Abstract
Objectives
This study aimed to assess the clinical characteristics, treatment and outcomes of the multisystem inflammatory syndrome in children (MIS-C) following COVID-19 in five different geographical regions of Iran.
Methods
In this multicenter observational study, patients <21 years were included between March 2020 and October 2021. By Disease Control and Prevention (CDC) checklist, demographic characteristics, comorbidities, clinical signs and symptoms, laboratory and radiology findings, and treatment were collected. Statistical analysis was using Chi-square and t-test in STATA14.
Results
In total 225 patients with median age of 55 (26–96) months were included that 59.56% boys. 57.33% were admitted to the PICU with a median of 7 days (4–10). 95.56% of patients were discharged with recovery and the rest died. All of the patients in our study were included based on the MIS-C criteria. However, some patients had Kawasaki symptoms, so we compared the clinical and epidemiological characteristics of the two groups. Conjunctival injection, cervical lymphadenopathy>1.5 cm diameter, and strawberry tongue in Kawasaki-like MIS-C patients were higher than of MIS-C patients, and this difference was significant(p<0.001). The most common comorbidity was obesity (24.86%). Most patients tested for COVID-19 and about 60% of the patients had a positive test by serology or reverse transcription-polymerase chain reaction (RT-PCR). Gastrointestinal (88.89%) and hematologic signs (84.44%) were most common. Most drugs used in patients were IVIG and steroids. 88.07% and 61.29% of the patients had at least one problem in echocardiography and lung CT, respectively.
Conclusions
The best outcome was seen in patients who were treated with both IVIG and steroids on the first days of admission. Myocarditis was common in two groups of patients. According to most patients had echocardiography abnormal, screening of heart function is recommended for patients.
Introduction
Worldwide, the urgent dissemination of a novel entity termed severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) has been stated as one of the most challenging health issues [1]. Initially, coronavirus disease 2019 (COVID-19) exhibited clinically various presentations ranging from asymptomatic manifestation to multiple organ dysfunction in critically ill patients [2]. In the spring of 2020, an unexpected phenomenon illustrating a hyperinflammatory syndrome with multi-organ involvement has been identified in clusters of children, possibly associated with COVID-19 [3, 4]. Afterward, as similar cases subsequently appeared globally, the Centers for Disease Control and Prevention (CDC) and World Health Organization (WHO) reached a consensus to announce this potentially life-threatening circumstance during COVID-19 as a multisystem inflammatory syndrome in children (MIS-C) [5]. As of October 2021, there have been approximately 5,217 cases of MIS-C, including 46 deaths reported in the United States [6]. Diagnostic criteria for MIS-C in critically ill patients necessitate fever, elevated inflammatory markers, and involvement of at least two organs, with evidence of COVID-19 infection or exposure within four weeks before symptoms onset, and exclusion of other obvious etiologies [7]. MIS-C may have similarities with Kawasaki Disease (KD), including mucocutaneous involvement, conjunctivitis, lymphadenopathy, and elevation of inflammatory markers. Since the emergence of MIS-C, debates regarding distinguishing between MIS-C and KD are ongoing among specialists globally [8].
Nevertheless, some distinct clinical features correlated with MIS-C make a considerable difference from KD, such as prominent gastrointestinal symptoms, lymphocytopenia, and prevalent cardiovascular implications that demanded the urgent multidisciplinary management in MIS-C [9]. The exact underlying pathological mechanism of MIS-C is not still elucidated.
Regarding the COVID-19 variants that continue to emerge, the severity and outcomes of MIS-C can be significantly affected. Geographic, genomic, and ethnic distributions of children with MIS-C need to be considered to identify the exact diagnostic criteria and optimal treatment guidelines. Further comprehensive studies are required to improve the insights into MIS-C manifestations, treatments, outcomes, and prevention in children. Hence, we performed this multicenter observational study to assess the spectrum of clinical characteristics and outcomes of MIS-C in children following COVID-19 in five referral hospitals in Iran during 2020–2021.
Materials and methods
The multicenter observational study included children <21 years who fulfilled the MIS-C criteria according to the CDC checklist [10]. The patients were hospitalized between March 2020 and September 2021 in five referral hospitals in Iran; including Ali Asghar children’s hospital of Tehran, Namazi hospital of Shiraz, Booali Sina hospital of Sari, Children’s hospital of Bandar Abbas, and Shafizadeh hospital of Babol. Patients with MIS-C were identified at each center by subspecialty physicians. Positive tests for current SARS-CoV-2 infection or exposure to COVID-19 case within four weeks prior to symptoms onset are a principal component of the CDC criteria for MIS-C. With regards to that, a nasopharyngeal reverse transcription-polymerase chain reaction (RT-PCR) assay was performed for most of the suspected SARS-CoV-2 patients. Furthermore, an enzyme-linked immunosorbent assay (ELISA) was done for identifying serum levels of anti-SARS-CoV-2 immunoglobulin G and M (Pishtaz Teb Kit). Since the beginning of the MIS-C emergence, adequate information about MIS-C was lacking, cases associated with multi-organ involvement manifestations with an epidemiological link to COVID-19 were considered suspected and included in our study without the requirement of a positive COVID-19 test.
