- •Acute respiratory distress syndrome ards
- •Incidence, mortalita
- •Fowler 1983, Pepe 1982
- •Zdroje mediátorů při ards
- •Komplikace
- •Základní složky léčby
- •Ventilační podpora - optimalizace ventilace a oxygenace
- •Neventilační posupy zlepšení výměny plynů
- •Novinky V ards (2001)
- •Klinická praxe hk
- •Ards 2007
- •0.92); Overall mortality was not significantly different if a plateau pressure
- •Is there evidence to support a phase II trial of inhaled corticosteroids in the treatment of incipient and persistent ards?
- •In vivo and In vitro effects of Salbutamol upon alveolar epithelial repair in acute lung injury.
- •Ards 2008
- •In the risk of mortality as well as relevant improvements in oxygenation and
- •Injury?
- •1 Unit may be warranted to reduce the risk of ards in injured patients.
- •Ventilator strategy using esophageal pressures to estimate the transpulmonary
- •Infection based on results of gram staining significantly reduced the incidences
- •Increase the incidence of ards in critically ill adults.
Ards 2008
Mesenchymální kmenové buňky intratracheálně za 4 hod po apliaci LPS – zlepšení klinického výsledku
Protective effects of propofol on acute lung injury induced by oleic acid in conscious rats. Crit Care Med. 2008 Apr;36(4):1214-21. CONCLUSIONS: Oleic acid resulted in sepsis-like responses including ALI, inflammatory reaction, and increased neutrophil-derived factors. It depressed the Na+-K+-ATPase activity but up-regulated inducible nitric oxide synthase. Treatment with propofol abrogated or reversed the oleic acid-induced changes.
Leukoreduction is associated with a decreased incidence of late onset acute respiratory distress syndrome after injury. Am Surg. 2008 Feb;74(2):117-23. NLR product exposure has an association with an increased incidence of late onset posttraumatic ARDS which is independent of large volume transfusions. Leukoreduction should be routinely included in an overall treatment strategy to furthermore mitigate this complication in critically ill trauma patients.
Nové mechanismy reparace ARDS Intensive Care Med. 2008 Apr;34(4):619-30. Epub 2008 Feb 9. Advances in mechanisms of repair and remodelling in acute lung injury.
Inhalační steroidy u časného ARDS ? Is there evidence to support a phase II trial of inhaled corticosteroids in the treatment of incipient and persistent ARDS? Crit Care Resusc. 2007 Sep;9(3):276-85
Steroidy a ARDS 2008 ?: Když nutno, tak:
co nejnižší dávka
ne později než 14 dní od vzniku ARDS
časné podání nízkých dávek redukuje dobu UPV a ICU
steroidy nelze doporučit jako rutinní postup u ARDS
Year Book of Intensive Care and Emergency Medicine 2008
The use of an inflammation-modulating diet in patients with acute lung injury or
acute respiratory distress syndrome: a meta-analysis of outcome data.
JPEN J Parenter Enteral Nutr. 2008 Nov-Dec;32(6):596-605.
Pontes-Arruda A, Demichele S, Seth A, Singer P.
Background: This meta-analysis of clinical trials compares an
inflammation-modulating diet enriched with eicosapentaenoic acid (EPA),
gamma-linolenic acid (GLA), and elevated antioxidants (EPA + GLA) vs a control
diet to determine the effectiveness of this specialized diet on oxygenation and
clinical outcomes in mechanically ventilated patients with acute lung injury
(ALI)/acute respiratory distress syndrome (ARDS). Methods: MEDLINE, EMBASE,
Cochrane Clinical Trials Register, and the U.S. National Institute of Health
Clinical Trials databases were searched. The outcome measures assessed were
28-day in-hospital mortality, 28-day ventilator-free and intensive care unit
(ICU)-free days, and the development of new organ failures. An evaluation of
oxygenation and ventilatory variables was also performed. Outcomes were analyzed
using both fixed-effects and random-effects models. Results: Three randomized
controlled studies (n = 411 patients) were included in this meta-analysis. Among
the most important findings of this evaluation is a significant reduction in the
risk of mortality (odds ratio [OR] = 0.40; 95% confidence interval [CI] =
0.24-0.68; P = .001), with significant reductions in the risk of developing new
organ failures (OR = 0.17; 95% CI = 0.08-0.34; P < .0001), time on mechanical
ventilation (standardized mean difference [SMD] = 0.56; 95% CI = 0.32-0.79; P <
.0001), and ICU stay (SMD = 0.51; 95% CI = 0.27-0.74; P < .0001) in patients who
received EPA + GLA. Conclusions: The meta-analysis showed a significant reduction
