J Reconstr Microsurg 2015; 31(01): 045-053
DOI: 10.1055/s-0034-1383821
Original Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Vascularized Osseous Flaps and Assessing Their Bipartate Perfusion Pattern via Intraoperative Fluorescence Angiography

Ian Valerio
1   Department of Plastic and Reconstructive Surgery, Walter Reed National Military Medical Center, Bethesda, Maryland
2   Department of Plastic Surgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania
3   Department of Plastic and Reconstructive Surgery, The Johns Hopkins University School of Medicine, Baltimore, Maryland
,
J. Marshall Green III
1   Department of Plastic and Reconstructive Surgery, Walter Reed National Military Medical Center, Bethesda, Maryland
,
Justin M. Sacks
3   Department of Plastic and Reconstructive Surgery, The Johns Hopkins University School of Medicine, Baltimore, Maryland
,
Shane Thomas
1   Department of Plastic and Reconstructive Surgery, Walter Reed National Military Medical Center, Bethesda, Maryland
,
Jennifer Sabino
1   Department of Plastic and Reconstructive Surgery, Walter Reed National Military Medical Center, Bethesda, Maryland
,
T. Oguz Acarturk
2   Department of Plastic Surgery, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania
› Author Affiliations
Further Information

Publication History

30 January 2014

07 May 2014

Publication Date:
03 December 2014 (online)

Abstract

Background Large segmental bone and composite tissue defects often require vascularized osseous flaps for definitive reconstruction. However, failed osseous flaps due to inadequate perfusion can lead to significant morbidity. Utilization of indocyanine green (ICG) fluorescence angiography has been previously shown to reliably assess soft tissue perfusion. Our group will outline the application of this useful intraoperative tool in evaluating the perfusion of vascularized osseous flaps.

Methods A retrospective review was performed to identify those osseous and/or osteocutaneous bone flaps, where ICG angiography was employed. Data analyzed included flap types, success and failure rates, and perfusion-related complications. All osseous flaps were evaluated by ICG angiography to confirm periosteal and endosteal perfusion.

Results Overall 16 osseous free flaps utilizing intraoperative ICG angiography to assess vascularized osseous constructs were performed over a 3-year period. The flaps consisted of the following: nine osteocutaneous fibulas, two osseous-only fibulas, two scapular/parascapular with scapula bone, two quadricep-based muscle flaps, containing a vascularized femoral bone component, and one osteocutaneous fibula revision. All flap reconstructions were successful with the only perfusion-related complication being a case of delayed partial skin flap loss.

Conclusions Intraoperative fluorescence angiography is a useful adjunctive tool that can aid in flap design through angiosome mapping and can also assess flap perfusion, vascular pedicle flow, tissue perfusion before flap harvest, and flap perfusion after flap inset. Our group has successfully extended the application of this intraoperative tool to assess vascularized osseous flaps in an effort to reduce adverse outcomes related to preventable perfusion-related complications.

Note

None of the authors has a financial interest in any of the products, devices, or drugs mentioned in this article. Justin M. Sacks is a consultant/speaker for LifeCell Corporation. The views expressed in this article are those of the authors and do not necessarily reflect the official policy or position of the Department of the Navy, Army, Department of Defense, or the United States Government.


This article was presented at the Annual Meeting of the Australian and New Zealand Head and Neck Cancer Society; October 2012; Brisbane, Australia and at the Annual Meeting of the Military Health System Research Symposium; August 2013; Ft Lauderdale, FL.