Data collection and analysis
Medical records were extracted from admission to discharge by skilled staff onto a checklist. Data concerning patient demographic characteristics, comorbidities, clinical signs and symptoms on admission and during hospitalization, laboratory assay results, radiology findings (Echocardiogram, Abdominal and Chest imaging), complications, diagnostic tests (SARS-CoV-2 PCR and serology tests), treatments and need for pediatric intensive care unit (PICU) admission were recorded.
Based on the CDC case definition, the following criteria were considered to define MIS-C patients: 1) age<21 years; 2) fever≥ 38.0°C (100,4°F) for >24 hours or report of subjective fever lasting> 24 hours; 3) a history of current SARS-CoV-2 infection by positive RT-PCR, serology, or antigen test or contact with a suspected or confirmed COVID-19 case within 4 weeks prior to the onset of symptoms; 4) signs and symptoms of multisystem (≥2) organ involvement including: cardiovascular (e.g. shock, elevated troponin), renal, gastrointestinal (e.g. abdominal pain, vomiting), hematologic (e.g. coagulopathy), neurologic (e.g. seizure, meningitis) and respiratory (e.g. pneumonia, pulmonary embolism); 5) positive inflammatory markers including elevated CRP, erythrocyte sedimentation rate (ESR), D-dimers, ferritin, interleukin 6 (IL-6), elevated neutrophils, lymphocytopenia, low albumin; 6) no apparent plausible diagnosis [10].
According to the CDC checklist, if the patient has one of the results of coronary artery aneurysms, including coronary artery dilation, cardiac dysfunction, mitral regulation (MR), tricuspid regulation (TR), pulmonary valve insufficiency, pericardial dysfunction, and low ejection fraction (EF) < 55%, were considered as abnormal results in echocardiography. Abdominal sonography was considered abnormal if the patient had one of the following criteria: free fluid, mesenteric lymphadenopathy or splenomegaly. Moreover, chest CT scans were reported as abnormal if one of the following were present: Ground-glass Opacity (GGO), consolidation, pneumonia, pleural effusion, or atelectasis.
Based on the WHO child growth standards, obesity was considered as the body mass index(BMI) at or over the 95th percentile for age and sex [9]. BMI was calculated as weight in kilograms divided by height in meters squared.
Ethics statement
This study was approved by the ethics committee of Mazandaran University of Medical Sciences (IR.MAZUMS.REC.1400.10565). Written consent was obtained from the parents or guardians of all patients. In addition, we got verbal consent from the 10 years and older patients.
Results were represented as mean ± standard deviation (SD) or median with interquartile range (IQR) for continuous variables and frequency with percentage for categorical variables. All of the patients met the MIS-C criteria; however, some patients had Kawasaki symptoms. Based on clinical manifestations and laboratory markers, the patients were divided into two groups: Kawasaki-like MIS-C and MIS-C. Kawasaki-like MIS-C is a child who meets the criteria for complete or incomplete KD with positive RT-PCR or increased IgM, IgG COVID-19.
Comparisons were assessed using the Chi-square and t-test (Mann-Whitney test) based on the data distribution. Statistical analyses were conducted using STATA14. A p-value less than 0.05 was considered significant.
Results
Study population and characteristics
A total of 225 patients were included in the study; 59.6% boys and 40.4% girls. The sex ratio of patients was 1.47 (134 males, 91 females). The median age of all patients was 55 months (26–96). Patients were included from Shafizadeh Children’s hospital (30.7%), Booali Sina hospital (27.6%), Ali Asghar hospital (17.8%), Namazi hospital (12.9%), and Bandar Abbas Children’s hospital (11.1%), respectively. 129/225 (57.3%) patients were admitted to the PICU with a median length of stay of seven days (4–10). Two hundred fifteen patients (95.6%) were discharged from the hospital with complete or partial recovery, and ten patients (4.44%) died (Table 1).
Table 1. The baseline characteristics and clinical outcome in MIS-C and Kawasaki- like MIS-C.
| Characteristic | Total(N = 225) | Kawasaki- like MIS-C | MIS-C | p-value |
|---|---|---|---|---|
| (n = 58) | (n = 167) | |||
| Age in month, median (IQR) | 55(26–96) | 56(32–89) | 54(24–96) | 0.94 |
| Gender, n (%) | ||||
| Male | 134(59.6) | 38(65.5) | 96(57.5) | 0.28 |
| Female | 91(40.4) | 20(34.5) | 71(42.5) | |
| Comorbid a | ||||
| Yes | 73(32.4) | 15(25.9) | 58(34.7) | 0.21 |
| No | 152(67.6) | 43(74.1) | 109(65.3) | |
| Type of comorbid a | ||||
| Obesity b | 44(24.9) | 7(14.3) | 37(28.9) | 0.04 |
| Seizures | 17(7.6) | 4(6.90) | 13(7.78) | 0.82 |
| Chronic lung disease | 12(5.33) | 5(8.62) | 7(4.19) | 0.19 |
| Immunosuppressive disorder malignancy | 3(1.33) | 0 | 3(1.80) | 0.57 |
| Type1 diabetes | 3(1.33) | 0 | 3(1.80) | 0.57 |
| G6PD insufficient | 16(7.11) | 5(8.62) | 11(6.59) | 0.60 |
| Hospital stay(days), median (IQR) | 9(7–13) | 9(7–12) | 9(7–13) | 0.82 |
| PICU admission | 129(57.3) | 33(56.9) | 96(57.5) | 0.93 |
| ICU stay(days), median (IQR) | 7(4–10) | 8(6–11) | 7(4–9.5) | 0.05 |
| Outcome | ||||
| Survived | 215(95·6) | 58(100) | 157(94.0) | 0.06 |
| Died | 10(4·44) | 0 | 10(5.99) |
a A patient may have at least one type of comorbid.
