Myopic shift and preoperative axial length after congenital cataract surgery in Peruvian patients - The Association for Research in Vision and Ophthalmology Meeting (ARVO) 2018 Honolulu, Hawaii - Poster presentation
Purpose: We report a rare case of a 2 - year-old child with ectopia lentis and potential Marfan syndrome (MFS) and discuss her management.
Methods: A 2 - year - old female with no signifi cant past medical history was brought in by her mother after complaints that the child has recently been holding everything close to her eyes while simultaneously shifting her head down. Her mother reported no history of pain or trauma. The child’s family history was negative for ectopia lentis or MFS.
This study evaluated the outcomes of implanting intrastromal corneal ring segments (ICRS) in 25 eyes of 20 patients with corneal ectasia after refractive surgery. Post-operatively, uncorrected distance visual acuity significantly improved from 20/185 to 20/66 on average and corrected distance visual acuity significantly improved from 20/125 to 20/40 on average. Keratometry and corneal asphericity values also significantly improved. The study found that ICRS implantation can effectively treat corneal ectasia after refractive surgery by improving vision and corneal shape.
This case report describes two patients presenting with anterior lentiglobus resulting from abnormalities in the posterior lens capsule. Patient 1 was a 6 week old girl diagnosed with persistent fetal vasculature in the right eye who had a flattened posterior capsule with a central dense fibrous plaque causing anterior doming of the lens. She underwent a successful lensectomy and vitrectomy. Patient 2 was a 1 month old boy with suspected familial exudative vitreoretinopathy. Both eyes showed peripheral capsular fibrosis and flattening causing anterior lentiglobus. The right eye also had a complete retinal detachment. Ultrasound biomicroscopy and Retcam imaging confirmed posterior capsular abnormalities resulting in anterior doming of the lens
Ocular Manifestations Of Cystinosis Case Report And Review Of Literature Dr. Jagannath Boramani
This document presents a case report of a 63-year-old male with non-nephropathic cystinosis who presented with longstanding photophobia, glare, and foreign body sensation in his eyes. On examination, punctate needle-shaped crystals were diffusely present throughout the cornea. Diagnosis was confirmed by an elevated level of serum cystine. The document also provides background on cystinosis as a rare metabolic disorder characterized by intracellular cystine accumulation. Corneal crystal deposition is a pathognomonic manifestation and advances with age, initially causing asymptomatic crystals and later photophobia, punctate keratopathy, and blurred vision. Treatment involves cysteamine therapy to reduce cystine levels.
This document discusses the ABCD staging system for diagnosing and monitoring progression of keratoconus. It begins with an overview of keratoconus and the need for early diagnosis and treatment. It then reviews prior classification and progression monitoring systems. The document introduces the Belin ABCD staging system, which uses tomographic pachymetry maps to assess four parameters (A= maximum keratometry, B= minimum keratometry, C= thickness, D= asymmetry) and stage disease. It presents evidence that the ABCD system can identify progressive keratoconus an average of 5 months earlier than prior methods, allowing for earlier intervention like corneal collagen cross-linking. The conclusion is that the ABCD system allows earlier diagnosis
Spinal cord injury without radiographic abnormalities (SCIWORA)SanchitUppal5
- SCIWORA refers to spinal cord injury without radiographic abnormality. It commonly occurs in children and involves the cervical spine.
- MRI is now considered the gold standard for diagnosis as it can detect abnormalities not seen on plain radiographs or CT scans like edema, hemorrhage or cord transection.
- Treatment involves immobilization, IV steroids may help, and surgery is indicated if MRI shows instability, compression or worsening neurological status. Prognosis depends on initial neurological status and MRI findings, with most patients showing improvement but some facing permanent impairments.
This document provides information on managing pediatric cataracts. It discusses that childhood cataracts are a major cause of blindness worldwide and disrupt visual development. Timely cataract removal and rehabilitation is important. Examination of pediatric cataract patients involves assessing visual acuity, eye alignment and function. Surgical techniques aim to remove the cataract while preserving the capsular bag for intraocular lens implantation. Post-operative care and amblyopia management are crucial to optimize visual outcomes. Complications include inflammation, glaucoma, posterior capsule opacification and membrane formation.
