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58. Surve A, Cottam D, Richards C, Medlin W, Belnap L.A matched cohort comparison of long-term outcomes of roux-en-Y gastric bypass (RYGB) versus single-anastomosis Duodeno-ileostomy with sleeve gastrectomy (SADI-S). Obes Surg. 2021;31:1438–48.
59. Brown WA, Ooi G, Higa K, Himpens J, Torres A. Single anastomosis duodenal-Ileal bypass with sleeve gastrectomy/one anastomosis duode­nal switch (SADI-S/OADS) IFSO position statement. Obes Surg. 2018;28:1207–16.
60. Kallies K, Rogers AM.ASMBS guidelines/statements American Society for Metabolic and Bariatric Surgery updated statement on single­anastomosis duodenal switch. Surg Obes Relat Dis. 2020;16:825–30.
61. Sudan R, Puri V, Sudan D.Robotically assisted biliary pancreatic diver­sion with a duodenal switch: a new technique. Surg Endosc. 2007;21:729–
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63. Biertho L, Lebel S, Marceau S, Hould FS, Lescelleur O, Moustarah F, Simard S, Biron S, Marceau P.Perioperative complications in a consecu­tive series of 1000 duodenal switches. Surg Obes Relat Dis. 2013;9:63–8.
64. Dorman RB, Rasmus NF, Al-Haddad BJS, Serrot FJ, Slusarek BM, Sampson BK, Buchwald H, Leslie DB, Ikramuddin S.Benets and com­plications of the duodenal switch/biliopancreatic diversion compared to the Roux-en-Y gastric bypass. Surgery. 2012;152:758–67.
65. Surve A, Zaveri H, Cottam D.Video case report a safer and simpler tech­nique of duodenal dissection and transection of the duodenal bulb for duodenal switch-NC-ND license. Surg Obes Relat Dis. 2016;12:923–4.
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67. Loske G, Liedke M, Schlöricke E, Herrmann T, Rucktaeschel F.Endoscopic negative-pressure therapy for duodenal leakage using new open- pore lm and polyurethane foam drains with the pull-through tech­nique. Endoscopy. 2017;49:E300–2.
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7 Use ofFluorescence Guidance inBariatric Surgery
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Use ofFluorescence Guidance
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inBreast Reconstruction
AcaraTurner, LuisQuiroga, SebastianBrooke, andKerriWoodberry
Introduction
The assessment of tissue perfusion is a critical step in the plan­ning and success of every plastic surgery procedure. Plastic sur­geons rely on the clinical evaluation of tissue perfusion, including tissue color, capillary rell, and bleeding at the edge of a ap. Recently, several objective assessment adjuncts have been developed in order to reduce complication rates of fat necrosis, mastectomy skin ap necrosis, and partial ap loss [1, 2]. These objective adjuncts utilize various surrogate markers via tissue oximetry measurements, ultrasound-based tools, dye-based and
Supplementary Information The online version contains supplementary material available at
https://doi.org/10.1007/978- 3- 031- 40685- 0_8.
8
A. Turner · L. Quiroga · S. Brooke · K. Woodberry (*) Department of Surgery, Division of Plastic, Reconstructive, and Hand Surgery, West Virginia University School of Medicine, Morgantown, WV, USA e-mail: acara.turner@hsc.wvu.edu; luis.quiroga@hsc.wvu.edu;
sebastian.brooke@hsc.wvu.edu; kerri.woodberry@hsc.wvu.edu
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023 N. Szoka et al. (eds.), The SAGES Manual of Fluorescence-Guided Surgery, https://doi.org/10.1007/978-3-031-40685-0_8
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non-dye- based angiography, or temperature as a relative measure­ment of well-perfused tissue. While these methods are more sophisticated than clinical evaluation, some are superior to others. For example, thermography has been found to be less reliable than others due to multiple factors that interfere with the accuracy of its reading [1]. On the other hand, uorescent angiography has proved to be a reliable and more accurate form of intraoperative perfusion assessment. Since the mid-1950s, indocyanine green (ICG) angiography has become a popular method to assess tissue perfusion with applications in multiple specialties [3]. ICG was rst used in plastic surgery in 1999 by Still etal. who used the technology as a tool to assess ap perfusion in burn reconstruc­tion. Since then, it has had multiple applications throughout the eld including management of diabetic ulcers, assessment of ap perfusion, lymph ow reconstruction, and breast reconstruction, with experimental use in face transplant preoperative planning. This chapter focuses on the application of ICG in breast recon­struction and treatment of associated lymphedema. We will dis­cuss its use in implant-based reconstruction, autologous reconstruction, and postmastectomy surgical correction of lymph­edema. More importantly, we will discuss the implications of its use in intraoperative decision-making, postoperative complica­tions, patient costs, and overall patient satisfaction. Overall, the use of ICG has been found to reduce rates of fat necrosis and partial ap necrosis, facilitate early detection of lymphedema in breast cancer reconstruction, reduce patient costs associated with management of complications, and improve patient satisfaction [2, 4, 5]. ICG angiography is not only a cost-effective adjunct to breast reconstruction but also an effective tool to assess tissue per­fusion in breast reconstruction.
