Introduction
Kawasaki disease (KD) is an acute febrile illness of an unknown cause characterized by fever, polymorphic rash, conjunctival congestion, redness of the lip mucosa, swollen neck lymph nodes, erythema, and edema of the extremities. It predominantly affects young children worldwide, with the highest incidence in East Asia. KD has become a leading cause of acquired cardiac disease in children in developed countries
1. Treatment for KD includes intravenous immunoglobulin (IVIG) and high doses of aspirin, which significantly reduce the risk of the coronary artery lesion (CAL) complication (CAL is assessed using echocardiographic z-score. A coronary artery with z-score more than 2 was considered as CAL.). Nonetheless, up to 20% of patients with KD fail to respond to IVIG treatment and remain or relapse fever after 24–48 h following completion of the first dose of IVIG, which is termed IVIG-resistance
2‐
4. According to the latest American College of Rheumatology (ACR) guideline for the management of KD
1, co-treatment with glucocorticoids or other immunosuppressants is recommended as the initial therapy for children at high risk of IVIG-resistant KD. Hence, identifying children with a high risk of IVIG-resistant KD is warranted for better management of KD.
Although several prediction models for IVIG resistance have been established, the performance of these predictive models lacks consistency in clinical practice in different regions or populations and is limited by the categorization of continuous variables
5,
6. In addition, potential predictors that have been considered vary in different relevant research
7‐
9. Up to now, there were no effective prediction models for the actual clinical practice in the Chinese population. This cohort study encompassed a comprehensive range of risk factors to evaluate IVIG resistance in children with KD in southeast China, and an effective predictive nomogram, which is a continuous scoring system estimating the risk probability of IVIG resistance for an individual child patient, was established.
Methods
Subjects
The study population was patients diagnosed with KD in Quanzhou Children’s Hospital between November 3, 2018 and February 24, 2023. This study was approved by the Ethics Committee of Quanzhou Children’s Hospital. Data were retrieved from the electronic medical records, and all patients were de-identified. The written informed consent was waived because of the retrospective and anonymous nature of the data.
Patients meeting the diagnostic criteria for complete or incomplete KD in accordance with the AHA guidance published in 20172 were included in this study. Patients who did not receive IVIG treatment in Quanzhou Children’s Hospital or those who received glucocorticoids or other immunosuppressants during or prior to the initial IVIG treatment were excluded. The patients were classified into IVIG responsive or resistant groups according to whether patients remained or relapsed fever after 36 h following completion of the first dose of IVIG. The IVIG dosage was 2 g per kilogram of body weight in a single administration. The upper limit for the dosage was capped at 30 g.
Statistical analysis and nomogram development
The data of demographic features (age and sex) and potential predictors (white blood cell counts, neutrophil-lymphocyte ratio, hematocrit, platelets, sodium ion, albumin, total bilirubin, alanine transaminase, aspartate aminotransferase, gamma-glutamyl transferase, lactate dehydrogenase, creatine kinase-myocardial band, blood urea nitrogen, creatinine, c-reactive protein, procalcitonin, erythrocyte sedimentation rate, DNA damage response, troponin, B-type natriuretic peptide, fever day before treatment, and coronary artery lesion status) were selected for further analysis.
To create a training and validation set, patients were divided based on the time of hospital admission. The earlier 70% of patients were selected as the training set, whereas the remaining 30% from a later period were designated as the validation set.
Missing data were handled by the multiple imputation method using MICE R-Package. Variables with more than 20% missing values were excluded from this study, which are BNP and troponin. Mean values with standard deviations were reported for continuous variables, while frequencies (expressed as percentages) were used for categorical variables.
Patient characteristics were compared between two groups: IVIG-responding and IVIG-resistant, in both the training and validation sets. For continuous baseline characteristics, comparisons were made using the independent Student’s t-test, whereas categorical data were compared using the Chi-square test.
A stepwise backward multivariable logistic analysis was employed to validate these potential risk factors for IVIG resistance using the entire dataset. The stepwise process was evaluated by the Akaike information criterion (AIC) statistics
10. The model with the lowest AIC was selected. Factors such as white blood cell counts, neutrophil-lymphocyte ratio, hematocrit, albumin, total bilirubin, lactate dehydrogenase, and creatinine were included to establish the nomogram model using the training dataset. Subsequently, the predictive model was validated internally using the bootstrap sampling method and externally in the validation dataset.
