Performance of Invasive Mode in Different Heated Humidification Systems With High-Flow Nasal Cannula.

BACKGROUND: Oxygen therapy via high-flow nasal cannula generates physiologic changes that impact ventilatory variables of patients. However, we know that there are detrimental effects on airway mucosa related to inhalation of gases. The objective of this study was to evaluate the performance in terms of absolute humidity, relative humidity, and temperature of different brands of heated humidifiers and circuits in the invasive mode during the use of high-flow oxygen therapy in flows between 30 and 100 L/min. METHODS: A prospective observational study conducted at the Sanatorio Anchorena equipment analysis laboratory; September 5 to October 20, 2019. RESULTS: A statistically significant interaction was found among the programmed flows and the different combinations of devices and circuits for the delivery of absolute humidity (P < .001). An effect of flow on delivered absolute humidity was found, regardless of the equipment and circuit combination (P < .001). However, in the invasive mode, the combination of the Fisher&Paykel MR850 heated humidifier with the Medtronic-Dar circuit, the Intersurgical circuit, and the AquaVENT circuit always reached or achieved absolute humidity values > 33 mg/L, even at flows up to 100 L/min. The combination of the Flexicare FL9000 heated humidifier with the Fisher&Paykel RT202 circuit, the Fisher&Paykel Evaqua 2 circuit, the Flexicare circuit, the AquaVENT circuit, and the GGM circuit achieved similar results. The mean (SD) of absolute humidity delivered in the invasive mode (36.2 ± 5.9 mg/L) was higher compared with the noninvasive mode (26.8 ± 7.2 mg/L) (P < .001), regardless of circuit and programmed flows. CONCLUSIONS: When heated humidifiers were used in the invasive mode for high-flow oxygen therapy, absolute humidity depended not only on the heated humidifiers and the combination of circuits but also on the programmed flow, especially at flows > 50 L/min. Moreover, the heated humidifiers exhibited different behaviors, in some cases inefficient, in delivering adequate humidification. However, some equipment improved performance when set to the invasive mode.

Performance of Different Active Humidification Systems in High-Flow Oxygen Therapy.

BACKGROUND: We sought to evaluate the performance in terms of absolute humidity (AH), relative humidity (RH), and temperature of different heated humidifiers (HH) and circuits that are commonly used to deliver high-flow oxygen therapy in conventional ranges (30-60 L/min) and unconventional ranges (70-100 L/min). METHODS: In this prospective, observational study, an electronic thermohygrometer was used to obtain the required measurements. A mechanical ventilator was used as a source for high-flow nasal cannula oxygen therapy. For active humidification, the following equipment was used: a HH with standard disposable water trap circuit, 3 servo-controlled HH, and 7 circuits with a heated wire. Data on environmental conditions (ie, temperature, RH, AH) were collected from the laboratory during each measurement; the temperature, RH, and AH resulting from the application of 8 flows (30-100 L/min) were also recorded. Variables were compared with analysis of variance for repeated measurements with Tukey post hoc tests. A value of P < .05 was assumed to be significant. RESULTS: During the study, a statistically significant difference was found in the average AH for each flow for the different devices (P < .005). The highest AH values were recorded with the Fisher & Paykel MR850 and the Medtronic-DAR circuit (AH = 40.8 mg/L with flow of 50 L/min, P < .005), and the lowest AH values were recorded with the Flexicare FL9000 HH and the Flexicare circuit (AH = 11.4 mg/L with 100 L/min flow, P < .005). For flows > 50 L/min, the best performance for all flows in terms of AH was found with the Fisher & Paykel MR850 HH, regardless of the circuit used. CONCLUSIONS: During oxygen therapy with very high gas flows, HH devices behave differently and in many cases are inefficient in delivering adequate humidification, even at conventional flows. Caution is therefore recommended when selecting the device and flow settings for the implementation of high-flow nasal cannula oxygen therapy.

Effects of High-Flow Nasal Cannula on End-Expiratory Lung Impedance in Semi-Seated Healthy Subjects.

