Dehan Celine, Kaiser Eric, Fourcade Laurent
Hôpital Laveran, 13 384 Marseille cedex 13, France.
Pan Afr Med J. 2013 Apr 9;14:141. doi: 10.11604/pamj.2013.14.141.2016. Print 2013.
Few data are available about pediatric cardiovascular disease (CVD) in the Horn of Africa. The objective of this study was to describe the spectrum of CVD in children in Djibouti.
Clinical features and management of Djiboutian children between 1 month-old and 15 year-old with CVD were prospectively recorded over a two-year period in Bouffard Military Hospital in Djibouti (January 2009- December 2010).
Clinical examination and echocardiography were performed on 156 patients: 32 of them (20%) had CVD. Three (10%) of them had Down's syndrome. The median age was 5 years (male 53%). Congenital heart disease was observed in 27 (84%) patients and dilated cardiomyopathy (DCM) in 5 (16%) patients including 2 patients with rheumatic valvular disease. Ventricular septal defect was frequent (28%). Other abnormalities were atrial septal defect (13%), Tetralogy of Fallot (9%), pulmonary stenosis (6%) and 3 other patients had multiple congenital anomalies condition. Surgical management was required in 22 (69%) patients and was performed on 15 (47%) cases. During follow up (mean 11.3 ± 6.8 months), 5 (16%) patients died. Absence of surgery was associated with significant mortality (p > 0.05) but age, sex and mean follow up were not.
Pediatric CVD is at least as common in this Djiboutian community as in other African cohorts. The absence of surgery was a major mortality risk factor. DCM was frequent in this study. Much work remains to be done to discover the size and nature of genetic and environmental contributions to these various forms of heart diseases in the Horn of Africa.
关于非洲之角地区小儿心血管疾病(CVD)的数据很少。本研究的目的是描述吉布提儿童心血管疾病的范围。
在吉布提的布法尔军事医院(2009年1月至2010年12月)对1个月至15岁患有心血管疾病的吉布提儿童进行了为期两年的前瞻性临床特征和治疗记录。
对156名患者进行了临床检查和超声心动图检查:其中32名(20%)患有心血管疾病。其中3名(10%)患有唐氏综合征。中位年龄为5岁(男性占53%)。27名(84%)患者患有先天性心脏病,5名(16%)患者患有扩张型心肌病(DCM),其中包括2名风湿性瓣膜病患者。室间隔缺损很常见(28%)。其他异常包括房间隔缺损(13%)、法洛四联症(9%)、肺动脉狭窄(6%),另外3名患者患有多种先天性异常疾病。22名(69%)患者需要手术治疗,15名(47%)患者接受了手术。在随访期间(平均11.3±6.8个月),5名(16%)患者死亡。未进行手术与显著的死亡率相关(p>0.05),但年龄、性别和平均随访时间与死亡率无关。
在这个吉布提社区,小儿心血管疾病至少与其他非洲人群一样常见。未进行手术是主要的死亡风险因素。在本研究中,扩张型心肌病很常见。要发现遗传和环境因素对非洲之角地区这些各种形式心脏病的影响程度和性质,仍有许多工作要做。