b The number of available patient height and weight information for calculating body mass was 177 patients.
Based on their clinical manifestations and laboratory markers, the patients were divided into two categories: Kawasaki-like MIS-C (n = 58) and MIS-C (n = 167).
The mean age of patients in MIS-C group was higher than Kawasaki-like MIS-C patients, [64 ± 48 months (range 2–180) compared to 59 ± 34 months (range 9–125)]. Regarding the comorbid variable, 34.7% of MIS-C patients had at least one type of comorbid disease compared to 25.9% of Kawasaki-like MIS-C. Obesity was the most common comorbid in both groups. This difference was statistically significant (p 0.044).
The median number of hospital stay in both groups was nine days. The median number of ICU hospitalization days was eight days in Kawasaki like MIS-C and seven days in MIS-C patients. This difference was marginally significant (p 0.059).
Clinical signs and symptoms
All patients had fever at the time of admission. The median duration of fever was eight days (6–10) with statistically significant difference between the two groups of patients (p 0.002). The most common signs and symptoms were gastrointestinal 88.9%, hematologic 84.4% and skin 61.3% of the patents. There was a significant difference between cardiac and skin symptoms, conjunctival injection, cervical lymphadenopathy, and strawberry tongue between the two groups of patients (p <0.05) (Table 2).
Table 2. Clinical signs and symptoms in Kawasaki- like MIS-C and MIS-C patients.
| Clinical Signs and Symptoms | Total(N = 225) | Kawasaki- like MIS-C | MIS-C | p-value |
|---|---|---|---|---|
| (n = 58) | (n = 167) | |||
| Fever | 225(100) | 58(100) | 167(100) | |
| Duration of fever(days), median (IQR) | 8(6–10) | 8(7–10) | 7(5–10) | 0.001 |
| Cardiac | ||||
| Yes | 109(48.4) | 20(34.5) | 89(53.3) | 0.01 |
| No | 116(51.6) | 38(65.5) | 78(46.7) | |
| Renal | ||||
| Yes | 83(36.9) | 24(41.4) | 59(35.3) | 0.41 |
| No | 142(63.1) | 34(58.6) | 108(64.7) | |
| Respiratory | ||||
| Yes | 121(53.8) | 32(55.2) | 89(53.3) | 0.80 |
| No | 104(46.2) | 26(44.4) | 78(46.7) | |
| Hematologic | ||||
| Yes | 190(84.4) | 48(82.7) | 142(85.0) | 0.68 |
| No | 35(15.6) | 10(17.2) | 25(14.9) | |
| Gastrointestinal | ||||
| Yes | 200(88.9) | 53(91.4) | 147(88.0) | 0.48 |
| No | 25(11.1) | 5(8.6) | 20(11.9) | |
| Skin | ||||
| Yes | 138(61.3) | 53(91.4) | 85(50.9) | <0.001 |
| No | 87(38.7) | 5(8.62) | 82(49.1) | |
| Neurologic | ||||
| Yes | 63(28) | 15(25.9) | 48(28.7) | 0.67 |
| No | 162(72) | 43(74.1) | 119(71.3) | |
| Other | ||||
| Conjunctival injection | 88(39.1) | 46(79.3) | 42(25.2) | <0.001 |
| Cervical lymphadenopathy >1.5 cm diameter | 21(9.33) | 13(22.4) | 8(4.8) | <0.001 |
| Strawberry tongue | 16(7.11) | 15(25.9) | 1(0.60) | <0.001 |
Complications
The most common complications were myocarditis in 35.1%, hypotension in 26.7%, and shock in 21.8%. There was a significant difference in hypotension, shock, arrhythmia, pneumonia, and congestive heart failure in Kawasaki- like MIS-C and MIS-C patients (p <0.05) (Table 3).
Table 3. Complication in Kawasaki- like MIS-c and MIS-c patients.
| Complication | Total(N = 225) | Kawasaki- like MIS-C | MIS-C | p-value |
|---|---|---|---|---|
| (n = 58) | (n = 167) | |||
| Myocarditis | 79(35.1) | 22(37.9) | 57(34.1) | 0.60 |
| Hypotension | 60(26.7) | 5(8.62) | 55(32.9) | <0.001 |
| Shock | 49(21.8) | 3(5.17) | 46(27.5) | <0.001 |
| Arrhythmia | 45(20) | 19(32.7) | 26(15.6) | 0.005 |
| Pneumonia | 45(20) | 4(6.90) | 41(24.5) | 0.004 |
| Congestive heart failure | 21(9.33) | 0 | 21(12.6) | 0.003 |
| ARDSa | 7(3.11) | 0 | 7(4.19) | 0.19 |
| Pericarditis | 6(2.67) | 0 | 6(3.59) | 0.34 |
a Acute respiratory distress syndrome.