BACKGROUND: High-flow nasal cannula (HFNC) enables delivery of humidified gas at high flow while controlling the FIO2 . Although its use is growing in patients with acute respiratory failure, little is known about the impact of HFNC on lung volume. Therefore, we aimed to assess lung volume changes in healthy subjects at different flows and positions. METHODS: This was a prospective physiological study performed in 16 healthy subjects. The changes in lung volumes were assessed by measuring end-expiratory lung impedance by using electrical impedance tomography. All the subjects successively breathed during 5 min in these following conditions: while in a supine position without HFNC (T0) and 3 measurements in a semi-seated position at 45° without HFNC (T1), and with HFNC at a flow of 30 L/min (T2), and 50 L/min (T3). RESULTS: Compared with the supine position, the values of end-expiratory lung impedance significantly increased with the subjects in a semi-seated position. End-expiratory lung impedance significantly increased after HFNC initiation in subjects in a semi-seated position and further increased by increasing flow at 50 L/min. When taking the end-expiratory lung impedance measurement in subjects in a semi-seated position (T1) as reference, the differences among the medians of global end-expiratory lung impedance were statistically significant (P < .001), which amounted to 1.05 units in T1; 1.12 units in T2; and 1.44 units in T3 (P < .05 for all comparisons, Wilcoxon test). The breathing frequency did not differ between the supine and semi-seated position (T0 and T1) but significantly decreased after initiation of HFNC and further decreased at high flow. T0 and T1 were not different (P = .13); whereas there was a statistically significant difference among T1, T2, and T3 (P < .05, post hoc test with Bonferroni correction). CONCLUSIONS: In healthy subjects, the semi-seated position and the use of HFNC increased end-expiratory lung impedance globally. These changes were accompanied by a significant decrease in the breathing frequency.

Ventilación mecánica en pacientes con falla respiratoria aguda hipoxémica / Mechanical ventilation in patients with acute hypoxemic respiratory failure

Objetivo: Describir las características clínicas de los pacientes internados en la UCI con requerimiento de VMi con FRAH-No SDRA. Evaluar la asociación de la mortalidad con diferentes variables. Diseño: Cohorte de comienzo. Ámbito: Estudio realizado en 2 UCIs argentinas del ámbito privado de la salud, entre el 01/07/2013 y 31/12/2014. Pacientes: De una muestra consecutiva de 2526 pacientes, se incluyeron a 229 mayores de 18 años, que ingresaron a la UCI con requirimiento de VMi por más de 24hs desarrollando FRAH-No SDRA. Variables de interés principales: Se registraron variables demográficas, estadía en VMi y en UCI, variables de programación inicial del respirador, variables de monitoreo y evolución al alta. También se registraron el número y tipo de complicaciones desarrolladas durante el periodo de VMi Resultados: El 70,7% de los ingresos fue por causa médica. El SAPS II fue de 42. El tiempo de VMi y de estadía en UCI fue mayor en los pacientes con delirio (p < 0,0001 en ambos). En el modelo de regresión logística ajustado por severidad de la hipoxemia, la edad (OR 1,02; IC95% 1,002-1,04: p = 0,033) y el shock (OR 2,37; IC95% 1,12-5: p = 0,023) resultaron predictores independientes de mortalidad. Conclusiones: En este grupo de pacientes que requirieron VMi por más de 24 hs y desarrollaron FRAH-No SDRA se encontró una distribución demográfica similar a la descripta por otros reportes. La mortalidad no se relacionó con la severidad de la hipoxemia, mientras que el shock y la edad fueron predictores independientes de mortalidad.

Mechanical ventilation in patients with acute hypoxemic respiratory failure

Objective: To describe the clinical characteristics of patients with AHRF (without ARDS) hospitalized in the ICU who require IMV. To evaluate the association between mortality and different variables. Design: Inception cohort. Scope: This study was conducted in two Argentine ICUs from the private health sector between 07/01/2013 and 12/31/2014. Patients: From a consecutive sample of 2526 patients, 229 individuals aged 18 and upwards were included in the study; they were admitted to the ICU requiring IMV for over 24 hours and developed AHRF (without ARDS). Primary endpoints: Demographic variables and variables associated with the number of days with IMV and at the ICU were documented, as well as the initial setting of the respirator, monitoring variables and evolution at discharge. Likewise, the number and type of complications developed during the period of IMV were documented. Results: 70.7% of admissions were for medical reasons. SAPS II score was 42. The period of IMV and at the ICU was higher in patients with delirium (p<0.0001 in both). In the logistic regression model adjusted by the severity of hypoxemia, age (OR 1.02; 95% CI 1.002-1.04: p = 0.033) and shock (OR 2.37; 95% CI 1.12-5: p = 0.023) acted as independent predictors of mortality. Conclusions: In this group of patients who required IMV for over 24 hours and who developed AHRF (without ARDS) there was a demographic distribution similar to that described in other reports. Mortality was not associated with the severity of hypoxemia, whereas shock and age were independent predictors of mortality.

