Therapeutic Drug Monitoring of Antibiotics Is Needed in the Treatment of Sepsis
https://doi.org/10.21292/2078-5658-2022-19-6-62-71
Abstract
The article presents the results of a prospective one-center observational clinical study.
The level of therapeutic drug monitoring antibiotics was studied in patients with sepsis.
The objective: to assess the impact of pharmacokinetics and pharmacodynamics parameters of the main classes of antibacterial drugs using specific indices to improve the effectiveness of ongoing antimicrobial therapy in patients with sepsis asscoaited with the infectious process with pan-resistant nosocomial microflora.
Subjects and Methods. A total of 8 patients with sepsis meetiing the criteria of Sepsis-3 were included. Carbapenems, oxazolidinones, and aminoglycosides were used in the treatment. Concentrations of drugs in blood plasma were studied by high-performance liquid chromatography with mass spectrometry. Analysis of the effectiveness of treatment was performed on the third day of therapy.
Results. The T > MIC index reached 40% of the time interval between the two administrations for MIC for Pseudomonas aeruginosa in only two cases for group II carbapenems.
In both cases, high peak concentrations of the drug (19.5 and 35.4 mg/L, respectively) were observed, a low static volume of antibiotic distribution (0.06 l/kg and 0,09 l/kg) and reduced total clearance of the drug (7.18 and 4.11 ml/hr) were noted. The peak concentration of amikacin was low (3.35 mg/l), while the time to achieve it and the level of static volume distribution (356.5 liters) increased. The peak concentration of linezolid was reduced in all observations and amounted to 4.04 and 3.35 mg/l. The time of its achievement was increased (3.27 and 6.6 hours), the ratio of AUC/MIC was low and made 76.8 and 59.2.
The resolution of organ dysfunction and reduction of manifestations of infectious intoxication were noted only in three patients on the third day of observation.
Conclusion. Static pharmacokinetic/pharmacodynamic criteria may serve as a guideline for antimicrobial therapy.
Limitations in changing the tactics of antimicrobial therapy based on the use instruction nevertheless allow optimizing treatment by controlling the volume of distribution of the drug, presence of renal or hepatic insufficiency that, however, does not guarantee treatment success. The volume of therapeutic drug monitoring of antibiotics sufficient for compilation of static pharmakinetic models, does not meet the requirements of modern intensive care.
About the Authors
G. P. PlotnikovRussian Federation
Georgiy P. Plotnikov - Doctor of Medical Sciences, Head of Anesthesiology and Intensive Care Department with Intensive Care Wards
27, Bolshaya Serpukhovskaya St., Moscow, 115093
Phone: +7 (499) 236–20–23
A. N. Kudryavtsev
Russian Federation
Anton N. Kudryavtsev - Candidate of Medical Sciences, Anesthesiologist and Emergency Physician of Anesthesiology and Intensive Care Department with Intensive Care Wards
27, Bolshaya Serpukhovskaya St., Moscow, 115093
Phone: +7 (499) 236–20–23
A. A. Kleuzovich
Russian Federation
Artem A. Kleuzovich - Anesthesiologist and Emergency Physician of Anesthesiology and Intensive Care Department with Intensive Care Wards
27, Bolshaya Serpukhovskaya St., Moscow, 115093
Phone: +7 (499) 236–20–23
A. G. Chizhov
Russian Federation
Andrey G. Chizhov - Candidate of Medical Sciences, Anesthesiologist and Emergency Physician of Anesthesiology and Intensive Care Department with Intensive Care Wards
