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20. Trencheva K, Morrissey KP, Wells M, Mancuso CA, Lee SW, Sonoda T, Michelassi F, Charlson ME, Milsom JW.Identifying important predictors for anastomotic leak after colon and rectal resection: prospective study on 616 patients. Ann Surg. 2013;257(1):108–13.
21. Markus PM, Martell J, Leister I, Horstmann O, Brinker J, Becker H.Predicting postoperative morbidity by clinical assessment. Br J Surg. 2005;92(1):101–6.
22. Karliczek A, Harlaar NJ, Zeebregts CJ, Wiggers T, Baas PC, van Dam GM.Surgeons lack predictive accuracy for anastomotic leakage in gas­trointestinal surgery. Int J Color Dis. 2009;24(5):569–76.
23. Boni L, David G, Mangano A, Dionigi G, Rausei S, Spampatti S, etal. Clinical applications of indocyanine green (ICG) enhanced uorescence in laparoscopic surgery. Surg Endosc. 2015;29(7):2046–55.
24. Boni L, David G, Dionigi G, Rausei S, Cassinotti E, Fingerhut A.Indocyanine green-enhanced uorescence to assess bowel perfusion during laparoscopic colorectal resection. Surg Endosc. 2016;30(7):2736–
42.
25. Mizrahi I, Abu-Gazala M, Rickles AS, Fernandez LM, Petrucci A, Wolf J, etal. Indocyanine green uorescence angiography during low anterior resection for low rectal cancer: results of a comparative cohort study. Tech Coloproctol. 2018;22(7):535–40.
26. Impellizzeri HG, Pulvirenti A, Inama M, Bacchion M, Marrano E, Creciun M, Casaril A, Moretto G.Near-infrared uorescence angiogra­phy for colorectal surgery is associated with a reduction of anastomotic leak rate. Updat Surg. 2020;72(4):991–8.
27. Ris F, Liot E, Buchs NC, Kraus R, Ismael G, Belfontali V, Douissard J, Cunningham C, Lindsey I, Guy R, Jones O, George B, Morel P, Mortensen NJ, Hompes R, Cahill RA, Near-Infrared Anastomotic Perfusion Assessment Network VOIR. Multicentre phase II trial of near-infrared imaging in elective colorectal surgery. Br J Surg. 2018;105(10):1359–67.
28. Siddighi S, Yune JJ, Hardesty J.Indocyanine green for intraoperative localization of ureter. Am J Obstet Gynecol. 2014;211(4):436.e1–2.
29. Soriano CR, Cheng RR, Corman JM, Moonka R, Simianu VV, Kaplan JA.Feasibility of injected indocyanine green for ureteral identication during robotic left-sided colorectal resections. Am J Surg. 2021:S0002­9610(21)00392-5.
30. Yeung TM. Fluorescence imaging in colorectal surgery. Surg Endosc. 2021;35(9):4956–63.
31. Jafari MD, Wexner SD, Martz JE, McLemore EC, Margolin DA, Sherwinter DA, Lee SW, Senagore AJ, Phelan MJ, Stamos MJ.Perfusion assessment in laparoscopic left-sided/anterior resection (PILLAR II): a multi-institutional study. J Am Coll Surg. 2015;220(1):82–92.e1.
32. Starker PM, Chinn B.Using outcomes data to justify instituting new tech­nology: a single institution’s experience. Surg Endosc. 2018;32(3):1586–
92.
M. R. Freund et al.
3 Use ofFluorescence Guidance inColorectal Surgery
https://t.me/medicina_free
33. De Nardi P, Elmore U, Maggi G, Maggiore R, Boni L, Cassinotti E, Fumagalli U, Gardani M, De Pascale S, Parise P, Vignali A, Rosati R.Intraoperative angiography with indocyanine green to assess anasto­mosis perfusion in patients undergoing laparoscopic colorectal resection: results of a multicenter randomized controlled trial. Surg Endosc. 2020;34(1):53–60.
34. Watanabe J, Ishibe A, Suwa Y, Suwa H, Ota M, Kunisaki C, Endo I.Indocyanine green uorescence imaging to reduce the risk of anas­tomotic leakage in laparoscopic low anterior resection for rectal can­cer: a propensity score-matched cohort study. Surg Endosc. 2020;34(1):202–8.
