Literature DB >> 31548437

Epidemiologic Features of Kawasaki Disease in Shanghai From 2013 Through 2017.

Li-Ping Xie1, Wei-Li Yan2, Min Huang3, Mei-Rong Huang4, Sun Chen5, Guo-Ying Huang1, Fang Liu1.   

Abstract

BACKGROUND: We sought to investigate epidemiologic features of Kawasaki disease (KD) in Shanghai from 2013 through 2017 and identify risk factors for coronary artery lesions (CAL).
METHODS: As in our previous three surveys, a set of questionnaires and diagnostic guidelines for KD were sent to 50 hospitals providing pediatric medical care in Shanghai. Medical records of KD patients diagnosed from January 2013 through December 2017 were retrospectively analyzed. Multivariate logistic regression analysis was performed to identify risk factors for CAL.
RESULTS: A total of 4,452 cases were enrolled. Male-to-female ratio was 1.7:1. The incidence of KD was 68.8 to 107.3 per 100,000 children aged <5 years from 2013 to 2017. Age at onset ranged from 15 days to 14.0 years (median: 1.8 years). KD occurred more frequently in spring and summer. Of 4,325 patients (97.0%) receiving intravenous immunoglobulin (IVIG), 362 (8.4%) were resistant to initial IVIG. CAL occurred in 406 (9.1%) patients, including 118 (2.7%) with medium aneurysms and 31 (0.7%) with giant aneurysms. Recurrent cases were 60 (1.3%). No death was found in this survey. Higher platelet levels, lower albumin levels, male sex, incomplete KD, IVIG resistance, and receiving initial IVIG ≤4 days or >10 days, were independently associated with CAL.
CONCLUSIONS: The incidence of KD in Shanghai had substantially increased while the proportion of CAL had substantially decreased as compared with our previous surveys. Higher platelet levels, lower albumin levels, male sex, incomplete KD, IVIG resistance, and receiving initial IVIG ≤4 days or >10 days, were risk factors for CAL.

Entities:  

Keywords:  Kawasaki disease; Shanghai; coronary artery lesion; epidemiology

Year:  2019        PMID: 31548437      PMCID: PMC7492704          DOI: 10.2188/jea.JE20190065

Source DB:  PubMed          Journal:  J Epidemiol        ISSN: 0917-5040            Impact factor:   3.211


INTRODUCTION

Kawasaki disease (KD) is an acute, self-limited febrile illness that predominantly affects children under 5 years of age. The etiology remains unclear. It is a systemic vasculitis mainly affecting coronary arteries[1] and is becoming the leading cause of childhood acquired heart disease both in developed countries and China.[2] The incidence of KD remains highest in Japan,[3] followed by South Korea,[4] Taiwan,[5] and mainland China,[6],[7] whereas it was much lower in European[8] and American countries.[9],[10] Actually, the incidence of KD has recently shown an increasing trend in many regions, especially in Asian countries.[3]–[5],[7] In Shanghai, a well-developed city in China, the incidence of KD increased from 16.8 to 55.5 per 100,000 children <5 years old from 1998 through 2012.[6],[11] Coronary artery lesions (CAL) are still the main factors affecting the long-term prognosis and mortality of KD. Fortunately, the proportion of CAL among KD patients showed a decreasing trend with the increasing administration of large dose of intravenous immunoglobulin (IVIG).[3],[4],[8],[9] In Shanghai, the proportion of CAL decreased from 19.8% to 15.9% from 1998 through 2012.[6],[11] We have conducted three epidemiologic surveys of KD in Shanghai since 1998 (once every 5 years). Considering that epidemiologic features of KD keeps changing since our first survey, especially the incidence of KD and the proportion of CAL, we continued to carry out the fourth survey to keep track of the latest changes. We aimed to provide the descriptive epidemiology of KD in Shanghai from 2013 through 2017 and identify independent risk factors for CAL.

