This document provides an overview of ocular wound healing. It begins with an introduction and history of wound healing concepts. It then describes the typical phases of wound healing (hemostasis, proliferation, and maturation) and how they apply to specific ocular tissues like the cornea, conjunctiva, sclera, iris and retina. Factors that can modify wound healing like suture choice, anti-inflammatories and anti-proliferative agents are also discussed. The presentation aims to explain the summation of processes involved in ocular healing and how they may differ based on the injured tissue.
The cornea is the transparent front part of the eye that transmits and focuses light. It has 3 main layers - an outer epithelial layer, a thick middle stromal layer made of collagen, and an inner single-cell endothelial layer. The cornea derives its strength and curvature from the orderly arrangement of collagen in the stroma. It remains transparent due to its regular structure without blood vessels and the deturgescent properties maintained by the endothelial pump. The cornea has a high metabolic rate powered by glucose and oxygen and is innervated by nerves for vision and protection.
1. Corneal wound healing involves an epithelial phase, stromal phase, and endothelial phase. The epithelial phase begins within 12-48 hours as the surface epithelium slides and replicates to form a plug. The stromal phase lasts several weeks as keratocytes transform and synthesize new collagen to bridge the wound. The endothelial phase can take up to 30 days as the monolayer remodels to form a functional barrier.
1. Dr. Reshma Peter discusses various lenses used in ophthalmology, including those for fundus examination, gonioscopy, and contact biomicroscopy of the fundus.
2. Indirect fundus biomicroscopy uses Volk lenses of +60D, +78D, and +90D attached to a slit lamp to provide an inverted and laterally reversed view of the retina.
3. Lenses for indirect ophthalmoscopy include +30D, +20D, and +15D lenses, which provide different levels of magnification, stereopsis, and field of view.
4. Contact lenses for fundus examination include Modified Koeppe's lens and Goldmann's three mirror contact
The document discusses the anatomy, embryology, and function tests of the macula lutea. It describes the macula lutea as a 5.5mm circular area at the posterior pole of the retina that subserves central vision. It notes the macula's delayed development until 8 months gestation and specialization of the fovea which contains the highest concentration of cones. The document outlines various macular function tests used to evaluate macular diseases, including visual acuity, Amsler grid, microperimetry, and electroretinography. It provides details on the anatomy and cell layers of the fovea centralis and techniques for assessing macular integrity with tests like the Maddox rod.
Techniques of tear film evaluation by Raju KaitiRaju Kaiti
The document summarizes techniques for evaluating the tear film, which has three layers: an outer lipid layer, intermediate aqueous layer, and inner mucous layer. Non-invasive techniques discussed include tear break-up time tests, lipid layer evaluation using interferometry, and inferior tear meniscus height measurements. Invasive techniques involve Schirmer's tests to evaluate tear secretion, fluorescein and rose bengal staining of the ocular surface, and conjunctival impression cytology to examine goblet cell density. The document provides details on procedures and normal results for each evaluation method.
The document provides information on the anatomy, physiology, and diseases of the lens. It discusses the lens's biconvex shape and ability to change shape to accommodate. The lens is divided into an anterior and posterior epithelium, cortex, and nucleus. It maintains transparency through organized fiber structure, hydration, and antioxidants. The lens focuses light and accommodates through changes in shape mediated by the ciliary body and zonules. Aging and various diseases can impact the lens's structure and function.
The uvea consists of the iris, ciliary body, and choroid. It develops from both neuroectoderm and vascular mesoderm. The iris develops fully by age 5, with pigmentation continuing after birth. The ciliary body appears by 9 weeks and is fully developed by 6 months gestation. The choroid layers are seen by 5 months gestation. The uvea regulates light entry and provides blood supply to the outer retina. Congenital anomalies include heterochromia, polycoria, persistent pupillary membranes, and colobomas. Uveitis is inflammation of the uveal tract.
Cycloplegic refraction involves temporarily paralyzing the ciliary muscle with eye drops in order to determine a person's full refractive error. This is important for children who accommodate too much. Common cycloplegic agents include atropine, homatropine, and cyclopentolate. Cyclopentolate is often the drug of choice due to its faster onset and shorter duration. A cycloplegic refraction allows an accurate assessment of refractive error, especially in children and other patients where accommodation can affect results.
The cornea is the transparent front part of the eye that transmits and focuses light. It has 3 main layers - an outer epithelial layer, a thick middle stromal layer made of collagen, and an inner single-cell endothelial layer. The cornea derives its strength and curvature from the orderly arrangement of collagen in the stroma. It remains transparent due to its regular structure without blood vessels and the deturgescent properties maintained by the endothelial pump. The cornea has a high metabolic rate powered by glucose and oxygen and is innervated by nerves for vision and protection.
1. Corneal wound healing involves an epithelial phase, stromal phase, and endothelial phase. The epithelial phase begins within 12-48 hours as the surface epithelium slides and replicates to form a plug. The stromal phase lasts several weeks as keratocytes transform and synthesize new collagen to bridge the wound. The endothelial phase can take up to 30 days as the monolayer remodels to form a functional barrier.
1. Dr. Reshma Peter discusses various lenses used in ophthalmology, including those for fundus examination, gonioscopy, and contact biomicroscopy of the fundus.
2. Indirect fundus biomicroscopy uses Volk lenses of +60D, +78D, and +90D attached to a slit lamp to provide an inverted and laterally reversed view of the retina.
3. Lenses for indirect ophthalmoscopy include +30D, +20D, and +15D lenses, which provide different levels of magnification, stereopsis, and field of view.
