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==Historical Perspective== | ==Historical Perspective== | ||
* | |||
* [[COVID-19]]-associated multisystem inflammatory syndrome was first reported as a new febrile pediatric entity began to appear in late April 2020 during the [[COVID-19]] pandemic in Western Eu<nowiki/>rope.<ref name=":0">Shulman, Stanford T. "Pediatric coronavirus disease-2019–associated multisystem inflammatory syndrome." ''Journal of the Pediatric Infectious Diseases Society'' (2020).</ref> | |||
* Cases of children with such symptoms were quickly identified in the New York City area, which was then the most heavily affected city in the U.S. by the [[COVID-19]] pandemic;<ref name=":0" /> | * Cases of children with such symptoms were quickly identified in the New York City area, which was then the most heavily affected city in the U.S. by the [[COVID-19]] pandemic;<ref name=":0" /> | ||
* A | * A repor<nowiki/>t of 8 cases from Evelina London Children's Hospital was published on 6 May 2020, showing very prominent markers of [[inflammation]] such as [[ferritin]], [[D-dimers]], [[triglycerides]], eleva<nowiki/>ted [[cardiac enzymes]], high [[NT-pro-BNP]] levels and [[troponin]], being empirically treated with [[IVIG]];<ref name=":0" /> | ||
* In 22 May, an article from the Journal of Pediatric Infectious Diseases Society addressed some of the similarities and differences of this new entity with [[Kawasaki's disease]], noting | * In 22 May, an article from the Journal of Pediatric Infectious Diseases Society addressed some of the similarities and differences of this new entity with [[Kawasaki's disease]], noting th<nowiki/>at the demographics affected was significantly different, as it was not seen in Asia despite the pandemic also affecting such countries, but it was affecting mostly children of African ethnicity. The author also differentiated some of the laboratory findings, resembling the [[macrophage activation syndrome]] and not [[Kawasaki's disease]].<ref name=":0" /> | ||
==Classification of Disease Severity of COVID-19-associated multisystem inflammatory syndrome == | ==Classification of Disease Severity of COVID-19-associated multisystem inflammatory syndrome == | ||
| Line 25: | Line 27: | ||
==Pathophysiology== | ==Pathophysiology== | ||
* The exact pathophysiological mechanism of COVID-19-associated multisystem inflammatory syndrome is unclear. | * The exact pathophysiological mechanism of [[COVID-19]]-associated multisystem inflammatory syndrome is unclear; | ||
*Since there is a lag time between COVID-19-associated multisystem inflammatory syndrome appearance and [[COVID-19]] infection ([[median]] time: 25 days)<ref name=":2">Feldstein, Leora R., et al. "Multisystem inflammatory syndrome in US children and adolescents." ''New England Journal of Medicine'' (2020).</ref> it is suspected to be a post-infectious phenomenon related to [[IgG]] antibody-mediated enhancement of disease. There are two arguments that support this theory: the presence of [[IgG]] [[antibodies]] against SARS-CoV2 and the presence of the lag time between [[COVID-19]] symptoms and COVID-19-associated multisystem inflammatory syndrome.<ref name=":3">Rowley, Anne H. "Understanding SARS-CoV-2-related multisystem inflammatory syndrome in children." ''Nature Reviews Immunology'' (2020): 1-2.</ref> | *It is thought that [[COVID-19]]-associated multisystem inflammatory syndrome is caused by either [[IgG]] [[antibody]]-mediated enhancement of the disease, an [[acute]] [[viral]] presentation, or due to [[cytokine storm]].<ref name=":3" /> | ||
*Since there is a lag time between [[COVID-19]]-associated multisystem inflammatory syndrome appearance and [[COVID-19]] infection ([[median]] time: 25 days)<ref name=":2">Feldstein, Leora R., et al. "Multisystem inflammatory syndrome in US children and adolescents." ''New England Journal of Medicine'' (2020).</ref> it is suspected to be a post-infectious phenomenon related to [[IgG]] antibody-mediated enhancement of disease. There are two arguments that support this theory: the presence of [[IgG]] [[antibodies]] against SARS-CoV2 and the presence of the lag time between [[COVID-19]] symptoms and COVID-19-associated multisystem inflammatory syndrome.<ref name=":3">Rowley, Anne H. "Understanding SARS-CoV-2-related multisystem inflammatory syndrome in children." ''Nature Reviews Immunology'' (2020): 1-2.</ref> | |||
