Department of Pediatrics, Hamamatsu University School of Medicine, 1 - 20 - 1 Handayama, Hamamatsu, Shizuoka, 431 - 3192, Japan.
BMC Pediatr. 2018 Nov 19;18(1):359. doi: 10.1186/s12887-018-1344-z.
Delayed diagnosis of critical congenital heart disease (CCHD) carries a serious risk of mortality, morbidity, and handicap. As echocardiography is commonly used to diagnose congenital heart disease (CHD), echocardiographic investigations in newborns may be helpful in detecting CCHD earlier and with higher sensitivity than when using other screening methods. The present study aimed to evaluate the effectiveness of echocardiographic screening for CCHD in a tertiary care center.
A retrospective chart review was conducted among newborns delivered at Hamamatsu University Hospital between June 2009 and May 2016. The study included consecutive newborns who underwent early echocardiographic screening (within the first 5 days of life) performed by pediatric cardiologists, were born at ≥36 weeks of gestation, had a birthweight ≥2300 g, and were cared for in the well-baby nursery. Newborns admitted to the neonatal intensive care unit, as well as those with prenatal diagnosis of CHD and/or clinical symptoms or signs of CHD were excluded. Four CHD outcome categories were defined: critical, serious, clinically significant, and clinically non-significant.
A total of 4082 live newborns were delivered during the study period. Of 3434 newborns who met the inclusion criteria and had complete echocardiography data, 104 (3.0%) were diagnosed as having CHD. Among these, none was initially diagnosed as having critical or serious CHD. Of the 95 newborns who continued follow-up with a cardiologist, 61 (64%) were determined to have non-significant CHDs that resolved within 6 months of life. Review of excluded newborns revealed nine cases of critical or serious CHD; among these newborns, six were diagnosed prenatally and three had some clinical signs of CHD prior to hospital discharge.
In our tertiary care center, echocardiography screening within the first 5 days of life did not help improve CCHD detection rate in newborns without prenatal diagnosis or clinical signs of CHD. Echocardiographic screening may be associated with increased rate of false-positives (defects resulting in clinically non-significant CHDs) in newborns without prenatal diagnosis or suspicion of CHD.
先天性心脏病(CHD)的延迟诊断存在严重的死亡、发病和残疾风险。由于超声心动图常用于诊断先天性心脏病(CHD),因此在新生儿中进行超声心动图检查可能有助于更早、更敏感地发现先天性心脏病(CHD),而不是使用其他筛查方法。本研究旨在评估在三级保健中心进行超声心动图筛查先天性心脏病(CHD)的效果。
本研究对 2009 年 6 月至 2016 年 5 月期间在滨松大学医院分娩的新生儿进行了回顾性病历审查。该研究包括连续的新生儿,他们接受了儿科心脏病专家在出生后 5 天内进行的早期超声心动图筛查,胎龄≥36 周,出生体重≥2300g,在新生儿重症监护病房中接受治疗。新生儿重症监护病房入院的新生儿,以及产前诊断为 CHD 和/或有 CHD 的临床症状或体征的新生儿被排除在外。定义了四种 CHD 结局类别:严重、严重、有临床意义和无临床意义。
在研究期间,共分娩了 4082 名活产新生儿。在符合纳入标准且具有完整超声心动图数据的 3434 名新生儿中,有 104 名(3.0%)被诊断为 CHD。其中,无一例最初被诊断为患有严重或严重的 CHD。在继续接受心脏病专家随访的 95 名新生儿中,有 61 名(64%)被确定患有 6 个月内可消退的非严重 CHD。对被排除的新生儿进行回顾发现有 9 例严重或严重的 CHD;其中,6 例在产前诊断,3 例在出院前有 CHD 的一些临床症状。
在我们的三级保健中心,在无产前诊断或无 CHD 临床体征的新生儿中,出生后 5 天内进行超声心动图筛查并未有助于提高 CCHD 的检出率。在无产前诊断或无 CHD 怀疑的新生儿中,超声心动图筛查可能与假阳性率(导致无临床意义的 CHD 的缺陷)的增加有关。