4. Contact lenses for fundus examination include Modified Koeppe's lens and Goldmann's three mirror contact
The document discusses the anatomy, embryology, and function tests of the macula lutea. It describes the macula lutea as a 5.5mm circular area at the posterior pole of the retina that subserves central vision. It notes the macula's delayed development until 8 months gestation and specialization of the fovea which contains the highest concentration of cones. The document outlines various macular function tests used to evaluate macular diseases, including visual acuity, Amsler grid, microperimetry, and electroretinography. It provides details on the anatomy and cell layers of the fovea centralis and techniques for assessing macular integrity with tests like the Maddox rod.
Techniques of tear film evaluation by Raju KaitiRaju Kaiti
The document summarizes techniques for evaluating the tear film, which has three layers: an outer lipid layer, intermediate aqueous layer, and inner mucous layer. Non-invasive techniques discussed include tear break-up time tests, lipid layer evaluation using interferometry, and inferior tear meniscus height measurements. Invasive techniques involve Schirmer's tests to evaluate tear secretion, fluorescein and rose bengal staining of the ocular surface, and conjunctival impression cytology to examine goblet cell density. The document provides details on procedures and normal results for each evaluation method.
The document provides information on the anatomy, physiology, and diseases of the lens. It discusses the lens's biconvex shape and ability to change shape to accommodate. The lens is divided into an anterior and posterior epithelium, cortex, and nucleus. It maintains transparency through organized fiber structure, hydration, and antioxidants. The lens focuses light and accommodates through changes in shape mediated by the ciliary body and zonules. Aging and various diseases can impact the lens's structure and function.
The uvea consists of the iris, ciliary body, and choroid. It develops from both neuroectoderm and vascular mesoderm. The iris develops fully by age 5, with pigmentation continuing after birth. The ciliary body appears by 9 weeks and is fully developed by 6 months gestation. The choroid layers are seen by 5 months gestation. The uvea regulates light entry and provides blood supply to the outer retina. Congenital anomalies include heterochromia, polycoria, persistent pupillary membranes, and colobomas. Uveitis is inflammation of the uveal tract.
Cycloplegic refraction involves temporarily paralyzing the ciliary muscle with eye drops in order to determine a person's full refractive error. This is important for children who accommodate too much. Common cycloplegic agents include atropine, homatropine, and cyclopentolate. Cyclopentolate is often the drug of choice due to its faster onset and shorter duration. A cycloplegic refraction allows an accurate assessment of refractive error, especially in children and other patients where accommodation can affect results.
Keratoconus is a non-inflammatory thinning of the cornea that causes it to take on a conical shape. It typically develops in adolescence and causes vision impairment due to irregular astigmatism. It is classified into four stages based on refractive error, corneal thickness and shape. While the exact cause is unknown, theories include genetic and enzymatic factors. It is often associated with eye rubbing and connective tissue disorders. Clinical features include corneal thinning, Fleischer's ring, Munson's sign, and scarring in advanced cases. Diagnosis involves topography, pachymetry and biomicroscopy to detect corneal shape changes.
Binocular single vision refers to simultaneous vision with two eyes that occurs when an individual fixates on an object. There are three grades of binocular vision: simultaneous perception, fusion, and stereopsis. Fusion is the ability to see a composite picture from two similar images, while stereopsis provides the impression of depth by superimposing images from slightly different angles. Tests for binocular vision include those for simultaneous perception, fusion, and stereopsis using instruments like the synaptophore. Binocular vision develops through infancy and childhood as the visual axes become coordinated to direct each fovea at the object of regard.
Dr. Monika Soni presented on the topic of tear film at the upgraded department of ophthalmology at MGMMC & MYH Indore. The presentation discussed the anatomy and physiology of tear film, including the three layers of the tear film, mechanisms of tear secretion and distribution, functions of the tear film, tests to evaluate tear film such as tear breakup time, Schirmer's test, and osmolarity. A variety of glands contribute secretions to form and maintain the tear film, which is essential for maintaining a clear cornea and proper vision.
This document discusses choroidal coloboma, beginning with definitions and epidemiology. It describes the embryonic development of the eye and how failure of fusion of the embryonic fissure can result in coloboma. Types of coloboma are classified based on location and presence of other anomalies. Complications like retinal detachment are discussed. Management of cataracts and other ocular issues in the context of coloboma are covered. The prognosis depends on factors like presence of microphthalmos, corneal diameter, and type and timing of surgery.
This document provides information about fundus fluorescein angiography (FFA). It begins with basic principles of FFA and the dyes used, including sodium fluorescein and indocyanine green. The purpose, indications, contraindications, technique, phases, and interpretation of FFA are described. Abnormal fluorescence patterns like hyperfluorescence and hypofluorescence are discussed. Recent advances in wide-field imaging and indocyanine green angiography are also summarized.
This document discusses the embryology and anatomy of the cornea. It describes how the cornea develops from surface ectoderm in the 4th-5th week of gestation, with mesenchymal cells forming the stroma and endothelium. The cornea continues developing through the fetal period, with layers such as Bowman's membrane forming between 12-26 weeks. The document also discusses the cellular components, functions, and common congenital anomalies of the cornea, including microcornea, megalocornea, cornea plana, keratoconus, and others.
This document provides information on the anatomy and physiology of the cornea. It describes the layers of the cornea including the epithelium, Bowman's membrane, stroma, Dua's layer, Descemet's membrane, and endothelium. It discusses the transparency of the cornea, metabolic processes, drug permeability, wound healing, and the effects of contact lens wear on corneal physiology. The cornea has several specialized functions including refracting light and protecting the interior of the eye.
