Evidence map›Paper›PMID 37398978›Full record

ArticleThe Lancet. Rheumatology2023

Post-COVID condition in patients with inflammatory rheumatic diseases: a prospective cohort study in the Netherlands.

Laura Boekel, Sadaf Atiqi, Maureen Leeuw, Femke Hooijberg, Yaëlle R Besten, Rosa Wartena, Maurice Steenhuis, Erik Vogelzang, Casper Webers, Annelies Boonen and 9 more

Abstract read
In one paragraph

Article in The Lancet. Rheumatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

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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

19 authors.

Laura BoekelDepartment of Rheumatology, Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam University Medical Center, Amsterdam, Netherlands.
Sadaf AtiqiDepartment of Rheumatology, Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam University Medical Center, Amsterdam, Netherlands.
Maureen LeeuwDepartment of Rheumatology, Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam University Medical Center, Amsterdam, Netherlands.
Femke HooijbergDepartment of Rheumatology, Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam University Medical Center, Amsterdam, Netherlands.
Yaëlle R BestenDepartment of Rheumatology, Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam University Medical Center, Amsterdam, Netherlands.
Rosa WartenaDepartment of Rheumatology, Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam University Medical Center, Amsterdam, Netherlands.
Maurice SteenhuisDepartment of Immunopathology, Sanquin Research and Landsteiner Laboratory, Amsterdam University Medical Center, Amsterdam, Netherlands.
Erik VogelzangDepartment of Medical Microbiology and Infection Control, Amsterdam University Medical Center, Amsterdam, Netherlands.
Casper WebersDepartment of Internal Medicine, Division of Rheumatology, Maastricht University Medical Center, Maastricht, Netherlands.
Annelies BoonenDepartment of Internal Medicine, Division of Rheumatology, Maastricht University Medical Center, Maastricht, Netherlands.
Martijn GerritsenDepartment of Rheumatology, Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam University Medical Center, Amsterdam, Netherlands.
Willem F LemsDepartment of Rheumatology, Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam University Medical Center, Amsterdam, Netherlands.
Sander W TasDepartment of Rheumatology and Clinical Immunology, Amsterdam Rheumatology and Immunology Center, University of Amsterdam, Amsterdam University Medical Center, Amsterdam, Netherlands.
Ronald F van VollenhovenDepartment of Rheumatology and Clinical Immunology, Amsterdam Rheumatology and Immunology Center, University of Amsterdam, Amsterdam University Medical Center, Amsterdam, Netherlands.
Alexandre E VoskuylDepartment of Rheumatology and Clinical Immunology, Amsterdam Rheumatology and Immunology Center, VU University Medical Center, Amsterdam University Medical Center, Amsterdam, Netherlands.
Irene van der Horst-BruinsmaDepartment of Rheumatic Diseases, Radboud, University Medical Center, Nijmegen, Netherlands.
Mike NurmohamedDepartment of Rheumatology, Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam University Medical Center, Amsterdam, Netherlands.
Theo RispensDepartment of Immunopathology, Sanquin Research and Landsteiner Laboratory, Amsterdam University Medical Center, Amsterdam, Netherlands.
Gertjan WolbinkDepartment of Rheumatology, Amsterdam Rheumatology and Immunology Center, Reade, Amsterdam University Medical Center, Amsterdam, Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Studies on long-term consequences of COVID-19, commonly referred to as post-COVID condition, in patients with inflammatory rheumatic diseases are scarce and inconclusive. Furthermore, classifying patients with inflammatory rheumatic diseases as having post-COVID condition is complicated because of overlapping symptoms. Therefore, we investigated the risk of post-COVID condition and time until recovery, and compared the prevalence of symptoms seen in post-COVID condition, between patients with inflammatory rheumatic diseases and healthy controls, with and without a history of COVID-19. Methods: In this substudy we used data from an ongoing prospective cohort study in the Netherlands. All adult patients with inflammatory rheumatic diseases from the Amsterdam Rheumatology and Immunology Center in Amsterdam, the Netherlands, were invited to participate in the study between April 26, 2020, and March 1, 2021. All patients were asked, but not obliged, to recruit their own control participant of the same sex, of comparable age (< 5 years), and without an inflammatory rheumatic disease. Demographic and clinical data, including data on the occurrence of SARS-CoV-2 infections, were collected via online questionnaires. On March 10, 2022, all study participants received a questionnaire on the occurrence, onset, severity, and duration of persistent symptoms during the first 2 years of the COVID-19 pandemic, independent of their history of SARS-CoV-2 infection. Additionally, we prospectively monitored a subset of participants who had a PCR or antigen confirmed SARS-CoV-2 infection in the 2-month period surrounding the questionnaire in order to assess COVID-19 sequelae. In line with WHO guidelines, post-COVID condition was defined as persistent symptoms that lasted at least 8 weeks, started after the onset and within 3 months of a PCR or antigen-confirmed SARS-CoV-2 infection, and could not be explained by an alternative diagnosis. Statistical analyses included descriptive statistics, logistic regression analyses, logistic-based causal mediation analyses, and Kaplan-Meier survival analyses for time until recovery from post-COVID condition. In exploratory analyses, E-values were calculated to investigate unmeasured confounding. Findings: A total of 1974 patients with inflammatory rheumatic disease (1268 [64%] women and 706 [36%] men; mean age 59 years [SD 13]) and 733 healthy controls (495 [68%] women and 238 [32%] men; mean age 59 years [12]) participated. 468 (24%) of 1974 patients with inflammatory rheumatic disease and 218 (30%) of 733 healthy controls had a recent SARS-CoV-2 omicron infection. Of those, 365 (78%) of 468 patients with inflammatory rheumatic disease and 172 (79%) of 218 healthy controls completed the prospective follow-up COVID-19 sequelae questionnaires. More patients than controls fulfilled post-COVID condition criteria: 77 (21%) of 365 versus 23 (13%) of 172 (odds ratio [OR] 1·73 [95% CI 1·04-2·87]; p=0·033). The OR was attenuated after adjusting for potential confounders (adjusted OR 1·53 [95% CI 0·90-2·59]; p=0·12). Among those without a history of COVID-19, patients with inflammatory diseases were more likely to report persistent symptoms consistent with post-COVID condition than were healthy controls (OR 2·52 [95% CI 1·92-3·32]; p<0·0001). This OR exceeded the calculated E-values of 1·74 and 1·96. Recovery time from post-COVID condition was similar for patients and controls (p=0·17). Fatigue and loss of fitness were the most frequently reported symptoms in both patients with inflammatory rheumatic disease and healthy controls with post-COVID condition. Interpretation: Post-COVID condition after SARS-CoV-2 omicron infections was higher in patients with inflammatory rheumatic disease than in healthy controls based on WHO classification guidelines. However, because more patients with inflammatory rheumatic disease than healthy controls without a history of COVID-19 reported symptoms that are commonly used to define a post-COVID condition during the first 2 years of the pandemic, it is likely that the observed difference in post-COVID condition between patients and controls might in part be explained by clinical manifestations in the context of underlying rheumatic diseases. This highlights the limitations of applying current criteria for post-COVID condition in patients with inflammatory rheumatic disease, and suggests it might be appropriate for physicians to keep a nuanced attitude when communicating the long-term consequences of COVID-19. Funding: ZonMw (the Netherlands organization for Health Research and Development) and Reade foundation.

Identifiers

PMID37398978
PMCPMC10292827

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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.