J Reconstr Microsurg 2017; 33(01): 040-044
DOI: 10.1055/s-0036-1587698
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Form and Size Matter: Increased Risk of Thrombosis in Microvessels with Surgically Created Endothelial Lesions

Thomas Mücke
1   Department of Oral and Maxillofacial Surgery, Technische Universität München, Klinikum rechts der Isar, Germany
,
Constantin Wolff
1   Department of Oral and Maxillofacial Surgery, Technische Universität München, Klinikum rechts der Isar, Germany
,
Monika von Düring
2   Department of Neuroanatomy, Ruhr University, Bochum, Germany
,
David A. Mitchell
1   Department of Oral and Maxillofacial Surgery, Technische Universität München, Klinikum rechts der Isar, Germany
,
Lucas M. Ritschl
1   Department of Oral and Maxillofacial Surgery, Technische Universität München, Klinikum rechts der Isar, Germany
,
Andreas M. Fichter
1   Department of Oral and Maxillofacial Surgery, Technische Universität München, Klinikum rechts der Isar, Germany
› Author Affiliations
Further Information

Publication History

29 April 2016

07 July 2016

Publication Date:
19 August 2016 (online)

Abstract

Background Atherosclerosis is a known risk factor for flap loss in microsurgery. Several microsurgical techniques, like plaque removal, have been proposed for atherosclerotic vessels, but these techniques often induce intimal injuries. The aim of this study was to investigate the impact of various endothelial defects on the risk of thrombosis in a rat acute intimal injury model.

Methods Endothelial defects of various forms and sizes were created in the abdominal aorta of 30 male Wistar rats following a strict protocol. Defect sizes were measured and classified as round, horizontal, or vertical based on their configuration. An hour after reestablishing the blood flow, the abdominal aorta was harvested and the operation site was assessed for signs of thrombosis clinically and using light microscopy. Univariate and multiple linear regression analysis were performed to identify possible influencing factors on thrombosis.

Results The mean defect size was 2.65 ± 1.19 mm2. Intimal lesions were classified as round in 36.7%, horizontal in 33.3%, and vertical in 30% of specimens. Thrombus formation was detected in 46.7% clinically and in 50% histologically. Univariate regression analysis revealed that defect size (p = 0.048) and vertical form (p = 0.017) were significantly associated with thrombus formation. Multiple regression analysis corroborated vertical defects as a risk factor for thrombosis (p = 0.03).

Conclusion Endothelial injuries are associated with a high risk of thrombosis with highest risks associated with vertical defects. Arteries should be carefully examined for intimal defects before microvascular anastomosis, especially in the atherosclerotic patient.

