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Dataset results
146 results for “membrane oxygenator”
ExtraCorporeal Membrane Oxygenation in the Therapy of Cardiogenic Shock
ClinicalTrials.gov study NCT02301819. IPD Sharing: UNDECIDED. Countries: 1. Publications: 3.
Definition and Management of Right Ventricular Injury in Adult Patients Receiving Extracorporeal Membrane Oxygenation
ClinicalTrials.gov study NCT05948332. IPD Sharing: NO. Countries: 1. Publications: 15.
Outcome of COVID-19 Patients After Extracorporeal Membrane Oxygenation for Acute Respiratory Distress Syndrome
ClinicalTrials.gov study NCT04383678. IPD Sharing: NO. Countries: 6. Publications: 1.
Extracorporal Membrane Oxygenation for Critically Ill Patients With COVID-19
ClinicalTrials.gov study NCT05158816. IPD Sharing: NO. Countries: 1. Publications: 2.
Long Term Follow up of Patients Who Were Treated With Extracorporeal Membrane Oxygenation for Pandemic Influenza A/H1N1 Induced Severe Respiratory Failure
ClinicalTrials.gov study NCT01763060. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Measurement of Recirculation During Venovenous Extracorporeal Membrane Oxygenation (VV ECMO)
ClinicalTrials.gov study NCT00920062. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Cytokine Adsorption in Patients With Severe COVID-19 Pneumonia Requiring Extracorporeal Membrane Oxygenation
ClinicalTrials.gov study NCT04385771. IPD Sharing: NO. Countries: 1. Publications: 3.
Treatment of Extracorporeal Membrane Oxygenation in Severe Poisoning
ClinicalTrials.gov study NCT05762029. IPD Sharing: Not stated. Countries: 1. Publications: 6.
Pharmacokinetics in Extracorporeal Membrane Oxygenation
ClinicalTrials.gov study NCT03766282. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Circulatory Changes During Venovenous (VV)- and Venoarterial (VA) Extracorporeal Membrane Oxygenation (ECMO)
ClinicalTrials.gov study NCT00622492. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Veno-venous Extracorporeal Membrane Oxygenation (VV-ECMO) Heparin Study
ClinicalTrials.gov study NCT04496362. IPD Sharing: NO. Countries: 1. Publications: 2.
Trendelenburg Maneuver Predicts Fluid Responsiveness in Patients With Extracorporeal Membrane Oxygenation (TEMPLE)
ClinicalTrials.gov study NCT03553459. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Risk Factors of Bleeding Under Veno Arterial Membrane Oxygenation
ClinicalTrials.gov study NCT03888833. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Early Versus Late Initiation of ECMO (Extracorporal Membrane Oxygenation) Trial (ELIEO-Trial)
ClinicalTrials.gov study NCT04208126. IPD Sharing: Not stated. Countries: 1. Publications: 0.
Cardioespiratory physiological perturbations after acute smoke-induced lung injury and during extracorporeal membrane oxygenation support in sheep
<p><span><b>Background:</b> Numerous successful therapies developed for human medicine involve animal experimentation. Animal studies that are focused solely on translational potential, may not sufficiently document unexpected outcomes. Considerable amounts of data from such studies could be used to advance veterinary science. For example, sheep are increasingly being used as models of intensive care and therefore, data arising from such models must be published. In this study, the hypothesis is that there is little information describing physiological data from sheep models of intensive care and the author aimed to analyse such data to provide biological information that is currently not available for sheep that received extracorporeal life support (ECLS) following acute smoke-induced lung injury. </span></p> <p><span><b>Methods:</b> Nineteen mechanically ventilated adult ewes undergoing intensive care during evaluation of a form of ECLS (treatment) for acute lung injury were used to collate clinical observations. Eight sheep were injured by acute smoke inhalation prior to treatment (injured/treated), while another eight were not injured but treated (uninjured/treated). Two sheep were injured but not treated (injured/untreated), while one received room air instead of smoke as the injury and was not treated (placebo/untreated). The data were then analysed for 11 physiological categories and compared between the two treated groups.</span></p> <p><span><b>Results:</b> Compared with the baseline, treatment contributed to and exacerbated the deterioration of pulmonary pathology by reducing lung compliance and the arterial oxygen partial pressure to fractional inspired oxygen (PaO<sub>2</sub>/FiO<sub>2</sub>) ratio. The oxygen extraction index changes mirrored those of the PaO<sub>2</sub>/FiO<sub>2</sub> ratio. Decreasing coronary perfusion pressure predicted the severity of cardiopulmonary injury. </span></p> <p><b>Conclusions:</b> These novel observations could help in understanding similar pathology such as that which occurs in animal victims of smoke inhalation from house or bush fires, aspiration pneumonia secondary to tick paralysis and in the management of the severe coronavirus disease 2019 (COVID-19) in humans.</p>
