Evaluation of intravenous voriconazole in patients with compromised renal function
<p<Abstract</p< <p<Background</p< <p<Incorporation of the solubilizing excipient, sulfobutylether-β-cyclodextrin (SBECD), in the intravenous (IV) formulation of voriconazole has resulted in the recommendation that this formulation be used with caution in patients with c...
Ausführliche Beschreibung
Autor*in: |
Lilly Craig M [verfasserIn] Welch Verna L [verfasserIn] Mayer Thomas [verfasserIn] Ranauro Paul [verfasserIn] Meisner Joanne [verfasserIn] Luke David R [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2013 |
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Schlagwörter: |
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Übergeordnetes Werk: |
In: BMC Infectious Diseases - BMC, 2003, 13(2013), 1, p 14 |
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Übergeordnetes Werk: |
volume:13 ; year:2013 ; number:1, p 14 |
Links: |
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DOI / URN: |
10.1186/1471-2334-13-14 |
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Katalog-ID: |
DOAJ008175918 |
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520 | |a <p<Abstract</p< <p<Background</p< <p<Incorporation of the solubilizing excipient, sulfobutylether-β-cyclodextrin (SBECD), in the intravenous (IV) formulation of voriconazole has resulted in the recommendation that this formulation be used with caution in patients with creatinine clearances (Cl<sub<cr</sub<) < 50 mL/min. This study evaluated the safety of IV voriconazole compared with two other IV antifungals not containing SBECD in patients with compromised renal function.</p< <p<Methods</p< <p<A total of 128 patients aged 11–93 years who had a baseline Cl<sub<cr</sub< < 50 mL/min between January 1, 2007 and December 31, 2010 were identified from a database of a university-affiliated inpatient healthcare system; of these, 55 patients received caspofungin, 54 patients received fluconazole, and 19 patients received voriconazole. Changes in serum creatinine (S<sub<cr</sub<) and Cl<sub<cr</sub< levels while on therapy were compared with baseline values and between groups.</p< <p<Results</p< <p<The groups had similar characteristics apart from the larger proportion of females that received fluconazole. Baseline S<sub<cr</sub< was higher in those receiving caspofungin, but maximal increases of S<sub<cr</sub< and decreases in Cl<sub<cr</sub< were greatest for the fluconazole group. Acute kidney injury (AKI), assessed by RIFLE criteria, was more frequent in the fluconazole <it<vs.</it< the caspofungin group (<it<p</it< < 0.01); incidence of AKI in the voriconazole group was not significantly different than found in the other two groups. The infecting organism was a predictor of AKI and formulation with SBECD was not.</p< <p<Conclusions</p< <p<Treatment of fungal infections in patients with compromised renal function with an SBECD-containing antifungal agent was not associated with AKI in clinical practice. Since the infecting organism was associated with AKI, decision on which antifungal to use should be determined by susceptibilities to the organism and not the incorporation of SBECD in the IV formulation.</p< | ||
650 | 4 | |a Voriconazole | |
650 | 4 | |a Caspofungin | |
650 | 4 | |a Fluconazole | |
650 | 4 | |a Renal dysfunction | |
650 | 4 | |a Sulfobutylether-β-cyclodextrin | |
650 | 4 | |a SBECD | |
650 | 4 | |a Acute kidney injury | |
653 | 0 | |a Infectious and parasitic diseases | |
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700 | 0 | |a Mayer Thomas |e verfasserin |4 aut | |
700 | 0 | |a Ranauro Paul |e verfasserin |4 aut | |
700 | 0 | |a Meisner Joanne |e verfasserin |4 aut | |
700 | 0 | |a Luke David R |e verfasserin |4 aut | |
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10.1186/1471-2334-13-14 doi (DE-627)DOAJ008175918 (DE-599)DOAJ989d1aa8d3c745fa9e79b8977bdbce76 DE-627 ger DE-627 rakwb eng RC109-216 Lilly Craig M verfasserin aut Evaluation of intravenous voriconazole in patients with compromised renal function 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<Incorporation of the solubilizing excipient, sulfobutylether-β-cyclodextrin (SBECD), in the intravenous (IV) formulation of voriconazole has resulted in the recommendation that this formulation be used with caution in patients with creatinine clearances (Cl<sub<cr</sub<) < 50 mL/min. This study evaluated the safety of IV voriconazole compared with two other IV antifungals not containing SBECD in patients with compromised renal function.