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You searched for:"Guillermo Bugedo"

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  • Editorial

    Thank you, Professor Gattinoni†, and have a good trip to eternity!

    Critical Care Science. 2025;37:e20250002
    02-21-2025

    Abstract

    Editorial

    Thank you, Professor Gattinoni†, and have a good trip to eternity!

    Critical Care Science. 2025;37:e20250002
    02-21-2025

    DOI 10.62675/2965-2774.20250002

    Views68
    Early years, the advent of computed tomography and the description of acute respiratory distress syndrome subphenotypes Professor Gattinoni began his research career by studying extracorporeal CO2 removal as a mechanism to rest the lung during respiratory failure. Luck and effort at the same time, as he himself described, led him to apply these concepts in […]
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    Thank you, Professor Gattinoni†, and have a good trip to eternity!
  • CLINICAL REPORT

    Adherence to low tidal volume in the transition to spontaneous ventilation in patients with acute respiratory failure in intensive care units in Latin America (SPIRAL): a study protocol

    Critical Care Science. 2024;36:e20240044en
    07-24-2024

    Abstract

    CLINICAL REPORT

    Adherence to low tidal volume in the transition to spontaneous ventilation in patients with acute respiratory failure in intensive care units in Latin America (SPIRAL): a study protocol

    Critical Care Science. 2024;36:e20240044en
    07-24-2024

    DOI 10.62675/2965-2774.20240044-en

    Views97

    ABSTRACT

    Objective:

    Patients with acute respiratory failure often require mechanical ventilation to reduce the work of breathing and improve gas exchange; however, this may exacerbate lung injury. Protective ventilation strategies, characterized by low tidal volumes (≤ 8mL/kg of predicted body weight) and limited plateau pressure below 30cmH2O, have shown improved outcomes in patients with acute respiratory distress syndrome. However, in the transition to spontaneous ventilation, it can be challenging to maintain tidal volume within protective levels, and it is unclear whether low tidal volumes during spontaneous ventilation impact patient outcomes. We developed a study protocol to estimate the prevalence of low tidal volume ventilation in the first 24 hours of spontaneous ventilation in patients with hypoxemic acute respiratory failure and its association with ventilator-free days and survival.

    Methods:

    We designed a multicenter, multinational, cohort study with a 28-day follow-up that will include patients with acute respiratory failure, defined as a partial oxygen pressure/fraction of inspired oxygen ratio < 300mmHg, in transition to spontaneous ventilation in intensive care units in Latin America.

    Results:

    We plan to include 422 patients in ten countries. The primary outcomes are the prevalence of low tidal volume in the first 24 hours of spontaneous ventilation and ventilator-free days on day 28. The secondary outcomes are intensive care unit and hospital mortality, incidence of asynchrony and return to controlled ventilation and sedation.

    Conclusion:

    In this study, we will assess the prevalence of low tidal volume during spontaneous ventilation and its association with clinical outcomes, which can inform clinical practice and future clinical trials.

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    Adherence to low tidal volume in the transition to spontaneous ventilation in patients with acute respiratory failure in intensive care units in Latin America (SPIRAL): a study protocol
  • Review Articles

    Does the use of high PEEP levels prevent ventilator-induced lung injury?

    Revista Brasileira de Terapia Intensiva. 2017;29(2):231-237
    01-01-2017

    Abstract

    Review Articles

    Does the use of high PEEP levels prevent ventilator-induced lung injury?

    Revista Brasileira de Terapia Intensiva. 2017;29(2):231-237
    01-01-2017

    DOI 10.5935/0103-507X.20170032

    Views60

    ABSTRACT

    Overdistention and intratidal alveolar recruitment have been advocated as the main physical mechanisms responsible for ventilator-induced lung injury. Limiting tidal volume has a demonstrated survival benefit in patients with acute respiratory distress syndrome and is recognized as the cornerstone of protective ventilation. In contrast, the use of high positive end-expiratory pressure levels in clinical trials has yielded conflicting results and remains controversial. In the present review, we will discuss the benefits and limitations of the open lung approach and will discuss some recent experimental and clinical trials on the use of high versus low/moderate positive end-expiratory pressure levels. We will also distinguish dynamic (tidal volume) from static strain (positive end-expiratory pressure and mean airway pressure) and will discuss their roles in inducing ventilator-induced lung injury. High positive end-expiratory pressure strategies clearly decrease refractory hypoxemia in patients with acute respiratory distress syndrome, but they also increase static strain, which in turn may harm patients, especially those with lower levels of lung recruitability. In patients with severe respiratory failure, titrating positive end-expiratory pressure against the severity of hypoxemia, or providing it in a decremental fashion after a recruitment maneuver, is recommended. If high plateau, driving or mean airway pressures are observed, prone positioning or ultraprotective ventilation may be indicated to improve oxygenation without additional stress and strain in the lung.

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    Does the use of high PEEP levels prevent ventilator-induced lung injury?
  • Case Report

    Hantavirus cardiopulmonary syndrome successfully treated with high-volume hemofiltration

    Revista Brasileira de Terapia Intensiva. 2016;28(2):190-194
    01-01-2016

    Abstract

    Case Report

    Hantavirus cardiopulmonary syndrome successfully treated with high-volume hemofiltration

    Revista Brasileira de Terapia Intensiva. 2016;28(2):190-194
    01-01-2016

    DOI 10.5935/0103-507X.20160032

    Views12

    ABSTRACT

    Hantavirus cardiopulmonary syndrome has a high mortality rate, and early connection to extracorporeal membrane oxygenation has been suggested to improve outcomes. We report the case of a patient with demonstrated Hantavirus cardiopulmonary syndrome and refractory shock who fulfilled the criteria for extracorporeal membrane oxygenation and responded successfully to high volume continuous hemofiltration. The implementation of high volume continuous hemofiltration along with protective ventilation reversed the shock within a few hours and may have prompted recovery. In patients with Hantavirus cardiopulmonary syndrome, a short course of high volume continuous hemofiltration may help differentiate patients who can be treated with conventional intensive care unit management from those who will require more complex therapies, such as extracorporeal membrane oxygenation.