Treatment
The most commonly prescribed medication were IVIG, steroids, antiplatelet and anticoagulant, with 94.2%, 77.8%, 68.4% and 54.7%, respectively. There was a statistically significant difference between the drugs used in the two groups of patients, including steroids, antiplatelet, antibiotic, antiviral, second IVIG, and high flow nasal cannula (P <0.05). Among the drugs steroids and IVIG were marginally significant in two groups of patients (p 0.054) (Table 4).
Table 4. Treatment in Kawasaki- like MIS-C and MIS-C patients.
| Treatment | Total(N = 225) | Kawasaki- like MIS-C | MIS-C | p-value |
|---|---|---|---|---|
| (n = 58) | (n = 167) | |||
| IVIG | 211(94.2) | 57(98.3) | 154(92.8) | 0.12 |
| Steroids | 175(77.8) | 37(63.8) | 138(82.6) | 0.003 |
| Steroids and IVIG | 161(71.9) | 36(62.1) | 125(75.3) | 0.05 |
| Antiplatelet | 154(68.4) | 49(84.5) | 105(62.8) | 0.002 |
| Anticoagulation | 123(54.7) | 27(46.5) | 96(57.5) | 0.15 |
| Antibiotics | 123(54.7) | 50(86.2) | 73(43.7) | <0.001 |
| Vasoactive medication | 100(44.4) | 26(44.8) | 74(44.3) | 0.94 |
| Low flow nasal cannula | 90(40) | 21(36.2) | 69(41.3) | 0.49 |
| Second IVIG | 38(16.9) | 4(6.90) | 34(20.4) | 0.01 |
| Antivirals | 38(16.9) | 20(34.5) | 18(10.8) | <0.001 |
| Intubation | 22(9.78) | 2(3.45) | 20(11.9) | 0.06 |
| Mechanical ventilation | 21(9.33) | 2(3.45) | 19(11.4) | 0.07 |
| High flow nasal cannula | 13(5.78) | 0 | 13(7.78) | 0.02 |
| Immune modulators | 12(5.33) | 1(1.72) | 11(6.59) | 0.15 |
| Noninvasive ventilation | 5(2.22) | 0 | 5(2.99) | 0.33 |
| Dialysis | 2(0.89) | 0 | 2(1.20) | 1 |
Imaging
Echocardiography was performed in 218/225 patients (96.9%), and at least one problem was detected in 88.1%. The most common complications were MR (88.7%), TR (64.1%), and cardiac dysfunction (51.6%), respectively. One hundred nine patients had both MR and TR. There was a statistically significant difference in TR, coronary artery dilatation, pulmonary valve insufficiency and low EF in these two groups (p <0.05), being more commonly in the MIS-C group. In this study, 146 patients (64.9%) underwent an abdominal ultrasound, and 54.1% of these patients had problems and the most common was free fluid (76.3%). A significant difference was in the presence of mesenteric lymphadenopathy between these two groups (p<0.05). Only 155 patients (68.9%) had spiral chest CT scans, and 61.3% of them had abnormal findings, the most commonly being ground-glass opacity and consolidation in 84.2% (Table 5).
Table 5. Characteristic of imaging in Kawasaki- like MIS-C and MIS-C patients.
| Total(N = 225) | Kawasaki- like MIS-C | MIS-C | p-value | |
|---|---|---|---|---|
| (n = 58) | (n = 167) | |||
| Echocardiography a | ||||
| Yes | 192(88.1) | 52(91.2) | 140(86.9) | 0·39 |
| No | 26(11.9) | 5(8.77) | 21(13.0) | |
| Mitral Regulation | 157(81.8) | 45(86.5) | 112(80) | 0.40 |
| Tricuspid regurgitation | 123(64.1) | 41(78.9) | 82(58.6) | 0.009 |
| Cardiac dysfunction | 99(51.6) | 24(46.2) | 75(53.6) | 0.31 |
| Ventricular dysfunction | 93(48.4) | 22(42.3) | 71(50.7) | 0.30 |
| Coronary artery dilatation | 62(32.3) | 25(48.1) | 37(26.4) | 0.004 |
| Pericardial Effusion | 60(31.3) | 20(38.5) | 40(28.6) | 0.18 |
| Brightness & PVB | 54(28.1) | 19(36.5) | 35(25) | 0.11 |
| Lack of tapering | 54(28.1) | 22(42.3) | 32(22.9) | 0.008 |
| Low EF | 51(26.6) | 21(40.4) | 30(21.4) | 0.008 |
| Pulmonary valve insufficiency | 36(18.8) | 19(36.6) | 17(12.1) | <0.001 |
| Coronary artery aneurysms | 2(1.04) | 1(1.92) | 1(0.71) | 0.46 |
| Abdominal Sonography a | ||||
| Yes | 79(54.1) | 24(63.2) | 55(50.9) | 0.19 |
| No | 67(45.9) | 14(36.2) | 53(49.1) | |
| Free fluid | 61(76.3) | 21(84) | 40(72.7) | 0.27 |
| Mesenteric lymphadenopathy | 34(42.5) | 6(25) | 28(50) | 0.03 |
| Splenomegaly | 6(7.50) | 1(4.17) | 5(8.93) | 0.66 |
| Spiral Chest CT scan a | ||||
| Yes | 95(61.3) | 21(70) | 74(59.2) | 0.27 |
| No | 60(38.7) | 9(30) | 51(40·8) | |
| Ground-glass Opacity (GGO) and Consolidation | 80(84.2) | 19(90.5) | 61(82.4) | 0.37 |
| Pleural Effusion | 40(42.1) | 10(47.6) | 30(40.5) | 0.56 |
| Atelectasis | 21(22.3) | 2(9.52) | 19(26.0) | 0.11 |
a A patient may have at least one type of abnormal results so; the total percentage is greater than 100.