</p< <p<Methods</p< <p<A total of 128 patients aged 11–93 years who had a baseline Cl<sub<cr</sub< < 50 mL/min between January 1, 2007 and December 31, 2010 were identified from a database of a university-affiliated inpatient healthcare system; of these, 55 patients received caspofungin, 54 patients received fluconazole, and 19 patients received voriconazole. Changes in serum creatinine (S<sub<cr</sub<) and Cl<sub<cr</sub< levels while on therapy were compared with baseline values and between groups.</p< <p<Results</p< <p<The groups had similar characteristics apart from the larger proportion of females that received fluconazole. Baseline S<sub<cr</sub< was higher in those receiving caspofungin, but maximal increases of S<sub<cr</sub< and decreases in Cl<sub<cr</sub< were greatest for the fluconazole group. Acute kidney injury (AKI), assessed by RIFLE criteria, was more frequent in the fluconazole <it<vs.</it< the caspofungin group (<it<p</it< < 0.01); incidence of AKI in the voriconazole group was not significantly different than found in the other two groups. The infecting organism was a predictor of AKI and formulation with SBECD was not.</p< <p<Conclusions</p< <p<Treatment of fungal infections in patients with compromised renal function with an SBECD-containing antifungal agent was not associated with AKI in clinical practice. Since the infecting organism was associated with AKI, decision on which antifungal to use should be determined by susceptibilities to the organism and not the incorporation of SBECD in the IV formulation.</p< Voriconazole Caspofungin Fluconazole Renal dysfunction Sulfobutylether-β-cyclodextrin SBECD Acute kidney injury Infectious and parasitic diseases Welch Verna L verfasserin aut Mayer Thomas verfasserin aut Ranauro Paul verfasserin aut Meisner Joanne verfasserin aut Luke David R verfasserin aut In BMC Infectious Diseases BMC, 2003 13(2013), 1, p 14 (DE-627)326645381 (DE-600)2041550-3 14712334 nnns volume:13 year:2013 number:1, p 14 https://doi.org/10.1186/1471-2334-13-14 kostenfrei https://doaj.org/article/989d1aa8d3c745fa9e79b8977bdbce76 kostenfrei http://www.biomedcentral.com/1471-2334/13/14 kostenfrei https://doaj.org/toc/1471-2334 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2013 1, p 14 |
spelling |
10.1186/1471-2334-13-14 doi (DE-627)DOAJ008175918 (DE-599)DOAJ989d1aa8d3c745fa9e79b8977bdbce76 DE-627 ger DE-627 rakwb eng RC109-216 Lilly Craig M verfasserin aut Evaluation of intravenous voriconazole in patients with compromised renal function 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<Incorporation of the solubilizing excipient, sulfobutylether-β-cyclodextrin (SBECD), in the intravenous (IV) formulation of voriconazole has resulted in the recommendation that this formulation be used with caution in patients with creatinine clearances (Cl<sub<cr</sub<) < 50 mL/min. This study evaluated the safety of IV voriconazole compared with two other IV antifungals not containing SBECD in patients with compromised renal function.</p< <p<Methods</p< <p<A total of 128 patients aged 11–93 years who had a baseline Cl<sub<cr</sub< < 50 mL/min between January 1, 2007 and December 31, 2010 were identified from a database of a university-affiliated inpatient healthcare system; of these, 55 patients received caspofungin, 54 patients received fluconazole, and 19 patients received voriconazole. Changes in serum creatinine (S<sub<cr</sub<) and Cl<sub<cr</sub< levels while on therapy were compared with baseline values and between groups.</p< <p<Results</p< <p<The groups had similar characteristics apart from the larger proportion of females that received fluconazole. Baseline S<sub<cr</sub< was higher in those receiving caspofungin, but maximal increases of S<sub<cr</sub< and decreases in Cl<sub<cr</sub< were greatest for the fluconazole group. Acute kidney injury (AKI), assessed by RIFLE criteria, was more frequent in the fluconazole <it<vs.</it< the caspofungin group (<it<p</it< < 0.01); incidence of AKI in the voriconazole group was not significantly different than found in the other two groups. The infecting organism was a predictor of AKI and formulation with SBECD was not.</p< <p<Conclusions</p< <p<Treatment of fungal infections in patients with compromised renal function with an SBECD-containing antifungal agent was not associated with AKI in clinical practice. Since the infecting organism was associated with AKI, decision on which antifungal to use should be determined by susceptibilities to the organism and not the incorporation of SBECD in the IV formulation.