A. Turner et al.
History
Indocyanine green was initially developed by Kodak during World War II and used as a forming layer of Technicolor lms. In the mid-1950s, an executive of Kodak offered to help Dr. Irwin Fox search for a biocompatible dye that could be detected in the blood.
8 Use ofFluorescence Guidance inBreast Reconstruction
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Kodak sent several dyes, including ICG, for testing. ICG showed a distinguished absorption of near-infrared light at 805nm (the same wavelength at which the optical densities of oxygenated and reduced hemoglobin in blood are approximately equal). In 1955, ICG dye was developed for near-infrared (NIR) photography by the Kodak research laboratories. It was then approved for clinical use in 1959 by the FDA.Hynson, Westcott & Dunning, a small pharmaceutical company in Baltimore, developed the stable lyophilized form in use today. ICG had its rst medical applica­tion in 1956in the eld of cardiology. By measuring the time­variant dilution of ICG in whole blood, cardiac output could be measured, and valvular septal defects could be determined. It was then discovered that the dye was excreted exclusively by the liver, leading to his application for measuring hepatic function. In 1969, Kogure and co-workers attempted the rst ICG angiography when they demonstrated infrared absorption of the canine brain vascu­lature following intra-arterial ICG injection. Since its initial use in burn patients, ICG angiography has become an important tool for assessing tissue perfusion and lymphatics. Today, the SPY Elite system is the most common and accessible indocyanine green angiography system in the USA.It was rst used in cardiac sur­gery to assess vascular ow and transplant surgery. In 2009, Newman and Samsom introduced the SPY Elite system as a tool to assess free ap perfusion. Jones and Pestana then described its ability to assess both mastectomy skin ap perfusion and micro­vascular anastomoses in autologous tissue transfer. These were the rst of many studies that have proven its efcacy in improving intraoperative decision-making and reducing postoperative complications.
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Mechanism ofAction
Indocyanine green is an anionic, hydrophobic tricarbocyanine mol­ecule. Immediately following IV injection, ICG rapidly binds to plasma proteins, especially lipoproteins with no known metabo­lites. ICG has a short half-life of only 2.5 to 3min as it is extracted rapidly by the liver without modications and excreted into the bile
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approximately 8 min after injection. When injected interstitially, ICG binds to protein and is then found in lymphatic channels. It can be found in the nearest draining lymph nodes within 15min and reaches regional lymph nodes within 1–2h. ICG absorbs light in the near-infrared region at 800 to 810nm in blood plasma and emits uorescent light at a slightly longer wavelength, with peak emis­sion at a wavelength of 830nm. The uorescence imaging devices provide external energy as near-infrared light for the indocyanine green to absorb. This causes excitation of the indocyanine greens and emits a uorescent light which is transferred from the eld to an image on the monitor. At this wavelength, ICG allows visualiza­tion of blood vessels at 2cm depth without signicant absorption by water, tissue, or hemoglobin. The dye is eventually taken up by the liver cells and secreted in the bile. The plasma fractional disap­pearance rate is 0.5mg/kg and is slightly higher in women than in men. The pharmacokinetic properties of ICG have two main bene­ts. First, it allows a practical application of ICG in bile system assessment during surgery. Second and more importantly, the short half-life of ICG enables repeated examinations via multiple injec­tions without reaching toxic levels, which is vital to plastic surgery applications. This property separates ICG from uorescein, which can only be used once as it remains within the tissues.