MATERIALS AND METHODS

Data collection

As in our previous three surveys, a set of questionnaires and diagnostic guidelines were sent to all hospitals providing pediatric medical care in Shanghai (50 in total). All patients discharged from these hospitals from January 1, 2013 through December 31, 2017 with an International Classification of Diseases (ICD) code for KD or mucocutaneous lymph node syndrome (ICD9 446.1 and ICD10 M30.3) were enrolled. Data were collected by pediatricians, including demographic information, clinical manifestations, prognosis, laboratory indices, treatment, and echocardiographic findings. The contents of the questionnaire were mildly modified, only with addition of erythema and induration at Bacillus Calmette-Guérin (BCG) sites, sites of valvular regurgitation, the presence of coronary stenosis and thrombosis, and some new laboratory indices including neutrophil count (NEUT), lymphocyte count (LYM), aspartate transaminase (AST), serum sodium (Na), and total bilirubin (TB). After all questionnaires were returned, two senior pediatric cardiologists were responsible for further verification. All eligible cases were entered into the KD database. This study was approved by the institutional review board of Children’s Hospital of Fudan University and requirements for informed consents were waived for this retrospective study.

Patients and definitions

KD was diagnosed according to the guidelines released by the Japanese Circulation Society.[12] The diagnostic criteria were as follows: (1) fever persisting for 5 days or longer (including cases in whom the fever has subsided before the 5th day in response to therapy); (2) bilateral conjunctival congestion; (3) polymorphous exanthema; (4) changes of lips and oral cavity: reddening of lips, strawberry tongue, diffuse injection of oral and pharyngeal mucosa; (5) changes of peripheral extremities: reddening of palms and soles in acute phase and membranous desquamation from fingertips in convalescent phase; and (6) acute non-purulent cervical lymphadenopathy. KD was diagnosed in the presence of at least 5 of the 6 principle symptoms. Incomplete KD, referring to KD patients with fewer than 5 principle symptoms, was diagnosed according to the algorithm in AHA guidelines.[1],[13] Between-hospital transfers during the same episode were identified and repeated cases were excluded. Patients who hospitalized only for further evaluation and treatment of cardiac sequelae (non-acute cases) were also excluded. IVIG resistance was defined as recurrent or persistent fever (>38°C) after 36 hours of completion of initial IVIG infusion.[1] Laboratory indices before initial IVIG infusion were recorded, including the highest values of C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), platelet count (PLT), white blood cell count (WBC), creatine kinase-muscle/brain (CK-MB), alanine aminotransferase (ALT), AST, and TB, and the lowest values of hemoglobin (HB), serum albumin (ALB), and Na if laboratory tests were performed more than once before initial IVIG. NEUT and LYM of the same blood test with highest WBC were also recorded. CAL, defined as coronary dilation or aneurysm, was evaluated using two-dimensional echocardiography. A patient was considered to have CAL if the luminal diameter of a coronary artery was >3.0 mm in children aged <5 years or >4.0 mm in those aged ≥5 years, or when the internal diameter of a segment was ≥1.5 times that of an adjacent segment.[14] A medium aneurysm was defined as an internal luminal diameter from 4 to 8 mm and a giant aneurysm was defined as an internal luminal diameter ≥8 mm. Coronary measurements of the most severe echocardiography were recorded if the measurement was performed more than once. Coronary thrombosis was assessed using echocardiography or angiography and coronary stenosis was assessed only using coronary angiography.

Statistical analysis

The incidence of KD was calculated by dividing the number of newly diagnosed KD patients <5 years old who inhabited Shanghai by the resident population of the corresponding age group in Shanghai. Census data were acquired from Shanghai Municipal Center for Disease Control and Prevention. Data were presented as mean (standard deviation) or median (interquartile range) for continuous variables, and count (percentage) for categorical variables. Continuous variables were compared between groups using unpaired Student’s t tests or Mann-Whitney U test. Categorical variables were compared using χ2 test or Fisher exact test. Univariate analysis was performed to explore potential risk factors for CAL, including age of onset, male sex, KD type, the dose and fever days of initial IVIG, and all 13 laboratory indices. Among them, CRP was divided into four groups based on quartiles due to the presence of truncated values. Multivariate logistic regressions were performed to identify risk factors independently associated with CAL.

RESULTS

Demographic data and prognosis

Fifty hospitals (100% response rate) returned the questionnaires by the deadline, with 4,533 cases reported. Among them, 37 non-acute cases and 44 repeated cases were excluded. Ultimately, 4,452 cases were enrolled, of which 2,824 (63.4%) were male and 1,628 (36.6%) were female. Male-to-female ratio was 1.7:1. Sixty patients (1.3%) recurred during this study period, of which 54 (1.2%) relapsed for the first time, 5 (0.1%) for the second, and 1 for the third. The average interval of the first, second, and third recurrence was 13.7 months (range: 0.5–60 months), 8.4 months (range: 1–21 months) and 32 months, respectively. No death was found in this survey.