The cornea is the transparent front part of the eye that allows light to enter. It has 6 layers - an epithelial layer, Bowman's membrane, a thick stromal layer, Duas layer, Descemet's membrane, and an endothelial layer. The stroma makes up around 90% of the cornea's thickness and contains collagen fibrils that give it strength and transparency. The cornea has no blood vessels and receives nutrients from vessels in the surrounding tissues. It has a rich nerve supply that provides its high sensitivity. The cornea refracts and helps focus light entering the eye and is essential for vision.
This document discusses the evaluation of ptosis, or drooping of the eyelids. It begins by defining ptosis and distinguishing between true and pseudo ptosis. True ptosis is classified as acquired or congenital, with acquired further divided into neurogenic, myogenic, aponeurotic, and mechanical types. The evaluation of ptosis involves a thorough history, measurement of margin-reflex distance, palpebral fissure height, levator function, and upper lid crease. Additional tests include assessing for fatigability, Cogan's twitch sign, and jaw winking phenomenon. Confirmatory tests include the ice test and edrophonium (Tensilon) test. Treatment options mentioned include eyelid
1. Vitreous humour is the jelly-like substance that fills the vitreous cavity behind the lens. It is composed of 99% water along with collagen, hyaluronic acid, and other proteins.
2. The vitreous humour can be divided into three parts - the outer hyaloid layer, the cortical vitreous, and the medullary vitreous. It attaches to structures around the eye including the retina, lens, and optic disc.
3. The biochemical composition of the vitreous humour allows it to maintain a high level of transparency and act as a viscoelastic gel within the eye.
This document provides information on the anatomy and diseases of the vitreous humor. It discusses that the vitreous humor is a jelly-like structure that fills the back of the eye and provides support. Common diseases include vitreous liquefaction, detachment, hemorrhage, and opacities. Vitreous liquefaction is the most common degenerative change and causes floaters. Posterior vitreous detachment often occurs in older individuals and may lead to retinal tears or breaks. Vitreous opacities can result from inflammatory cells, aggregates, tumors or hemorrhages. Vitreous hemorrhage usually stems from retinal vessels and can cause vision loss.
Gonioscopy allows visualization of the anterior chamber angle to evaluate for angle closure and diagnose glaucoma. It was pioneered in the early 20th century with the introduction of contact lenses to eliminate total internal reflection at the cornea. Direct gonioscopy uses contact lenses for a straight view, while indirect gonioscopy uses prisms for an inverted image at the slit lamp. Examination of angle structures like the trabecular meshwork and classification systems help diagnose angle closure and glaucoma. Gonioscopy is used for diagnostic and therapeutic purposes like laser and surgery.
The document summarizes the structure and function of the tear film. It consists of three layers - an outer lipid layer, middle aqueous layer, and inner mucin layer. The lipid layer prevents evaporation and overflow of tears. The aqueous layer hydrates the cornea and contains nutrients. The mucin layer lubricates the eye surface. Tears are produced through basal and reflex secretion and drained through the lacrimal system into the nose. Blinking helps spread and replenish the tear film layers, which must be continuously renewed to maintain a smooth optical surface and protect the cornea.
The document provides information on the anatomy and physiology of the lens. It discusses the position, dimensions, surfaces, parts and zones of the lens. It describes the biochemistry of the lens including its water, protein, amino acid, carbohydrate and lipid content. It explains the metabolic activities of the lens such as glucose metabolism and protein synthesis and breakdown. It discusses permeability, transport mechanisms and the role of various components in maintaining lens transparency.
Indirect ophthalmoscopy has evolved since its introduction in the 1850s to become an indispensable tool for examining the retina. It allows examination of the peripheral retina through the use of a condensing lens held close to the eye. The observer views an enlarged, inverted image of the retina. Several advantages include the ability to compensate for a patient's refractive error, good illumination, and use with scleral indentation to examine the far periphery. Adjustments of the lens diopter and observation distance allow viewing different areas of the retina with varying magnification and field of view. Proper technique involves adjusting the headband-mounted binocular scope and positioning the condensing lens.
Retinoscopy is an objective refraction technique used to determine a patient's refractive error. Dynamic retinoscopy is performed with the patient fixating on a near target. Several methods of dynamic retinoscopy have been developed, including MEM, Bell retinoscopy, Nott's retinoscopy, and Book retinoscopy. The movements observed during dynamic retinoscopy - with, against, and neutral - provide information about a patient's accommodative response and ability. The document discusses the procedures, interpretations, limitations, and histories of various dynamic retinoscopy techniques.
Accommodation is the mechanism by which the eye changes refractive power to focus on objects at different distances. It involves changes in the shape of the elastic lens, controlled by the ciliary muscle. The amplitude of accommodation declines with age as the lens loses elasticity, causing presbyopia. Accommodation is measured using methods like push-up and minus lens, which determine the near and far points of clear vision. The range between these points indicates how much accommodation is available. Accommodation abilities normally decline with age according to established formulas.
The document summarizes the Amsler grid, a diagnostic tool used since 1945 to screen for and monitor macular diseases. It consists of a grid with a central dot that patients look at to detect any distortions, gaps, or blurred areas in their central vision. Various versions are available, including ones with different colors, patterns of lines, or dot sizes to test specific parts of the visual field and detect different types of visual abnormalities that could indicate conditions like macular degeneration or glaucoma. The procedure involves having patients view the grid with each eye separately at 16 inches and report any anomalies in the lines of the grid.
Keratoconus is a non-inflammatory, progressive thinning and protrusion of the cornea that results in irregular astigmatism and decreased vision. It typically presents after puberty with no gender or racial predilection. Diagnosis is made based on corneal thinning, Fleischer ring, Vogt's striae, and irregular astigmatism seen on keratometry and topography. Mild cases are managed with spectacles while more severe cases require rigid gas permeable contact lenses, Intacs, or corneal transplantation.