A. Turner et al.
Indications inPlastic Surgery
The use of indocyanine green angiography in breast reconstruc­tion has increased in the past 20years as a useful tool to assess mastectomy skin and autologous tissue viability with real-time imaging. Complication rates associated with assessment of ap perfusion via clinical assessment alone highlighted the need for an improved means of skin ap and autologous tissue evaluation [1, 6]. Indocyanine green angiography in implant-based and autologous breast reconstruction is a useful tool that has been associated with decreased rates of mastectomy skin necrosis, par­tial ap loss, and fat necrosis by guiding intraoperative decision­making [6]. Its use allows surgeons to excise poorly perfused tissue, place implants in the proper plane, and determine the
8 Use ofFluorescence Guidance inBreast Reconstruction
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appropriate timeline for breast reconstruction. ICG angiography provides surgeons with visual evidence of poor perfusion that may not manifest clinically until several days postoperatively, thereby allowing surgeons to excise specic areas of poor tissue perfusion (Video 8.1). In implant-based reconstruction, ICG angi­ography provides an objective assessment of mastectomy skin ap perfusion that helps determine which plane is most appropri­ate for implant placement. This is especially important in high­risk patients, such as those who are smokers, those with a BMI greater than 30, or those who have undergone radiotherapy. In autologous reconstruction, ICG angiography centers around the assessment of autologous tissue perfusion and patency of micro­vascular anastomoses, which has led to decreased rates of fat necrosis and partial ap loss, as poorly perfused tissue can be pri­marily excised. For patients who have undergone axillary lymph node surgery with resultant lymphedema, ICG angiography has been found to outperform lymphoscintigraphy, which is currently the main lymphatic imaging modality [4, 7]. Lymphoscintigraphy does not provide the detailed characteristics or real-time dynamic ow needed to perform lymphatic surgery. ICG angiography eval­uates lymphatic channels in order to determine the adequate tim­ing of surgical intervention and guide preoperative planning and intraoperative performance of lymphedema surgery. Overall, indocyanine green angiography has become a useful tool in breast reconstruction that has decreased overall complication rates.
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Implant-Based Reconstruction
Immediate Reconstruction
Immediate breast reconstruction with a direct-to-implant (DTI) reconstruction has the clear advantage of a single operation, which is offset by higher complication rates especially in the early postoperative period. Early complications include mastectomy skin necrosis, infection, delayed wound healing, and implant exposure—the majority of which are due to inadequate tissue per­fusion. Having a tool for objective assessment of tissue perfusion
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A. Turner et al.
to complement clinical evaluation allows surgeons to make intra­operative decisions based on ICG angiography ndings. The use of ICG angiography guides two main surgical decisions:
1. The quantity and location of mastectomy skin ap excision based on surface area of tissue perfusion.
2. The feasibility of direct-to-implant reconstruction versus tis­sue expander placement based on skin ap vascular integrity.
In immediate breast reconstruction with direct-to-implant reconstruction, implants may be placed in the prepectoral plane or in the submuscular plane with total coverage or partial coverage by the pectoralis major muscle, the serratus muscle, or an acellu­lar dermal matrix. While submuscular placement has historically been the predominant location of implants, prepectoral placement has increased in popularity as patients experience less postopera­tive pain and have lower rates of animation distortion seen in sub­muscular placement. The use of SPY angiography allows patients to undergo DTI reconstruction in the prepectoral plane with lower rates of postoperative complications [6]. Using this tool permits surgeons to assess the vascular integrity of mastectomy skin aps, thereby guiding intraoperative decision-making. When mastec­tomy skin aps display an adequate percentage of skin perfusion, surgeons may move forward with prepectoral implant placement. However, when mastectomy skin aps display a lack of vascular integrity proven by SPY uorescent imaging, prepectoral placement is no longer the best option and necessitates conversion to submuscular implant or expander. Following movement of the implant, a repeated vascular assessment according to the SPY ELITE or SPY Portable Handheld Imager protocol can then be used to conrm the absence of implant-induced vascular compro­mise. In both planes of implant placement, the use of acellular dermal matrix is important. Its use in the prepectoral plane pro­vides superior pole fullness and provides adequate coverage that is comparable to the pectoralis major muscle coverage. In the sub­muscular plane, the acellular dermal matrix provides lower pole coverage, often needed during the tissue expansion process which muscular coverage is inadequate [6].
