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14 Use ofFluorescence Guidance inCardiothoracic Surgery
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33. Hills KD, Smith PK, Bittl JL, et al. 2100 ACCF/AHA Guidelines for coronary artery bypass graft surgery. A report of the American College of Cardiology Foundation/American Heart Association task force on prac­tice guidelines. Developed in collaboration with the American Association for Thoracic Surgery. Society of Cardiovascular Anesthesiologist, and Society of Thoracic Surgeons. J Am Coll Cardiol. 2011;58(24):e123–
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34. Kogon B, Fernandez J, Kanter K, et al. The role of intraoperative Indocyanine green uorescence angiography in pediatric surgery. Ann Thorac Surg. 2009;88:632–6.
35. Feins EN, Si MS, Baird CW, Emani SM.Intraoperative coronary artery imaging for planning. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2021;23(C):11–6.
36. Muehrcke DD, Shimp W, Casillas M.Intraoperative angiogrphy to nd an intramyocardial artery. Clin Surg. 2021;6:3025.
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Use ofFluorescence Guidance
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inUrologic Surgery
DavidZekan, AndrewWilliams, AmrElbakry, andAdamLuchey
Introduction
Anastomoses are a vital part of urologic surgery cases, used for urinary diversions, ureteral reimplantation, and other upper and lower urinary tract reconstruction. However, a considerable com­plication that can arise is anastomotic leak and stricture. While many factors have been implicated, a major cause of anastomotic leak and strictures is poor blood ow leading to tissue ischemia [1, 2]. The quality of organ perfusion is often only assessed by the surgeon’s impression, taking into account the active bleeding margin, palpable pulsation, and lack of discoloration [3, 4], which, unfortunately, have low predictive value for risk of anastomotic leakage [5]. Recent advancements have led to a promising alter­native: SPY uorescence imaging. SPY-ELITE and its portable handheld model SPY-PHI are uorescent imaging machines that are able to better assess blood ow in vessels and tissue when
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D. Zekan (*) · A. Elbakry · A. Luchey West Virginia University Department of Urology, Morgantown, WV, USA e-mail: dszekan@hsc.wvu.edu
A. Williams West Virginia University School of Medicine, Morgantown, WV, USA
© 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_15
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used with near-infrared uorescent dyes [1]. Such assessment of perfusion is widely applicable in urologic surgery, expanding uses far beyond just anastomotic analysis. The most commonly used immunouorescent dye is indocyanine green (ICG), most com­monly given intravenously (IV) and active for only 150–180 s before being excreted into the bile [6]. The IV dose of ICG has very low rates of adverse side effects with only 0.05% of patients having mild allergic reactions [7]. With the use of ICG and SPY, the recommended dose is 0.02mg/kg body weight, but this can vary based on intended use as outlined below [8]. ICG is water soluble and binds almost exclusively to plasma proteins concen­trating the uorescence mostly to vasculature [4]. The uorophore operates within the near-infrared spectrum, absorbing light in the 805nm wavelength and emitting at 835nm [4]. Most human tis­sue is relatively transparent at these wavelengths allowing for visualization depth of 10–20mm, which is generally sufcient for use in urologic surgery [4]. The various camera recording options available on the SPY systems allow for detection of even small perfusion decits within tissues and anastomoses while offering beautifully crisp images of the organs [4]. When ICG rst became available, it was described as a “hammer looking for a nail,” and its intended function was well-established in its ability to nd and display perfusion; however, its clinical benet and overall practi­cality were still underreported [6]. Recently, ICG and SPY tech­nologies have been utilized in urologic surgery in an attempt to improve patient outcomes and streamline surgeries [6]. Here, we outline the various uses of ICG and SPY technologies in urologic cases and specic methods for replicability.
D. Zekan et al.
Ureteral Identication
Although a majority of its uses are intravenous, ICG injected ret­rograde into the ureters also provides promise for ureteral identi­cation. This is crucial when working in conjunction with colorectal and gynecologic surgery, who traditionally rely on ure­teral stent placement for ureteral identication and prevention of iatrogenic ureteral injuries. However, stenting vs. no stenting
15 Use ofFluorescence Guidance inUrologic Surgery
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shows no difference in prevention of ureteral injury but aids in identication of an injury after it occurs. These injuries are increasing in incidence with use of laparoscopic and robotic tech­nology to aid in pelvic surgeries [9]. Bilateral ureters are known to uoresce green when injected intraluminally with methylene blue. However, studies vary with respect to reliability of uores­cence, reporting 50–91% visualization when viewed under NIRF (near-infrared uorescence). The use of intraluminal ICG as described below (with injection through an open-ended ureteral catheter, nephrostomy tube, or both) boasts a 100% success rate for ureteral visualization in both colorectal and gynecologic sur­gery [9].
