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Methylprednisolone pulses as an initial treatment in hyperinflammatory syndrome after COVID-19 in children: evaluation of laboratory data, serial echocardiography and outcome: a case series

Intensive Care Medicine Experimental volume 10, Article number: 56 (2022) Cite this article

Abstract

Background

Hyper-inflammatory syndrome in children and young adult occur 2–6 weeks after COVID-19 infection or closed contact with COVID-19 persons. In this study, the laboratory data and echocardiography and abdominal ultrasonography assessments were evaluated before and after Methylprednisolone pulse as an initial treatment of hyper-inflammatory syndrome. Therefore, the aim of this study is to assessment the clinical manifestations and laboratory data and outcome after methylprednisolone pulse as an initial treatment.

Method

In this retrospective study, the demographic status, clinical features, laboratory data, echocardiography, abdominal ultrasound, treatment and outcome of 31 pediatric patients under 16 years old, with inflammatory process after COVID-19 were evaluated. The clinical assessments, laboratory data, sonography and echocardiography were evaluated before and after methylprednisolone pulse. The patients were divided in two age group < and ≥ 7 years old and the clinical manifestations were compared with each other. The Mann–Whitney U test was used to assess the difference in quantitative variables between two groups. To compare pre- and post- treatment values, Wilcoxol test was used. To assess the correlation between qualitative variables chi-square test was used. The level of significant was considered 0.05. These patients with fever and hyper-inflammation features admitted to the referral pediatric rheumatology ward in Children Medical Center of Tehran University of medical sciences, from April 2020 to May 2021 were assessed.

Result

The mean age ± SD were (5.94 ± 3) and 51.6% (16) patients were male and 48.4% (15) patients were female. The most documented of previous COVID infection were antibody positive in about 27 (87%) patients. Moreover, 1 (3.8%) was PCR positive, 2 (7.7%) were positive in both PCR and serology and 3(11.5%) had closed contact with COVID-19 patients. About 9(29%) of patients were admitted in Intensive Care Unit (ICU). There were significant correlation between days of delay in starting treatment and ICU admission (P-value = 0.02). The mortality rate was negative in patients and no re-hospitalization was documented. There were significant differences (P-value < 0.05) between lymphocytes, platelet, Erythrocyte Sedimentation rate, C-reactive protein, Aspartate transaminase, Alanine transaminase and ferritin before and after treatment. Skin rashes and cardiac involvement totally as carditis (myocarditis, vulvulitis and pericarditis) (33.3%) and coronary involvements (53.3%) were the most prominent initial presentation in patients. There were near significant correlation (P-value = 0.066) between ferritin level and carditis before treatment. Cervical lymphadenopathy was seen significantly more in ≥ 7 years old (P-value = 0.01).

Conclusion

Multisystem inflammatory system in children as a hyperinflammatory syndrome could be treated with first step methylprednisolone pulse with decreasing inflammation in laboratory data and cardiac involvements and good outcome. Furthermore, the ferritin level may be one of the predictor of severe hyper-inflammatory syndrome leading to aggressive and urgent treatment with methylprednisolone pulse.

Introduction

Coronavirus in children and young patients may present in different features from adult patients. Although the mortality and morbidity are higher in adult, some serious complications of SARS-COV2 can also be seen in children. About two third of infected children are asymptomatic. Some children, especially with background disease, have severe COVID infection with pulmonary involvements [1]. The other involved children or closed contacts with infected person have inflammatory features with two or more organ involvements about 2–6 weeks after COVID infection [2]. The COVID PCR is usually negative with lower pulmonary involvement in this group [1]. The severe inflammatory responses as a result of cytokine releases could be consisted of gastrointestinal, hematologic, renal, central nervous system, cutaneous, nervous system and especially cardiac manifestations such as carditis, valvulitis, coronary involvements, and even the cardiogenic shock with a hyper-inflammatory process with two or more organ involvements; named Multi-system inflammatory syndrome in children (MISC) [2].

On the other hand, conjunctivitis, mucocutaneous manifestations and coronary involvements can be seen with the same features like atypical Kawasaki disease, so called Kawasaki-like syndrome [3].

Some articles separated these two post hyper-inflammatory conditions after COVID-19, but the others considered the two as one syndrome with a hyper-inflammatory process and various organ involvements [4].

