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Prognosis Related to Induced Thrombopenia With Heparin Under Venoarterial ECMO in Reanimation

Prognosis Related to Induced Thrombopenia With Heparin Under Venoarterial ECMO in Reanimation

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03979625
Acronym
TIH ECMO
Enrollment
39
Registered
2019-06-07
Start date
2016-01-01
Completion date
2018-04-30
Last updated
2019-06-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heparin-induced Thrombocytopenia

Brief summary

Thrombocytopenia is a frequent and serious adverse event in patients treated with veno-arterial extracorporeal membrane oxygenation (VA-ECMO) for refractory cardiogenic shock. Similarly to postcardiac surgery patients, heparin-induced thrombocytopenia (HIT) could represent the causative underlying mechanism. However, the epidemiology as well as related mortality regarding HIT and VA-ECMO remains largely unknown. The investigators aimed to define the prevalence and associated 90-day mortality of HIT diagnosed under VA-ECMO.This retrospective study included patients under VA-ECMO from 20 French centers between 2012 and 2016.

Interventions

OTHERHospitalization for more than 3 days with high clinical suspicion of HIT and positive anti-PF4/heparin antibodies

Patients are classified according to results of functional tests as having either Confirmed or Excluded HIT.

Sponsors

Central Hospital, Nancy, France
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥ 18 years * Patient hospitalized in intensive care for a cardiovascular failure requiring the setting up of an ECMO-VA * ECMO-VA duration ≥ 3 days * HIT confirmed by immunological tests * Patient affiliated to a Social Security scheme

Exclusion criteria

* Known antecedent of TIH prior to cannulation * Pregnant woman * ECMO-VA following cardiopulmonary arrest or septic shock

Design outcomes

Primary

MeasureTime frame
Death90 days after inclusion

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026