Implantation of left ventricular assist device complicated by undiagnosed thrombophilia

Tex Heart Inst J. 2012;39(5):615-7.

Abstract

A patient with dilated cardiomyopathy and no history of thromboembolic events received a surgically implanted axial-flow left ventricular assist device. After implantation, transesophageal echocardiography revealed a giant thrombus on the lateral and anterior aspects of the left ventricle. The inflow cannula inserted through the apex of the left ventricle was not obstructed, and the device generated satisfactory blood flow. Laboratory screening for thrombophilia showed protein S deficiency, heterozygous factor V Leiden mutation, and heterozygous MTHFR C667T mutation. During the entire duration of circulatory support, no significant suction events were detected, and the patient was listed for heart transplantation. Ventricular assist device implantation can unmask previously undiagnosed thrombophilia; therefore, it should be necessary to identify thrombophilic patients before cardiac support implantation.

Keywords: Anticoagulants/therapeutic use; blood coagulation disorders/complications; factor V Leiden; factor V/genetics; left ventricular assist device; perioperative care; postoperative complications; thrombophilia/genetics; thrombus/etiology/prevention & control.

Publication types

  • Case Reports

MeSH terms

  • Cardiomyopathy, Dilated / complications*
  • Cardiomyopathy, Dilated / physiopathology
  • DNA Mutational Analysis
  • Echocardiography, Doppler, Color
  • Echocardiography, Doppler, Pulsed
  • Echocardiography, Transesophageal
  • Factor V / genetics
  • Fatal Outcome
  • Genetic Predisposition to Disease
  • Genetic Testing / methods
  • Heart Diseases / blood
  • Heart Diseases / diagnostic imaging
  • Heart Diseases / etiology*
  • Heart Diseases / genetics
  • Heart Failure / diagnostic imaging
  • Heart Failure / etiology
  • Heart Failure / physiopathology
  • Heart Failure / therapy*
  • Heart-Assist Devices / adverse effects*
  • Humans
  • Male
  • Methylenetetrahydrofolate Reductase (NADPH2) / genetics
  • Middle Aged
  • Mutation
  • Predictive Value of Tests
  • Prosthesis Design
  • Prosthesis-Related Infections / etiology
  • Protein S Deficiency / complications
  • Protein S Deficiency / diagnosis
  • Protein S Deficiency / genetics
  • Stroke Volume
  • Thrombophilia / blood
  • Thrombophilia / complications*
  • Thrombophilia / diagnosis
  • Thrombophilia / genetics
  • Thrombosis / blood
  • Thrombosis / diagnostic imaging
  • Thrombosis / etiology*
  • Thrombosis / genetics
  • Ventricular Function, Left*

Substances

  • factor V Leiden
  • Factor V
  • MTHFR protein, human
  • Methylenetetrahydrofolate Reductase (NADPH2)

Supplementary concepts

  • Thrombophilia, hereditary