*There is, however, another theory that states that it is still an [[acute]] [[viral]] presentation of the disease due to the fact that children presenting with such symptoms undergone exploratory [[laparotomy]] which found [[mesenteric adenitis]], supporting GI infection. SARS-CoV2 is also known to easily infect [[enterocytes]]. Another interesting point to consider is that the worsening of illness has not been seen in patients with [[COVID-19]] who are treated with convalescent plasma, which could have occurred if it was an antibody-mediated enhancement.<ref name=":3" /> | *There is, however, another theory that states that it is still an [[acute]] [[viral]] presentation of the disease due to the fact that children presenting with such symptoms undergone exploratory [[laparotomy]] which found [[mesenteric adenitis]], supporting GI infection. SARS-CoV2 is also known to easily infect [[enterocytes]]. Another interesting point to consider is that the worsening of illness has not been seen in patients with [[COVID-19]] who are treated with convalescent plasma, which could have occurred if it was an antibody-mediated enhancement.<ref name=":3" /> | ||
*There is another hypothesis for the [[cytokine storm]] seen on children with COVID-19-associated multisystem inflammatory syndrome is originated from the known ability of [[coronaviruses]] to block type I and type III [[interferon]] responses, delaying the [[cytokine storm]] in patients that could not control the [[viral replication]] on earlier phases of the disease.<ref name=":3" /> | *There is another hypothesis for the [[cytokine storm]] seen on children with COVID-19-associated multisystem inflammatory syndrome is originated from the known ability of [[coronaviruses]] to block type I and type III [[interferon]] responses, delaying the [[cytokine storm]] in patients that could not control the [[viral replication]] on earlier phases of the disease.<ref name=":3" /> | ||
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==Differentiating Any Disease from other disease== | ==Differentiating Any Disease from other disease== | ||
* Children who met criteria for COVID-19-associated multisystem inflammatory syndrome presented features that overlapped with the ones seen on [[Kawasaki's disease]] and [[toxic shock syndrome]], such as [[conjunctival injection]], [[oropharyngeal]] findings (red and/or cracked lips, [[strawberry tongue]]), [[rash]], [[Swelling|swollen]] and/or [[erythematous]] hands and feet, and cervical [[lymphadenopathy]].<ref name=":1">Whittaker E, Bamford A, Kenny J, et al; PMIS-TS Study Group; EUCLIDS and PERFORM Consortia. Clinical and laboratory characteristics of 58 children with a pediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2. JAMA. doi:10.1001/jama.2020.10369</ref> | *[[COVID-19]]-associated multisystem inflammatory syndrome must be differentiated from [[Kawasaki's disease]] and [[toxic shock syndrome]]. | ||
*Children who met criteria for COVID-19-associated multisystem inflammatory syndrome presented features that overlapped with the ones seen on [[Kawasaki's disease]] and [[toxic shock syndrome]], such as [[conjunctival injection]], [[oropharyngeal]] findings (red and/or cracked lips, [[strawberry tongue]]), [[rash]], [[Swelling|swollen]] and/or [[erythematous]] hands and feet, and cervical [[lymphadenopathy]].<ref name=":1">Whittaker E, Bamford A, Kenny J, et al; PMIS-TS Study Group; EUCLIDS and PERFORM Consortia. Clinical and laboratory characteristics of 58 children with a pediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2. JAMA. doi:10.1001/jama.2020.10369</ref> | |||
*[[PCR]] tests for SARS-CoV-2 were positive in the minority of cases (26%), while the [[IgG]] [[antibody]] was positive in most patients (87%)<ref name=":1" /> and it remains as the preferred laboratory test for differentiating such diseases; | *[[PCR]] tests for SARS-CoV-2 were positive in the minority of cases (26%), while the [[IgG]] [[antibody]] was positive in most patients (87%)<ref name=":1" /> and it remains as the preferred laboratory test for differentiating such diseases; | ||
