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Does Earlier Cannulation With Veno-Venous Extracorporeal Membrane Oxygenation in Adult Patients With Acute Respiratory Distress Syndrome Decrease Duration of Artificial Mechanical Ventilation? / Hartner, Christine; Ochsenreither, Jacqueline; Miller, Kenneth; Weiss, Michael

Material type: Continuing resourceContinuing resourceISSN: 2380-9418Subject(s): acute respiratory distress syndrome | extracorporeal membrane oxygenation | mechanical ventilation In: Journal of Doctoral Nursing Practice -- 2020, v. 13, 2, p. 148-155Summary: Acute respiratory distress syndrome (ARDS) is characterized by an acute, diffuse, inflammatory lung injury, leading to increased alveolar capillary permeability, increased lung weight, and loss of aerated lung tissue (Fan, Brodie, & Slutsky, 2018). Primary treatment for ARDS is artificial mechanical ventilation (AMV) (Wu, Huang, Wu, Wang, & Lin, 2016). Given recent advances in technology, the use of veno-venous extracorporeal membrane oxygenation (VV-ECMO) to treat severe ARDS is growing rapidly (Combes et al., 2014). Objective: This 49-month quantitative, retrospective inpatient EMR chart review compared if cannulation with VV-ECMO up to and including 48 hours of admission and diagnosis in adult patients 30 to 65 years of age diagnosed with ARDS, decreased duration on AMV, as compared to participants who were cannulated after 48 hours of admission and diagnosis with ARDS. Methods: A total of 110 participants were identified as receiving VV-ECMO during the study timeframe. Of the 58 participants who met all inclusion criteria, 39 participants were cannulated for VV-ECMO within 48 hours of admission and diagnosis with ARDS, and 19 participants were cannulated with VV-ECMO after 48 hours of admission and diagnosis with ARDS. Results: Data collected identified no statistically significant (p < 0.579) difference in length of days on AMV between participant groups. Conclusions: Further studies are needed to determine if earlier initiation of VV-ECMO in adult patients with ARDS decrease time on AMV
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PP Propolis nasal spray effectively improves recovery from infectious acute rhinitis and common cold symptoms in children: a pilot study / PP Veno-venöse extrakorporale Membranoxygenierung (ECMO) mit heparinbeschichtetem Bypass-System = Eine effektive Erweiterung bei der Behandlung des akuten Lungenversagens (ARDS): Eine effektive Erweiterung bei der Behandlung des akuten Lungenversagens (ARDS) / PP Treatment of acute adult respiratory distress syndrome = Traitement du syndrome de détresse respiratoire aiguë de l'adulte (SDRA) / PP Does Earlier Cannulation With Veno-Venous Extracorporeal Membrane Oxygenation in Adult Patients With Acute Respiratory Distress Syndrome Decrease Duration of Artificial Mechanical Ventilation? / PP Clinical outcomes according to cannula confgurations in patients with acute respiratory distress syndrome under veno-venous extracorporeal membrane oxygenation: a Korean multicenter study / PP Burns. 26 / PP Analysis of a Silent Voice A Qualitative Inquiry of Embroidery Created by a Patient with Schizophrenia /

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Acute respiratory distress syndrome (ARDS) is characterized by an acute, diffuse, inflammatory lung injury, leading to increased alveolar capillary permeability, increased lung weight, and loss of aerated lung tissue (Fan, Brodie, & Slutsky, 2018). Primary treatment for ARDS is artificial mechanical ventilation (AMV) (Wu, Huang, Wu, Wang, & Lin, 2016). Given recent advances in technology, the use of veno-venous extracorporeal membrane oxygenation (VV-ECMO) to treat severe ARDS is growing rapidly (Combes et al., 2014). Objective: This 49-month quantitative, retrospective inpatient EMR chart review compared if cannulation with VV-ECMO up to and including 48 hours of admission and diagnosis in adult patients 30 to 65 years of age diagnosed with ARDS, decreased duration on AMV, as compared to participants who were cannulated after 48 hours of admission and diagnosis with ARDS. Methods: A total of 110 participants were identified as receiving VV-ECMO during the study timeframe. Of the 58 participants who met all inclusion criteria, 39 participants were cannulated for VV-ECMO within 48 hours of admission and diagnosis with ARDS, and 19 participants were cannulated with VV-ECMO after 48 hours of admission and diagnosis with ARDS. Results: Data collected identified no statistically significant (p < 0.579) difference in length of days on AMV between participant groups. Conclusions: Further studies are needed to determine if earlier initiation of VV-ECMO in adult patients with ARDS decrease time on AMV

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