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Complications of Therapeutic Plasma Exchange in Pediatric Neuroimmune Disorders

Bibliographic Data

ID15717559
AuthorsKaty Eichinger (0000-0003-4623-7014, Medical University of Vienna), Markus Breu (0000-0003-3825-5749, Medical University of Vienna), Marleen Renken (Medical University of Vienna), Sandy Siegert (0000-0002-8022-7736, Medical University of Vienna), Emily N Hilz (0000-0002-1380-4919, Medical University of Vienna), Sarah Glatter (0000-0002-0372-4317, Medical University of Vienna), Dagmar Csaicsich (Medical University of Vienna), Michael Böehm (0000-0003-4897-6953, Medical University of Vienna), Christian Lechner (0000-0003-2721-4407, Innsbruck Medical University), Barbara Kornek (0000-0002-1851-6967, Medical University of Vienna), Rainer Seidl (0000-0003-1455-6491, Medical University of Vienna, corresponding author)
Year2025
Volume12
Issue11
Pages1457-1457
Publication date2025-10-27
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueChildren (JOURNAL)
Journal identifiersISSN: 2227-9067 • E-ISSN: 2227-9067
PublisherMultidisciplinary Digital Publishing Institute (PUBLISHER • CH)
DOI10.3390/children12111457
PMID41300575
OpenAlexW4415612858
LanguageEN

Background: Therapeutic plasma exchange (TPE) is an established treatment for immune-mediated neurological diseases in adults, but pediatric-specific data remain limited. This retrospective single-center study investigates the safety, complication profile, and clinical outcomes of TPE in children with pediatric neuroimmunological disorders (PNID). Methods: Medical records of pediatric patients who underwent TPE at the Medical University of Vienna between April 2006 and October 2022 were reviewed. Inclusion criteria required TPE initiation before the age of 18 years. Data collected included diagnoses, pre-TPE therapy, TPE characteristics, complications and clinical outcomes based on retrospective documentation. Results: A total of 53 patients (60% female, median age 13 years) were included and underwent 378 TPE procedures. Most common diagnoses were pediatric-onset multiple sclerosis (23%) and autoimmune encephalitis (19%). TPE was preceded by corticosteroids and/or intravenous immunoglobulin in 83% of patients. Complications occurred in 81% of patients and 23% of procedures and were predominantly rated mild to moderate (CTCAE I-II), including nausea, hypotension, and catheter-related issues. Severe complications (CTCAE III-IV) occurred in 11% of patients; no deaths were reported. Clinical improvement was documented in 84% of patients, with 42% showing significant improvement. Conclusions: TPE is a generally well-tolerated and effective treatment in PNID, with a high rate of clinical improvement and predominantly mild complications. The higher reported complication rate compared to other studies likely reflects more comprehensive documentation of minor adverse events. These findings support the use of TPE in PNID, particularly in cases refractory to first-line therapies. Standardized reporting of outcomes and complications is essential to improve comparability across studies and guide future clinical practice

Adverse effect · Complication · Medical record · Multiple sclerosis · Refractory (planetary science · Retrospective cohort study · Therapeutic plasma exchange · Complement system in diseases · Multiple Sclerosis Research Studies · Peripheral Neuropathies and Disorders

Citation velocityhistorical
Highly citedNo
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