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Ureteral Reconstruction
The use of ICG in upper tract reconstruction comes in two forms: intraluminal use of ICG to visualize ureters and areas of stricture and IV use to determine ureteral viability prior to reconstruction. Bjurlin etal. describe its IV use in robotic pyeloplasties, ureteral reimplants, ureterolysis, and ureteroureterostomies (UU) per the protocol outlined below. In all cases described (42in total), they boast an overall 95.2% success rate with a 100% symptomatic (ank pain) and radiographic (hydroureteronephrosis) success rate in included cases aside from ureterolysis (71.4%), which is known to be less efcacious at baseline. Clavien grade 1–3 com­plications occurred in 14.3% of patients, including transient lower extremity weakness (one patient), enterotomy requiring small bowel resection (one patient), ureteral stone requiring nephros­tomy tube (one patient), postoperative bleed requiring surgical exploration (one patient), and ureteral stent migration requiring repositioning (two patients) [10] (Fig.15.1).
Lee et al. describe use of intraluminal ICG in UUs treating short ureteral strictures robotically in the hands of a single sur­geon. Intraluminal injection was performed as described below, with injection above and below the level of stricture using a ure­teral catheter, nephrostomy tube, or combination of the two. In a case series including seven patients with short mid-ureteral stric-
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Fig. 15.1 Intraluminal injection of ICG for ureteral identication under NIRF [11]
Fig. 15.2 Use of NIRF with IV ICG to differentiate diseased (ischemic) ure­teral segment from healthy ureteral segment during robotic ureteral reimplan­tation for benign uretero-anastomotic stricture [13]
D. Zekan et al.
tures, they demonstrate the ability to delineate disease from healthy ureteral segments in all patients, with mean excision length of 1.6±0.7cm. A single patient with dense peri-hepatic adhesions experienced gallbladder laceration at the time of sur­gery, requiring robotic cholecystectomy, with no attributable complications to ICG administration. At follow-up (mean
5.9 ± 1.5 months), no patient had clinical or radiographic evi­dence of continued stricture [12]. Thus, both IV (Fig.15.2) and intraluminal (Fig.15.3) use of ICG during benign ureteral recon­struction is feasible, and its addition to the case presents minimal, if any, risk to the patient. Needed are long-term studies comparing outcomes (persistence and recurrence of stricture) between open, laparoscopic, and robotic techniques for benign reconstruction with and without the use of ICG.
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Fig. 15.3 Use of NIRF to differentiate diseased from healthy ureter during UU [12]
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D. Zekan et al.
Partial Nephrectomy
The use of ICG and SPY angiography for upper tract pathology extends beyond just pyeloplasties and UUs, also aiding in partial nephrectomies. Partial nephrectomy offers superior functional outcomes compared to radical nephrectomy in small renal masses [14]. To minimize ischemia to healthy tissue, SPY angiography can be used to properly identify hilar vessels and tumor-specic vasculature to be clamped before resection [15]. Furthermore, tumors are often well demarcated on the SPY imaging, appearing hypouorescent compared to surrounding parenchyma [15]. The use of ICG dye allows for better localization of malignant tissue for more precise resections [16]. Mitsui etal. utilized ICG dye and uorescent imaging to visualize the tumor margins during surgery and validated these margins ex vivo. They found that even in complex cases, ICG allowed for easy discrimination between normal and cancerous tissues [16]. Their case series demonstrates 100% exvivo differentiation within 60min of ICG injection in 16 cases, with 14 of 16 tumors showing hypouores­cence invivo. The remaining two were endophytic with overly­ing normal parenchyma. High and low uorescence were both used to rule out residual tumor, which was conrmed on patho­logic specimens [16]. Similarly, Angell etal. describe the ability to achieve differential uorescence between renal tumors and surrounding normal parenchyma with a test dose of ICG and then re-dose at the time of tumor resection. Differential uorescence was achieved in 65 of 70 tumors (82%), excluding tumors that could not be visualized as they were completely endophytic [17]. While the difference in tissue uorescence between tumors and normal kidney parenchyma is easily discernable, tissue uores­cence of the tumor itself cannot adequately determine malignant and benign masses [18].
The use of uorescent imaging also allows for better postop­erative renal function when compared to conventional methods [14, 19]. Borofsky etal. utilized ICG dye to visualize renal vascu­lature during partial nephrectomy allowing them to more speci­cally cross-clamp distal vessels feeding the tumor (“zero
15 Use ofFluorescence Guidance inUrologic Surgery
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ischemia” partial nephrectomy), rather than conventional cross­clamping of the main renal artery [14]. They demonstrated suc­cessful selective clamping in 27 of 34 patients (79.4%). While this method did lead to increased operating time, it also led to signi­cantly better postoperative kidney function with a reduction in glomerular ltration rate (GFR) of only 1.8% compared to 14.9% reduction in the renal artery cross-clamp at a mean follow-up of about 13days [14]. Shao et al. found similar signicant results with 3-month postoperative GFR decrease of 16.7% in multiple feeder clamping compared to 26.2% decrease in GFR for renal artery clamping [19]. Fluorescent imaging also allows the sur­geon to conrm that the tumor vasculature has been restricted fol­lowing arterial clamping by assessing the change in parameters produced with SPY imaging analysis (quantitatively) and the visual uorescence of the tissue [14]. When all the feeders to the tumor are properly cross-clamped, the tumor and surrounding parenchyma should hypouoresce. Overall, uorescent imaging of renal vasculature during partial nephrectomies allows for a more directed approach for tumor resection, leading to less over­all damage to normal kidney parenchyma and better patient out­comes.
