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
9 Use of Fluorescence Guidance in Plastic and Reconstructive…
https://t.me/medicina_free
• Relative percentage provides information about the uorescence of a selected area relative to a pre-selected reference
point that represents an ideal perfusion of 100%. In general, a
percentage of 15–20% or less indicates poor perfusion which
indicates higher chance of tissue necrosis.
• Absolute measurement utilizing a 255-level grayscale system
which depends on signal intensity. The level reported ranges
from 0 to 255 with a higher level indicating higher perfusion
and a lower level (generally 6.0) indicating lower perfusion.
With the use of optical technologies such as ICG angiography,
there has been signicant improvement in the capacity of:
• Preoperative planning by identifying tissue viability (e.g., perfusion during debridement of bone, muscle perfusion before
and during reconstruction)
• Intraoperative reconstruction by optimizing ap design
• Postoperative evaluation of areas of poor ap perfusion and
anticipation of possible areas of subsequent tissue necrosis
269
Timing ofDye Administration: Preoperative
Considerations
Methylene blue and lymphazurin blue will interfere with imaging.
Likewise, vasoconstrictors such as epinephrine will decrease blood
ow and interfere with imaging. A delay of at least 2h after administration of epinephrine is required before imaging [23], (level of
evidence 5). Factors associated with ischemia include previous
surgery, previous radiation treatment, current smoking, obesity,
diabetes, vasculopathy, chronic steroid use, and thin aps [24, 25].
Timing ofDye Administration: Intraoperative
Considerations
The intraoperative use of image-guided technologies such as ICG
angiography at the time of ap design, ap elevation, ap inset,
and nal closure allows for intraoperative modications such as

270
https://t.me/medicina_free
angiosome mapping (especially useful in random, propeller aps),
excision of distal ap segments with poor perfusion, ap inset
modications (ischemic incision closures, especially in closures
under tension, or in cases of a skin/tissue bridge), or evaluation of
free ap anastomoses, which will all allow for improvement in
reconstructive surgeries.
In our institution, we have been using both SPY-PHI and SPYElite uorescence imaging systems by Stryker/LifeCell. SPY-PHI
refers to the “Portable Handheld Imager.” The imaging head is
positioned prior to the anesthesiologist giving the ICG.The ICG
(25mg) is reconstituted with 10ml of sterile water. This yields a
2.5mg/ml solution of ICG.For plastic, reconstructive, and microsurgery cases, the volume of ICG for images which are acquired
through the patient’s skin is 3–4 ml [7]. ICG is administered
through a peripheral IV and ushed with 10ml of saline immediately prior to imaging. It is often given prior to closing in order to
assess skin perfusion. It can also be utilized preoperatively during
ap design, intraoperatively to assess ap perfusion prior to insetting, and after completion of surgery. We will sometimes use uorescence angiography two or three times during the operation.
Recordings are performed according to the owner’s manual for
SPY-PHI or SPY-Elite [24, 25].
Z. A. Koenig et al.
Timing ofDye Administration: Postoperative
Considerations
In addition to the described traditional methods for evaluation of
tissue perfusion (physical examination, Doppler ultrasound, tactile
feedback), technologies such as the SPY-Q system can provide
objective data of tissue perfusion and vascular anastomosis patency
(such as use to evaluate venous thrombosis at the anastomosis) and
even allow evaluation of neovascularization of a ap to determine
if a pedicled ap is ready for division and insetting [26], (level of
evidence 4).
Our institutional experience and literature review shows that
the use of ICG uorescence angiography allows early detection of
tissue with compromised vascularity and minimizes the risks of

