دورية أكاديمية
Incidence of acute kidney injury (AKI) and its impact on patient outcomes among adult hospitalized patients with carbapenem-resistant Gram-negative infections who received targeted treatment with a newer β-lactam or β-lactam/β-lactamase inhibitor-, polymyxin- or aminoglycoside-containing regimen.
العنوان: | Incidence of acute kidney injury (AKI) and its impact on patient outcomes among adult hospitalized patients with carbapenem-resistant Gram-negative infections who received targeted treatment with a newer β-lactam or β-lactam/β-lactamase inhibitor-, polymyxin- or aminoglycoside-containing regimen. |
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المؤلفون: | Lodise TP; Albany College of Pharmacy and Health Sciences, Department of Pharmacy Practice, 106 New Scotland Avenue, Albany, NY, USA., Yucel E; Merck & Co., Inc., 2025 E Scott Ave, Rahway, NJ, USA., Obi EN; Merck & Co., Inc., 2025 E Scott Ave, Rahway, NJ, USA., Watanabe AH; Merck & Co., Inc., 2025 E Scott Ave, Rahway, NJ, USA., Nathanson BH; OptiStatim LLC, 25 Willow Circle, Longmeadow, MA, USA. |
المصدر: | The Journal of antimicrobial chemotherapy [J Antimicrob Chemother] 2024 Jan 03; Vol. 79 (1), pp. 82-95. |
نوع المنشور: | Observational Study; Journal Article |
اللغة: | English |
بيانات الدورية: | Publisher: Oxford University Press Country of Publication: England NLM ID: 7513617 Publication Model: Print Cited Medium: Internet ISSN: 1460-2091 (Electronic) Linking ISSN: 03057453 NLM ISO Abbreviation: J Antimicrob Chemother Subsets: MEDLINE |
أسماء مطبوعة: | Publication: 1997- : London : Oxford University Press Original Publication: London, New York, Academic Press. |
مواضيع طبية MeSH: | beta-Lactamase Inhibitors*/adverse effects , Acute Kidney Injury*/chemically induced, Adult ; Humans ; beta-Lactams ; Carbapenems/therapeutic use ; Polymyxins ; Lactams ; Aminoglycosides/adverse effects ; Retrospective Studies ; Incidence ; Anti-Bacterial Agents/pharmacology |
مستخلص: | Background: Limited comparative data exist on acute kidney injury (AKI) risk and AKI-associated outcomes in hospitalized patients with carbapenem-resistant Gram-negative infections (CR-GNIs) treated with a newer β-lactam/β-lactam-β-lactamase inhibitor (BL/BL-BLI)-, polymyxin (PB)- or aminoglycoside (AG)-containing regimen. This study quantified the risk of AKI and AKI-related outcomes among patients with CR-GNIs treated with a newer BL/BL-BLI-, PB- or AG-containing regimen. Methods: A multicentre, retrospective, observational study was performed (2016-20). The study included adult hospitalized patients with (i) baseline estimated glomerular filtration rates ≥30 mL/min/1.73 m2; (ii) CR-GN pneumonia, complicated urinary tract infection or bloodstream infection; and (iii) receipt of newer BL/BL-BLI, PG or AG within 7 days of index CR-GN culture for ≥3 days. Outcomes included AKI, in-hospital mortality and hospital costs. Results: The study included 750 patients and most (48%) received a newer BL/BL-BLI. The median (IQR) treatment duration was 8 (5-11), 5 (4-8) and 7 (4-8) days in the newer BL/BL-BLI group, AG group and PB group, respectively. The PB group had the highest adjusted AKI incidence (95% CI) (PB: 25.1% (15.6%-34.6%) versus AG: 8.9% (5.7%-12.2%) versus newer BL/BL-BLI: 11.9% (8.1%-15.7%); P = 0.001). Patients with AKI had significantly higher in-hospital mortality (AKI: 18.5% versus 'No AKI': 5.6%; P = 0.001) and mean hospital costs (AKI: $49 192 versus 'No AKI': $38,763; P = 0.043). Conclusions: The AKI incidence was highest among PB patients and patients with AKI had worse outcomes. Healthcare systems should consider minimizing the use of antibiotics that augment AKI risk as a measure to improve outcomes in patients with CR-GNIs. (© The Author(s) 2023. Published by Oxford University Press on behalf of British Society for Antimicrobial Chemotherapy.) |
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معلومات مُعتمدة: | Merck Sharp & Dohme LLC; Merck & Co., Inc. |
المشرفين على المادة: | 0 (beta-Lactamase Inhibitors) 0 (beta-Lactams) 0 (Carbapenems) 0 (Polymyxins) 0 (Lactams) 0 (Aminoglycosides) 0 (Anti-Bacterial Agents) |
تواريخ الأحداث: | Date Created: 20231114 Date Completed: 20240104 Latest Revision: 20240104 |
رمز التحديث: | 20240104 |
مُعرف محوري في PubMed: | PMC10761276 |
DOI: | 10.1093/jac/dkad351 |
PMID: | 37962080 |
قاعدة البيانات: | MEDLINE |
تدمد: | 1460-2091 |
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DOI: | 10.1093/jac/dkad351 |