35. Marquardt C, Kalev G, Schiedeck T.Intraoperative uorescence angiog­raphy with indocyanine green: retrospective evaluation and detailed anal­ysis of our single-center 5-year experience focused on colorectal surgery. Innov Surg Sci. 2020;5(1–2):35–42.
36. Hasegawa H, Tsukada Y, Wakabayashi M, Nomura S, Sasaki T, Nishizawa Y, Ikeda K, Akimoto T, Ito M.Impact of intraoperative indocyanine green uorescence angiography on anastomotic leakage after laparoscopic sphincter-sparing surgery for malignant rectal tumors. Int J Color Dis. 2020;35(3):471–80.
37. Yanagita T, Hara M, Osaga S, Nakai N, Maeda Y, Shiga K, Hirokawa T, Matsuo Y, Takahashi H, Takiguchi S.Efcacy of intraoperative ICG uo­rescence imaging evaluation for preventing anastomotic leakage after left-sided colon or rectal cancer surgery: a propensity score-matched analysis. Surg Endosc. 2021;35(5):2373–85.
38. Kudszus S, Roesel C, Schachtrupp A, Höer JJ.Intraoperative laser uo­rescence angiography in colorectal surgery: a noninvasive analysis to reduce the rate of anastomotic leakage. Langenbeck’s Arch Surg. 2010;395(8):1025–30.
39. Dip F, Boni L, Bouvet M, Carus T, Diana M, Falco J, Gurtner GC, Ishizawa T, Kokudo N, Lo Menzo E, Low PS, Masia J, Muehrcke D, Papay FA, Pulitano C, Schneider-Koraith S, Sherwinter D, Spinoglio G, Stassen L, Urano Y, Vahrmeijer A, Vibert E, Warram J, Wexner SD, White K, Rosenthal RJ.Consensus conference statement on the general use of near-infrared uorescence imaging and indocyanine green guided sur­gery: results of a modied Delphi study. Ann Surg. 2022;275(4):685–91.
40. Wexner S, Abu-Gazala M, Boni L, etal. Use of uorescence imaging and indocyanine green during colorectal surgery: results of an intercontinen­tal Delphi survey. Surgery. 2022;172(6S):S38–45.
41. Jafari MD, Pigazzi A, McLemore EC, Mutch MG, Haas E, Rasheid SH, Wait AD, Paquette IM, Bardakcioglu O, Safar B, Landmann RG, Varma MG, Maron DJ, Martz J, Bauer JJ, George VV, Fleshman JW Jr, Steele SR, Stamos MJ.Perfusion assessment in left-sided/Low anterior resec­tion (PILLAR III): a randomized, controlled, parallel, multicenter study assessing perfusion outcomes with PINPOINT near-infrared uorescence
117
118
https://t.me/medicina_free
imaging in low anterior resection. Dis Colon Rectum. 2021;64(8):995–
1002.
42. Jacquet P, Sugarbaker PH.Clinical research methodologies in diagnosis and staging of patients with peritoneal carcinomatosis. Cancer Treat Res. 1996;82:359–74.
43. Quenet F, Elias D, Roca L, Goere D, Ghouti L, Pocard M, et al. Cytoreductive surgery plus hyperthermic intraperitoneal chemotherapy versus cytoreductive surgery alone for colorectal peritoneal metastases (PRODIGE 7): a multicentre, randomised, open-label, phase 3 trial. Lancet Oncol. 2021;22(2):256–66.
44. Esquivel J.Cytoreductive surgery and hyperthermic intraperitoneal che­motherapy for colorectal cancer: survival outcomes and patient selection. J Gastrointest Oncol. 2016;7(1):72–8.
45. Vassos N, Piso P.Metastatic colorectal cancer to the peritoneum: current treatment options. Curr Treat Options in Oncol. 2018;19(10):49.
46. Liberale G, Bourgeois P, Larsimont D, Moreau M, Donckier V, Ishizawa T.Indocyanine green uorescence-guided surgery after IV injection in metastatic colorectal cancer: a systematic review. Eur J Surg Oncol. 2017;43(9):1656–67.
47. De Vos N, Goethals I, Ceelen W.Clinical value of (18)F-FDG- PET-CT in the preoperative staging of peritoneal carcinomatosis from colorectal origin. Acta Chir Belg. 2014;114(6):370–5.
