Evidence map›Paper›PMID 32172462›Full record

Observational studyRheumatology international2020

Peripheral neuropathy and health-related quality of life in patients with primary Sjögren's syndrome: a preliminary report.

Marta Jaskólska, Magdalena Chylińska, Anna Masiak, Katarzyna Nowicka-Sauer, Mariusz Siemiński, Marcin Ziętkiewicz, Zenobia Czuszyńska, Zbigniew Zdrojewski

Open access · hybridAbstract readObservational Study
In one paragraph

Observational study in Rheumatology international, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 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

8 authors at 1 institution in 1 country.

Marta JaskólskaDepartment of Internal Medicine, Connective Tissue Diseases and Geriatrics, Medical University of Gdansk, Gdańsk, Poland. jaskolskamm@gmail.com.ORCID http://orcid.org/0000-0002-1408-4490
Magdalena ChylińskaDepartment of Adult Neurology, Medical University of Gdansk, Gdańsk, Poland.ORCID http://orcid.org/0000-0002-9374-3430
Anna MasiakDepartment of Internal Medicine, Connective Tissue Diseases and Geriatrics, Medical University of Gdansk, Gdańsk, Poland.ORCID http://orcid.org/0000-0001-6687-2408
Katarzyna Nowicka-SauerDepartment of Family Medicine, Medical University of Gdansk, Gdańsk, Poland.ORCID http://orcid.org/0000-0002-7510-5478
Mariusz SiemińskiDepartment of Adult Neurology, Medical University of Gdansk, Gdańsk, Poland.ORCID http://orcid.org/0000-0001-8219-2912
Marcin ZiętkiewiczDepartment of Internal Medicine, Connective Tissue Diseases and Geriatrics, Medical University of Gdansk, Gdańsk, Poland.ORCID http://orcid.org/0000-0002-0186-4009
Zenobia CzuszyńskaDepartment of Internal Medicine, Connective Tissue Diseases and Geriatrics, Medical University of Gdansk, Gdańsk, Poland.ORCID http://orcid.org/0000-0002-6583-0860
Zbigniew ZdrojewskiDepartment of Internal Medicine, Connective Tissue Diseases and Geriatrics, Medical University of Gdansk, Gdańsk, Poland.ORCID http://orcid.org/0000-0001-8889-697X
Gdańsk Medical University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sjögren's syndrome (SS) is a chronic autoimmune disease with a wide spectrum of possible organ involvement. Peripheral (PNS) and central nervous system (CNS)-related symptoms may occur in the course of the disease. The aim of this study was to compare the health-related quality of life (HR-QOL) in SS patients with and without peripheral neuropathy. The study involved 50 patients with primary Sjögren's syndrome (pSS). All patients underwent neurological clinical examination followed by nerve conduction studies (NCS) and rheumatological examination. Thirty-six-item Short Form Health Survey (SF-36) was used for evaluating HR-QOL. To assess pSS activity, the EULAR Sjögren's Syndrome Disease Activity Index (ESSDAI) and EULAR Sjögren's Syndrome Patient Reported Index (ESSPRI) were used. For the assessment of clinical disability due to peripheral neuropathy, the Overall Disability Sum Score scale (ODSS) was used. Additional evaluation of pain was performed with the use of the Visual Analogue Scale (VAS) and a semistructured interview. Twenty-three (46%) patients were diagnosed with peripheral neuropathy. The most common PNS manifestation was sensorimotor neuropathy (47%). Neurological symptoms preceded the diagnosis of pSS in eight patients. The following domains of the SF-36 form were significantly lower scored by patients with peripheral nervous system involvement: role-physical [0 (0-100) vs. 75 (0-100)], role-emotional [67 (0-100) vs. 100 (0-100)], vitality [40 (10-70) vs. 50 (20-75)], bodily pain [45 (10-75) vs. 55 (0-100)], and general health [20 (5-50) vs. 30 (0-50)] (p ≤ 0.05). Our study showed that peripheral neuropathy was a common organ-specific complication in SS patients. In pSS patients, coexisting neurological involvement with symptoms such as pain and physical disability may be responsible for diminished HR-QOL.

Indexed as

Quality of LifeAdultAgedCase-Control StudiesCross-Sectional StudiesDisability EvaluationFemaleHumansMaleMiddle AgedPeripheral Nervous System DiseasesSeverity of Illness IndexSjogren's SyndromeSurveys and QuestionnairesAutoimmune neuropathyHealth-related quality of lifePatient-reported outcomesPeripheral nervous system involvementSjögren’s syndrome

Identifiers

PMID32172462
PMCPMC7316843
OpenAlexW3011031161

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.