Nowadays, because of limitation in studies on urgent and life-saving management of severely features of cytokines releases, the selected treatment process are based on the treatments of hyper-inflammatory process such as macrophage activation syndrome [5, 6], Kawasaki disease shock syndrome [7], secondary Hemophagocytic Lymphohistiocytosis (HLH), toxic shock syndrome; immunomodulatory agents, such as IVIG (Intravenous Immunoglobulin) [8], Glucocorticoids [9] in low to high dose as pulse therapy and Biologics [10].

In this study, methyl prednisolone pulse for one to three days was administered as the first step of treatment in hyper-inflammatory syndrome after SARS-COV2 infection [11]. Clinical manifestations, laboratory data and echocardiography (echo) and abdominal sonography, before and after treatment and the outcome of patients 1–2 weeks after discharge were evaluated. The clinical features were compared in two groups, < and ≥ 7 years old.

Methods

In this retrospective study, the demographic status, clinical features, laboratory data, echocardiography, abdominal ultrasound, treatment and outcome of 31 pediatric patients under 16 years old, with inflammatory process after COVID-19 were evaluated. The previous positive COVID-19 were approved by PCR (Polymerase Chain Reaction), antibodies and history of closed contact in 1–2 recent months. Since, the accurate definition for inflammatory process is not demonstrated, each inflammatory condition according to CDC [2] and WHO [12] criteria of MISC and also the Kawasaki-like manifestations in pediatric patients after COVID-19 were intended. The criteria consisted of; documented fever ≥ 24 h, at least two organ involvement of cardiovascular, respiratory, renal, neurologic, hematologic, gastrointestinal, dermatologic, laboratory evidence of inflammation, any of the following: elevated CRP(C-Reactive Protein), elevated ESR(Erythrocyte Sedimentation Rate), elevated fibrinogen, elevated procalcitonin, elevated D-dimer, elevated ferritin, elevated LDH(Lactate dehydrogenase), elevated IL-6 (Interleukin6), Neutrophilia, Lymphocytopenia, hypoalbuminemia and sever condition requiring hospitalization. The Sars-cov2 infection confirmed by positive serology, positive PCR and the history of closed contact exposure within 4 -6 weeks. Hence, the pediatric patients with fever and hyper-inflammation features were admitted to the referral pediatric rheumatology ward in Children Medical Center of Tehran University of medical sciences, from April 2020 to May 2021 were evaluated. There were excluded from the PCR positive patients admitted in infectious ward of hospital. The study were reviewed and approved by Institutional Review Board of Children Medical Center (Tehran University of Medical Sciences).The patients provided written informed consent to participate in this study.

The demographic data, laboratory data, duration from clinical manifestations to hospitalization, the duration from hospitalization to first treatment, the duration of hospitalization, were documented. Echocardiography was done for all admitted patients in first hours, the second echo was done after 2–3 days after treatment and depends on patients´ condition the others echocardiography and follow up echocardiography were done 1–2 weeks after discharge. Cardiac involvements consisted: pericarditis (The inflammation of pericardia with effusion diagnosed with echocardiography), valvulitis (The inflammation of valves that could not closed completely, become leaky, named regurgitation), myocarditis (The inflammation of myocardia known with elevated troponin/BNP (Brain Natriuretic Peptide), ck-mb and/or Decreased ejection fraction and cardiogenic shock). Carditis consisted of one or more than one inflammation of pericardia, myocardia and endocardia as vulvulitis. The coronary involvements defined as ectesia (the dilation of internal luminal diameter > 2.5 z-score without aneurysm) and coronary aneurysm (The dilation of internal luminal diameter ≥ 1.5 times more than the adjuvant segment). If the patients did not have cardiac involvement, about four normal echocardiography should be documented. All echocardiographies were done by one expert pediatric cardiologist. The abdominal ultrasound was done for all patients.

The initial laboratory data in first hours of admission such as white blood cell count (WBC), polymorphonuclear (PMN), and lymphocyte absolute count, Hemoglobin, Platelet, Ferritin, Alanine transaminase (ALT), Aspartate transaminase (AST). These laboratory data were named as WBC1, PMN1, and so forth. The same laboratory data were also documented one day after methylprednisolone pulse named as WBC2, PMN2, and so forth. The dynamic changes in these variables were also calculated by subtracting the second from the first.

The other laboratory data such as fibrinogen, procalcitonin, Interleukin 6, the cardiac enzyme, Amylase, Lipase, uric acid, D dimer and the others were documented as an initial laboratory data before treatment.

According to prevalence of Kawasaki disease in < 5 years old with lower expansion to 7 years and the prevalence of MISC in teenage ages with CDC definition under 21 years old [13].

