Useful predictors of Kawasaki disease without complications before initial acute-phase treatment

Authors

  • Toshimasa Nakada Department of Pediatrics, Aomori Prefectural Central Hospital, 030-8553 Higashi- tukurimiti 2-1-1, Aomori City, Aomori Prefecture, Japan.

DOI:

https://doi.org/10.30574/gscarr.2021.7.3.0122

Keywords:

Kawasaki disease, Neutrophil-to-lymphocyte ratio, Predictors, Intravenous immunoglobulin therapy resistance, Coronary artery lesions

Abstract

Kawasaki disease (KD) is an acute febrile systemic vasculitis that primarily affects children younger than 5 years, with coronary artery lesions (CALs) as its severe complications. Intravenous immunoglobulin (IVIG) therapy resistance has been implicated in CAL development, and its known predictors are as follows: Egami score, Kobayashi score, C-reactive protein (CRP), albumin, CRP-to-albumin ratio, and neutrophil-to-lymphocyte ratio (NLR). However, the most useful predictor for IVIG resistance in patients with KD without complications before initial acute-phase treatment remains unclear. Therefore, this study aimed to determine the most useful predictor for IVIG resistance in such patients. This retrospective study included data from 202 patients with KD who underwent acute-phase treatment from January 2009 to March 2021. Among 46 IVIG-resistant patients, 22 patients required rescue therapy (rescued patients), while the remaining 24 received no rescue therapy for resistance and had no CALs. Among the 6 indices, NLR had the highest sensitivity and specificity for the detection of all IVIG-resistant patients and rescued patients (0.724 and 0.728, respectively), and logistic regression analysis showed that the NLR was the sole independent predictor both for the IVIG-resistant patients and for the rescued patients (P < 0.001 and = 0.002, Odds ratio = 5.797 and 5.814, 95% confidence interval = 2.687–12.504 and 1.954–17.299, respectively). NLR was the useful predictor for all IVIG-resistant patients and rescued patients among those with KD without complications before initial acute-phase treatment.

Metrics

Metrics Loading ...

References

Kawasaki T, Kosaki F, Okawa S, Shigematsu I, Yanagawa H. A new infantile acute febrile mucocutaneous lymph node syndrome (MLNS) prevailing in Japan. Pediatrics. 1974; 54: 271–6.

Fukazawa R, Kobayashi J, Ayusawa M, Hamada H, Miura M, Mitani Y, et al. JCS/JSCS 2020 Guideline on Diagnosis and Management of Cardiovascular Sequelae in Kawasaki Disease. Circ J. 2020; 84: 1348–407.

Nakada T. Acute phase treatment for prevention of coronary artery stenosis caused in Kawasaki disease: a single center retrospective study. J Adv Res Med. 2018; 5(4): 1–7.

Nakada T. Intravenous Immunoglobulin Therapy for Prevention of Coronary Artery Stenosis Caused in Kawasaki Disease. International Journal of Advances in Medical Sciences. 2018; 3(6): 1–13.

Nakada T. Risk stratification after initial therapy for intravenous immunoglobulin-resistant Kawasaki disease. Research Journal of Life Sciences, Bioinformatics, Pharmaceutical and Chemical Sciences. 2019; 5(5): 1–13.

Chbeir D, Gaschignard J, Bonnefoy R, Beyler C, Melki I, Faye A, et al. Kawasaki disease: abnormal initial echocardiogram is associated with resistance to IV Ig and development of coronary artery lesions. Pediatr Rheumatol Online J. 2018; 16(1): 48.

Miyata K, Kaneko T, Morikawa Y, Sakakibara H, Matsushima T, Misawa M, et al. Efficacy and safety of intravenous immunoglobulin plus prednisolone therapy in patients with Kawasaki disease (Post RAISE): a multicentre, prospective cohort study. Lancet Child Adolesc Health. 2018; 2(12): 855–862.

Makino N, Nakamura Y, Yashiro M, Kosami K, Matsubara Y, Ae R, et al. Nationwide epidemiologic survey of Kawasaki disease in Japan, 2015–2016. Pediatr Int. 2019; 61: 397–403.

Nakada T. Acute Phase Treatment and Medium-Term Outcomes in Kawasaki Disease. European Journal of Medical and Health Sciences. 2020; 2 (4): 1–7.

Kobayashi T, Inoue Y, Takeuchi K, OkadaY, Tamura K, Tomomasa T, et al. Prediction of intravenous immunoglobulin unresponsiveness in patients with Kawasaki disease. Circulation. 2006; 113: 2606–12.