This document discusses healing and repair processes in the body. It explains that healing involves regeneration, where original tissue is restored, or repair through fibrosis and scarring. The stages of wound healing like inflammation, granulation tissue formation, and remodeling are described. Factors influencing healing like infection, nutrition and movement are also covered. Healing of specialized tissues like bone, muscle and skin wounds are explained in detail.
Keratoconus is a non-inflammatory thinning of the cornea that causes it to take on a conical shape. It typically develops in adolescence and causes vision impairment due to irregular astigmatism. It is classified into four stages based on refractive error, corneal thickness and shape. While the exact cause is unknown, theories include genetic and enzymatic factors. It is often associated with eye rubbing and connective tissue disorders. Clinical features include corneal thinning, Fleischer's ring, Munson's sign, and scarring in advanced cases. Diagnosis involves topography, pachymetry and biomicroscopy to detect corneal shape changes.
Binocular single vision refers to simultaneous vision with two eyes that occurs when an individual fixates on an object. There are three grades of binocular vision: simultaneous perception, fusion, and stereopsis. Fusion is the ability to see a composite picture from two similar images, while stereopsis provides the impression of depth by superimposing images from slightly different angles. Tests for binocular vision include those for simultaneous perception, fusion, and stereopsis using instruments like the synaptophore. Binocular vision develops through infancy and childhood as the visual axes become coordinated to direct each fovea at the object of regard.
Dr. Monika Soni presented on the topic of tear film at the upgraded department of ophthalmology at MGMMC & MYH Indore. The presentation discussed the anatomy and physiology of tear film, including the three layers of the tear film, mechanisms of tear secretion and distribution, functions of the tear film, tests to evaluate tear film such as tear breakup time, Schirmer's test, and osmolarity. A variety of glands contribute secretions to form and maintain the tear film, which is essential for maintaining a clear cornea and proper vision.
This document discusses choroidal coloboma, beginning with definitions and epidemiology. It describes the embryonic development of the eye and how failure of fusion of the embryonic fissure can result in coloboma. Types of coloboma are classified based on location and presence of other anomalies. Complications like retinal detachment are discussed. Management of cataracts and other ocular issues in the context of coloboma are covered. The prognosis depends on factors like presence of microphthalmos, corneal diameter, and type and timing of surgery.
This document provides information about fundus fluorescein angiography (FFA). It begins with basic principles of FFA and the dyes used, including sodium fluorescein and indocyanine green. The purpose, indications, contraindications, technique, phases, and interpretation of FFA are described. Abnormal fluorescence patterns like hyperfluorescence and hypofluorescence are discussed. Recent advances in wide-field imaging and indocyanine green angiography are also summarized.
This document discusses the embryology and anatomy of the cornea. It describes how the cornea develops from surface ectoderm in the 4th-5th week of gestation, with mesenchymal cells forming the stroma and endothelium. The cornea continues developing through the fetal period, with layers such as Bowman's membrane forming between 12-26 weeks. The document also discusses the cellular components, functions, and common congenital anomalies of the cornea, including microcornea, megalocornea, cornea plana, keratoconus, and others.
This document provides information on the anatomy and physiology of the cornea. It describes the layers of the cornea including the epithelium, Bowman's membrane, stroma, Dua's layer, Descemet's membrane, and endothelium. It discusses the transparency of the cornea, metabolic processes, drug permeability, wound healing, and the effects of contact lens wear on corneal physiology. The cornea has several specialized functions including refracting light and protecting the interior of the eye.
The cornea is the transparent front part of the eye that allows light to enter. It has 6 layers - an epithelial layer, Bowman's membrane, a thick stromal layer, Duas layer, Descemet's membrane, and an endothelial layer. The stroma makes up around 90% of the cornea's thickness and contains collagen fibrils that give it strength and transparency. The cornea has no blood vessels and receives nutrients from vessels in the surrounding tissues. It has a rich nerve supply that provides its high sensitivity. The cornea refracts and helps focus light entering the eye and is essential for vision.
This document discusses the evaluation of ptosis, or drooping of the eyelids. It begins by defining ptosis and distinguishing between true and pseudo ptosis. True ptosis is classified as acquired or congenital, with acquired further divided into neurogenic, myogenic, aponeurotic, and mechanical types. The evaluation of ptosis involves a thorough history, measurement of margin-reflex distance, palpebral fissure height, levator function, and upper lid crease. Additional tests include assessing for fatigability, Cogan's twitch sign, and jaw winking phenomenon. Confirmatory tests include the ice test and edrophonium (Tensilon) test. Treatment options mentioned include eyelid
1. Vitreous humour is the jelly-like substance that fills the vitreous cavity behind the lens. It is composed of 99% water along with collagen, hyaluronic acid, and other proteins.
2. The vitreous humour can be divided into three parts - the outer hyaloid layer, the cortical vitreous, and the medullary vitreous. It attaches to structures around the eye including the retina, lens, and optic disc.
3. The biochemical composition of the vitreous humour allows it to maintain a high level of transparency and act as a viscoelastic gel within the eye.
This document provides information on the anatomy and diseases of the vitreous humor. It discusses that the vitreous humor is a jelly-like structure that fills the back of the eye and provides support. Common diseases include vitreous liquefaction, detachment, hemorrhage, and opacities. Vitreous liquefaction is the most common degenerative change and causes floaters. Posterior vitreous detachment often occurs in older individuals and may lead to retinal tears or breaks. Vitreous opacities can result from inflammatory cells, aggregates, tumors or hemorrhages. Vitreous hemorrhage usually stems from retinal vessels and can cause vision loss.