Purpose: We report a rare case of a 2 - year-old child with ectopia lentis and potential Marfan syndrome (MFS) and discuss her management.
Methods: A 2 - year - old female with no signifi cant past medical history was brought in by her mother after complaints that the child has recently been holding everything close to her eyes while simultaneously shifting her head down. Her mother reported no history of pain or trauma. The child’s family history was negative for ectopia lentis or MFS.
This study evaluated the outcomes of implanting intrastromal corneal ring segments (ICRS) in 25 eyes of 20 patients with corneal ectasia after refractive surgery. Post-operatively, uncorrected distance visual acuity significantly improved from 20/185 to 20/66 on average and corrected distance visual acuity significantly improved from 20/125 to 20/40 on average. Keratometry and corneal asphericity values also significantly improved. The study found that ICRS implantation can effectively treat corneal ectasia after refractive surgery by improving vision and corneal shape.
This case report describes two patients presenting with anterior lentiglobus resulting from abnormalities in the posterior lens capsule. Patient 1 was a 6 week old girl diagnosed with persistent fetal vasculature in the right eye who had a flattened posterior capsule with a central dense fibrous plaque causing anterior doming of the lens. She underwent a successful lensectomy and vitrectomy. Patient 2 was a 1 month old boy with suspected familial exudative vitreoretinopathy. Both eyes showed peripheral capsular fibrosis and flattening causing anterior lentiglobus. The right eye also had a complete retinal detachment. Ultrasound biomicroscopy and Retcam imaging confirmed posterior capsular abnormalities resulting in anterior doming of the lens
Ocular Manifestations Of Cystinosis Case Report And Review Of Literature Dr. Jagannath Boramani
This document presents a case report of a 63-year-old male with non-nephropathic cystinosis who presented with longstanding photophobia, glare, and foreign body sensation in his eyes. On examination, punctate needle-shaped crystals were diffusely present throughout the cornea. Diagnosis was confirmed by an elevated level of serum cystine. The document also provides background on cystinosis as a rare metabolic disorder characterized by intracellular cystine accumulation. Corneal crystal deposition is a pathognomonic manifestation and advances with age, initially causing asymptomatic crystals and later photophobia, punctate keratopathy, and blurred vision. Treatment involves cysteamine therapy to reduce cystine levels.
This document discusses the ABCD staging system for diagnosing and monitoring progression of keratoconus. It begins with an overview of keratoconus and the need for early diagnosis and treatment. It then reviews prior classification and progression monitoring systems. The document introduces the Belin ABCD staging system, which uses tomographic pachymetry maps to assess four parameters (A= maximum keratometry, B= minimum keratometry, C= thickness, D= asymmetry) and stage disease. It presents evidence that the ABCD system can identify progressive keratoconus an average of 5 months earlier than prior methods, allowing for earlier intervention like corneal collagen cross-linking. The conclusion is that the ABCD system allows earlier diagnosis
Spinal cord injury without radiographic abnormalities (SCIWORA)SanchitUppal5
- SCIWORA refers to spinal cord injury without radiographic abnormality. It commonly occurs in children and involves the cervical spine.
- MRI is now considered the gold standard for diagnosis as it can detect abnormalities not seen on plain radiographs or CT scans like edema, hemorrhage or cord transection.
- Treatment involves immobilization, IV steroids may help, and surgery is indicated if MRI shows instability, compression or worsening neurological status. Prognosis depends on initial neurological status and MRI findings, with most patients showing improvement but some facing permanent impairments.
This document provides information on managing pediatric cataracts. It discusses that childhood cataracts are a major cause of blindness worldwide and disrupt visual development. Timely cataract removal and rehabilitation is important. Examination of pediatric cataract patients involves assessing visual acuity, eye alignment and function. Surgical techniques aim to remove the cataract while preserving the capsular bag for intraocular lens implantation. Post-operative care and amblyopia management are crucial to optimize visual outcomes. Complications include inflammation, glaucoma, posterior capsule opacification and membrane formation.