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    Hantavirus cardiopulmonary syndrome successfully treated with high-volume hemofiltration
  • Review Article

    Therapeutic hypothermia as a bridge to transplantation in patients with fulminant hepatic failure

    Revista Brasileira de Terapia Intensiva. 2015;27(1):72-76
    03-01-2015

    Abstract

    Review Article

    Therapeutic hypothermia as a bridge to transplantation in patients with fulminant hepatic failure

    Revista Brasileira de Terapia Intensiva. 2015;27(1):72-76
    03-01-2015

    DOI 10.5935/0103-507X.20150012

    Views18

    The most important topics in fulminant hepatic failure are cerebral edema and intracranial hypertension. Among all therapeutic options, systemic induced hypothermia to 33 - 34ºC has been reported to reduce the high pressure and increase the time during which patients can tolerate a graft. This review discusses the indications and adverse effects of hypothermia.

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    Therapeutic hypothermia as a bridge to transplantation in patients with fulminant hepatic failure
  • Original Articles

    The implementation of an analgesia-based sedation protocol reduced deep sedation and proved to be safe and feasible in patients on mechanical ventilation

    Revista Brasileira de Terapia Intensiva. 2013;25(3):188-196
    01-01-2013

    Abstract

    Original Articles

    The implementation of an analgesia-based sedation protocol reduced deep sedation and proved to be safe and feasible in patients on mechanical ventilation

    Revista Brasileira de Terapia Intensiva. 2013;25(3):188-196
    01-01-2013

    DOI 10.5935/0103-507X.20130034

    Views72

    INTRODUCTION:

    Deep sedation in critically ill patients is associated with a longer duration of mechanical ventilation and a prolonged length of stay in the intensive care unit. Several protocols have been used to improve these outcomes. We implement and evaluate an analgesia-based, goal-directed, nurse-driven sedation protocol used to treat critically ill patients who receive mechanical ventilation.

    METHODS:

    We performed a prospective, two-phase (before-after), non-randomized multicenter study that involved 13 intensive care units in Chile. After an observational phase (observational group, n=155), we designed, implemented and evaluated an analgesia-based, goal-directed, nurse-driven sedation protocol (intervention group, n=132) to treat patients who required mechanical ventilation for more than 48 hours. The primary outcome was to achieve ventilator-free days by day 28.

    RESULTS:

    The proportion of patients in deep sedation or in a coma decreased from 55.2% to 44.0% in the interventional group. Agitation did not change between the periods and remained approximately 7%. Ventilator-free days to day 28, length of stay in the intensive care unit and mortality were similar in both groups. At one year, post-traumatic stress disorder symptoms in survivors were similar in both groups.

    CONCLUSIONS:

    We designed and implemented an analgesia-based, goal-directed, nurse-driven sedation protocol in Chile. Although there was no improvement in major outcomes, we observed that the present protocol was safe and feasible and that it resulted in decreased periods of deep sedation without increasing agitation.

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    The implementation of an analgesia-based sedation protocol reduced deep sedation and proved to be safe and feasible in patients on mechanical ventilation
  • Original Articles - Clinical Research

    Positive end-expiratory pressure increases strain in patients with ALI/ARDS

    Revista Brasileira de Terapia Intensiva. 2012;24(1):43-51
    04-24-2012

    Abstract

    Original Articles - Clinical Research

    Positive end-expiratory pressure increases strain in patients with ALI/ARDS

    Revista Brasileira de Terapia Intensiva. 2012;24(1):43-51
    04-24-2012

    DOI 10.1590/S0103-507X2012000100007

    Views15

    OBJECTIVE: The objective of this study was to assess the effects of positive end-expiratory pressure on recruitment, cyclic recruitment and derecruitment and strain in patients with acute lung injury and acute respiratory distress syndrome using lung computed tomography. METHODS: This is an open, controlled, non-randomized interventional study of ten patients with acute lung injury and acute respiratory distress syndrome. Using computed tomography, single, basal slices of the lung were obtained during inspiratory and expiratory pauses at a tidal volume of 6 ml/kg and a positive end-expiratory pressure of 5, 10, 15 and 20 cmH2O. The densities of the lung parenchyma were measured in Hounsfield units. The values for positive end-expiratory pressure-induced recruitment, cyclic recruitment and derecruitment and strain were then calculated. RESULTS: Increasing levels of positive end-expiratory pressure were correlated with increased recruitment and global strain (p < 0.01), which was significantly correlated with plateau pressure (r² = 0.97, p < 0.01). In addition, increasing levels of positive end-expiratory pressure systematically increased strain along the sternovertebral axis. CONCLUSION: While strain is an adverse effect of positive end-expiratory pressure, the decision use positive end-expiratory pressure with any patient should be balanced against the potential benefits of recruitment. Due to the small number of patients in this study, the present data should be treated as hypothesis generating and is not intended to limit the clinical application of a high level of positive end-expiratory pressure in patients with severe hypoxemia.

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    Positive end-expiratory pressure increases strain in patients with ALI/ARDS

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