Você pesquisou por y - Critical Care Science (CCS)
Abstract
Rev Bras Ter Intensiva. 2010;22(4):315-320
DOI 10.1590/S0103-507X2010000400001
OBJECTIVE: Limb movements, passively performed by a physiotherapist, have been shown to result in significant increases in critically ill patients' metabolic and hemodynamic variables. This study objective was to determine whether passive cycling leg movement increases hemodynamic and metabolic variables in sedated mechanical ventilation dependent patients. METHODS: Five sedated mechanical ventilation dependent patients in a 18-bed intensive care unit of a university hospital were evaluated. Passive cycling leg movements were performed for 10min at a 30 movements/min rate. Complete hemodynamical data were recorded and arterial and mixed venous blood sample were collected 5 minutes before and after 5 minutes after the maneuver completion. RESULTS: All patients had increased oxygen consumption (VO2). The VO2 increase occurred with a concomitant drop in mixed venous blood saturation (SvO2), likely from both oxygen extraction ratio (O2ER) and cardiac index (CI) increase. CONCLUSION: passive cycling leg movements may influence hemodynamical and metabolic status in sedated mechanical ventilation-dependent patients.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):315-320
DOI 10.1590/S0103-507X2010000400001
OBJECTIVE: Limb movements, passively performed by a physiotherapist, have been shown to result in significant increases in critically ill patients' metabolic and hemodynamic variables. This study objective was to determine whether passive cycling leg movement increases hemodynamic and metabolic variables in sedated mechanical ventilation dependent patients. METHODS: Five sedated mechanical ventilation dependent patients in a 18-bed intensive care unit of a university hospital were evaluated. Passive cycling leg movements were performed for 10min at a 30 movements/min rate. Complete hemodynamical data were recorded and arterial and mixed venous blood sample were collected 5 minutes before and after 5 minutes after the maneuver completion. RESULTS: All patients had increased oxygen consumption (VO2). The VO2 increase occurred with a concomitant drop in mixed venous blood saturation (SvO2), likely from both oxygen extraction ratio (O2ER) and cardiac index (CI) increase. CONCLUSION: passive cycling leg movements may influence hemodynamical and metabolic status in sedated mechanical ventilation-dependent patients.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):321-326
DOI 10.1590/S0103-507X2010000400002
PURPOSE: Sepsis severity and mortality risk require aggressive therapy which includes hemodynamic support. The best fluid for volume replacement, however, is controversial. This study aimed to compare 0.9% isotonic saline solution versus 7.5% hypertonic saline solution as volume replacement fluid in sepsis induced by cecum ligation plus puncture rats. METHODS: This experimental trial included 30 rats divided into three groups: Control group (CG, n = 10), isotonic (ISG, n = 10) and hypertonic solution (HSG, n = 10). Fifteen hours after cecum ligation and puncture, all animals underwent respiratory rate, mean arterial pressure, renal and hepatic blood flow and weight evaluation, plus blood collection for TNF-α measurement. The ISG and HSG treatment groups received volume replacement 60 minutes before the procedure with either 0.9% or 7.5% saline solution, respectively. RESULTS: Two animals died. Significant differences were found for the animals' mean weight after 15 hours (p=0.018), particularly relevant when ISG and HSG are compared (p=0.003). Renal blood flow was also significantly different for the CG versus HSG (p=0.002) and CG versus ISG (p=0.008), but not significantly different for ISG versus HSG. No mean arterial pressure improvement was found for HSG (0.054). Other variables were not significant. CONCLUSIONS: Although no mean blood pressure, hepatic flow or TNF-α improvements were detected, the rats with sepsis 15 hours after cecum ligation and puncture showed significantly increased renal blood flow which was 0.9% isotonic saline solution or of 7.5% hypertonic solution use independent.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):321-326
DOI 10.1590/S0103-507X2010000400002
