Добавил:
Sekretar
kiopkiopkiop18@yandex.ru
t.me/Prokururor I Вовсе не секретарь, но почту проверяю
Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз:
Предмет:
Файл:Ординатура / Хирургия / @xirurgi_2025 / @xirurgi_2025 - 715 - файл
.pdf
10 Use ofFluorescence Guidance inBurn Surgery
https://t.me/medicina_free
299
Conclusion
Using ICGA precise marking to guide indeterminate burn excision resulted in an excellent rate of complete wound closure and
an improvement in short-term and long-term wound outcomes.
Therefore, ICGA is an effective method to aid decision-making in
burn surgeries of the indeterminate areas. The current level of evidence in using ICGA in burn excision is III.The future direction
should pursue in the randomization of using versus not using
ICGA in the treatment of burn.
References
1. Forjuoh SN. Burns in low- and middle-income countries: a review of
available literature on descriptive epidemiology, risk factors, treatment,
and prevention. Burns. 2006;32(5):529–37.
2. Peck MD, Kruger GE, van der Merwe AE, Godakumbura W, Ahuja
RB. Burns and res from non-electric domestic appliances in low and
middle income countries Part I. The scope of the problem. Burns.
2008;34(3):303–11.
3. James SL, Lucchesi LR, Bisignano C, Castle CD, Dingels ZV, Fox JT,
etal. Epidemiology of injuries from re, heat and hot substances: global,
regional and national morbidity and mortality estimates from the Global
Burden of Disease 2017 study. Inj Prev. 2020;26(Supp 1):i36–45.
4. Peck MD.Epidemiology of burns throughout the world. Part I: distribution and risk factors. Burns. 2011;37(7):1087–100.
5. Jeschke MG, van Baar ME, Choudhry MA, Chung KK, Gibran NS,
Logsetty S.Burn injury. Nat Rev Dis Primers. 2020;6(1):11.
6. Saavedra PAE, De Oliveira Leal JV, Areda CA, Galato D.The costs of
burn victim hospital care around the world: a systematic review. Iran J
Public Health. 2021;50(5):866–78.
7. Kaddoura I, Abu-Sittah G, Ibrahim A, Karamanoukian R, Papazian
N.Burn injury: review of pathophysiology and therapeutic modalities in
major burns. Ann Burns Fire Disasters. 2017;30(2):95–102.
8. Rowan MP, Cancio LC, Elster EA, Burmeister DM, Rose LF, Natesan S,
etal. Burn wound healing and treatment: review and advancements. Crit
Care. 2015;19:243.
9. Orgill DP, Solari MG, Barlow MS, O’Connor NE.A nite-element model
predicts thermal damage in cutaneous contact burns. J Burn Care Rehabil.
1998;19(3):203–9.

300
https://t.me/medicina_free
10. Cheng W, Shen C, Zhao D, Zhang H, Tu J, Yuan Z, etal. The epidemiology and prognosis of patients with massive burns: a multicenter study of
2483 cases. Burns. 2019;45(3):705–16.
11. Uzun I, Akyildiz E, Inanici MA.Histopathological differentiation of skin
lesions caused by electrocution, ame burns and abrasion. Forensic Sci
Int. 2008;178(2–3):157–61.
12. Robins EV. Burn shock. Crit Care Nurs Clin North Am. 1990;2(2):
299–307.
13. Aulick LH, Wilmore DW, Mason AD Jr, Pruitt BA Jr. Inuence of the
burn wound on peripheral circulation in thermally injured patients. Am J
Phys. 1977;233(4):H520–6.
14. Mertens DM, Jenkins ME, Warden GD. Outpatient burn management.
Nurs Clin North Am. 1997;32(2):343–64.
15. Neligan PC.Plastic surgery. 4th ed. Toronto, ON: Elsevier; 2018.
16. Singer AJ, Clark RA. Cutaneous wound healing. N Engl J Med.
1999;341(10):738–46.
17. Tabas I, Glass CK.Anti-inammatory therapy in chronic disease: challenges and opportunities. Science. 2013;339(6116):166–72.
18. Claudinot S, Nicolas M, Oshima H, Rochat A, Barrandon Y.Long-term
renewal of hair follicles from clonogenic multipotent stem cells. Proc
Natl Acad Sci U S A. 2005;102(41):14677–82.
