Antibiotic Therapy Optimization in Special Populations

A special issue of Antibiotics (ISSN 2079-6382).

Deadline for manuscript submissions: closed (30 September 2022) | Viewed by 5452

Special Issue Editors


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Guest Editor
Division of Clinical Pharmacy/Infectious Diseases Pharmacotherapy, Department of Pharmacy, College of Pharmacy, Kyung Hee University, Seoul, Korea
Interests: clinical pharmacokinetics; pharmacodynamics; clinical pharmacometrics; critical care; sepsis; obesity; drug therapy optimization

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Guest Editor
Department of Obstetrics and Gynecology and Division of Clinical Pharmacology, Department of Medicine, Indiana University School of Medicine, Indianapolis, IN, USA
Interests: obstetric clinical pharmacology; pharmacometrics; drug metabolism; pediatric pharmacology; pharmacokinetics; pharmacodynamics; physiologically based pharmacokinetic modeling, drug-drug interactions, personalized medicine

Special Issue Information

Dear Colleagues,

In the era of antibiotic resistance, with few novel antimicrobial agents in the clinical pipeline, the importance of appropriate antibiotic use cannot be emphasized enough. One of the contributing factors to inappropriate antibiotic use is inadequate consideration of patient characteristics to design an individualized dosing regimen. Failure of the “one size fits all” theory to achieve optimal clinical outcomes is now evident, and the practice of medicine is moving toward individualized precision medicine. The primary reason for the failure of the “one size fits all” theory is substantial pharmacokinetic and pharmacodynamic variability among various patient populations.

Individualized precision antibiotic therapy is critical to optimize treatment outcomes because sufficient antimicrobial concentrations are imperative to achieve maximal killing activity, but excessive concentrations should be avoided in order to minimize antibiotic-associated toxicities. However, the design of optimal individualized antibiotic therapy regimen is particularly complicating for the patient populations whose gradual or acute pathophysiologic alterations substantially impact antimicrobial pharmacokinetics and pharmacodynamics. These patient populations are collectively called special populations and include critically ill patients, elderly populations, obese individuals, pediatric populations, immunocompromised patients, pregnant individuals, and patients with impaired organ functions. In these special populations, antibiotic clearance and volume of distribution are substantially different compared to general populations, requiring alternative antimicrobial dosing regimen. Additionally, change in their disease course over time affects intra-individual pharmacokinetic variability, resulting in continuous dosage adjustment in these patient populations. With the advancement of data computation technology and elaborate understanding of pathophysiology, scientific data contributing to the design of optimal antibiotic therapy are exponentially increasing.

In this Special Issue, scientific advances in designing optimal antibiotic therapy considering various patient characteristics will be discussed focusing on the aforementioned special patient populations. The multidisciplinary efforts in the field of antibiotic pharmacotherapy such as clinical pharmacokinetics and pharmacodynamics will provide insight for clinician scientists and healthcare professionals regarding the optimal antimicrobial therapy for special patient populations.

We look forward to your contributions to this important area of clinical practice and research.

Dr. Eun Kyoung Chung
Prof. Dr. Sara K. Quinney
Guest Editors

Manuscript Submission Information

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Keywords

  • clinical pharmacometrics
  • PK/PD optimization of antibiotic therapy
  • special populations
  • critically ill patients
  • elderly populations
  • obesity
  • immunocompromised patients
  • pediatric populations
  • pregnancy
  • patients with impaired organ function

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Published Papers (1 paper)

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Research

10 pages, 2478 KiB  
Article
Comparative Risk of Acute Kidney Injury Following Concurrent Administration of Vancomycin with Piperacillin/Tazobactam or Meropenem: A Systematic Review and Meta-Analysis of Observational Studies
by Abdulmajeed M. Alshehri, Mohammed Y. Alzahrani, Mohammed A. Abujamal, Mariam H. Abdalla, Shuroug A. Alowais, Osamah M. Alfayez, Majed S. Alyami, Abdulaali R. Almutairi and Omar A. Almohammed
Antibiotics 2022, 11(4), 526; https://doi.org/10.3390/antibiotics11040526 - 14 Apr 2022
Cited by 9 | Viewed by 4414
Abstract
The study aims to comparatively assess the nephrotoxicity of vancomycin when combined with piperacillin-tazobactam (V + PT) or meropenem (V + M) in adult patients hospitalized in general wards or intensive care units. We searched MEDLINE, Google Scholar, and Web of Science for [...] Read more.
The study aims to comparatively assess the nephrotoxicity of vancomycin when combined with piperacillin-tazobactam (V + PT) or meropenem (V + M) in adult patients hospitalized in general wards or intensive care units. We searched MEDLINE, Google Scholar, and Web of Science for observational studies evaluating incidences of AKI in adult patients receiving V + PT or V + M for at least 48 h in general wards or intensive care units. The primary outcome was AKI events, while the secondary outcomes were hospital length of stay, need for renal replacement therapy (RRT), and mortality events. The odds ratio (OR), or mean difference for the hospital length of stay, with a corresponding 95% confidence interval (CI) from the inverse variance weighting random-effects model were estimated for the risk of AKI, RRT, and mortality. Of the 112 studies identified, twelve observational studies were included in this meta-analysis with a total of 14,511 patients. The odds of having AKI were significantly higher in patients receiving V + PT compared with V + M (OR = 2.31; 95%CI 1.69–3.15). There were no differences between V + PT and V + M in the hospital length of stay, RRT, or mortality outcomes. Thus, clinicians should be vigilant while using V + PT, especially in patients who are at high risk of AKI. Full article
(This article belongs to the Special Issue Antibiotic Therapy Optimization in Special Populations)
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