According to Children Medical Centre (CMC) protocol of Tehran University of Medical Sciences Methylprednisolone pulses 30 mg/kg/dose infused in one to three doses were prescribed as first line treatment [11]. oral prednisolone were continued 2–3 weeks after discharged and tapered gradually according to patients conditions in each visit. If the coronary arteries were involved, according to (AHA2017) [13] guidelines, IVIG 2gr/kg were initiated.

The cardiac outcome, mortality and morbidity were followed for one month.

Statistical analysis

The statistical analysis was performed with SPSS version 20 (SPSS Inc., Chicago, IL). The Mann–Whitney U test was used to assess the difference in quantitative variables between two groups. To compare pre- and post- treatment values, Wilcoxol test was used. To assess the correlation between qualitative variables chi-square test was used. The level of significant was considered 0.05.

Result

Thirty one patients were included in this study. One patient was excluded because the ultimately diagnosis in following up were systemic Juvenile Idiopathic Arthritis. The characteristic data were shown in Table 1. The most documented of previous COVID infection were antibody positive in about 27 (87%) patients. Moreover, 1(3.8%) was PCR positive, 2(7.7%) were positive in both PCR and serology and 3(11.5%) had closed contact with COVID-19 patients. About 8(25.8%) patients were referred to our hospital as a tertiary center. Duration from the first day of symptoms to diagnosis was about 8.16 ± 6.16 (1–30) days. The day of initial treatment of Methyl- prednisolone pulse was about 8.8 ± 6.5 (2–30) days from the first day of manifestations. The duration of corticosteroid treatment (methylprednisolone IV + oral prednisolone) was about 10.76 ± 4.83 (16–7) days. The duration of hospitalization was approximately 6.1 ± 2.7 (3–15) days. About 9(29%) of patients were admitted in Intensive Care Unit (ICU). There were significantly different in days of delay in starting principle treatment and ICU admission (P-value = 0.02). The mortality rate was negative in patients and no re-hospitalization was documented. Thus, no patient had renal involvement.

Table 1 The demographic characteristic of patients
Full size table

The mean ± standard deviation (minimum –maximum) of laboratory data were shown in Table 2. According to Table 2 there are significant differences (P-value < 0.05) between lymphocytes, platelet, Erythrocyte Sedimentation rate (ESR), C-reactive protein (CRP), Aspartate transaminase (AST), Alanine transaminase (ALT) and ferritin before and after treatment.

Table 2 The mean, standard deviation, maximum and minimum ranges of laboratory data and P-value of comparing of some laboratory data before and after treatment
Full size table

Skin rashes and cardiac involvement (33.3%) [Pericardial involvement, myocarditis and valvulitis] and coronary involvements (53.3%) were the most prominent initial presentation in patients (Table 3). One patient from another center was referred with myocarditis in first echocardiography, diffuse coronary ectasia in second echo and viral encephalopathy without good response to two IVIG infusions. So, three Methylprednisolone pulses were initiated in following echo the coronary involvement and carditis were resolved with residue encephalopathy. Hence, with initiation of Infliximab the patient´s consciousness was improved with nearly good responses.

Table 3 The percentage of clinical manifestations in hyper-inflammatory features of pediatric patients after COVID-19
Full size table

The echocardiography and abdominal ultra-sonography were shown in Table 4. Coronary involvement ectasia are the most presentation in all three tandem echocardiography. The initial echocardiography were normal in 14 patients, then the second echo 2–4 days after treatment were normal in 20 patients. Ultimately 28 patients had normal echocardiography in follow up echocardiography 1–2 weeks after discharge. One patient despite the progressive treatment included three Methylprednisolone pulses and IVIG, the coronary ectasia and aneurysm had not good response. So, Infiliximab (Tumor Necrosis Factorα inhibitor) was prescribed with nearly good responses in following echocardiography. About one patient had residual coronary involvement 1–2 month after discharge.

Table 4 The echocardiography and abdominal sonography findings of pediatric patients with hyper-inflammatory features after COVID-19
Full size table

There were near significant corellation (P-value = 0.066) between higher ferritin level and carditis. However, the significant difference were not found between CRP, ESR and coronary involvements and carditis respectively (P-value: 0.7, 0.38, 0.92, 0. 35). Also, there were no significant difference between Ferritin level and coronary involvement. (P-value = 0.74).The patients were divided in two subgroup less than 7 years old and more than 7 years old. Although the initial presentations especially the gastrointestinal manifestations in less than7 group were more than other group, there were no significant difference between two groups. Cervical lymphadenopathy in more than 7 years old were more than the other group with significant difference (P-value = 0.01). Thus, there were significantly different between AST level and cervical lymphadenopathy (P-value = 0.02). However, there were no significantly different between cervical lymphadenopathy and ALT, CRP, ESR, Ferritin, respectively (P-value: 0.16, 0.88, 0.2,0.47).