*The first cases of COVID-19-associated multisystem inflammatory syndrome presented with: unrelenting [[fever]] (38–40°C), [[conjunctivitis]], cutaneous [[rash]], [[peripheral edema]], extremity pain and remarkable [[gastrointestinal]] symptoms. Most didn't have any respiratory symptoms, and all progressed to warm vasoplegic [[Shock (circulatory)|shock]], refractory to volume resuscitation demanding [[vasopressors]] for [[hemodynamic]] support.<ref name=":4">Riphagen, Shelley, et al. "Hyperinflammatory shock in children during COVID-19 pandemic." ''The Lancet'' 395.10237 (2020): 1607-1608.</ref> | *The first cases of COVID-19-associated multisystem inflammatory syndrome presented with: unrelenting [[fever]] (38–40°C), [[conjunctivitis]], cutaneous [[rash]], [[peripheral edema]], extremity pain and remarkable [[gastrointestinal]] symptoms. Most didn't have any respiratory symptoms, and all progressed to warm vasoplegic [[Shock (circulatory)|shock]], refractory to volume resuscitation demanding [[vasopressors]] for [[hemodynamic]] support.<ref name=":4">Riphagen, Shelley, et al. "Hyperinflammatory shock in children during COVID-19 pandemic." ''The Lancet'' 395.10237 (2020): 1607-1608.</ref> | ||
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'''Gender''' | '''Gender''' | ||
* Most of the cases | * Most of the cases seem to happen in boys.<ref name=":4" /><ref name=":1" /> | ||
'''Race''' | '''Race''' | ||
Revision as of 15:40, 14 July 2020
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Harmeet Kharoud M.D.[2] José Eduardo Riceto Loyola Junior, M.D.[3] Sahar Memar Montazerin, M.D.[4]
Synonyms and keywords: Multisystem Inflammatory Syndrome in Children (MIS-C)
Overview
COVID-19-associated multisystem inflammatory syndrome (also known as PIMS-TS - pediatric inflammatory multisystem syndrome temporally with SARS-CoV2 infection or MIS-C - multisystem inflammatory syndrome in children) is an uncommon clinical entity caused by SARS-CoV2 and seen mostly on children. It presents with: fever > 3 days and elevated markers of inflammation and 2 of the following 5 criteria: rash or conjunctivitis; hypotension or shock; myocardial dysfunction, pericarditis, valvulitis or coronary abnormalities; evidence of coagulopathy and/or acute gastrointestinal problems along with evidence of COVID-19. It seems to be a severe form of COVID-19 in children presenting with symptoms that can be challenging to differentiate from other pediatric infectious diseases such as toxic shock syndrome and Kawasaki disease. The pathophysiology of this form of SARS-CoV2 infection remains unknown.
Historical Perspective
- COVID-19-associated multisystem inflammatory syndrome was first reported as a new febrile pediatric entity began to appear in late April 2020 during the COVID-19 pandemic in Western Europe.[1]
- Cases of children with such symptoms were quickly identified in the New York City area, which was then the most heavily affected city in the U.S. by the COVID-19 pandemic;[1]
- A report of 8 cases from Evelina London Children's Hospital was published on 6 May 2020, showing very prominent markers of inflammation such as ferritin, D-dimers, triglycerides, elevated cardiac enzymes, high NT-pro-BNP levels and troponin, being empirically treated with IVIG;[1]
- In 22 May, an article from the Journal of Pediatric Infectious Diseases Society addressed some of the similarities and differences of this new entity with Kawasaki's disease, noting that the demographics affected was significantly different, as it was not seen in Asia despite the pandemic also affecting such countries, but it was affecting mostly children of African ethnicity. The author also differentiated some of the laboratory findings, resembling the macrophage activation syndrome and not Kawasaki's disease.[1]
Classification of Disease Severity of COVID-19-associated multisystem inflammatory syndrome
- There is no established system for the classification of COVID-19-associated multisystem inflammatory syndrome.
