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Double filtration plasmapheresis for children with different types of critical kidney diseases: a single-center retrospective cohort study

BACKGROUND: Double filtration plasmapheresis (DFPP) was initially used to facilitate the conduction of ABO-incompatible renal transplantation. The applicability of DFPP has recently expanded to cover the removal of various antibodies in adults with immune-mediated diseases. However, DFPP is seldom u...

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Autores principales: Zhang, Yu, Xie, Qing, Chen, Yaxian, Yang, Juanjuan, Huang, Shi, Deng, Linxia, Zhou, Jianhua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080493/
https://www.ncbi.nlm.nih.gov/pubmed/37035407
http://dx.doi.org/10.21037/tp-22-322
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author Zhang, Yu
Xie, Qing
Chen, Yaxian
Yang, Juanjuan
Huang, Shi
Deng, Linxia
Zhou, Jianhua
author_facet Zhang, Yu
Xie, Qing
Chen, Yaxian
Yang, Juanjuan
Huang, Shi
Deng, Linxia
Zhou, Jianhua
author_sort Zhang, Yu
collection PubMed
description BACKGROUND: Double filtration plasmapheresis (DFPP) was initially used to facilitate the conduction of ABO-incompatible renal transplantation. The applicability of DFPP has recently expanded to cover the removal of various antibodies in adults with immune-mediated diseases. However, DFPP is seldom used in children, with few reports addressing its efficacy and safety in this population. This study aimed to explore the efficacy and adverse effects of DFPP for pediatric patients with renal indications. METHODS: Children who received DFPP between December 2017 and December 2020 at Tongji Hospital were retrospectively studied, and sub-grouped for analysis according to the types of disease. All children received 3 to 6 DFPP sessions within 2 to 3 weeks, and were assessed for clinical outcomes according to glomerular filtration rate, proteinuria and extra-renal symptoms. Pre- and post-DFPP plasma were collected to measure the levels of pathogenic autoantibodies, immunoglobulins, fibrinogen, albumin, calcium, etc. In-hospital complications were also recorded. RESULTS: Totally there were 10 children receiving 44 sessions of DFPP, including 2 males and 8 females, with a median age of 11.2 years old (5–13 years) and a median weight of 42.1 kg (20–59 kg). Five patients were treated for systemic lupus erythematosus (SLE), three patients for antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), one for C3 glomerulopathy and one for ABO-incompatible renal transplantation. Plasma autoantibodies decreased substantially by 93% and 89% in those with SLE and AAV after the last session, respectively. Complete or partial responses were achieved in 80%, 33.3%, 100% and 100% of patients with SLE, AAV, C3 glomerulopathy, and ABO-incompatible renal transplantation, respectively. The proportion of cumulative IgG, fibrinogen, and albumin removal at the end of the last sessions were 58.8%, 67.69%, and 14.05% respectively. The removal of calcium, potassium and creatinine were not statistically significant. A few episodes (4.55%) of hypotension were observed when fresh frozen plasma was used as the replacement fluid, and no bleeding nor severe anaphylaxis was noted. CONCLUSIONS: The efficacy and safety of DFPP treatment in children with SLE, AAV, C3 glomerulopathy and ABO-incompatible renal transplantation were described in the present study. DFPP is proven to be a safe apheresis method for children weighing more than 20 kg.
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spelling pubmed-100804932023-04-08 Double filtration plasmapheresis for children with different types of critical kidney diseases: a single-center retrospective cohort study Zhang, Yu Xie, Qing Chen, Yaxian Yang, Juanjuan Huang, Shi Deng, Linxia Zhou, Jianhua Transl Pediatr Original Article BACKGROUND: Double filtration plasmapheresis (DFPP) was initially used to facilitate the conduction of ABO-incompatible renal transplantation. The applicability of DFPP has recently expanded to cover the removal of various antibodies in adults with immune-mediated diseases. However, DFPP is seldom used in children, with few reports addressing its efficacy and safety in this population. This study aimed to explore the efficacy and adverse effects of DFPP for pediatric patients with renal indications. METHODS: Children who received DFPP between December 2017 and December 2020 at Tongji Hospital were retrospectively studied, and sub-grouped for analysis according to the types of disease. All children received 3 to 6 DFPP sessions within 2 to 3 weeks, and were assessed for clinical outcomes according to glomerular filtration rate, proteinuria and extra-renal symptoms. Pre- and post-DFPP plasma were collected to measure the levels of pathogenic autoantibodies, immunoglobulins, fibrinogen, albumin, calcium, etc. In-hospital complications were also recorded. RESULTS: Totally there were 10 children receiving 44 sessions of DFPP, including 2 males and 8 females, with a median age of 11.2 years old (5–13 years) and a median weight of 42.1 kg (20–59 kg). Five patients were treated for systemic lupus erythematosus (SLE), three patients for antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), one for C3 glomerulopathy and one for ABO-incompatible renal transplantation. Plasma autoantibodies decreased substantially by 93% and 89% in those with SLE and AAV after the last session, respectively. Complete or partial responses were achieved in 80%, 33.3%, 100% and 100% of patients with SLE, AAV, C3 glomerulopathy, and ABO-incompatible renal transplantation, respectively. The proportion of cumulative IgG, fibrinogen, and albumin removal at the end of the last sessions were 58.8%, 67.69%, and 14.05% respectively. The removal of calcium, potassium and creatinine were not statistically significant. A few episodes (4.55%) of hypotension were observed when fresh frozen plasma was used as the replacement fluid, and no bleeding nor severe anaphylaxis was noted. CONCLUSIONS: The efficacy and safety of DFPP treatment in children with SLE, AAV, C3 glomerulopathy and ABO-incompatible renal transplantation were described in the present study. DFPP is proven to be a safe apheresis method for children weighing more than 20 kg. AME Publishing Company 2023-03-15 2023-03-31 /pmc/articles/PMC10080493/ /pubmed/37035407 http://dx.doi.org/10.21037/tp-22-322 Text en 2023 Translational Pediatrics. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Zhang, Yu
Xie, Qing
Chen, Yaxian
Yang, Juanjuan
Huang, Shi
Deng, Linxia
Zhou, Jianhua
Double filtration plasmapheresis for children with different types of critical kidney diseases: a single-center retrospective cohort study
title Double filtration plasmapheresis for children with different types of critical kidney diseases: a single-center retrospective cohort study
title_full Double filtration plasmapheresis for children with different types of critical kidney diseases: a single-center retrospective cohort study
title_fullStr Double filtration plasmapheresis for children with different types of critical kidney diseases: a single-center retrospective cohort study
title_full_unstemmed Double filtration plasmapheresis for children with different types of critical kidney diseases: a single-center retrospective cohort study
title_short Double filtration plasmapheresis for children with different types of critical kidney diseases: a single-center retrospective cohort study
title_sort double filtration plasmapheresis for children with different types of critical kidney diseases: a single-center retrospective cohort study
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10080493/
https://www.ncbi.nlm.nih.gov/pubmed/37035407
http://dx.doi.org/10.21037/tp-22-322
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