[Drug monitoring of the antibacterial drug Vancomycin in patients with purulent-inflammatory diseases of the maxillofacial region]. 2023

N M Khelminskaya, and V I Kravets, and A V Posadskaya, and D A Eremin, and A V Martirosov, and Sh M Bugaev
Pirogov Russian National Research Medical University, Moscow, Russia.

OBJECTIVE To evaluate the change in the level of concentration of the antibacterial drug Vancomycin registered in the purulent focus area (facial vein) and in the peripheral blood flow (cubital vein) in patients with phlegmon of the maxillofacial region (MFR). METHODS The clinical material of the study was 12 patients with phlegmon of MFR who were being treated in the maxillofacial department of the N.I. Pirogov State Clinical Hospital No. 1 of the Moscow Medical Center. The drainage of phlegmons was performed on the day of admission of the patient 2-3 days after the onset of the disease. The phlegmons involved two or more spaces of the MFR. As an antimicrobial drug, 500 mg of Vancomycin in 400 ml of saline solution was used intravenously. Quantitative registration of Vancomycin was carried out 2 hours after intravenous infusion. Blood sampling was carried out from the cubital and facial veins in an amount of 7-8 ml intraoperatively at the opening of the phlegmon, under endotracheal anesthesia. The concentration of the antibiotic was determined by high-performance liquid crystal chromatography. CONCLUSIONS The study found that the concentration of Vancomycin in the facial vein exceeds similar indicators obtained from the cubital vein. The difference in the percentage ratio averaged 19.2±7.3%. In 10 patients with phlegmons of various localization, it was found that the penetration of the antibacterial drug into the tissues of the inflammatory focus is higher compared to the periphery. However, in a number of patients, the concentration of the drug did not exceed the minimum suppressive concentration recommended for obtaining a therapeutic effect (for Vancomycin, it is at least 2 mcg / ml). CONCLUSIONS To achieve the therapeutic effect of phlegmon treatment, it is necessary to select an individual dose of the drug for each patient.

UI MeSH Term Description Entries
D002481 Cellulitis An acute, diffuse, and suppurative inflammation of loose connective tissue, particularly the deep subcutaneous tissues, and sometimes muscle, which is most commonly seen as a result of infection of a wound, ulcer, or other skin lesions. Phlegmon
D006257 Head The upper part of the human body, or the front or upper part of the body of an animal, typically separated from the rest of the body by a neck, and containing the brain, mouth, and sense organs. Heads
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000900 Anti-Bacterial Agents Substances that inhibit the growth or reproduction of BACTERIA. Anti-Bacterial Agent,Anti-Bacterial Compound,Anti-Mycobacterial Agent,Antibacterial Agent,Antibiotics,Antimycobacterial Agent,Bacteriocidal Agent,Bacteriocide,Anti-Bacterial Compounds,Anti-Mycobacterial Agents,Antibacterial Agents,Antibiotic,Antimycobacterial Agents,Bacteriocidal Agents,Bacteriocides,Agent, Anti-Bacterial,Agent, Anti-Mycobacterial,Agent, Antibacterial,Agent, Antimycobacterial,Agent, Bacteriocidal,Agents, Anti-Bacterial,Agents, Anti-Mycobacterial,Agents, Antibacterial,Agents, Antimycobacterial,Agents, Bacteriocidal,Anti Bacterial Agent,Anti Bacterial Agents,Anti Bacterial Compound,Anti Bacterial Compounds,Anti Mycobacterial Agent,Anti Mycobacterial Agents,Compound, Anti-Bacterial,Compounds, Anti-Bacterial
D014640 Vancomycin Antibacterial obtained from Streptomyces orientalis. It is a glycopeptide related to RISTOCETIN that inhibits bacterial cell wall assembly and is toxic to kidneys and the inner ear. AB-Vancomycin,Diatracin,VANCO-cell,Vanco Azupharma,Vanco-saar,Vancocin,Vancocin HCl,Vancocine,Vancomicina Abbott,Vancomicina Chiesi,Vancomicina Combino Phar,Vancomicina Norman,Vancomycin Hexal,Vancomycin Hydrochloride,Vancomycin Lilly,Vancomycin Phosphate (1:2),Vancomycin Phosphate (1:2), Decahydrate,Vancomycin Sulfate,Vancomycin-ratiopharm,Vancomycine Dakota,Hydrochloride, Vancomycin,Sulfate, Vancomycin
D016903 Drug Monitoring The process of observing, recording, or detecting the effects of a chemical substance administered to an individual therapeutically or diagnostically. Monitoring, Drug,Therapeutic Drug Monitoring,Drug Monitoring, Therapeutic,Monitoring, Therapeutic Drug

Related Publications

N M Khelminskaya, and V I Kravets, and A V Posadskaya, and D A Eremin, and A V Martirosov, and Sh M Bugaev
January 1975, Stomatologiia,
N M Khelminskaya, and V I Kravets, and A V Posadskaya, and D A Eremin, and A V Martirosov, and Sh M Bugaev
January 2015, Stomatologiia,
N M Khelminskaya, and V I Kravets, and A V Posadskaya, and D A Eremin, and A V Martirosov, and Sh M Bugaev
January 2008, Stomatologiia,
N M Khelminskaya, and V I Kravets, and A V Posadskaya, and D A Eremin, and A V Martirosov, and Sh M Bugaev
April 1978, Voenno-meditsinskii zhurnal,
N M Khelminskaya, and V I Kravets, and A V Posadskaya, and D A Eremin, and A V Martirosov, and Sh M Bugaev
November 1968, Arzneimittel-Forschung,
N M Khelminskaya, and V I Kravets, and A V Posadskaya, and D A Eremin, and A V Martirosov, and Sh M Bugaev
January 1987, Stomatologiia,
N M Khelminskaya, and V I Kravets, and A V Posadskaya, and D A Eremin, and A V Martirosov, and Sh M Bugaev
January 2008, Stomatologiia,
N M Khelminskaya, and V I Kravets, and A V Posadskaya, and D A Eremin, and A V Martirosov, and Sh M Bugaev
January 1973, Stomatologiia. Stomatology,
N M Khelminskaya, and V I Kravets, and A V Posadskaya, and D A Eremin, and A V Martirosov, and Sh M Bugaev
January 1974, Stomatologiia,
N M Khelminskaya, and V I Kravets, and A V Posadskaya, and D A Eremin, and A V Martirosov, and Sh M Bugaev
January 2000, Zhurnal mikrobiologii, epidemiologii i immunobiologii,
Copied contents to your clipboard!