Evidence map›Paper›PMID 30607566›Full record

ArticlePediatric nephrology (Berlin, Germany)2019

Clinical and histopathological prognostic factors affecting the renal outcomes in childhood ANCA-associated vasculitis.

Gül Özçelik, Hafize Emine Sönmez, Sezgin Şahin, Ayşim Özağarı, Meral Torun Bayram, Rümeysa Yasemin Çiçek, Evrim Kargın Çakıcı, Elif Çomak, Kenan Barut, Nihal Şahin and 16 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

26 authors.

Gül ÖzçelikDepartment of Pediatric Nephrology, SBÜ. Sisli Hamidiye Etfal Training and Research Hospital, Istanbul, Turkey.
Hafize Emine SönmezDepartment of Pediatric Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Sezgin ŞahinDepartment of Pediatric Rheumatology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey.
Ayşim ÖzağarıDepartment of Pathology, SBÜ. Sisli Etfal Training and Research Hospital, Istanbul, Turkey.
Meral Torun BayramDepartment of Pediatric Nephrology, Dokuz Eylul University Faculty of Medicine, İzmir, Turkey.
Rümeysa Yasemin ÇiçekDepartment of Pediatric Nephrology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey.
Evrim Kargın ÇakıcıDepartment of Pediatric Nephrology, SBÜ. Dr. Sami Ulus Training and Research Hospital, Istanbul, Turkey.
Elif ÇomakDepartment of Pediatric Nephrology, Akdeniz University Faculty of Medicine, Antalya, Turkey.
Kenan BarutDepartment of Pediatric Rheumatology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey.
Nihal ŞahinDepartment of Pediatric Nephrology and Rheumatology, Erciyes University Faculty of Medicine, Kayseri, Turkey.
Sevcan BakkaloğluDepartment of Pediatric Nephrology, Gazi University Faculty of Medicine, Ankara, Turkey.
İbrahim GökçeDepartment of Pediatric Nephrology, Marmara University Faculty of Medicine, İstanbul, Turkey.
Ali DüzovaDepartment of Pediatric Nephrology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Yelda BilginerDepartment of Pediatric Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Ceyhun AçarıDepartment of Pediatric Rheumatology, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey.
Engin MelekDepartment of Pediatric Nephrology, Çukurova University Faculty of Medicine, Adana, Turkey.
Beltinge Demircioğlu KılıçDepartment of Pediatric Nephrology, Gaziantep University Faculty of Medicine, Gaziantep, Turkey.
Semanur ÖzdelDepartment of Pediatric Rheumatology, SBÜ. Dr. Sami Ulus Training and Research Hospital, Istanbul, Turkey.
Amra AdroviçDepartment of Pediatric Rheumatology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey.
Özgür KasapçopurDepartment of Pediatric Rheumatology, Cerrahpasa Medical School, Istanbul University, Istanbul, Turkey.
Erbil ÜnsalDepartment of Pediatric Rheumatology, Dokuz Eylul University Faculty of Medicine, Izmir, Turkey.
Harika AlpayDepartment of Pediatric Nephrology, Marmara University Faculty of Medicine, İstanbul, Turkey.
Diclehan OrhanDepartment of Pediatrics, Division of Rheumatology, Hacettepe University Faculty of Medicine, 06100, Ankara, Turkey.
Rezan TopaloğluDepartment of Pediatric Nephrology, Hacettepe University Faculty of Medicine, Ankara, Turkey.
Ruhan DüşünselDepartment of Pediatric Nephrology and Rheumatology, Erciyes University Faculty of Medicine, Kayseri, Turkey.
Seza ÖzenDepartment of Pediatric Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey. sezaozen@hacettepe.edu.tr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAntineutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) are very rare in childhood with an increased risk of morbidity and mortality. We aimed to evaluate renal prognostic factors in childhood AAV from the perspective of ANCA serotype, histopathological classification, and five-factor score (FFS).

methodsPediatric AAV patients from 11 referral centers in Turkey had been included to the study. The demographics, clinical findings, AAV subtypes, outcomes, and FFS were evaluated retrospectively. Kidney biopsies were classified histopathologically.

resultsTotally, 39 patients were enrolled in the study. Among all patients, 74.4% had renal involvement, 56.4% ear-throat-nose involvement, and 51.3% had musculoskeletal involvement. Proteinase 3 (PR3)-ANCA was positive in 48.7%, and myeloperoxidase (MPO)-ANCA was positive in 30.8%. 69.2% of patients had impaired renal function, and 28.2% had progressed to end-stage renal disease (ESRD) during the follow-up. At the time of diagnosis, FFS was ≥ 2 in 53.8%. The most common histopathologic classifications were as follows: crescentic type in 40.7% and sclerotic type in 25.9%. Gastrointestinal and renal involvement, MPO-ANCA positivity, serum creatinine levels, and impaired renal function during the follow-up were significantly higher in patients with FFS ≥ 2, compared to patients with FFS < 2. Patients with FFS ≥ 2 had more common crescentic, mixed and sclerotic histopathologic findings in biopsies. By logistic regression analysis forward method, the strongest single-risk factor among all the parameters was the initial level of creatinine in patients with ESRD, compared to the other patients (p = 0,007).

conclusionsEvaluation of the FFS, ANCA serology, and the creatinine levels may help to predict renal prognosis.

Indexed as

AdolescentAntibodies, Antineutrophil CytoplasmicAnti-Neutrophil Cytoplasmic Antibody-Associated VasculitisBiopsyChildCreatinineDisease ProgressionFemaleFollow-Up StudiesGlomerulonephritisHumansKidney Failure, ChronicKidney GlomerulusMaleMyeloblastinPeroxidaseAntibodies, Antineutrophil CytoplasmicCreatinineMyeloblastinPeroxidaseANCAAntineutrophil cytoplasmic antibody–associated vasculitidesFive-factor scoreHistopathologyRenal involvement

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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.