9 Use of Fluorescence Guidance in Plastic and Reconstructive…
https://t.me/medicina_free
postoperative partial or total necrosis, which can lead to further
surgeries, surgical revisions, poor outcomes, and increased morbidity.
271
Documentation andMedical Coding
Appropriate coding and documentation are essential for reimbursement for uorescence angiography. The American Medical
Association Current Professional Terminology (CPT) Professional
Codebook 2022 lists 15,860 as the appropriate code. CPT code
15860 is dened as “intravenous injection of agent (e.g., uorescein) to test vascular ow in ap or graft.” In this case, the agent
is ICG.There are no additional codes for the intraoperative laser
angiography. CPT codes 99,240 and 99,242 refer to ICG angiography specically for ophthalmology and are not appropriate for
aps elsewhere on the body [27].
According to the 2022 National Physician Fee Schedule
Relative Value File, CPT code 15860 has a corresponding work
relative value unit (RVU) of 1.95 and a facility total RVU of 3.14
[28]. To best ensure reimbursement, copies of intraoperative angiography images must be retained and placed in the patient’s medical record.
Conclusion
The use of image-guided surgery such as SPY-Q system in
extremity reconstruction, not only by plastic surgeons but also by
surgeons in associated departments such as orthopedic surgery,
general surgery, trauma surgery, vascular surgery, and otolaryngology, allows improvement in tissue salvage through reliable
debridement, improvement in function, and better treatment planning. Such technologies are useful in all settings (preoperatively,
intraoperatively, and postoperatively) and help facilitate decisions
of ap design, ap assessment, and early detection of potential
tissue necrosis, decreasing additional surgeries and morbidity.

272
https://t.me/medicina_free
Z. A. Koenig et al.
Overall, the use of uorescence angiography reduces complications and improves outcomes [29].
References
1. Burns PB, Rohrich RJ, Chung KC.The levels of evidence and their role
in evidence-based medicine. Plast Reconstr Surg. 2011;128(1):305–10.
https://doi.org/10.1097/PRS.0b013e318219c171.
2. Lohman RF, Ozturk CN, Ozturk C, Jayaprakash V, Djohan R. An analysis of
current techniques used for intraoperative ap evaluation. Ann Plast Surg.
2015;75(6):679–85. https://doi.org/10.1097/SAP.0000000000000235.
3. Ludolph I, Horch RE, Arkudas A, Schmitz M.Enhancing safety in reconstructive microsurgery using intraoperative indocyanine green angiography. Front Surg. 2019;6:39. https://doi.org/10.3389/fsurg.2019.00039.
4. Obana A, Miki T, Hayashi K, etal. Survey of complications of indocyanine green angiography in Japan. Am J Ophthalmol. 1994;118(6):749–
53. https://doi.org/10.1016/s0002- 9394(14)72554- 1.
5. Holm C, Tegeler J, Mayr M, Becker A, Pfeiffer UJ, Mühlbauer
W.Monitoring free aps using laser-induced uorescence of indocyanine
green: a preliminary experience. Microsurgery. 2002;22(7):278–87.
https://doi.org/10.1002/micr.10052.
6. Hitier M, Cracowski JL, Hamou C, Righini C, Bettega G.Indocyanine
green uorescence angiography for free ap monitoring: a pilot study. J
Craniomaxillofac Surg. 2016;44(11):1833–41. https://doi.org/10.1016/j.
jcms.2016.09.001.
7. Mothes H, Dönicke T, Friedel R, Simon M, Markgraf E, Bach
O.Indocyanine- green uorescence video angiography used clinically to
evaluate tissue perfusion in microsurgery. J Trauma. 2004;57(5):1018–
24. https://doi.org/10.1097/01.ta.0000123041.47008.70.
8. Dietz MJ, Hare JT, Ueno C, Prud’homme BJ, Boyd JW. Laser-assisted
uorescent angiography to assess tissue perfusion in the setting of traumatic elbow dislocation. Wounds Compend Clin Res Pract.
2018;30(10):E93–7.
9. Green JM, Sabino J, Fleming M, Valerio I. Intraoperative plastic and
reconstructive surgery: a review of applications and outcomes in warrelated trauma. Mil Med. 2015;180(3 Suppl):37–43. https://doi.
org/10.7205/MILMED- D- 14- 00632.
10. Graham BH, Walton RL, Elings VB, Lewis FR.Surface quantication of
injected uorescein as a predictor of ap viability. Plast Reconstr Surg.
1983;71(6):826–33. https://doi.org/10.1097/00006534-
198306000- 00016.
11. Still J, Law E, Dawson J, Bracci S, Island T, Holtz J.Evaluation of the
circulation of reconstructive aps using laser-induced uorescence of