All the patients received methylprednisolone pulse and Aspirin and approximately 8 patients (25.8%) received IVIG. Also, Enoxaparin was prescribed for 8 (25.8%) of patients. Infliximab was prescribed in two patients because of aneurysm in coronary artery and CNS involvement.

Discussion

The hyper- inflammatory syndrome because of severe cytokine release occur about 3–6 weeks after SARS-COV2 infection or closed contact with COVID-19. The antibodies against SARS-COV2 were more important than PCR in this study like the other articles. These antibodies probably display the function of acquired immune system against auto-antigens and lead to activation of the other immune cells; such as T-cell, macrophages, neutrophils and ultimately result in cytokine storm with multiple organs involvement [14]. With considering hyperinflammatory syndrome as a cytokine storm could be treat with methylprednisolone pulse, we evaluated the laboratory data, echocardiography results before and after methylprednisolone pulse treatment in MISC patients.

The mean age was lower than the other studies and the male to female ratio was nearly similar to other studies. The differences were due to selection of patients with one to two positive laboratory data and at least two organs involvement and echocardiography- and sonography-positive data [15, 16].

Multisystem inflammatory syndrome in children (MISC) and Kawasaki-like syndrome both illustrate the hyper- inflammatory syndrome. Some articles emphasize that MISC is a novel disease after COVID -19 pandemic in children with older age and more gastrointestinal manifestations and myocarditis [17]. On the other hand, there are some reports about more Kawasaki-like syndrome, with features of atypical Kawasaki disease and coronary abnormalities, after SARS-COV2 [18, 19].

Furthermore, there are some similarities between MISC and Kawasaki disease. Cytokine storm lead to hyperinflammatory condition with myocarditis in both of them [20]. In addition, high level of ferritin can be seen in both MISC and MAS in Kawasaki disease [20, 21]. Moreover, autoantibodies in MISC patients have some special target auto-antigens on endothelial cells and myocardial cells leading to small and medium-sized vasculitis similar to KD [22]. These auto-antigens were also reported in KD [23]. However, the exact pathogenesis of MISC still remains unclear.

The mucocutaneous involvement, conjunctivitis, lymphadenopathy are seen in both MISC and atypical KD. The cardiac manifestations such as coronary and myocardial involvement have the same presentation in MISC and atypical-KD, especially myocarditis in Kawasaki disease shock syndrome (KDSS). The KDSS in acute phase of Kawasaki disease is IVIG-resistant with higher level of inflammatory cytokines such as IL6, TNFα, and IL1 and good response to methylprednisolone pulses [7, 24]. Nowadays, the researchers work on methyl prednisolone pulses instead of IVIG treatment in acute phase of Kawasaki disease. In acute phase of Kawasaki disease, the innate immune system are involved with cytokines released as a hyper-inflammatory process [25, 26].

The mucocutaneous involvement and cardiac manifestations were the most clinical presentations. The patients were divided in two groups of less or more than 7 years old. The majority of Kawasaki disease are in the age of 2–5 years old with mucocutaneous- lymph node syndrome. The MISC patients are older with more prominent organ involvement; gastrointestinal, myocarditis and shock. The purpose was to separate these two phenomena according to special presentations. However, there were no significantly difference in gastrointestinal and cardiac involvement between two age groups. So, MISC and KD- like disease may be the similar hyper-inflammatory syndromes with wide spectrum of organ involvements [4, 27, 28]. These findings may be against assumption of difference between MISC and Kawasaki-like disease based on age ranges and organ involvements [1, 3].

Cervical lymphadenopathy was more frequently seen in ≥ 7 years old group. First-Node Kawasaki Disease (FNKD) in an unusual presentation of atypical Kawasaki disease in older ages, similar to this study [29, 30]. The FNKD patients have more hyper-inflammatory process with more coronary involvements and IVIG- resistance. In NFKD, the IL6, AST, CRP, ESR are in higher levels in comparison with other atypical Kawasaki disease [29]. This study, with evaluation of hyper-inflammatory syndrome after SARS-COV-2, found significant correlation between AST and cervical lymphadenopathy (p-value = 0.02). So, the reticuloendothelial system involvement may be more prominent in these age group.

