Mice were anesthetized with a mixture of xylazine (6 mg/kg) and ketamine (100 mg/kg), and pupils were dilated with topical drops of Cyclomydril (Alcon Laboratories, Fort Worth, TX). Two minutes after pupil dilation, lubricating eye drops (Alcon Laboratories) were applied to the cornea. The fundus was viewed with an imaging camera, and laser photocoagulation was induced using the image-guided laser system (Micron IV, Phoenix Research Laboratories, Pleasanton, CA). The fundus image as well as the aiming beam can be observed on the monitor screen. Four laser burns at equal distance from the optic nerve were induced one by one in each eye by a green Argon laser pulse with a wavelength of 532 nm, a fixed diameter of 50 μm, duration of 70 ms, and varying power levels from 180 mW to 360 mW. If necessary, an orienting laser shot can also be generated approximately three times of the diameter of the optic nerve to help determine the relative positions of the lesions in an eye. After laser photocoagulation, the eyes were gently rinsed with sterile saline to remove the lubricating eye drops and treated with an antibiotic ointment, erythromycin (Fougera, Melville, NY). Mice were then placed on a pre-warmed warming plate at 35°C after the laser treatment until they awakened.
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Therapeutic or Preventive Procedure
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Light Coagulation
Light Coagulation
Light coagulation is a medical procedure that uses focused light energy to precisely target and coagulate, or fuse, specific tissue.
This technique is commonly used in ophthalmology, dermatology, and other medical fields to treat a variety of conditions, such as retinal tears, vascular lesions, and skin conditions.
The process involves directing a controlled beam of light, such as a laser, onto the targeted area, causing the tissue to heat up and fuse together.
Light coagulation is a minimally invasive procedure that can often be performed on an outpatient basis, with a relatively quick recovery time for the patient.
It is an important tool in the clinician's arsenal for diagnosing and treating a range of medical issues in a targeted and effeictive manner.
This technique is commonly used in ophthalmology, dermatology, and other medical fields to treat a variety of conditions, such as retinal tears, vascular lesions, and skin conditions.
The process involves directing a controlled beam of light, such as a laser, onto the targeted area, causing the tissue to heat up and fuse together.
Light coagulation is a minimally invasive procedure that can often be performed on an outpatient basis, with a relatively quick recovery time for the patient.
It is an important tool in the clinician's arsenal for diagnosing and treating a range of medical issues in a targeted and effeictive manner.
Most cited protocols related to «Light Coagulation»
Antibiotics
Argon Ion Lasers
Burns
Cornea
Erythromycin
Eye
Eye Drops
Ketamine
Light Coagulation
Lubricant Eye Drops
Mice, House
Mydriasis
Ointments
Optic Nerve
Pulse Rate
Pupil
Saline Solution
Sterility, Reproductive
Xylazine
Disease Progression
Eligibility Determination
Eye
Light Coagulation
Ranibizumab
Triamcinolone
Visual Acuity
Animals
Argon Ion Lasers
Bruch Membrane
Contact Lenses
Exanthema
Food
Ketamine
Light Coagulation
Mice, House
Mice, Inbred C57BL
Molar
Needles
Optic Nerve
Phenylephrine Hydrochloride
Pupil
Sulfate, Atropine
Tail
Treatment Protocols
Veins
Vision
Xylazine
FFA to determine leakage (not to determine lesion size) was performed with the retinal imaging microscope (Micron IV, Phoenix Research Laboratories) 6 days after laser photocoagulation. Mice were anesthetized, pupils dilated, and intraperitoneally injected with fluorescein AK-FLUOR (Akorn, Lake Forest, IL) at 5 μg/g body weight. Fluorescent fundus images were taken with the retinal imaging microscope at 5 and 10 minutes after fluorescein injection. The fluorescent intensity of CNV lesions was graded using ImageJ (National Institutes of Health, Bethesda, MD) by masked researchers [12 (link)], and the difference of fluorescent intensity between 5 and 10 minute images were recorded as an indicator of CNV vascular leakage.