Incidence of KD

The incidence of KD was 68.8–107.3 per 100,000 children aged <5 years from 2013 to 2017, with an average of 94.7 (112.7 for males and 75.4 for females; Table 1). It had increased substantially from 2013 to 2015, but remained stable in 2016 and 2017. Generally, the incidence of KD in Shanghai was on the rise since our first survey in 1998 (Figure 1).
Table 1.

Incidence of Kawasaki Disease in Shanghai, China, from 2013 through 2017 (per 100,000 children younger than 5 years)

YearMalesFemalesTotal



Number of KD casesTotal populationAnnual incidence (/100,000)Number of KD casesTotal populationAnnual incidence (/100,000)Number of KD casesTotal populationAnnual incidence (/100,000)
2013240256,33893.6103241,93742.6343498,27568.8
2014247244,986100.8154231,27166.6401476,25784.2
2015321262,719122.2216246,97887.5537509,697105.4
2016324274,484118.0247257,50595.9571531,989107.3
2017370293,919125.9225274,90481.8595568,823104.6
Total1,5021,332,446112.79451,252,59575.42,4472,585,04194.7

KD, Kawasaki disease.

Figure 1.

Incidence rate of Kawasaki disease in Shanghai, China from 1998 through 2017.

KD, Kawasaki disease.

Age of onset

Age at onset of KD ranged from 15 days to 14.0 years (median: 1.8 years), peaking at 1 year of age. A total of 464 cases (10.4%) occurred before 6 months old, 1,133 cases (25.4%) before 1 year old, 2,460 cases (55.3%) before 2 years old, and 3,985 cases (89.5%) before 5 years old. Only one patient, a 15-day-old boy, was a neonate. Males and females shared similar age distribution with the total population (Figure 2).
Figure 2.

Age distribution of onset of Kawasaki disease in Shanghai, China from 2013 through 2017.

Seasonal distribution

Similar to our previous surveys, KD occurred more frequently in spring (March to May; 1,137 cases, 25.5%) and summer (June to August; 1,235 cases, 27.7%), as compared with autumn (September to November; 1,045 cases, 23.5%) and winter (December to February; 1,035 cases, 23.2%). There was a clear peak in May, which fell to baseline in September after maintaining for 3 months (Figure 3). There were 1,713 cases (38.5%) occurring between May and August.
Figure 3.

Seasonal distribution of Kawasaki disease in Shanghai, China from 2013 through 2017.

Clinical manifestations

The most common manifestation was fever persisting for 5 days or longer (4,304 cases, 96.7%), followed by bilateral conjunctival congestion (3,933 cases, 88.3%), changes in the lips and oral cavity (3,757 cases, 84.4%), polymorphous exanthema (3,502 cases, 78.7%), cervical lymphadenopathy (3,256 cases, 73.1%), and changes in peripheral extremities (2,221 cases, 49.9%). Crissum desquamate (667 cases, 15.0%), and erythema and induration at BCG sites (191 cases, 4.3%) occurred less frequently. BCG reaction occurred more frequently in children under 1 year old (113/1,131 cases, 10.0%) than in those over 1 year old (78/3,321 cases, 2.3%; OR 4.62; 95% confidence interval [CI], 3.43–6.21; P < 0.001). Among the patients, 1,564 (35.1%) presented as incomplete KD, of which 1,020 (65.2%) had four principal signs, 352 (22.5%) had three, and 192 (12.3%) had two. Manifestations of other systems mainly included the involvement of respiratory system (1,291 cases, 29.0%), digestive system (681 cases, 15.3%), hematologic system (159 cases, 3.6%), urinary system (99 cases, 2.2%), skin (71 cases, 1.6%), joint (13 cases, 0.3%), and nervous system (33 cases, 0.7%).

Treatment

IVIG was administrated to 4,320 cases (97.0%; 6.9 ± 3.4 days, range: 2–55 days), including regimens of 2 g/kg once (2,232 cases, 51.7%), 1 g/kg for two consecutive days (1,671 cases, 38.7%), 1 g/kg once (394 cases, 9.1%) and irregular usage (23 cases, 0.5%). However, 362 (8.4%) patients failed to respond to the initial treatment. For secondary treatment (354 patients in total because of 8 patients missing further treatment information), a second dose of IVIG (314 cases, 88.7%) was administered most, followed by steroids (41 cases, 11.6%; 1–2 mg/kg, 68.3%) and infliximab (2 cases, 0.6%). Seventy-seven patients (21.8%) were not sensitive to secondary treatment. For third-line or subsequent treatment, steroids (63 cases, 81.8%; ≥10 mg/kg, 55.6%) were administered most, followed by IVIG (28 cases, 36.4%) and infliximab (3 cases, 3.9%). Fever eventually resolved in all patients.

