Literature DB >> 32349999

Intrathecal Antibacterial and Antifungal Therapies.

Roland Nau1,2, Claudia Blei3, Helmut Eiffert4,5.   

Abstract

Intrathecal administration of anti-infectives is indicated in central nervous system infections by multiresistant pathogens when drugs that can reach adequate cerebrospinal fluid (CSF) concentrations by systemic therapy are not available. Antibiotics that readily pass the blood-brain and blood-CSF barriers and/or that have low toxicity allowing an increase in the daily dosage should not be used for intrathecal therapy. Intrathecal therapy is accompanied by systemic treatment. Antibacterials indispensable for intrathecal therapy include aminoglycosides, colistin, daptomycin, tigecycline, and vancomycin. Limited experience suggests the utility of the antifungals amphotericin B and caspofungin. Intraventricular administration ensures distribution throughout the CSF compartment, whereas intralumbar dosing often fails to attain adequate antibiotic concentrations in the ventricles. The individual dose is determined by the estimated size of the CSF space and by the estimated clearance from CSF. For moderately lipophilic anti-infectives with a molecular weight above approximately 1,000 g/mol, as well as for hydrophilic drugs with a molecular weight above approximately 400 g/mol, one daily dose is normally adequate. The ventricular drain should be clamped for 15 to 120 min to facilitate the distribution of the anti-infective in the CSF space. Therapeutic drug monitoring of the trough levels is necessary only in cases of therapeutic failure.
Copyright © 2020 American Society for Microbiology.

Entities:  

Keywords:  antibiotics; antifungal agents; brain abscess; cerebrospinal fluid; intrathecal; intraventricular; meningitis; ventricular shunt; ventriculitis

Mesh:

Substances:

Year:  2020        PMID: 32349999      PMCID: PMC7194852          DOI: 10.1128/CMR.00190-19

Source DB:  PubMed          Journal:  Clin Microbiol Rev        ISSN: 0893-8512            Impact factor:   26.132


  136 in total

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2.  Development and validation of an LC-MS/MS method for the determination of tigecycline in human plasma and cerebrospinal fluid and its application to a pharmacokinetic study.

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4.  Pharmacokinetics and pharmacodynamics of antibiotics in central nervous system infections.

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5.  Multidrug-Resistant Acinetobacter baumannii Ventriculostomy-Related Infection, Treated by a Colistin, Tigecycline, and Intraventricular Fibrinolysis.

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Journal:  World Neurosurg       Date:  2018-10-10       Impact factor: 2.104

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7.  Relationship between structure and convulsant properties of some beta-lactam antibiotics following intracerebroventricular microinjection in rats.

Authors:  A De Sarro; D Ammendola; M Zappala; S Grasso; G B De Sarro
Journal:  Antimicrob Agents Chemother       Date:  1995-01       Impact factor: 5.191

8.  Successful treatment of extensively drug-resistant Acinetobacter baumannii ventriculitis and meningitis with intraventricular colistin after application of a loading dose: a case series.

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9.  Treatment of cerebrospinal fluid shunt infections with teicoplanin.

Authors:  M L Fernández Guerrero; M de Górgolas; R Fernández Roblas; J M Campos
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Journal:  Antimicrob Resist Infect Control       Date:  2018-01-19       Impact factor: 4.887

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2.  Clinical Pharmacogenetics Implementation Consortium Guideline for the Use of Aminoglycosides Based on MT-RNR1 Genotype.

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Review 3.  Efficacy of Vancomycin and Meropenem in Central Nervous System Infections in Children and Adults: Current Update.

Authors:  Franziska Schneider; André Gessner; Nahed El-Najjar
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Review 4.  Current Perspectives on the Diagnosis and Management of Healthcare-Associated Ventriculitis and Meningitis.

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Review 5.  Conventional Antifungals for Invasive Infections Delivered by Unconventional Methods; Aerosols, Irrigants, Directed Injections and Impregnated Cement.

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Review 6.  Spatial and temporal variation of routine parameters: pitfalls in the cerebrospinal fluid analysis in central nervous system infections.

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8.  Population pharmacokinetic model of vancomycin in postoperative neurosurgical patients.

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