Literature DB >> 34188987

Use of Indocyanine Green Fluorescent Imaging in the Assessment of a Tongue Flap After Lateral Hemiglossectomy.

Lisandro Montorfano1, Stephen J Bordes2,3, Ryan Azarkhail4, Mauricio Sarmiento Cobos1, Michael Medina5.   

Abstract

Indocyanine green (ICG) angiography is a real-time imaging modality that can be used to assess intraoperative tissue perfusion. ICG dye has proven to be feasible, safe, and cost-effective, especially for muscle flaps during complex reconstructions. To our knowledge, we discuss the first use of ICG angiography for the real-time assessment of a tongue flap following left lateral hemiglossectomy. ICG angiography showed excellent perfusion of the tongue and tongue flap, which subsequently led to an uncomplicated postoperative recovery.
Copyright © 2021, Montorfano et al.

Entities:  

Keywords:  hemiglossectomy; icg angiography; indocyanine green; squamous cell carcinoma (scc); tongue flap

Year:  2021        PMID: 34188987      PMCID: PMC8232998          DOI: 10.7759/cureus.15248

Source DB:  PubMed          Journal:  Cureus        ISSN: 2168-8184


Introduction

Reconstruction after tongue cancer surgery can be challenging due to the complex anatomy and physiology of the tongue, depending on the location and extension of the tumor. When surgery is performed, adequate margins (>1 cm) are needed to decrease local recurrence [1]. Patients are often left with a cosmetic deformity. Reconstructions can be completed with local/regional flaps or free flaps. The goal is to achieve the best possible functional and oncologic outcomes. Various technologies have been developed to provide an objective assessment of flap perfusion, including indocyanine green (ICG) fluorescence. ICG is a helpful and safe tool for the assessment of flap perfusion as it is a relatively safe and nontoxic tricarbocyanine dye that allows for real-time visualization [2-4]. We discuss the use of ICG fluorescence for a tongue flap following a lateral hemiglossectomy.

Case presentation

A 51-year-old Caucasian woman, with a history of celiac disease and squamous cell carcinoma of the tongue, came to our institution for a left lateral hemiglossectomy with reconstruction. The patient was brought to the operating room and placed on the table in the supine position. General anesthesia was administered, and the patient was intubated. The patient’s face and neck were then prepped and draped in a sterile fashion. A side gag was placed opposite the tumor. A penetrating towel clamp was used to retract the tongue anteriorly and away from the tumor. We marked a 1 cm margin around the primary lesion. Using a CO2 laser system, we performed a left lateral hemiglossectomy (Figure 1). Hemostasis was attained with cautery (bipolar and monopolar) and 3-0 vicryl suture ligatures for branches of the lingual artery. Once the primary lesion was removed, we resected peripheral mucosal margins and sent them to the pathology department for the frozen section. The frozen sections showed no signs of cancer.
Figure 1

Left lateral hemiglossectomy.

Subsequently, we used ICG fluorescence to determine the viability of the left anterior tongue due to concerns for perfusion, especially at the tip, as an extensive resection across the midline was performed. During the procedure, 1 cc of ICG was administered intravenously followed by a 10 cc flush of normal saline. The tongue was assessed immediately after injection using a Stryker SPY-PHI (Stryker Corporation, Kalamazoo, MI) portable handheld imaging system. ICG fluorescence showed good perfusion of the tongue (Figure 2). We then rotated the tongue posteriorly to cover the defect. This local flap was sutured in place using 3-0 vicryl interrupted sutures (Figure 3). We then used ICG angiography to reassess the flap. The reconstructed tongue had good perfusion (Figure 4). We subsequently performed a bilateral neck dissection. The wounds were irrigated copiously with water and saline. Two 19-French Blake round drains were placed in the neck and secured with 2-0 nylon sutures. Closure of the skin was performed in layers with 3-0 vicryl sutures for the platysma layer and staples for the skin. The patient was awakened and transferred to the recovery room in stable condition. Two weeks later, the patient was seen in the office. No complications from the reconstruction were reported.
Figure 2

ICG angiography showing perfusion of the tongue following left lateral hemiglossectomy.

