Walton Mollie, Raghuveer Geetha, Harahsheh Ashraf, Portman Michael A, Lee Simon, Khoury Michael, Dahdah Nagib, Fabi Marianna, Dionne Audrey, Harris Tyler H, Choueiter Nadine, Garrido-Garcia Luis Martin, Jain Supriya, Dallaire Frédéric, Misra Nilanjana, Hicar Mark D, Giglia Therese M, Truong Dongngan T, Tierney Elif Seda Selamet, Thacker Deepika, Nowlen Todd T, Szmuszkovicz Jacqueline R, Norozi Kambiz, Orr William B, Farid Pedrom, Manlhiot Cedric, McCrindle Brian W
Children's Mercy Hospital, Kansas City, MO, USA.
Division of Pediatric Cardiology, Ward Family Heart Center, Children's Mercy Hospital, 2401 Gillham Road, Kansas City, MO, 61408, USA.
Pediatr Cardiol. 2025 Jan;46(1):116-126. doi: 10.1007/s00246-023-03338-z. Epub 2023 Dec 29.
Kawasaki disease (KD) and Multisystem Inflammatory Syndrome in Children (MIS-C) associated with COVID-19 show clinical overlap and both lack definitive diagnostic testing, making differentiation challenging. We sought to determine how cardiac biomarkers might differentiate KD from MIS-C. The International Kawasaki Disease Registry enrolled contemporaneous KD and MIS-C pediatric patients from 42 sites from January 2020 through June 2022. The study population included 118 KD patients who met American Heart Association KD criteria and compared them to 946 MIS-C patients who met 2020 Centers for Disease Control and Prevention case definition. All included patients had at least one measurement of amino-terminal prohormone brain natriuretic peptide (NTproBNP) or cardiac troponin I (TnI), and echocardiography. Regression analyses were used to determine associations between cardiac biomarker levels, diagnosis, and cardiac involvement. Higher NTproBNP (≥ 1500 ng/L) and TnI (≥ 20 ng/L) at presentation were associated with MIS-C versus KD with specificity of 77 and 89%, respectively. Higher biomarker levels were associated with shock and intensive care unit admission; higher NTproBNP was associated with longer hospital length of stay. Lower left ventricular ejection fraction, more pronounced for MIS-C, was also associated with higher biomarker levels. Coronary artery involvement was not associated with either biomarker. Higher NTproBNP and TnI levels are suggestive of MIS-C versus KD and may be clinically useful in their differentiation. Consideration might be given to their inclusion in the routine evaluation of both conditions.
川崎病(KD)和与新型冠状病毒肺炎(COVID-19)相关的儿童多系统炎症综合征(MIS-C)表现出临床重叠,且两者均缺乏明确的诊断检测方法,这使得鉴别诊断具有挑战性。我们试图确定心脏生物标志物如何区分KD和MIS-C。国际川崎病登记处纳入了2020年1月至2022年6月期间来自42个地点的同期KD和MIS-C儿科患者。研究人群包括118名符合美国心脏协会KD标准的KD患者,并将他们与946名符合2020年疾病控制与预防中心病例定义的MIS-C患者进行比较。所有纳入的患者至少进行了一次氨基末端脑钠肽前体(NTproBNP)或心肌肌钙蛋白I(TnI)检测以及超声心动图检查。采用回归分析来确定心脏生物标志物水平、诊断和心脏受累之间的关联。就诊时NTproBNP(≥1500 ng/L)和TnI(≥20 ng/L)升高与MIS-C相关,而与KD相关的特异性分别为77%和89%。较高的生物标志物水平与休克和入住重症监护病房相关;较高的NTproBNP与较长的住院时间相关。左心室射血分数降低,在MIS-C中更为明显,也与较高的生物标志物水平相关。冠状动脉受累与这两种生物标志物均无关。较高的NTproBNP和TnI水平提示为MIS-C而非KD,可能在它们的鉴别诊断中具有临床应用价值。可考虑将它们纳入这两种疾病的常规评估中。