Evidence map›Paper›PMID 36028582›Full record

ArticleAnnals of hematology2022

Amyloidosis and COVID-19: experience from an amyloid program in Canada.

Ellen Lewis, Nowell Fine, Robert J H Miller, Christopher Hahn, Sameer Chhibber, Etienne Mahe, Jason Tay, Peter Duggan, Sylvia McCulloch, Nizar Bahlis and 2 more

Abstract read
In one paragraph

Article in Annals of hematology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
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

12 authors.

Ellen LewisDivision of Hematology, Department of Medicine, University of Calgary, Calgary, AB, Canada.
Nowell FineDivision of Cardiology, Department of Cardiac Sciences, Libin Cardiovascular Institute, University of Calgary, Calgary, AB, Canada.
Robert J H MillerDivision of Cardiology, Department of Cardiac Sciences, Libin Cardiovascular Institute, University of Calgary, Calgary, AB, Canada.
Christopher HahnDivision of Neurology, Department of Clinical Neurosciences, University of Calgary, Calgary, AB, Canada.
Sameer ChhibberDivision of Neurology, Department of Clinical Neurosciences, University of Calgary, Calgary, AB, Canada.
Etienne MaheDepartment of Pathology and Lab Medicine, University of Calgary, Calgary, AB, Canada.
Jason TayDivision of Hematology, Department of Medicine, University of Calgary, Calgary, AB, Canada.
Peter DugganDivision of Hematology, Department of Medicine, University of Calgary, Calgary, AB, Canada.
Sylvia McCullochDivision of Hematology, Department of Medicine, University of Calgary, Calgary, AB, Canada.
Nizar BahlisDivision of Hematology, Department of Medicine, University of Calgary, Calgary, AB, Canada.
Paola NeriDivision of Hematology, Department of Medicine, University of Calgary, Calgary, AB, Canada.
Victor H Jimenez-ZepedaDivision of Hematology, Department of Medicine, University of Calgary, Calgary, AB, Canada. Victor.Zepeda@albertahealthservices.ca.ORCID http://orcid.org/0000-0002-9294-9437

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus (SARS-CoV2) and associated COVID-19 infection continue to impact patients globally. Patients with underlying health conditions are at heightened risk of adverse outcomes from COVID-19; however, research involving patients with rare health conditions remains scarce. The amyloidoses are a rare grouping of protein deposition diseases. Light-chain and transthyretin amyloidosis are the most common disease forms, often present with systemic involvement of vital organs including the heart, nerves, kidneys, and GI tracts of affected individuals. The Amyloidosis Program of Calgary examined 152 ATTR patients and 103 AL patients analyzing rates of vaccination, COVID-19 testing, infection outcomes, influence referrals, and excess deaths. Results showed 15 total PCR-confirmed COVID-19 infections in the tested population of amyloid patients, with a higher frequency of infections among patient with AL compared to the ATTR cohort (26.2% vs 5.1%). Four patients (26.6%) required hospital admission for COVID-19 infection, 2 ATTR, and 2 AL patients. Of the confirmed cases, 1 (0.07%) unvaccinated ATTR patient died of a COVID-19 infection. An excess of deaths was found in both the ATTR and AL cohorts when comparing pre-pandemic years 2018 and 2019 to the pandemic years of 2020 and 2021. The finding suggests that amyloidosis patients are likely at a high risk for severe COVID-19 infection and mortality, especially those of advanced age, those on an active treatment with chemotherapy, and those with concomitant B-cell or plasma cell disorder. The impact of virtual healthcare visits and pandemic measures on the excess of deaths observed requires further research.

Indexed as

Amyloid Neuropathies, FamilialCOVID-19AmyloidCOVID-19 TestingHumansRNA, ViralSARS-CoV-2AmyloidRNA, ViralAmyloidCOVID-19Light-chain amyloidosisSARS CoV2Transthyretin amyloidosis

Identifiers

PMID36028582
PMCPMC9417080

What OpenQuestion holds

Textmetadata
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.