Systemic Inflammatory Response Syndrome
Conditions
Keywords
Immunoglobulins, inhibitor proteins, human albumin, systemic inflammatory response syndrome, interleukins, standardized serum-protein solution
Brief summary
Morbidity and mortality in patients suffering from systemic inflammatory response syndrome (SIRS) remain high. The primary aim of the present study is to assess the efficacy of a standardized 5% serum-protein solution containing immunoglobulins on serum cytokine levels. The secondary aim is to evaluate survival of the patients.
Detailed description
Out of 40 patients randomised, 18 patients received albumin, 20 patients received Biseko and 2 patients died before receiving the complete study medication. During days 1-6 of the study period, serum-levels of IL-1ß were significantly lower in patients with Biseko-therapy compared to patients receiving albumin (IL-1ß-Area under the curve 65.04 ± 71.09 days.pg/ml and 111.05 ± 156.97 days.pg/ml respectively, P=0.03). No difference could be found in serum-levels of IL-6, TNF-α and TNF-R between both groups. While a statistically not significant trend towards better survival was observed in the Biseko-group on day 28, the survival rate on day 180 was significantly higher in the Biseko-group \[9/18 (50%)\] vs. albumin- group \[2/20 (10%), (P=0.008)\]. Conclusion: Data suggest that Biseko treatment was associated with significantly lower IL-1ß plasma concentrations (d1 to 6) and improved long-term survival rates. The data provided in our study are the first to be collected in a randomized, controlled trial. Certainly, the small number of patients and the variety of diseases limit our study, however, the variety of diseases reflects the realistic large scale of morbidity in the medical intensive care unit.
Interventions
5% albumin was given intravenously at a volume of 1,000 ml on the first day and 500 ml/day during the following four days.
DRUGBiseko
Standardised 5% serum-protein solution (Biseko, Biotest, Dreieich, Germany) was given intravenously at a volume of 1,000 ml on the first day and 500 ml/day during the following four days.
Sponsors
Medical University of Vienna
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No
Inclusion criteria
* Patients aged between 18 and 85 years fulfilling at least two of the four SIRS criteria: * body temperature \> 38°C or \< 36°C * tachycardia \> 90/min * tachypnea \> 20/min with spontaneous respiration * leucocytosis \> 12,000/mcl * leucopenia \< 4,000/mcl or more than 10 % immature granulocytes were included \[8,21,22\]
Exclusion criteria
* Patients with proven intolerance against homologous protein solutions * Patients with known liver failure * Pregnant patients * Patients with absolute IgA deficiency were excluded
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary aim of the present study is to assess the efficacy of a standardized 5% serum-protein solution containing immunoglobulins on serum cytokine levels. | 3 years |
Secondary
| Measure | Time frame |
|---|---|
| The secondary aim is to evaluate survival of the patients. | 3 years |
Countries
Austria
Outcome results
None listed