Blood Vessel
Body Weight
Fluorescein
Forests
Light Coagulation
Microscopy
Mus
Pupil
Retina
Angina, Unstable
Blindness
Cardiovascular System
Cerebrovascular Accident
Committee Members
Congestive Heart Failure
Continuous Renal Replacement Therapy
Creatinine
Diabetes Mellitus
EGFR protein, human
Heart
Hemoglobin, Glycosylated
Hospitalization
Kidney
Kidney Diseases
Light Coagulation
Myocardial Infarction
Neoplasms
Pancreatitis
PER1 protein, human
Retina
Retinal Diseases
Serum
Vitreous Hemorrhage
Most recents protocols related to «Light Coagulation»
The records of 352 patients who underwent PRP due to PDR in one eye Department of Retina Beyoglu Eye Training and Research Hospital between January and March 2021 were reviewed retrospectively. Patients who underwent PRP in one eye but not in the other eye were included in the study. Patients who had previous ocular surgery, patients using steroids or other anti-inflammatory drugs, patients who received anti-VEGF therapy in the past month, patients with a history of ocular trauma/uveitis, and patients with vitreous hemorrhage, macular edema, tractional retinal detachment, and patients with HbA1c higher than 8.0 were excluded from the study. PRP applied eyes were taken as the study group and the other PRP-naive eyes were taken as the control group.
The study was carried out in accordance with the Declaration of Helsinki and was approved by the University of Health Sciences Hamidiye Scientific Research Ethics Committee with the decision number 13/2 on May 13, 2022. Informed consent was obtained from all patients in the study.
All patients underwent a full ophthalmologic examination before retinal photocoagulation. The best corrected visual acuity, IOP measured by Goldmann applanation tonometry, biomicroscopy, and dilated fundus examination findings were recorded. The other systemic/ocular diseases, surgeries, and drug use were questioned.
Retinal photocoagulation was performed with the pattern scan laser (PASCAL) system (PASCAL Synthesis, Topcon Medical Laser Systems, Santa Clara, CA) with a 200 micron spot size and an exposure time of 20–30 ms. The laser power was started with 200 mW and increased until a gray-white lesion was formed on the retina. 1000–1200 numbers of pulse were made in a single session. Any medication was not administered after PRP.
The laser flare meter (FC-700, Kowa Co. Ltd, Tokyo, Japan) was used to measure flare of aqueous humor. Measurements were performed by the same clinician. The mean of five consecutive reliable measurements was taken as the aqueous flare value. The values of flare meter were expressed as photon counts per millisecond (pc/ms).
Laser flare photometry and Goldmann applanation tonometry were both performed just before PRP and at the 1st and 24th h after PRP. At each visit, measurements were performed in both eyes consecutively and the other eye was accepted as the control eye.
“Statistical Package for the Social Sciences” version 20 software was used for statistical analysis. Continuous variables were reported as mean, standard deviation, and range. Categorical variables were expressed as absolute numbers and percentages. After evaluating the normality of the data with the Shapiro–Wilk test; the repeated measures analysis of variance (ANOVA) test with Greenhouse-Geisser correction was used to compare the values before and after retinal photocoagulation. If there was a significant difference with the repeated measures ANOVA test, Bonferroni correction was used to adjust of pairwise comparisons. Comparisons with the control eyes were made using an independent sample t-test. The correlation between variables was evaluated with the Pearson correlation coefficient. If p<0.05, the difference between values was considered statistically significant.
The study was carried out in accordance with the Declaration of Helsinki and was approved by the University of Health Sciences Hamidiye Scientific Research Ethics Committee with the decision number 13/2 on May 13, 2022. Informed consent was obtained from all patients in the study.
All patients underwent a full ophthalmologic examination before retinal photocoagulation. The best corrected visual acuity, IOP measured by Goldmann applanation tonometry, biomicroscopy, and dilated fundus examination findings were recorded. The other systemic/ocular diseases, surgeries, and drug use were questioned.
Retinal photocoagulation was performed with the pattern scan laser (PASCAL) system (PASCAL Synthesis, Topcon Medical Laser Systems, Santa Clara, CA) with a 200 micron spot size and an exposure time of 20–30 ms. The laser power was started with 200 mW and increased until a gray-white lesion was formed on the retina. 1000–1200 numbers of pulse were made in a single session. Any medication was not administered after PRP.
The laser flare meter (FC-700, Kowa Co. Ltd, Tokyo, Japan) was used to measure flare of aqueous humor. Measurements were performed by the same clinician. The mean of five consecutive reliable measurements was taken as the aqueous flare value. The values of flare meter were expressed as photon counts per millisecond (pc/ms).
Laser flare photometry and Goldmann applanation tonometry were both performed just before PRP and at the 1st and 24th h after PRP. At each visit, measurements were performed in both eyes consecutively and the other eye was accepted as the control eye.