Cardiovascular abnormalities

A total of 4,447 patients (99.9%) underwent echocardiography within 1 month of onset, of which 406 (9.1%) developed CAL. Except for 26 cases missing coronary measurements, the remaining 380 cases included 231 (5.2%) of dilation and small aneurysms, 118 (2.7%) of medium aneurysms, and 31 (0.7%) of giant aneurysms. Furthermore, the left main coronary artery (LMCA; 287 cases, 75.5%) was the most commonly involved, followed by the right coronary artery (RCA; 187 cases, 49.2%), the left anterior descending artery (LAD; 150 cases, 39.5%), and the left circumflex artery (LCX; 28 cases, 7.4%). Two hundred and ten cases (55.3%) involved one site, 89 cases (23.4%) involved two sites, 60 cases (15.8%) involved three sites, and 21 cases (5.5%) involved four sites simultaneously. Nine (0.2%) of 4,447 patients had coronary thrombosis, including the involvement of RCA in 6 cases, LMCA in 3 cases, LAD in 2 cases, and LCX in 2 cases. Five of the 9 patients had giant aneurysms and 4 had moderate aneurysms. Coronary stenosis occurred in 14 (0.3%) of 4,447 patients, including the involvement of RCA in 9 cases, LMCA in 7 cases, LAD in 7 cases, and LCX in 1 case. Three patients had severe stenosis, all accompanied with giant aneurysms. Other cardiovascular abnormalities included cardiomegaly (402 cases, 9.0%), cardiac dysfunction (19 cases, 0.4%), valvular regurgitation (653 cases, 14.7%), and pericardial effusion (408 cases, 9.2%). More specifically, 638 patients (97.7%) had mitral regurgitation (630 mild and 8 moderate cases) and 16 patients (2.5%) had moderate tricuspid regurgitation.

Risk factors for coronary artery lesions

The laboratory and clinical findings of KD patients with and without CAL were summarized in Table 2. Compared with the none-CAL group, the CAL group had higher levels of CRP, ESR, PLT, and LYM, and lower levels of HB, ALB, and CK-MB. Male sex, incomplete KD, and IVIG resistance were more common in the CAL group. The dose and fever days of initial IVIG also differed between the two groups. WBC, NEUT, ALT, AST, Na, TB, and age of onset were not significantly different.
Table 2.

Univariate analysis of relevant factors for coronary artery lesions

VariablesTotal cases(CAL/none CAL)CALNone CALP
CRP ≥105 mg/L, n (%)a387/4,022118 (30.5)1,004 (25.0)0.017
ESR, mm/h, mean (SD)358/3,82373.9 (34.1)70.3 (31.1)0.041
PLT, 1012/L, mean (SD)387/4,018465.5 (206.7)393.7 (163.9)<0.001
WBC, 109/L, mean (SD)388/4,02715.0 (7.4)14.7 (6.1)0.679
NEUT, 109/L, mean (SD)385/3,9289.8 (7.0)9.5 (5.5)0.310
LYM, 109/L, mean (SD)377/3,8833.9 (2.1)3.7 (2.0)0.032
HB, g/L, mean (SD)384/4,012106.4 (14.2)108.8 (12.4)<0.001
ALB, g/L, mean (SD)374/3,90233.7 (4.5)35.2 (4.2)<0.001
ALT, U/L, median (Q1, Q3)376/3,95625.0 (13.0, 50.5)22.0 (12.0, 51.0)0.175
AST, U/L, median (Q1, Q3)375/3,94227.0 (18.0, 42.5)26.0 (18.0, 39.0)0.277
CK-MB, IU/L, median (Q1, Q3)351/3,68616.0 (12.0, 21.0)18.0 (13.5, 24.0)<0.001
Na, mmol/L, mean (SD)366/3,845136.6 (3.9)136.2 (5.5)0.171
TB, µmol/L, median (Q1, Q3)366/3,8686.1 (3.9, 10.0)6.1 (4.1, 9.4)0.688
Age of onset, years, median (Q1, Q3)406/4,0411.8 (0.9, 3.5)1.8 (1.0, 3.2)0.611
Male, n (%)406/4,041291 (71.7)2,530 (62.6)<0.001
Incomplete KD, n (%)406/4,041181 (44.6)1,381 (34.2)<0.001
IVIG resistance, n (%)385/3,93163 (16.4)299 (7.6)<0.001
Fever days at initial IVIG, n (%)385/3,931  <0.001
 ≤4 days 45 (11.7)389 (9.9) 
 5–10 days 253 (65.7)3,328 (84.7) 
 >10 days 87 (22.6)214 (5.4) 
Initial IVIG treatment dose, n (%)385/3,931  <0.001
 2 g/kg × 1 197 (51.2)2,034 (51.7) 
 1 g/kg × 2 141 (36.6)1,527 (38.8) 
 1 g/kg × 1 35 (9.1)359 (9.1) 
 Irregular usage 12 (3.1)11 (0.3) 

