Risk Factors for Invasive Fungal Infection in Lung Transplant Recipients on Universal Antifungal Prophylaxis.
| dc.contributor.author | Huggins, Jonathan P | |
| dc.contributor.author | Arthur, David | |
| dc.contributor.author | Chow, Shein-Chung | |
| dc.contributor.author | Pease, Robert | |
| dc.contributor.author | Stanly, Kelly | |
| dc.contributor.author | Workman, Adrienne | |
| dc.contributor.author | Reynolds, John | |
| dc.contributor.author | Alexander, Barbara D | |
| dc.date.accessioned | 2025-12-01T14:39:42Z | |
| dc.date.available | 2025-12-01T14:39:42Z | |
| dc.date.issued | 2024-02 | |
| dc.description.abstract | BackgroundMany centers use universal antifungal prophylaxis after lung transplant, but risk factors for invasive fungal infection (IFI) in this setting are poorly described.MethodsThis retrospective, single-center cohort study including 603 lung transplant recipients assessed risk factors for early (within 90 days of transplant) invasive candidiasis (IC) and invasive mold infection (IMI) and late (90-365 days after transplant) IMI using Cox proportional hazard regression.ResultsIn this cohort, 159 (26.4%) patients had 182 IFIs. Growth of yeast on donor culture (hazard ratio [HR], 3.30; 95% CI, 1.89-5.75) and prolonged length of stay (HR, 1.02; 95% CI, 1.01-1.03) were associated with early IC risk, whereas transplantation in 2016 or 2017 (HR, 0.21; 95% CI, 0.06-0.70; HR, 0.25; 95% CI, 0.08-0.80, respectively) and female recipient sex (HR, 0.53; 95% CI, 0.30-0.93) were associated with reduced risk. Antimold therapy (HR, 0.21; 95% CI, 0.06-0.78) was associated with lower early IMI risk, and female donor sex (HR, 0.40; 95% CI, 0.22-0.72) was associated with lower late IMI risk. Recent rejection was a risk factor for late IMI (HR, 1.73; 95% CI, 1.02-2.95), and renal replacement therapy predisposed to early IC, early IMI, and late IMI (HR, 5.67; 95% CI, 3.01-10.67; HR, 7.54; 95% CI, 1.93-29.45; HR, 5.33; 95% CI, 1.46-19.49, respectively).ConclusionsIn lung transplant recipients receiving universal antifungal prophylaxis, risk factors for early IC, early IMI, and late IMI differ. | |
| dc.identifier | ofad640 | |
| dc.identifier.issn | 2328-8957 | |
| dc.identifier.issn | 2328-8957 | |
| dc.identifier.uri | ||
| dc.language | eng | |
| dc.publisher | Oxford University Press (OUP) | |
| dc.relation.ispartof | Open forum infectious diseases | |
| dc.relation.isversionof | 10.1093/ofid/ofad640 | |
| dc.rights.uri | ||
| dc.subject | amphotericin B | |
| dc.subject | antifungals | |
| dc.subject | invasive fungal infection | |
| dc.subject | lung transplant | |
| dc.subject | prophylaxis | |
| dc.title | Risk Factors for Invasive Fungal Infection in Lung Transplant Recipients on Universal Antifungal Prophylaxis. | |
| dc.type | Journal article | |
| duke.contributor.orcid | Arthur, David|0000-0003-0839-3294 | |
| duke.contributor.orcid | Reynolds, John|0000-0003-4766-8852 | |
| duke.contributor.orcid | Alexander, Barbara D|0000-0001-5868-0529 | |
| pubs.begin-page | ofad640 | |
| pubs.issue | 2 | |
| pubs.organisational-group | Duke | |
| pubs.organisational-group | School of Medicine | |
| pubs.organisational-group | Basic Science Departments | |
| pubs.organisational-group | Clinical Science Departments | |
| pubs.organisational-group | Institutes and Centers | |
| pubs.organisational-group | Biostatistics & Bioinformatics | |
| pubs.organisational-group | Medicine | |
| pubs.organisational-group | Pathology | |
| pubs.organisational-group | Medicine, Infectious Diseases | |
| pubs.organisational-group | Medicine, Pulmonary, Allergy, and Critical Care Medicine | |
| pubs.organisational-group | Duke Cancer Institute | |
| pubs.organisational-group | Biostatistics & Bioinformatics, Division of Biostatistics | |
| pubs.publication-status | Published | |
| pubs.volume | 11 |
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