Evidence map›Paper›PMID 35984290›Full record

ArticleRheumatology (Oxford, England)2023

Survival in Swedish patients with systemic sclerosis: a nationwide population-based matched cohort study.

Majd Bairkdar, Enoch Yi-Tung Chen, Paul W Dickman, Roger Hesselstrand, Helga Westerlind, Marie Holmqvist

Open access · hybridAbstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2023. 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
0.7field-weighted citation impact, top 30% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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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

6 authors at 2 institutions in 1 country.

Majd BairkdarDivision of Clinical Epidemiology, Department of Medicine, Solna.ORCID 0000-0001-6269-2792
Enoch Yi-Tung ChenDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm.
Paul W DickmanDepartment of Medical Epidemiology and Biostatistics, Karolinska Institutet, Stockholm.
Roger HesselstrandDepartment of Clinical Sciences Lund, Section for Rheumatology, Lund University and Skåne University Hospital, Lund.
Helga WesterlindDivision of Clinical Epidemiology, Department of Medicine, Solna.ORCID 0000-0003-3380-5342
Marie HolmqvistDivision of Clinical Epidemiology, Department of Medicine, Solna.ORCID 0000-0001-8996-5260
Karolinska Institutet · SELund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo conduct the first-ever nationwide, population-based cohort study investigating survival patterns of all patients with incident SSc in Sweden compared with matched individuals from the Swedish general population.

methodsWe used the National Patient Register to identify patients with incident SSc diagnosed between 2004 and 2015 and the Total Population Register to identify comparators (1:5), matched on sex, birth year and residential area. We followed them until death, emigration or the end of 2016. Follow-up of the general population comparators started the same date as their matched patients were included. We estimated all-cause survival using the Kaplan-Meier method, crude mortality rates and hazard ratios (HRs) using flexible parametric models.

resultsWe identified 1139 incident patients with SSc and 5613 matched comparators. The median follow-up was 5.0 years in patients with SSc and 6.0 years for their comparators. During follow-up, 268 deaths occurred in patients with SSc and 554 in their comparators. The 5-year survival was 79.8% and the 10-year survival was 67.7% among patients with SSc vs 92.9% and 84.8%, respectively, for the comparators (P < 0.0001). The mortality rate in patients with SSc was 42.1 per 1000 person-years and 15.8 per 1000 person-years in their comparators, corresponding to an HR of 3.7 (95% CI 2.9, 4.7) at the end of the first year of follow-up and 2.0 (95% CI 1.4, 2.8) at the end of the follow-up period.

conclusionDespite advances in understanding the disease and in diagnostic methods over the past decades, survival is still severely impacted in Swedish patients diagnosed with SSc between 2004 and 2015.

Indexed as

Scleroderma, SystemicCohort StudiesHumansProportional Hazards ModelsSwedenmortalitySScsurvival

Identifiers

PMID35984290
PMCPMC9977125
OpenAlexW4292364265

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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.