Most patients had been tested for COVID-19, and 60% had a positive test by serology or RT-PCR. Moreover, 76.8% of patients had exposure to confirmed COVID-19 cases. Thirteen patients (6.70%) had positive both RT-PCR and serology for SARS-CoV-2. Leukopenia, ESR >30, elevated troponin and D-dimer >1000 were statistically significant in two group of patients (P<0.05). NT Pro-BNP ≥110 in Kawasaki-like MIS-C and MIS-C patients was marginally significant (p 0.059). In this study, NT pro-BNP, troponin, IL6, fibrinogen and ferritin were only evaluated in some patients (Table 6).
Table 6. Laboratory features in Kawasaki- like MIS-C and MIS-C patients.
| laboratory Features | N (%) | Kawasaki- like MIS-C (n = 58) | MIS-C (n = 167) | P-value |
|---|---|---|---|---|
| COVID-19 Test Results | ||||
| Yes | 116(59.8) | 26(50.9) | 90(62.9) | 0.13 |
| No | 78(40.2) | 25(49.0) | 53(37.0) | |
| Positive RT-PCR | 49(25.3) | 14(27.5) | 35(24.5) | 0.67 |
| Positive Serology | 79(40.7) | 20(39.2) | 59(41.3) | 0.79 |
| Positive RT-PCR & Serology | 13(6.70) | 8(15.7) | 5(3.50) | 0.003 |
| Exposure to COVID-19 | 172(76.8) | 46(79.3) | 126(75.9) | 0.59 |
| WBC<4000a (highest) (n = 220) | 8(3.64) | 3(5.26) | 5(3.07) | 0.44 |
| WBC<4000a (lowest) (n = 184) | 40(21.7) | 5(10.6) | 35(25.6) | 0.03 |
| WBC > = 10000b (highest) (n = 220) | 158(71.8) | 44(77.2) | 114(69.9) | 0.29 |
| WBC > = 10000b (lowest) (n = 184) | 28(15.2) | 7(14.9) | 21(15.3) | 0.94 |
| PLT<100000c (highest) (n = 221) | 7(3.17) | 0 | 7(4.27) | 0.19 |
| PLT<100000c (lowest) (n = 187) | 64(34.2) | 13(27.1) | 51(36.7) | 0.22 |
| PLT> = 450000d (highest) (n = 221) | 81(36.6) | 23(40.4) | 58(35.4) | 0.50 |
| PLT> = 450000d (lowest) (n = 187) | 17(9.09) | 5(10.4) | 12(8.63) | 0.71 |
| ESR>30 (highest) (n = 135) | 122(90.4) | 51(98.1) | 71(85.5) | 0.01 |
| ESR>30 (lowest) (n = 73) | 42(57.5) | 14(46.7) | 28(65.1) | 0.11 |
| ESR>100 (highest) (n = 135) | 29(21.5) | 8(15.4) | 21(25.3) | 0.17 |
| ESR>100 (lowest) (n = 73) | 4(5.48) | 0 | 4(9.30) | 0.13 |
| D-Dimer >1000 (n = 169) | 120(71.0) | 34(87.9) | 86(66.2) | 0.01 |
| CRP (mg/L)> = 10 (n = 222) | 205(92.3) | 56(96.6) | 149(90.9) | 0.16 |
| Ferritin <12 & >135(n = 123) | 104(84.6) | 22(88) | 82(83.7) | 0.59 |
| Fibrinogen<200 & >400(n = 63) | 37(58.7) | 2(28.6) | 35(62.5) | 0.08 |
| NT pro BNP> = 110(n = 167) | 97(58.1) | 37(68.5) | 60(53.1) | 0.05 |
| Troponin> = 0.3(n = 136) | 52(38.2) | 4(14.3) | 48(44.4) | 0.003 |
| IL6> = 5.9(n = 18) | 16(88.9) | 2(100) | 14(87.5) | 1 |
a leukopenia
b Leukocytosis
c Thrombocytopenia
d Thrombocytosis.
