Factors associated with subtherapeutic levels of oral posaconazole tablet: a detailed analysis from a tertiary care center in India
Diarrhea
0303 health sciences
Antifungal Agents
Administration, Oral
Proton Pump Inhibitors
Infectious and parasitic diseases
RC109-216
Triazoles
Antifungal
3. Good health
Tertiary Care Centers
03 medical and health sciences
Humans
Posaconazole
Infection
Retrospective Studies
Tablets
DOI:
10.1016/j.ijid.2022.09.004
Publication Date:
2022-09-09T07:17:23Z
AUTHORS (9)
ABSTRACT
Posaconazole is a broad-spectrum triazole antifungal, with activity against various clinically important fungi. The delayed release (DR) tablet of posaconazole has been shown to have a superior pharmacokinetic profile in comparison with the oral suspension.We retrospectively analyzed the factors associated with posaconazole levels <1.25 μg/ml in 164 patients receiving the DR tablet for therapeutic purposes.Of the 164 patients, 53 (32.3%) showed subtherapeutic trough levels of posaconazole. The use of proton pump inhibitors (95% CI 1.41-3.91; P-value = 0.028) and the presence of diarrhea (95% CI 1.95-6.93; P-value = 0.001) were significantly associated with subtherapeutic levels. A total of 13 of the 21 patients receiving posaconazole tablets through a nasogastric tube had therapeutic levels.This is the largest study from India that analyzed factors associated with subtherapeutic levels of the DR tablet of posaconazole. These findings reinforce the importance of therapeutic drug monitoring. Unlike in previous studies, obesity and hypoalbuminemia were not found to be significant factors in our settings. The use of proton pump inhibitors and diarrhea remained significant factors, as found in previous studies. Administering the DR tablet of posaconazole through a nasogastric tube may be a viable option.
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