Pathophysiology
- The exact pathophysiological mechanism of COVID-19-associated multisystem inflammatory syndrome is unclear;
- It is thought that COVID-19-associated multisystem inflammatory syndrome is caused by either IgG antibody-mediated enhancement of the disease, an acute viral presentation, or due to cytokine storm.[2]
- Since there is a lag time between COVID-19-associated multisystem inflammatory syndrome appearance and COVID-19 infection (median time: 25 days)[3] it is suspected to be a post-infectious phenomenon related to IgG antibody-mediated enhancement of disease. There are two arguments that support this theory: the presence of IgG antibodies against SARS-CoV2 and the presence of the lag time between COVID-19 symptoms and COVID-19-associated multisystem inflammatory syndrome.[2]
- There is, however, another theory that states that it is still an acute viral presentation of the disease due to the fact that children presenting with such symptoms undergone exploratory laparotomy which found mesenteric adenitis, supporting GI infection. SARS-CoV2 is also known to easily infect enterocytes. Another interesting point to consider is that the worsening of illness has not been seen in patients with COVID-19 who are treated with convalescent plasma, which could have occurred if it was an antibody-mediated enhancement.[2]
- There is another hypothesis for the cytokine storm seen on children with COVID-19-associated multisystem inflammatory syndrome is originated from the known ability of coronaviruses to block type I and type III interferon responses, delaying the cytokine storm in patients that could not control the viral replication on earlier phases of the disease.[2]
Differentiating Any Disease from other disease
- COVID-19-associated multisystem inflammatory syndrome must be differentiated from Kawasaki's disease and toxic shock syndrome.
- Children who met criteria for COVID-19-associated multisystem inflammatory syndrome presented features that overlapped with the ones seen on Kawasaki's disease and toxic shock syndrome, such as conjunctival injection, oropharyngeal findings (red and/or cracked lips, strawberry tongue), rash, swollen and/or erythematous hands and feet, and cervical lymphadenopathy.[4]
- PCR tests for SARS-CoV-2 were positive in the minority of cases (26%), while the IgG antibody was positive in most patients (87%)[4] and it remains as the preferred laboratory test for differentiating such diseases;
- The first cases of COVID-19-associated multisystem inflammatory syndrome presented with: unrelenting fever (38–40°C), conjunctivitis, cutaneous rash, peripheral edema, extremity pain and remarkable gastrointestinal symptoms. Most didn't have any respiratory symptoms, and all progressed to warm vasoplegic shock, refractory to volume resuscitation demanding vasopressors for hemodynamic support.[5]
- Serum IL-6 level was elevated in most patients. IL-2R, IL-18, and CXCL 9 levels were elevated in all patients of a cohort and mildly increased IFN-γ and IL-8 levels in some.
- TNF-α, IL-1b, IL-2, IL-4, IL-5, and IL-13 levels remained normal in one in a series of cases from New York City.[6]
| Parameters | COVID-19-associated multisystem inflammatory syndrome (PIMS-TS) | Kawasaki Disease (KD) | Kawasaki Disease Shock (KDS) | Toxic Shock Syndrome (TSS) |
|---|---|---|---|---|
| Age (median, IQR) | 9 (5.7-14) | 2.7 (1.4-4.7) | 3.8 (0.2-18) | 7.38 (2.4-15.4) |
| Total white cell count (*10^9/L) | 17 (12-22) | 13.4 (10.5-17.3) | 12.1 (7.9-15.5) | 15.6 (7.5-20) |
| Neutrophil count (*10^9/L) | 13 (10-19) | 7.2 (5.1-9.9) | 5.5 (3.2-10.3) | 16.4 (12-22) |
| Lymphocyte count (*10^9/L) | 0.8 (0.5-1.5) | 2.8 (1.5-4.4) | 1.6 (1-2.5) | 0.63 (0.41, 1.13) |
| Hemoglobin (g/L) | 92 (83-103) | 111.0 (105-119) | 107 (98-115) | 114 (98-130) |
| Platelet number (10^9/L) | 151 (104-210) | 365.0 (288-462) | 235 (138-352) | 155 (92- 255) |
