P-1246. Evaluation of the Effectiveness of Administering Posaconazole and Isavuconazole via Enteral Feeding Tubes

Abstract Background Invasive fungal infections are a significant source of morbidity and mortality in immunocompromised and critically ill patients. Posaconazole and isavuconazole are commonly used for prophylaxis and treatment of invasive fungal infections in these populations. Oral therapy has many advantages over IV, including convenience and decreased IV-associated complications. Limited studies exist assessing the appropriateness of administering these medications via enteral feeding tube (EFT), but recent case series show feasibility in achieving therapeutic levels.Table 1.Primary and Secondary Outcomes Methods A single center retrospective chart review was performed for adult patients who received posaconazole or isavuconazole via EFT between January 1st 2020 and August 31st 2024. Key exclusion criteria included patients who received the antifungals via other routes of administration, no trough levels, or non-true trough levels (drawn too early or drawn before five days of therapy). For statistical analysis, continuous variables were reported as medians with interquartile ranges and compared using Mann-Whitney U tests. Categorical variables were reported as counts and percents and were compared utilizing Fisher’s exact tests. All statistical comparisons used a two-tailed alpha of 0.05. Results Eighty-six patients were reviewed for inclusion, and 29 patients were included in the final data analysis. Forty-nine percent of patients were receiving these medications for prophylaxis, and the remainder for treatment. Overall achievement of target trough levels was successful in 50% of patients who received posaconazole delayed release tablets (DRT), 56% of patients that received posaconazole suspension, and 100% of patients that received isavuconazole (p = 0.031; Table 1). Posaconazole patients also had lower rates of target trough attainment with first level drawn and took longer to achieve the first therapeutic trough level. No differences in 30-day mortality were found between treatment groups. Conclusion This study suggests that isavuconazole capsules, but not posaconazole, can be administered via EFT with adequate level attainment. Crushed posaconazole in DRT or suspension form was significantly less likely to reach therapeutic trough levels compared to isavuconazole when administered through EFT. Disclosures Emir Kobic, BCIDP, Shionogi: Honoraria

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Journal
Open Forum Infectious Diseases
Published
2026-01-01
DOI
https://doi.org/10.1093/ofid/ofaf695.1438
Primary Topic
Clinical Nutrition and Gastroenterology
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article
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article

P-1246. Evaluation of the Effectiveness of Administering Posaconazole and Isavuconazole via Enteral Feeding Tubes

Emir Kobic, Blake Williams, Michelle Potter, Mallory Yan
Open Forum Infectious Diseases
Clinical Nutrition and Gastroenterology
article

P-1246. Evaluation of the Effectiveness of Administering Posaconazole and Isavuconazole via Enteral Feeding Tubes

Emir Kobic, Blake Williams, Michelle Potter, Mallory Yan
article en

Abstract

Abstract Background Invasive fungal infections are a significant source of morbidity and mortality in immunocompromised and critically ill patients. Posaconazole and isavuconazole are commonly used for prophylaxis and treatment of invasive fungal infections in these populations. Oral therapy has many advantages over IV, including convenience and decreased IV-associated complications. Limited studies exist assessing the appropriateness of administering these medications via enteral feeding tube (EFT), but recent case series show feasibility in achieving therapeutic levels.Table 1.Primary and Secondary Outcomes Methods A single center retrospective chart review was performed for adult patients who received posaconazole or isavuconazole via EFT between January 1st 2020 and August 31st 2024. Key exclusion criteria included patients who received the antifungals via other routes of administration, no trough levels, or non-true trough levels (drawn too early or drawn before five days of therapy). For statistical analysis, continuous variables were reported as medians with interquartile ranges and compared using Mann-Whitney U tests. Categorical variables were reported as counts and percents and were compared utilizing Fisher’s exact tests. All statistical comparisons used a two-tailed alpha of 0.05. Results Eighty-six patients were reviewed for inclusion, and 29 patients were included in the final data analysis. Forty-nine percent of patients were receiving these medications for prophylaxis, and the remainder for treatment. Overall achievement of target trough levels was successful in 50% of patients who received posaconazole delayed release tablets (DRT), 56% of patients that received posaconazole suspension, and 100% of patients that received isavuconazole (p = 0.031; Table 1). Posaconazole patients also had lower rates of target trough attainment with first level drawn and took longer to achieve the first therapeutic trough level. No differences in 30-day mortality were found between treatment groups. Conclusion This study suggests that isavuconazole capsules, but not posaconazole, can be administered via EFT with adequate level attainment. Crushed posaconazole in DRT or suspension form was significantly less likely to reach therapeutic trough levels compared to isavuconazole when administered through EFT. Disclosures Emir Kobic, BCIDP, Shionogi: Honoraria

Open Forum Infectious DiseasesVol. 13(Supplement_1)
University of Arizona (US), Banner - University Medical Center Phoenix (US), Phoenix College (US)
Good health and well-being
Openalex Percentile: Top 91%
Clinical Nutrition and Gastroenterology
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