19. Franz MG, Steed DL, Robson MC. Optimizing healing of the acute
wound by minimizing complications. Curr Probl Surg. 2007;44(11):
691–763.
20. Church D, Elsayed S, Reid O, Winston B, Lindsay R.Burn wound infections. Clin Microbiol Rev. 2006;19(2):403–34.
21. Coban YK. Infection control in severely burned patients. World J Crit
Care Med. 2012;1(4):94–101.
22. Branski LK, Al-Mousawi A, Rivero H, Jeschke MG, Sanford AP, Herndon
DN.Emerging infections in burns. Surg Infect. 2009;10(5):389–97.
23. Shupp JW, Pavlovich AR, Jeng JC, Pezzullo JC, Oetgen WJ, Jaskille AD,
etal. Epidemiology of bloodstream infections in burn-injured patients: a
review of the national burn repository. J Burn Care Res. 2010;31(4):
521–8.
24. Hart DW, Wolf SE, Chinkes DL, Beauford RB, Mlcak RP, Heggers JP,
etal. Effects of early excision and aggressive enteral feeding on hypermetabolism, catabolism, and sepsis after severe burn. J Trauma.
2003;54(4):755–61; discussion 61–4.
25. Andel H, Kamolz LP, Horauf K, Zimpfer M. Nutrition and anabolic
agents in burned patients. Burns. 2003;29(6):592–5.
26. Dolp R, Rehou S, Pinto R, Trister R, Jeschke MG.The effect of diabetes
on burn patients: a retrospective cohort study. Crit Care. 2019;23(1):28.
27. Goutos I, Nicholas RS, Pandya AA, Ghosh SJ.Diabetes mellitus and
burns. Part I-basic science and implications for management. Int J Burns
Trauma. 2015;5(1):1–12.
A. Wongkietkachorn et al.

10 Use ofFluorescence Guidance inBurn Surgery
https://t.me/medicina_free
28. Casqueiro J, Casqueiro J, Alves C.Infections in patients with diabetes
mellitus: a review of pathogenesis. Indian J Endocrinol Metab.
2012;16(Suppl 1):S27–36.
29. Goutos I, Sadideen H, Pandya AA, Ghosh SJ.Obesity and burns. J Burn
Care Res. 2012;33(4):471–82.
30. Neaman KC, Andres LA, McClure AM, Burton ME, Kemmeter PR, Ford
RD. A new method for estimation of involved BSAs for obese and
normal- weight patients with burn injury. J Burn Care Res. 2011;32(3):
421–8.
31. Keck M, Lumenta DB, Andel H, Kamolz LP, Frey M.Burn treatment in
the elderly. Burns. 2009;35(8):1071–9.
32. Lewandowski R, Pegg S, Fortier K, Skimmings A.Burn injuries in the
elderly. Burns. 1993;19(6):513–5.
33. Hunt JL, Purdue GF. The elderly burn patient. Am J Surg.
1992;164(5):472–6.
34. Monstrey S, Hoeksema H, Verbelen J, Pirayesh A, Blondeel P.Assessment
of burn depth and burn wound healing potential. Burns. 2008;34(6):
761–9.
35. Heimbach D, Engrav L, Grube B, Marvin J.Burn depth: a review. World
J Surg. 1992;16(1):10–5.
36. Devgan L, Bhat S, Aylward S, Spence RJ.Modalities for the assessment
of burn wound depth. J Burns Wounds. 2006;5:e2.
37. Güler Gürsu K. An experimental study for diagnosis of burn depth.
Burns. 1977;4(2):97–103.
38. Still JM, Law EJ, Klavuhn KG, Island TC, Holtz JZ.Diagnosis of burn
depth using laser-induced indocyanine green uorescence: a preliminary
clinical trial. Burns. 2001;27(4):364–71.
39. Jaskille AD, Ramella-Roman JC, Shupp JW, Jordan MH, Jeng JC.Critical
review of burn depth assessment techniques: part II.Review of laser doppler technology. J Burn Care Res. 2010;31(1):151–7.
40. Sharma VP, O’Boyle CP, Jeffery SL.Man or machine? The clinimetric
properties of laser Doppler imaging in burn depth assessment. J Burn
Care Res. 2011;32(1):143–9.
