Bacterial sepsis: Diagnostics and calculated antibiotic therapy

被引:0
|
作者
Richter, D. C. [1 ]
Heininger, A. [2 ]
Brenner, T. [1 ]
Hochreiter, M. [1 ]
Bernhard, M. [3 ]
Briegel, J. [4 ]
Dubler, S. [1 ]
Grabein, B. [5 ]
Hecker, A. [6 ]
Kruger, W. A. [7 ]
Mayer, K. [8 ]
Pletz, M. W. [9 ]
Storzinger, D. [8 ]
Pinder, N. [8 ]
Hoppe-Tichy, T. [2 ]
Weiterer, S. [1 ]
Zimmermann, S. [2 ]
Brinkmann, A. [10 ]
Weigand, M. A. [1 ]
Lichtenstern, C. [1 ]
机构
[1] Heidelberg Univ Hosp, Dept Anesthesiol, Neuenheimer Feld 110, D-69120 Heidelberg, Germany
[2] Univ Klinikum Heidelberg, Sekt Krankenhaus & Umwelthyg, Zentrum Infektiol, Heidelberg, Germany
[3] Univ Klinikum Leipzig, Zent Notaufnahme, Leipzig, Germany
[4] Klinikum Univ Munchen, Klin Anasthesiol, Munich, Germany
[5] Klinikum Univ Munchen, Stabsstelle Klin Mikrobiol & Krankenhaushyg, Munich, Germany
[6] Univ Klinikum Giessen & Marburg, Klin Allgemein Viszeral Thorax Transplantat & Kin, Giessen, Germany
[7] Klinikum Konstanz, Klin Anasthesiol & Operat Intens Med, Gesundheitsverbund Landkreis Konstanz, Constance, Germany
[8] Univ Klinikums Heidelberg, Apotheke, Heidelberg, Germany
[9] Univ Klinikum Jena, Zentrum Infekt Med & Krankenhaushyg, Jena, Germany
[10] Klinikum Heidenheim, Klin Anasthesie Operat Intens Med & Spezielle Sch, Heidenheim, Germany
来源
ANAESTHESIST | 2019年 / 68卷
关键词
Drug resistance; multiple; bacterial; Lactams; Prolonged and continuous -lactam infusion; Therapeutic drug monitoring; Patient care bundles; VENTILATOR-ASSOCIATED PNEUMONIA; BLOOD-STREAM INFECTION; INTERNATIONAL CONSENSUS DEFINITIONS; SYSTEMIC INFLAMMATORY RESPONSE; COMPLICATED INTRAABDOMINAL INFECTION; INADEQUATE ANTIMICROBIAL TREATMENT; STAPHYLOCOCCUS-AUREUS INFECTIONS; RANDOMIZED CONTROLLED-TRIAL; OPTIMIZING DRUG EXPOSURE; BETA-LACTAM ANTIBIOTICS;
D O I
10.1007/s00101-017-0396-z
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
The mortality of patients with sepsis and septic shock is still unacceptably high. An effective calculated antibiotic treatment within 1h of recognition of sepsis is an important target of sepsis treatment. Delays lead to an increase in mortality; therefore, structured treatment concepts form a rational foundation, taking relevant diagnostic and treatment steps into consideration. In addition to the assumed infection and individual risks of each patient, local resistance patterns and specific problem pathogens must be taken into account during the selection of anti-infective treatment. Many pathophysiologic alterations influence the pharmacokinetics (PK) of antibiotics during sepsis. The principle of standard dosing should be abandoned and replaced by an individual treatment approach with stronger weighting of the pharmacokinetics/pharmacodynamics (PK/PD) index of the substance groups. Although this is not yet the clinical standard, prolonged (or continuous) infusion of -lactam antibiotics and therapeutic drug monitoring (TDM) can help to achieve defined PK targets. Prolonged infusion is sufficient without TDM, but for continuous infusion, TDM is generally necessary. Afurther argument for individual PK/PD-oriented antibiotic approaches is the increasing number of infections due to multidrug-resistant (MDR) pathogens in the intensive care unit. For effective treatment, antibiotic stewardship teams (ABS teams) are becoming more established. Interdisciplinary cooperation of the ABS team with infectious disease (ID) specialists, microbiologists, and clinical pharmacists leads not only to rational administration of antibiotics, but also has a positive influence on treatment outcome. The gold standards for pathogen identification are still culture-based detection and microbiologic resistance testing for the various antibiotic groups. Despite the rapid investigation time, novel polymerase chain reaction(PCR)-based procedures for pathogen identification and resistance determination are currently only an adjunct to routine sepsis diagnostics, due to the limited number of studies, high costs, and limited availability. In complicated septic courses with multiple anti-infective therapies or recurrent sepsis, PCR-based procedures can be used in addition to treatment monitoring and diagnostics. Novel antibiotics represent potent alternatives in the treatment of MDR infections. Due to the often defined spectrum of pathogens and the practically (still) absent resistance, they are suitable for targeted treatment of severe MDR infections (therapy escalation). (Contribution available free of charge by Free Access [https://link.springer.com/article/10.1007/s00101-017-0396-z].)
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收藏
页码:40 / 62
页数:23
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