The sensitivity and specificity of this predictive nomogram and independent predictors were evaluated by operating characteristic curve (ROC). The calibration curve was used to assess the agreement between the predicted result and the observed value. Decision curve analysis was performed to evaluate the clinical utility of this predictive model. Software R (version 4.20,
www.r-project.org) was used for the statistical analysis.
Discussion
Combinations of initial IVIG therapy and glucocorticoids or other immunosuppressants have been reported to effectively reduce the incidence of the coronary artery lesion (CAL) complication for children at high risk of IVIG-resistant KD
11‐
13, and therefore are recommended by the latest American College of Rheumatology (ACR) guideline for management of KD
1. Hence, it is imperative to develop an accurate predictive model for IVIG resistance. However, the inconsistency of the scoring systems in clinical practice in different regions or populations limits its application in general population. For example, the Japanese scoring system, Kobayashi, Egami and Sano, have a high predictive value in Japanese population but exhibit low sensitivities or specificities in other populations
7,
8,
14. It is of great significance in developing an effective scoring system for IVIG resistance in the Chinese population. Recently, researchers have developed several prediction models based on the Chinese population
15,
16. Nonetheless, these models have limitations, and none of them were officially accepted by any formal medical association. The continuous variables in these models were converted to categorical variables, losing within-category information so as to reduce the prediction accuracy. This study, in contrast, kept the continuous variables continuous. As the continuous variables included in this nomogram, such as WBC, N/L ratio, HCT, ALB, TBIL, LDH, and Cr, have been reported to have a monotonicity relation with IVIG resistance
17‐
19, this makes our predictive model more precise and reliable
20.
The nomogram is an invaluable computational model for prognostic prediction due to its ability to provide a visual representation of a statistical predictive model and generate a precise numerical probability for clinical events
21. It surpasses the conventional method that relies on odds ratios, offering enhanced accuracy
22. Herein, we developed a novel nomogram capable of estimating the risk probability of IVIG resistance in patients with KD. The parameters utilized in our model are readily accessible in medical centers, enabling a quick assessment of patients with KD before the determination of initial treatment strategies.
This study identified WBC, N/L ratio, HCT, ALB, TBIL, LDH, and Cr as significant predictors for IVIG resistance. WBC, as an essential serum biomarker related to inflammation and infection, has previously been reported to be associated with IVIG resistance in patients with KD. However, it is debatable how these parameters were correlated to IVIG resistance, and some studies even showed opposite results
23‐
25. In this study, the WBC was negatively correlated to the IVIG resistance risk. Regarding the debatable results from different studies, we assume that there might be some confounding variables that affect both WBC and IVIG resistance risk, which requires further investigation. On the other hand, the significance of N/L ratio, HCT, ALB, TBIL, LDH, and Cr as predictors of IVIG resistance was further confirmed in this study, whereas other characteristics, which were previously reported to be risk factors, were not found to be significantly associated with IVIG resistance, probably attributing to the sample size, different populations, or different local clinical practices.
Notably, recent studies reported that incomplete KD was closely related to IVIG responsiveness
16,
26. Although incomplete KD was not included as an independent risk factor in this study, the factors in the diagnostic criteria of complete or incomplete KD were analyzed. Nonetheless, further investigation on the association between incomplete KD and IVIG resistance is required.
Meanwhile, there are several limitations of this study. First, the present study is a retrospective observational study rather than a randomized controlled clinical study, which does not possess strong capabilities to establish causality
27. Second, other confounding variables may be present that were not measured. Third, this study, as a single-center study, is more susceptible to local clinical practices, limiting the validity and generalizability of our findings.
Conclusions
Overall, this study identified WBC, N/L ratio, HCT, ALB, TBIL, LDH, and Cr as the independent risk factors for IVIG resistance in patients with KD. The proposed novel nomogram with a high level of accuracy may benefit the clinical decision-making upon treatment initiation.
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