Data from: Electrospinning preparation of oxygen-deficient nano TiO2-x/carbon fibre membrane as a self-standing high performance anode for Li-ion batteries
Improving the specific capacity and electronic conductivity of TiO2 can boost its practical application as a promising anode material for lithium ion batteries. In this work, a three-dimensional networking oxygen-deficient nano TiO2-x/carbon fibre membrane was achieved by combining the electrospinning process with a hot-press sintering method and directly used as a self-standing anode. With the synergistic effects of three-dimensional conductive networks, surface oxygen deficiency, high specific surface area and high porosity, binder-free and self-standing structure, etc., the nano TiO2-x/carbon fibre membrane electrode displays a high electrochemical reaction kinetics and a high specific capacity. The reversible capacity could be jointly generated from porous carbon, full-lithiation of TiO2 and interfacial lithium storage. At a current density of 100 mA g−1, the reversible discharge capacity can reach 464 mA h g−1. Even at 500 mA g−1, the discharge capacity still remains at 312 mA h g−1. Compared with pure carbon fibre and TiO2 powder, the TiO2-x/C fibre membrane electrode also exhibits an excellent cycle performance with a discharge capacity of 209 mA h g−1 after 700 cycles at the current density of 300 mA g−1, and the coulombic efficiency always remains at approximately 100%.
Data from: Prognostic value of cerebral tissue oxygen saturation during neonatal extracorporeal membrane oxygenation
Objectives: Extracorporeal membrane oxygenation support is indicated in severe and refractory respiratory or circulatory failures. Neurological complications are typically represented by acute ischemic or hemorrhagic lesions, which induce higher morbidity and mortality. The primary goal of this study was to assess the prognostic value of cerebral tissue oxygen saturation (StcO2) on mortality in neonates and young infants treated with ECMO. A secondary objective was to evaluate the association between StcO2 and the occurrence of cerebral lesions. Study Design: This was a prospective study in infants < 3 months of age admitted to a pediatric intensive care unit and requiring ECMO support. Measurements: The assessment of cerebral perfusion was made by continuous StcO2 monitoring using near-infrared spectroscopy (NIRS) sensors placed on the two temporo-parietal regions. Neurological lesions were identified by MRI or transfontanellar echography. Results: Thirty-four infants <3 months of age were included in the study over a period of 18 months. The ECMO duration was 10±7 days. The survival rate was 50% (17/34 patients), and the proportion of brain injuries was 20% (7/34 patients). The mean StcO2 during ECMO in the non-survivors was reduced in both hemispheres (p = 0.0008 right, p = 0.03 left) compared to the survivors. StcO2 was also reduced in deceased or brain-injured patients compared to the survivors without brain injury (p = 0.002). Conclusion: StcO2 appears to be a strong prognostic factor of survival and of the presence of cerebral lesions in young infants during ECMO.
"Continuous Positive Airway Pressure on Venovenous extracorporeaL Membrane Oxygenation for Acute respIratory Distress syndrOme"
ClinicalTrials.gov study NCT06814340. IPD Sharing: YES. Countries: 1. Publications: 0.
Volatile Anesthetic Pharmacokinetics During Extracorporeal Membrane Oxygenation
ClinicalTrials.gov study NCT05680545. IPD Sharing: UNDECIDED. Countries: 0. Publications: 9.
Observational Cohort Study of a National Extracorporeal Membrane Oxygenation Service for Adults With Respiratory Failure: the NHS ECMO Study.
ClinicalTrials.gov study NCT03979222. IPD Sharing: UNDECIDED. Countries: 0. Publications: 1.
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