PURPOSE: Sepsis severity and mortality risk require aggressive therapy which includes hemodynamic support. The best fluid for volume replacement, however, is controversial. This study aimed to compare 0.9% isotonic saline solution versus 7.5% hypertonic saline solution as volume replacement fluid in sepsis induced by cecum ligation plus puncture rats. METHODS: This experimental trial included 30 rats divided into three groups: Control group (CG, n = 10), isotonic (ISG, n = 10) and hypertonic solution (HSG, n = 10). Fifteen hours after cecum ligation and puncture, all animals underwent respiratory rate, mean arterial pressure, renal and hepatic blood flow and weight evaluation, plus blood collection for TNF-α measurement. The ISG and HSG treatment groups received volume replacement 60 minutes before the procedure with either 0.9% or 7.5% saline solution, respectively. RESULTS: Two animals died. Significant differences were found for the animals' mean weight after 15 hours (p=0.018), particularly relevant when ISG and HSG are compared (p=0.003). Renal blood flow was also significantly different for the CG versus HSG (p=0.002) and CG versus ISG (p=0.008), but not significantly different for ISG versus HSG. No mean arterial pressure improvement was found for HSG (0.054). Other variables were not significant. CONCLUSIONS: Although no mean blood pressure, hepatic flow or TNF-α improvements were detected, the rats with sepsis 15 hours after cecum ligation and puncture showed significantly increased renal blood flow which was 0.9% isotonic saline solution or of 7.5% hypertonic solution use independent.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):327-332
DOI 10.1590/S0103-507X2010000400003
OBJECTIVE: Homocysteine and sepsis are both associated with inflammation and endothelial activation. Therefore this study was aimed to evaluate if the plasma homocystein level is related with the septic patient clinical severity. METHODS: Severe sepsis or septic shock patients, with less than 48 hours from organ dysfunction start, were admitted to this prospective observational study. Homocysteine levels were determined by the time of study admission and then on the Days 3, 7 and 14. The homocysteine association with the Sequential Organ Failure Assessment (SOFA) score was evaluated using the Sperman test, and its association with mortality using the Mann-Whitney test. A p<0.05 value was considered statistically significant. RESULTS: Twenty one patients were enrolled, and 60 blood samples were collected to measure total homocysteine [median 6.92 (5.27 - 9.74 μmol/L)]. The Sperman correlation test showed no association between homocysteine and SOFA ( r=0.15 and p=0.26). Also no correlation was found for the homocysteine level by the study admission time and the difference between the Day 3 SOFA score versus by study admission (deltaSOFA) (r=0.04 and p=0.87). Homocysteine variation between the Day 3 and the study admission (deltaHmc) and SOFA score variation in the same period were not correlated (r=-0.11 and p=0.66). Homocysteine by the study admission was not correlated with death in intensive care unit rate (p= 0.46) or in-hospital death rate (p = 0.13). This was also true for deltaHmc (p=0.12 and p=0.99, respectively). CONCLUSION: Baseline homocysteine levels and its variations within the first dysfunction days were not related with septic patients' worsened organ function parameters or mortality.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):327-332
DOI 10.1590/S0103-507X2010000400003
OBJECTIVE: Homocysteine and sepsis are both associated with inflammation and endothelial activation. Therefore this study was aimed to evaluate if the plasma homocystein level is related with the septic patient clinical severity. METHODS: Severe sepsis or septic shock patients, with less than 48 hours from organ dysfunction start, were admitted to this prospective observational study. Homocysteine levels were determined by the time of study admission and then on the Days 3, 7 and 14. The homocysteine association with the Sequential Organ Failure Assessment (SOFA) score was evaluated using the Sperman test, and its association with mortality using the Mann-Whitney test. A p<0.05 value was considered statistically significant. RESULTS: Twenty one patients were enrolled, and 60 blood samples were collected to measure total homocysteine [median 6.92 (5.27 - 9.74 μmol/L)]. The Sperman correlation test showed no association between homocysteine and SOFA ( r=0.15 and p=0.26). Also no correlation was found for the homocysteine level by the study admission time and the difference between the Day 3 SOFA score versus by study admission (deltaSOFA) (r=0.04 and p=0.87). Homocysteine variation between the Day 3 and the study admission (deltaHmc) and SOFA score variation in the same period were not correlated (r=-0.11 and p=0.66). Homocysteine by the study admission was not correlated with death in intensive care unit rate (p= 0.46) or in-hospital death rate (p = 0.13). This was also true for deltaHmc (p=0.12 and p=0.99, respectively). CONCLUSION: Baseline homocysteine levels and its variations within the first dysfunction days were not related with septic patients' worsened organ function parameters or mortality.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):333-338
DOI 10.1590/S0103-507X2010000400004
