Background
Tamoxifen citrate (tamoxifen) has been associated with increased rates of thromboembolic events, which have prompted concerns that tamoxifen may increase the risk of complications after microvascular breast reconstruction. Some centers have implemented protocols to temporarily stop tamoxifen before microvascular breast reconstruction. We sought to determine whether this practice is warranted.
Methods
We retrospectively compared rates of microvascular flap complications and pulmonary emboli between patients who were and were not receiving tamoxifen at the time of reconstruction in 670 patients who underwent delayed microsurgical breast reconstruction at our institution between January 2000 and April 2010.
Results
Two hundred five patients received tamoxifen within 28 days before reconstruction (these were considered to be receiving tamoxifen at reconstruction); 465 patients did not. Patients who received tamoxifen were significantly younger (p < 0.0001) and thinner (p = 0.0025) with less cardiovascular morbidity (p = 0.04) and shorter durations of surgery (p = 0.05). Despite fewer comorbidities, microvascular flap complications were significantly more common in patients who received tamoxifen (21.5% versus 15%; p = 0.04). Patients who received tamoxifen had 1.7 times the risk of complications (p = 0.015) and 1.8 times the risk of follow-up complications (p = 0.03) than patients in the no-tamoxifen group. In tamoxifen-group patients, cardiovascular co-morbidities significantly increased the risk of flap complications (p = 0.002). Tamoxifen-group patients had a significantly increased rate of immediate total flap loss (p = 0.041) and a lower rate of flap salvage (p = 0.023). Tamoxifen did not appear to increase the risk of pulmonary embolus during or after delayed microvascular breast reconstruction.
Conclusions
Tamoxifen may increase the risk of microvascular flap complications. Surgeons should consider temporarily stopping the drug 14-days before microsurgical breast reconstruction.