“Statistical Package for the Social Sciences” version 20 software was used for statistical analysis. Continuous variables were reported as mean, standard deviation, and range. Categorical variables were expressed as absolute numbers and percentages. After evaluating the normality of the data with the Shapiro–Wilk test; the repeated measures analysis of variance (ANOVA) test with Greenhouse-Geisser correction was used to compare the values before and after retinal photocoagulation. If there was a significant difference with the repeated measures ANOVA test, Bonferroni correction was used to adjust of pairwise comparisons. Comparisons with the control eyes were made using an independent sample t-test. The correlation between variables was evaluated with the Pearson correlation coefficient. If p<0.05, the difference between values was considered statistically significant.
Anabolism
Anti-Inflammatory Agents
Aqueous Flare
Edema, Macular
Ethics Committees, Research
Eye
Eye Injuries
Light Coagulation
Operative Surgical Procedures
Patients
Pharmaceutical Preparations
Photometry
Pulse Rate
Radionuclide Imaging
Retina
Retinal Detachment
Slit Lamp
Steroids
Therapeutics
Tonometry, Ocular
Traction
Uveitis
Vascular Endothelial Growth Factors
Vision
Visual Acuity
Vitreous Hemorrhage
This study was a retrospective consecutive case series of patients diagnosed with treatment-naïve unilateral CRVO between January 2010 and September 2017 at the Hangil Eye Hospital. The inclusion criteria for this study were as follows: (1) symptomatic CRVO in which retinal hemorrhage and retinal edema involved the macula, (2) foveal thickness greater than 300 μm as measured by OCT at initial visits, and (3) macular edema treated with intravitreal bevacizumab. An intravitreal injection of bevacizumab was administered in the same manner as reported previously28 (link). All patients were treated using a pro-re-nata regimen. The diagnosis of CRVO was based on the findings from fundus examination and fluorescein angiography. CRVO with a non-perfusion area larger than 10 disc areas on fluorescein angiography was defined as ischemic CRVO. Visual acuity improvement of 2 lines or more in the CRVO eyes following treatment was defined as a functional responder.
The exclusion criteria of the study included patients with any coexisting ocular diseases, such as age-related macular degeneration, diabetic retinopathy, and uveitis, as well as eyes that had received focal/grid laser photocoagulation, pan-retinal photocoagulation, prior intravitreal injections (e.g., intravitreal corticosteroids, intravitreal anti-VEGF agents), or prior ocular surgery (except cataract surgery). Patients were also excluded if they had refractive disorders greater than ± 3D.
Patient charts were reviewed for the following data: age, sex, medical history (hypertension and diabetes mellitus), best-corrected visual acuity (BCVA), axial length (measured with the IOL master; Carl Zeiss Meditec, Dublin, California, USA), anti-VEGF injection dates, and number of intravitreal injections. BCVA was converted to the logarithm of the minimum angle of resolution (logMAR). The BCVA, IOP, and SFCT were compared between CRVO eyes and fellow eyes at each follow-up visit.
The exclusion criteria of the study included patients with any coexisting ocular diseases, such as age-related macular degeneration, diabetic retinopathy, and uveitis, as well as eyes that had received focal/grid laser photocoagulation, pan-retinal photocoagulation, prior intravitreal injections (e.g., intravitreal corticosteroids, intravitreal anti-VEGF agents), or prior ocular surgery (except cataract surgery). Patients were also excluded if they had refractive disorders greater than ± 3D.
Patient charts were reviewed for the following data: age, sex, medical history (hypertension and diabetes mellitus), best-corrected visual acuity (BCVA), axial length (measured with the IOL master; Carl Zeiss Meditec, Dublin, California, USA), anti-VEGF injection dates, and number of intravitreal injections. BCVA was converted to the logarithm of the minimum angle of resolution (logMAR). The BCVA, IOP, and SFCT were compared between CRVO eyes and fellow eyes at each follow-up visit.
