Exploratory Use of Glycoprotein IIb/IIIa Inhibition in Prevention of Blalock-Taussig Shunt Thrombosis

Pediatr Crit Care Med. 2022 Sep 1;23(9):727-735. doi: 10.1097/PCC.0000000000003011. Epub 2022 Jun 10.

Abstract

Objectives: Morbidity and mortality related to modified Blalock-Taussig shunt (mBTTS) thrombosis remain a significant risk. Platelet inhibition following mBTTS may reduce this risk. However, oral antiplatelet agents have variable absorption following surgery. We determine risk factors for mBTTS thrombosis and hypothesize that IV glycoprotein IIb/IIIa inhibitor (tirofiban) as a bridge to oral aspirin reduces the rate of shunt thrombosis in the immediate postoperative period. End points within the 14-day follow-up period include mBTTS thrombosis, overall thrombosis, bleeding, length of stay, and mortality.

Design: Retrospective, Institutional Review Board-approved cohort study.

Setting: Single-center cardiac ICU.

Patients: Patients under the age of 18 who had an mBTTS placed within the study period of January 2008 to December 2018 were included.

Interventions: Patients were divided into two groups: standard of care (SOC) anticoagulation alone and SOC with tirofiban as a bridge to oral aspirin.

Measurements and main results: Freedom from mBTTS thrombosis was estimated using the Kaplan-Meier method. A multivariable predictive model using the four most significant risk factors was developed using logistic regression. A total of 272 patients were included: 36 subjects in the SOC/tirofiban group and 236 in the SOC group. Shunt thrombosis occurred in 26 (11%) SOC group with zero in SOC/tirofiban group ( p = 0.03). The median time to thrombosis was 0 days (range, 0-12 d). The area under the curve for the predictive model (anticoagulation group, history of coagulopathy, intraoperative shunt clipping, and shunt size/weight ratio) is 0.790 ( p < 0.001). Prevalence of bleeding and mortality was not significantly different between the groups.

Conclusions: Highest risk for shunt thrombosis following mBTTS occurs within the first few days after surgical procedure. Tirofiban is a safe addition to SOC and may be an effective strategy to prevent early mBTTS thrombosis.

MeSH terms

  • Anticoagulants
  • Aspirin / therapeutic use
  • Blalock-Taussig Procedure* / adverse effects
  • Cohort Studies
  • Fibrinolytic Agents* / therapeutic use
  • Hemorrhage / etiology
  • Humans
  • Integrin alpha2* / metabolism
  • Integrin beta3* / metabolism
  • Platelet Aggregation Inhibitors* / therapeutic use
  • Platelet Glycoprotein GPIIb-IIIa Complex* / metabolism
  • Retrospective Studies
  • Thrombosis* / etiology
  • Thrombosis* / prevention & control
  • Tirofiban* / therapeutic use
  • Treatment Outcome

Substances

  • Anticoagulants
  • Fibrinolytic Agents
  • ITGA2B protein, human
  • Integrin alpha2
  • Integrin beta3
  • Platelet Aggregation Inhibitors
  • Platelet Glycoprotein GPIIb-IIIa Complex
  • Tirofiban
  • Aspirin