Evidence map›Paper›PMID 42714965›Full record

Observational studyRheumatology (Oxford, England)2026

Therapeutic plasma exchange in paediatric ANCA-associated vasculitis: a multicentre real-world experience.

Bengisu Menentoğlu, Batuhan Küçükali, Fatma Gül Demirkan, Gülşah Kılbaş, Şeyma Türkmen, Elif Küçük, Mehveş Işıklar Ekici, Ayşenur Alkaya, Mehmet Emin Menentoğlu, Figen Çakmak and 10 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Rheumatology (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Bengisu MenentoğluDivision of Pediatric Rheumatology, Department of Pediatrics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.ORCID 0000-0003-2774-9591
Batuhan KüçükaliDepartment of Pediatric Rheumatology, Gazi University Faculty of Medicine, Ankara, Turkey.ORCID 0000-0002-4268-8603
Fatma Gül DemirkanDepartment of Pediatric Rheumatology, Kanuni Sultan Süleyman Training and Research Hospital, Istanbul, Turkey.ORCID 0000-0001-9950-2489
Gülşah KılbaşDepartment of Pediatric Rheumatology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
Şeyma TürkmenDepartment of Pediatric Rheumatology, University of Health Sciences, Umraniye Training and Research Hospital, Istanbul, Turkey.ORCID 0000-0002-2318-0361
Elif KüçükDepartment of Pediatric Rheumatology, Istanbul Medeniyet University, Istanbul, Turkey.ORCID 0009-0004-1063-7459
Mehveş Işıklar EkiciDivision of Pediatric Rheumatology, Department of Pediatrics, University of Health Sciences, Ankara Bilkent City Hospital, Ankara, Turkey.
Ayşenur AlkayaDepartment of Pediatric Rheumatology, Etlik City Hospital, Ankara, Turkey.
Mehmet Emin MenentoğluDepartment of Pediatric Intensive Care, University of Health Sciences Bakirkoy Dr. Sadi Konuk Training and Research Hospital, Istanbul, Turkey.
Figen ÇakmakDepartment of Rheumatology, Başakşehir Çam and Sakura City Hospital, İstanbul, Turkey.ORCID 0000-0002-1667-2480
Özlem AkgünDivision of Pediatric Rheumatology, Department of Pediatrics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.
Esra ŞevketoğluDepartment of Pediatric Intensive Care, University of Health Sciences Bakirkoy Dr. Sadi Konuk Training and Research Hospital, Istanbul, Turkey.
Kübra ÖztürkDepartment of Pediatric Rheumatology, Istanbul Medeniyet University, Istanbul, Turkey.ORCID 0000-0003-0466-0228
Semanur ÖzdelDepartment of Pediatric Rheumatology, Etlik City Hospital, Ankara, Turkey.ORCID 0000-0001-5602-4595
Serkan TürkuçarDepartment of Pediatric Rheumatology, Faculty of Medicine, Pamukkale University, Denizli, Turkey.
Selçuk YükselDepartment of Pediatric Nephrology and Pediatric Rheumatology, School of Medicine, Canakkale Onsekiz Mart University, Canakkale, Turkey.ORCID 0000-0001-9415-1640
Banu Çelikel AcarDivision of Pediatric Rheumatology, Department of Pediatrics, University of Health Sciences, Ankara Bilkent City Hospital, Ankara, Turkey.
Betül SözeriDepartment of Pediatric Rheumatology, University of Health Sciences, Umraniye Training and Research Hospital, Istanbul, Turkey.ORCID 0000-0002-5079-5644
Sevcan A BakkaloğluDepartment of Pediatric Rheumatology, Gazi University Faculty of Medicine, Ankara, Turkey.ORCID 0000-0001-6530-9672
Nuray Aktay AyazDivision of Pediatric Rheumatology, Department of Pediatrics, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey.ORCID 0000-0003-3594-7387

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesAnti-neutrophil cytoplasmic antibody-associated vasculitis (AAV) is a rare but potentially life-threatening condition in children, often presenting with severe multi-organ involvement. Although standard induction therapy includes cyclophosphamide or rituximab with glucocorticoids, the role of therapeutic plasma exchange (TPE) in paediatric AAV remains uncertain. This study sought to describe the clinical characteristics, indications and outcomes of paediatric AAV patients treated with TPE in real-world practice and to compare them with patients managed without TPE.

methodsThis retrospective multicentre study included children (<18 years) diagnosed with AAV according to EULAR/PRINTO/PRES criteria. Patients were classified into TPE-treated (TPE+) and non-TPE-treated (TPE-) groups. Demographic features, organ involvement, laboratory parameters, Paediatric Vasculitis Activity Score (PVAS), treatments, adverse events and outcomes were analysed.

resultsTwenty-six paediatric AAV patients were included, of whom 11 (42.3%) underwent TPE. At diagnosis, the TPE+ group had significantly higher disease activity (median PVAS 12 vs 7, P = 0.004) and more severe kidney involvement, with higher serum creatinine and lower estimated glomerular filtration rate. Severe pulmonary, gastrointestinal, cardiovascular and cutaneous manifestations occurred predominantly in the TPE+ group. The primary indication for TPE was severe kidney involvement. TPE was associated with a significant reduction in PVAS (median 12.0-4.5, P = 0.007). Clinical improvement was observed in most acute organ-threatening manifestations, although persistent abnormalities remained common among patients with severe baseline kidney involvement. One patient died from catheter-related Pseudomonas aeruginosa sepsis during treatment.

conclusionTPE is selectively used as an adjunctive therapy in children with severe or refractory AAV, particularly in those with advanced kidney involvement. Although disease activity and acute organ-threatening manifestations improved following TPE, persistent renal abnormalities remained frequent, reflecting the severity of baseline kidney disease.

Indexed as

Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisPlasma ExchangeAdolescentChildChild, PreschoolFemaleHumansImmunosuppressive AgentsMaleRetrospective StudiesSeverity of Illness IndexTreatment OutcomeImmunosuppressive Agentsanti-neutrophil cytoplasmic antibody-associated vasculitisplasma exchangesmall vesselsystemic vasculitisvasculitis

Identifiers

PMID42714965
PMCPMC13596060

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.