COVID-19 in Moscow patients on peritoneal dialysis: clinical phenotypes
- Authors: Frolova N.F.1,2, Berdinsky V.A.1, Zubkin M.L.1,3, Dushkin A.D.1, Chernov A.A.1, Kobzar M.V.1, Kumakhova L.A.1, Lysenko M.A.1,2, Gautier S.V.4
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Affiliations:
- Moscow Clinical Science and Research Center 52
- The Russian National Research Medical University named after N.I. Pirogov
- Moscow Scientific Research Institute of Epidemiology and Microbiology named after G.N. Gabrichevsky
- V.I. Shumakov National Medical Research Center for Transplantology and Artificial Organs
- Issue: Vol 30, No 3 (2025)
- Pages: 157-167
- Section: Original study articles
- URL: https://ogarev-online.ru/1560-9529/article/view/373789
- DOI: https://doi.org/10.17816/EID677542
- EDN: https://elibrary.ru/KEJIVA
- ID: 373789
Cite item
Abstract
BACKGROUND: The COVID-19 pandemic has greatly altered the management of patients with chronic conditions, including those receiving renal replacement therapy (hemodialysis and peritoneal dialysis) for end-stage renal disease.
AIM: This study aimed to identify the clinical phenotypes of patients with peritoneal dialysis and COVID-19, determine the risk factors for adverse outcomes (including death), and evaluate their impact on the progression of end-stage renal disease.
METHODS: The work presents a retrospective analysis of the clinical data of patients on peritoneal dialysis diagnosed with COVID-19 and hospitalized at Moscow City Clinical Hospital No. 52 between March 2020 and July 2023. The most frequently observed factors in adverse and fatal cases were assessed. Agglomerative clustering identified three distinct phenotypes in patients with COVID-19 and peritoneal dialysis, which differed in clinical characteristics and associated outcomes.
RESULTS: A total of 149 patients undergoing peritoneal dialysis for end-stage renal disease were hospitalized with a diagnosis of COVID-19. Of those, 38 deaths (25.5%) were reported. Deaths were associated with longer durations of renal replacement therapy, higher levels of C-reactive protein, lactate dehydrogenase, and procalcitonin, lower potassium levels at admission, and lower lymphocyte levels during hospitalization. Agglomerative clustering identified three phenotypes in patients with different outcomes. The mortality rate was 2.6% in patients with phenotype 1, 32.4% in patients with phenotype 2, and 64.1% in patients with phenotype 3. Patients with phenotype 3 (the least favorable) were older and had a higher comorbidity index. They had also received renal replacement therapy for a longer period and initially suffered from severe COVID-19 pneumonia. Patients with phenotypes 1 and 2 did not differ in terms of age or comorbidities. However, patients with phenotype 2 had more severe baseline lung lesions, as determined by computed tomography, and higher levels of systemic inflammation markers (C-reactive protein, lactate dehydrogenase, procalcitonin, and ferritin).
CONCLUSION: By predicting the progression of the COVID-19 in patients on peritoneal dialysis, we can distinguish three phenotypes characterized by differences in treatment duration, levels of inflammation markers (C-reactive protein and lactate dehydrogenase), and severity of pneumonia. These findings support the need for early risk stratification and multicenter studies to optimize clinical decisions.
Keywords
About the authors
Nadiya F. Frolova
Moscow Clinical Science and Research Center 52; The Russian National Research Medical University named after N.I. Pirogov
Email: nadiya.frolova@yandex.ru
ORCID iD: 0000-0002-6086-5220
SPIN-code: 3866-5560
MD, Cand. Sci. (Medicine)
Russian Federation, Moscow; MoscowVitaly A. Berdinsky
Moscow Clinical Science and Research Center 52
Email: gkb52@zdrav.mos.ru
ORCID iD: 0000-0001-5966-0415
SPIN-code: 7649-8358
MD
Russian Federation, MoscowMikhail L. Zubkin
Moscow Clinical Science and Research Center 52; Moscow Scientific Research Institute of Epidemiology and Microbiology named after G.N. Gabrichevsky
Email: m-zubkin@yandex.ru
ORCID iD: 0000-0001-5271-1902
SPIN-code: 6950-8080
MD, Dr. Sci. (Medicine), Professor
Russian Federation, Moscow; MoscowAlexander D. Dushkin
Moscow Clinical Science and Research Center 52
Author for correspondence.
Email: alex@drdushkin.ru
ORCID iD: 0000-0002-8013-5276
SPIN-code: 3857-0010
MD, Cand. Sci. (Medicine)
Russian Federation, MoscowAnton A. Chernov
Moscow Clinical Science and Research Center 52
Email: sbornay1med@yandex.ru
ORCID iD: 0000-0001-6209-387X
SPIN-code: 5893-5394
MD, Cand. Sci. (Medicine)
Russian Federation, MoscowMargarita V. Kobzar
Moscow Clinical Science and Research Center 52
Email: m.v.kobzar@yandex.ru
ORCID iD: 0009-0004-0236-653X
MD
Russian Federation, MoscowLiana A. Kumakhova
Moscow Clinical Science and Research Center 52
Email: gkb52@zdrav.mos.ru
SPIN-code: 9712-5247
MD
Russian Federation, MoscowMariana A. Lysenko
Moscow Clinical Science and Research Center 52; The Russian National Research Medical University named after N.I. Pirogov
Email: gkb52@zdrav.mos.ru
ORCID iD: 0000-0001-6010-7975
SPIN-code: 3887-6250
MD, Dr. Sci. (Medicine), Professor
Russian Federation, Moscow; MoscowSergey V. Gautier
V.I. Shumakov National Medical Research Center for Transplantology and Artificial Organs
Email: gautier@list.ru
ORCID iD: 0000-0003-0633-678X
SPIN-code: 5969-5749
MD, Dr. Sci. (Medicine), Professor
Russian Federation, MoscowReferences
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