9 Use of Fluorescence Guidance in Plastic and Reconstructive…
https://t.me/medicina_free
indocyanine green. Ann Plast Surg. 1999;42(3):266–74. https://doi.
org/10.1097/00000637- 199903000- 00007.
12. Holzbach T, Taskov C, Henke J, et al. Evaluation of perfusion in skin
aps by laser-induced indocyanine green uorescence. Handchir
Mikrochir Plast Chir. 2005;37(6):396–402. https://doi.
org/10.1055/s- 2005- 872986.
13. Krishnan KG, Schackert G, Steinmeier R.The role of near-infrared angiography in the assessment of post-operative venous congestion in random
pattern, pedicled Island and free aps. Br J Plast Surg. 2005;58(3):330–8.
https://doi.org/10.1016/j.bjps.2004.10.003.
14. Yano T, Okazaki M, Tanaka K, Tsunoda A, Aoyagi M, Kishimoto S.Use
of intraoperative uorescent indocyanine green angiography for real-time
vascular evaluation of pericranial aps. Ann Plast Surg. 2016;76(2):198–
204. https://doi.org/10.1097/SAP.0000000000000519.
15. Nergård S, Mercer JB, de Weerd L.Impact on abdominal skin perfusion
following abdominoplasty. Plast Reconstr Surg Glob Open.
2021;9(1):e3343. https://doi.org/10.1097/GOX.0000000000003343.
16. Patel KM, Bhanot P, Franklin B, Albino F, Nahabedian MY.Use of intraoperative indocyanin-green angiography to minimize wound healing
complications in abdominal wall reconstruction. J Plast Surg Hand Surg.
2013;47(6):476–80. https://doi.org/10.3109/2000656X.2013.787085.
17. Swanson E.Comparison of limited and full dissection abdominoplasty
using laser uorescence imaging to evaluate perfusion of the abdominal
skin. Plast Reconstr Surg. 2015;136(1):31e–43e. https://doi.org/10.1097/
PRS.0000000000001376.
18. Mayr M, Holm C, Höfter E, Becker A, Pfeiffer U, Mühlbauer W.Effects
of aesthetic abdominoplasty on abdominal wall perfusion: a quantitative
evaluation. Plast Reconstr Surg. 2004;114(6):1586–94. https://doi.
org/10.1097/01.prs.0000138757.33998.ee.
19. Colavita PD, Wormer BA, Belyansky I, etal. Intraoperative indocyanine
green uorescence angiography to predict wound complications in complex ventral hernia repair. Hernia. 2016;20(1):139–49. https://doi.
org/10.1007/s10029- 015- 1411- 4.
20. Burnier P, Niddam J, Bosc R, Hersant B, Meningaud JP. Indocyanine
green applications in plastic surgery: a review of the literature. J Plast
Reconstr Aesthetic Surg. 2017;70(6):814–27. https://doi.org/10.1016/j.
bjps.2017.01.020.
21. Cornelissen AJM, van Mulken TJM, Graupner C, et al. Near-infrared
uorescence image-guidance in plastic surgery: a systematic review. Eur
J Plast Surg. 2018;41(3):269–78. https://doi.org/10.1007/s00238- 018-
1404- 5.
22. Holm C, Mayr M, Höfter E, Becker A, Pfeiffer UJ, Mühlbauer
W. Intraoperative evaluation of skin-ap viability using laser-induced
uorescence of indocyanine green. Br J Plast Surg. 2002;55(8):635–44.
https://doi.org/10.1054/bjps.2002.3969.
273