</p< Voriconazole Caspofungin Fluconazole Renal dysfunction Sulfobutylether-β-cyclodextrin SBECD Acute kidney injury Infectious and parasitic diseases Welch Verna L verfasserin aut Mayer Thomas verfasserin aut Ranauro Paul verfasserin aut Meisner Joanne verfasserin aut Luke David R verfasserin aut In BMC Infectious Diseases BMC, 2003 13(2013), 1, p 14 (DE-627)326645381 (DE-600)2041550-3 14712334 nnns volume:13 year:2013 number:1, p 14 https://doi.org/10.1186/1471-2334-13-14 kostenfrei https://doaj.org/article/989d1aa8d3c745fa9e79b8977bdbce76 kostenfrei http://www.biomedcentral.com/1471-2334/13/14 kostenfrei https://doaj.org/toc/1471-2334 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2013 1, p 14 |
allfields_unstemmed |
10.1186/1471-2334-13-14 doi (DE-627)DOAJ008175918 (DE-599)DOAJ989d1aa8d3c745fa9e79b8977bdbce76 DE-627 ger DE-627 rakwb eng RC109-216 Lilly Craig M verfasserin aut Evaluation of intravenous voriconazole in patients with compromised renal function 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<Incorporation of the solubilizing excipient, sulfobutylether-β-cyclodextrin (SBECD), in the intravenous (IV) formulation of voriconazole has resulted in the recommendation that this formulation be used with caution in patients with creatinine clearances (Cl<sub<cr</sub<) < 50 mL/min. This study evaluated the safety of IV voriconazole compared with two other IV antifungals not containing SBECD in patients with compromised renal function.</p< <p<Methods</p< <p<A total of 128 patients aged 11–93 years who had a baseline Cl<sub<cr</sub< < 50 mL/min between January 1, 2007 and December 31, 2010 were identified from a database of a university-affiliated inpatient healthcare system; of these, 55 patients received caspofungin, 54 patients received fluconazole, and 19 patients received voriconazole. Changes in serum creatinine (S<sub<cr</sub<) and Cl<sub<cr</sub< levels while on therapy were compared with baseline values and between groups.</p< <p<Results</p< <p<The groups had similar characteristics apart from the larger proportion of females that received fluconazole. Baseline S<sub<cr</sub< was higher in those receiving caspofungin, but maximal increases of S<sub<cr</sub< and decreases in Cl<sub<cr</sub< were greatest for the fluconazole group. Acute kidney injury (AKI), assessed by RIFLE criteria, was more frequent in the fluconazole <it<vs.</it< the caspofungin group (<it<p</it< < 0.01); incidence of AKI in the voriconazole group was not significantly different than found in the other two groups. The infecting organism was a predictor of AKI and formulation with SBECD was not.</p< <p<Conclusions</p< <p<Treatment of fungal infections in patients with compromised renal function with an SBECD-containing antifungal agent was not associated with AKI in clinical practice. Since the infecting organism was associated with AKI, decision on which antifungal to use should be determined by susceptibilities to the organism and not the incorporation of SBECD in the IV formulation.</p< Voriconazole Caspofungin Fluconazole Renal dysfunction Sulfobutylether-β-cyclodextrin SBECD Acute kidney injury Infectious and parasitic diseases Welch Verna L verfasserin aut Mayer Thomas verfasserin aut Ranauro Paul verfasserin aut Meisner Joanne verfasserin aut Luke David R verfasserin aut In BMC Infectious Diseases BMC, 2003 13(2013), 1, p 14 (DE-627)326645381 (DE-600)2041550-3 14712334 nnns volume:13 year:2013 number:1, p 14 https://doi.org/10.1186/1471-2334-13-14 kostenfrei https://doaj.org/article/989d1aa8d3c745fa9e79b8977bdbce76 kostenfrei http://www.biomedcentral.com/1471-2334/13/14 kostenfrei https://doaj.org/toc/1471-2334 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2013 1, p 14 |
