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Tytuł pozycji:

Antimicrobial Dosing in Specific Populations and Novel Clinical Methodologies: Obesity.

Tytuł:
Antimicrobial Dosing in Specific Populations and Novel Clinical Methodologies: Obesity.
Autorzy:
Pai MP; Department of Clinical Pharmacy, College of Pharmacy, University of Michigan, Ann Arbor, Michigan, USA.
Źródło:
Clinical pharmacology and therapeutics [Clin Pharmacol Ther] 2021 Apr; Vol. 109 (4), pp. 942-951. Date of Electronic Publication: 2021 Feb 28.
Typ publikacji:
Journal Article; Review
Język:
English
Imprint Name(s):
Publication: 2015- : Hoboken, NJ : Wiley
Original Publication: St. Louis : C.V. Mosby
MeSH Terms:
Drug Dosage Calculations*
Anti-Bacterial Agents/*administration & dosage
Obesity/*epidemiology
Body Surface Area ; Body Weight ; Dose-Response Relationship, Drug ; Humans ; Metabolic Clearance Rate ; Phenotype ; Skin Diseases, Infectious/drug therapy ; Skin Diseases, Infectious/epidemiology
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Grant Information:
P30 CA046592 United States CA NCI NIH HHS; R01 HS027183 United States HS AHRQ HHS
Substance Nomenclature:
0 (Anti-Bacterial Agents)
Entry Date(s):
Date Created: 20210201 Date Completed: 20210824 Latest Revision: 20220219
Update Code:
20240104
PubMed Central ID:
PMC8855475
DOI:
10.1002/cpt.2181
PMID:
33523485
Czasopismo naukowe
Obesity and its related comorbidities can negatively influence the outcomes of certain infectious diseases. Specific dosing recommendations are often lacking in the product label for patients with obesity that leads to unclear guidance in practice. Higher rates of therapeutic failure have been reported with some fixed dose antibiotics and pragmatic approaches to dose modification are limited for orally administered agents. For i.v. antimicrobials dosed on weight, alternate body size descriptors (ABSDs) have been used to reduce the risk of overdosing. These ABSDs are mathematical transformations of height and weight that represent fat-free weight and follow the same principles as body surface area (BSA)-based dosing of cancer chemotherapy. However, ABSDs are rarely studied in pivotal phase III studies and so can risk the underdosing of antimicrobials in patients with obesity when incorrectly applied in the real-world setting. Specific case examples are presented to highlight these risks. Although general principles may be considered by clinicians, a universal approach to dose modification in obesity is unlikely. Studies that can better distinguish human body phenotypes may help reduce our reliance on height and weight to define dosing. Simple and complex technologies exist to quantify individual body composition that could improve upon our current approach. Early evidence suggests that body composition parameters repurposed from medical imaging data may improve upon height and weight as covariates of drug clearance and distribution. Clinical trials that can integrate human body phenotyping may help us identify new approaches to optimal dose selection of antimicrobials in patients with obesity.
(© 2021 The Authors. Clinical Pharmacology & Therapeutics © 2021 American Society for Clinical Pharmacology and Therapeutics.)

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