Evidence map›Paper›PMID 26092519›Full record

ArticleJournal of neurology2015

Non-systemic vasculitic neuropathy: single-center follow-up of 60 patients.

Nurcan Üçeyler, Anna Geng, Karlheinz Reiners, Klaus V Toyka, Claudia Sommer

Abstract read
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In one paragraph

Article in Journal of neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Localized Forms of Vasculitis.Current rheumatology reports · 2021
    Review
  7. Article
  8. Article
  9. Review
  10. Macrophage Depletion Ameliorates Peripheral Neuropathy in Aging Mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  11. Article
  12. [Immune-mediated neuropathies].Der Nervenarzt · 2016
    Review
  13. Article
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

5 authors.

Nurcan ÜçeylerDepartment of Neurology, University of Würzburg, Josef-Schneider-Str. 11, 97080, Würzburg, Germany. ueceyler_n@ukw.de.
Anna GengDepartment of Neurology, University of Würzburg, Josef-Schneider-Str. 11, 97080, Würzburg, Germany.
Karlheinz ReinersDepartment of Neurology, University of Würzburg, Josef-Schneider-Str. 11, 97080, Würzburg, Germany.
Klaus V ToykaDepartment of Neurology, University of Würzburg, Josef-Schneider-Str. 11, 97080, Würzburg, Germany.
Claudia SommerDepartment of Neurology, University of Würzburg, Josef-Schneider-Str. 11, 97080, Würzburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The objective of this study is to report the clinical presentation and long-term outcome of patients with non-systemic vasculitic neuropathy (NSVN) seen at our neuromuscular center. In this retrospective analysis, we assessed medical records of 60 patients with biopsy-proven NSVN (39 men, 21 women; median age: 64 years, 24-80), who were seen at our department between 1999 and 2008 and were followed up until 2014. The initial neurological findings, laboratory and neurophysiological data, treatment regimens, and outcome were analyzed in all patients. NSVN was mostly asymmetric (48/60, 80%), sensorimotor (45/60, 75%), and painful (38/60, 63%), with walking impairment as one major sign (51/60, 85%). No compound action potentials could be recorded in 29/60 (48%) sural nerves (later biopsied side) and in 6/60 (10%) tibial (motor) nerves. Pathology of sural nerve was informative in all cases irrespective of neurophysiological findings and prior immunosuppression. After initial treatment with i.v. methylprednisolone, all patients reported overall improvement. Of the 46 patients who were followed for >1 year, those with mild to moderate affliction were stable with azathioprine (19/46, 41%), while 18/46 (39%) patients were treated with cyclophosphamide and other immunosuppressants due to progression or relapse. At 4 years, 24/46 (52%) patients had either discontinued (n = 21) or had primarily refused immunosuppressive treatment (n = 3) without relapse. Age younger than the group median of 64 years was associated with better outcome. No patient evolved to systemic vasculitis. NSVN is a potentially treatable disorder of the peripheral nervous system.

Indexed as

Action PotentialsAdultAgedAged, 80 and overCyclophosphamideFemaleFollow-Up StudiesHumansImmunosuppressive AgentsMaleMethylprednisoloneMiddle AgedPolyneuropathiesRetrospective StudiesSural NerveTreatment OutcomeCyclophosphamideImmunosuppressive AgentsMethylprednisoloneCatamnesisImmunosuppressantsNeuropathic painNon-systemic vasculitic neuropathy

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Registered trials

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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.