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Early Clostridioides difficile infection characterizations, risks, and outcomes in allogeneic hematopoietic stem cell and solid organ transplant recipients.

Authors :
Obeid, Karam M.
Sapkota, Smarika
Cao, Qing
Richmond, Steven
Watson, Allison P.
Karadag, Fatma Keklik
Young, Jo‐Anne H.
Pruett, Timothy
Weisdorf, Daniel J.
Ustun, Celalettin
Source :
Transplant Infectious Disease. Feb2022, Vol. 24 Issue 1, p1-10. 10p.
Publication Year :
2022

Abstract

Background: Clostridioides difficile infection (CDI) frequently complicates allogeneic hematopoietic stem cell (allo‐HCT) and solid organ transplantation (SOT). Methods: We retrospectively analyzed risk factors and outcomes of CDI occurring within 30 days of transplant. Results: Between March 2010 and June 2015, 466 allo‐HCT and 1454 SOT were performed. The CDI cumulative incidence (95% CI) was 10% (8–13) and 4% (3–5), following allo‐HCT and SOT, respectively (p <.01), occurring at a median (range) 7.5 days (1–30) and 11 (1–30), respectively (p =.18). In multivariate analysis, fluoroquinolones use within 14 days pre‐transplantation was a risk factor for CDI following allo‐HCT (HR 4.06 [95% CI 1.31–12.63], p =.02), and thoracic organ(s) transplantation was a risk factor for CDI following SOT (HR 3.03 [95% CI 1.31–6.98]) for lung and 3.90 (1.58–9.63) for heart and heart/kidney transplant, p =.02. Compared with no‐CDI patients, the length of stay (LOS) was prolonged in both allo‐HCT (35 days [19–141] vs. 29 [13–164], p <.01) and SOT with CDI (16.5 [4–101] vs. 7 [0–159], p <.01), though not directly attributed to CDI. In allo‐HCT, severe acute graft‐versus‐host disease (aGVHD) occurred more frequently in patients with CDI (33.3% vs. 15.8% without CDI, p =.01) and most aGVHD (87.5%) followed CDI. Non‐relapse mortality or overall survival, not attributed to CDI, were also similar in both allo‐HCT and SOT. Conclusions: Early post‐transplant CDI is frequent, associated with fluoroquinolones use in allo‐HCT and the transplanted organ in SOT, and is associated with longer LOS in both the groups without difference in survival but with increased aGVHD in allo‐HCT. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
13982273
Volume :
24
Issue :
1
Database :
Academic Search Index
Journal :
Transplant Infectious Disease
Publication Type :
Academic Journal
Accession number :
155130615
Full Text :
https://doi.org/10.1111/tid.13720