OBJECTIVES: To describe the clinical features and outcomes of patients admitted with influenza A (H1N1) infection in two private hospitals' intensive care units in São Paulo, Brazil, during the 2009 pandemics. METHODS: A retrospective cohort study was conducted to evaluate demographic data, initial clinical presentation, prognostic scores [Simplified Acute Physiology Score (SAPS) 3 and Sequential Organ Failure Assessment (SOFA)], comorbidities, outcomes and treatment of patients with confirmed pandemic influenza diagnosis from July to September 2009. RESULTS: 22 patients were admitted. Median age was 30 (25-43.5) years. Median SAPS 3 and SOFA were 42 (37-49) and 2 (1-3.5), respectively. Comorbidities were common (45.4%), especially obesity (22.7%). Two (9.1%) patients were pregnant. Five (22.7%) patients required invasive mechanical ventilation, with high positive end expiratory pressures (median of 16 cmH2O, interquartile range 10-25cmH2O). There was a 50% incidence of non-invasive ventilation failure. Most (77.2%) of patients were treated with oseltamivir. Hospital mortality was 4.5%. Initial SAPS 3, SOFA and PaO2/FiO2 ratio were associated with mechanical ventilation requirement (p<0.01). CONCLUSIONS: Pandemic influenza infection mainly affected young and obese patients. In this study, patients were less severe than those previously described, what explains our low mortality and mechanical ventilation needs. However, high positive end expiratory pressures were required for mechanically ventilated patients.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):333-338
DOI 10.1590/S0103-507X2010000400004
OBJECTIVES: To describe the clinical features and outcomes of patients admitted with influenza A (H1N1) infection in two private hospitals' intensive care units in São Paulo, Brazil, during the 2009 pandemics. METHODS: A retrospective cohort study was conducted to evaluate demographic data, initial clinical presentation, prognostic scores [Simplified Acute Physiology Score (SAPS) 3 and Sequential Organ Failure Assessment (SOFA)], comorbidities, outcomes and treatment of patients with confirmed pandemic influenza diagnosis from July to September 2009. RESULTS: 22 patients were admitted. Median age was 30 (25-43.5) years. Median SAPS 3 and SOFA were 42 (37-49) and 2 (1-3.5), respectively. Comorbidities were common (45.4%), especially obesity (22.7%). Two (9.1%) patients were pregnant. Five (22.7%) patients required invasive mechanical ventilation, with high positive end expiratory pressures (median of 16 cmH2O, interquartile range 10-25cmH2O). There was a 50% incidence of non-invasive ventilation failure. Most (77.2%) of patients were treated with oseltamivir. Hospital mortality was 4.5%. Initial SAPS 3, SOFA and PaO2/FiO2 ratio were associated with mechanical ventilation requirement (p<0.01). CONCLUSIONS: Pandemic influenza infection mainly affected young and obese patients. In this study, patients were less severe than those previously described, what explains our low mortality and mechanical ventilation needs. However, high positive end expiratory pressures were required for mechanically ventilated patients.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):339-345
DOI 10.1590/S0103-507X2010000400005
OBJECTIVES: The length of stay after prolonged cardiac surgery has been associated with poor immediate outcomes and increased costs. This study aimed to evaluate the predictive power of the Ambler Score to anticipate the length of stay in the intensive care unit. METHODS: This was a retrospective cohort study based on data collected from 110 patients undergoing valve replacement surgery alone or in combination with other procedures. Additive and logistic Ambler Scores were obtained and their predictive performances calculated using the Receiver Operating Characteristic curve. The normal length stay in the intensive care unit was assumed to be <3 days and prolonged >3 days. The areas under the receiver operating curves for both the additive and logistic models were compared using the Hanley-MacNeil test. RESULTS: The mean intensive care unit length of stay was 4.2 days. Sixty-three patients were male. The logistic model showed areas under the receiver operating characteristic curve of 0.73 and 0.79 for hospitalization > 3 days and < 3 days, respectively, showing good discriminative power. For the additive model, the areas were 0.63 and 0.59 for hospitalization > 3 days and < 3 days, respectively, a poor discriminative power. CONCLUSIONS: In our database, prolonged length of stay in the intensive care unit was positively correlated with the logistic Ambler score. The performance of the logistic Ambler Score had good discriminative power for correlation with the intensive care unit length of stay.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):339-345
DOI 10.1590/S0103-507X2010000400005