 
  • References

  • 1 Bui DT, Cordeiro PG, Hu QY, Disa JJ, Pusic A, Mehrara BJ. Free flap reexploration: indications, treatment, and outcomes in 1193 free flaps. Plast Reconstr Surg 2007; 119 (7) 2092-2100
  • 2 Mücke T, Wolff KD, Wagenpfeil S, Mitchell DA, Hölzle F. Immediate microsurgical reconstruction after tumor ablation predicts survival among patients with head and neck carcinoma. Ann Surg Oncol 2010; 17 (1) 287-295
  • 3 Bozec A, Poissonnet G, Chamorey E , et al. Free-flap head and neck reconstruction and quality of life: a 2-year prospective study. Laryngoscope 2008; 118 (5) 874-880
  • 4 Chen HC, Coskunfirat OK, Ozkan O , et al. Guidelines for the optimization of microsurgery in atherosclerotic patients. Microsurgery 2006; 26 (5) 356-362
  • 5 Mücke T, Rau A, Weitz J , et al. Influence of irradiation and oncologic surgery on head and neck microsurgical reconstructions. Oral Oncol 2012; 48 (4) 367-371
  • 6 Hanasono MM, Barnea Y, Skoracki RJ. Microvascular surgery in the previously operated and irradiated neck. Microsurgery 2009; 29 (1) 1-7
  • 7 Shum J, Markiewicz MR, Park E , et al. Low prealbumin level is a risk factor for microvascular free flap failure. J Oral Maxillofac Surg 2014; 72 (1) 169-177
  • 8 Suh JD, Sercarz JA, Abemayor E , et al. Analysis of outcome and complications in 400 cases of microvascular head and neck reconstruction. Arch Otolaryngol Head Neck Surg 2004; 130 (8) 962-966
  • 9 Kolbenschlag J, Hellmich S, Germann G, Megerle K. Free tissue transfer in patients with severe peripheral arterial disease: functional outcome in reconstruction of chronic lower extremity defects. J Reconstr Microsurg 2013; 29 (9) 607-614
  • 10 Henrita van Zanten G, Saelman EU, Schut-Hese KM , et al. Platelet adhesion to collagen type IV under flow conditions. Blood 1996; 88 (10) 3862-3871
  • 11 Ritschl LM, Fichter AM, Häberle S , et al. Ketamine-Xylazine anesthesia in rats: intraperitoneal versus intravenous administration using a microsurgical femoral vein access. J Reconstr Microsurg 2015; 31 (5) 343-347
  • 12 Rasband WS. ImageJ. In, U S National Institutes of Health, Bethesda, Maryland, USA. Available at: http://imagej.nih.gov/ij/ 1997 –2009
  • 13 Scholz M, Mücke T, Düring Mv, Pechlivanis I, Schmieder K, Harders AG. Microsurgically induced aneurysm models in rats, part I: techniques and histological examination. Minim Invasive Neurosurg 2008; 51 (2) 76-82
  • 14 Ritschl LM, Fichter AM, von Düring M, Mitchell DA, Wolff KD, Mücke T. Introduction of a microsurgical in-vivo embolization-model in rats: the aorta-filter model. PLoS ONE 2014; 9 (2) e89947
  • 15 Chow SP. The histopathology of microvascular anastomosis: a study of the incidence of various tissue changes. Microsurgery 1983; 4 (1) 5-9
  • 16 Barker JH, Anderson GL, Gu JM, Wyllie F, Acland RD. Experimental study of the relationship between alterations in tissue perfusion and anastomotic patency. Microsurgery 1993; 14 (6) 409-415
  • 17 O'Shaughnessy M, Anderson GL, Acland RD, Barker JH. Platelet-derived thromboxane A2 decreases microvascular perfusion after arterial repair. Plast Reconstr Surg 1997; 99 (3) 834-841
  • 18 Froemel D, Fitzsimons SJ, Frank J, Sauerbier M, Meurer A, Barker JH. A review of thrombosis and antithrombotic therapy in microvascular surgery. Eur Surg Res 2013; 50 (1) 32-43
  • 19 Kesting MR, Hölzle F, Wolff KD , et al. Use of microvascular flap technique in older adults with head and neck cancer: a persisting dilemma in reconstructive surgery?. J Am Geriatr Soc 2011; 59 (3) 398-405
  • 20 Adriaensen ME, Kock MC, Stijnen T , et al. Peripheral arterial disease: therapeutic confidence of CT versus digital subtraction angiography and effects on additional imaging recommendations. Radiology 2004; 233 (2) 385-391
  • 21 Sharpe RY, Walker J, Bown MJ, Naylor MB, Evans DH, Naylor AR. Identifying the high-risk patient with clinically relevant embolisation after carotid endarterectomy. Eur J Vasc Endovasc Surg 2009; 37 (1) 1-7
  • 22 Painter TA, Hertzer NR, O'Hara PJ, Krajewski LP, Beven EG. Symptomatic internal carotid thrombosis after carotid endarterectomy. J Vasc Surg 1987; 5 (3) 445-451
  • 23 Clagett GP, Robinowitz M, Youkey JR , et al. Morphogenesis and clinicopathologic characteristics of recurrent carotid disease. J Vasc Surg 1986; 3 (1) 10-23
  • 24 Johnson BL, Gupta AK, Bandyk DF, Shulman C, Jackson M. Anatomic patterns of carotid endarterectomy healing. Am J Surg 1996; 172 (2) 188-190
  • 25 O'Donnell Jr TF, Callow AD, Scott G, Shepard AD, Heggerick P, Mackey WC. Ultrasound characteristics of recurrent carotid disease: hypothesis explaining the low incidence of symptomatic recurrence. J Vasc Surg 1985; 2 (1) 26-41
  • 26 Rosenthal D, Archie Jr JP, Avila MH , et al. Secondary recurrent carotid stenosis. J Vasc Surg 1996; 24 (3) 424-428 , discussion 428–429
  • 27 Bürrig KF. The morphology of the carotid artery after uncomplicated endarterectomy. J Cardiovasc Surg (Torino) 1994; 35 (5) 413-418
  • 28 Savoie FH, Cooley BC, Gould JS. Evaluation of the effect of pharmacologic agents on crush-avulsion arterial injuries: a scanning electron microscopy study. Microsurgery 1991; 12 (4) 292-300
  • 29 Wolff KD, Hölzle F, Wysluch A, Mücke T, Kesting M. Incidence and time of intraoperative vascular complications in head and neck microsurgery. Microsurgery 2008; 28 (3) 143-146
  • 30 Cooley BC, Hansen FC. Microvascular repair following local crush and avulsion vascular injury. Microsurgery 1985; 6 (1) 46-48
  • 31 Miller MJ, Schusterman MA, Reece GP, Kroll SS. Interposition vein grafting in head and neck reconstructive microsurgery. J Reconstr Microsurg 1993; 9 (3) 245-251 , discussion 251–252
  • 32 Nelson JA, Fischer JP, Grover R , et al. Vein grafting your way out of trouble: Examining the utility and efficacy of vein grafts in microsurgery. J Plast Reconstr Aesthet Surg 2015; 68 (6) 830-836
  • 33 Hashimoto I, Nakanishi H, Shono Y, Yamano M, Toda M. The features of thrombus in a microvessel injury model and the antithrombotic efficacy of heparin, urokinase, and prostaglandin E1. Plast Reconstr Surg 2003; 111 (7) 2307-2314
  • 34 Zimmermann A, Roenneberg C, Wendorff H, Holzbach T, Giunta RE, Eckstein HH. Early postoperative detection of tissue necrosis in amputation stumps with indocyanine green fluorescence angiography. Vasc Endovascular Surg 2010; 44 (4) 269-273
  • 35 Munabi NC, Olorunnipa OB, Goltsman D, Rohde CH, Ascherman JA. The ability of intra-operative perfusion mapping with laser-assisted indocyanine green angiography to predict mastectomy flap necrosis in breast reconstruction: a prospective trial. J Plast Reconstr Aesthet Surg 2014; 67 (4) 449-455