Endosc Int Open 2016; 04(03): E371-E377
DOI: 10.1055/s-0042-101752
Original article
© Georg Thieme Verlag KG Stuttgart · New York

Gastrointestinal angiodysplasia is associated with significant gastrointestinal bleeding in patients with continuous left ventricular assist devices

Justin Cochrane
1   Assistant Clinical Associate Professor University of Washington Medical School, Providence Sacred Heart Medical Center Internal Medicine Residency Spokane, Washington, United States
,
Christian Jackson
2   Loma Linda University Medical Center, Department of Medicine, Section of Gastroenterology, Loma Linda, California, United States
,
Greg Schlepp
3   Spokane Digestive Disease Center Spokane, Washington, United States
,
Richard Strong
2   Loma Linda University Medical Center, Department of Medicine, Section of Gastroenterology, Loma Linda, California, United States
› Author Affiliations
Further Information

Publication History

submitted: 01 June 2015

accepted after revision: 05 January 2016

Publication Date:
18 March 2016 (online)

Background and study aims: Patients with a continuous-flow left ventricular assist device (LVAD) have a 65 % incidence of bleeding events within the first year. The majority of gastrointestinal bleeding (GIB) is from gastrointestinal angiodyplasia (GIAD). The primary aim of the study was to determine whether GIAD was associated with a higher rate of significant bleeding, an increased number of bleeding events per year, and a higher rate of transfusion compared to non-GIAD sources.

Patients and methods: This retrospective cohort study included 118 individuals who received a LVAD at a tertiary medical center from 2006 through 2014. Patients were subdivided into GIB and non-GIB for comparison of patient demographics, comorbid conditions, and laboratory data. GIB was further divided into sources of GIB, GIAD, obscure, or non-GIAD to establish severity of bleeding, rate of re-bleeding, and transfusion rate.

Results: GIAD is associated with an increased number of bleeding events compared to non-GIAD sources of GIB (2.07 vs 1.23, P = 0.01) and a higher number of bleeding events per year (0.806 vs. 0.455 P = 0.001). GIAD compared to non-GIAD sources of GIB was associated with an increased incidence of major bleeding (100 % vs 60 %, P = 0.006) and increased rates of transfusion (8.8 vs 2.95 units, P = 0.0004). Cox Regression analysis between non-GIB and GIAD demonstrated increased risk with age (P = 0.001), history of chronic kidney disease (P = 0.005), and length of stay after LVAD implantation of more than 45 days (P = 0.04). History of hypertension (P = 0.045), diabetes mellitus (P = 0.016), and male gender was associated with decreased risk (P = 0.04).

Conclusion: Patients with a continuous-flow LVAD who develop a GIB secondary to GIAD have a higher rate of major bleeding, multiple bleeding events, and require more transfusions to achieve stabilization compared to patients who do not have GIAD.