This document discusses the case of a 57-year-old female patient with von Hippel-Lindau (VHL) disease who presented with decreased vision in her left eye due to retinal hemangioblastoma. She underwent two unsuccessful laser treatments but photodynamic therapy (PDT) resulted in significant resolution of the serous retinal detachment and cystoid macular edema. PDT was concluded to be an effective treatment for exudative retinal detachment caused by retinal hemangioblastomas in patients with VHL disease.
Posterior vitreous detachment (PVD) involves the separation of the vitreous gel from the retina. It occurs normally with aging as the vitreous liquefies through the processes of synchysis and syneresis. Incomplete PVD can result in vitreomacular adhesion (VMA) which may lead to vitreomacular traction (VMT) or macular hole (MH). Left untreated, VMT and MH can cause severe vision loss or blindness. The current standard treatment is vitrectomy surgery, but pharmacologic therapies offer an alternative to observation in early disease.
This is a presentation given at the teaching programme for Ophthalmologists in training at the Royal Victoria Eye and Ear Hospital, March 2011. It covers new developments in the treatment of Retinopathy of Prematurity.
Retinopathy of prematurity, Therapy Modalities, BIUMS, Dr Joobin Khadamy, 1st...Joobin Khadamy . MD
Retinopathy of Prematurity, Pain Management, BIUMS, Dr Joobin Khadamy, 1st feb 2018
It review current available therapies and future of therapy in management of retinopathy of prematurity.
This document discusses idiopathic juxtafoveolar telangiectasia (IJFT), including its classification and stages. It describes IJFT types 1 and 2, with type 1 being congenital and aneurysmal and type 2 being acquired and perifoveal. Type 2 is further classified into 5 stages based on angiographic and imaging findings. The document also presents three case studies where anti-VEGF therapy with ranibizumab was used to treat neovascularization associated with types 1 and 2 IJFT, showing improvements in leakage and vision. While anti-VEGF therapy may help reduce leakage, preexisting photoreceptor damage from IJFT may limit improvements in visual acuity.
Tomographic fundus features in Pseudoxanthoma Elasticum Abdallah Ellabban
This study analyzed optical coherence tomography (OCT) scans of 52 eyes from 27 patients with pseudoxanthoma elasticum (PXE) and compared features between those with choroidal neovascularization (CNV) secondary to angioid streaks (AS) vs CNV secondary to age-related macular degeneration (AMD). Unique lesions were more common in PXE patients, including outer retinal tubulation (ORT) seen in 70.5% of eyes with CNV secondary to AS vs 34.1% of AMD eyes, and Bruch's membrane undulation seen in 70.8% vs 11.4% respectively. ORT appeared as round or ovoid structures beneath the outer plexiform layer.
A brief description of different methods (in use or proposed) of radiological assessment of X-linked ALD.
By Felice D'Arco Pediatric neuroradiology consultant Great Ormond Street Hospital London
This document summarizes recent developments in retinopathy of prematurity (ROP). It discusses that ROP cases are increasing in the US due to declining infant mortality. Imaging techniques now allow wide-angle retinal imaging. Telemedicine enables remote diagnosis of ROP. Anti-VEGF treatments show promise but require more research on dosage and side effects. Future areas of study include genetics, epigenetics, stem cells, and using artificial intelligence for remote image grading to manage increasing ROP cases.
This document discusses the use of multimodal imaging to diagnose and monitor MacTel-2, a progressive retinal disease. It describes how digital color fundus photography, multicolor scanning laser fundus photography, optical coherence tomography, and dye-based angiography can be combined to identify early disease features like loss of foveal autofluorescence and subtle retinal changes. Over time, imaging reveals complications such as subretinal neovascularization and macular holes. By concurrently assessing different retinal structures, multimodal imaging improves understanding, evaluation, and treatment of MacTel-2.