OBJECTIVES: The length of stay after prolonged cardiac surgery has been associated with poor immediate outcomes and increased costs. This study aimed to evaluate the predictive power of the Ambler Score to anticipate the length of stay in the intensive care unit. METHODS: This was a retrospective cohort study based on data collected from 110 patients undergoing valve replacement surgery alone or in combination with other procedures. Additive and logistic Ambler Scores were obtained and their predictive performances calculated using the Receiver Operating Characteristic curve. The normal length stay in the intensive care unit was assumed to be <3 days and prolonged >3 days. The areas under the receiver operating curves for both the additive and logistic models were compared using the Hanley-MacNeil test. RESULTS: The mean intensive care unit length of stay was 4.2 days. Sixty-three patients were male. The logistic model showed areas under the receiver operating characteristic curve of 0.73 and 0.79 for hospitalization > 3 days and < 3 days, respectively, showing good discriminative power. For the additive model, the areas were 0.63 and 0.59 for hospitalization > 3 days and < 3 days, respectively, a poor discriminative power. CONCLUSIONS: In our database, prolonged length of stay in the intensive care unit was positively correlated with the logistic Ambler score. The performance of the logistic Ambler Score had good discriminative power for correlation with the intensive care unit length of stay.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):346-350
DOI 10.1590/S0103-507X2010000400006
OBJECTIVES: Different conditions require that critically ill patients to receive lower than prescribed enteral nutrition volumes, energy and protein. This study objective was to evaluate the prescribed versus administered enteral nutrition difference in adults admitted to an intensive care unit. METHODS: In 2009, patients were followed for 30 days from the start of enteral nutrition to its discontinuation, or discharge from the intensive care unit. Parametric and nonparametric tests were used to evaluate prescribed versus administered differences. RESULTS: Eighty five patients were enrolled; mean age was 58.6±18.0 years and 40% were male. The patients remained in hospital for 29.5 days (IQ: 15.2 - 48.7) and were under enteral nutrition for 10 (IQ: 4.2 - 27.5) days. Lower than enteral nutrition prescribed volume (-428±243ml/day), energy (-665±412 Kcal/day) and protein (-30±19 g protein/day) was received. Individual patients' evaluation demonstrated that about 40% of the prescribed volume was not actually given. The main reasons for enteral nutrition interruptions were nausea and vomiting, abdominal distension, constipation and clinical complications (52%); diagnostic procedures (41.6%); and transition to oral feeding (5.6%). CONCLUSION: Patients admitted to intensive care unit receive less than the prescribed enteral nutrition. The routine care and gastrointestinal tract complications lead to enteral nutrition interruptions, contributing to less than prescribed calories administration.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):346-350
DOI 10.1590/S0103-507X2010000400006
OBJECTIVES: Different conditions require that critically ill patients to receive lower than prescribed enteral nutrition volumes, energy and protein. This study objective was to evaluate the prescribed versus administered enteral nutrition difference in adults admitted to an intensive care unit. METHODS: In 2009, patients were followed for 30 days from the start of enteral nutrition to its discontinuation, or discharge from the intensive care unit. Parametric and nonparametric tests were used to evaluate prescribed versus administered differences. RESULTS: Eighty five patients were enrolled; mean age was 58.6±18.0 years and 40% were male. The patients remained in hospital for 29.5 days (IQ: 15.2 - 48.7) and were under enteral nutrition for 10 (IQ: 4.2 - 27.5) days. Lower than enteral nutrition prescribed volume (-428±243ml/day), energy (-665±412 Kcal/day) and protein (-30±19 g protein/day) was received. Individual patients' evaluation demonstrated that about 40% of the prescribed volume was not actually given. The main reasons for enteral nutrition interruptions were nausea and vomiting, abdominal distension, constipation and clinical complications (52%); diagnostic procedures (41.6%); and transition to oral feeding (5.6%). CONCLUSION: Patients admitted to intensive care unit receive less than the prescribed enteral nutrition. The routine care and gastrointestinal tract complications lead to enteral nutrition interruptions, contributing to less than prescribed calories administration.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):351-357
DOI 10.1590/S0103-507X2010000400007
OBJECTIVE: To identify the relevant differences between portable blood glucose meter readings in different sampling accesses blood and laboratory analysis. METHODS: Quantitative validity study. Daily samples were collected from capillary blood, central venous access catheter and arterial catheter and the blood glucose values checked using portable blood glucose meter and laboratory analysis. The findings were analyzed with the Statistical Package for the Social Sciences - SPSS software. RESULTS: Central venous catheter samples blood glucose meter readings were found to have the best correlation with the laboratory analysis results, considered as the gold-standard. CONCLUSION: Hemodynamically unstable patients' capillary blood samples may provide false blood glucose results, and lead to inappropriate insulin solution management. Therefore, ideal blood glucose sampling is relevant to prevent insulin solution management errors.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):351-357