Adrenal Cortex Hormones
Age-Related Macular Degeneration
Anti-Anxiety Agents
Bevacizumab
Cataract Extraction
Diabetes Mellitus
Diabetic Retinopathy
Diagnosis
Edema, Macular
Eye
Fluorescein Angiography
High Blood Pressures
Light Coagulation
Macula Lutea
N-acetyltryptophanamide
Patients
Perfusion
Refractive Errors
Retina
Retinal Edema
Retinal Hemorrhage
Treatment Protocols
Uveitis
Vascular Endothelial Growth Factors
Vision
Visual Acuity
Protocol full text hidden due to copyright restrictions
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Adrenal Cortex Hormones
Anesthesia
Antibiotics
Aqueous Humor
Betamethasone
Chambers, Anterior
Eye
Eye Drops
Infection
Inflammation
Injections, Intraperitoneal
Ketamine
Light Coagulation
Mus
Ocular Hypertension
Ointments
Pharmaceutical Preparations
Phenylephrine Hydrochloride
Pupil
Tropicamide
Xylazine
Protocol full text hidden due to copyright restrictions
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Administration, Ophthalmic
Eye
Light Coagulation
Microscopy, Fluorescence
Mus
Optic Disk
paraform
Pharmaceutical Preparations
Phosphates
Pressure
Retina
Saline Solution
This prospective interventional study was approved by the Institutional Ethics Committee of the Graduate School of Medicine and the Faculty of Medicine at the University of Tokyo (#11986). Written informed consent was obtained from all patients. The procedures were conducted in accordance with the tenets of the Declaration of Helsinki.
Consecutive patients were recruited from the Department of Ophthalmology at the University of Tokyo Hospital between March 2019 and June 2020. The inclusion criteria were clinically significant DME with apparent leaking MAs and eligibility for FA. Each patient was informed about the treatment options, including anti-VEGF and steroid therapies, and the risks and benefits of laser photocoagulation. Patients who were reluctant to use anti-VEGF therapy for economic or psychological reasons, had recurrent DME despite previous treatments, and were eligible for laser photocoagulation treatment were recruited to the study. All enrolled patients underwent comprehensive ophthalmologic examinations. The best-corrected visual acuity (BCVA) was measured at baseline before laser photocoagulation and at the 1- and 3-month follow-ups. The major exclusion criteria were previous pars plana vitrectomy, intraocular surgery in the last 6 months, treatment for macular edema in the last 6 months, significant media opacities, and a diagnosis or history of any ocular disease that might influence the study results, including age-related macular degeneration, inflammatory eye disease, neurodegenerative disease, and vitreomacular traction syndrome.
Consecutive patients were recruited from the Department of Ophthalmology at the University of Tokyo Hospital between March 2019 and June 2020. The inclusion criteria were clinically significant DME with apparent leaking MAs and eligibility for FA. Each patient was informed about the treatment options, including anti-VEGF and steroid therapies, and the risks and benefits of laser photocoagulation. Patients who were reluctant to use anti-VEGF therapy for economic or psychological reasons, had recurrent DME despite previous treatments, and were eligible for laser photocoagulation treatment were recruited to the study. All enrolled patients underwent comprehensive ophthalmologic examinations. The best-corrected visual acuity (BCVA) was measured at baseline before laser photocoagulation and at the 1- and 3-month follow-ups. The major exclusion criteria were previous pars plana vitrectomy, intraocular surgery in the last 6 months, treatment for macular edema in the last 6 months, significant media opacities, and a diagnosis or history of any ocular disease that might influence the study results, including age-related macular degeneration, inflammatory eye disease, neurodegenerative disease, and vitreomacular traction syndrome.
Age-Related Macular Degeneration
Diagnosis
Edema, Macular
Eligibility Determination
Eye Disorders
Faculty, Medical
Inflammation
Institutional Ethics Committees
Light Coagulation
Neurodegenerative Disorders
Operative Surgical Procedures
Patients
Physical Examination
Planum
Poly(ADP-ribose) Polymerases
Steroids
Syndrome
Traction
Vascular Endothelial Growth Factors
Vision
Visual Acuity
Vitrectomy
Top products related to «Light Coagulation»
Sourced in United States
The Micron IV is a compact and versatile laboratory equipment designed for a range of scientific applications. It features a high-precision fluid delivery system capable of accurately measuring and dispensing small volumes of liquids. The Micron IV is suitable for a variety of tasks, including sample preparation, reagent addition, and automated liquid handling.
Sourced in United States, Germany
The Constellation Vision System is a surgical platform designed for ophthalmic procedures. It provides advanced control and precision for the surgeon during operations. The system integrates multiple components to support the surgical workflow.
Sourced in United States, Spain, Switzerland, Denmark, Australia, Belgium
Tropicamide is a synthetic chemical compound used in ophthalmic applications. It is a pupil dilator that temporarily enlarges the pupil of the eye. Tropicamide is commonly used in eye examinations and diagnostic procedures to facilitate the examination of the inside of the eye.
Sourced in Germany, United States, United Kingdom, Japan
The Spectralis OCT is a high-resolution optical coherence tomography (OCT) imaging system designed for clinical use. It provides detailed, cross-sectional images of the eye's internal structures, enabling healthcare professionals to diagnose and monitor a variety of ocular conditions.