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Urothelial Carcinoma andUrinary Diversion
Fluorescent imaging has two main potential uses in urothelial car­cinoma of the bladder: the rst is to map out regional lymph nodes associated with resected masses and the other is to ensure well­vascularized anastomoses, viable bowel, and identication of stricture should they occur at the anastomotic site.
Standard treatment for muscle-invasive bladder cancer remains radical cystectomy with pelvic lymph node dissection (PLND) [20]. SPY angiography may allow for quicker and more easy identication of SLN.ICG can be administered IV to visualize vasculature, but it can also be injected into the sub­mucosa and smooth muscle to be taken up into the lymphatics [21]. This technique allows for easy identication of sentinel
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lymph nodes, which require resection in all cystectomies per­formed for malignancy [22].
Manny etal. describe the use of submucosal and detrusor ICG injected circumferentially with a cystoscope in 10 patients under­going robotic radical cystectomy. Intraoperative identication of tumor was possible in 90% of patients using NIRF, only not achieved in a single patient noted to have circumferential bladder wall thickening, with bladder wall measuring >2cm in thickness. Sentinel lymph node drainage was also identied in 90% of patients, all of whom had multiple areas of drainage, with bilat­eral sentinel drainage in eight of nine patients. Importantly, of the three patients with node positive disease on nal pathology, nodal uorescence was 100% sensitive, but only 47% specic for iden­tication of node positivity [21]. While this technique does allow for a quick and simple understanding of tissue, its use for extended lymph node dissections may be less dependable [23]. The main constraint of ICG in identifying lymph nodes is its ability to ow easily through the lymphatic vessels. One potential problem with high tumor burden is that vessels may become obstructed by met­astatic disease, leading to areas of hypo-uorescence where metastases are present [23]. The sensitivity for ICG and uores­cent dye’s use in SNL dissection ranges widely from 44% to 100% depending on the study and for that reason should not be used alone for identication and resection lymph nodes [2325]. Overall, uorescent imaging of tissue lymphatics is an emerging eld, and as more advancements in technology and surgical tech­nique arise, its practicality and utility will become more apparent.
As often used intraoperatively by general surgeons, IV ICG can be utilized to visualize mesenteric vasculature in both the laparoscopic and open setting when performing urinary diversion, be it in the form of a neobladder, ileal conduit, or otherwise. The above group who utilized submucosa ICG for sentinel node iden­tication also describes use of IV ICG for identication of mesen­teric arcades when performing robotic intracorporeal diversion. Real-time visualization of vasculature guides stapling of the bowel and mesentery, and in 100% of cases (eight total), no com­plications related to diversion ischemia were observed, including anastomotic stricture and stomal stenosis [21].
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Another advancing use of SPY imaging is allowing for better visualization and quantitative assessment of vasculature in anas­tomoses. For instance, ureteroenteric strictures (UES) are a com­mon consequence of radical cystectomies and any surgery involving ureteral diversions [1]. Various surgical techniques have been developed to reduce stricture, but few have led to any substantial risk reduction, maintaining a complication rate of approximately 9% [1, 26, 27]. Ischemia is thought to be a major contributing factor to the development of UES.Thus, it was theo­rized that by assessing distal perfusion at each on the anastomoses using SPY angiography, fewer strictures may occur [1]. Shen et al. compared UES rates before (47 patients) and after (47 patients) implementing SPY into their practice for radical cystec­tomies. The stricture rate for patients prior to SPY implementa­tion was 7.5%, diagnosed with either hydronephrosis, lack of reux on loopogram, or Lasix renal scan showing t
1/2
>20min. After implementation of SPY and ICG, 0% of cases developed UES over a 12-month period. Through the use of SPY’s vascula­ture analysis, their team identied poor distal perfusion in 34.4% of ureters requiring a more proximal anastomosis; however, use of SPY did not lead to a signicantly more proximal anastomosis [1]. Doshi etal. conducted a similar study assessing rates of stric­ture in patients with or without the use of SPY imaging (n= 31 and 30, respectively). They found that only 3.2% of patients (n=1) developed stricture when uorescent imaging was used, compared to 13% (n = 5) with conventional methods [28]. Robotic-specic data is provided by Ahmadi etal., who analyzed 179 patients who underwent robotic-assisted laparoscopic radical cystectomy with intracorporeal diversion. When comparing the 132 patients in the non-ICG group to the 47in the ICG group, those in the ICG group were likely to have more ureter excised based on concern for ischemia and were more likely to have long segment (>5cm) ureteral excision. However, at 14 and 12months average follow-up, respectively, no UESs were noted in the ICG group, compared to a per-patient stricture rate of 10.6% and per­ureter stricture rate of 6.6% in the non-ICG group [29]. This prac­tice for assessing ureteral anastomoses can also be applied when creating a neobladder to prevent anastomotic leak.
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