The initial treatment was methyl-prednisolone pulse, in contrast with the other articles using IVIG in FNKD. There was no significant correlation between coronary involvements and cervical lymphadenopathy (P-value = 0.6). Therefore, the cervical lymphadenopathy may predict the IVIG-resistant hyper-inflammatory syndrome with good responses to methylprednisolone pulses. In addition, the earlier use of pulse in our study might decrease the coronary involvement [29, 30].

Macrophage activation syndrome (MAS) is a cytokine storm with increased level of ferritin produced by activated macrophages [5, 31]. Secondary HLH like MAS, primary HLH and probably MISC, may initially have different mechanisms in stimulation of inflammatory pathway, nevertheless all of them lead to activated macrophages, neutrophils, histiocytes and the other cells and subsequently elevated ferritin level and ultimately cytokine storm with some organ damages [32]. In addition, the acute phase of Kawasaki disease is presented with activation of innate immune system as a cytokine storm, especially in KDSS with myocarditis and elevated ferritin level [7, 33].

The correlation between ferritin level and carditis were near-significant. With more sample size, the correlation can be significant. So, Ferritin level may be a valuable predictor of carditis, with effect on decision for aggressive treatment.

One to three doses of Methylprednisolone pulses were the initial treatment. In previous study, methylprednisolone pulse was not prescribed alone without IVIG [10, 17, 34,35,36,37]. In some studies, Biologic treatments were used in resistant patients more than this study [10, 17, 34]. IVIG and low dose glucocorticoid were the principle treatment in these studies [35,36,37]. However, one study demonstrated no significant differences between IVIG and glucocorticoid and high dose glucocorticoid alone as first-line treatment [39]. In our study, the biologic treatment were prescribed in only two patients and the mortality were zero. However, one patient presented persistent aneurysm in 1–2 weeks following echocardiography.

There were significant differences between inflammatory laboratory data before and after methylprednisolone pulses treatment with rapid decrease within two to three days after methyl prednisolone pulses. On the other hand, the delayed initiation methyl prednisolone pulses were associated by more ICU admission. So, decreasing inflammatory parameter might have an effect on low rate of complications and lower use of Biologic treatments [36,37,38].

The mainweakness of this study were low sample size and retrospective design without control group. Higher sample size and prospective study would be more valuable. Furthermore, the presence of control group will yield more accurate result. Further clinical trials for evaluation of selected treatments should be considered.

In conclusion,.we have shown methylprednisolone pulse as the first step of treatment in MISC patients with considering the hyperinflammatory syndrome could decrease the clinical, laboratory and cardiac inflammation with good outcome. However, control group with more sample size would be more valuable in future studies.

Furthermore, the ferritin level may be one of the predictor of severe hyper-inflammatory syndrome leading to aggressive and urgent treatment with methylprednisolone pulse.

Availability of data and materials

The data sets study are available from the corresponding author on reasonable written request.

References

  1. Whittaker E, Bamford A, Kenny J, Kaforou M, PIMS-TS Study Group and EUCLIDS and PERFORM Consortia et al (2020) Clinical characteristics of 58 children with a pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2. JAMA 324(3):259–269

    Article  CAS  Google Scholar 

  2. CDC Health Alert Network [Internet] (2020) https://emergency.cdc.gov/han/2020/han00432.asp. Accessed 22 May 2020.

  3. Toubiana J, Poirault C, Corsia A, Bajolle F, Fourgeaud J, Angoulvant F et al (2020) Kawasaki-like multisystem inflammatory syndrome in children during the covid-19 pandemic in Paris, France: prospective observational study. BMJ 369:m2094. https://doi.org/10.1136/bmj.m2094

    Article  Google Scholar 

  4. Matucci-Cerinic C, Caorsi R, Consolaro A, Rosina S, Civino A, Ravelli A (2021) Multisystem inflammatory syndrome in children: unique disease or part of the Kawasaki disease spectrum? Front Pediatr. 9:680813. https://doi.org/10.3389/fped.2021.680813

    Article  Google Scholar 

  5. Ravelli A, Davì S, Minoia F, Martini A, Cron RQ (2015) Macrophage activation syndrome. Hematol Oncol Clin North Am 29(5):927–941. https://doi.org/10.1016/j.hoc.2015.06.010

    Article  Google Scholar 

  6. Assari R, Sadeghi P, Mirmohammadsadeghi A, Ebadi F, Ziaee V (2020) Macrophage activation syndrome as a complication of rheumatologic disorders, a report from Iran. Reumatismo 71(4):189–198. https://doi.org/10.4081/reumatismo.2019.1204