274
https://t.me/medicina_free
23. Gurtner GC, Jones GE, Neligan PC, etal. Intraoperative laser angiography using the SPY system: review of the literature and recommendations
for use. Ann Surg Innov Res. 2013;7:1. https://doi.org/10.1186/1750-
1164- 7- 1.
24. SPY Elite imaging system (Lifecell) operator’s manual. Stryker. 2013.
https://www.stryker.com/us/en/endoscopy/products/spy- elite.html.
Accessed 16 Feb 2022.
25. SPY Portable Hand Imaging System (PHI) operator’s manual. Stryker.
2019. https://www.stryker.com/us/en/endoscopy/products/spy- phi.html.
Accessed 16 Feb 2022.
26. Mandelbaum M, Lakhiani C, Lenert JJ.Is 21 days too short? Utility of
indocyanine green angiography in predicting successful cross-leg ap
division in the compromised lower extremity. Plast Reconstr Surg.
2021;147(5):919e–20e. https://doi.org/10.1097/PRS.0000000000007872.
27. CPT Professional 2022. American Medical Association (AMA); 2021.
28. 2022 National Physician Fee Schedule Relative Value File. Centers for
Medicare and Medicaid Services. 2021. https://www.cms.gov/
medicaremedicare- fee- service- paymentphysicianfeeschedpfs- relativevalue- les/rvu22a. Accessed 16 Feb 2022.
29. Liu DZ, Mathes DW, Zenn MR, Neligan PC.The application of indocyanine green uorescence angiography in plastic surgery. J Reconstr
Microsurg. 2011;27(6):355–64. https://doi.org/10.1055/s- 0031- 1281515.
Z. A. Koenig et al.

Use ofFluorescence
https://t.me/medicina_free
Guidance inBurn Surgery
ApinutWongkietkachorn,
PalakornSurakunprapha,
SupawichWongkietkachorn,
SarinyaBoonpoapichart,
andPhacharaLongmeewong
Introduction
Burn injuries are a signicant global public health issue because
of their high frequency and potentially severe physical, emotional,
and economical effects on people, households, and communities
[1, 2]. Burns from re, heat, and hot substances rank fourth among
all civilian traumatic injuries in the globe, after falls, trafc accidents, and interpersonal violence [2]. According to the estimation,
there are between 7 and 12 million people (up to 33,000 every
Supplementary Information The online version contains supplementary
material available at
https://doi.org/10.1007/978- 3- 031- 40685- 0_10.
10
A. Wongkietkachorn (*)
Division of Plastic and Reconstructive Surgery, Department of Surgery,
Faculty of Medicine, Mae Fah Luang University, Chiang Rai, Thailand
P. Surakunprapha · S. Boonpoapichart · P. Longmeewong
Division of Plastic and Reconstructive Surgery, Department of Surgery,
Faculty of Medicine, Khon Kaen University, Khon Kaen, Thailand
e-mail: palsur@kku.ac.th; L_phachara@kkumail.com
S. Wongkietkachorn
Department of Surgery, Police General Hospital, Bangkok, Thailand
© 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_10
275

276
https://t.me/medicina_free
day) suffering each year from burn injuries that necessitate medical attention, cause extended absences from work or school, or
even result in death [3]. In contrast, the incidence of burn injuries
is higher than the combined incidence of tuberculosis and human
immunodeciency virus (HIV/AIDS), and it is close to the incidence of all malignant neoplasms [4].
Burns result in high morbidity and cost [5]. Nonfatal burns are
the main cause of morbidity, which includes extended hospital
stays, disgurement, and disability, frequently with associated
rejection and social stigmata [2]. According to a recent study, burn
injuries have an impact on morbidity and mortality for at least 5 to
10years following the injury [5]. The overall cost of hospital care
per patient ranged from US$ 10.58 to US$ 125,597.86 [6]. The
cost of 1% of total body surface area burned varied from US$ 2.65
to US$ 11,245.04, and the cost of hospital care per day varied
from US$ 24.23 to US$ 4125.50 [6].
This chapter will discuss on the knowledge of burn wound
evaluation, various methods of burn determination, the limitation
of burn depth determination, and a thorough review of the development, fundamentals, and evidence base for using ICGA precise
marking for burn wound evaluation and excision in clinical
practice.
A. Wongkietkachorn et al.
Pathophysiology ofBurn Wounds
Burn wounds result from accidental injury to the human body by
various etiologies such as heat, electricity, friction, chemicals, or
radiation [7]. Thermal injury is reported to be the most common [8].
The extent of thermal injury correlates with the contact time, temperature, and skin thickness of the damaged area [9]. Thermal burns
can be produced by ames, hot objects, liquids, and steam [10].
The pathophysiology of burns can be classied into two levels: local changes and systemic changes [7]. Local tissues are
damaged when the tissue came into contact with the thermal
source resulting in heat transfer. This induces coagulative necrosis, intraepidermal separation, or dermoepidermal separation
[11]. Burns lead to systemic changes when the injury reaches

