Evidence map›Paper›PMID 40315194›Full record

ArticlePloS one2025

Impact of COVID-19 on mucormycosis presentation and laboratory values: A comparative analysis.

Sepideh Hejazi, Ali Gholampour Kargar, Sahar Ravanshad, Arash Ziaee, Maryam Emadzadeh, Mona Kabiri, Reza Khoshbakht, Mohammad Hossein Ahmadi, Masoumeh Hosseinpoor, Hamed Khosravi and 2 more

Abstract readComparative Study
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Sepideh HejaziLung Diseases Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Ali Gholampour KargarStudent Research Committee, Mashhad University of Medical Sciences, Mashhad, Iran.
Sahar RavanshadDepartment of Internal Medicine, Faculty of Medicine, Mashhad University of Medical Science, Mashhad, Iran.
Arash ZiaeeStudent Research Committee, Mashhad University of Medical Sciences, Mashhad, IranIran.
Maryam EmadzadehDepartment of Community Medicine, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.ORCID https://orcid.org/0000-0002-1526-3765
Mona KabiriNanotechnology Research Center, Pharmaceutical Technology Institute, Mashhad University of Medical Sciences, Mashhad, Iran.
Reza KhoshbakhtDepartment of Laboratory Sciences, School of Paramedical Sciences, Mashhad University of Medical Sciences, Mashhad, Iran.
Mohammad Hossein AhmadiDepartment of Laboratory Sciences, Faculty of Paramedical and Rehabilitation Sciences, Mashhad University of Medical Sciences, Mashhad.
Masoumeh HosseinpoorSinus and Surgical Endoscopic Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Hamed KhosraviDepartment of Industrial & Management Systems Engineering, West Virginia University, Morgantown.
Imtiaz AhmedDepartment of Industrial & Management Systems Engineering, West Virginia University, Morgantown.ORCID https://orcid.org/0000-0003-1577-7384
Mehdi BakhshaeeSinus and Surgical Endoscopic Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.ORCID https://orcid.org/0000-0001-9590-4798

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe COVID-19 pandemic has led to an alarming increase in mucormycosis coinfections and its rapid progression. The overlapping risk factors and symptoms between COVID-19 and mucormycosis further complicate prompt detection, which is crucial for patient survival. This study aims to investigate potential differences in mucormycosis progression, initial symptom presentation, and laboratory value alterations in mucormycosis patients with COVID-19 history to enhance diagnostic accuracy and improve outcomes in this complex clinical scenario. METHODOLOGY: This retrospective cohort study, conducted from April 1, 2021, to March 31, 2022, examined 102 patients diagnosed with mucormycosis at two primary teaching hospitals. Patients were categorized into two groups based on COVID-19 history. Variables included demographic information, clinical parameters, laboratory results, and outcomes. The study compared patient laboratory studies and presentation symptoms between COVID-19 history-positive and COVID-19 history-negative groups, with a particular focus on mortality rates and associated comorbidities such as diabetes, cancer and immunosuppressive treatment.

resultsInitial clinical presentations differed significantly, eneralized Estimating Equations (GEE) analysis, adjusted for comorbidities, revealed COVID-19 history was associated with increased platelet counts (P = 0.0311) and decreased facial swelling (P = 0.049) and fever symptom reporting (P < 0.001). Cancer history, diabetes, and immunosuppressive treatment also showed significant associations with various clinical and laboratory parameters. Laboratory analysis revealed significant differences between mucormycosis patients with and without COVID-19 history. The COVID-19 history-positive group showed lower WBC counts (P = 0.002), and higher hemoglobin levels (P < 0.001) compared to controls. Diabetes was more prevalent in COVID-19 history-positive patients, while cancer history was more common in controls.

conclusionThis study reveals intricate relationships between COVID-19 history, mucormycosis, patient presentation, challenging earlier findings. Mucormycosis patients with COVID-19 history exhibited higher platelet counts and altered symptom presentation. The research highlights varied symptom patterns across patient subgroups and underscores the complexity of interactions between COVID-19, cancer, and diabetes in mucormycosis cases. These findings advocate multivariate analytical approaches to better understand these multifaceted relationships.

Indexed as

COVID-19MucormycosisAdultAgedComorbidityFemaleHumansMaleMiddle AgedRetrospective StudiesRisk FactorsSARS-CoV-2

Identifiers

PMID40315194
PMCPMC12047787

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.