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Levosimendan Efficacy for Veno-arterial ECMO Weaning: a Retrospective Study

Conditions
Cardiogenic Shock
Registration Number
NCT03346824
Lead Sponsor
University Hospital, Strasbourg, France
Brief Summary

Failure of Weaning from ECMO is a serious complication, reaching an incidence between 29 and 58%. Inotrops are frequently used to help separating patient from ECMO. Levosimendan is an ino-dilatatory medication and was used in different clinical settings. The aim of this study was to evaluate the benefit with levosimendan when used in weaning process.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
65
Inclusion Criteria
  • Age over 18
  • Patient requiring the need for short-term assistance
  • Patient who has agreed to use his medical data for research purposes
Exclusion Criteria
  • Refusal to participate in the study
  • Non-weaning attempts due to a death under assistance or a relay by a long-term assistance or heart transplant
  • Non-cardiac indications of assistance (indication of pulmonary replacement)
  • Subject under guardianship or curatorship

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Comparison of the incidence of weaning failure between patients with levosimendan and othersData were recorded from admission until 48 hours after weaning from ECMO
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Service Réanimation chirurgicale cardiovasculaire-NHC

🇫🇷

Strasbourg, France

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