Clinical efficacy of novel combinations of older beta-lactam and beta-lactamase inhibitors: Where are the evidences?
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作者:
Veeraraghavan, Balaji
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Christian Med Coll & Hosp, Dept Clin Microbiol, Vellore, Tamil Nadu, IndiaChristian Med Coll & Hosp, Dept Clin Microbiol, Vellore, Tamil Nadu, India
Veeraraghavan, Balaji
[1
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Bakthavatchalam, Yamuna Devi
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Christian Med Coll & Hosp, Dept Clin Microbiol, Vellore, Tamil Nadu, IndiaChristian Med Coll & Hosp, Dept Clin Microbiol, Vellore, Tamil Nadu, India
Bakthavatchalam, Yamuna Devi
[1
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Kandasamy, Subramani
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Christian Med Coll & Hosp, Crit Care Div, Vellore, Tamil Nadu, IndiaChristian Med Coll & Hosp, Dept Clin Microbiol, Vellore, Tamil Nadu, India
Kandasamy, Subramani
[2
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Iyadurai, Ramya
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Christian Med Coll & Hosp, Dept Med, Vellore, Tamil Nadu, IndiaChristian Med Coll & Hosp, Dept Clin Microbiol, Vellore, Tamil Nadu, India
Iyadurai, Ramya
[3
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机构:
[1] Christian Med Coll & Hosp, Dept Clin Microbiol, Vellore, Tamil Nadu, India
[2] Christian Med Coll & Hosp, Crit Care Div, Vellore, Tamil Nadu, India
[3] Christian Med Coll & Hosp, Dept Med, Vellore, Tamil Nadu, India
India is well known for the rampant growth of ESBLs that jeopardized the clinical utility of standalone betalactam. Pharmaceutical organizations fancied to rescue these beta-lactams by combining them with generic beta-lactamase inhibitors despite such combinations were never investigated in non-clinical or clinical studies. Lack of stringency in regulatory review practices allowed the market entry of these combinations. CSE 1034 (ceftriaxone, sulbactam and EDTA) and cefoperazone sulbactam are the most irrational antibiotics in clinical use. The effectiveness of such combinations relies on multiple factors such as relative beta-lactamase stability of the standalone beta-lactam, the inhibitory potency of the beta-lactamase inhibitor and more importantly the adequacy of the dose incorporated in the formulation. Unfortunately, none of the unconventional BL-BLI inhibitor combinations marketed in India has been subjected to such evaluations. Therefore, their therapeutic utility is uncertain. Besides questionable therapeutic utility, sub-optimal exposures would lead to the selection of resistant clones.
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Univ Paris Diderot, PRESS Sorbonne Cite, CHU Bichat Claude Bernard, AP HP,Dept Anethesie Reanimat,INSERM,UMR 1152, Paris, FranceUniv Paris Diderot, PRESS Sorbonne Cite, CHU Bichat Claude Bernard, AP HP,Dept Anethesie Reanimat,INSERM,UMR 1152, Paris, France
Montravers, Philippe
Bassetti, Matteo
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Univ Udine, Dept Med, Infect Dis Div, Udine, Italy
Azienda Sanitaria Univ Integrata Udine, Udine, ItalyUniv Paris Diderot, PRESS Sorbonne Cite, CHU Bichat Claude Bernard, AP HP,Dept Anethesie Reanimat,INSERM,UMR 1152, Paris, France
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Univ Calif San Francisco, Sch Pharm, 533 Parnassus Ave,U-503 Box 0622, San Francisco, CA 94143 USAUniv Calif San Francisco, Sch Pharm, 533 Parnassus Ave,U-503 Box 0622, San Francisco, CA 94143 USA
Ho, Stephanie
Lynn Nguyen
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Univ Calif San Francisco, Med Ctr, San Francisco, CA USAUniv Calif San Francisco, Sch Pharm, 533 Parnassus Ave,U-503 Box 0622, San Francisco, CA 94143 USA
Lynn Nguyen
Trang Trinh
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Univ Calif San Francisco, Sch Pharm, 533 Parnassus Ave,U-503 Box 0622, San Francisco, CA 94143 USAUniv Calif San Francisco, Sch Pharm, 533 Parnassus Ave,U-503 Box 0622, San Francisco, CA 94143 USA
Trang Trinh
MacDougall, Conan
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Univ Calif San Francisco, Sch Pharm, 533 Parnassus Ave,U-503 Box 0622, San Francisco, CA 94143 USAUniv Calif San Francisco, Sch Pharm, 533 Parnassus Ave,U-503 Box 0622, San Francisco, CA 94143 USA