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Photodynamic eye

Manufactured by Hamamatsu Photonics
Sourced in Japan

The Photodynamic Eye is a specialized lab equipment designed for photometric and spectroscopic analysis. It features a sensitive photodetector and optical system for precise measurement and characterization of light-based phenomena.

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14 protocols using photodynamic eye

1

ICG Lymphography-Guided Lymphaticovenous Anastomosis

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Preoperative ICG lymphography was performed as reported previously. First, 0.2 mL of ICG (Diagnogreen 0.25%; Daiichi Sankyo Pharmaceuticals, Tokyo, Japan) was injected subcutaneously into the bilateral lower extremities of the first and fourth web spaces of the foot and into the lateral and medial malleolus [12 (link),14 (link)]. After the ICG injection, circumferential fluorescent images of lymphatic drainage channels were obtained using an infrared camera system (Photodynamic Eye; Hamamatsu Photonics K.K., Hamamatsu, Japan). LVA was planned in the site with a linear pattern, just distal to the beginning of the dermal backflow region. The subcutaneous vein was detected near the planned area using ultrasonography [15 (link)].
After the skin incision, the lymphatic vessel was identified using an infrared camera system (Photodynamic Eye; Hamamatsu Photonics K.K., Hamamatsu, Japan, LIGHTVISION; Shimazu Corporation, Kyoto, Japan), and was anastomosed to the vein using 12-0 nylon (Figure 1).
The anastomoses were performed with either the conventional technique or the suture-stent technique. After confirmation of the patency of the anastomosis site, the incision site was closed.
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2

Perfusion and Angiographic Assessment of Vascularized Composite Tissue

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Machine perfusion parameters (flow, pressure, pump speed, and temperature) were assessed hourly during perfusion. Core temperature was measured using a 15-mm needle temperature probe (Myocardial 400 needle temp. probe; MTS40015; Smith Medical, Rosmalen, the Netherlands) after flap harvest and after the ex-vivo preservation period. Flaps were weighed after harvest, after the ex-vivo preservation period, and at 7 days after replantation, as both ischemia-reperfusion injury and ex-vivo perfusion could potentially contribute to weight increase of the vascularized composite tissue.30 (link) Flap perfusion was appraised using a near-infrared fluorescence angiography camera (PhotoDynamic Eye; Hamamatsu Photonics, Japan) that recorded the surgical field after each intravenous injection of 5 mg fluorescent marker indocyanine-green (ICG, 5mg/mL, Verdye, Diagnostic Green GmbH, Germany). Spatial distribution of recorded fluorescence intensity throughout the flap was assessed using an algorithm in MATLAB (MathWorks Inc, Natick, Mass.). Near-infrared fluorescence angiography was performed after flap harvest, directly after replantation, and 3 and 7 days after replantation.
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3

ICG Lymphography Characterization of Lymphedema

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ICG lymphography was performed in all cases as follows. First, 0.2 mL of ICG (Diagnogreen 0.25%; Daiichi Sankyo, Tokyo, Japan) was injected subcutaneously into each lower extremity at the first web space of the foot and at the lateral border of the Achilles tendon. Circumferential fluorescent images of the lymphatic drainage channels were then obtained using an infrared camera system (Photodynamic Eye; Hamamatsu Photonics K.K., Hamamatsu, Japan). ICG lymphography images were recorded in the plateau phase (12–18 hours after injection; ie, on the following day) when no further changes in the images obtained would be expected. All ICG lymphography images were reviewed by 2 plastic surgeons working independently. The characteristic lymphography patterns in the thigh and lower leg were then categorized according to anthropometric characteristics. The patients in the obese and nonobese groups were categorized according to whether the lymphedema was primary or secondary.
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4

Lymphedema Evaluation and Treatment

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A small amount (0.25 mg/0.1 mL) of ICG (Diagnogreen Injection, Daiichi Pharmaceutical, Tokyo, Japan) was injected subcutaneously into the first web space in upper extremity lymphedema, lateral malleolus, and the lateral side of the superior edge of the knee in lower extremity lymphedema. Furthermore, 12–18 h after the injection, we observed the ICG lymphography results using a near-infrared imaging device (Photodynamic Eye; Hamamatsu Photonics, Hamamatsu, Japan) and classified them into types Ⅰ to Ⅴ, as reported previously.17 (link) LVA was performed under local anesthesia in all cases along a linear pattern or along the ulnar side of the upper extremity in upper extremity lymphedema, and greater saphenous vein course in lower extremity lymphedema in the area of the dermal backflow pattern.58 (link) The LVA procedures were performed in an end-to-end manner using 11-0 or 12-0 nylon micro sutures under a surgical microscope (Figures S4C and S4D).9 (link)
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5