DOI 10.1590/S0103-507X2010000400007
OBJECTIVE: To identify the relevant differences between portable blood glucose meter readings in different sampling accesses blood and laboratory analysis. METHODS: Quantitative validity study. Daily samples were collected from capillary blood, central venous access catheter and arterial catheter and the blood glucose values checked using portable blood glucose meter and laboratory analysis. The findings were analyzed with the Statistical Package for the Social Sciences - SPSS software. RESULTS: Central venous catheter samples blood glucose meter readings were found to have the best correlation with the laboratory analysis results, considered as the gold-standard. CONCLUSION: Hemodynamically unstable patients' capillary blood samples may provide false blood glucose results, and lead to inappropriate insulin solution management. Therefore, ideal blood glucose sampling is relevant to prevent insulin solution management errors.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):358-362
DOI 10.1590/S0103-507X2010000400008
BACKGROUND: Hyperglycemia is frequent in the critically ill patient, and is a risk factor for unfavorable clinical outcomes, including mortality. During the recent years, intensive blood glucose control using intravenous insulin infusion has gained a prominent role in the critically ill patient management. There is important concern on insulin solution continued efficacy over the time, as little the literature available on this subject is poor. Lack of evidence is known to lead to inappropriate practices. This study aimed to compare the blood glucose levels between two different protocols in an intensive care unit in Porto Alegre, using the same solution concentration and two different replacement times during the first 24 hours, and additionally to assess the protocol-related hypoglycemia rate. METHODS: The medical charts of 80 patients under insulin therapy for over 24 hours during 2008 were revised; 40 patients had their insulin solution replaced every 6 hours and for 40 patients the insulin solution was replaced after 24 hours. RESULTS: The causes for admission to the intensive care unit included more frequently hypertensive (68.8%) and diabetic (45%) patients. No significant capillary blood glucose differences were seen for the every 6 or 24 hours solution replacement groups. Only 3 mild hypoglycemia cases were observed in the every 6 hours replacement group, and no hypoglycemia was seen in the 24 hours replacement group. CONCLUSION: We concluded that keeping insulin infusion, replacing the solution every 24 hours is feasible. However, longer infusion time studies are required to check for possible hypoglycemic events as insulin therapy advances.
Abstract
Rev Bras Ter Intensiva. 2010;22(4):358-362
DOI 10.1590/S0103-507X2010000400008
BACKGROUND: Hyperglycemia is frequent in the critically ill patient, and is a risk factor for unfavorable clinical outcomes, including mortality. During the recent years, intensive blood glucose control using intravenous insulin infusion has gained a prominent role in the critically ill patient management. There is important concern on insulin solution continued efficacy over the time, as little the literature available on this subject is poor. Lack of evidence is known to lead to inappropriate practices. This study aimed to compare the blood glucose levels between two different protocols in an intensive care unit in Porto Alegre, using the same solution concentration and two different replacement times during the first 24 hours, and additionally to assess the protocol-related hypoglycemia rate. METHODS: The medical charts of 80 patients under insulin therapy for over 24 hours during 2008 were revised; 40 patients had their insulin solution replaced every 6 hours and for 40 patients the insulin solution was replaced after 24 hours. RESULTS: The causes for admission to the intensive care unit included more frequently hypertensive (68.8%) and diabetic (45%) patients. No significant capillary blood glucose differences were seen for the every 6 or 24 hours solution replacement groups. Only 3 mild hypoglycemia cases were observed in the every 6 hours replacement group, and no hypoglycemia was seen in the 24 hours replacement group. CONCLUSION: We concluded that keeping insulin infusion, replacing the solution every 24 hours is feasible. However, longer infusion time studies are required to check for possible hypoglycemic events as insulin therapy advances.