41. Mileski WJ, Atiles L, Purdue G, Kagan R, Safe JR, Herndon DN, etal.
Serial measurements increase the accuracy of laser Doppler assessment
of burn wounds. J Burn Care Rehabil. 2003;24(4):187–91.
42. Grunwald TB, Garner WL. Acute burns. Plast Reconstr Surg.
2008;121(5):311e–9e.
43. Johnson RM, Richard R.Partial-thickness burns: identication and management. Adv Skin Wound Care. 2003;16(4):178–87; quiz 88–9.
44. Kahn AM, McCrady VL, Rosen VJ.Burn wound biopsy. Multiple uses in
patient management. Scand J Plast Reconstr Surg. 1979;13(1):53–6.
45. Singer AJ, Berruti L, Thode HC Jr, McClain SA. Standardized burn
model using a multiparametric histologic analysis of burn depth. Acad
Emerg Med. 2000;7(1):1–6.
301

302
https://t.me/medicina_free
46. Chvapil M, Speer DP, Owen JA, Chvapil TA.Identication of the depth
of burn injury by collagen stainability. Plast Reconstr Surg.
1984;73(3):438–41.
47. Watts AM, Tyler MP, Perry ME, Roberts AH, McGrouther DA.Burn
depth and its histological measurement. Burns. 2001;27(2):154–60.
48. Saranto JR, Rubayi S, Zawacki BE.Blisters, cooling, antithromboxanes,
and healing in experimental zone-of-stasis burns. J Trauma.
1983;23(10):927–33.
49. Robson MC, Kucan JO, Paik KI, Eriksson E.Prevention of dermal ischemia after thermal injury. Arch Surg. 1978;113(5):621–5.
50. Mladick R, Georgiade N, Thorne F.A clinical evaluation of the use of
thermography in determining degree of burn injury. Plast Reconstr Surg.
1966;38(6):512–8.
51. Lawson RN, Gaston JP.Temperature measurements of localized pathological processes. Ann N Y Acad Sci. 1964;121:90–8.
52. Cole RP, Jones SG, Shakespeare PG.Thermographic assessment of hand
burns. Burns. 1990;16(1):60–3.
53. Liddington MI, Shakespeare PG. Timing of the thermographic assessment of burns. Burns. 1996;22(1):26–8.
54. Goans RE, Cantrell JH Jr, Meyers FB.Ultrasonic pulse-echo determination of thermal injury in deep dermal burns. Med Phys. 1977;4(3):259–
63.
55. Brink JA, Sheets PW, Dines KA, Etchison MR, Hanke CW, Sadove
AM.Quantitative assessment of burn injury in porcine skin with highfrequency ultrasonic imaging. Investig Radiol. 1986;21(8):645–51.
56. Foster FS, Zhang MY, Zhou YQ, Liu G, Mehi J, Cherin E, etal. A new
ultrasound instrument for invivo microimaging of mice. Ultrasound Med
Biol. 2002;28(9):1165–72.
57. Pape SA, Skouras CA, Byrne PO.An audit of the use of laser Doppler
imaging (LDI) in the assessment of burns of intermediate depth. Burns.
2001;27(3):233–9.
58. Essex TJ, Byrne PO.A laser Doppler scanner for imaging blood ow in
skin. J Biomed Eng. 1991;13(3):189–94.
59. Holloway GA Jr, Watkins DW.Laser Doppler measurement of cutaneous
blood ow. J Invest Dermatol. 1977;69(3):306–9.
60. Green HA, Bua D, Anderson RR, Nishioka NS.Burn depth estimation
using indocyanine green uorescence. Arch Dermatol. 1992;128(1):
43–9.
61. Meyerholz DK, Piester TL, Sokolich JC, Zamba GK, Light
TD. Morphological parameters for assessment of burn severity in an
acute burn injury rat model. Int J Exp Pathol. 2009;90(1):26–33.
62. DSouza AV, Lin H, Henderson ER, Samkoe KS, Pogue BW.Review of
uorescence guided surgery systems: identication of key performance
capabilities beyond indocyanine green imaging. J Biomed Opt.
2016;21(8):080901.
A. Wongkietkachorn et al.

10 Use ofFluorescence Guidance inBurn Surgery
https://t.me/medicina_free
63. Moyer HR, Losken A.Predicting mastectomy skin ap necrosis with
indocyanine green angiography: the gray area dened. Plast Reconstr
Surg. 2012;129(5):1043–8.