    Article  CAS  Google Scholar 

  7. Li Y, Zheng Q, Zou L, Wu J, Guo L, Teng L, Zheng R, Jung LKL, Lu M (2019) Kawasaki disease shock syndrome: clinical characteristics and possible use of IL-6, IL-10 and IFN-γ as biomarkers for early recognition. Pediatr Rheumatol Online J 17(1):1. https://doi.org/10.1186/s12969-018-0303-4

    Article  Google Scholar 

  8. Jonat B, Gorelik M, Boneparth A et al (2021) Multisystem inflammatory syndrome in children associated with coronavirus disease 2019 in a Children’s Hospital in New York City: patient characteristics and an institutional protocol for evaluation, management, and follow-up. Pediatr Crit Care Med 22(3):e178–e191. https://doi.org/10.1097/PCC.0000000000002598

    Article  Google Scholar 

  9. McArdle AJ, Vito O, Patel H, Seaby EG, Shah P, Wilson C et al (2021) Treatment of multisystem inflammatory syndrome in children. N Engl J Med 385(1):11–22. https://doi.org/10.1056/NEJMoa2102968

    Article  CAS  Google Scholar 

  10. Abdel-Haq N, Asmar BI, Deza Leon MP, McGrath EJ, Arora HS, Cashen K, Tilford B, CharafEddine A, Sethuraman U, Ang JY (2021) SARS-CoV-2-associated multisystem inflammatory syndrome in children: clinical manifestations and the role of infliximab treatment. Eur J Pediatr 180(5):1581–1591. https://doi.org/10.1007/s00431-021-03935-1

    Article  CAS  Google Scholar 

  11. Ziaee V, Assari R, Mamishi S, Zeinaloo A, Mohammadpour M et al (2020) An Algorithmic approach to multisystem inflammatory syndrome in children with COVID-19: Tehran children’s medical center protocol. Iran J Pediatr. 30(5):e108617. https://doi.org/10.5812/ijp.108617

    Article  Google Scholar 

  12. World Health Organization. Director-General's remarks at the media briefing on 2019-nCoV on 11 February 2020. http://www.who.int/dg/speeches/detail/who-director-general-s-remarks-at-the-media-briefing-on-2019-ncov-on-11-february-2020. Accessed 12 Feb 2020.

  13. McCrindle BW, Rowley AH, Newburger JW, Burns JC et al (2017) American Heart Association diagnosis, treatment, and long-term management of Kawasaki disease: a scientific statement for health professionals from the American Heart Association. Circulation 135(17):e927–e999. https://doi.org/10.1161/CIR.0000000000000484. (Epub 2017 Mar 29. Erratum in: Circulation. 2019 Jul 30;140 (5):e181-e184)

    Article  Google Scholar 

  14. Consiglio CR, Cotugno N, Sardh F, Pou C, Amodio D et al (2020) The immunology of multisystem inflammatory syndrome in children with COVID-19. Cell. https://doi.org/10.1016/j.cell.2020.09.016

    Article  Google Scholar 

  15. Kurz H, Gombala T (2021) Multisystem inflammatory syndrome in children (MIS-C)-a case series in December 2020 in Vienna, Austria. Front Pediatr 9:656768. https://doi.org/10.3389/fped.2021.656768

    Article  Google Scholar 

  16. Akca UK, Kesici S, Ozsurekci Y, Aykan HH, Batu ED, Atalay E, Demir S, Sag E, Vuralli D, Bayrakci B, Bilginer Y, Ozen S (2020) Kawasaki-like disease in children with COVID-19. Rheumatol Int 40(12):2105–2115. https://doi.org/10.1007/s00296-020-04701-6

    Article  CAS  Google Scholar 

  17. Sood M, Sharma S, Sood I, Sharma K, Kaushik A (2021) Emerging evidence on multisystem inflammatory syndrome in children associated with SARS-CoV-2 infection: a systematic review with meta-analysis. SN Compr Clin Med 7:1–10. https://doi.org/10.1007/s42399-020-00690-6

    Article  CAS  Google Scholar 

  18. Akca UK, Kesici S, Ozsurekci Y et al (2020) Kawasaki-like disease in children with COVID-19. Rheumatol Int 40(12):2105–2115. https://doi.org/10.1007/s00296-020-04701-6

