Evidence map›Paper›PMID 34712516›Full record

ArticleAmerican journal of neurodegenerative disease2021

Parsonage-Turner syndrome: a firsthand experience of an uncommon malady.

Vinod P Jerath, Vikram K Mahajan

Open access · greenAbstract read
In one paragraph

Article in American journal of neurodegenerative disease, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 33% 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

6 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. 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

2 authors at 2 institutions in 2 countries.

Vinod P JerathDr Jerath's Skin, VD and Allergy Centre Jalandhar 144001, Punjab, India.
Vikram K MahajanDepartment of Dermatology, Venereology & Leprosy, Dr. Rajendra Prasad Government Medical College Kangra (Tanda) 176001, Himachal Pradesh, India.
Allergy and Asthma Federation · FIDr. Rajendra Prasad Government Medical College · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parsonage Turner Syndrome (syn. idiopathic brachial plexopathy, neurologic amyotrophy) is a rare syndrome of poorly understood etiology with a reported incidence of 1.64 in 1 lakh persons per year. It affects men more often than women with a highest incidence in the third and seventh decades of life. Its pathophysiology is obscure and the syndrome has been reported in the postoperative, post infectious and recent viral illness, and post-vaccination settings. Trauma from manipulation of tissues and various positioning techniques used to facilitate surgical techniques, or immune-mediated inflammation remains the most common associated risk factor. It mostly remains under diagnosed for lack of clinical suspicion and specific diagnostic tools. Herein, we share a personal experience of this uncommon disorder by the first author, a healthy 67-year-old man, having no significant medical or surgical disorder and presenting with several weeks of weakness of right shoulder. The diagnosis was made after its aggravation following stretch injury sustained from a fall with upper limbs in full abduction. Treatment with high dose dexamthasone (100 mg in 200 ml 5% dextrose given once by slow i.v. infusion), NSAIDs (as needed) and physiotherapy given over 12 months was remittive.

Indexed as

Brachial plexusbrachial plexus neuropathyidiopathic brachial plexopathyneurologic amyotrophy

Identifiers

PMID34712516
PMCPMC8546633
OpenAlexW3209845245

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.