Evidence map›Paper›PMID 34505902›Full record

ArticleRheumatology (Oxford, England)2022

Utility of interval kidney biopsy in ANCA-associated vasculitis.

Gavin B Chapman, Tariq E Farrah, Fiona A Chapman, Dan Pugh, Christopher O C Bellamy, Rashmi Lahiri, Eve Miller-Hodges, David C Kluth, Robert W Hunter, Neeraj Dhaun

Open access · hybridAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.1field-weighted citation impact, top 12% of its field
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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Gavin B ChapmanUniversity of Edinburgh/British Heart Foundation Centre of Research Excellence, Centre for Cardiovascular Science, The Queen's Medical Research Institute.
Tariq E FarrahUniversity of Edinburgh/British Heart Foundation Centre of Research Excellence, Centre for Cardiovascular Science, The Queen's Medical Research Institute.
Fiona A ChapmanUniversity of Edinburgh/British Heart Foundation Centre of Research Excellence, Centre for Cardiovascular Science, The Queen's Medical Research Institute.
Dan PughUniversity of Edinburgh/British Heart Foundation Centre of Research Excellence, Centre for Cardiovascular Science, The Queen's Medical Research Institute.
Christopher O C BellamyDepartment of Pathology, Royal Infirmary of Edinburgh, Edinburgh, UK.
Rashmi LahiriDepartment of Pathology, Royal Infirmary of Edinburgh, Edinburgh, UK.
Eve Miller-HodgesUniversity of Edinburgh/British Heart Foundation Centre of Research Excellence, Centre for Cardiovascular Science, The Queen's Medical Research Institute.
David C KluthDepartment of Renal Medicine.
Robert W HunterUniversity of Edinburgh/British Heart Foundation Centre of Research Excellence, Centre for Cardiovascular Science, The Queen's Medical Research Institute.ORCID 0000-0003-2344-8978
Neeraj DhaunUniversity of Edinburgh/British Heart Foundation Centre of Research Excellence, Centre for Cardiovascular Science, The Queen's Medical Research Institute.ORCID 0000-0001-9128-6603
British Heart Foundation · GBEdinburgh Royal Infirmary · GB

Funding

Chief Scientist Office CAF/19/01Chief Scientist Office SCAF/19/02
6 · The paper itself

Abstract

objectivesANCA-associated vasculitis (AAV) is a rare autoimmune disorder that commonly involves the kidney. Early identification of kidney involvement, assessing treatment-response and predicting outcome are important clinical challenges. Here, we assessed the potential utility of interval kidney biopsy in AAV.

methodsIn a tertiary referral centre with a dedicated vasculitis service, we identified patients with AAV who had undergone interval kidney biopsy, defined as a repeat kidney biopsy (following an initial biopsy showing active AAV) undertaken to determine the histological response in the kidney following induction immunosuppression. We analysed biochemical, histological and outcome data, including times to kidney failure and death for all patients.

resultsWe identified 57 patients with AAV who underwent at least one interval kidney biopsy (59 interval biopsies in total; median time to interval biopsy ∼130 days). Of the 59 interval biopsies performed, 24 (41%) patients had clinically suspected active disease at time of biopsy which was confirmed histologically in only 42% of cases; 35 (59%) patients were in clinical disease-remission, and this was correct in 97% of cases. The clinician's impression was incorrect in one in four patients. Hematuria at interval biopsy did not correlate with histological activity. Interval biopsy showed fewer acute lesions and more chronic damage compared with initial biopsy and led to immunosuppressive treatment-change in 75% (44/59) of patients. Clinical risk prediction tools tended to operate better using interval biopsy data.

conclusionInterval kidney biopsy is useful for determining treatment-response and subsequent disease management in AAV. It may provide better prognostic information than initial kidney biopsy and should be considered for inclusion into future clinical trials and treatment protocols for patients with AAV.

Indexed as

Anti-Neutrophil Cytoplasmic Antibody-Associated VasculitisKidney Failure, ChronicAntibodies, Antineutrophil CytoplasmicBiopsyFemaleHumansImmunosuppressive AgentsKidneyMaleRetrospective StudiesAntibodies, Antineutrophil CytoplasmicImmunosuppressive AgentsANCA vasculitishematuriainterval kidney biopsy

Identifiers

PMID34505902
PMCPMC9071515
OpenAlexW3198004411

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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.