Kim So Youn, Han Mi Young, Cha Sung-Ho, Jeon Yang Bin
Department of Pediatrics, Kyunghee University School of Medicine, 26 Kyungheedae-ro, Dongdaemun-gu, Seoul, 130-701, South Korea.
Pediatr Cardiol. 2013;34(8):1837-43. doi: 10.1007/s00246-013-0724-2. Epub 2013 Jun 7.
Intravenous immunoglobulin (IVIG) administered in the acute stage of Kawasaki disease (KD) is the standard therapy. Few reports describe nonresponders to initial treatment with IVIG in KD, which remains the most consistent risk factor for coronary artery lesions (CALs). This study aimed to investigate whether the serum level of N-terminal pro-brain natriuretic peptide (NT-proBNP) can be a predictive indicator for identifying patients with KD at higher risk of IVIG treatment failure. In this study, 135 patients with a diagnosis of KD admitted for IVIG treatment were retrospectively enrolled for analysis. Of these 135 patients, 22 were nonresponders who received additional rescue therapy because they had an elevated body temperature 36 h after completion of initial IVIG treatment. The NT-proBNP concentration was significantly higher in the nonresponder group (2,465.36 ± 3,293.24 pg/mL) than in the responder group (942.38 ± 1,293.48 pg/mL) (p < 0.05). The optimal sensitivity and specificity cutoff point for predicted nonresponders was 1,093.00 pg/mL or higher. The sensitivity and specificity for prediction of IVIG response were respectively 70.0 and 76.5 %. The findings show that NT-proBNP is a helpful marker in determining patients at risk for not responding to initial IVIG treatment. The authors suggest that patients with an NT-proBNP level of 1,093.00 pg/dL or higher are likely to fail initial IVIG and may require further rescue therapy.
静脉注射免疫球蛋白(IVIG)用于川崎病(KD)急性期治疗是标准疗法。关于KD患者对初始IVIG治疗无反应的报道较少,而这仍是冠状动脉病变(CALs)最一致的风险因素。本研究旨在调查N末端脑钠肽前体(NT-proBNP)血清水平是否可作为识别KD患者IVIG治疗失败风险较高的预测指标。在本研究中,回顾性纳入了135例因IVIG治疗入院的KD确诊患者进行分析。在这135例患者中,22例为无反应者,他们在初始IVIG治疗结束后36小时体温仍升高,因此接受了额外的抢救治疗。无反应者组的NT-proBNP浓度(2,465.36 ± 3,293.24 pg/mL)显著高于反应者组(942.38 ± 1,293.48 pg/mL)(p < 0.05)。预测无反应者的最佳敏感性和特异性截断点为1,093.00 pg/mL及以上。预测IVIG反应的敏感性和特异性分别为70.0%和76.5%。研究结果表明,NT-proBNP是确定初始IVIG治疗无反应风险患者的有用标志物;作者建议,NT-proBNP水平为1,093.00 pg/dL及以上的患者初始IVIG治疗可能失败,可能需要进一步的抢救治疗。