 
  • References

  • 1 Miller LW, Pagnani ED, Russell SD et al. Use of continuous-flow devices in patients awaiting heart transplant. NEJM 2007; 357: 885-896
  • 2 Crow S, Chen D, Milano C et al. Acquired von Willebrand syndrome in continuous-flow ventricular assist device recipients. Ann Thorac Surg 2010; 90: 1263-1269
  • 3 John R, Kamdar F, Liao K et al. Improved survival and decreasing incidence of adverse events with the HeartMate II left ventricular assist device as bridge-to-transplant therapy. Ann Thorac Surg 2008; 86: 1227-1234
  • 4 Kirklin JK, Naftel DC, Kormos RL et al. Second INTERMACS annual report: more than 1000 primary left ventricular assist device implants. J Heart Lung Transplant 2010; 29: 1-10
  • 5 Crow S, John R, Boyle A et al. Gastrointestinal bleeding rates in recipients of nonpulsatile and pulsatile left ventricular assist devices. J Thorac Cardiovasc Surg 2009; 137: 208-215
  • 6 Aggarwal A, Pant R, Kumar S et al. Incidence and management of gastrointestinal bleeding with continuous flow assist devices. Ann Thorac Surg 2012; 93: 1534-1540
  • 7 Uriel N, Pak SW, Jorde UP et al. Acquired von Willebrand syndrome after continuous-flow mechanical device support contributes to a high prevalence of bleeding during long-term support and at the time of transplantation. J Am Coll Cardiol 2010; 56: 1207-1213
  • 8 Wever-Pinzon O, Selzman CH, Drakos SG et al. Pulsatility and the risk of nonsurgical bleeding in patients supported with the continuous-flow left ventricular assist device HeartMate II. Circ Heart Fail 2013; 6: 517-526
  • 9 Heyde EC. Gastrointestinal bleeding in aortic stenosis. N Eng J Med 1958; 259: 196
  • 10 Demirozu ZT, Radovanceivic R, Hochman LF et al. Arteriovenous malformation and gastrointestinal bleeding in patients with Heartmate II left ventricular device. J Heart Lung Transplant 2011; 30: 849-853
  • 11 Pennington DG, Mcbride LR, Peigh PS et al. Eight years experience with bridging to cardiac transplantation. J Thoracic Cardiovasc Surg 1994; 107: 472-481
  • 12 Draper KV, Huang RJ, Gerson LB. GI bleeding in patients with continuous-flow left ventricular assist devices: a systematic review and meta-analysis. Gastrointest Endosc 2014; 80: 435-446
  • 13 Kushnir VM, Sharma S, Ewald GA et al. Evaluation of GI bleeding after implantation of left ventricular assist device. Gastrointest Endosc 2012; 75: 973-979
  • 14 Singh G, Albeldawi M, Kalra S et al. Features of Patients with Gastrointestinal Bleeding After Implantation of an Assist Device. Clin Gastr Hepat 2015; 13: 107-114
  • 15 Tsiouris A, Paone G, Nemeh HW et al. Factors determining post-operative readmissions after left ventricular assist device implantation. Heart Lung Transplant 2014; 33: 1041-1047
  • 16 Forest SJ, Bello R, Friedmann P et al. Readmissions after ventricular assist device: etiologies, patterns, and days out of hospital. Ann Thorac Surg 2013; 95: 1276-1281
  • 17 Sarosiek K, Bogar L, Conn MI et al. An old problem with a new therapy: gastrointestinal bleeding in ventricular assist device patients and deep overtube-assisted enteroscopy. ASAIO J 2013; 59: 384-389
  • 18 Jackson CS, Gerson LB. Management of Gastrointestinal Angiodysplastic Lesions (GIADs): A Systematic Review and Meta-Analysis. Am J Gastroenterol 2014; 109: 474-483
  • 19 Uriel N, Pak SW, Jorde UP et al. Acquired von Willebrand syndrome after continuous-flow mechanical device support contributes to a high prevalence of bleeding during long-term support and at the time of transplantation. J Am Coll Cardiol 2010; 56: 1207-1213
  • 20 Randi AM, Laffan MA, Starke RD. Von Willebrand factor, angiodysplasia and angiogenesis. Mediterr J Hematol Infect Dis 2013; 5 (1)
  • 21 Daly C, Eicthen A, Castanaro C et al. Angiopoeitin-2 functions as a Tie2 agonist in tumor models, where it limits the effects of VEGF inhibition. Cancer Res 2013; 73: 108-118
  • 22 Starke RD, Ferraro F, Paschalaki KE et al. Endothelial von Willebrand factor regulates angiogenesis. Blood 2011; 117: 1071-1080
  • 23 Veyradier A, Balian A, Wolf M et al. Abnormal von Willebrand factor in bleeding angiodysplasias of the digestive tract. Gastroenterology 2001; 120: 346-353
  • 24 Hoog CM, Brostrom O, Lindahl TL et al. Bleeding from gastrointestinal angioectasias is not related to bleeding disorders- a case control study. BMC Gastroenterol 2010; 10: 113
  • 25 Junquera F, Saperas E, de Torres I et al. Increased expression of angiogenic factors in human colonic angiodysplasia. Am J Gastroenterol 1999; 94: 1070-1076
  • 26 Ge ZZ, Chen HM, Gao YJ et al. Efficacy of thalidomide for refractors gastrointestinal bleeding from vascular malformation. Gastroenterology 2011; 14: 1629-1637
  • 27 Laine L, Takeuchi K, Tarnawski A. Gastric mucosal defense and cytoprotection: Bench to bedside. Gastroenterology 2008; 135: 41-60