Successful perfusion is noted by fluorescent green emission. Arrows point to both the tip of the tongue and the left anterior tongue.

ICG: indocyanine green

Figure 3

Tongue flap reconstruction.

Figure 4

Tongue flap perfusion with ICG.

Arrow points to the tip of the tongue.

ICG: indocyanine green

ICG angiography showing perfusion of the tongue following left lateral hemiglossectomy.

Successful perfusion is noted by fluorescent green emission. Arrows point to both the tip of the tongue and the left anterior tongue. ICG: indocyanine green

Tongue flap perfusion with ICG.

Arrow points to the tip of the tongue. ICG: indocyanine green

Discussion

ICG angiography has revolutionized surgeons’ ability to assess tissue perfusion in the operating room. First introduced in the 1950s, ICG is a unique tricarbocyanine dye that allows real-time targeted anatomical visualization due to its high level of contrast against the background, innate ability to be taken up in small concentrations, rapid excretion into the bile, ease of use for prospective clinicians and researchers, low toxicity potential, and affordability [5-7]. Due to its amphiphilic characteristics, ICG has a nonspecific affinity for plasma proteins and blood lipoproteins [8]. The resulting interactions and competition for binding causes aggregation, which subsequently permits ICG to affect the emission spectrum and results in its fluorescent capabilities [8]. ICG fluorescence is best observed within a few seconds of intravenous injection between the wavelengths of 820 and 830 nm on the emission spectrum in vitro [8]. To achieve a plasma concentration of 100 mg/mL, dosages are calculated at 0.5 mg/kg body weight [9]. Furthermore, ICG has demonstrated a rapid clearance (half-life of 3-5 minutes) from the body via first-order kinetics in the form of nonconjugated bile [2,5]. ICG also has a very low toxicity profile, with reported cases of 1/40,000 [6,7,9]. ICG stands as a frontier for further surgical utilization, research, and clinical usage. The application of this imaging modality first gained traction through its vascular applications in ophthalmology, cardiology, and neurosurgery [10]. As continued research and case studies reveal, ICG has proven to be versatile across many specialties. Investigations have highlighted the potential for ICG to be used in postoperative wound care, lymph node biopsy, cancer treatment and detection, evaluation of liver function, and plastic surgery reconstruction [6,7,10]. Vascular patency and quality blood flow are vital for the long-term success and sustainability of any flap. This principle holds particularly true for muscle-only flaps, which exhibit the lowest salvage rate of all flap types [11]. Our case demonstrates the utility of ICG angiography for the real-time intraoperative vascular assessment of a rotational tongue flap following lateral hemiglossectomy. While several studies have described flap perfusion assessment with ICG, our study is the first to highlight the application of ICG angiography exclusively for tongue reconstruction. Upon the initial phase of reconstruction, ICG was used to evaluate blood flow of the left anterior tongue following left lateral hemiglossectomy to rule out any potential vascular compromise. ICG was then used to reassess the vascularization of the tongue following reconstruction. Our patient experienced no postoperative complications. Our study not only asserted the effectiveness of ICG for tongue flap reconstruction but also revealed its potential superiority to pinprick testing. Although simple, quick, and conventional, pinprick testing is largely dependent on physician experience due to the subjective nature of the results [12]. Additionally, bruising at the site can develop in patients who have undergone repeated testing, jeopardizing the reliability of the examination [12]. In the setting of free-flap vascular complications in patients who have undergone microvascular reconstruction, ICG was able to identify intraoperative and postoperative complications at an earlier rate than clinical examination alone; however, data on locoregional flaps is limited [13]. Successful salvage is fundamentally reliant on early detection of potential complications, such as those related to hypoperfusion of tissues. [14]. Our case highlights the feasibility, safety, and efficacy of ICG angiography in determining short-term and long-term flap viability. As ICG angiography continues to grow in use and popularity, future investigations are necessary to accrue clinical outcome data with greater study power and compare ICG angiography to other intraoperative assessment modalities for locoregional tongue flaps.

