Laser-Doppler flowmetry in the monitoring of the human intestinal allograft: a preliminary report

Transplant Proc. 2006 Jul-Aug;38(6):1723-5. doi: 10.1016/j.transproceed.2006.05.001.

Abstract

During acute rejection, graft endothelium becomes a prime target for recipient immune cells. Animal studies have shown reduced microvascular perfusion, probably due to increased endothelial-leukocyte interaction and endothelial impairment, leading to graft damage. Using laser-Doppler flowmetry (LDF), we correlated the microvascular blood flow in the intestinal mucosa of five patients receiving multivisceral grafts with clinical events and pathology results. Measurements (n = 75) were performed during the first 4 weeks posttransplantation by inserting the LDF flexible probe through the ileostomy for 25 to 30 cm. Forty-six of the 75 measurements were performed within 24 hours of endoscopy and biopsy. In uncomplicated cases, we recorded a gradual increase in mucosal perfusion during the first week posttransplantation that presumably reflected regeneration after reperfusion injury. Increased mucosal perfusion did not seem to correlate with rejection or other adverse clinical events. Sudden and sustained decreases in mucosal perfusion by 30% or more compared to the previous measurements were associated with septic episodes, rejection, or both. LDF revealed a good sensitivity in monitoring the intestinal microcirculation. It was able to indicate perfusion changes associated with acute rejection. The relatively low specificity of LDF may be compensated by the low invasivity, allowing frequent investigation. LDF may be an additional tool for routine monitoring of intestinal allografts.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Female
  • Graft Rejection
  • Humans
  • Intestinal Mucosa / blood supply*
  • Intestines / transplantation*
  • Laser-Doppler Flowmetry
  • Male
  • Microcirculation / diagnostic imaging*
  • Middle Aged
  • Monitoring, Physiologic
  • Transplantation, Homologous / physiology*
  • Treatment Outcome
  • Ultrasonography
  • Viscera / transplantation*