Evidence map›Paper›PMID 34203480›Full record

ReviewBiomolecules2021

Instruments for Outcome Evaluation of Specific Domains in Primary Sjögren's Syndrome.

Nicoletta Del Papa, Antonina Minniti, Wanda Maglione, Francesca Pignataro, Roberto Caporali, Claudio Vitali

Abstract readReview
In one paragraph

Review in Biomolecules, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

6 authors.

Nicoletta Del PapaDepartment of Rheumatology, Azienda Socio Sanitaria Territoriale Gaetano Pini-Centro Traumatologico Ortopedico, 20122 Milano, Italy.ORCID 0000-0003-1549-8852
Antonina MinnitiDepartment of Rheumatology, Azienda Socio Sanitaria Territoriale Gaetano Pini-Centro Traumatologico Ortopedico, 20122 Milano, Italy.
Wanda MaglioneDepartment of Rheumatology, Azienda Socio Sanitaria Territoriale Gaetano Pini-Centro Traumatologico Ortopedico, 20122 Milano, Italy.
Francesca PignataroDepartment of Rheumatology, Azienda Socio Sanitaria Territoriale Gaetano Pini-Centro Traumatologico Ortopedico, 20122 Milano, Italy.
Roberto CaporaliDepartment of Rheumatology, Azienda Socio Sanitaria Territoriale Gaetano Pini-Centro Traumatologico Ortopedico, 20122 Milano, Italy.
Claudio VitaliRheumatology Outpatient Clinics, Mater Domini Humanitas Hospital, 21053 Castellanza, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary Sjögren's syndrome (pSS) is a systemic autoimmune disorder characterized by very heterogeneous features. The spectrum of this disorder may vary from benign but disabling symptoms such as dryness, due to lachrymal and salivary involvement, pain and fatigue, to systemic, potentially severe, manifestations that may involve any organ. In recent decades, the arrival of biotechnological therapy has offered new opportunities for the treatment of this-until now-orphan disease. Currently, the possible use of these new drugs in therapeutic trials has made it necessary to have reliable outcome measures to evaluate their efficacy in this disease. A great effort has been made in multicenter, often multinational, studies to develop and validate instruments capable of assessing the different disease-related features. The adoption in therapeutic trials of the newly developed outcome measures aimed at assessing systemic features and patient reported symptoms has often yielded disappointing results. These negative data have been ascribed, on the one hand, to the trial design not being completely appropriate, and, on the other hand, to the fact that a single instrument may be not sufficient to cover the great clinical heterogeneity of the disease features. There is now growing belief that composite end points that include instruments that are able to assess the various aspects of the disease may be more properly and successfully used in future therapeutic trials.

Indexed as

Patient Outcome AssessmentQuality of LifeSeverity of Illness IndexFatigueHumansOutcome Assessment, Health CareSjogren's Syndromedisease activityoutcome measuressicca symptomsSjogren’s syndrome

Identifiers

PMID34203480
PMCPMC8301983

What OpenQuestion holds

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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.