Cangrelor As Treatment for Cardiac Surgery Associated With Heparin Induced Thrombocytopenia

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorSociété Française d'Anesthésie et de Réanimation

About this trial

Heparin-induced thrombocytopenia (HIT) is a rare but serious immune complication of heparin exposure that paradoxically increases the risk of thrombosis. In patients undergoing cardiac surgery with cardiopulmonary bypass (CPB), heparin is essential to prevent circuit clotting, yet contraindicated in HIT. Available alternatives carry significant limitations. Cangrelor, an intravenous reversible P2Y12 inhibitor, has shown promise in case reports and small series in this context, but no multicenter study exists. CATCH-IT is a multicenter retrospective observational study conducted across 11 French cardiac surgery centers, aiming to describe the safety and efficacy of cangrelor combined with heparin during CPB in confirmed HIT patients, by estimating the incidence of major bleeding and thrombotic events within 7 days after surgery.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years

Confirmed or highly probable HIT: 4T score ≥ 3 AND positive anti-PF4 antibodies (ELISA or equivalent), and when available, positive functional platelet test

Cardiac or aortic surgery with cardiopulmonary bypass (CPB)

Cangrelor administered in the perioperative period

Disqualifiers

None

Trial population

* Age \< 18 years * HIT not confirmed or ruled out * Patient objection to data use * Surgery performed without CPB * Requirement for continued cangrelor in the postoperative period * Post-cardiotomy ECMO

Trial design

Design model

Other

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Incidence of major hemorrhagic and/or thrombotic events

Proportion of patients experiencing at least one major hemorrhagic event (BARC grade ≥3, including hemoglobin drop ≥3 g/dL, red blood cell transfusion attributed to bleeding, need for interventional procedure, hemorrhagic shock, or documented intracranial hemorrhage) and/or thrombotic complication (imaging-confirmed ischemic stroke, acute mesenteric ischemia requiring surgery, acute limb ischemia, or vascular thrombosis) within 7 days after surgery.

Time frame
7 days postoperatively

Secondary outcomes

1

Cangrelor dosing modalities

Description of dose used during CPB (cardiopulmonary bypass)

Time frame
intraoperative period.
2

Cangrelor dosing modalities

Description monitoring during CPB (cardiopulmonary bypass)

Time frame
intraoperative period.
3

Cangrelor dosing modalities

Description of dose adjustments during CPB (cardiopulmonary bypass)

Time frame
intraoperative period.
4

Cangrelor dosing modalities

Description of duration of drug during CPB (cardiopulmonary bypass)

Time frame
intraoperative period.

Other outcomes

Sponsors and contacts

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