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1.
Resuscitation ; 94: 1-7, 2015 Sep.
Article in English | MEDLINE | ID: mdl-26095301

ABSTRACT

BACKGROUND: Survival is less than 10% for pediatric patients following out-of-hospital cardiac arrest. It is not known if more time on the scene of the cardiac arrest and advanced life support interventions by emergency services personnel are associated with improved survival. AIM: This study was performed to determine which times on the scene and which prehospital interventions were associated with improved survival. METHODS: We studied patients aged 3 days to 19 years old with out-of-hospital cardiac arrest, using the Resuscitation Outcomes Consortium cardiac arrest database from 11 North American regions, from 2005 to 2012. We evaluated survival to hospital discharge according to on-scene times (<10, 10 to 35 and >35 min). RESULTS: Data were available for 2244 patients (1017 infants, 594 children and 633 adolescents). Infants had the lowest rate of survival (3.7%) compared to children (9.8%) and adolescents (16.3%). Survival improved over the 7 year study period especially among adolescents. Survival was highest in the 10 to 35 min on-scene time group (10.2%) compared to the >35 min. group (6.9%) and the <10 min. group (5.3%, p=0.01). Intravenous or intra-osseous access attempts and fluid administration were associated with improved survival, whereas advanced airway attempts were not associated with survival and resuscitation drugs were associated with worse survival. CONCLUSIONS: In this observational study, a scene time of 10 to 35 min was associated with the highest survival, especially among adolescents. Access for fluid resuscitation was associated with increased survival but advanced airway and resuscitation drugs were not.


Subject(s)
Cardiopulmonary Resuscitation/methods , Emergency Medical Services/methods , Out-of-Hospital Cardiac Arrest/therapy , Adolescent , Canada/epidemiology , Child , Child, Preschool , Female , Follow-Up Studies , Humans , Infant , Infant, Newborn , Male , Out-of-Hospital Cardiac Arrest/mortality , Prognosis , Retrospective Studies , Survival Rate/trends , Time Factors , United States/epidemiology , Young Adult
2.
Crit Care Med ; 39(7): 1655-62, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21423000

ABSTRACT

OBJECTIVES: Administration of eicosapentaenoic acid and docosahexanoic acid, omega-3 fatty acids in fish oil, has been associated with improved patient outcomes in acute lung injury when studied in a commercial enteral formula. However, fish oil has not been tested independently in acute lung injury. We therefore sought to determine whether enteral fish oil alone would reduce pulmonary and systemic inflammation in patients with acute lung injury. DESIGN: Phase II randomized controlled trial. SETTING: Five North American medical centers. PATIENTS: Mechanically ventilated patients with acute lung injury ≥18 yrs of age. INTERVENTIONS: Subjects were randomized to receive enteral fish oil (9.75 g eicosapentaenoic acid and 6.75 g docosahexanoic acid daily) or saline placebo for up to 14 days. MEASUREMENTS AND MAIN RESULTS: Bronchoalveolar lavage fluid and blood were collected at baseline (day 0), day 4 ± 1, and day 8 ± 1. The primary end point was bronchoalveolar lavage fluid interleukin-8 levels. Forty-one participants received fish oil and 49 received placebo. Enteral fish oil administration was associated with increased serum eicosapentaenoic acid concentration (p < .0001). However, there was no significant difference in the change in bronchoalveolar lavage fluid interleukin-8 from baseline to day 4 (p = .37) or day 8 (p = .55) between treatment arms. There were no appreciable improvements in other bronchoalveolar lavage fluid or plasma biomarkers in the fish oil group compared with the control group. Similarly, organ failure score, ventilator-free days, intensive care unit-free days, and 60-day mortality did not differ between the groups. CONCLUSIONS: Fish oil did not reduce biomarkers of pulmonary or systemic inflammation in patients with acute lung injury, and the results do not support the conduct of a larger clinical trial in this population with this agent. This experimental approach is feasible for proof-of-concept studies evaluating new treatments for acute lung injury.


Subject(s)
Acute Lung Injury/drug therapy , Bronchoalveolar Lavage Fluid/chemistry , Docosahexaenoic Acids/therapeutic use , Eicosapentaenoic Acid/therapeutic use , Enteral Nutrition , Interleukin-8/analysis , Acute Lung Injury/blood , Acute Lung Injury/mortality , Adult , Aged , Biomarkers/analysis , Biomarkers/blood , Body Weight/drug effects , Cell Count , Chemokine CCL2/analysis , Docosahexaenoic Acids/adverse effects , Docosahexaenoic Acids/blood , Drug Therapy, Combination , Eicosapentaenoic Acid/adverse effects , Eicosapentaenoic Acid/blood , Female , Hospital Mortality , Humans , Interleukin-6/analysis , Interleukin-6/blood , Interleukin-8/blood , Leukotriene B4/analysis , Leukotriene B4/blood , Male , Middle Aged , Neutrophils , Pneumonia/drug therapy , Positive-Pressure Respiration, Intrinsic , Pulmonary Surfactant-Associated Protein D/blood , Tidal Volume/drug effects , von Willebrand Factor/analysis , von Willebrand Factor/metabolism
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