64. Jerath MR, Schomacker KT, Sheridan RL, Nishioka NS.Burn wound
assessment in porcine skin using indocyanine green uorescence. J
Trauma. 1999;46(6):1085–8.
65. Dissanaike S, Abdul-Hamed S, Griswold JA.Variations in burn perfusion
over time as measured by portable ICG uorescence: a case series. Burns
Trauma. 2014;2(4):201–5.
66. Wongkietkachorn A, Surakunprapha P, Winaikosol K, Waraasawapati S,
Chaiwiriyakul S, Eua-Angkanakul K, etal. Indocyanine green dye angiography as an adjunct to assess indeterminate burn wounds: a prospective, multicentered, triple-blinded study. J Trauma Acute Care Surg.
2019;86(5):823–8.
67. Alander JT, Kaartinen I, Laakso A, Patila T, Spillmann T, Tuchin VV,
etal. A review of indocyanine green uorescent imaging in surgery. Int J
Biomed Imaging. 2012;2012:940585.
68. Hope-Ross M, Yannuzzi LA, Gragoudas ES, Guyer DR, Slakter JS,
Sorenson JA, et al. Adverse reactions due to indocyanine green.
Ophthalmology. 1994;101(3):529–33.
69. Fourman MS, Phillips BT, Crawford L, McClain SA, Lin F, Thode HC Jr,
etal. Indocyanine green dye angiography accurately predicts survival in
the zone of ischemia in a burn comb model. Burns. 2014;40(5):940–6.
70. Hirche C, Engel H, Kolios L, Cognie J, Hunerbein M, Lehnhardt M, etal.
An experimental study to evaluate the Fluobeam 800 imaging system for
uorescence-guided lymphatic imaging and sentinel node biopsy. Surg
Innov. 2013;20(5):516–23.
71. McUmber H, Dabek RJ, Bojovic B, Driscoll DN.Burn depth analysis
using indocyanine green uorescence: a review. J Burn Care Res.
2019;40(4):513–6.
72. Wongkietkachorn A, Surakunprapha P, Winaikosol K, Eua-Angkanakul
K, Wongkietkachorn N, Punyavong P, etal. Quantitative burn depth analysis using indocyanine green angiography. J Burn Care Res.
2019;40(5):725.
73. Engrav LH, Heimbach DM, Reus JL, Harnar TJ, Marvin JA.Early excision and grafting vs. nonoperative treatment of burns of indeterminant
depth: a randomized prospective study. J Trauma. 1983;23(11):1001–4.
74. Wongkietkachorn A, Surakunprapha P, Winaikosol K, Wongkietkachorn
N, Wongkietkachorn S.Precise marking for burn excision by using indocyanine green angiography. Plast Reconstr Surg. 2020;145(1):229e–30e.
75. Arturson G. Pathophysiology of the burn wound. Ann Chir Gynaecol.
1980;69(5):178–90.
76. Wongkietkachorn A, Surakunprapha P, Jenwitheesuk K, Winaikosol K,
Punyavong P, Chowchuen B, etal. Improvement in interpretation of indocyanine green angiography. J Plast Reconstr Aesthet Surg. 2019;73:608.
303

304
https://t.me/medicina_free
77. Wongkietkachorn A, Surakunprapha P, Jenwitheesuk K, Eua-Angkanakul
K, Winaikosol K, Punyavong P, etal. An inconvenient truth of clinical
assessment and indocyanine green angiography precise marking for indeterminate burn excision. Plast Reconstr Surg Glob Open. 2021;9(3):e3497.
78. Wongkietkachorn A, Surakunprapha P, Jenwitheesuk K, Eua-angkanakul
K, Winaikosol K, Punyavong P, etal. An inconvenient truth of clinical
assessment of indeterminate burns and indocyanine green dye angiography precise marking for burn excision: a prospective, multicentered,
triple- blinded study. Plast Reconstr Surg Glob Open. 2020;8(9
Suppl):145–6. https://doi.org/10.1097/01.GOX.0000721084.58676.5d.
79. Cubison TC, Pape SA, Parkhouse N.Evidence for the link between healing time and the development of hypertrophic scars (HTS) in paediatric
burns due to scald injury. Burns. 2006;32(8):992–9.
