Cerebrospinal Fluid Concentrations of Meropenem and Vancomycin in Ventriculitis Patients Obtained by TDM-Guided Continuous Infusion.
cerebrospinal fluid
critical care
meropenem
pharmacokinetics
therapeutic drug monitoring
vancomycin
ventriculitis
Journal
Antibiotics (Basel, Switzerland)
ISSN: 2079-6382
Titre abrégé: Antibiotics (Basel)
Pays: Switzerland
ID NLM: 101637404
Informations de publication
Date de publication:
20 Nov 2021
20 Nov 2021
Historique:
received:
25
10
2021
revised:
17
11
2021
accepted:
18
11
2021
entrez:
27
11
2021
pubmed:
28
11
2021
medline:
28
11
2021
Statut:
epublish
Résumé
Effective antibiotic therapy of cerebral infections such as meningitis or ventriculitis is hindered by low penetration into the cerebrospinal fluid (CSF). Because continuous infusion of meropenem and vancomycin and routine therapeutic drug monitoring (TDM) have been proposed to optimize antimicrobial exposure in ventriculitis patients, an individualized dosing strategy was implemented in our department. We present a retrospective analysis of meropenem and vancomycin concentrations in serum and CSF in the first nine ventriculitis patients treated with continuous infusion and TDM-guided dose optimization aiming at 20-30 mg/L. Median initial dosing was 8.8 g/24 h meropenem and 4.25 g/24 h vancomycin, respectively, resulting in median serum concentrations of 21.3 mg/L for meropenem and 24.5 mg/L for vancomycin and CSF concentrations of 3.4 mg/L for meropenem and 1.7 mg/L for vancomycin. Median CSF penetration was 15% for meropenem and 7% for vancomycin. With initial dosing, all but one patient achieved CSF concentrations above 1 mg/L. Dose adjustment according to TDM ensured sufficient CSF concentrations in all patients within 48 h of treatment. Given the limited penetration, continuous infusion of meropenem and vancomycin based on renal function and TDM-guided dose optimization appears a reasonable approach to attain sufficient CSF concentrations in ventriculitis patients.
Identifiants
pubmed: 34827359
pii: antibiotics10111421
doi: 10.3390/antibiotics10111421
pmc: PMC8614961
pii:
doi:
Types de publication
Journal Article
Langues
eng
Références
Acta Neurochir (Wien). 2017 Feb;159(2):317-323
pubmed: 27928632
J Antimicrob Chemother. 2017 Oct 1;72(10):2891-2897
pubmed: 29091190
Antimicrob Agents Chemother. 2012 Dec;56(12):6343-8
pubmed: 23045356
Clin Infect Dis. 2014 Apr;58(8):1072-83
pubmed: 24429437
Int J Artif Organs. 2015 Jan;38(1):17-22
pubmed: 25633891
Int J Antimicrob Agents. 2015 Apr;45(4):385-92
pubmed: 25656151
Clin Pharmacokinet. 2018 Apr;57(4):439-454
pubmed: 28905331
Anesth Analg. 2010 Dec;111(6):1505-10
pubmed: 21048095
Intensive Care Med. 2020 Jun;46(6):1127-1153
pubmed: 32383061
Clin Infect Dis. 2017 Mar 15;64(6):e34-e65
pubmed: 28203777
Antimicrob Agents Chemother. 2020 Dec 16;65(1):
pubmed: 33077649
Acta Neurochir (Wien). 2018 Nov;160(11):2099-2105
pubmed: 30242495
Clin Pharmacokinet. 2017 Dec;56(12):1479-1490
pubmed: 28528396
Am J Health Syst Pharm. 2020 May 19;77(11):835-864
pubmed: 32191793
J Antimicrob Chemother. 2012 Jan;67(1):17-24
pubmed: 22028203
J Antimicrob Chemother. 2018 May 1;73(5):1330-1339
pubmed: 29425283
Pharmacotherapy. 2015 Apr;35(4):e32-6
pubmed: 25884534
Ann Clin Microbiol Antimicrob. 2018 Dec 29;17(1):47
pubmed: 30594199
Nephron. 1976;16(1):31-41
pubmed: 1244564
Clin Infect Dis. 2004 Nov 1;39(9):1267-84
pubmed: 15494903
Crit Care. 2016 Oct 24;20(1):343
pubmed: 27776537
J Antimicrob Chemother. 2019 Apr 1;74(4):991-996
pubmed: 30689877