Gonioscopy allows visualization of the anterior chamber angle to evaluate for angle closure and diagnose glaucoma. It was pioneered in the early 20th century with the introduction of contact lenses to eliminate total internal reflection at the cornea. Direct gonioscopy uses contact lenses for a straight view, while indirect gonioscopy uses prisms for an inverted image at the slit lamp. Examination of angle structures like the trabecular meshwork and classification systems help diagnose angle closure and glaucoma. Gonioscopy is used for diagnostic and therapeutic purposes like laser and surgery.
The document summarizes the structure and function of the tear film. It consists of three layers - an outer lipid layer, middle aqueous layer, and inner mucin layer. The lipid layer prevents evaporation and overflow of tears. The aqueous layer hydrates the cornea and contains nutrients. The mucin layer lubricates the eye surface. Tears are produced through basal and reflex secretion and drained through the lacrimal system into the nose. Blinking helps spread and replenish the tear film layers, which must be continuously renewed to maintain a smooth optical surface and protect the cornea.
The document provides information on the anatomy and physiology of the lens. It discusses the position, dimensions, surfaces, parts and zones of the lens. It describes the biochemistry of the lens including its water, protein, amino acid, carbohydrate and lipid content. It explains the metabolic activities of the lens such as glucose metabolism and protein synthesis and breakdown. It discusses permeability, transport mechanisms and the role of various components in maintaining lens transparency.
Indirect ophthalmoscopy has evolved since its introduction in the 1850s to become an indispensable tool for examining the retina. It allows examination of the peripheral retina through the use of a condensing lens held close to the eye. The observer views an enlarged, inverted image of the retina. Several advantages include the ability to compensate for a patient's refractive error, good illumination, and use with scleral indentation to examine the far periphery. Adjustments of the lens diopter and observation distance allow viewing different areas of the retina with varying magnification and field of view. Proper technique involves adjusting the headband-mounted binocular scope and positioning the condensing lens.
Retinoscopy is an objective refraction technique used to determine a patient's refractive error. Dynamic retinoscopy is performed with the patient fixating on a near target. Several methods of dynamic retinoscopy have been developed, including MEM, Bell retinoscopy, Nott's retinoscopy, and Book retinoscopy. The movements observed during dynamic retinoscopy - with, against, and neutral - provide information about a patient's accommodative response and ability. The document discusses the procedures, interpretations, limitations, and histories of various dynamic retinoscopy techniques.
Accommodation is the mechanism by which the eye changes refractive power to focus on objects at different distances. It involves changes in the shape of the elastic lens, controlled by the ciliary muscle. The amplitude of accommodation declines with age as the lens loses elasticity, causing presbyopia. Accommodation is measured using methods like push-up and minus lens, which determine the near and far points of clear vision. The range between these points indicates how much accommodation is available. Accommodation abilities normally decline with age according to established formulas.
The document summarizes the Amsler grid, a diagnostic tool used since 1945 to screen for and monitor macular diseases. It consists of a grid with a central dot that patients look at to detect any distortions, gaps, or blurred areas in their central vision. Various versions are available, including ones with different colors, patterns of lines, or dot sizes to test specific parts of the visual field and detect different types of visual abnormalities that could indicate conditions like macular degeneration or glaucoma. The procedure involves having patients view the grid with each eye separately at 16 inches and report any anomalies in the lines of the grid.
Keratoconus is a non-inflammatory, progressive thinning and protrusion of the cornea that results in irregular astigmatism and decreased vision. It typically presents after puberty with no gender or racial predilection. Diagnosis is made based on corneal thinning, Fleischer ring, Vogt's striae, and irregular astigmatism seen on keratometry and topography. Mild cases are managed with spectacles while more severe cases require rigid gas permeable contact lenses, Intacs, or corneal transplantation.
This document discusses healing and repair processes in the body. It explains that healing involves regeneration, where original tissue is restored, or repair through fibrosis and scarring. The stages of wound healing like inflammation, granulation tissue formation, and remodeling are described. Factors influencing healing like infection, nutrition and movement are also covered. Healing of specialized tissues like bone, muscle and skin wounds are explained in detail.
The document discusses wound healing and provides details about the different phases of wound healing: inflammatory, proliferative, and remodeling. It defines wounds and outlines factors that influence wound healing. The three main phases of wound healing - inflammatory, proliferative, and remodeling - are described in detail including the key cell types and processes involved in each phase such as hemostasis, granulation, angiogenesis, and epithelialization. Chronic wounds are defined as wounds that fail to progress through the normal healing stages and factors that can impair wound healing are also outlined.
Wound healing is a complex physiological process involving three overlapping phases: inflammatory, proliferative, and remodeling. The inflammatory phase aims to stop bleeding and remove debris through neutrophil and macrophage activity. During proliferation, granulation tissue forms through angiogenesis, collagen deposition, and epithelialization. Remodeling involves tissue remodeling and increased strength over months. Factors like infection, poor nutrition, and diabetes can impair healing. New treatments include negative pressure wound therapy, growth factors, and tissue engineering to enhance healing.
The document discusses wounds and the wound healing process. It defines a wound as a break in the skin or tissue integrity caused by injury. Wounds are classified based on various factors like cleanliness, depth, and type. The healing process involves three phases - inflammatory, proliferative, and remodeling. The inflammatory phase prepares the wound for healing. In proliferation, new tissue is formed through granulation. Remodeling provides increased strength over months. Healing occurs through regeneration or repair, with the former restoring original tissue and the latter resulting in scar tissue. Growth factors play important roles in the complex cellular cascade of wound healing.