80. Wongkietkachorn A, Surakunprapha P, Jenwitheesuk K, Eua-Angkanakul
K, Winaikosol K, Punyavong P, etal. Indocyanine Green angiography
precise marking for indeterminate burn excision: a prospective, multicentered, double-blinded study. Plast Reconstr Surg Glob Open.
2021;9(4):e3538.
81. Tenenhaus M, Bhavsar D, Rennekampff HO.Treatment of deep partial
thickness and indeterminate depth facial burn wounds with water-jet
debridement and a biosynthetic dressing. Injury. 2007;38(Suppl 5):S39–
45.
82. Karim AS, Shaum K, Gibson ALF. Indeterminate-depth burn injuryexploring the uncertainty. J Surg Res. 2020;245:183–97.
83. Israel JS, Greenhalgh DG, Gibson AL.Variations in burn excision and
grafting: a survey of the American Burn Association. J Burn Care Res.
2017;38(1):e125–e32.
84. Gurnkel R, Rosenberg L, Cohen S, Cohen A, Barezovsky A, Cagnano E,
etal. Histological assessment of tangentially excised burn eschars. Can J
Plast Surg. 2010;18(3):e33–6.
85. Esselman PC.Burn rehabilitation: an overview. Arch Phys Med Rehabil.
2007;88(12 Suppl 2):S3–6.
86. Goel A, Shrivastava P. Post-burn scars and scar contractures. Indian J
Plast Surg. 2010;43(Suppl):S63–71.
87. Tredget EE, Levi B, Donelan MB.Biology and principles of scar management and burn reconstruction. Surg Clin North Am. 2014;94(4):793–
815.
88. Ong YS, Samuel M, Song C. Meta-analysis of early excision of burns.
Burns. 2006;32(2):145–50.
89. Singer AJ, Boyce ST.Burn wound healing and tissue engineering. J Burn
Care Res. 2017;38(3):e605–e13.
90. Gottrup F, Apelqvist J, Price P.Outcomes in controlled and comparative
studies on non-healing wounds: recommendations to improve the quality
of evidence in wound management. J Wound Care. 2010;19(6):237–68.
A. Wongkietkachorn et al.

10 Use ofFluorescence Guidance inBurn Surgery
https://t.me/medicina_free
91. Gould L, Li WW.Dening complete wound closure: closing the gap in
clinical trials and practice. Wound Repair Regen. 2019;27(3):201–24.
92. Muntean MV, Ardelean F, Strilciuc S, Pestean C, Georgescu AV, Muntean
V.Flap warming improves intraoperative indocyanine green angiography
(ICGA) assessment of perfusion. An experimental study. J Plast Reconstr
Aesthet Surg. 2019;72(7):1150–6.
93. Hettiaratchy S, Dziewulski P.ABC of burns: pathophysiology and types
of burns. BMJ. 2004;328(7453):1427–9.
94. Nielson CB, Duethman NC, Howard JM, Moncure M, Wood JG.Burns:
pathophysiology of systemic complications and current management. J
Burn Care Res. 2017;38(1):e469–e81.
95. Gurtner GC, Jones GE, Neligan PC, Newman MI, Phillips BT, Sacks JM,
etal. Intraoperative laser angiography using the SPY system: review of
the literature and recommendations for use. Ann Surg Innov Res.
2013;7(1):1.
305

Use ofFluorescence
https://t.me/medicina_free
Guidance inAcute Care
11
Surgery andTrauma
ElwinTham, JenniferKnight,
andNovaSzoka
Introduction
Fluorescence-guided surgery (FGS) is a medical imaging technique that uses a uorescent dye or a near-infrared-emitting light
source to identify anatomic structures during surgical procedures.
The present chapter will describe the history and mechanism of
action of indocyanine green (ICG) dye as well as review the use
of uorescence guidance in acute care surgery (ACS) and trauma
surgery. Two of the primary applications of FGS in ACS are ICG
cholangiography during cholecystectomy to dene anatomic
Supplementary Information The online version contains supplementary
material available at
https://doi.org/10.1007/978- 3- 031- 40685- 0_11.