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10.1186/1471-2334-13-14 doi (DE-627)DOAJ008175918 (DE-599)DOAJ989d1aa8d3c745fa9e79b8977bdbce76 DE-627 ger DE-627 rakwb eng RC109-216 Lilly Craig M verfasserin aut Evaluation of intravenous voriconazole in patients with compromised renal function 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<Incorporation of the solubilizing excipient, sulfobutylether-β-cyclodextrin (SBECD), in the intravenous (IV) formulation of voriconazole has resulted in the recommendation that this formulation be used with caution in patients with creatinine clearances (Cl<sub<cr</sub<) < 50 mL/min. This study evaluated the safety of IV voriconazole compared with two other IV antifungals not containing SBECD in patients with compromised renal function.</p< <p<Methods</p< <p<A total of 128 patients aged 11–93 years who had a baseline Cl<sub<cr</sub< < 50 mL/min between January 1, 2007 and December 31, 2010 were identified from a database of a university-affiliated inpatient healthcare system; of these, 55 patients received caspofungin, 54 patients received fluconazole, and 19 patients received voriconazole. Changes in serum creatinine (S<sub<cr</sub<) and Cl<sub<cr</sub< levels while on therapy were compared with baseline values and between groups.</p< <p<Results</p< <p<The groups had similar characteristics apart from the larger proportion of females that received fluconazole. Baseline S<sub<cr</sub< was higher in those receiving caspofungin, but maximal increases of S<sub<cr</sub< and decreases in Cl<sub<cr</sub< were greatest for the fluconazole group. Acute kidney injury (AKI), assessed by RIFLE criteria, was more frequent in the fluconazole <it<vs.</it< the caspofungin group (<it<p</it< < 0.01); incidence of AKI in the voriconazole group was not significantly different than found in the other two groups. The infecting organism was a predictor of AKI and formulation with SBECD was not.</p< <p<Conclusions</p< <p<Treatment of fungal infections in patients with compromised renal function with an SBECD-containing antifungal agent was not associated with AKI in clinical practice. Since the infecting organism was associated with AKI, decision on which antifungal to use should be determined by susceptibilities to the organism and not the incorporation of SBECD in the IV formulation.</p< Voriconazole Caspofungin Fluconazole Renal dysfunction Sulfobutylether-β-cyclodextrin SBECD Acute kidney injury Infectious and parasitic diseases Welch Verna L verfasserin aut Mayer Thomas verfasserin aut Ranauro Paul verfasserin aut Meisner Joanne verfasserin aut Luke David R verfasserin aut In BMC Infectious Diseases BMC, 2003 13(2013), 1, p 14 (DE-627)326645381 (DE-600)2041550-3 14712334 nnns volume:13 year:2013 number:1, p 14 https://doi.org/10.1186/1471-2334-13-14 kostenfrei https://doaj.org/article/989d1aa8d3c745fa9e79b8977bdbce76 kostenfrei http://www.biomedcentral.com/1471-2334/13/14 kostenfrei https://doaj.org/toc/1471-2334 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2013 1, p 14 |
allfieldsSound |
10.1186/1471-2334-13-14 doi (DE-627)DOAJ008175918 (DE-599)DOAJ989d1aa8d3c745fa9e79b8977bdbce76 DE-627 ger DE-627 rakwb eng RC109-216 Lilly Craig M verfasserin aut Evaluation of intravenous voriconazole in patients with compromised renal function 2013 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier <p<Abstract</p< <p<Background</p< <p<Incorporation of the solubilizing excipient, sulfobutylether-β-cyclodextrin (SBECD), in the intravenous (IV) formulation of voriconazole has resulted in the recommendation that this formulation be used with caution in patients with creatinine clearances (Cl<sub<cr</sub<) < 50 mL/min. This study evaluated the safety of IV voriconazole compared with two other IV antifungals not containing SBECD in patients with compromised renal function.</p< <p<Methods</p< <p<A total of 128 patients aged 11–93 years who had a baseline Cl<sub<cr</sub< < 50 mL/min between January 1, 2007 and December 31, 2010 were identified from a database of a university-affiliated inpatient healthcare system; of these, 55 patients received caspofungin, 54 patients received fluconazole, and 19 patients received voriconazole. Changes in serum creatinine (S<sub<cr</sub<) and Cl<sub<cr</sub< levels while on therapy were compared with baseline values and between groups.</p< <p<Results</p< <p<The groups had similar characteristics apart from the larger proportion of females that received fluconazole. Baseline S<sub<cr</sub< was higher in those receiving caspofungin, but maximal increases of S<sub<cr</sub< and decreases in Cl<sub<cr</sub< were greatest for the fluconazole group. Acute kidney injury (AKI), assessed by RIFLE criteria, was more frequent in the fluconazole <it<vs.</it< the caspofungin group (<it<p</it< < 0.01); incidence of AKI in the voriconazole group was not significantly different than found in the other two groups. The infecting organism was a predictor of AKI and formulation with SBECD was not.