Abstract
The mortality of septic patients is still very high. Sepsis is caused by the host
response to invasive microbial infections and arises when the body’s response to an
infection injures its own tissues and organs. Sepsis is diagnosed by a mosaic of clinical
and laboratory parameters. Therapy consists of antimicrobial and surgical measures
for source control, supportive intensive care therapy and adjunctive therapies. Sepsis
is an emergency that requires immediate antimicrobial and supportive therapy. Goals
for hemodynamic stabilization are (CVP ≥ 8/≥ 12 mmHg under mechanical ventilation,
MAP ≥ 65 mmHg, ScvO2 ≥ 70 %) to achieve an adequate cellular oxygen supply. Further supportive measures
are lung protective ventilation (6 ml/kg predicted body weight in patients with ARDS/ALI),
and organsupportive measures as necessary. Recombined activated Protein C and Selenium
can be considered for adjunctive therapy. Low dose corticosteroids may be only administered
in patients with refractory septic shock despite high dose vasopressor support.
Kernaussagen
Die Sepsis ist trotz aller medizinischen Fortschritte noch immer eine der häufigsten
Todesursachen auf deutschen Intensivstationen. Bei der Genese dieser Erkrankung spielt
das Zusammenwirken von Infektion und Immunantwort eine entscheidende Rolle. Dabei
sind alle Mikroorganismen wie Bakterien, Pilze, Viren oder Parasiten in der Lage,
eine Sepsis auszulösen. Die Diagnose „Sepsis” beruht auf einem Mosaik von klinischen
und laborchemischen Parametern.
Bei der Therapie unterscheidet man einerseits die kausalen antimikrobiellen bzw. operativen
interventionellen Maßnahmen zur Herdsanierung und andererseits die elementare supportive
(organbezogene) intensivmedizinische Therapie sowie adjunktive (potenziell zusätzliche)
therapeutische Ansätze. Hierbei hat die kausale antimikrobielle Therapie bzw. die
chirurgische Herdsanierung die höchste Priorität.
Bei den supportiven Maßnahmen ist die hämodynamische Stabilisierung (ZVD ≥ 8, unter
Beatmung ≥ 12 mmHg, MAD ≥ 65 mmHg, ScvO2 ≥ 70 %) mit Volumen- und Katecholamintherapie mit dem Ziel eines adäquaten zellulären
Sauerstoffangebots von großer Bedeutung. Nicht zu vernachlässigen sind eine adäquate
Beatmungstherapie (6 ml/kgKG), eine frühzeitige Organersatztherapie und eine suffiziente
Ernährungstherapie. Zu den adjunktiven therapeutischen Therapieansätzen gehören das
rekombinierte aktivierte Protein C, Selen und Hydrokortison, deren endgültiger Stellenwert
erst nach weiteren Studien zu beurteilen ist.
Literatur
- 1
Engel C, Brunkhorst F, Bone H.
Epidemiology of sepsis in Germany: Results from a national prospective multicenter
study.
Intensive Care Med.
2007;
33
606-618
- 2
Lucioni C, Mazzi S, Currado I.
Sepsis costs in Italy.
Intensive Care Med.
2001;
Suppl. 2
580
- 3
Bone R, Sprung C, Sibbald W.
Definition for sepsis and organ failure.
Crit Care Med.
1992;
20
724-726
- 4
Clec'h C, Ferriere F, Karoubi P et al.
Diagnostic and prognostic value of procalcitonin in patients with septic shock.
Crit Care Med.
2004;
32
1166-1169
- 5
Bloos F, Hinder F, Becker K et al.
A multicenter trial to compare blood culture with polymerase chain reaction in severe
human sepsis.
Intensive Care Med.
2010;
36
241-247
- 6
Reinhart K, Brunkhorst F, Bone H et al.
Prävention, Diagnose, Therapie und Nachsorge der Sepsis; 1. Revision der S2k-Leitlinien
der Deutschen Sepsis-Gesellschaft e. V. (DSG) und der Deutschen Interdisziplinären
Vereinigung für Intensiv- und Notfallmedizin (DIVI).
Intensiv News.
2010;
Sonderausgabe
- 7
Rivers E, Nguyen P, Havstad S E.
Early goal-directed therapy in the treatment of severe sepsis and septic shock.
N Engl J Med.
2001;
345
1368-1377
- 8
Brunkhorst F, Engel C, Bloos F et al.
Intensive Insulin therapy and pentastarch resuscitation in severe sepsis.
N Engl J Med.
2008;
358
125-139
- 9
Dart A B, Mutter T C, Ruth C A et al.
Hydroxyethyl starch (HES) versus other fluid therapies: effects on kidney function.
Cochrane Database Syst Rev.
2010;
CD007594
- 10
Finfer S, Bellomo R, Boyce N et al.
