Abstract
Backgrounds: Multisystem inflammatory syndrome in children (MIS-C) is a rare but dangerous complication of COVID-19. The pathophysiology, immunology and long-term clinical outcomes are not yet fully known, and further research is required. The aim of our study is to identify and understand long-term outcomes of MIS-C.
Methods: In this prospective cohort study conducted from January 2021 to December 2021, 30 patients with MIS-C were enrolled. To identify the outcomes, all patients were evaluated in face-to-face visits 2 weeks, 8 weeks, and 6 months after diagnosis using clinical assessment, laboratory testing and cardiological examination.
Results: During the two-week follow up visit 20% (n=6) of children had abnormal clinical findings. Notably, significant increase was seen in these findings at 8-week follow-up (63,3%, n=14). Most often reported symptoms at 8-weeks were cognitive, musculoskeletal and neurological sequelae. At 6-month follow-up only 30% (n=9) of patients had any abnormal clinical findings. During the 2-week visit, 90% (n=27) of patients had abnormal complete blood cell and platelet counts, but 60% (n=18) of children had abnormal inflammatory parameters (D-dimers, ferritin, CRP, Il-6). Significant improvement of hematologic and inflammatory parameters was seen at 8-week (6.7%, n=2) and 6-month (3.3%, n=1) follow-up. In addition, at 2-week follow-up 60% (n=18) of patients had abnormal electrocardiograms, but 13,3% (n=4) patients had abnormal echocardiography, including two patients with diagnosed coronary artery involvement. At 8 week and 6-month follow-up visits all patients had normal cardiological findings.
Conclusions/Learning Points: Abnormal clinical, laboratory and cardiological findings were seen in majority of patients two weeks after MIS-C with significant improvement in following weeks
Methods: In this prospective cohort study conducted from January 2021 to December 2021, 30 patients with MIS-C were enrolled. To identify the outcomes, all patients were evaluated in face-to-face visits 2 weeks, 8 weeks, and 6 months after diagnosis using clinical assessment, laboratory testing and cardiological examination.
Results: During the two-week follow up visit 20% (n=6) of children had abnormal clinical findings. Notably, significant increase was seen in these findings at 8-week follow-up (63,3%, n=14). Most often reported symptoms at 8-weeks were cognitive, musculoskeletal and neurological sequelae. At 6-month follow-up only 30% (n=9) of patients had any abnormal clinical findings. During the 2-week visit, 90% (n=27) of patients had abnormal complete blood cell and platelet counts, but 60% (n=18) of children had abnormal inflammatory parameters (D-dimers, ferritin, CRP, Il-6). Significant improvement of hematologic and inflammatory parameters was seen at 8-week (6.7%, n=2) and 6-month (3.3%, n=1) follow-up. In addition, at 2-week follow-up 60% (n=18) of patients had abnormal electrocardiograms, but 13,3% (n=4) patients had abnormal echocardiography, including two patients with diagnosed coronary artery involvement. At 8 week and 6-month follow-up visits all patients had normal cardiological findings.
Conclusions/Learning Points: Abnormal clinical, laboratory and cardiological findings were seen in majority of patients two weeks after MIS-C with significant improvement in following weeks
Original language | English |
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Pages | 957 |
Number of pages | 1 |
Publication status | Published - May 2022 |
Event | 40th Meeting of the European Society for Paediatric Infectious Diseases - Athens, Greece Duration: 9 May 2022 → 13 May 2022 Conference number: 40 https://2022.espidmeeting.org |
Meeting
Meeting | 40th Meeting of the European Society for Paediatric Infectious Diseases |
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Abbreviated title | ESPID |
Country/Territory | Greece |
City | Athens |
Period | 9/05/22 → 13/05/22 |
Internet address |
Keywords*
- COVID-19
- multisystem inflammatory syndrome in children (MIS-C)
- long term outcomes
Field of Science*
- 3.2 Clinical medicine
Publication Type*
- 3.4. Other publications in conference proceedings (including local)