| C-reactive protein (mg/L) | 229 (156-338) | 67.0(40-150) | 193 (83-237) | 201 (122, 317) |
| ALT (IU/L) | 42 (26-95) | 42.0 (24-112) | 73 (34-107) | 30.00 (22.10, 49.25) |
| Albumin (g/L) | 24 (21-27) | 38.0 (35-41) | 30 (27-35) | 27.00 (21.00, 31.00) |
| Ferritin (ug/L) | 610 (359-1280) | 200 (143-243) | 301 (228-337) | - |
| NT-Pro-BNP (pg/ml) | 788 (174-10548) | 41 (12-102) | 396 (57-1520) | - |
| Troponin (ng/L) | 45 (8-294) | 10.0 (10-20) | 10 (10-30) | - |
| D-dimer (ng/ml) | 3578 (2085- 8235) | 1650 (970-2660) | 2580 (1460- 2990) | - |
- Most patients presented with the following findings: elevated erythrocyte sedimentation rate or C-reactive protein level, elevated ferritin level, lymphocytopenia, hypoalbuminemia, neutrophilia, elevated alanine aminotransferase level, anemia, thrombocytopenia prolonged INR, elevated d-dimer level, or elevated fibrinogen level.[3]
- To view the differential diagnosis of COVID-19, click here.
Epidemiology and Demographics
Age
- Children aged age over 5 years seem to have a worse prognosis than younger ones.[7]
- The median age found out in a study published by JAMA was 9 years.[4]
Gender
Race
Comorbidities
- Clinical evidence of association with underlying diseases is still scarce since it is a rare presentation of COVID-19 in children and teenagers.[8]
Natural History, Complications, and Prognosis
Complications of COVID-19-associated multisystem inflammatory syndrome include:[9][10][11][12][13][14]
- Ventricular dysfunction
- Coronary artery changes
- Atrioventricular valve regurgitation
- Pericardial effusions
- Shock
- Venous thromboembolic events
- Cytokine storm syndrome
Diagnosis
Diagnostic Criteria
The table below describes various diagnostic criteria for COVID-19-associated multisystem inflammatory syndrome:[15][16][17]
| Features | World Health Organization
Criteria |
Royal College of Paediatrics and Child Health
(United Kingdom) Criteria |
Centers for Disease Control and Prevention
(United States) Criteria |
|---|---|---|---|
| Age |
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| Clinical Features |
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| 1. Rash or non-purulent conjunctival injection or mucocutaneous involvement |
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| 2. Low blood pressure/Shock | |||
| 3. Findings consistent with myocarditis, pericarditis, valvulitis or coronary involvement | |||
| 4. Acute gastrointestinal symptoms | |||
| Laboratory Findings | 5. Laboratory evidence of coagulopathy |
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| Diagnosis of SARS-CoV-2 |
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| Others |
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History and Symptoms
COVID-19 associated multisystem inflammatory syndrome is associated with the following symptoms:[15][14]
- Fever lasting 24 hours or longer.
- Vomiting
- Diarrhea
- Abdominal pain
- Difficulty Breathing
- Chest pain
- Headache
- Sore throat
- New onset confusion
Physical Examination
COVID-19 associated multisystem inflammatory syndrome is associated with the following physical examination findings:[15]
- Skin rash
- Conjuctivitis
- Redness or swelling of the lips and tongue
- Redness or swelling of the hands or feet
- Lymphadenopathy
- Lethargy
- Cyanosis
Laboratory Findings
COVID-19 associated multisystem inflammatory syndrome is associated with the following laboratory findings:[15][18]
Less common laboratory findings include:
- Abnormal fibrinogen
- Hypoalbuminaemia
- Elevated creatiine kinase (CK)
- Elevated LDH
- Elevated triglycerides
Inflammatory biomarkers
Elevation of inflammatory markers including erythrocyte sedimentation rate, reactive protein, and procalcitonin are usually seen in MIS-C. Increased level of Interleukin-6 (IL-6), Interleukin-10 (IL-10) d-dimer, serum ferritin, prothrombin time have also been seen in MIS-C.