ALB, serum albumin; ALT, alanine aminotransferase; AST, aspartate transaminase; CAL, coronary artery lesions; CK-MB, creatine kinase-muscle/brain; CRP, C-reactive protein; ESR, erythrocyte sedimentation rate; HB, hemoglobin; IVIG, intravenous immunoglobulin; KD, Kawasaki disease; LYM: lymphocyte count; Na, serum sodium; NEUT, neutrophil count; PLT, blood platelet count; Q1, quartile 1; Q3, quartile 3; SD, standard deviations; TB, total bilirubin; WBC, white blood cell count.

aCRP was converted to a dichotomous variable by the upper quartile due to the presence of truncated values.

ALB, serum albumin; ALT, alanine aminotransferase; AST, aspartate transaminase; CAL, coronary artery lesions; CK-MB, creatine kinase-muscle/brain; CRP, C-reactive protein; ESR, erythrocyte sedimentation rate; HB, hemoglobin; IVIG, intravenous immunoglobulin; KD, Kawasaki disease; LYM: lymphocyte count; Na, serum sodium; NEUT, neutrophil count; PLT, blood platelet count; Q1, quartile 1; Q3, quartile 3; SD, standard deviations; TB, total bilirubin; WBC, white blood cell count. aCRP was converted to a dichotomous variable by the upper quartile due to the presence of truncated values. Therefore, 12 significant variables from the univariate analysis, including CRP, ESR, PLT, LYM, HB, ALB, CK-MB, male sex, incomplete KD, the dose and fever days of initial IVIG, and IVIG resistance, were included in the multivariate analysis to identify risk factors for CAL. It was shown that a higher platelet level, a lower albumin level, male sex, incomplete KD, IVIG resistance, and receiving initial IVIG within 4 days or over 10 days, were independent risk factors for CAL (Table 3).
Table 3.

Multivariate logistic regression analysis of risk factors for coronary artery lesions (3,627 cases)

VariablesOdds Ratio95% Confidence IntervalP
PLT, 1012/L1.0021.001–1.003<0.001
ALB, g/L0.930.90–0.95<0.001
Male sex1.641.24–2.15<0.001
Incomplete KD1.631.26–2.09<0.001
IVIG resistance2.441.72–3.46<0.001
Fever days at initial IVIG  <0.001
 ≤4 days1.621.11–2.440.014
 5–10 daysRef.Ref. 
 >10 days4.443.14–6.28<0.001

ALB, serum albumin; IVIG, intravenous immunoglobulin; KD, Kawasaki disease; PLT, blood platelet count.

ALB, serum albumin; IVIG, intravenous immunoglobulin; KD, Kawasaki disease; PLT, blood platelet count.