Factores de riesgo para el fracaso de destete en una población de pacientes con EPOC en ventilación mecánica prolongada / Risk Factors for Weaning Failure in Patients with Chronic Obstructive Pulmonary Disease in Prolonged Mechanical Ventilation

Introducción: Los pacientes con EPOC experimentan episodios de falla respiratoria que requieren de asistencia ventilatoria mecánica (AVM). Debido al compromiso pulmonar, muscular y nutricional, experimentan dificultad en el destete. Hay escasa información de los factores que puedan predecir el fracaso del destete en pacientes con EPOC en VM prolongada (VMP). El objetivo de este trabajo es encontrar factores de riesgo para el fracaso del destete en pacientes con EPOC y evaluar mortalidad según éxito o fracaso en el destete. Materiales y Métodos: El estudio se realizó en un centro de weaning (CW) y se incluyeron pacientes internados en una unidad de terapia intensiva (UTI) por reagudización de su EPOC derivados a nuestro CW traqueostomizados con requerimiento de AVM. Resultados: Se recolectaron los datos de 40 pacientes, de los cuales 21 finalizaron AVM de manera exitosa y 19 fracasaron. El análisis univariado arrojó 4 variables asociadas al fracaso del destete: Pimax (p = 0.035), días de AVM en el CW (p = 0.005), pH (p = 0.039) y la PaCO2 (p = 0.002). Sin embargo, solo la PaCO2 a las 12hs de la prueba de respiración espontánea (PRE) fue predictor de fracaso de destete (p = 0.007). No se encontraron predictores de mortalidad. Conclusión: Encontrar factores de riesgo que permitan identificar el fracaso en la desvinculación de la VM puede contribuir en la decisión de insistir con el destete, o bien, plantear un programa de internación domiciliaria con la finalidad de mejorar la calidad de vida. La única variable asociada al fracaso de destete fue la PaCO2 a las 12hs de comenzada la PRE.

Introduction: Patients suffering from chronic obstructive pulmonary disease (COPD) have an airflow limitation and require mechanical ventilation (MV). Because of deteriorated lung function, respiratory muscles weakness and malnutrition, patients also present difficulties in the weaning process. Information on the factors that can predict weaning failure in patients with COPD after prolonged MV is scarce. To identify risk factors for weaning failure in patients with COPD and evaluate the mortality depending on weaning success or failure. Materials and Methods: This study was carried out at a weaning center in Buenos Aires, Argentina. We evaluated patients admitted to an intensive care unit (ICU) and referred to the weaning center as a result of COPD exacerbation, after tracheostomy and in need of mechanical ventilation. Results: Data from 40 patients were collected; 21 were successfully weaned from MV and 19 failed the weaning process. Univariate analysis showed 4 variables associated with weaning failure: maximum inspiratory pressure (MIP) (p = 0.035), length of MV at weaning center (p = 0.005), pH (p = 0.039) and PaCO2 (p = 0.002). However, only PaCO2 twelve hours after the spontaneous breathing trial (SBT) was a predictor of weaning failure (p=0.007). Mortality predictors were not found. Conclusion: The only predictive variable associated with weaning failure was PaCO2 twelve hours after SBT. Finding risk factors for failure in discontinuing MV may provide information to decide whether to insist in the weaning process or choose home MV to improve life quality.

Factores de riesgo para el fracaso de destete en una población de pacientes con EPOC en ventilación mecánica prolongada

Introducción: Los pacientes con EPOC experimentan episodios de falla respiratoria que requieren de asistencia ventilatoria mecánica (AVM). Debido al compromiso pulmonar, muscular y nutricional, experimentan dificultad en el destete. Hay escasa información de los factores que puedan predecir el fracaso del destete en pacientes con EPOC en VM prolongada (VMP). El objetivo de este trabajo es encontrar factores de riesgo para el fracaso del destete en pacientes con EPOC y evaluar mortalidad según éxito o fracaso en el destete. Materiales y Métodos: El estudio se realizó en un centro de weaning (CW) y se incluyeron pacientes internados en una unidad de terapia intensiva (UTI) por reagudización de su EPOC derivados a nuestro CW traqueostomizados con requerimiento de AVM. Resultados: Se recolectaron los datos de 40 pacientes, de los cuales 21 finalizaron AVM de manera exitosa y 19 fracasaron. El análisis univariado arrojó 4 variables asociadas al fracaso del destete: Pimax (p = 0.035), días de AVM en el CW (p = 0.005), pH (p = 0.039) y la PaCO2 (p = 0.002). Sin embargo, solo la PaCO2 a las 12hs de la prueba de respiración espontánea (PRE) fue predictor de fracaso de destete (p = 0.007). No se encontraron predictores de mortalidad. Conclusión: Encontrar factores de riesgo que permitan identificar el fracaso en la desvinculación de la VM puede contribuir en la decisión de insistir con el destete, o bien, plantear un programa de internación domiciliaria con la finalidad de mejorar la calidad de vida. La única variable asociada al fracaso de destete fue la PaCO2 a las 12hs de comenzada la PRE.(AU)