    Article  CAS  Google Scholar 

  19. Kabeerdoss J, Pilania RK, Karkhele R, Kumar TS, Danda D, Singh S (2021) Severe COVID-19, multisystem inflammatory syndrome in children, and Kawasaki disease: immunological mechanisms, clinical manifestations and management. Rheumatol Int 41(1):19–32. https://doi.org/10.1007/s00296-020-04749-4

    Article  CAS  Google Scholar 

  20. Pouletty M, Borocco C, Ouldali N, Caseris M et al (2020) Paediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2 mimicking Kawasaki disease (Kawa-COVID-19): a multicentre cohort. Ann Rheum Dis 79(8):999–1006. https://doi.org/10.1136/annrheumdis-2020-217960

    Article  CAS  Google Scholar 

  21. Yamamoto N, Sato K, Hoshina T, Kojiro M, Kusuhara K (2015) Utility of ferritin as a predictor of the patients with Kawasaki disease refractory to intravenous immunoglobulin therapy. Mod Rheumatol 25(6):898–902. https://doi.org/10.3109/14397595.2015.1038430

    Article  CAS  Google Scholar 

  22. Consiglio CR, Cotugno N, Sardh F, Pou C, Amodio D et al (2020) The immunology of multisystem inflammatory syndrome in children with COVID-19. Cell. https://doi.org/10.1016/j.cell.2020.09.016

    Article  Google Scholar 

  23. Sakurai Y (2019) Autoimmune aspects of Kawasaki disease. J Investig Allergol Clin Immunol 29(4):251–261. https://doi.org/10.18176/jiaci.0300

    Article  CAS  Google Scholar 

  24. Hur G, Song MS, Sohn S et al (2019) Infliximab treatment for intravenous immunoglobulin-resistant Kawasaki disease: a multicenter study in Korea. Korean Circ J 49(2):183–191

    Article  CAS  Google Scholar 

  25. Aslani N, Raeeskarami SR, Aghaei-Moghadam E, Tahghighi F, Assari R, Sadeghi P, Ziaee V (2022) Intravenous methylprednisolone pulse therapy versus intravenous immunoglobulin in the prevention of coronary artery disease in children with Kawasaki disease: a randomized controlled trial. Cureus 14(6):e26252. https://doi.org/10.7759/cureus.26252

    Article  Google Scholar 

  26. Wardle AJ, Connolly GM, Seager MJ, Tulloh RM (2017) Corticosteroids for the treatment of Kawasaki disease in children. Cochrane Database Syst Rev 1(1):CD011188. https://doi.org/10.1002/14651858.CD011188.pub2

    Article  Google Scholar 

  27. Diorio C, Henrickson SE, Vella LA, McNerney KO, Chase J et al (2020) Multisystem inflammatory syndrome in children and COVID-19 are distinct presentations of SARS-CoV-2. J Clin Invest 130(11):5967–5975. https://doi.org/10.1172/JCI140970

    Article  CAS  Google Scholar 

  28. Yeung RS, Ferguson PJ (2020) Is multisystem inflammatory syndrome in children on the Kawasaki syndrome spectrum? J Clin Invest 130(11):5681–5684. https://doi.org/10.1172/JCI141718

    Article  CAS  Google Scholar 

  29. Kanegaye JT, Van Cott E, Tremoulet AH, Salgado A, Shimizu C, Kruk P, Hauschildt J, Sun X, Jain S, Burns JC (2013) Lymph-node-first presentation of Kawasaki disease compared with bacterial cervical adenitis and typical Kawasaki disease. J Pediatr. https://doi.org/10.1016/j.jpeds.2012.11.064

    Article  Google Scholar 

  30. Kim JO, Kim YH, Hyun MC (2016) Comparison between Kawasaki disease with lymph-node-first presentation and Kawasaki disease without cervical lymphadenopathy. Korean J Pediatr 59(2):54–58. https://doi.org/10.3345/kjp.2016.59.2.54

    Article  CAS  Google Scholar 

  31. Assari R, Ziaee V, Mirmohammadsadeghi A, Moradinejad MH (2015) Dynamic changes, cut-off points, sensitivity, and specificity of laboratory data to differentiate macrophage activation syndrome from active disease. Dis Markers. https://doi.org/10.1155/2015/424381

    Article  Google Scholar 

  32. Krei JM, Møller HJ, Larsen JB (2021) The role of interleukin-18 in the diagnosis and monitoring of hemophagocytic lymphohistiocytosis/macrophage activation syndrome—a systematic review. Clin Exp Immunol 203(2):174–182. https://doi.org/10.1111/cei.13543