48. Dromain C, Leboulleux S, Auperin A, Goere D, Malka D, Lumbroso J, et al. Staging of peritoneal carcinomatosis: enhanced CT vs. PET/CT Abdom Imaging. 2008;33(1):87–93.
49. Pasqual EM, Bertozzi S, Bacchetti S, Londero AP, Basso SM, Santeufemia DA, et al. Preoperative assessment of peritoneal carcinomatosis in patients undergoing hyperthermic intraperitoneal chemotherapy follow­ing cytoreductive surgery. Anticancer Res. 2014;34(5):2363–8.
50. Liberale G, Vankerckhove S, Caldon MG, Ahmed B, Moreau M, Nakadi IE, et al. Fluorescence imaging after indocyanine green injection for detection of peritoneal metastases in patients undergoing cytoreductive surgery for peritoneal carcinomatosis from colorectal cancer: a pilot study. Ann Surg. 2016;264(6):1110–5.
51. Lieto E, Auricchio A, Cardella F, Mabilia A, Basile N, Castellano P, etal. Fluorescence-guided surgery in the combined treatment of peritoneal car­cinomatosis from colorectal cancer: preliminary results and consider­ations. World J Surg. 2018;42(4):1154–60.
52. Barabino G, Klein JP, Porcheron J, Grichine A, Coll JL, Cottier M.Intraoperative near-infrared uorescence imaging using indocyanine green in colorectal carcinomatosis surgery: proof of concept. Eur J Surg Oncol. 2016;42(12):1931–7.
53. Baiocchi GL, Gheza F, Molno S, Arru L, Vaira M, Giacopuzzi S. Indocyanine green uorescence-guided intraoperative detection of peritoneal carcinomatosis: systematic review. BMC Surg. 2020;20(1):158.
M. R. Freund et al.
3 Use ofFluorescence Guidance inColorectal Surgery
https://t.me/medicina_free
54. Robinson JR, Newcomb PA, Hardikar S, Cohen SA, Phipps AI.Stage IV colorectal cancer primary site and patterns of distant metastasis. Cancer Epidemiol. 2017;48:92–5.
55. van Gestel YR, de Hingh IH, van Herk-Sukel MP, van Erning FN, Beerepoot LV, Wijsman JH, etal. Patterns of metachronous metastases after curative treatment of colorectal cancer. Cancer Epidemiol. 2014;38(4):448–54.
56. Fong Y, Fortner J, Sun RL, Brennan MF, Blumgart LH.Clinical score for predicting recurrence after hepatic resection for metastatic colorectal cancer: analysis of 1001 consecutive cases. Ann Surg. 1999;230(3):309– 18; discussion 18–21.
57. Van Cutsem E, Cervantes A, Adam R, Sobrero A, Van Krieken JH, Aderka D, etal. ESMO consensus guidelines for the management of patients with metastatic colorectal cancer. Ann Oncol. 2016;27(8):1386–422.
58. Adam R, De Gramont A, Figueras J, Guthrie A, Kokudo N, Kunstlinger F, et al. The oncosurgery approach to managing liver metastases from colorectal cancer: a multidisciplinary international consensus. Oncologist. 2012;17(10):1225–39.
59. Rees M, Tekkis PP, Welsh FK, O’Rourke T, John TG.Evaluation of long­term survival after hepatic resection for metastatic colorectal cancer: a multifactorial model of 929 patients. Ann Surg. 2008;247(1):125–35.
60. Mao Y, Chen B, Wang H, Zhang Y, Yi X, Liao W, etal. Diagnostic perfor­mance of magnetic resonance imaging for colorectal liver metastasis: a systematic review and meta-analysis. Sci Rep. 2020;10(1):1969.
61. Ellebaek SB, Fristrup CW, Mortensen MB.Intraoperative ultrasound as a screening modality for the detection of liver metastases during resection of primary colorectal cancer- a systematic review. Ultrasound Int Open. 2017;3(2):E60–E8.
62. Reinhart MB, Huntington CR, Blair LJ, Heniford BT, Augenstein VA. Indocyanine green: historical context, current applications, and future considerations. Surg Innov. 2016;23(2):166–75.
