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MULTISYSTEM INFLAMMATORY SYNDROME IN CHILDREN: DIAGNOSTIC MARKERS AND FEATURES OF PHARMACOTHERAPY

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Relevance. In 2020, children were hospitalized with fever and multisystem inflammation throughout the world during the COVID-19 pandemic. In the United States, this condition is called MIS-C (Multisystem Inflammatory Syndrome in Children). This syndrome is thought to be similar to the severe course of COVID-19 in adults (cytokine storm). The objective of the work is to evaluate the features of the course and pharmacotherapy of multisystem inflammatory syndrome in children. Materials and methods. The study included 17 children (10 boys and 7 girls) aged 3-16 years (on average – 9.5±3.4 years). Diagnosis of coronavirus infection was performed by polymerase chain reaction with real-time detection, determined the level of immunoglobulins M and G before coronavirus infection. Results. The duration of fever in patients was 5-21 days (average 8.1±4.0 days), the duration of inpatient treatment – 7-35 days (average 15.7±7.0 days). Blood albumin levels were reduced in 53.8% of children; the level of fibrinogen was increased in 88.2% of children, the level of C-reactive protein, ferritin, and D-dimer – in all patients. 15 (88.2%) children had pathology of the digestive system, 13 (76.5%) – cardiovascular system (7 children were diagnosed with carditis, 2 – dilation of coronary arteries, 7 – cardiac arrhythmia). Acute respiratory distress -syndrome was found in a 13-year-old girl, shock - in an 11-year-old boy, 11 children (64.7%) were diagnosed with the pathology of the respiratory system (pleurisy, pneumonia), skin and mucous membranes, and 4 children (23.5%) there were manifestations of central nervous system disorders (meningism, decreased reflexes, ataxia), in 2 (11.8%) – renal failure. On average, each patient had lesions of 3.9 ±1.2 systems. Conclusions. MIS-C was manifested by prolonged fever, high levels of laboratory markers of inflammation, hypoalbuminemia, hypercoagulation, often – pathological manifestations of the cardiovascular, digestive, respiratory systems, skin, and mucous membranes. The treatment included intravenous immunoglobulin, steroids, anticoagulant, and antibacterial therapy and was effective.
Title: MULTISYSTEM INFLAMMATORY SYNDROME IN CHILDREN: DIAGNOSTIC MARKERS AND FEATURES OF PHARMACOTHERAPY
Description:
Relevance.
In 2020, children were hospitalized with fever and multisystem inflammation throughout the world during the COVID-19 pandemic.
In the United States, this condition is called MIS-C (Multisystem Inflammatory Syndrome in Children).
This syndrome is thought to be similar to the severe course of COVID-19 in adults (cytokine storm).
The objective of the work is to evaluate the features of the course and pharmacotherapy of multisystem inflammatory syndrome in children.
Materials and methods.
The study included 17 children (10 boys and 7 girls) aged 3-16 years (on average – 9.
5±3.
4 years).
Diagnosis of coronavirus infection was performed by polymerase chain reaction with real-time detection, determined the level of immunoglobulins M and G before coronavirus infection.
Results.
The duration of fever in patients was 5-21 days (average 8.
1±4.
0 days), the duration of inpatient treatment – 7-35 days (average 15.
7±7.
0 days).
Blood albumin levels were reduced in 53.
8% of children; the level of fibrinogen was increased in 88.
2% of children, the level of C-reactive protein, ferritin, and D-dimer – in all patients.
15 (88.
2%) children had pathology of the digestive system, 13 (76.
5%) – cardiovascular system (7 children were diagnosed with carditis, 2 – dilation of coronary arteries, 7 – cardiac arrhythmia).
Acute respiratory distress -syndrome was found in a 13-year-old girl, shock - in an 11-year-old boy, 11 children (64.
7%) were diagnosed with the pathology of the respiratory system (pleurisy, pneumonia), skin and mucous membranes, and 4 children (23.
5%) there were manifestations of central nervous system disorders (meningism, decreased reflexes, ataxia), in 2 (11.
8%) – renal failure.
On average, each patient had lesions of 3.
9 ±1.
2 systems.
Conclusions.
MIS-C was manifested by prolonged fever, high levels of laboratory markers of inflammation, hypoalbuminemia, hypercoagulation, often – pathological manifestations of the cardiovascular, digestive, respiratory systems, skin, and mucous membranes.
The treatment included intravenous immunoglobulin, steroids, anticoagulant, and antibacterial therapy and was effective.

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