The document discusses wound healing and fibrosis. It describes that wound healing occurs in three phases: inflammation, proliferation, and maturation. It also discusses primary and secondary wound healing. Primary healing involves wounds with opposed edges that heal with a thin scar, while secondary healing involves wounds with tissue loss that heal with more scarring and contracture. The document also discusses factors that influence wound healing and complications that can arise. It provides details on cutaneous wound healing and fracture healing processes. Finally, it discusses fibrosis, describing that it is excessive collagen deposition in tissue during repair. It notes the role of macrophages and TGF-beta in promoting fibrosis.
1. Wound healing is the body's complex biological response to tissue injury. It involves regeneration and repair processes to restore tissue integrity and function.
2. There are four main phases of wound healing: hemostasis, inflammation, proliferation, and remodeling. Various cell types and mediators are involved in each phase to clean the wound and promote new tissue growth.
3. Wounds can heal through primary intention, secondary intention, or tertiary intention depending on factors like cleanliness and tissue loss. Primary intention involves direct wound edge approximation while secondary intention involves healing from the base up without suturing.
Management of ulcers,physical therapy interventions, characteristics, how to asses different ulcer,examination, prognosis, evidence based medicine, drug therapy and other therapies
This document discusses wound healing processes in various ocular tissues, including the cornea, sclera, uvea, lens, retina, vitreous, and eyelid. It describes the typical sequence of wound healing, from blood clot formation and neutrophil migration to re-epithelialization and collagen deposition. Healing outcomes like scarring are also addressed. Proper specimen handling techniques are reviewed, including fixation, orientation, gross dissection, and sectioning to include relevant anatomical structures.
1. The document discusses normal wound healing which occurs in three phases - inflammatory, proliferative, and remodeling. The inflammatory phase begins immediately after injury and lasts 2-3 days.
2. It also discusses abnormal wound healing such as delayed healing and discusses managing acute wounds which involves thorough debridement to remove all contaminated and devitalized tissue.
3. The document provides details on the classification of wounds as tidy or untidy and discusses various types of wounds like bites, puncture wounds, and degloving injuries as well as their management.
The document discusses wound healing and provides details on the various phases of healing. It describes the healing process, which involves regeneration or repair through scar formation depending on the tissue type. The main phases of healing are the inflammatory phase, proliferative phase, and remodeling phase. The inflammatory phase lasts 3-5 days and involves coagulation and an immune response. The proliferative phase lasts up to 3 weeks and includes granulation tissue formation, re-epithelialization, and collagen deposition. The remodeling phase can last years and involves matrix remodeling and strengthening of the scar tissue. Complications can arise if this delicate process is disrupted.
This document discusses wound healing, defining wounds and classifying them. It covers the definition and process of wound healing, involving hemostasis, inflammation, proliferation, and maturation phases. Factors that influence and delay wound healing are addressed. Management of wounds involves cleaning, debridement if needed, approximating edges, dressing, and antibiotics if infected. The goal of wound healing treatment is satisfactory repair.
The document discusses the processes of wound healing through regeneration and repair. Regeneration involves the proliferation of parenchymal cells to restore original tissues, while repair involves proliferation of connective tissue elements and fibrosis. Repair was described as occurring through granulation tissue formation and wound contraction. The phases of wound healing were explained as inflammation, clearance and ingrowth of granulation tissue. Primary and secondary wound healing were also summarized.
This document discusses surgical wounds, their classifications, wound healing process, and complications. It outlines wound classifications based on degree of contamination and aetiology. The phases of wound healing are haemostasis, inflammation, proliferation, and remodeling. Factors affecting healing include age, nutrition, site vascularity, and sepsis. Clinical applications to promote healing include analgesics, antibiotics, dressings, rest, and wound closure. Complications can be early like infection or late like hypertrophic scarring. A thorough understanding of wound healing is important for surgical practice.
The document summarizes wound healing and physical therapy interventions for wound management. It describes the three overlapping phases of wound healing - inflammatory, proliferative, and maturation. Various physical therapy modalities that can be used for wound treatment are discussed, including ultrasound therapy, electrical stimulation, whirlpool bath, ionozone therapy, infrared therapy, iontophoresis, TENS, negative pressure wound therapy, and shortwave diathermy. All aim to accelerate wound healing by reducing inflammation and infection, promoting granulation and collagen formation.
Wound healing occurs through three phases: inflammation, proliferation, and maturation. During inflammation, blood vessels constrict and immune cells are attracted to the wound to remove debris. Proliferation involves new blood vessel formation through angiogenesis, collagen deposition by fibroblasts, and re-epithelialization of the epidermis. Maturation is marked by remodeling of collagen and decreased vascularity. Scars can form after healing and include atrophic, hypertrophic, or keloid types. Treatment depends on the scar but may involve pressure, silicone gel, steroid injections, or surgery combined with radiation.
A series of case studies showed that an integrated approach using Dialklycaramoyl chloride (DACC) to control bacteria and inflammation combined with a new bioactive native collagen scaffold to control excess MMPs addressed challenges in healing chronic wounds. Specifically:
- Case 1 involved a surgical wound in a diabetic female that was treated with DACC followed by the collagen scaffold, resulting in granulation and re-epithelialization.
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Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
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Basavarajeeyam - Ayurvedic heritage book of Andhra pradesh
Ocular wound healing
1. OCULAR WOUND
HEALING
PRESENTER – BEMNET T.(R2)
MODERATOR – DR.YARED A.