8 Use ofFluorescence Guidance inBreast Reconstruction
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There are special considerations that the plastic surgeon should address when following this decision-making algorithm. They are based on the angiography assessment as well as patient factors. Cutoffs for skin perfusion values that necessitate conversion to sub­muscular range from 25% to 45% relative perfusion. Skin with 25% or less relative tissue perfusion is nonviable in most patients, and skin with 45% relative tissue perfusion will survive in most patients. Therefore, a gray area exists between these values. Moyer etal. studied this “gray area” and found that the use of a 33% cutoff is associated with a positive predictive value of removing nonviable skin of 88% with a negative predictive value of removing healthy skin of 16% [8]. These values, however, should be determined on an individual basis after evaluating the patient’s risk factors for increased mastectomy skin ap necrosis. The main risk factors that affect skin ap necrosis and therefore contribute to angiography success in predicting skin ap necrosis are smoking status, BMI, and mastectomy weight [9]. In patients who are smokers, have a BMI greater than 30, and have a mastectomy weight greater than 800g, rates of mastectomy skin ap necrosis are higher compared to nonsmokers, patients with a BMI less than 30, or patients with lower mastectomy weights [9]. After accounting for values of tissue perfusion and patient risk factors, the plastic surgeon can then determine an adequate amount of tissue that can be excised without compromising the skin envelope. SPY angiography provides both qualitative and quantitative assessments that allow plastic surgeons to make informed decisions regarding patient eligibility for DTI reconstruction. In doing so, it guides excision of poorly perfused areas and determination of the best plane of implant placement. When factoring in patient factors, these two surgical decisions lead to reduced rates of mastectomy skin ap necrosis and reduce the need for subsequent surgical revision.
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Tissue Expander Reconstruction
In patients who undergo immediate or delayed breast recon­struction with tissue expanders, SPY angiography serves to maximize tissue expansion and allows surgeons to assess the
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amount of initial ll of the tissue expander. In immediate breast reconstruction, the tissue expander can be lled to a signicant volume—particularly with the use of ADM—which speeds the overall timing of expansion. The use of acellular dermal matrix and skin sparing mastectomies has allowed greater intraopera­tive lling of expanders. Delayed breast reconstruction occurs for multiple reasons, including patient preference, need for radiotherapy, or inadequate tissue perfusion in the immediate setting. In patients who undergo tissue expander placement after mastectomy, the initial ll of the tissue expander is vital to skin ap perfusion throughout expansion. Following intraoperative tissue expander ll, SPY angiography may be used to assess skin ap perfusion [2] (Video 8.2). If the tissue is shown to have inadequate perfusion, saline should be removed, and the skin ap should be reassessed. This should be repeated until tissue perfusion is adequate, after which closure can take place. While not a requirement, SPY angiography may be used in the intraop­erative setting to determine safe rates of tissue expander ll [9].
A. Turner et al.
Autologous Reconstruction
For patients who choose to undergo breast reconstruction but do not want to undergo implant-based reconstruction, autologous reconstruction is an alternative option. Autologous reconstruction, though associated with longer operative times and length of hos­pital stay, touts the benets of a breast mound with a more natural shape and feel without the use of a foreign body. Complications of fat necrosis associated with autologous reconstruction can include either partial or complete fat necrosis. Fat necrosis after autolo­gous breast reconstruction not only is a source of patient discom­fort and anxiety but also leads to contour abnormalities that may construe the breast exam. Fat necrosis, in addition to partial and total ap loss, has many implications ranging from the need for biopsy to surgical excision.
SPY angiography in autologous breast reconstruction can be used to assess ap perfusion based on perforators present [5, 10]. When used to assess ap perfusion, the plastic surgeon should use
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