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Clinical predictors of nephrotoxicity associated with teicoplanin: Meta-analysis and meta-regression
Toshinori Hirai1, Keiko Hosohata2, Yukari Ogawa3
1Department of Pharmacy, Mie University Hospital, Faculty of Medicine, Mie University, Tsu, Mie, Japan.
Abstract:
Teicoplanin is a glycopeptide antibiotic against methicillin-resistant Staphylococcus aureus infections. However, the impact of clinical characteristics on nephrotoxicity associated with teicoplanin has not been determined. This meta-analysis aimed to investigate the relationship between clinical characteristics and nephrotoxicity associated with teicoplanin. We identified clinical research published from January 1975 to June 2021 using PubMed, Cochrane Library, and Scopus, which described the nephrotoxicity associated with teicoplanin. Meta-analysis determined the incidence of nephrotoxicity. Using meta-regression analysis, we evaluated the impact of clinical characteristics on outcomes. Of the 567 articles, eight articles including 634 patients were analysed. The overall incidence of nephrotoxicity associated with teicoplanin was 11.0% (95% confidence interval: 8.0-13.0) for the fixed-effect model. Additionally, patients with >65 years had a high trend for the risk of nephrotoxicity compared to those with ≤65 years (>65 years; 12.0% [95% confidence interval: 9.0-15.0] vs. ≤65 years; 7.0% [95% confidence interval: 3.0-12.0], p = 0.09) for the fixed-effect model. Meta-regression analysis demonstrated that only serum albumin level negatively correlated with the risk of nephrotoxicity (y = -17.0 x + 56.7, r = 0.74, p = 0.01). This meta-analysis ascertained that hypoalbuminemia leads to nephrotoxicity associated with teicoplanin.
Insights
This study found that low serum albumin levels increase the risk of teicoplanin-induced nephrotoxicity. Hypoalbuminemia is a key factor in teicoplanin
Area of Science:
- Pharmacology and Toxicology
- Infectious Diseases
- Nephrology
Background:
- Teicoplanin is a critical glycopeptide antibiotic for treating methicillin-resistant Staphylococcus aureus (MRSA) infections.
- The clinical factors influencing teicoplanin-associated nephrotoxicity remain incompletely understood.
- Understanding these factors is crucial for optimizing patient safety and treatment efficacy.
Purpose of the Study:
- To investigate the relationship between various clinical characteristics and the incidence of nephrotoxicity.
- To identify specific patient factors that may predict or correlate with teicoplanin-induced kidney damage.
- To provide evidence-based insights for safer teicoplanin prescribing practices.
Main Methods:
- A comprehensive meta-analysis of clinical studies published between January 1975 and June 2021.
- Databases searched included PubMed, Cochrane Library, and Scopus for relevant research on teicoplanin and nephrotoxicity.
- Meta-regression analysis was employed to evaluate the impact of clinical characteristics on nephrotoxicity outcomes.
Main Results:
- The overall incidence of teicoplanin-associated nephrotoxicity was 11.0% across eight analyzed studies (634 patients).
- A trend towards increased nephrotoxicity risk was observed in patients over 65 years old (12.0% vs. 7.0%).
- Meta-regression revealed a significant negative correlation between serum albumin levels and nephrotoxicity risk (p=0.01).
Conclusions:
- Hypoalbuminemia is a significant risk factor contributing to teicoplanin-induced nephrotoxicity.
- Clinical monitoring of serum albumin levels may be essential in patients receiving teicoplanin.
- Further research should focus on proactive management strategies for patients with hypoalbuminemia to mitigate kidney injury.
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