DISCUSSION

The incidence of KD in Shanghai was on the rise since 1998, similar to the other Asian countries and regions.[3]–[5],[7] The highest ever record in Shanghai was 107.3 per 100,000 children aged <5 years in 2016, which was still much lower than that in Japan in 2015[3] (330.2 per 100,000 children aged <5 years) and in South Korea in 2013[4] (194.9 per 100,000 children aged <5 years), but was for the first time higher than that in Taiwan in 2010[5] (82.8 per 100,000 children aged <5 years). The incidence of KD in Shanghai remained stable in 2016 and 2017. It requires continuous surveillance, whether or not a 3-year plateau period implies no further increase. Compared with the high prevalence of fever and five principal symptoms, crissum desquamate (15.0%) and erythema and induration at BCG site (4.3%) occurred less frequently. Not all patients had been checked for BCG site, which might be a reason for the lower rate of BCG site reaction in our study. Changes at the BCG site is increasingly recognized as a specific diagnostic tool for KD in Japan, especially in infants with incomplete KD.[15],[16] In our study, we also found that BCG site reaction was more prevalent in infants (59.2% for age <1 year). In addition, of 191 patients with positive BCG site reaction, 151 (79.1%) had polymorphous exanthema whereas 40 (20.9%) did not have. Considering the high specificity of BCG reaction in KD patients, we suggest that BCG reaction be added as a supplementary criterion for polymorphous exanthema when diagnosing KD. The proportion of IVIG administration increased from 71.8% to 97.0% since our first survey in 1998.[6],[11],[17] In addition, 90.3% of patients received 2 g/kg IVIG as initial treatment and 93.0% received IVIG within 10 days, indicating the standard treatment has been universally adopted in Shanghai. The proportion of IVIG resistance reported so far in Shanghai was 4.9% in 2008–2012[6] and 8.4% in 2013–2017. The only two reports were not enough to show the trend in our view. Therefore, continuous surveillance is needed. However, the proportion of IVIG resistance was lower than that in Japan[3] (17.8%), South Korea[4] (11.8%), and other reported countries (16.3% in the United States,[18] 9–14% in Canada,[19] 16.5% in Australia,[20] 26.8% in German,[21] and 23.1% in the Netherlands[22]), which may partially be attributed to genetic factors. In addition, studies have shown that administration of IVIG with chemical modifications (such as β-propiolactone and enzyme digestion) led to a higher incidence of IVIG nonresponse than with other manufacturing techniques.[23],[24] The IVIG used in Shanghai were all pH4 and prepared with acidification rather than chemical modifications, which may also explain the lower incidence of IVIG nonresponse. Given that the mechanism of IVIG action and IVIG resistance remains unclear, it is really difficult to explain the reasons for these discrepancies. More genetic and basic research is needed to clarify it. Fortunately, the proportion of CAL has substantially decreased from 19.8% to 9.1% since 1998,[11] possibly attributed to the increasing proportion of IVIG administration and early treatment during the acute phase. Similarly, the proportion of coronary dilation and aneurysm showed a decreasing trend in Japan[3],[25] (from 10.0% to 6.5%, 2007–2016) and in South Korea[4],[26] (from 18.5% to 12.5%, 2006–2014). However, the proportion of both medium aneurysms and giant aneurysms lack a significant decrease in Shanghai. In this survey, severe coronary stenosis (all 3 cases) and thrombosis (5 of 9 cases) mainly occurred on the basis of giant aneurysms, increasing the risk of myocardial ischemia and sudden death. Therefore, further prevention of the development of giant aneurysms remains the top priority in the future. Previous frequently reported risk factors for CAL, such as a higher platelet level,[27],[28] a lower albumin level,[28],[29] male sex,[6],[28]–[30] IVIG resistance[6],[29],[31] and receiving initial IVIG beyond 10 days,[6],[27],[28],[32] were also demonstrated in our findings. As for incomplete KD, study results were contradictory even in multivariate analyses. One study showed that incomplete KD was more common in the CAL group due to delayed diagnosis rather than the low number of presenting symptoms.[33] However, consistent with other two studies,[31],[34] our study identified incomplete KD itself as an independent risk factor for CAL, despite the presence of delayed IVIG treatment. The last risk factor, receiving initial IVIG within 4 days, was identified beyond expectations. Nomura et al reported that KD patients treated with IVIG before 5 days had a higher incidence of aneurysms than those treated at the fifth day or after (15.2% vs 1.3%; P = 0.004).[35] We also found that patients treated within 4 days had a higher incidence of IVIG resistance (21.4% vs 9.1%; P < 0.001), a younger age of onset (1.4 vs 1.8 years; P < 0.001), higher levels of CRP (71 vs 62 mg/L; P = 0.001), ALT (28 vs 22 U/L; P < 0.001), AST (29 vs 26 U/L; P < 0.001) and TB (7.3 vs 6.0 µmol/L; P < 0.001), and lower levels of Na (135.7 vs 136.2 mmol/L; P < 0.001). Considering these, although infusion of IVIG within 4 days was identified as an independent risk factor for CAL in our analysis, it should be interpreted as a sign of severity of KD, which is consistent with Nomura’s views.[35] Therefore, KD patients diagnosed within 4 days should be treated as early as possible, and may need more aggressive treatment (such as combination with steroids or infliximab). Further prospective studies are needed to confirm this. There were a couple of limitations in our current study. First, Japanese diagnostic criteria for CAL could lead to underdiagnosis due to the failure of taking patients’ size into account.[36] Z score, a normalization of coronary dimensions for body surface area, maybe more suitable to evaluate CAL.[37],[38] Since Z score has not been widely implemented in Shanghai, we still use coronary diameters to evaluate CAL in this survey and the proportion of CAL could be underestimated, although it is encouraging to see its decline in the current survey. Second, epidemiological surveys in Shanghai could to some extent but not completely reflect epidemiologic features of KD in China. We hope to conduct a nationwide sample survey in the future. In conclusion, the incidence of KD in Shanghai has substantially increased over 20 years. Although the occurrence of CAL has substantially decreased, the proportion of giant aneurysms has remained the same. Higher platelet levels, lower albumin levels, male sex, incomplete KD, IVIG resistance, and receiving initial IVIG within 4 days or beyond 10 days, were independent risk factors for CAL. Continuous epidemiological investigations are still necessary.
  37 in total