Introduction: Patients suffering from chronic obstructive pulmonary disease (COPD) have an airflow limitation and require mechanical ventilation (MV). Because of deteriorated lung function, respiratory muscles weakness and malnutrition, patients also present difficulties in the weaning process. Information on the factors that can predict weaning failure in patients with COPD after prolonged MV is scarce. To identify risk factors for weaning failure in patients with COPD and evaluate the mortality depending on weaning success or failure. Materials and Methods: This study was carried out at a weaning center in Buenos Aires, Argentina. We evaluated patients admitted to an intensive care unit (ICU) and referred to the weaning center as a result of COPD exacerbation, after tracheostomy and in need of mechanical ventilation. Results: Data from 40 patients were collected; 21 were successfully weaned from MV and 19 failed the weaning process. Univariate analysis showed 4 variables associated with weaning failure: maximum inspiratory pressure (MIP) (p = 0.035), length of MV at weaning center (p = 0.005), pH (p = 0.039) and PaCO2 (p = 0.002). However, only PaCO2 twelve hours after the spontaneous breathing trial (SBT) was a predictor of weaning failure (p=0.007). Mortality predictors were not found. Conclusion: The only predictive variable associated with weaning failure was PaCO2 twelve hours after SBT. Finding risk factors for failure in discontinuing MV may provide information to decide whether to insist in the weaning process or choose home MV to improve life quality.(AU)

Decanulación después de la estadía en UCI: Análisis de 181 pacientes traqueotomizados / Decannulation after the ICU Stay. Analysis of 181 Tracheostomized Patients

Objetivo: Encontrar predictores de decanulación en pacientes traqueostomizados y desvinculados de la asistencia ventilatoria mecánica. Analizar la mortalidad en el centro de weaning y supervivencia al alta. Materiales y métodos: Estudio retrospectivo. Se revisaron historias clínicas de pacientes que ingresaron al centro de weaning entre enero de 2004 y junio de 2011. Se estudiaron diferentes variables como posibles predictores de decanulación. Se analizó la mortalidad y se realizó seguimiento al alta. Resultados: Se incluyeron 181 pacientes con una media de 62 años. Se logró decanular al 44.2% de los pacientes (mediana 20 días). El análisis univariado encontró 6 variables asociadas al fracaso de decanulación: sexo masculino, antecedentes respiratorios, antecedentes cardiovasculares, albúmina al ingreso al centro de weaning, días de internación en centro de weaning y días de internación en Unidad de Cuidados Intensivos + centro de weaning. La regresión logística encontró como predictores independientes: sexo masculino y antecedentes respiratorios. En el análisis de regresión logística la decanulación fue un factor protectivo con respecto a la mortalidad. El 80% de los pacientes decanulados y el 15,8% de los no decanulados obtuvieron alta médica. La mediana de supervivencia de los decanulados fue de 45.47 meses y los no decanulados de 10.87. Conclusiones: Los pacientes de sexo masculino y aquellos con antecedentes respiratorios se asocian con fracaso de decanulación. Los pacientes decanulados tienen menor riesgo de muerte durante la internación.

Objective: Find predictors of decannulation in tracheostomized patients and without mechanical ventilation. A secondary objective was the analysis of mortality in the weaning center and survival at discharge. Material and methods: We reviewed, retrospectively, the medical records of patients admitted to the weaning center with tracheostomy and without mechanical ventilation between January 2004 and June 2011. Different variables as possible predictors of decannulation were studied. Mortality at weaning center and outcomes during follow up after discharge were analyzed. Results: We included 181 patients with an average age of 62 years old. Decannulation was carried out in 44.2% of the patients. The decannulation process took 20 days. The univariate analysis found six variables associated with decannulation failure: male gender, respiratory or cardiovascular history, albumin at admission to the weaning center, days of hospitalization in the weaning center and admission to intensive care units plus the weaning center. Logistic regression analysis found that male sex and respiratory history were independent predictors. Regarding mortality during hospitalization, logistic regression analysis found that decannulation was a protective factor. Another finding was that 80% of patients decannulated were discharged; only 15.8% of the group was not decannulated. The average survival was 45.47 months among the decannulated patients and 10.87 months for the non decannulated patients. Conclusions: We found that male sex and a history of respiratory failure were factors associated with unsuccessful decannulation. Decannulated patients had lower risk of death during hospitalization.