63. Ishizawa T, Fukushima N, Shibahara J, Masuda K, Tamura S, Aoki T, etal. Real-time identication of liver cancers by using indocyanine green uorescent imaging. Cancer. 2009;115(11):2491–504.
64. van der Vorst JR, Schaafsma BE, Hutteman M, Verbeek FP, Liefers GJ, Hartgrink HH, et al. Near-infrared uorescence- guided resection of colorectal liver metastases. Cancer. 2013;119(18):3411–8.
65. Okusanya OT, Holt D, Heitjan D, Deshpande C, Venegas O, Jiang J, etal. Intraoperative near-infrared imaging can identify pulmonary nodules. Ann Thorac Surg. 2014;98(4):1223–30.
66. Handgraaf HJM, Boogerd LSF, Hoppener DJ, Peloso A, Sibinga Mulder BG, Hoogstins CES, etal. Long-term follow- up after near-infrared uo­rescence-guided resection of colorectal liver metastases: a retrospective multicenter analysis. Eur J Surg Oncol. 2017;43(8):1463–71.
119
120
https://t.me/medicina_free
67. Achterberg FB, Sibinga Mulder BG, Meijer RPJ, Bonsing BA, Hartgrink HH, Mieog JSD, etal. Real-time surgical margin assessment using ICG­uorescence during laparoscopic and robot-assisted resections of colorec­tal liver metastases. Ann Transl Med. 2020;8(21):1448.
68. Aoki T, Murakami M, Koizumi T, Matsuda K, Fujimori A, Kusano T, etal. Determination of the surgical margin in laparoscopic liver resec­tions using infrared indocyanine green uorescence. Langenbeck’s Arch Surg. 2018;403(5):671–80.
69. Tashiro Y, Aoki T, Hirai T, Koizumi T, Mansou DA, Kusano T, et al. Pathological validity of using near-infrared uorescence imaging for securing surgical margins during liver resection. Anticancer Res. 2020;40(7):3873–82.
70. Keating J, Newton A, Venegas O, Nims S, Zeh R, Predina J, etal. Near­infrared intraoperative molecular imaging can locate metastases to the lung. Ann Thorac Surg. 2017;103(2):390–8.
71. Tuech JJ, Pessaux P, Regenet N, Bergamaschi R, Colson A. Sentinel lymph node mapping in colon cancer. Surg Endosc. 2004;18(12):1721–9.
72. Morton DL, Wen DR, Wong JH, Economou JS, Cagle LA, Storm FK, et al. Technical details of intraoperative lymphatic mapping for early stage melanoma. Arch Surg. 1992;127(4):392–9.
73. Rozenholc A, Samouelian V, Warkus T, Gauthier P, Provencher D, Sauthier P, etal. Green versus blue: randomized controlled trial compar­ing indocyanine green with methylene blue for sentinel lymph node detection in endometrial cancer. Gynecol Oncol. 2019;153(3):500–4.
74. Concin N, Matias-Guiu X, Vergote I, Cibula D, Mirza MR, Marnitz S, etal. ESGO/ESTRO/ESP guidelines for the management of patients with endometrial carcinoma. Int J Gynecol Cancer. 2020;31(1):12–39.
75. Emile SH, Elfeki H, Shalaby M, Sakr A, Sileri P, Laurberg S, et al. Sensitivity and specicity of indocyanine green near-infrared uores­cence imaging in detection of metastatic lymph nodes in colorectal can­cer: systematic review and meta-analysis. J Surg Oncol. 2017;116(6):730–40.
76. van der Zaag ES, Bouma WH, Tanis PJ, Ubbink DT, Bemelman WA, Buskens CJ.Systematic review of sentinel lymph node mapping proce­dure in colorectal cancer. Ann Surg Oncol. 2012;19(11):3449–59.
77. Cahill RA, Bembenek A, Sirop S, Waterhouse DF, Schneider W, Leroy J, etal. Sentinel node biopsy for the individualization of surgical strategy for cure of early-stage colon cancer. Ann Surg Oncol. 2009;16(8):2170–
80.
78. Handgraaf HJ, Boogerd LS, Verbeek FP, Tummers QR, Hardwick JC, Baeten CI, etal. Intraoperative uorescence imaging to localize tumors and sentinel lymph nodes in rectal cancer. Minim Invasive Ther Allied Technol. 2016;25(1):48–53.