1.  Kawasaki Disease in Germany: A Prospective, Population-based Study Adjusted for Underreporting.

Authors:  André Jakob; Jane Whelan; Matthaeus Kordecki; Reinhard Berner; Brigitte Stiller; Raoul Arnold; Rudiger von Kries; Elena Neumann; Nicholas Roubinis; Mirna Robert; Jochen Grohmann; René Höhn; Markus Hufnagel
Journal:  Pediatr Infect Dis J       Date:  2016-02       Impact factor: 2.129

2.  Predictive risk factors for coronary artery abnormalities in Kawasaki disease.

Authors:  Taeyeun Kim; Wooksun Choi; Chan-Wook Woo; Byungmin Choi; Junghwa Lee; Kwangchul Lee; Changsung Son; Joowon Lee
Journal:  Eur J Pediatr       Date:  2006-10-11       Impact factor: 3.183

3.  A new scoring system to predict Kawasaki disease with coronary artery lesions.

Authors:  Wang Hua; Feiyue Ma; Ying Wang; Songling Fu; Wei Wang; Chunhong Xie; Yiying Zhang; Fangqi Gong
Journal:  Clin Rheumatol       Date:  2018-12-06       Impact factor: 2.980

4.  Clinical responses of patients with Kawasaki disease to different brands of intravenous immunoglobulin.

Authors:  Ming-Han Tsai; Yhu-Chering Huang; Meng-Hsiu Yen; Chung-Chen Li; Cheng-Hsun Chiu; Pen-Yi Lin; Tzou-Yien Lin; Luan-Yin Chang
Journal:  J Pediatr       Date:  2006-01       Impact factor: 4.406

Review 5.  Diagnosis, Treatment, and Long-Term Management of Kawasaki Disease: A Scientific Statement for Health Professionals From the American Heart Association.

Authors:  Brian W McCrindle; Anne H Rowley; Jane W Newburger; Jane C Burns; Anne F Bolger; Michael Gewitz; Annette L Baker; Mary Anne Jackson; Masato Takahashi; Pinak B Shah; Tohru Kobayashi; Mei-Hwan Wu; Tsutomu T Saji; Elfriede Pahl
Journal:  Circulation       Date:  2017-03-29       Impact factor: 29.690

6.  Nationwide epidemiologic survey of Kawasaki disease in Japan, 2015-2016.

Authors:  Nobuko Makino; Yosikazu Nakamura; Mayumi Yashiro; Koki Kosami; Yuri Matsubara; Ryusuke Ae; Yasuko Aoyama; Hiroshi Yanagawa
Journal:  Pediatr Int       Date:  2019-04-16       Impact factor: 1.524

7.  Erythema and induration of the Bacillus Calmette-Guérin site for diagnosing Kawasaki disease.

Authors:  Ann Loh; Phek Hui Jade Kua; Ze Lei Tan
Journal:  Singapore Med J       Date:  2018-07-16       Impact factor: 1.858

8.  Delayed intravenous immunoglobulin treatment increased the risk of coronary artery lesions in children with Kawasaki disease at different status.