A Variety of Anatomical and Clinical Manifestations of Myelinated Retinal Ner...inventionjournals
Introduction: Myelinated Retinal Nerve Fibers (MRNF) represent a developmental anomaly that occurs in about 1% of the population. They appear as different in size, well demarcated white striated lesions along the retinal nerve fibers mainly in contiguity with the optic nerve head. The MRNF may be an isolated asymptomatic finding or associated with other ocular or systemic abnormalities, causing mild to significant visual loss. Purpose: To present a variety of anatomical and clinical manifestations of MRNF. Patients and methods: Between 2011 and 2016 nine patients (six children and three adults) with MRNF were admitted to the Eye clinic of the University Alexandrovska hospital in Sofia, Bulgaria. Full orthoptic and ophthalmologic examination was performed. Results: Eight patients had unilateral MRNF, seven with the left eye and one - with the right eye involved. Two of them had the triad of MRNF, axial myopia and amblyopia (Straatsma syndrome). One patient had bilateral MRNF and hyperopia („reverse” Straatsma syndrome). Two adult patients were asymptomatic. The rest had a substantial visual impairment because of anisometropia, strabismus or massive myelinated lesions. Conclusion: There is a great variety of anatomical and clinical manifestations of MRNF and their effect on the visual function depends on both organic and amblyogenic factors
Retinopathy of Prematurity, Pain Management, BIUMS, Dr Joobin Khadamy, 1st fe...Joobin Khadamy . MD
Retinopathy of Prematurity, Pain Management, BIUMS, Dr Joobin Khadamy, 1st feb 2018
It review current approach in management of pain during retinopathy of prematurity screening.
Irregular Astigmatism after DSAEK in case of Congenital Hereditary Endothelial Distrophy with Intrastromal Vacuolization - L. Avoni, L. Cappuccini, M. Busin
Gene therapy shows promise for treating previously incurable hereditary retinal degenerations like Leber Congenital Amaurosis (LCA). Clinical trials of gene therapy using an AAV2 vector carrying the RPE65 gene for LCA caused by RPE65 mutations demonstrated safety and modest efficacy. However, subfoveal injections carried some risk and provided no benefit, as patients with better foveal structure lost retinal thickness and acuity. While gene therapy is sufficiently safe and efficacious in the extrafoveal retina for LCA caused by RPE65 mutations, treating the fovea requires more research due to risks.
Intrastromal corneal ring segments are devices used to correct mild to moderate myopia by flattening the cornea. They are inserted through a peripheral incision and come in various thicknesses to determine the degree of correction. Intrastromal corneal ring segments work by shortening the corneal cord length and producing flattening across the entire cornea. They are indicated for mild myopia up to -3.00 diopters with minimal astigmatism in patients over 21 with stable refraction, and can also be used to treat keratoconus and post-LASIK ectasia. Complications are generally rare and reversible.
This document discusses retinopathy of prematurity (ROP), including aggressive posterior ROP (AP-ROP). It provides details on:
1. The classification system for ROP which stages the disease based on location and severity. AP-ROP is noted as a rapidly progressive form of posterior ROP.
2. Treatment options for ROP including laser ablation therapy which destroys retinal tissue, and anti-VEGF therapy which aims to reduce abnormal blood vessel growth.
3. A case study on 10 preterm infants with AP-ROP who were treated with intravitreal ranibizumab injections followed by laser therapy, with results showing regression of ROP and no complications.
Case Review #8: 62 year old female with cervical spinal stenosisRobert Pashman
62 year old female with neck pain and left arm weakness. On MRI, the patient was found to have spinal stenosis. Dr. Pashman treated the patient with an Anterior Cervical Discecomy and fusion C4-/7.
Leber congenital amaurosis (LCA) is a rare inherited retinal disease present from birth that causes severe vision loss. It is caused by mutations in genes critical for the visual cycle, preventing the retina from responding normally to light. Diagnosis involves assessing lack of retinal response on electroretinogram and genetic testing to identify the specific mutation. While currently no treatment can restore lost vision, gene therapy targeting the RPE65 gene has been approved for LCA type 2 based on clinical trials demonstrating improved light sensitivity.