E. Tham · N. Szoka (*)
Department of Surgery, West Virginia University, Morgantown,
WV, USA
e-mail: elwinjennhui.tham@hsc.wvu.edu; nova.szoka@hsc.wvu.edu
J. Knight
Department of Surgery, The Ohio State University,
Werner Medical Center, Columbus, OH, USA
e-mail: Jennifer.knightdavis@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_11
307

308
https://t.me/medicina_free
structures and ICG angiography to evaluate bowel perfusion. In
addition, an evolving area of use for uorescence guidance in
acute care surgery is in the management of wounds and soft tissue
infections. In trauma surgery, the primary application of ICG is
for evaluating tissue perfusion following traumatic injury; however, there are evolving applications for the assessment of other
types of traumatic injuries. ICG dosing and administration, as
well as coding and reimbursement, will be discussed for each
respective procedure.
E. Tham et al.
History andPhysiology ofIndocyanine
GreenDye
Originally employed for the quantitative measurement of hepatic
and cardiac function as early as the mid-1950s, indocyanine
green (ICG) is a nontoxic, uorescent iodide dye with rapid
hepatic clearance. In the initial studies, research centered around
the measurement of serum ICG levels as a method to assess
hepatic and cardiac function. Later studies in the 1970s expanded
the use of ICG to the eld of ophthalmology for macular hole
surgery. Due to technological limitations, the development of
ICG into ICG uorescence angiography did not occur until the
mid-1990s. With further technological advancement in the early
2000s, the development of improved digital imaging resolution
that paralleled lm-based photography resulted in the widespread
acceptance of ICG angiography [1]. Since then, the utility of ICG
angiography for assessing tissue perfusion has been studied, with
numerous ongoing studies assessing other applications of this
compound [1].
ICG is an amphiphilic, tricarbocyanine iodide dye that can be
reconstituted into an aqueous solution of pH 6.5 for intravenous
injection in patients. Once injected, ICG binds to plasma proteins
taken up by the liver and later excreted in bile. Typically, 98% of
injected ICG is plasma protein-bound, while the remaining 2%
remains free in the serum. Free ICG is then transported into the bile
via the enzyme glutathione S-transferase, while bound ICG remains
in the intravascular space for a longer period of time [2–6].
Due to its well-tolerated biopharmacological prole, ICG can be
used in a wide variety of medical applications and has a low inci-

11 Use of Fluorescence Guidance in Acute Care Surgery…
https://t.me/medicina_free
dence of adverse reactions [7]. Adverse reactions from ICG are
commonly mild, with nausea and urticaria being the most common.
The main contraindication to ICG use is iodine allergy. Typical dosing of ICG varies with the procedure, with standard vials containing
25mg of ICG that are reconstituted in 10ml sterile water and each
single milliliter containing 2.5mg of ICG.Individual doses range in
size from 2.5 to 15mg. Standard dosing is far below the lethal dose
(LD50) for this drug, which is 50–80mg/kg [2–8].
Once injected, ICG uorescence has high contrast and sensitivity as the near-infrared light used to measure uorescence makes
tissues appear more translucent allowing visualization through
several millimeters of tissue compared to visible light wavelengths.
This is achieved by the excitation of the molecule via an external
laser or light source, causing it to uoresce at near- infrared wavelengths (750–800nm with a maximum peak of 832nm) [2, 3]. The
near-infrared camera then captures the images and reveals realtime perfusion in the tissue assessed by quantifying the dye’s uorescence, providing objective information regarding which regions
have the best blood supply. Real-time viewing of these images via
video angiography also allows clinicians to make decisions immediately without the need for additional studies [2, 9].
ICG is cleared by the liver at a rate of 18–24% per min. With a
half-life of 3 to 4min, the dye is cleared from the intravascular
space in the rst 10 to 20min after application. The rapid clearance rate allows ICG to be used for multiple injections during a
procedure yielding signicant benets over other analogous substances. Following initial metabolism, the drug clearance rate
slows, allowing trace amounts of ICG to remain in the plasma for
more than an hour [2, 3, 10]. Due to ICG’s hepatic clearance and
excretion into bile, ICG can effectively be used to visualize biliary
anatomy in cholecystectomy [11, 12].
309
Fluorescence Guidance inAcute Care Surgery
ICG inLaparoscopic Cholecystectomy
ICG is being applied as an adjunct to many procedures due to its
ability to improve visualization of surgical anatomy via augmented reality; one such area is minimally invasive cholecystec-
Соседние файлы в папке @xirurgi_2025