Authors:  Huixian Qiu; Yuee He; Xing Rong; Yue Ren; Lulu Pan; Maoping Chu; Rongzhou Wu; Hongying Shi
Journal:  Postgrad Med       Date:  2018-05-10       Impact factor: 3.840

9.  Epidemiologic features of Kawasaki disease in Japan: results of the 2007-2008 nationwide survey.

Authors:  Yosikazu Nakamura; Mayumi Yashiro; Ritei Uehara; Atsuko Sadakane; Izumi Chihara; Yasuko Aoyama; Kazuhiko Kotani; Hiroshi Yanagawa
Journal:  J Epidemiol       Date:  2010-06-05       Impact factor: 3.211

10.  Epidemiologic features of Kawasaki disease in acute stages in Taiwan, 1997-2010: effect of different case definitions in claims data analysis.

Authors:  Ming-Chih Lin; Mei-Shu Lai; Sheng-Ling Jan; Yun-Ching Fu
Journal:  J Chin Med Assoc       Date:  2015-01-28       Impact factor: 2.743

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1.  [Pediatric expert consensus on the application of aspirin in Kawasaki disease].

Authors: 
Journal:  Zhongguo Dang Dai Er Ke Za Zhi       Date:  2022-06-15

2.  Melatonin alleviates vascular endothelial cell damage by regulating an autophagy-apoptosis axis in Kawasaki disease.

Authors:  Yuanzheng Zheng; Saihua Huang; Jialing Zhang; Jia Hou; Fang Wu; Wenji Wang; Xiao Han; Yonghao Gui
Journal:  Cell Prolif       Date:  2022-05-17       Impact factor: 8.755

3.  Is Short-Term Exposure to PM2.5 Relevant to Childhood Kawasaki Disease?

Authors:  Jongmin Oh; Ji Hyen Lee; Eunji Kim; Soontae Kim; Hae Soon Kim; Eunhee Ha
Journal:  Int J Environ Res Public Health       Date:  2021-01-21       Impact factor: 3.390

4.  Ambient Air Pollution and Kawasaki Disease in Korean Children: A Study of the National Health Insurance Claim Data.

Authors:  Dayoon Kwon; Young June Choe; Sun-Young Kim; Byung Chul Chun; Seung-Ah Choe
Journal:  J Am Heart Assoc       Date:  2022-04-27       Impact factor: 6.106

5.  A New Scoring System for Prediction of Intravenous Immunoglobulin Resistance of Kawasaki Disease in Infants Under 1-Year Old.

Authors:  Shu Wu; Yuan Long; Selena Chen; Yaqian Huang; Ying Liao; Yan Sun; Qingyou Zhang; Chunyu Zhang; Hui Yan; Jianguang Qi; Xueqin Liu; Yonghong Chen; Yong Zhang; Junbao Du
Journal:  Front Pediatr       Date:  2019-12-11       Impact factor: 3.418

Review 6.  Correct identification of incomplete Kawasaki disease.

Authors:  Tianhua Li; Jie Feng; Na Li; Tingting Liu
Journal:  J Int Med Res       Date:  2021-03       Impact factor: 1.671

7.  The Most Common Clinical Features of Kawasaki Disease Patients in King Abdulaziz Medical City.

Authors:  Khalid Talal Alghamdi; Rahaf Abdulmalik Waggass; Syed Sameer Aga; Abdulaziz Ahmed Alrohaili; Ali Hassan Alaidroos; Mohammed Dakhilallah Alghamdi; Mohannd Khalid Algamdi; Ashwaq Talal Alghamdi
Journal:  Cureus       Date:  2021-05-19

8.  Neutropenia Is Not Associated With the Outcomes in Patients With Kawasaki Disease.

Authors:  Yunjia Tang; Miao Gang; Weiguo Qian; Jin Ma; Qiuqin Xu; Haitao Lv
Journal:  Front Pediatr       Date:  2021-06-04       Impact factor: 3.418

Review 9.  What Lies Ahead for Young Hearts in the 21st Century - Is It Double Trouble of Acute Rheumatic Fever and Kawasaki Disease in Developing Countries?

Authors:  Aaqib Zaffar Banday; Sanjib Mondal; Prabal Barman; Archan Sil; Rajni Kumrah; Pandiarajan Vignesh; Surjit Singh
Journal:  Front Cardiovasc Med       Date:  2021-06-24

10.  Factors affecting the duration of coronary artery lesions in patients with the Kawasaki disease: a retrospective cohort study.

Authors:  Xuting Zhang; Yuee He; Yiping Shao; Biyao Hang; Zhipeng Xu; Maoping Chu
Journal:  Pediatr Rheumatol Online J       Date:  2021-06-26       Impact factor: 3.054

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