Conclusions

The use of ICG angiography for the real-time assessment of blood flow is a valuable and feasible tool for the intraoperative assessment of perfusion in extended hemiglossectomies with local flap reconstruction. It may be especially beneficial in cases involving complex reconstructions, and when regional organ hypoperfusion is suspected.
  14 in total

1.  Intraoperative near-infrared fluorescence imaging in perforator flap reconstruction: current research and early clinical experience.

Authors:  Bernard T Lee; Aya Matsui; Merlijn Hutteman; Samuel J Lin; Joshua H Winer; Rita G Laurence; John V Frangioni
Journal:  J Reconstr Microsurg       Date:  2009-12-21       Impact factor: 2.873

2.  Indocyanine green fluorescence angiography for free flap monitoring: A pilot study.

Authors:  Marine Hitier; Jean-Luc Cracowski; Cynthia Hamou; Christian Righini; Georges Bettega
Journal:  J Craniomaxillofac Surg       Date:  2016-09-10       Impact factor: 2.078

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Authors:  Andrea De Gasperi; Ernestina Mazza; Manlio Prosperi
Journal:  World J Hepatol       Date:  2016-03-08

Review 4.  Fluorescence properties and metabolic features of indocyanine green (ICG) as related to angiography.

Authors:  T Desmettre; J M Devoisselle; S Mordon
Journal:  Surv Ophthalmol       Date:  2000 Jul-Aug       Impact factor: 6.048

5.  Analysis of risk factors for flap loss and salvage in free flap head and neck reconstruction.

Authors:  Edward I Chang; Hong Zhang; Jun Liu; Peirong Yu; Roman J Skoracki; Matthew M Hanasono
Journal:  Head Neck       Date:  2015-07-18       Impact factor: 3.147

6.  Endoscopic measurements of free-flap perfusion in the head and neck region using red-excited Indocyanine Green: preliminary results.

Authors:  C S Betz; S Zhorzel; H Schachenmayr; H Stepp; M Havel; V Siedek; A Leunig; C Matthias; C Hopper; U Harreus
Journal:  J Plast Reconstr Aesthet Surg       Date:  2008-11-25       Impact factor: 2.740

7.  Use of Indocyanine Green Angiography for Real-Time Assessment of a Sternocleidomastoid Muscle Flap During Complex Facial Reconstruction.

Authors:  Lisandro Montorfano; Stephen J Bordes; Mauricio Sarmiento Cobos; Emmanuel Alejandro Garcia Lopez; Michael Medina
Journal:  Cureus       Date:  2021-03-18

8.  Utility of Indocyanine Green Angiography to Identify Clinical Factors Associated With Perfusion of Paramedian Forehead Flaps During Nasal Reconstruction Surgery.

Authors:  Mohamed Abdelwahab; Cherian K Kandathil; Sam P Most; Emily A Spataro
Journal:  JAMA Facial Plast Surg       Date:  2019-05-01       Impact factor: 4.611

9.  Intraoperative laser angiography using the SPY system: review of the literature and recommendations for use.

Authors:  Geoffrey C Gurtner; Glyn E Jones; Peter C Neligan; Martin I Newman; Brett T Phillips; Justin M Sacks; Michael R Zenn
Journal:  Ann Surg Innov Res       Date:  2013-01-07

10.  A review of indocyanine green fluorescent imaging in surgery.

Authors:  Jarmo T Alander; Ilkka Kaartinen; Aki Laakso; Tommi Pätilä; Thomas Spillmann; Valery V Tuchin; Maarit Venermo; Petri Välisuo
Journal:  Int J Biomed Imaging       Date:  2012-04-22
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