Добавил:
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
Скачиваний:
0
Добавлен:
29.08.2026
Размер:
16 Мб
Скачать
10 Use ofFluorescence Guidance inBurn 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, etal. 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, etal. 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, etal. 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. Inuence 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-inammatory 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, etal. 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, etal. 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 ofFluorescence Guidance inBurn 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, Safe JR, Herndon DN, etal. 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: identication 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.Identication 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, etal. A new ultrasound instrument for invivo 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: identication of key performance capabilities beyond indocyanine green imaging. J Biomed Opt. 2016;21(8):080901.
A. Wongkietkachorn et al.
10 Use ofFluorescence Guidance inBurn Surgery
https://t.me/medicina_free
63. Moyer HR, Losken A.Predicting mastectomy skin ap necrosis with indocyanine green angiography: the gray area dened. 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, etal. 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, etal. 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, etal. 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, etal. 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, etal. 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, etal. 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, etal. 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, etal. 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, etal. 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. Gurnkel R, Rosenberg L, Cohen S, Cohen A, Barezovsky A, Cagnano E, etal. 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 ofFluorescence Guidance inBurn Surgery
https://t.me/medicina_free
91. Gould L, Li WW.Dening 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, etal. 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 ofFluorescence
https://t.me/medicina_free
Guidance inAcute Care
11
Surgery andTrauma
ElwinTham, JenniferKnight, andNovaSzoka
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 dene 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 andPhysiology ofIndocyanine GreenDye
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 [26].
Due to its well-tolerated biopharmacological prole, 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 25mg of ICG that are reconstituted in 10ml sterile water and each single milliliter containing 2.5mg of ICG.Individual doses range in size from 2.5 to 15mg. Standard dosing is far below the lethal dose (LD50) for this drug, which is 50–80mg/kg [28].
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 (750–800nm with a maximum peak of 832nm) [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 4min, the dye is cleared from the intravascular space in the rst 10 to 20min after application. The rapid clear­ance rate allows ICG to be used for multiple injections during a procedure yielding signicant benets 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 inAcute Care Surgery
ICG inLaparoscopic 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