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Observational Study
. 2021 May 1;22(5):e285-e293.
doi: 10.1097/PCC.0000000000002728.

Association Between Treatments and Short-Term Biochemical Improvements and Clinical Outcomes in Post-Severe Acute Respiratory Syndrome Coronavirus-2 Inflammatory Syndrome

Affiliations
Observational Study

Association Between Treatments and Short-Term Biochemical Improvements and Clinical Outcomes in Post-Severe Acute Respiratory Syndrome Coronavirus-2 Inflammatory Syndrome

Patrick Davies et al. Pediatr Crit Care Med. .

Abstract

Objectives: To 1) analyze the short-term biochemical improvements and clinical outcomes following treatment of children with post-severe acute respiratory syndrome coronavirus-2 inflammatory syndrome (multisystem inflammatory syndrome in children/pediatric inflammatory multisystem syndrome temporally associated with severe acute respiratory syndrome coronavirus-2) admitted to U.K. PICUs and 2) collate current treatment guidance from U.K. PICUs.

Design: Multicenter observational study.

Setting: Twenty-one U.K. PICUs.

Patients: Children (< 18 yr) admitted to U.K. PICUs between April 1, 2020, and May 10, 2020, fulfilling the U.K. case definition of pediatric inflammatory multisystem syndrome temporally associated with severe acute respiratory syndrome coronavirus-2.

Interventions: None.

Measurements and main results: Routinely collected, deidentified data were analyzed. Propensity score and linear mixed effects models were used to analyze the effect of steroids, IV immunoglobulin, and biologic agents on changes in C-reactive protein, platelet counts, and lymphocyte counts over the course of PICU stay. Treatment recommendations from U.K. clinical guidelines were analyzed. Over the 6-week study period, 59 of 78 children (76%) received IV immunoglobulin, 57 of 78 (73%) steroids, and 18 of 78 (24%) a biologic agent. We found no evidence of a difference in response in clinical markers of inflammation between patients with multisystem inflammatory syndrome in children/pediatric inflammatory multisystem syndrome temporally associated with severe acute respiratory syndrome coronavirus-2 who were treated with IV immunoglobulin, steroids, or biologics, compared with those who were not. By the end of the study period, most patients had received immunomodulation. The 12 patients who did not receive any immunomodulators had similar decrease in inflammatory markers as those treated. Of the 14 guidelines analyzed, the use of IV immunoglobulin, steroids, and biologics was universally recommended.

Conclusions: We were unable to identify any short-term benefit from any of the treatments, or treatment combinations, administered. Despite a lack of evidence, treatment guidelines for multisystem inflammatory syndrome in children/pediatric inflammatory multisystem syndrome temporally associated with severe acute respiratory syndrome coronavirus-2 have become very similar in advising step-wise treatments. Retaining clinical equipoise regarding treatment will allow clinicians to enroll children in robust clinical trials to determine the optimal treatment for this novel important condition.

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Conflict of interest statement

Dr. Prayle’s institution received funding from the Thrasher Research Fund, Action for Ataxia-Telangiectasia, and the Sir Jules Thorn Trust, and he disclosed the off-label product use of drugs for multisystem inflammatory syndrome in children/pediatric inflammatory multisystem syndrome temporally associated with severe acute respiratory syndrome coronavirus-2. All authors have completed the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. The remaining authors have disclosed that they do not have any potential conflicts of interest.

Figures

Figure 1.
Figure 1.
Linear mixed effect model estimates of 5 d progression of C-reactive protein (CRP), lymphocyte count, and platelet count dependent on whether the patient had been given steroids, IV immunoglobulin (IVIG), the combination of steroids plus IVIG, biologic agents, or all three treatments, compared with no treatment. Brown lines are average (mean) response with 95% CIs of no treatment, blue lines are mean and 95% CIs of treatment. The model estimates are not adjusted for baseline risk; adjusted estimates are plotted in Supplementary Figure 1 (http://links.lww.com/PCC/B740; legend, http://links.lww.com/PCC/B743).

References

    1. Royal College of Paediatrics and Child Health (RCPCH): Guidance: Paediatric Multisystem Inflammatory Syndrome Temporally Associated With COVID-19. 2020. Available at: https://%20inflammatory%20syndrome-20200501.pdf. Accessed July 30, 2020
    1. Centers for Disease Control and Prevention: Multisystem Inflammatory Syndrome in Children (MIS-C) Associated with Coronavirus Disease 2019 (COVID-19). CDCHAN-00432, 2020. Available at: https://emergency.cdc.gov/han/2020/han00432.asp. Accessed July 30, 2020
    1. Kanthimathinathan HK, Scholefield BR: Pediatric inflammatory multisystem syndrome: Time to collaborate. J Pediatric Infect Dis Soc 2020. Sep 18. [online ahead of print 2020] - PMC - PubMed
    1. Whittaker E, Bamford A, Kenny J, et al. ; PIMS-TS Study Group and EUCLIDS and PERFORM Consortia: Clinical characteristics of 58 children with a pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2. JAMA 2020; 324:259–269 - PMC - PubMed
    1. Dufort EM, Koumans EH, Chow EJ, et al. ; New York State and Centers for Disease Control and Prevention Multisystem Inflammatory Syndrome in Children Investigation Team: Multisystem inflammatory syndrome in children in New York State. N Engl J Med 2020; 383:347–358 - PMC - PubMed

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