(MD ,MPH, ASSOCIATE PROFESSOR OF OPHTHALMOLOGY,
SUBSPECIALTY IN ANTERIOR SEGMENT AND CORNEAL DISEASE)
DR.YORDANOS T.(SENIOR RESIDENT)
12/31/2020
1
2. OUTLINE
Introduction
History of wound healing
Types of wound healing
Phases of wound healing
Specific ocular structure wound healing
Dermal/conjunctival
Corneal
Scleral
Uveal
Modifying wound healing 12/31/2020 2
3. INTRODUCTION
In human regeneration is limited to epithelium and the liver; most tissues
heal by repair resulting in scarring.
Wound healing is the summation of a number of processes that follow injury
Healing in ophthalmic surgery involve different tissue with different
characteristics
Even if almost all tissues have common feature they vary accordingly
12/31/2020 3
4. HISTORY OF WOUND HEALING
Sumerians – were the earliest to be accounted for wound healing around
2000 B.C
Egyptians - were the first to differentiate between infected and noninfected
wounds
The Greeks – classify wounds as acute and chronic
Galen of Pergamum – emphasized on maintaining moist env’t to fasten
wound healing 12/31/2020 4
5. Louis Pasteur (1822–1895) - proving that germs were always introduced
into the wound from the environment
Joseph Lister – began soaking his instruments in phenol and spraying the
operating rooms
Robert Wood Johnson – produce antiseptic dressing in the form of cotton
gauze impregnated with iodoform
12/31/2020 5
6. TYPES OF WOUND HEALING
Traditionally there are three types of wound healing. These are:
1. Healing by first intention/ primary closure
Wound will be approximated or closed using sutures, strips, graft or
flaps
Minimal basement membrane interruption , tissue loss, and cellular
damage
12/31/2020 6
7. Cont.…
2. Healing by secondary/spontaneous intention
No active intent to seal the wound
Contaminated and wounds that have extensive tissue loss
Closure is by re- epitelazation ….. Wound contracture
12/31/2020 7
8. Cont.…
3. Tertiary intention /delayed primary closure
Contaminated wound will be treated using repeated debridement , ABX and
negative pressure
Close the wound using primary methods once the wound is ready
12/31/2020 8
9. PHASES OF WOUND HEALING
• Classically its divided into three continues and overlapping phases
• Are differentiated depending on the type of cells and chemicals involved
12/31/2020 9
10. Cont.….
1. Hemostasis and inflammatory phase
Represents an attempt to limit damage by stopping the bleeding, sealing
the surface of the wound, and removing any necrotic tissue, foreign
debris, or bacteria present
First hemostasis ensue
• Vascular Constriction – local myogenic constriction, platelet derived
autacoids and nervous reflex
• Formation of the Platelet Plug
• Formation of blood clot
• Growth of fibrous tissue
12/31/2020 10
13. Cont.…
PMN are the first to infiltrate the wound site
Infiltration of neutrophil…….phagocytosis and debride necrotic tissue
Infiltration of macrophages….. Debridement of necrotic tissue ,
microbial stasis and also activate and recruit other cell
Macrophages also involve in proliferation, matrix synthesis, and
angiogenesis
T lymphocytes – are bridge the transition from the inflammatory to the
proliferative phase
12/31/2020 13
17. Cont.….
2. Proliferation phase
Consists of re-epithelialization, matrix synthesis, and
neovascularization
Tissue re-continuity established
Cells that are involved in this phase are:
Fibroblasts …….secret connective tissue proteins (collagen type 1,111
and proteoglycan)
Vascular endothelial cells…….initiate the process of angiogenesis.
Epithelial cells………migrate over the wound surface
Myofibroblasts……….contract the wound and facilitate wound closure.
12/31/2020 17
19. Cont.….
3. Maturation and remodeling
Characterized by a reorganization of previously synthesized collagen to re-
establishment of extracellular matrix
Fibroblasts ……….continue to secrete the structural proteins and protease
MMP is the major enzyme that involve in this phase
Net wound collagen ….result of a balance between collagenolysis and
collagen synthesis
12/31/2020 19
20. Cont.…..
Wound strength and mechanical integrity……. quantity and quality of the
newly deposited collagen
The deposition of matrix at the wound site follows a characteristic
pattern:
Fibronectin and collagen type III
Glycosaminoglycan's and proteoglycans and
Collagen type I is the final matrix
12/31/2020 20
21. Cont.…..
By several weeks postinjury the amount of collagen in the wound
reaches a plateau
The tensile strength continues to increase for several more months
The mechanical strength of the scar never achieves that of the uninjured
tissue
Re-epithelialization………by rapid mitotic activity of migrating epithelial
cells
12/31/2020 21
22. Cont.….
Factors affecting the wound healing processes are :
Age
Medical conditions
Medications
Vascularity
Availability of chemoattractant factors and
Cellular proliferation rates
Heritable Diseases of Connective Tissue
Ehlers-Danlos syndrome,
Marfan syndrome,
Osteogenesis imperfecta,
Epidermolysis bullosa, and acrodermatitis enteropathica 12/31/2020 22
23. Ocular wound healing
CONJUNCTIVAL WOUND HEALING
• Is highly vascularized structure
• Have similarity in wound healing with skin
• Healing could be accomplished in both primary and secondary
intension
• In general primary wound healing is preferable
• Re-epitelazation will be achieved with in days
• It depend on:
• Type of suture material – Vicryl or gut sutures.
• Type of suture placed.
12/31/2020 23
24. Cont.….
Corneal wound healing
• Has no vascular stage
• No granulation tissue rather there is fibroblastic tissue
• Healing differ in each layer
Epithelial wound/ abrasions healing
• Migration of epithelial cells from wound margin ….. 1hr post injury
at 60 to 80um per hr.
