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Lessons learned from awake ECMO approach in Covid-19-related acute respiratory distress syndrome - a scoping review

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00843989%3A_____%2F25%3AE0111684" target="_blank" >RIV/00843989:_____/25:E0111684 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://www.dovepress.com/lessons-learned-from-awake-ecmo-approach-in-covid-19-related-acute-res-peer-reviewed-fulltext-article-TCRM" target="_blank" >https://www.dovepress.com/lessons-learned-from-awake-ecmo-approach-in-covid-19-related-acute-res-peer-reviewed-fulltext-article-TCRM</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2147/TCRM.S507120" target="_blank" >10.2147/TCRM.S507120</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Lessons learned from awake ECMO approach in Covid-19-related acute respiratory distress syndrome - a scoping review

  • Popis výsledku v původním jazyce

    Abstract: During the COVID-19 pandemic, specific COVID-19-related conditions renewed interest in the full-awake venovenous extracorporeal membrane oxygenation (faV–V ECMO) approach, in which ECMO is applied to awake, cooperative, and non-intubated patients. This scoping review aims to provide a descriptive overview of faV–V ECMO in patients with COVID-19-related acute respiratory distress syndrome (CARDS). We searched the PubMed, Web of Science, and Scopus databases using the keywords “awake ECMO” or “spontaneous breathing AND ECMO”, combined with “COVID-19”, “SARS-CoV-2” or “coronavirus”, utilizing the Boolean operator “AND”. The search included papers published from November 1, 2019, to December 31, 2024. Sixty-four papers were assessed for eligibility at the abstract level, and fourteen articles (seven small-sample cohort studies and seven case reports) comprising 95 patients were included in the final analysis. The most frequent reasons for preferring faV-V ECMO over mechanical ventilation were barotrauma and patient refusal of intubation and mechanical ventilation. The faV-V ECMO strategy was successful (ie, patients not intubated, disconnected from ECMO, and discharged from the hospital) in 36.4% of cases (cohort studies only). The incidence of defined severe adverse events (bleeding, thrombosis, cannula malposition, delirium, and progression of barotrauma) was considered low. The mortality rate for CARDS patients treated with faV-V ECMO (including only patients from cohort studies) reached 33.0%, notably lower than the 48% reported for CARDS patients treated with V-V ECMO in the ELSO registry. Patients who were intubated due to worsening respiratory failure during faV-V ECMO had significantly higher mortality. Infectious complications, sepsis, and multiorgan failure were the most frequent causes of death. However, significant heterogeneity in the definitions and reporting of management, ECMO-related complications, and outcomes was observed across the paper...

  • Název v anglickém jazyce

    Lessons learned from awake ECMO approach in Covid-19-related acute respiratory distress syndrome - a scoping review

  • Popis výsledku anglicky

    Abstract: During the COVID-19 pandemic, specific COVID-19-related conditions renewed interest in the full-awake venovenous extracorporeal membrane oxygenation (faV–V ECMO) approach, in which ECMO is applied to awake, cooperative, and non-intubated patients. This scoping review aims to provide a descriptive overview of faV–V ECMO in patients with COVID-19-related acute respiratory distress syndrome (CARDS). We searched the PubMed, Web of Science, and Scopus databases using the keywords “awake ECMO” or “spontaneous breathing AND ECMO”, combined with “COVID-19”, “SARS-CoV-2” or “coronavirus”, utilizing the Boolean operator “AND”. The search included papers published from November 1, 2019, to December 31, 2024. Sixty-four papers were assessed for eligibility at the abstract level, and fourteen articles (seven small-sample cohort studies and seven case reports) comprising 95 patients were included in the final analysis. The most frequent reasons for preferring faV-V ECMO over mechanical ventilation were barotrauma and patient refusal of intubation and mechanical ventilation. The faV-V ECMO strategy was successful (ie, patients not intubated, disconnected from ECMO, and discharged from the hospital) in 36.4% of cases (cohort studies only). The incidence of defined severe adverse events (bleeding, thrombosis, cannula malposition, delirium, and progression of barotrauma) was considered low. The mortality rate for CARDS patients treated with faV-V ECMO (including only patients from cohort studies) reached 33.0%, notably lower than the 48% reported for CARDS patients treated with V-V ECMO in the ELSO registry. Patients who were intubated due to worsening respiratory failure during faV-V ECMO had significantly higher mortality. Infectious complications, sepsis, and multiorgan failure were the most frequent causes of death. However, significant heterogeneity in the definitions and reporting of management, ECMO-related complications, and outcomes was observed across the paper...

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30221 - Critical care medicine and Emergency medicine

Návaznosti výsledku

  • Projekt

  • Návaznosti

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Ostatní

  • Rok uplatnění

    2025

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Therapeutics and Clinical Risk Management

  • ISSN

    1176-6336

  • e-ISSN

    1178-203X

  • Svazek periodika

    21

  • Číslo periodika v rámci svazku

    may

  • Stát vydavatele periodika

    NZ - Nový Zéland

  • Počet stran výsledku

    14

  • Strana od-do

    655-668

  • Kód UT WoS článku

    001490311400001

  • EID výsledku v databázi Scopus

    2-s2.0-105006743197