    Article  CAS  Google Scholar 

  33. Roh DE, Kwon JE, Choi HJ, Kim YH (2021) Importance of serum ferritin level for early diagnosis and differentiation in patients with Kawasaki disease with macrophage activation syndrome. Children (Basel) 8(4):269. https://doi.org/10.3390/children8040269

    Article  Google Scholar 

  34. Son MBF, Murray N, Friedman K, Young CC, Newhams MM et al (2021) Multisystem inflammatory syndrome in children—initial therapy and outcomes. N Engl J Med 385(1):23–34. https://doi.org/10.1056/NEJMoa2102605

    Article  CAS  Google Scholar 

  35. Dove ML, Jaggi P, Kelleman M, Abuali M, Ang JY et al (2021) Multisystem inflammatory syndrome in children: survey of protocols for early hospital evaluation and management. J Pediatr 229:33–40. https://doi.org/10.1016/j.jpeds.2020.10.026

    Article  CAS  Google Scholar 

  36. Belhadjer Z, Auriau J, Méot M, Oualha M, Renolleau S, Houyel L, Bonnet D (2020) Addition of corticosteroids to immunoglobulins is associated with recovery of cardiac function in multi-inflammatory syndrome in children. Circulation 142(23):2282–2284. https://doi.org/10.1161/CIRCULATIONAHA.120.050147

    Article  CAS  Google Scholar 

  37. Ouldali N, Toubiana J, Antona D, Javouhey E, Madhi F et al (2021) Association of intravenous immunoglobulins plus methylprednisolone vs immunoglobulins alone with course of fever in multisystem inflammatory syndrome in children. JAMA 325(9):855–864. https://doi.org/10.1001/jama.2021.0694. (Erratum in: JAMA. 2021 Jul 6;326(1):90)

    Article  CAS  Google Scholar 

  38. Edalatifard M, Akhtari M, Salehi M, Naderi Z, Jamshidi A et al (2020) Intravenous methylprednisolone pulse as a treatment for hospitalised severe COVID-19 patients: results from a randomised controlled clinical trial. Eur Respir J 56(6):2002808. https://doi.org/10.1183/13993003.02808-2020

    Article  CAS  Google Scholar 

  39. McArdle AJ, Vito O, Patel H, Seaby EG, Shah P, Wilson C et al (2021) Treatment of multisystem inflammatory syndrome in children. N Engl J Med 385(1):11–22. https://doi.org/10.1056/NEJMoa2102968

    Article  CAS  Google Scholar 

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Acknowledgements

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Funding

No funding resources support this study.

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Authors and Affiliations

  1. Department of Pediatric Rheumatology, Pediatric Center of Excellence, Children’s Medical Center of Tehran University of Medical Science, No 63, Gharib Ave., Keshavarz Blv., Tehran, Iran

    Payman Sadeghi, Raheleh Assari, Fatemeh Tahghighi & Vahid Ziaee

  2. Department of Pediatric Cardiology, Pediatric Center of Excellence, Children’s Medical Center of Tehran University of Medical Science, Tehran, Iran

    Mojtaba Gorji

  3. Department of Pediatric Rheumatology, Imam Khomeini Hospital Complex, Tehran University of Medical Science, Tehran, Iran

    Seyed Reza Raeeskarami

Authors
  1. Payman Sadeghi
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  2. Mojtaba Gorji
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  3. Raheleh Assari
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  4. Fatemeh Tahghighi
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  5. Seyed Reza Raeeskarami
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  6. Vahid Ziaee
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Contributions

PS performed data gathering, contributed to the conception and design of the study. SR and FT contributed to the conception and design of the study, and clinical expertise. RA analysed data, interpretation of the clinical data and drafting of the manuscript, contributed to the conception and design of the study. MG performed echocardiography and contributed to interpretation of the clinical data. VZ provided the concept the survey, interpretation of the clinical data, critical revision of the final draft of manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Raheleh Assari.

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Ethics approval and consent to participate

This research was performed in accordance with the Declaration of Helsinki. All authors read and approved the final version of the manuscript. Informed consent was obtained from all study subjects. The protocol and informed consent were approved by Institutional Review board of Children Medical Center of Tehran University of Medical Sciences.

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Not applicable.

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The authors declare that they have no competing interests.

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Sadeghi, P., Gorji, M., Assari, R. et al. Methylprednisolone pulses as an initial treatment in hyperinflammatory syndrome after COVID-19 in children: evaluation of laboratory data, serial echocardiography and outcome: a case series. ICMx 10, 56 (2022). https://doi.org/10.1186/s40635-022-00484-1

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