A Critical Review of Cephalexin and Cefadroxil for the Treatment of Acute Uncomplicated Lower Urinary Tract Infection in the Era of "Bad Bugs, Few Drugs".
Adolescent
Adult
Aged
Aged, 80 and over
Anti-Bacterial Agents
/ pharmacokinetics
Cefadroxil
/ pharmacokinetics
Cephalexin
/ pharmacokinetics
Child
Drug Resistance, Multiple, Bacterial
/ physiology
Enterobacteriaceae
/ drug effects
Female
Humans
Male
Microbial Sensitivity Tests
Middle Aged
Urinary Tract Infections
/ drug therapy
Young Adult
beta-Lactamases
/ metabolism
Urinary tract infection (UTI)
cephalosporins
pharmacodynamics
pharmacokinetics
Journal
International journal of antimicrobial agents
ISSN: 1872-7913
Titre abrégé: Int J Antimicrob Agents
Pays: Netherlands
ID NLM: 9111860
Informations de publication
Date de publication:
Oct 2020
Oct 2020
Historique:
received:
19
04
2020
revised:
16
06
2020
accepted:
05
07
2020
pubmed:
14
7
2020
medline:
28
5
2021
entrez:
14
7
2020
Statut:
ppublish
Résumé
First-generation oral cephalosporins (cephalexin and cefadroxil) have traditionally been considered second-line treatment options for uncomplicated lower urinary tract infections (uLUTIs). However, in the current age of "bad bugs, few drugs", where there are increasingly limited oral options against resistant Enterobacteriaceae, there is an urgent need to rethink how best to utilize the available antibiotic armamentarium. This review examines the historical clinical trials and experimental studies of cephalexin and cefadroxil, particularly through the modern lens of pharmacokinetics/pharmacodynamics (PK/PD), to better appreciate the efficacy of these drugs in uLUTIs. Furthermore, newer cefazolin-cephalexin surrogate testing, as recommended by the Clinical and Laboratory Standards Institute (CLSI) and the United States Committee on Antimicrobial Susceptibility Testing (USCAST), has recategorized cephalexin in many instances from resistant to susceptible. We conclude that cephalexin and cefadroxil have very good early bacteriological and clinical cures in uLUTIs due to non-extended-spectrum beta-lactamase-producing (ESBL) Enterobacteriaceae comparable to many traditionally first-line agents. Cephalexin can be conveniently administered as 500 mg twice or thrice daily, similar to cefadroxil (500 mg twice daily); therefore, either agent may be used as a fluoroquinolone-sparing alternative. Cephalexin may be the more practical choice for many clinicians because reliable antimicrobial susceptibility test interpretative criteria (STIC) are provided by CLSI, USCAST, and the European Committee on Antimicrobial Susceptibility Testing (EUCAST), whereas direct cefadroxil STIC is offered only by EUCAST.
Identifiants
pubmed: 32659466
pii: S0924-8579(20)30255-7
doi: 10.1016/j.ijantimicag.2020.106085
pii:
doi:
Substances chimiques
Anti-Bacterial Agents
0
Cefadroxil
280111G160
beta-Lactamases
EC 3.5.2.6
Cephalexin
OBN7UDS42Y
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
106085Informations de copyright
Copyright © 2020 Elsevier Ltd. All rights reserved.