Flap Perfusion Monitoring and Evaluation

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Flap monitoring (skin colour, temperature and capillary refill) was performed hourly. In the case of abnormal controls, the pedicle was visually inspected and intervention took place if necessary. To visualise the perfusion of flaps, indocyanine-green (ICG) fluorescence angiography was used. ICG is a fluorescent dye that remains in the intravascular compartment after injection. The fluorescent signal can be visualised with a hand-held camera using near-infrared emission (PhotoDynamic Eye, Hamamatsu Photonics, Hamamatsu, Japan) [22 (link)]. A dose of 0.15 mg/kg was administered through the femoral artery line at 30 min, 4 h, 8 h and 12 h after replantation. The percentage of the fluorescent surface was recorded. Porcine arterial blood samples were taken at 1, 6 and 12 h after replantation for analysis of cytokines, CK and blood gas. Flaps were explanted after euthanizing the pigs, weight was recorded and flaps were fixed in buffered formaldehyde for histological sampling.
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6

Lymphatic Imaging of Roxadustat Effects

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Lymphatic structures in the hindlimbs of the control and roxadustat groups were compared by fluorescent lymphography every week for 4 weeks postoperatively (n = 6 per group). Prior to imaging, isoflurane was used to anesthetize the mice and their residual fur was removed. A 5-μL volume of indocyanine green solution (2.5 mg/mL Diagnogreen in distilled water; Daiichi Sankyo Company, Ltd., Tokyo, Japan;) was subcutaneously injected into both paws with a 26-gauge needle. Imaging was performed indocyanine green using a near-infrared fluorescence camera system (Photodynamic Eye; Hamamatsu Photonics, Hamamatsu, Japan) 15 min after indocyanine green injection. The coverage of the fluorescent area (i.e., the dermal backflow at the thigh) was measured using ImageJ software (National Institutes of Health).
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7

Intraoperative Graft Flow Assessment: A Comprehensive Approach

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Intraoperative graft flow measurement was performed using a transit time flow meter (TTFM; VeriQ System, Medistim, Oslo, Norway). Graft flow assessment was performed just before chest closure, and after hemodynamic stabilization, systolic blood pressure was controlled around 120 mmHg and the heart rate was controlled from 60 to 80 bpm. The parameters evaluated with TTFM were MGF (mL/min) and pulsatility index (PI; absolute value, maximal flow − minimal flow/mean flow). We routinely measured MGF and PI with a 3-mm probe and checked the flow pattern and acoustic coupling index (ACI; as a correlate of the quality or reliability of the TTFM measurements) >30%.20) (link) If we thought inappropriate measurements, we changed the probe to a 2- or 4-mm probe as appropriate and checked good flow pattern and ACI >30%.
All grafts were evaluated with intraoperative fluorescence graft imaging with Photodynamic Eye (Hamamatsu Photonics K.K., Shizuoka, Japan) to check whether or not the grafts were successful.
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8

ICG Lymphography Imaging Technique

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A small amount (0.1 mL) of ICG (Diagnogreen Injection, Daiichi Pharmaceutical, Tokyo, Japan) was injected subcutaneously into the first web space, lateral malleolus, and the lateral side of the superior edge of the knee [10 (link)]. Furthermore, 12 to 18 h after the injection, we observed the ICG lymphography results using a near-infrared camera (Photodynamic Eye; Hamamatsu Photonics, Hamamatsu, Japan) and classified them into types I to V, as previously published (Figure 3) [3 (link)].
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9

Infrared Fluorescence Imaging of ICG

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Testing was carried out at a room temperature of 20 °C-25 °C with the patient resting in a supine position; 25 mg ICG (Diagnogreen ™ ; Daiichi-Sankyo Pharmaceutical, Tokyo, Japan) was dissolved in 25 mL distilled water (Otsuka distilled water ™ ; Otsuka Pharmaceutical, Tokyo, Japan) and 0.1 mg/kg of the mixture was injected via the cubital vein. Fluorescence photography was then immediately conducted using an infrared camera system (Photodynamic Eye ™ , Hamamatsu Photonics K.K., Hamamatsu, Japan). Infrared rays activate ICG and emit light weaker than 820 nm (10) . A light-emitting diode of 760 nm was used as the light source to irradiate ICG, with a charge-coupled device (CCD) camera used as the detector. The camera system was placed in a position approximately 20 cm from the skin of the feet, filming was carried out for 5 min following ICG injection, and real-time fluorescence imaging was shown on a monitor and recorded using an audio video interweave system. Thereby, the time-intensity curve was measured. ICG is non-toxic and side effects rarely occur (1/40,000); no abnormalities in the hemodynamics were observed in any case, and the pulse and blood pressure were within normal ranges (11) .
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10

Lymphatic Flow Visualization Protocol

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The injection sites were covered with non-porous black tape to avoid oversaturation of the camera, spreading of ICG on the skin, and an undesirable fluorescent background in the images. Fluorescence imaging of the lymphatic flow was observed by fixing the camera (Photo Dynamic Eye, Hamamatsu®) 15 cm above the investigation field (see supplementary video; supplementary material is available online at www.liebertpub.com/lrb).
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