10 Use ofFluorescence Guidance inBurn Surgery
https://t.me/medicina_free
277
approximately 20% of total body surface area (TBSA) [12]. The
consequences are signicant hypovolemia and the release of
numerous inammatory mediators resulting in a cardiovascular
insufciency known as burn shock [12, 13]. Burn shock is a com-
plicated circulatory and microcirculatory failure process that
causes generalized edema in both injured and uninjured body
parts. Although the patient is appropriately resuscitated, the burn
shock remains irreversible in some severe cases.
Burn wounds are categorized based on the depth of tissue
injury, which determines the burn management to be either conservative or operative. Burn depth is classied into four categories: epidermal, supercial partial-thickness, deep
partial-thickness, and full-thickness skin loss [14, 15]. Epidermal
burns involve only the epidermis. The typical etiology is sunburn.
The wounds appear erythematous, painful, and blanch with pressure. Supercial partial-thickness burns affect the supercial part
of the dermis, with scald burn being the most frequent etiology.
These wounds are erythematous and tender, and blisters can
appear up to 24h after the injury. Deep partial-thickness burns
involve the deep part of the dermis, where hair follicles and glandular tissue are located. This kind of burn wound is not painful
unless the burn area is pressured with signicant force. These
wounds contain variously mottled colorization from patchy white
to red, and they were not blanched with the pressure. Finally, fullthickness burns, the deepest degree, involve the epidermis and all
layers of the dermis. A diverse wound color can be observed, such
as waxy white, leathery gray, charred, and dark black. The wound
is dry, inelastic, and painless. It does not blanched with pressure.
There are several factors affecting the treatment of burn wounds.
Inammatory and anti-inammatory medications can disturb the
healing process [16, 17]. Inammation is the early phase of wound
healing. When the inammatory mediators are released, they stimulate immune signals, causing the engagement of leukocytes and
macrophages, which primarily start the proliferation phase of
inammation [16]. These cytokines from the inammatory process activate keratinocytes and broblasts to migrate from the hair
follicles to the injury area, consequently aiding wound reepithelialization [18]. Thus, inammation is vital for the success of burn

278
https://t.me/medicina_free
A. Wongkietkachorn et al.
wound healing. Anti-inammatory treatments can worsen the
wound healing mechanism and prolong the healing process [17].
For example, conventional anti- inammatory therapy, such as
nonsteroidal anti-inammatory drugs or steroids, inhibits prostaglandin synthesis, which inevitably impairs wound healing [19].
Infection can also impair burn wound healing [20]. The skin is
a vital organ, which serves as a barrier to protect the external environment, maintain body temperature and homeostasis, provide
sensory detection, and provide metabolic and immunological support. Destruction of this vital organ damages the innate immunological response and increases the risk of infection [20]. Therefore,
burn patients are certainly at a higher risk of infection [21]. When
burn patients are hospitalized long enough to get infected by
drug-resistant organisms, the infection process prolongs the hospital stay, delays the wound healing, increases hospital cost, and
increases mortality [22, 23].
Nutrition contributes to proper burn wound healing [24].
Minimizing the consequence of hypermetabolism and supplying
adequate nutritional support are the main components that contribute to the appropriate wound healing process and recovery [25].
The following health factors can also impact burn severity and
the burn recovery process: diabetes, obesity, and geriatric status.
Diabetes mellitus signicantly affects burn patients [26]. It impairs
the body’s ability to deal with stress due to glucose- related cell,
end-organ, and vascular damage, which deteriorates clinical outcomes in admitted patients [27]. The hyperglycemic state injures
the immune cells causing their function to be impaired. This distinctly leads to a greater risk of infection in diabetic patients [28],
which is one of the lethal complications in burns [20].
Patients with excessive adiposity can also have altered physiological responses in burns, thus are considered a challenge in
burn treatment [29]. Burn patients with obesity usually have multiple comorbidities, including diabetes mellitus, hypertension,
cardiovascular disease, and lung disease [29]. Even with a burn
assessment tool, for example, the Lund-Browder chart, the body
surface area can be misinterpreted due to the deviated body mass
distribution in obesity [30].
Соседние файлы в папке @xirurgi_2025