A Comparison of Albumin and Saline for Fluid Resuscitation in the Intensive Care Unit.
N Engl J Med.
2004;
350
2247-2256
- 11
Annane D F.
Norepinephrine plus dobutamine versus epinephrine alone for management of septic shock:
a randomised trial.
Lancet.
2007;
370
676-684
- 12
Russel J, Wally K, Singer J et al.
Vasopressin versus norepinephrine infusion in patients with septic shock.
N Engl J Med.
2008;
358
877-887
- 13
De Backer D, Biston P, Devriendt J et al.
Comparison of Dopamine and Norepinephrine in the Treatment of Shock.
N Engl J Med.
2010;
362
779-789
- 14
Bellomo R, Chapman M, Finfer S.
Low-dose dopamine in patients with early renal dysfunction: A placebo-controlled randomised
trial. Australian and New Zealand Intensive Care Society (ANZICS) Clinical Trials
Group.
Lancet.
2000;
356
2139-2143
- 15
Dellinger R, Carlet J, Masur H et al.
Surviving Sepsis Campaign for management of severe sepsis and septic shock.
Crit Care Med.
2004;
32
858-872
- 16
Shah M, Hasselblad V, Stevenson L E.
Impact of the pulmonary artery catheter in critically ill patients: Meta-analysis
of randomized clinical trials.
JAMA.
2005;
294
1664-1670
- 17
Hebert P, Wells G, Blaichman M E.
A multicenter, randomized, controlled clinical trial of transfusion requirements in
critical care. Transfusion Requirements in Critical Care Investigators, Canadian Critical
Care Trials Group.
N Engl J Med.
1999;
340
409-417
- 18
Brower R, Lanken P, MacIntyre N.
Higher versus Lower Positive End-Expiratory Pressures in Patients with the Acute Respiratory
Distress Syndrome.
N Engl J Med.
2004;
351
327-336
- 19
Amato M, Barbas C, Medeiros D.
Effect of a Protective-Ventilation Strategy on Mortality in the Acute Respiratory
Distress Syndrome.
N Engl J Med.
1998;
338
347-354
- 20
Oppert M, Engel C, Brunkhorst F.
Acute renal failure in patients with severe sepsis and septic shock – A significant
independent risk factor for mortality.
Nephrol Dial Transplant.
2008;
23
904-909
- 21
Bertolini G, Lapichino G, Radrizzani D E.
Early enteral immunonutrition in patients with severe sepsis: Results of an interim
analysis of a randomized multicentre clinical trial.
Intensive Care Med.
2003;
29
834-840
- 22
Abraham E, Laterre P, Garg R E.
Drotrecogin alfa (activated) for adults with severe sepsis and a low risk of death.
N Engl J Med.
2005;
353
1332-1341
- 23
Bernard G, Vincent J, Laterre P E.
Efficacy and safety of recombinant human activated protein C for severe sepsis.
N Engl J Med.
2001;
344
699-709
- 24
Nadel S, Goldstein B, Williams M D et al.
Drotrecogin alfa (activated) in children with severe sepsis: a multicentre phase III
randomised controlled trial.
Lancet.
2007;
369
836-843
- 25
Annane D, Sebille V, Charpentier C.
Effect of treatment with low doses of hydrocortisone and flurocortisone on mortality
in patients with septic shock.
JAMA.
2002;
28
862-871
- 26
Sprung C, Annane D, Keh D.
Hydrocortisone therapy for patients with septic shock.
N Engl J Med.
2008;
358
111-124
- 27
Wiener R, Wiener D, Larson R.
Benefits and Risks of Tight Glucose Control in Critically Ill Adults – A Meta-analysis.
JAMA.
2008;
300
933-944
- 28
Forceville X, Laviolle B, Annane D.
Effects of high doses of selenium, as sodium selenite, in septic shock: a placebo-controlled,
randomized, double-blind, phase II study.
Critical Care.
2007;
11R
73
- 29
Alejandria M M, Lansang M AD, Dans L F, Mantaring I II.
Intravenous immunoglobulin for treating sepsis, severe sepsis and septic shock (Review).
The Cochrane Database of Systematic Reviews.
2010;
1
CD001090
- 30
Warren B, Eid A, Singer P.
High-dose antithrombin III in severe sepsis: a randomized controlled trial.
JAMA.
2001;
286
1869-1878
- 31 Reinhart K, Bloos F, Meier-Hellmann A. Sepsis und septischer Schock.. In: van Aken H,
Reinhart K, Zimpfer M, Welte T, Hrsg Intensivmedizin.. Stuttgart: Thieme; 2006: 825-854
Dr. med. Ole Bayer
Friedrich-Schiller-Universität Jena
Klinik für Anästhesiologie und Intensivtherapie
Erlanger Allee 101
07747 Jena
Email: Ole.Bayer@med.uni-jena.de