| Literature DB >> 29110351 |
D Stelzer1,2,3, A Weber3, F Ihle1,2, S Matthes1,2, F Ceelen1,2, G Zimmermann1,2, N Kneidinger1,2, R Schramm4, H Winter5, M Zoller6, M Vogeser7, J Behr1,2, C Neurohr1,2.
Abstract
Posaconazole is an extended-spectrum triazole antifungal used in the treatment and prophylaxis of Aspergillus infections. It is available as oral suspension (POS-Liq) and delayed-release tablets (POS-Tab). The aim of this longitudinal, retrospective study was to compare the clinical effectiveness, toxicity and pharmacokinetics of POS-Liq vs POS-Tab in lung transplant recipients (LTx-recipients), who were treated with both formulations subsequently. Twenty-four consecutive LTx-recipients with 191 documented posaconazole trough levels (PTLs) for POS-Liq or POS-Tab were included. The administered daily doses were 300 mg for POS-Tab and 600 mg (prophylaxis) or 800 mg (therapy) for POS-Liq. Target PTLs were ≥700 ng/mL (prophylaxis) and ≥1250 ng/mL (therapy). The overall prophylactic and therapeutic response rates were 78% and 67%, respectively. No cases of hepatotoxicity or QT-prolongation were observed with either formulation. The achieved target PTLs were tripled under POS-Tab compared to POS-Liq with fewer risk factors for sub-therapeutic PTLs. Concomitant administration of POS-Tab significantly reduced the tacrolimus concentration-to-dose ratio (P = .001). We suggest the use of POS-Tab is appropriate for prophylaxis and therapy of Aspergillus infections in LTx-recipients, since POS-Tab displayed more reliable PTLs with no added adverse events. However, we recommend regular drug monitoring for POS-Liq and for therapy with POS-Tab and that immunosuppressant levels are monitored closely when the posaconazole formulation is switched.Entities:
Keywords: antifungal agents; dosage form; invasive fungal infection; lung transplantation; posaconazole; therapeutic drug monitoring
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Year: 2017 PMID: 29110351 DOI: 10.1111/myc.12724
Source DB: PubMed Journal: Mycoses ISSN: 0933-7407 Impact factor: 4.377