• If entire cornea is injured ….source of epithelial cells is limbal
stem cell and will take 48 to 72 hr
• Epithelial mitotic division and stratification ……re-establish corneal
12/31/2020 24
25. Cont.….
Wound involving bowman layer and superficial stroma
• Do not heal by fibrous proliferation of the stroma
• The gap will be filled by the proliferating epithelial cells ……Epithelial
facet
12/31/2020 25
26. Cont.….
Stromal wound healing
• First the proliferating epithelial cell will fill the gap
• Corneal stromal swelling
• Keratocytes start to produce collagen and proteoglycan……scar
12/31/2020 26
27. Cont.….
Full thickness corneal wound healing
• Proteinaceous coagulum(fibrin and fibronectin) will seal the posterior gap
• Migration of endothelial cells
• Polymegatism and polymorphisim
• In young individual there could be a mitotic activity
• Descemet will be produced by endothelial cells
12/31/2020 27
28. Cont.….
Practical consideration
• Partial and full thickness corneal wounds have to be heal by primary
intention
• Epithelial wounds will be left to heal by secondary intention
• The two factors that affect corneal wound healing are:
• Type of suture……. nylon monofilaments
• Technique ………. Interrupted sutures
• Topical steroid ……retard cellular response and scar formation
12/31/2020 28
29. Cont.….
Scleral wound healing
• The healing is by granulation formation
Partial wound healing
• External….. Tissues for granulation are derived from episclera
• Internal ….. Tissues are derived from uveal tissue
Full thickness wound healing
• Granulation tissue will originate from both episclera tissue and uveal tract
12/31/2020 29
31. Cont.….
Practical consideration
• Healing by primary intention is important
• Prevention of scar formation is less important
• Choice of suturing material depends size and anatomic location of the wound
• Small and/or anterior wounds……absorbable sutures
• Large and/or posterior wounds……non absorbable nylon monofilaments.
12/31/2020 31
32. Cont.….
Surgical limbus healing
• Involve features of corneal, conjunctival and scleral wound healing
• Conjunctival epithelium will seal the wound by granulation tissue
derived from conjunctiva and episclera
• The rest healing processes is similar to external scleral wound
healing
• Internally there is no granulation tissue due to no involvement of uveal
tract
• Internal wound will be sealed by migration of endothelial cells and
reformation of descemet
12/31/2020 32
34. Cont.….
Uveal wound healing
• Posterior uveal tract heal by granulation and subsequent scar formation
• Iris wound healing is different and depend on the anatomy of the lesion
• Perpendicular lesions
• Allows the radial muscle to pull the wound edges apart……gaping
the wound
• Wound healing does not extend across the gap
12/31/2020 34
35. Cont.….
• Parallel lesion
• Wound edges are
approximated
• Epithelium migrate and cover
the wound
• Stroma produce collagen and
ground substance
12/31/2020 35
36. Cont.….
Lens healing
• Proliferation and fibrous metaplasia of epithelium will close small capsular
defects
• Most wounds to the lens, small and large, result in cataracts.
Injury fibromyoblastic transformation of the epithelium
Transformed epithelium produce type I and type III collagen and GAG……
opacities
Eg. PCO after ECCE and pheco
12/31/2020 36
37. Cont.….
Retinal healing
• Wound healing of the neurosensory retina follows the principles of wound
healing.
• Removal of necrotic tissue
• Migration and proliferation
• Astrocytes will migrate from periphery to wound site and
proliferate down to subretinal space
• RPE will migrate from periphery to wound site and proliferate up
to subretinal space
• When the two proliferating cell types unite, a tight chorioretinal bond
12/31/2020 37
38. Cont.….
Vitreous healing
• Vitreous has few cells and no blood vessels.
• However it contain large amount of collagen fibrils
• This collagens act as a scaffold for glial and fibro vascular tissue from the
retina and uveal tract to grow and extend into the vitreous to proliferate as
membranes
12/31/2020 38
39. Modifying wound healing
• Scarring of any ocular tissue can result in decreased vision and
increase morbidity.
• Methods of modifying wound healing are:
Suture Materials
• Is a simply way of modifying wound healing
• If rapid healing is desired …. Use sutures capable of inducing
inflammatory response
• This include Vicryl , gut, and silk.
12/31/2020 39
40. Cont.….
• If inflammation is not desired ….use monofilament
sutures such as Prolene and nylon
• In some surgeries we can use both sutures
Eg. Limbal based trabeculectomy
12/31/2020 40
42. Cont.….
Anti- inflammatory
• Corticosteroid affect all stages of wound healing
• In acute stage affect neutrophil adherence and migration
• In late stages it affect production of plasmin no degradation of fibrin
• NSAIDs
• In early stage affect some cell adhesion interaction and migration
• It also non specifically inhibit COX affect production of PG Affect
leucocyte migration
12/31/2020 42
43. Cont.….
Anti - proliferative agents
The two most common anti- proliferative agents that is used are:
Fluorouracil (5-FU)
• Fluorinated pyrimidine nucleoside analogue that blocks production of
thymidylate synthase
• Interrupts normal cellular DNA and RNA synthesis
12/31/2020 43
44. Cont.…..
• Cause cellular thymine deficiency and resultant cell death.
• The effect is most pronounced on rapidly growing cells
• Used postoperatively as a sub conjunctival injection and
intraoperatively as a topical application to the trabeculectomy site
12/31/2020 44
45. Cont.….
Mitomycin C
• Compound isolated from the fungus streptomyces caespitosus
• Becomes a bifunctional alkylating agent after enzymatic alteration within
the cell
• Inhibits DNA synthesis by DNA cross-linkage
• Weak immunosuppressive but a potent inhibitor of fibroblast proliferation
12/31/2020 45