Invasive fusariosis after allogeneic hematopoietic cell transplantation: clinical features and prognostic value of serum β-D-glucan in a nationwide Japanese registry study

Clicks: 3
ID: 337849
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This article has not been analysed, so there is no overall score — reader engagement is measured and shown alongside.
AI Quality Assessment
Not analyzed
Readership in this journal
Emerging

Ranked #186 of 187 articles by views in medical mycology

Most read Least read

Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 187 in total.

Mint this article as an NFT
Not yet minted

Create a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.

5 SUSD one-off · no wallet required
Abstract
Abstract Invasive fusariosis is a rare but often fatal infection in immunocompromised patients. However, data in allogeneic hematopoietic cell transplantation (HCT) are limited. Using a nationwide Japanese transplant registry database, we identified patients who underwent allogeneic HCT between 2008 and 2021 and subsequently developed invasive fusariosis. We conducted questionnaire survey to characterize invasive fusariosis and identify factors associated with early mortality. Thirty-one patients were included. Invasive fusariosis developed at a median of 24 days after HCT. Neutropenia was present in 23 patients (74.2%), and corticosteroids were administered to 23 patients (74.2%). The most commonly involved sites were the bloodstream (71.0%), skin (54.8%), and the respiratory tract (35.5%). Serum (1→3)-β-D-glucan (BDG) was positive in 26 of 31 patients (83.9%) within 2 weeks after diagnosis, whereas BDG positivity preceded the diagnosis in only 15 of 29 evaluable patients (51.7%). Twenty-two (71.0%) died within 30 days after the diagnosis. BDG value normalized to the upper limit of normal (BDG/ULN) within 1 week before diagnosis was significantly lower in 30-day survivors than in non-survivors (median, survivor 0.55 vs. non-survivor 2.94). A pre-diagnostic BDG/ULN of 1.27 predicted 30-day mortality with a sensitivity of 85.7% and a specificity of 81.0%. Among 23 patients who developed invasive fusariosis during neutropenia, all seven 30-day survivors achieved neutrophil recovery, whereas none of the non-survivors did. In conclusion, invasive fusariosis after allogeneic HCT was associated with extremely poor outcomes, particularly in patients with persistent neutropenia. Elevated BDG levels around the time of diagnosis were strongly associated with early mortality.
Reference Key
openalex_W7224997220 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors
Journal medical mycology
Year 2026
DOI
10.1093/mmy/myag118
URL
Keywords Keywords not found

Citations

No citations found. To add a citation, contact the admin at info@scimatic.org

No comments yet. Be the first to comment on this article.