</p< <p<Conclusions</p< <p<Treatment of fungal infections in patients with compromised renal function with an SBECD-containing antifungal agent was not associated with AKI in clinical practice. Since the infecting organism was associated with AKI, decision on which antifungal to use should be determined by susceptibilities to the organism and not the incorporation of SBECD in the IV formulation.</p< Voriconazole Caspofungin Fluconazole Renal dysfunction Sulfobutylether-β-cyclodextrin SBECD Acute kidney injury Infectious and parasitic diseases Welch Verna L verfasserin aut Mayer Thomas verfasserin aut Ranauro Paul verfasserin aut Meisner Joanne verfasserin aut Luke David R verfasserin aut In BMC Infectious Diseases BMC, 2003 13(2013), 1, p 14 (DE-627)326645381 (DE-600)2041550-3 14712334 nnns volume:13 year:2013 number:1, p 14 https://doi.org/10.1186/1471-2334-13-14 kostenfrei https://doaj.org/article/989d1aa8d3c745fa9e79b8977bdbce76 kostenfrei http://www.biomedcentral.com/1471-2334/13/14 kostenfrei https://doaj.org/toc/1471-2334 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_11 GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_31 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_702 GBV_ILN_2001 GBV_ILN_2003 GBV_ILN_2005 GBV_ILN_2006 GBV_ILN_2008 GBV_ILN_2009 GBV_ILN_2010 GBV_ILN_2011 GBV_ILN_2014 GBV_ILN_2015 GBV_ILN_2020 GBV_ILN_2021 GBV_ILN_2025 GBV_ILN_2031 GBV_ILN_2038 GBV_ILN_2044 GBV_ILN_2048 GBV_ILN_2050 GBV_ILN_2055 GBV_ILN_2056 GBV_ILN_2057 GBV_ILN_2061 GBV_ILN_2111 GBV_ILN_2113 GBV_ILN_2190 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 13 2013 1, p 14 |
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Lilly Craig M misc RC109-216 misc Voriconazole misc Caspofungin misc Fluconazole misc Renal dysfunction misc Sulfobutylether-β-cyclodextrin misc SBECD misc Acute kidney injury misc Infectious and parasitic diseases Evaluation of intravenous voriconazole in patients with compromised renal function |
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RC109-216 Evaluation of intravenous voriconazole in patients with compromised renal function Voriconazole Caspofungin Fluconazole Renal dysfunction Sulfobutylether-β-cyclodextrin SBECD Acute kidney injury |
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Evaluation of intravenous voriconazole in patients with compromised renal function |
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Evaluation of intravenous voriconazole in patients with compromised renal function |
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evaluation of intravenous voriconazole in patients with compromised renal function |
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Evaluation of intravenous voriconazole in patients with compromised renal function |
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<p<Abstract</p< <p<Background</p< <p<Incorporation of the solubilizing excipient, sulfobutylether-β-cyclodextrin (SBECD), in the intravenous (IV) formulation of voriconazole has resulted in the recommendation that this formulation be used with caution in patients with creatinine clearances (Cl<sub<cr</sub<) < 50 mL/min. This study evaluated the safety of IV voriconazole compared with two other IV antifungals not containing SBECD in patients with compromised renal function.</p< <p<Methods</p< <p<A total of 128 patients aged 11–93 years who had a baseline Cl<sub<cr</sub< < 50 mL/min between January 1, 2007 and December 31, 2010 were identified from a database of a university-affiliated inpatient healthcare system; of these, 55 patients received caspofungin, 54 patients received fluconazole, and 19 patients received voriconazole. Changes in serum creatinine (S<sub<cr</sub<) and Cl<sub<cr</sub< levels while on therapy were compared with baseline values and between groups.</p< <p<Results</p< <p<The groups had similar characteristics apart from the larger proportion of females that received fluconazole. Baseline S<sub<cr</sub< was higher in those receiving caspofungin, but maximal increases of S<sub<cr</sub< and decreases in Cl<sub<cr</sub< were greatest for the fluconazole group. Acute kidney injury (AKI), assessed by RIFLE criteria, was more frequent in the fluconazole <it<vs.</it< the caspofungin group (<it<p</it< < 0.01); incidence of AKI in the voriconazole group was not significantly different than found in the other two groups. The infecting organism was a predictor of AKI and formulation with SBECD was not.</p< <p<Conclusions</p< <p<Treatment of fungal infections in patients with compromised renal function with an SBECD-containing antifungal agent was not associated with AKI in clinical practice. Since the infecting organism was associated with AKI, decision on which antifungal to use should be determined by susceptibilities to the organism and not the incorporation of SBECD in the IV formulation.</p< |
