The impact of the COVID-19 pandemic on the incidence and clinical course of IgA vasculitis in paediatric patients

Author:

Poplicha Karol1ORCID,Ufniarski Tomasz1ORCID,Ucieklak Jarosław1ORCID,Podsiadły Edyta2ORCID,Jerzykowska Monika3,Mizerska-Wasiak Małgorzata4ORCID

Affiliation:

1. Student’s Scientific Association of General Paediatrics, Department of Paediatrics and Nephrology, Medical University of Warsaw, Warsaw, Poland

2. Department of Dental Microbiology, Microbiology Laboratory UCML, UCK WUM, Warsaw, Poland

3. Laboratory of the Józef Polikarp Brudziński Children’s Clinical Hospital in Warsaw, Medical University of Warsaw, Warsaw, Poland

4. Department of Paediatrics and Nephrology, Medical University of Warsaw, Warsaw, Poland

Abstract

Introduction and objective: Immunoglobulin A vasculitis is an autoimmune disorder resulting from immune complex accumulation in small blood vessels, causing skin, joint, abdominal, and kidney manifestations. This study evaluated the impact of the COVID-19 pandemic on the incidence and clinical course of immunoglobulin A vasculitis in paediatric patients. Materials and methods: A retrospective analysis of medical records from a single university paediatric hospital was performed to compare 117 patients presenting with immunoglobulin A vasculitis before and 57 after the COVID-19 epidemic announcement in Poland on 20 March 2020. Laboratory results, hospitalisation duration, preceding infections, clinical presentation, history of allergies and COVID-19 vaccinations, and the proportion of immunoglobulin A vasculitis patients among all admissions were analysed. Results: The study of 174 patients showed that their average age during the pandemic (5.51 ± 3.10) was significantly lower than pre-pandemically (6.98 ± 3.67) (p < 0.05). Before the pandemic, more hospitalised patients had immunoglobulin A vasculitis (1.14%) compared to during the pandemic (0.47%) (p < 0.05). Food allergies were also more common during the pandemic (20.8%) than before (8.8%) (p < 0.05). No significant differences were found in hospitalisation duration, and the incidence of immunoglobulin A vasculitis nephritis and abdominal symptoms (p = 0.194, p = 0.381, p = 0.968, respectively). Three patients had COVID-19 infection at admission. Conclusions: The pandemic led to fewer immunoglobulin A vasculitis hospitalisations but did not alter the clinical course of the disease or the incidence of immunoglobulin A vasculitis nephritis. In the context of the resurgence of COVID-19 infections, it is important to consider them as potential factors affecting immunoglobulin A vasculitis. Ongoing research is essential to understand these dynamics and guide effective clinical management of immunoglobulin A vasculitis amidst the evolving COVID-19 setting.

Funder

Warszawski Uniwersytet Medyczny

Publisher

Medical Communications Sp. z.o.o.

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