Discussion
Since the appearance of MIS-C, physicians have been encountering challenges in diverse manifestations of MIS-C that could lead to misdiagnosis. In this observational study, we described the clinical, laboratory and demographic characteristics of MIS-C and Kawasaki like MIS-C in 225 children and adolescents <21 years in Iran. Although, MIS-C and KD share similarities through clinical presentations, laboratory findings, and treatment; there are particular distinctions between MIS-C and KD that potentially facilitates prompt diagnosis and multidisciplinary management in critically ill patients.
In our study, the median age of the patients with MIS-C and Kawasaki like MIS-C was 4.5 and 4.6 years, respectively. However, some reports have shown that MIS-C tends to affect all age groups, especially children older than five years, with a median age ranging from 6 to 12 years [11, 12].
Consistently with other studies [13–15], a male predominance was detected among our MIS-C patients. Biological dissimilarities between males and females may impact the immune reaction to SARS-CoV-2, as has been discussed in KD [16]. However, the effect of gender on the prevalence, severity and mortality of MIS-C needs to be clarified by larger studies.
Initially, it was presumed that as most patients diagnosed with MIS-C were previously healthy, underlying comorbid diseases were not substantially associated with MIS-C. Nevertheless, in line with study by Abram et al. in our study, obesity was the most prevalent comorbidity, counting for 24.9% of the MIS-C patients [17].
In the current study, the median duration of hospital stay was similar in both MIS-C and Kawasaki-like MIS-C groups, with a median duration of 9 (7–13) days. In the literature, the median length of hospital stay in MIS-C patients ranged from 6 to 13 days [18–20]. It is important to notice that initial treatment can impact the average duration of hospitalization. In our study, most patients received IVIG and steroids as the main treatments and it is in agreement with other studies [14, 21]. Regarding the more utilization of steroids plus IVIG in the MIS-C group, we found that the median duration of PICU stay was shorter in these patients. About 17% of the patients needed a second dose of IVIG due to persistent major signs and symptoms. These patients had a fever for more than five days. In children with Kawasaki-like MIS-C, there was a clinical reassessment 36 hours after IVIG infusion and if they did not respond to IVIG treatment, they received a second dose of IVIG.
In a systematic review by Kaushik et al. MIS-C was associated with favorable outcomes in most of patients and 11 (1.7%) MIS-C related deaths were observed among 655 patients [14]. However, we observed that the mortality ratio in our patients was 4.8%. Importantly, diverse factors including age, ethnicity, gender, prompt diagnosis, and accurate treatment may potentially impact the prognosis of MIS-C [22, 23].
With regards to the symptoms, fever is encountered as the most common characteristic in MIS-C and KD patients [24]. We noticed that duration of fever was longer in Kawasaki-like MIS-C, compared to the MIS-C group. Likewise, Bar-Meir et al. reported the same duration of fever in patients who met both MIS-C and KD criteria’s [11].
Our observations about clinical manifestations of MIS-C were in agreement with those in the literature [14, 25]. However, respiratory and renal involvement was more common in our study. Cardiac involvement was reported as a more frequent feature in patients with MIS-C compared to the Kawasaki-like MIS-C group. Specially, we found that classic presentations of KD, including the strawberry tongue, lymphadenopathy, and conjunctivitis, were less frequent in the MIS-C group compared to the Kawasaki-like MIS-C group.
In our study, 88% of the patients had abnormal echocardiographic results, which were higher in the Kawasaki-like MIS-C patients and MR was the most common problem. In the Blumfield et al. study, 81% of patients had abnormal echocardiographic results that were almost similar to our study [26]. In a Mamishi et al. study, 56% of the patients had cardiac involvement [21]. It should be noted that the reasons for the difference in results can be operator-dependent. Also, according to the hospital policy, not all patients may have an echocardiogram and only seriously ill patients underwent it. On lung CT scan, 61.3% of the patients had one of the problems including GGO or consolidation, pleural effusion, or atelectasis. In the Kwak et al. study, 13 to 41% of patients reported opacity and infiltration, while in our study, GGO and consolidation were commonly reported (84.21%) [27].
In agreement with some studies, most of our patients had positive COVID-19 tests or contact with a COVID-19 positive person [21, 27].
Our findings of high inflammatory markers, including ESR and CRP at the time of admission, were similar to those in other studies [14, 27].
In the current study, D-dimers over 1000 were reported in 71% of the patients and there was a significant difference between the two groups. Also, seven out of 10 patients who died had D-dimer over 1000. In several studies D-dimer has been demonstrated as a biomarker for disease severity and mortality in COVID-19 patients [28, 29]. Ferritin was abnormal in 84.5% of our patients. Ina study, abnormal ferritin was found in 73% [21]. Ferritin is not evaluated routinely for all patients because its role in monitoring inflammation is still not very clear. In a systematic review and meta-analysis, most patients had leukopenia with marked Lymphopenia [30]. In our study, leukopenia was higher in MIS-C patients, and this difference was statistically significant. In another study, patients had leukopenia but did not see a significant difference in leukopenia at the time of admission in patients [31].