 
  • References

  • 1 Christensen JM, Baumann DP, Myers JN, Buretta K, Sacks JM. Indocyanine green near-infrared laser angiography predicts timing for the division of a forehead flap. Eplasty 2012; 12: e41
  • 2 Sacks JM, Nguyen AT, Broyles JM, Yu P, Valerio IL, Baumann DP. Near-infrared laser-assisted indocyanine green imaging for optimizing the design of the anterolateral thigh flap. Eplasty 2012; 12: e30
  • 3 Holm C, Mayr M, Höfter E, Becker A, Pfeiffer UJ, Mühlbauer W. Intraoperative evaluation of skin-flap viability using laser-induced fluorescence of indocyanine green. Br J Plast Surg 2002; 55 (8) 635-644
  • 4 Harris L, Goldstein D, Hofer S, Gilbert R. Impact of vasopressors on outcomes in head and neck free tissue transfer. Microsurgery 2012; 32 (1) 15-19
  • 5 Fox IJ, Wood EH. Applications of dilution curves recorded from the right side of the heart or venous circulation with the aid of a new indicator dye. Proc Staff Meet Mayo Clin 1957; 32 (19) 541-550
  • 6 U. S. Food and Drug Administration. Indocyanine Green (IC-Green). Available at: http://www.accessdata.fda.gov/scripts/cder/drugsatfda/index.cfm?fuseaction=Search.DrugDetails Accessed 10 June, 2012
  • 7 Schneider DS, Wu V, Wax MK. Indications for pedicled pectoralis major flap in a free tissue transfer practice. Head Neck 2012; 34 (8) 1106-1110
  • 8 Landsman MLJ, Kwant G, Mook GA, Zijlstra WG. Light-absorbing properties, stability, and spectral stabilization of indocyanine green. J Appl Physiol 1976; 40 (4) 575-583
  • 9 Siedek V, Waggershauser T, Berghaus A, Matthias C. Intraoperative monitoring of intraarterial paraganglioma embolization by indocyaningreen fluorescence angiography. Eur Arch Otorhinolaryngol 2009; 266 (9) 1449-1454
  • 10 Maus EA, Tan IC, Rasmussen JC , et al. Near-infrared fluorescence imaging of lymphatics in head and neck lymphedema. Head Neck 2012; 34 (3) 448-453
  • 11 Betz CS, Zhorzel S, Schachenmayr H , et al. Endoscopic measurements of free-flap perfusion in the head and neck region using red-excited Indocyanine Green: preliminary results. J Plast Reconstr Aesthet Surg 2009; 62 (12) 1602-1608
  • 12 Dzurinko VL, Gurwood AS, Price JR. Intravenous and indocyanine green angiography. Optometry 2004; 75 (12) 743-755
  • 13 Pestana IA, Coan B, Erdmann D, Marcus J, Levin LS, Zenn MR. Early experience with fluorescent angiography in free-tissue transfer reconstruction. Plast Reconstr Surg 2009; 123 (4) 1239-1244
  • 14 Phillips BT, Lanier ST, Conkling N , et al. Intraoperative perfusion techniques can accurately predict mastectomy skin flap necrosis in breast reconstruction: results of a prospective trial. Plast Reconstr Surg 2012; 129 (5) 778e-788e
  • 15 Woodard CR, Most SP. Intraoperative angiography using laser-assisted indocyanine green imaging to map perfusion of forehead flaps. Arch Facial Plast Surg 2012; 14 (4) 263-269
  • 16 Green III JM, Thomas S, Sabino J , et al. Use of intraoperative fluorescent angiography to assess and optimize free tissue transfer in head and neck reconstruction. J Oral Maxillofac Surg 2013; 71 (8) 1439-1449
  • 17 Hunter W. Of the structure and disease of articulating cartilages. 1743. Clin Orthop Relat Res 1995; (317) 3-6
  • 18 Barkow JCL. Comparative Morphologiedes des Menschen und der Thiere, Theil 6. Breslau: Hirt; 1868
  • 19 Testut L. Vaisseaux et nerfs des tissus conjonctifs fibreux, sereux, et osseux. These d'agregation. Paris: Octave Doin; 1880
  • 20 Drinker CK, Drinker KR, Lund CC. The circulation in the mammalian bone marrow. Am J Physiol 1922; 62: 1-92
  • 21 Johnson Jr RW. A physiological study of the blood supply of the diaphysis. Clin Orthop Relat Res 1968; 56 (56) 5-11
  • 22 Brookes M, Harrison RG. The vascularization of the rabbit femur and tibio-fibula. J Anat 1957; 91 (1) 61-72
  • 23 Oni OO, Stafford H, Gregg PJ. An experimental study of the patterns of periosteal and endosteal damage in tibial shaft fractures using a rabbit trauma model. J Orthop Trauma 1989; 3 (2) 142-147
  • 24 Wei FC, Chen HC, Chuang CC, Noordhoff MS. Fibular osteoseptocutaneous flap: anatomic study and clinical application. Plast Reconstr Surg 1986; 78 (2) 191-200
  • 25 Taylor GI, Miller GD, Ham FJ. The free vascularized bone graft. A clinical extension of microvascular techniques. Plast Reconstr Surg 1975; 55 (5) 533-544
  • 26 Menck J, Sander A. [Periosteal and endosteal blood supply of the human fibula and its clinical importance]. Acta Anat (Basel) 1992; 145 (4) 400-405
  • 27 Nguyen JT, Ashitate Y, Buchanan IA , et al. Bone flap perfusion assessment using near-infrared fluorescence imaging. J Surg Res 2012; 178 (2) e43-e50
  • 28 Hölzle F, Loeffelbein DJ, Nolte D, Wolff KD. Free flap monitoring using simultaneous non-invasive laser Doppler flowmetry and tissue spectrophotometry. J Craniomaxillofac Surg 2006; 34 (1) 25-33
  • 29 Prantl L, Pfeifer C, Geis S, Gosau M, Jung EM. Osteocutaneous free flaps: a critical analysis of quantitative evaluation of bone microcirculation with contrast-enhanced high resolution ultrasound (hrCEUS) and TIC analysis. Clin Hemorheol Microcirc 2011; 49 (1-4) 251-259
  • 30 Müller S, Gosau M, Strobel D , et al. Assessment of bone microcirculation by contrast-enhanced ultrasound (CEUS) and [18F]-positron emission tomography/computed tomography in free osseous and osseocutaneus flaps for mandibular reconstruction: preliminary results. Clin Hemorheol Microcirc 2011; 49 (1-4) 115-128
  • 31 Zaretski A, Amir A, Meller I , et al. Free fibula long bone reconstruction in orthopedic oncology: a surgical algorithm for reconstructive options. Plast Reconstr Surg 2004; 113 (7) 1989-2000
  • 32 Wei FC, Celik N, Yang WG, Chen IH, Chang YM, Chen HC. Complications after reconstruction by plate and soft-tissue free flap in composite mandibular defects and secondary salvage reconstruction with osteocutaneous flap. Plast Reconstr Surg 2003; 112 (1) 37-42
  • 33 Kroll SS, Schusterman MA, Reece GP , et al. Choice of flap and incidence of free flap success. Plast Reconstr Surg 1996; 98 (3) 459-463