79. Noura S, Ohue M, Seki Y, Tanaka K, Motoori M, Kishi K, etal. Feasibility of a lateral region sentinel node biopsy of lower rectal cancer guided by
M. R. Freund et al.
3 Use ofFluorescence Guidance inColorectal Surgery
https://t.me/medicina_free
indocyanine green using a near-infrared camera system. Ann Surg Oncol. 2010;17(1):144–51.
80. Liberale G, Vankerckhove S, Galdon MG, Donckier V, Larsimont D, Bourgeois P.Fluorescence imaging after intraoperative intravenous injec­tion of indocyanine green for detection of lymph node metastases in colorectal cancer. Eur J Surg Oncol. 2015;41(9):1256–60.
81. Liberale G, Galdon MG, Moreau M, Vankerckhove S, El Nakadi I, Larsimont D, etal. Ex vivo detection of tumoral lymph nodes of colorec­tal origin with uorescence imaging after intraoperative intravenous injection of indocyanine green. J Surg Oncol. 2016;114(3):348–53.
82. Liberale G, Vankerckhove S, Bouazza F, Gomez Galdon M, Larsimont D, Moreau M, etal. Systemic sentinel lymph node detection using uores­cence imaging after Indocyanine green intravenous injection in colorectal cancer: protocol for a feasibility study. JMIR Res Protoc. 2020;9(8):e17976.
83. Cao Y, Wang P, Wang Z, Zhang W, Lu Q, Butch CJ, etal. A pilot study of near-infrared uorescence guided surgery for primary tumor localization and lymph node mapping in colorectal cancer. Ann Transl Med. 2021;9(16):1342.
84. Hernot S, van Manen L, Debie P, Mieog JSD, Vahrmeijer AL. Latest developments in molecular tracers for uorescence image- guided cancer surgery. Lancet Oncol. 2019;20(7):e354–e67.
85. Gutowski M, Framery B, Boonstra MC, Garambois V, Quenet F, Dumas K, etal. SGM-101: an innovative near-infrared dye- antibody conjugate that targets CEA for uorescence-guided surgery. Surg Oncol. 2017;26(2):153–62.
86. Meijer RPJ, de Valk KS, Deken MM, Boogerd LSF, Hoogstins CES, Bhairosingh SS, etal. Intraoperative detection of colorectal and pancre­atic liver metastases using SGM-101, a uorescent antibody targeting CEA.Eur J Surg Oncol. 2021;47(3 Pt B):667–73.
87. Harlaar NJ, Koller M, de Jongh SJ, van Leeuwen BL, Hemmer PH, Kruijff S, etal. Molecular uorescence-guided surgery of peritoneal car­cinomatosis of colorectal origin: a single-centre feasibility study. Lancet Gastroenterol Hepatol. 2016;1(4):283–90.
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Use ofFluorescence
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Guidance in Cholecystectomy
RyanC.Broderick, DavidRenton, andSantiagoHorgan
Introduction
Laparoscopic cholecystectomy (LC) is widely accepted as the standard of care for cholecystectomy. It is currently the most commonly performed procedure performed by general sur­geons in the United States. Bile duct injuries in the era of lapa­roscopic cholecystectomy range from 0.03% to 0.5% [14]. While infrequent, they represent a signicant patient and healthcare burden when these injuries occur. Cost of treating bile duct injuries can be 4.5 to 26 times the cost of an uncom­plicated procedure with an average 32-day hospitalization and signicant mortality rate [5].
4
Supplementary Information The online version contains supplementary material available at
R. C. Broderick (*) · S. Horgan Division of Minimally Invasive Surgery, Department of Surgery, University of California San Diego, La Jolla, CA, USA e-mail: rbroderick@health.ucsd.edu; shorgan@health.ucsd.edu
D. Renton Center for Minimally Invasive Surgery, The Ohio State University Wexner Medical Center, Columbus, OH, USA e-mail: david.renton@osumc.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_4
https://doi.org/10.1007/978- 3- 031- 40685- 0_4.
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R. C. Broderick et al.