We had some limitations that should be noted. First, data collection in some hospitals was from the medical records of hospitalized patients, so there was no access to information and variables that needed to be checked in other hospitals. Second, imaging was not performed on all patients, or we did not have an imaging document of patients to be evaluated by two separate radiologists for agreement percentage.
Conclusion
All of the patients in our study met the MIS-C criteria; however some patients had Kawasaki symptoms, so we compared the clinical and epidemiological characteristics of the two groups. Myocarditis was common in two groups of patients. Conjunctival injection, cervical lymphadenopathy>1.5 cm diameter, and strawberry tongue in Kawasaki-like MIS-C patients were higher than of MIS-C patients. The most common symptom in patients was gastrointestinal symptoms. The best outcome was seen in patients who were treated with both IVIG and steroids on the first days of admission. According to most patients who had echocardiography abnormal, screening of heart function is recommended for patients.
Acknowledgments
The authors would like to express their appreciation to the patients, their parents and guardians for their good cooperation.
Data Availability
Because of ethical and legal restrictions on sharing a de-identified data set we cannot share the data that has been imposed by ethics committee of Mazandaran University of medical sciences. However, we provided the contact information of the ethics committee as below: Email: pajoheshi@mazums.ac.ir Tel: +98 11 33257230.
Funding Statement
The Vice-Chancellor of Research in Mazandaran University of Medical Sciences provided partial funding and supported data collection and analysis for this study. No additional external funding was received for this study.
References
- 1.Phelan AL, Katz R, Gostin LO. The Novel Coronavirus Originating in Wuhan, China: Challenges for Global Health Governance. JAMA. 2020;323(8):709–10. 10.1001/JAMA.2020.1097. [DOI] [PubMed] [Google Scholar]
- 2.Mokhtari T, Hassani F, Ghaffari N, et al. COVID-19 and multiorgan failure: A narrative review on potential mechanisms. J Mol Histol. 2020;51(6):613–28. doi: 10.1007/s10735-020-09915-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Whittaker E, Bamford A, Kenny J, et al. Clinical characteristics of 58 children with a pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2. JAMA. 2020;324(3):259–69. doi: 10.1001/jama.2020.10369 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.https://www.who.int/publications/i/item/multisystem-inflammatory-syndrome-in-children-and-adolescents-with-covid-19.
- 5.Zhang QY, Xu BW, Du JB. Similarities and differences between multiple inflammatory syndrome in children associated with COVID-19 and Kawasaki disease: clinical presentations, diagnosis, and treatment. World J Pediatr. 2021;17(4):335–40. doi: 10.1007/s12519-021-00435-y [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Jones VG, Mills M, Suarez D, et al. COVID-19 and Kawasaki Disease: Novel Virus and Novel Case. Hosp Pediatr. 2020;10(6):537–40. doi: 10.1542/hpeds.2020-0123 [DOI] [PubMed] [Google Scholar]
- 7.Wu EY, Campbell MJ. Cardiac Manifestations of Multisystem Inflammatory Syndrome in Children (MIS-C) Following COVID-19. Curr Cardiol Rep 2021;23(11):168. doi: 10.1007/s11886-021-01602-3 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Sperotto F, Friedman KG, Son MBF, et al. Cardiac manifestations in SARS-CoV-2-associated multisystem inflammatory syndrome in children: a comprehensive review and proposed clinical approach. Eur J Pediatr. 2021;180(2):307–22. doi: 10.1007/s00431-020-03766-6 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Whitlock EP, Williams SB, Gold R, Smith PR, Shipman SA. Screening and interventions for childhood overweight: a summary of evidence for the US Preventive Services Task Force. Pediatrics. 2005;116(1):e125–44. doi: 10.1542/peds.2005-0242 [DOI] [PubMed] [Google Scholar]
- 10.gov/han/2020/han00432.asp. Accessed June 20, 2020. CfDCaPMisicMCawcdChec.
