Paediatric Cardiology Services, Royal Brompton Hospital, London, UK.
National Heart and Lung Institute, Imperial College, London, UK.
Cardiol Young. 2023 Jul;33(7):1177-1183. doi: 10.1017/S1047951122002414. Epub 2022 Aug 3.
Multi-system inflammatory syndrome in children and Kawasaki disease have overlapping clinical features but comparative echocardiographic studies are lacking.
We reviewed echocardiography findings of all multi-system inflammatory syndrome cases between 1st April and 31st July, 2020 and typical Kawasaki disease patients with coronary arteries abnormalities consecutively followed between 1st October, 2016 and June 30th, 2019.
We included 40 multi-system inflammatory syndrome children (25 males, 62.5%) and 45 Kawasaki disease patients (31 males, 68.9%) at a mean age of 6.4 years old and 8 years old, respectively. Four out of 40 multi-system inflammatory syndrome children had coronary arteries abnormalities. Left ventricle ejection fraction was normal in both groups. Global longitudinal strain was normal although Kawasaki disease group had significantly lower values (-20.0 versus -21.7%; p = 0.02). Basal segments were the most affected in Kawasaki disease patients with significant differences in the basal anterior, anterolateral, and anteroseptal strain: -18.2 versus -23.0% (p = 0.002), -16.7 versus -22.0% (p < 0.001), -16.7 versus -19.5% (p = 0.034), respectively. The basal anterolateral and anteroseptal segments in Kawasaki disease patients were the only ones with an absolute reduction of longitudinal strain (-16.7% both) consistent with the greater left main coronary involvement in this cohort.
Our findings are consistent with the transient cardiac involvement in multi-system inflammatory syndrome, as opposed to the subtle and chronic myocardial involvement in Kawasaki disease children with coronary arteries abnormalities. We speculate that the mechanism of cardiac impairment in the few multi-system inflammatory syndrome children with reduced global longitudinal strain is not related to coronary arteries abnormalities.
儿童多系统炎症综合征和川崎病具有重叠的临床特征,但缺乏比较性的超声心动图研究。
我们回顾了 2020 年 4 月 1 日至 7 月 31 日期间所有多系统炎症综合征病例的超声心动图检查结果,以及 2016 年 10 月 1 日至 2019 年 6 月 30 日期间连续随访的伴有冠状动脉异常的典型川崎病患者。
我们纳入了 40 例多系统炎症综合征患儿(25 例男性,占 62.5%)和 45 例川崎病患儿(31 例男性,占 68.9%),平均年龄分别为 6.4 岁和 8 岁。40 例多系统炎症综合征患儿中有 4 例存在冠状动脉异常。两组左心室射血分数均正常。尽管川崎病组的整体纵向应变值明显较低(-20.0%对-21.7%;p=0.02),但整体纵向应变仍正常。基底段是川崎病患者中受影响最严重的部位,前壁基底段、前侧壁基底段和前间隔基底段的应变差异有统计学意义:-18.2%对-23.0%(p=0.002)、-16.7%对-22.0%(p<0.001)、-16.7%对-19.5%(p=0.034)。川崎病患者的基底前侧壁和前间隔段是唯一出现纵向应变绝对值降低的节段(均为-16.7%),这与该队列中左主干冠状动脉受累更大有关。
我们的研究结果与多系统炎症综合征的短暂性心脏受累一致,而不是伴有冠状动脉异常的川崎病患儿的细微和慢性心肌受累。我们推测,少数多系统炎症综合征患儿出现整体纵向应变降低的心脏损害机制与冠状动脉异常无关。