Rearch Committee of the Japanese Society of Pediatric Cardiology; Cardiac Surgery Committee for Development of Guidelines for Medical Treatment of Acute Kawasaki Disease. Guidelines for medical treatment of acute Kawasaki disease: report of the Research Committee of the Japanese Society of Pediatric Cardiology and Cardiac Surgery (2012 revised version). Pediatr Int. 2014; 56: 135–58.

Egami K, Muta H, Ishii M, Suda K, Sugahara Y, Iemura M, et al. Prediction of resistance to intravenous immunoglobulin treatment in patients with Kawasaki disease, J Pediatr. 2006; 149: 237–40.

Tsai CM, Yu HR, Tang KS, Huang YH, Kuo HC. C-Reactive Protein to Albumin Ratio for Predicting Coronary Artery Lesions and Intravenous Immunoglobulin Resistance in Kawasaki Disease. Front Pediatr. 2020; 8: 607631.

Liu X, Wang L, Zhou K, Shao S, Hua Y, Wu M, et al. Predictive value of C-reactive protein to albumin ratio as a biomarker for initial and repeated intravenous immunoglobulin resistance in a large cohort of Kawasaki disease patients: a prospective cohort study. Pediatric Rheumatology. 2021; 19: 24.

Ha KS, Lee J, Jang GY, Lee J, Lee KC, Son CS, et al. Value of neutrophil-lymphocyte ratio in predicting outcomes in Kawasaki disease. Am J Cardiol. 2015; 116: 301–6.

Xie T, Wang Y, Fu S, Wang W, Xie C, Zhang Y, et al. Predictors for intravenous immunoglobulin resistance and coronary artery lesions in Kawasaki disease. Pediatric Rheumatology. 2017; 15: 17.

Cho HJ, Bak SY, Kim SY, Yoo R, Baek HS, Yang S, et al. High neutrophil: lymphocyte ratio is associated with refractory Kawasaki disease. Pediatr Int. 2017; 59: 669–74.

Ayusawa M, Sonobe T, Uemura S, Ogawa S, Nakamura Y, Kiyosawa N, et al. Revision of diagnostic guidelines for Kawasaki disease (the 5th revised edition). Pediatr Int. 2005; 47: 232–4.

Nakada T. Effects of anti-inflammatory drugs on intravenous immunoglobulin therapy in the acute phase of Kawasaki disease. Pediatr Cardiol. 2015; 36: 335–9.

Zahorec R. Ratio of neutrophil to lymphocyte counts–rapid and simple parameters of systemic inflammation and stress in critically ill. Bratisl Lek Listy. 2001; 102: 5–14.

Chang LS, Lin YJ, Yan JH, Guo MMH, Lo MH, Kuo HC. Neutrophil-to-lymphocyte ratio and scoring system for predicting coronary artery lesions of Kawasaki disease. BMC Pediatrics. 2020; 20: 398.

Nakada T. Usefulness of the neutrophil to lymphocyte ratio for risk stratification after initial intravenous immunoglobulin therapy in Kawasaki disease. Research Journal of Life Sciences, Bioinformatics, Pharmaceutical and Chemical Sciences. 2017; 2(5): 1–17.

Nakada T. Usefulness of an Initial Single Intravenous Immunoglobulin Infusion with Delayed Use of Aspirin against Kawasaki Disease Relapse: a single center retrospective study. J Adv Res Med. 2019; 6(1): 18–24.

Seo YM, Kang HM, Lee SC, Yu JW, Kil HR, Rhim JW, et al. Clinical implications in laboratory parameter values in acute Kawasaki disease for early diagnosis and proper treatment. Korean J Pediatr. 2018; 61(5): 160–6.

Chaudhary H, Nameirakpam J, Kumrah R, Pandiarajan V, Suri D, Rawat A, et al. Biomarkers for Kawasaki Disease: Clinical Utility and the Challenges Ahead. Front Pediatr. 2019; 7: 242.

Nakada T. Combined Usefulness of Serum Albumin and C-Reactive Protein for Guiding Rescue Therapy for Intravenous Immunoglobulin-Resistant Kawasaki Disease. International Journal of Advances in Medical Sciences. 2018; 3(39): 1–7.

Rigante D, Andreozzi L, Fastiggi M, Bracci B, Natale MF, Esposito S, et al. Critical overview of the risk scoring systems to predict non-responsiveness to intravenous immunoglobulin in Kawasaki syndrome. Int J Mol Sci. 2016.

Nakada T. Background factors associated with the complications of coronary artery lesions caused by Kawasaki disease. Clinical Medicine Research. 2015; 4: 127–31.

Downloads

Published

2021-06-30

How to Cite

Nakada, T. (2021). Useful predictors of Kawasaki disease without complications before initial acute-phase treatment. GSC Advanced Research and Reviews, 7(3), 018–027. https://doi.org/10.30574/gscarr.2021.7.3.0122

Issue

Section

Original Article