Indocyanine green (ICG) dye is a water-soluble dye with spec­tral absorption at 800 nm. It has been described visualizing the biliary tree since 2008 [6]. When injected intravenously, ICG binds plasma proteins before being rapidly metabolized by hepatocytes and excreted exclusively into the bile; protein-bound ICG uo­resces green when illuminated with near-infrared (NIR) light [6
9]. The excretion of ICG into the biliary tree peaks at 2–4h after
intravenous injection [10]. Dynamic, real-time NIR light capabil­ity is built-in to many modern laparoscopic and robotic cameras. As described elsewhere in this manual, there are also cameras designed to image ICG in open surgery. These cameras are able to toggle between white-light and NIR light with the push of a button, allowing real-time imaging without disrupting surgical workow, especially in the case of laparoscopic or robotic surgery (Figs.4.1,
4.2, and 4.3; video clip attached for video chapter). The technol-
ogy incorporates smoothly into the operation without increased need for stafng or additional supplies in the operative theater.
Through constant reassessment of the anatomy with NIR imaging, surgeons may continuously identify the position of criti­cal biliary structures; these structures are often identiable prior to dissection of peritoneal layer of the gallbladder, providing a safe dissection starting point as well as areas of critical impor­tance. FC offers the potential detailed anatomical mapping of extrahepatic biliary structures and can be a useful adjunct to the critical view of safety [614]. FC allows for surgeons to identify either normal anatomy or anatomic variation prior to dissection
Fig. 4.1 Top panel: white-light laparoscopic view of gallbladder during cho­lecystectomy. Bottom panel: “overlay mode” ICG view of same patient show­ing cystic duct and common bile duct junction
4 Use ofFluorescence Guidance inCholecystectomy
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Fig. 4.2 Top panel: white-light laparoscopic view of gallbladder during cho­lecystectomy prior to peritoneal dissection. Bottom panel: “gray mode” ICG view of same image showing cystic duct, common bile duct, and junction
Fig. 4.3 Use of uorescence cholangiography in robotic surgery. Left panel is traditional bright light view. Right panel is ICG mode highlighting cystic duct, CBD, and CD-CBD junction
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and during active dissection. In contrast, IOC can be time con­suming and involves exposure of the patient and ancillary staff to radiation, with associated increases in cost [15].
Literature Review
Ishizawa etal. described their laparoscopic experience with pre­operative ICG injection for cholangiography during cholecystec­tomy, demonstrating a 100% visualization of the cystic duct and 96% visualization of the common hepatic duct prior to any dissec­tion, which improved to 100% visualization of both structures with dissection [7]. Several other groups have demonstrated simi-
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Table 4.1 Fluorescence cholangiography in laparoscopic cholecystectomy in literature. Reported common bile duct injuries and level of evidence for each study
First author (year)
Ishizawa (2010) 52 0 0 IV Boni (2015) 52 0 0 IV Dip (2015) 45 0 0 IV Osayi (2015) 82 0 0 IV van Dam
(2015) Dip (2016) 70 0 0 0 IV Dip (2019) 318 0 0 1 II Hiwatashi
(2018) Broderick
(2022)
Total patients
37 0 0 IV
65 0 0 7 IV
828 0 0 6 III
Bile duct injuries
Adverse reactions
R. C. Broderick et al.
Conversions to open
Level of evidence
lar ndings during laparoscopic cholecystectomy, as well as dur­ing robotic-assisted laparoscopic cholecystectomy, including in obese individuals [621]. With a growing body of literature, some surgeons have advocated for FC to become the standard of care in laparoscopic cholecystectomy in both elective and emergent cho­lecystectomy.
The highest level evidence conrming uorescent visualization of extrahepatic biliary anatomy was shown in two studies. Dip etal. in 2019 published a single-blind randomized controlled trial comparing FC (n=312) vs LC (n=318) demonstrating that FC was statistically superior in identifying extrahepatic biliary structures [13]. Bile duct injury was zero in FC and two patients in LC; operative times and other complications were not reported. Lim etal. performed a meta­analysis of seven studies comparing biliary anatomy visualization with IOC versus FC.Rates of extrahepatic biliary anatomy identica­tion included cystic duct, common bile duct, CD-CBD junction, and common hepatic duct. FC was safe and effective [14].
Tables 4.1 and 4.2 feature studies evaluating uorescence chol­angiography (FC) during cholecystectomy to evaluate common bile duct injury and operative times. The studies listed are mostly
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