27, Bolshaya Serpukhovskaya St., Moscow, 115093
Phone: +7 (499) 236–20–23
A. A. Ponomarev
Russian Federation
Anatoliy A. Ponomarev - Anesthesiologist and Emergency Physician
of Anesthesiology and Intensive Care Department with Intensive Care Wards
27, Bolshaya Serpukhovskaya St., Moscow, 115093
Phone: +7 (499) 236–20–23
S. S. Larin
Russian Federation
Sergey S. Larin - Candidate of Biological Sciences, Deputy Director of the Higher School of Molecular and Experimental Medicine
1, Samory Mashela St., GSP-7, Moscow, 117997
Phone: +7 (495) 287–65–70
E. A. Litvin
Russian Federation
Evgeniy A. Litvin - Candidate of Biological Sciences, Researcher of Laboratory of Experimental and Clinical Pharmacology
1, Samory Mashela St., GSP-7, Moscow, 117997
Phone: +7 (495) 287–65–70
L. A. Anastasevich
Russian Federation
Lyudmila A. Anastasevich - Candidate of Medical Sciences, Head of Higher Professional Education Department, Expert in Clinical Trials of the Testing Center
1, Samory Mashela St., GSP-7, Moscow, 117997
Phone: +7 (495) 287–65–70
References
1. Beloborodov V.B., Gusarov V.G., Dekhnich A.V. et al. Diagnostics and antimicrobial therapy of the infections caused by multiresistant microorganisms. Guidelines. Messenger of Anesthesiology and Resuscitation, 2020, vol. 17, no. 1, pp. 52-83. (In Russ.) doi: 10.21292/2078-5658-2020-17-1-52-83.
2. Rudnov V.A., Kulabukhov V.V. Evolving understanding of sepsis: the ongoing story. Infeksii v Khirurgii, 2015, no. 2, pp. 6-10. (In Russ.)
3. Adembri C., Fallani S., Cassetta M.I. et al. Linezolid pharmacokinetic/pharmacodynamic profile in critically ill septic patients: intermittent versus continuous infusion. Int. J. Antimicr. Agents, 2008, vol. 31, no. 2, pp. 122-129. doi:10.1016/j.ijantimicag.2007.09.009.
4. Evans L., Rhodes A., Alhazzani W. et al. sepsis campaign: international guidelines for management of sepsis and septic shock 2021. Int. Care Med., 2021, vol. 47, no. 11, pp. 1181-1247. doi: 10.1186/s13613-021-00862-0.
5. Roberts J.A., Paul S.K., Akova M. et al. DALI: defining antibiotic levels in intensive care unit patients: are current beta-lactam antibiotic doses sufficient for critically ill patients? Clin. Infect. Dis., 2014, vol. 58, no. 8, pp. 1072-1083. doi: 10.1093/cid/ciu027.
6. Singer M., Deuschman C.S., Seymour C.W. et al. The Third International Consensus definitions for Sepsis and Septic Shock (Sepsis-3). JAMA, 2016, vol. 315, no. 8, pp. 801-810. doi: 10.1001/jama.2016.0287.
7. Taccone F.S., Laterre P.F., Spapen H. et al. Revisiting the loading dose of amikacin for patients with severe sepsis and septic shock. Crit. Care, 2010, vol. 14, no. 2, pp. 53. doi: 10.1186/cc8945.
8. Van Zanten A.R.H., Oudijk M., Nohlmans‐Paulssen M.K.E. et al. Continuous vs. intermittent cefotaxime administration in patients with chronic obstructive pulmonary disease and respiratory tract infections: pharmacokinetics/pharmacodynamics, bacterial susceptibility and clinical efficacy. Brit. J. Clin. Pharmacol., 2007, vol. 63, no. 1, pp. 100-109. doi: 10.1111/j.1365-2125.2006.02730.x. Epub 2006 Jul 21.
Review
For citations:
Plotnikov G.P., Kudryavtsev A.N., Kleuzovich A.A., Chizhov A.G., Ponomarev A.A., Larin S.S., Litvin E.A., Anastasevich L.A. Therapeutic Drug Monitoring of Antibiotics Is Needed in the Treatment of Sepsis. Messenger of ANESTHESIOLOGY AND RESUSCITATION. 2022;19(6):62-71. (In Russ.) https://doi.org/10.21292/2078-5658-2022-19-6-62-71