- 11.Bar-Meir M, Guri A, Godfrey ME, et al. Characterizing the differences between multisystem inflammatory syndrome in children and Kawasaki disease. Sci Rep. 2021;11(1):13840. doi: 10.1038/s41598-021-93389-0 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Alkan G, Sert A, Oz SKT, Emiroglu M, Yılmaz R. Clinical features and outcome of MIS-C patients: an experience from Central Anatolia. Clin Rheumatol. 2021;40(10):4179–89. doi: 10.1007/s10067-021-05754-z [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Payne AB, Gilani Z, Godfred-Cato S, et al. Incidence of Multisystem Inflammatory Syndrome in Children Among US Persons Infected With SARS-CoV-2. JAMA Netw Open. 2021;4(6):e2116420–e. doi: 10.1001/jamanetworkopen.2021.16420 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Kaushik A, Gupta S, Sood M, Sharma S, Verma S. A Systematic Review of Multisystem Inflammatory Syndrome in Children Associated With SARS-CoV-2 Infection. Pediatr Infect Dis J. 2020;39(11). doi: 10.1097/INF.0000000000002888 [DOI] [PubMed] [Google Scholar]
- 15.Mohsin SS, Abbas Q, Chowdhary D, et al. Multisystem inflammatory syndrome (MIS-C) in Pakistani children: A description of the phenotypes and comparison with historical cohorts of children with Kawasaki disease and myocarditis. PLOS ONE. 2021;16(6):e0253625. doi: 10.1371/journal.pone.0253625 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Fernandez-Cooke E, Barrios Tascón A, Sánchez-Manubens J, et al. Epidemiological and clinical features of Kawasaki disease in Spain over 5 years and risk factors for aneurysm development. (2011–2016): KAWA-RACE study group. PLOS ONE. 2019;14(5):e0215665. doi: 10.1371/journal.pone.0215665 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Abrams JY, Oster ME, Godfred-Cato SE, et al. Factors linked to severe outcomes in multisystem inflammatory syndrome in children (MIS-C) in the USA: a retrospective surveillance study. Lancet Child Adolesc Health. 2021;5(5):323–31. doi: 10.1016/S2352-4642(21)00050-X [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Feldstein LR, Rose EB, Horwitz SM, et al. Multisystem Inflammatory Syndrome in U.S. Children and Adolescents. N Engl J Med. 2020;383(4):334–46. doi: 10.1056/NEJMoa2021680 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Merckx J, Cooke S, Tal TE, et al. Multicenter cohort study of multisystem inflammatory syndrome in children (MIS-C). medRxiv. 2021:2021.05.14.21257058. 10.1101/2021.05.14.21257058. [DOI] [Google Scholar]
- 20.Tolunay O, Çelik Ü, Arslan İ, et al. Multisystem Inflammatory Syndrome in Children (MIS-C) Associated with COVID-19: A Case Series Experience in a Tertiary Care Hospital of Southern Turkey. J Trop Pediatr. 2021;67(2). 10.1093/tropej/fmab050. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Mamishi S, Movahedi Z, Mohammadi M, et al. Multisystem inflammatory syndrome associated with SARS-CoV-2 infection in 45 children: a first report from Iran. Epidemiol Infect. 2020;148. doi: 10.1017/S095026882000196X [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Chou J, Platt CD, Habiballah S, et al. Mechanisms underlying genetic susceptibility to multisystem inflammatory syndrome in children (MIS-C). J Allergy Clin Immunol. 2021;148(3):732–8 e1. doi: 10.1016/j.jaci.2021.06.024 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Bowen A, Miller AD, Zambrano LD, et al. Demographic and Clinical Factors Associated With Death Among Persons <21 Years Old With Multisystem Inflammatory Syndrome in Children—United States, February 2020–March 2021. Open Forum Infect Dis 2021;8(8). 10.1093/ofid/ofab388. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Sharma C, Ganigara M, Galeotti C, et al. Multisystem inflammatory syndrome in children and Kawasaki disease: a critical comparison. Nat Rev Rheumatol. 2021;17(12):731–48. doi: 10.1038/s41584-021-00709-9 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Ahmed M, Advani S, Moreira A, et al. Multisystem inflammatory syndrome in children: A systematic review. EClinicalMedicine. 2020;26:100527. doi: 10.1016/j.eclinm.2020.100527 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Blumfield E, Levin TL, Kurian J, Lee EY, Liszewski MC. Imaging Findings in Multisystem Inflammatory Syndrome in Children (MIS-C) Associated With Coronavirus Disease (COVID-19). AJR Am J Roentgenol. 2021;216(2):507–17. doi: 10.2214/AJR.20.24032 [DOI] [PubMed] [Google Scholar]
- 27.Kwak JH, Lee S-Y, Choi J-W. Clinical features, diagnosis, and outcomes of multisystem inflammatory syndrome in children associated with coronavirus disease 2019. Clin Exp Pediatr. 2021;64(2):68. doi: 10.3345/cep.2020.01900 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Zou Y, Guo H, Zhang Y, et al. Analysis of coagulation parameters in patients with COVID-19 in Shanghai, China. Bios Trends. 2020. doi: 10.5582/bst.2020.03086 [DOI] [PubMed] [Google Scholar]
- 29.Yao Y, Cao J, Wang Q, et al. D-dimer as a biomarker for disease severity and mortality in COVID-19 patients: a case control study. J Intensive Care. 2020;8(1):1–11. doi: 10.1186/s40560-020-00466-z [DOI] [PMC free article] [PubMed] [Google Scholar]
- 30.Mardi P, Esmaeili M, Iravani P, et al. Characteristics of children with Kawasaki Disease-like signs in COVID-19 pandemic: A systematic review. Front pediatr. 2021;9. doi: 10.3389/fped.2021.625377 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Attia Bari AC, Iqbal Bano NS. Is leukopenia and lymphopenia a characteristic feature of COVID-19 in children? Pak J Med Sci. 2021;37(3):869. doi: 10.12669/pjms.37.3.3848 [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
Because of ethical and legal restrictions on sharing a de-identified data set we cannot share the data that has been imposed by ethics committee of Mazandaran University of medical sciences. However, we provided the contact information of the ethics committee as below: Email: pajoheshi@mazums.ac.ir Tel: +98 11 33257230.