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Rompun is a veterinary drug used as a sedative and analgesic for animals. It contains the active ingredient xylazine hydrochloride. Rompun is designed to induce a state of sedation and pain relief in animals during medical procedures or transportation.
Sourced in Germany, United States, United Kingdom, Japan, Switzerland, Ireland
The Spectralis is an optical coherence tomography (OCT) imaging device developed by Heidelberg Engineering. It captures high-resolution, cross-sectional images of the retina and optic nerve using near-infrared light. The Spectralis provides detailed structural information about the eye, which can aid in the diagnosis and management of various eye conditions.
Sourced in Japan, China, Belgium, Germany
Tropicamide is a mydriatic and cycloplegic agent used in ophthalmic examinations and procedures. It is a pharmaceutical product designed to temporarily dilate the pupil and temporarily paralyze the ciliary muscle, which controls the eye's focusing ability.
Sourced in France, United States, Italy, Australia, Germany, China, Thailand, Cameroon, United Kingdom, Netherlands, New Zealand
Zoletil is a general anesthetic and analgesic used in veterinary medicine. It is a combination of two active compounds, tiletamine and zolazepam, that work together to induce a state of deep sedation and pain relief in animals. The product is administered by injection and is commonly used for a variety of veterinary procedures, including surgery, diagnostic imaging, and minor treatments. Zoletil is intended for use under the supervision of licensed veterinary professionals.
Sourced in Japan, Germany
Mydrin-P is a laboratory product used for ophthalmic purposes. It functions as a mydriatic agent, intended to dilate the pupil.
Sourced in Germany, France, Japan, United States, Brazil, Spain, Canada, Switzerland, Cameroon, Australia, United Kingdom
Xylazine is a pharmaceutical product used as a sedative and analgesic in veterinary medicine. It is a central alpha-2 adrenergic agonist that produces a calming effect and pain relief in animals. Xylazine is used to facilitate handling, examination, and minor surgical procedures in various animal species.
More about "Light Coagulation"
Light Coagulation: A Versatile Medical Procedure for Targeted Tissue Fusion.
Also known as laser coagulation or photocoagulation, this minimally invasive technique utilizes focused light energy to precisely treat a variety of conditions in fields like ophthalmology, dermatology, and beyond.
From retinal tears to vascular lesions, skin conditions, and more, light coagulation offers clinicians an effective diagnostic and treatment option with a quick recovery time for patients.
Key Subtopics and Related Terms: - Laser Coagulation: The use of laser light to induce tissue coagulation and fusion. - Photocoagulation: A broader term encompassing various light-based coagulation methods. - Ophthalmic Applications: Treating retinal tears, diabetic retinopathy, and other eye conditions using Micron IV, Constellation Vision System, Spectralis OCT, etc. - Dermatological Uses: Addressing vascular lesions, skin tags, and other skin issues through light-based coagulation. - Anesthesia Considerations: Mydrin-P, Zoletil, Xylazine, and Rompun may be used to facilitate light coagulation procedures. - Research Optimization: Platforms like PubCompare.ai can enhance light coagulation research by identifying optimal protocols and products from published literature, preprints, and patents.
Discover the versatility and precision of light coagulation in modern medical practice, and explore the cutting-edge tools and techniques driving advancements in this field.
Also known as laser coagulation or photocoagulation, this minimally invasive technique utilizes focused light energy to precisely treat a variety of conditions in fields like ophthalmology, dermatology, and beyond.
From retinal tears to vascular lesions, skin conditions, and more, light coagulation offers clinicians an effective diagnostic and treatment option with a quick recovery time for patients.
Key Subtopics and Related Terms: - Laser Coagulation: The use of laser light to induce tissue coagulation and fusion. - Photocoagulation: A broader term encompassing various light-based coagulation methods. - Ophthalmic Applications: Treating retinal tears, diabetic retinopathy, and other eye conditions using Micron IV, Constellation Vision System, Spectralis OCT, etc. - Dermatological Uses: Addressing vascular lesions, skin tags, and other skin issues through light-based coagulation. - Anesthesia Considerations: Mydrin-P, Zoletil, Xylazine, and Rompun may be used to facilitate light coagulation procedures. - Research Optimization: Platforms like PubCompare.ai can enhance light coagulation research by identifying optimal protocols and products from published literature, preprints, and patents.
Discover the versatility and precision of light coagulation in modern medical practice, and explore the cutting-edge tools and techniques driving advancements in this field.