Cardiac biomarkers
Elevation of cardic enzymes including cardiac troponins (cardiac troponin I(cTnI) and cardiac troponin T (cTnT)) and Brain natriuretic peptide (BNP)) has been observed in MIS-C patients.
- To view the complete physical examination in COVID-19, click here.
- To view the laboratory findings on COVID-19, click here.
X-ray
X-ray of patients with COVID-19 associated multiorgan system inflammatory syndrome may be normal. When abnormal, findings may include the followings:[19]
- Peribronchial cuffing
- Perihilar interstitial thickening
- Perihilar opacification
- Perihilar consolidation
- Low volume pleural effusion affecting both lungs
- Left lower lobe atelectasis
Echocardiography or Ultrasound
Abdominal ultrasound imaging of patients with COVID-19 associated multiorgan system inflammatory syndrome may include the following findings:[19]
- Free-fluid
- Localised inflammatory change within the right iliac fossa
- A combination of echogenic expanded mesenteric fat and enlarged lymph nodes
- Bowel wall thickening of parts of ileum and cecum
- Gall bladder wall thickening and edema
To view the echocardiographic findings on COVID-19, click here.
CT scan
Chest CT scan of patients with COVID-19-associated multisystem inflammatory syndrome includes the following patterns:[19]
- Consolidation and collapse of the lung bases
- Pleural effusions
- Diffuse bilateral ground-glass opacities with dense, patchy consolidation
Abdominal CT scan may show the following abnormalities:
- Intestinal wall thickening particularly in the terminal ileum and cecum
To view the CT scan findings on COVID-19, click here.
MRI
- To view the MRI findings on COVID-19, click here.
Other Imaging Findings
- To view other imaging findings on COVID-19, click here.
Other Diagnostic Studies
- To view other diagnostic studies for COVID-19, click here.
Treatment
Medical Therapy
Treatment of patients with COVID-19-associated multisystem inflammatory syndrome includes:[14]
- Antibiotics: broad-spectrum antibiotics are recommended initially.
- If the symptoms are mild, ceftriaxone may be sufficient.
- If the gastrointestinal symptoms are predominant, then metronidazole is recommended.
- In case of severe symptoms including shock] the following antibiotics have been recommended:
- Vancomycin, clindamycin, and cefepime
- Vancomycin, meropenem, and gentamicin
- Remdesivir is indicated in children with PCR positive COVID-19 and/or with a presentation consistent with typical COVID-19.
- It should be administered 5 mg/kg loading dose IV once (max dose 200 mg) on day 1, then 2.5 mg/kg (100 mg max dose) IV daily for nine days.
- Cardiac and respiratory support is recommended for patients presenting with shock.
- IVIG and aspirin for Kawasaki-like disease
Patients with KD-like illness in high-risk categories should receive IVIG with other agents. The high-risk category includes:
- Infants
- Those with KD shock syndrome
- Those with CRP > 130 g/dL
- Those with admission echo Z score > 2.5 or aneurysms
- Asian race
The following treatment regimen is recommended for patients with KD-like illness in high-risk categories:
- IVIG 2 g/kg as a single infusion with three-day pulse methylprednisolone. If fails, then:
- The second dose of IVIG or infliximab (a Tumor necrosis factor (TNF)-alpha inhibitor)
- Venous thromboembolism prophylaxis may be indicated as well.
- Few studies have reported that interleukin-1 inhibitors may be effective in the treatment of severe cases.[20]
- Tocilizumab (interleukin-6 inhibitor) is another agent that has been used in some cases.
Prevention
- MIS-C can be prevented by reducing the risk of child exposure to COVID-19 infection.
References
- ↑ 1.0 1.1 1.2 1.3 Shulman, Stanford T. "Pediatric coronavirus disease-2019–associated multisystem inflammatory syndrome." Journal of the Pediatric Infectious Diseases Society (2020).
- ↑ 2.0 2.1 2.2 2.3 Rowley, Anne H. "Understanding SARS-CoV-2-related multisystem inflammatory syndrome in children." Nature Reviews Immunology (2020): 1-2.