abstractGer |
<p<Abstract</p< <p<Background</p< <p<Incorporation of the solubilizing excipient, sulfobutylether-β-cyclodextrin (SBECD), in the intravenous (IV) formulation of voriconazole has resulted in the recommendation that this formulation be used with caution in patients with creatinine clearances (Cl<sub<cr</sub<) < 50 mL/min. This study evaluated the safety of IV voriconazole compared with two other IV antifungals not containing SBECD in patients with compromised renal function.</p< <p<Methods</p< <p<A total of 128 patients aged 11–93 years who had a baseline Cl<sub<cr</sub< < 50 mL/min between January 1, 2007 and December 31, 2010 were identified from a database of a university-affiliated inpatient healthcare system; of these, 55 patients received caspofungin, 54 patients received fluconazole, and 19 patients received voriconazole. Changes in serum creatinine (S<sub<cr</sub<) and Cl<sub<cr</sub< levels while on therapy were compared with baseline values and between groups.</p< <p<Results</p< <p<The groups had similar characteristics apart from the larger proportion of females that received fluconazole. Baseline S<sub<cr</sub< was higher in those receiving caspofungin, but maximal increases of S<sub<cr</sub< and decreases in Cl<sub<cr</sub< were greatest for the fluconazole group. Acute kidney injury (AKI), assessed by RIFLE criteria, was more frequent in the fluconazole <it<vs.</it< the caspofungin group (<it<p</it< < 0.01); incidence of AKI in the voriconazole group was not significantly different than found in the other two groups. The infecting organism was a predictor of AKI and formulation with SBECD was not.</p< <p<Conclusions</p< <p<Treatment of fungal infections in patients with compromised renal function with an SBECD-containing antifungal agent was not associated with AKI in clinical practice. Since the infecting organism was associated with AKI, decision on which antifungal to use should be determined by susceptibilities to the organism and not the incorporation of SBECD in the IV formulation.</p< |
abstract_unstemmed |
<p<Abstract</p< <p<Background</p< <p<Incorporation of the solubilizing excipient, sulfobutylether-β-cyclodextrin (SBECD), in the intravenous (IV) formulation of voriconazole has resulted in the recommendation that this formulation be used with caution in patients with creatinine clearances (Cl<sub<cr</sub<) < 50 mL/min. This study evaluated the safety of IV voriconazole compared with two other IV antifungals not containing SBECD in patients with compromised renal function.</p< <p<Methods</p< <p<A total of 128 patients aged 11–93 years who had a baseline Cl<sub<cr</sub< < 50 mL/min between January 1, 2007 and December 31, 2010 were identified from a database of a university-affiliated inpatient healthcare system; of these, 55 patients received caspofungin, 54 patients received fluconazole, and 19 patients received voriconazole. Changes in serum creatinine (S<sub<cr</sub<) and Cl<sub<cr</sub< levels while on therapy were compared with baseline values and between groups.</p< <p<Results</p< <p<The groups had similar characteristics apart from the larger proportion of females that received fluconazole. Baseline S<sub<cr</sub< was higher in those receiving caspofungin, but maximal increases of S<sub<cr</sub< and decreases in Cl<sub<cr</sub< were greatest for the fluconazole group. Acute kidney injury (AKI), assessed by RIFLE criteria, was more frequent in the fluconazole <it<vs.</it< the caspofungin group (<it<p</it< < 0.01); incidence of AKI in the voriconazole group was not significantly different than found in the other two groups. The infecting organism was a predictor of AKI and formulation with SBECD was not.</p< <p<Conclusions</p< <p<Treatment of fungal infections in patients with compromised renal function with an SBECD-containing antifungal agent was not associated with AKI in clinical practice. Since the infecting organism was associated with AKI, decision on which antifungal to use should be determined by susceptibilities to the organism and not the incorporation of SBECD in the IV formulation.</p< |
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