Evidence map›Paper›PMID 35813704›Full record

ArticleQatar medical journal2022

Risk of Severe SARS-CoV-2 Infection in Patients with Autoimmune Rheumatic Diseases in Qatar: A Cohort Matched Study.

Omar Alsaed, Samar Alemadi, Eman Satti, Karima Becetti, Rawan Saleh, Hadil Ashour, Miral Hamed, Fiaz Alam, Yousef Alrimawi, Joanne Nader and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Qatar medical journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 50% 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, 1 synthesis or guideline pooled it, 2 citations in OpenAlex.

  1. Pooled it
  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

13 authors at 1 institution in 1 country.

Omar AlsaedDivision of Rheumatology, Department of Medicine, Hamad Medical Corporation, Doha, Qatar E-mail: Oalsaed@hamad.qa.
Samar AlemadiDivision of Rheumatology, Department of Medicine, Hamad Medical Corporation, Doha, Qatar E-mail: Oalsaed@hamad.qa.
Eman SattiDivision of Rheumatology, Department of Medicine, Hamad Medical Corporation, Doha, Qatar E-mail: Oalsaed@hamad.qa.
Karima BecettiDivision of Rheumatology, Department of Medicine, Hamad Medical Corporation, Doha, Qatar E-mail: Oalsaed@hamad.qa.
Rawan SalehDivision of Rheumatology, Department of Medicine, Hamad Medical Corporation, Doha, Qatar E-mail: Oalsaed@hamad.qa.
Hadil AshourDivision of Rheumatology, Department of Medicine, Hamad Medical Corporation, Doha, Qatar E-mail: Oalsaed@hamad.qa.
Miral HamedDivision of Rheumatology, Department of Medicine, Hamad Medical Corporation, Doha, Qatar E-mail: Oalsaed@hamad.qa.
Fiaz AlamDivision of Rheumatology, Department of Medicine, Hamad Medical Corporation, Doha, Qatar E-mail: Oalsaed@hamad.qa.
Yousef AlrimawiDivision of Rheumatology, Department of Medicine, Hamad Medical Corporation, Doha, Qatar E-mail: Oalsaed@hamad.qa.
Joanne NaderDivision of Infectious Disease, Department of Medicine, Hamad Medical Corporation, Doha, Qatar.
Masautso ChapondaDivision of Infectious Disease, Department of Medicine, Hamad Medical Corporation, Doha, Qatar.
Basem AwadhDivision of Rheumatology, Department of Medicine, Hamad Medical Corporation, Doha, Qatar E-mail: Oalsaed@hamad.qa.
Mohammad HammoudehDivision of Rheumatology, Department of Medicine, Hamad Medical Corporation, Doha, Qatar E-mail: Oalsaed@hamad.qa.
Hamad Medical Corporation · QA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt remains unclear whether patients with autoimmune rheumatic diseases (ARDs) are at a higher risk of poor outcomes from a SARS-CoV-2 infection. We evaluated whether patients with an ARDs infected with SARS-CoV-2 were at a higher risk of a poorer outcome than those without an ARDs.

methodsPatients with an ARDs infected with SARS-CoV-2 were matched to control patients without a known ARDs. Matching was performed according to age ( ± 6 years) and sex at a case-to-control ratio of 1:3. Demographic and clinical data were extracted from the databases and were compared between the two groups. Severe SARS-CoV-2 infection was the primary outcome and was defined as the requirement for oxygen therapy support, the need for invasive or noninvasive mechanical ventilation, or the use of glucocorticoids.

resultsA total of 141 patients with an ARDs were matched to 398 patients who formed the control group. The mean ages (SD) of the ARDs and non-ARDs groups were 44.4 years (11.4) and 43.4 years (12.2). Women accounted for 58.8% of the ARDs group and 56.3% of the control group (p = 0.59). Demographics and comorbidities were balanced between the groups. ARDs included connective tissue disease in 43 (30.3%) patients, inflammatory arthritis in 92 (65.2%), and other ARDs in 8 (5.7%). ARDs medications included biological/targeted synthetic disease-modifying antirheumatic drugs (b/ts-DMARDs) in 28 (15.6%) patients, conventional synthetic DMARDs in 95 (67.4%), and immunosuppressive antimetabolites in 13 (9.2%). The ARDs group had more respiratory and gastrointestinal symptoms related to SARS-CoV-2 infection than the control group (24.8% and 20.6% vs. 10% and 5.3%, respectively; p <  0.001 for both). Severe SARS-CoV-2 infection was more common in the ARDs group than in the control group (14.9% vs. 5.8%; p <  0.001).

conclusionsIn this single-center matched cohort study, patients with an ARDs experienced more respiratory and gastrointestinal symptoms related to SARS-CoV-2 infection and had more severe infection than those from the control group. Therefore, patients with an ARDs require close observation during the coronavirus disease 2019 pandemic.

Indexed as

Autoimmune rheumatic disease, Disease-modifying antirheumatic drugs, Poor prognostic factors, Severe acute respiratory syndrome coronavirus 2

Identifiers

PMID35813704
PMCPMC9234511
OpenAlexW4283722520

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.