Decanulación después de la estadía en UCI: Análisis de 181 pacientes traqueotomizados

Objetivo: Encontrar predictores de decanulación en pacientes traqueostomizados y desvinculados de la asistencia ventilatoria mecánica. Analizar la mortalidad en el centro de weaning y supervivencia al alta. Materiales y métodos: Estudio retrospectivo. Se revisaron historias clínicas de pacientes que ingresaron al centro de weaning entre enero de 2004 y junio de 2011. Se estudiaron diferentes variables como posibles predictores de decanulación. Se analizó la mortalidad y se realizó seguimiento al alta. Resultados: Se incluyeron 181 pacientes con una media de 62 años. Se logró decanular al 44.2% de los pacientes (mediana 20 días). El análisis univariado encontró 6 variables asociadas al fracaso de decanulación: sexo masculino, antecedentes respiratorios, antecedentes cardiovasculares, albúmina al ingreso al centro de weaning, días de internación en centro de weaning y días de internación en Unidad de Cuidados Intensivos + centro de weaning. La regresión logística encontró como predictores independientes: sexo masculino y antecedentes respiratorios. En el análisis de regresión logística la decanulación fue un factor protectivo con respecto a la mortalidad. El 80% de los pacientes decanulados y el 15,8% de los no decanulados obtuvieron alta médica. La mediana de supervivencia de los decanulados fue de 45.47 meses y los no decanulados de 10.87. Conclusiones: Los pacientes de sexo masculino y aquellos con antecedentes respiratorios se asocian con fracaso de decanulación. Los pacientes decanulados tienen menor riesgo de muerte durante la internación.(AU)

Objective: Find predictors of decannulation in tracheostomized patients and without mechanical ventilation. A secondary objective was the analysis of mortality in the weaning center and survival at discharge. Material and methods: We reviewed, retrospectively, the medical records of patients admitted to the weaning center with tracheostomy and without mechanical ventilation between January 2004 and June 2011. Different variables as possible predictors of decannulation were studied. Mortality at weaning center and outcomes during follow up after discharge were analyzed. Results: We included 181 patients with an average age of 62 years old. Decannulation was carried out in 44.2% of the patients. The decannulation process took 20 days. The univariate analysis found six variables associated with decannulation failure: male gender, respiratory or cardiovascular history, albumin at admission to the weaning center, days of hospitalization in the weaning center and admission to intensive care units plus the weaning center. Logistic regression analysis found that male sex and respiratory history were independent predictors. Regarding mortality during hospitalization, logistic regression analysis found that decannulation was a protective factor. Another finding was that 80% of patients decannulated were discharged; only 15.8% of the group was not decannulated. The average survival was 45.47 months among the decannulated patients and 10.87 months for the non decannulated patients. Conclusions: We found that male sex and a history of respiratory failure were factors associated with unsuccessful decannulation. Decannulated patients had lower risk of death during hospitalization.(AU)

Evaluation of tracheal cuff pressure variation in spontaneously breathing patients.

BACKGROUND: Most of the studies referring cuff tubes' issues were conducted on intubated patients. Not much is known about the cuff pressure performance in chronically tracheostomized patients disconnected from mechanical ventilation. OBJECTIVE: To evaluate cuff pressure (CP) variation in tracheostomized, spontaneously breathing patients in a weaning rehabilitation center. MATERIALS AND METHODS: Experimental setup to test instruments in vitro, in which the gauge (TRACOE) performance at different pressure levels was evaluated in six tracheostomy tubes, and a clinical setupin which CP variation over 24 h, every 4 h, and for 6 days was measured in 35 chronically tracheostomized clinically stable, patients who had been disconnected from mechanical ventilation for at least 72 h. The following data were recorded: Tube brand, type, and size; date of the tube placed; the patient's body position; the position of the head; axillary temperature; pulse and respiration rates; blood pressure; and pulse oximetry. RESULTS: In vitro difference between the initial pressure (IP) and measured pressure (MP) was statistically significant (P < 0.05). The difference between the IP and MP was significant when selecting for various tube brands (P < 0.05). In the clinical set-up, 207 measurements were performed and the CP was >30 cm H2O in 6.28% of the recordings, 20-30 cm H2O in 42.0% of the recordings, and <20 cm H2O in 51.69% of the recordings. CONCLUSION: The systematic CP measurement in chronically tracheostomized, spontaneously breathing patients showed high variability, which was independent of tube brand, size, type, or time of placement. Consequently, measurements should be made more frequently.