- ↑ 3.0 3.1 Feldstein, Leora R., et al. "Multisystem inflammatory syndrome in US children and adolescents." New England Journal of Medicine (2020).
- ↑ 4.0 4.1 4.2 4.3 4.4 4.5 Whittaker E, Bamford A, Kenny J, et al; PMIS-TS Study Group; EUCLIDS and PERFORM Consortia. Clinical and laboratory characteristics of 58 children with a pediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2. JAMA. doi:10.1001/jama.2020.10369
- ↑ 5.0 5.1 5.2 Riphagen, Shelley, et al. "Hyperinflammatory shock in children during COVID-19 pandemic." The Lancet 395.10237 (2020): 1607-1608.
- ↑ Cheung, Eva W., et al. "Multisystem Inflammatory Syndrome Related to COVID-19 in Previously Healthy Children and Adolescents in New York City." JAMA (2020).
- ↑ 7.0 7.1 Pouletty, Marie, et al. "Paediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2 mimicking Kawasaki disease (Kawa-COVID-19): a multicentre cohort." Annals of the Rheumatic Diseases (2020).
- ↑ "World Health Organization - Multisystem inflammatory syndrome in children and adolescents temporally related to COVID-19". WHO. 07/13/2020. Check date values in:
|date=(help) - ↑ Riphagen, Shelley; Gomez, Xabier; Gonzalez-Martinez, Carmen; Wilkinson, Nick; Theocharis, Paraskevi (2020). "Hyperinflammatory shock in children during COVID-19 pandemic". The Lancet. 395 (10237): 1607–1608. doi:10.1016/S0140-6736(20)31094-1. ISSN 0140-6736.
- ↑ DeBiasi, Roberta L.; Song, Xiaoyan; Delaney, Meghan; Bell, Michael; Smith, Karen; Pershad, Jay; Ansusinha, Emily; Hahn, Andrea; Hamdy, Rana; Harik, Nada; Hanisch, Benjamin; Jantausch, Barbara; Koay, Adeline; Steinhorn, Robin; Newman, Kurt; Wessel, David (2020). "Severe COVID-19 in Children and Young Adults in the Washington, DC Metropolitan Region". The Journal of Pediatrics. doi:10.1016/j.jpeds.2020.05.007. ISSN 0022-3476.
- ↑ Verdoni, Lucio; Mazza, Angelo; Gervasoni, Annalisa; Martelli, Laura; Ruggeri, Maurizio; Ciuffreda, Matteo; Bonanomi, Ezio; D'Antiga, Lorenzo (2020). "An outbreak of severe Kawasaki-like disease at the Italian epicentre of the SARS-CoV-2 epidemic: an observational cohort study". The Lancet. 395 (10239): 1771–1778. doi:10.1016/S0140-6736(20)31103-X. ISSN 0140-6736.
- ↑ Belhadjer, Zahra; Méot, Mathilde; Bajolle, Fanny; Khraiche, Diala; Legendre, Antoine; Abakka, Samya; Auriau, Johanne; Grimaud, Marion; Oualha, Mehdi; Beghetti, Maurice; Wacker, Julie; Ovaert, Caroline; Hascoet, Sebastien; Selegny, Maëlle; Malekzadeh-Milani, Sophie; Maltret, Alice; Bosser, Gilles; Giroux, Nathan; Bonnemains, Laurent; Bordet, Jeanne; Di Filippo, Sylvie; Mauran, Pierre; Falcon-Eicher, Sylvie; Thambo, Jean-Benoît; Lefort, Bruno; Moceri, Pamela; Houyel, Lucile; Renolleau, Sylvain; Bonnet, Damien (2020). "Acute heart failure in multisystem inflammatory syndrome in children (MIS-C) in the context of global SARS-CoV-2 pandemic". Circulation. doi:10.1161/CIRCULATIONAHA.120.048360. ISSN 0009-7322.
- ↑ Klok, F.A.; Kruip, M.J.H.A.; van der Meer, N.J.M.; Arbous, M.S.; Gommers, D.; Kant, K.M.; Kaptein, F.H.J.; van Paassen, J.; Stals, M.A.M.; Huisman, M.V.; Endeman, H. (2020). "Confirmation of the high cumulative incidence of thrombotic complications in critically ill ICU patients with COVID-19: An updated analysis". Thrombosis Research. 191: 148–150. doi:10.1016/j.thromres.2020.04.041. ISSN 0049-3848.
- ↑ 14.0 14.1 14.2 Hennon, Teresa R.; Penque, Michelle D.; Abdul-Aziz, Rabheh; Alibrahim, Omar S.; McGreevy, Megan B.; Prout, Andrew J.; Schaefer, Beverly A.; Ambrusko, Steven J.; Pastore, John V.; Turkovich, Stephen J.; Gomez-Duarte, Oscar G.; Hicar, Mark D. (2020). "COVID-19 associated Multisystem Inflammatory Syndrome in Children (MIS-C) guidelines; a Western New York approach". Progress in Pediatric Cardiology. 57: 101232. doi:10.1016/j.ppedcard.2020.101232. ISSN 1058-9813.
- ↑ 15.0 15.1 15.2 15.3 Feldstein, Leora R.; Rose, Erica B.; Horwitz, Steven M.; Collins, Jennifer P.; Newhams, Margaret M.; Son, Mary Beth F.; Newburger, Jane W.; Kleinman, Lawrence C.; Heidemann, Sabrina M.; Martin, Amarilis A.; Singh, Aalok R.; Li, Simon; Tarquinio, Keiko M.; Jaggi, Preeti; Oster, Matthew E.; Zackai, Sheemon P.; Gillen, Jennifer; Ratner, Adam J.; Walsh, Rowan F.; Fitzgerald, Julie C.; Keenaghan, Michael A.; Alharash, Hussam; Doymaz, Sule; Clouser, Katharine N.; Giuliano, John S.; Gupta, Anjali; Parker, Robert M.; Maddux, Aline B.; Havalad, Vinod; Ramsingh, Stacy; Bukulmez, Hulya; Bradford, Tamara T.; Smith, Lincoln S.; Tenforde, Mark W.; Carroll, Christopher L.; Riggs, Becky J.; Gertz, Shira J.; Daube, Ariel; Lansell, Amanda; Coronado Munoz, Alvaro; Hobbs, Charlotte V.; Marohn, Kimberly L.; Halasa, Natasha B.; Patel, Manish M.; Randolph, Adrienne G. (2020). "Multisystem Inflammatory Syndrome in U.S. Children and Adolescents". New England Journal of Medicine. doi:10.1056/NEJMoa2021680. ISSN 0028-4793.
- ↑ "Guidance - Paediatric multisystem inflammatory syndrome temporally associated with COVID-19 (PIMS) | RCPCH".
- ↑ Cheung, Eva W.; Zachariah, Philip; Gorelik, Mark; Boneparth, Alexis; Kernie, Steven G.; Orange, Jordan S.; Milner, Joshua D. (2020). "Multisystem Inflammatory Syndrome Related to COVID-19 in Previously Healthy Children and Adolescents in New York City". JAMA. doi:10.1001/jama.2020.10374. ISSN 0098-7484.
- ↑ 19.0 19.1 19.2 Hameed, Shema; Elbaaly, Heba; Reid, Catriona E. L.; Santos, Rui M. F.; Shivamurthy, Vinay; Wong, James; Jogeesvaran, K. Haran (2020). "Spectrum of Imaging Findings on Chest Radiographs, US, CT, and MRI Images in Multisystem Inflammatory Syndrome in Children (MIS-C) Associated with COVID-19". Radiology: 202543. doi:10.1148/radiol.2020202543. ISSN 0033-8419.
- ↑ Shah, Satish K.; Munoz, Alvaro Coronado (2020). "Multisystem Inflammatory Syndrome in Children in COVID-19 Pandemic". The Indian Journal of Pediatrics. doi:10.1007/s12098-020-03440-7. ISSN 0019-5456.