Pediatric cervical spine clearance: A review and understanding of the conceptsApollo Hospitals
Cervical spine injuries are uncommon in pediatric trauma
patients. Delayed or missed diagnosis is usually attributed to failure to suspect an injury to the cervical spine, or to inadequate cervical spine radiology and incorrect interpretation of radiographs. New imaging techniques have become available, but did not solve the problem, adding their own ‘baggage’, such as cost, availability, logistic difficulties, radiation dosage, lack of specificity and evidence of effectiveness or safety.
This document summarizes considerations for intraocular lens (IOL) power calculation in children. It discusses that children's eyes continue growing post-surgery, unlike adult eyes. This growth normally leads to increasing myopia. Studies show a myopic shift of several diopters on average after IOL implantation in young children, with the greatest shifts in infants. There is no consensus on the ideal postoperative refractive goal in children, though many surgeons aim for hyperopia in younger children and emmetropia or mild myopia in older children.
This study investigated the effect of under-correcting myopia on myopic progression by analyzing clinical refraction data from 275 visits of 76 myopic patients. The results showed a significant positive correlation between the degree of under-correction and myopic progression, with greater under-correction associated with greater progression. Myopic progression also correlated positively with the degree of myopia. However, progression did not correlate with age or gender. The findings suggest that under-correcting myopia may induce small increases in myopic progression compared to full correction.
This study evaluated the long-term safety and efficacy of Ferrara intrastromal corneal ring segments for keratoconus treatment. The records of 36 eyes of 30 patients who received ICRS from 1996-2002 were reviewed. At the 5-year follow-up, uncorrected and corrected visual acuity significantly improved, and keratometry and corneal thickness values significantly decreased. At the 10-year follow-up, these improvements were maintained without significant changes, demonstrating the long-term effectiveness and stability of ICRS for keratoconus. This is the longest reported follow-up of ICRS for keratoconus correction.
This document discusses the case of a 57-year-old female patient with von Hippel-Lindau (VHL) disease who presented with decreased vision in her left eye due to retinal hemangioblastoma. She underwent two unsuccessful laser treatments but photodynamic therapy (PDT) resulted in significant resolution of the serous retinal detachment and cystoid macular edema. PDT was concluded to be an effective treatment for exudative retinal detachment caused by retinal hemangioblastomas in patients with VHL disease.
Posterior vitreous detachment (PVD) involves the separation of the vitreous gel from the retina. It occurs normally with aging as the vitreous liquefies through the processes of synchysis and syneresis. Incomplete PVD can result in vitreomacular adhesion (VMA) which may lead to vitreomacular traction (VMT) or macular hole (MH). Left untreated, VMT and MH can cause severe vision loss or blindness. The current standard treatment is vitrectomy surgery, but pharmacologic therapies offer an alternative to observation in early disease.
This is a presentation given at the teaching programme for Ophthalmologists in training at the Royal Victoria Eye and Ear Hospital, March 2011. It covers new developments in the treatment of Retinopathy of Prematurity.
Retinopathy of prematurity, Therapy Modalities, BIUMS, Dr Joobin Khadamy, 1st...Joobin Khadamy . MD
Retinopathy of Prematurity, Pain Management, BIUMS, Dr Joobin Khadamy, 1st feb 2018
It review current available therapies and future of therapy in management of retinopathy of prematurity.
This document discusses idiopathic juxtafoveolar telangiectasia (IJFT), including its classification and stages. It describes IJFT types 1 and 2, with type 1 being congenital and aneurysmal and type 2 being acquired and perifoveal. Type 2 is further classified into 5 stages based on angiographic and imaging findings. The document also presents three case studies where anti-VEGF therapy with ranibizumab was used to treat neovascularization associated with types 1 and 2 IJFT, showing improvements in leakage and vision. While anti-VEGF therapy may help reduce leakage, preexisting photoreceptor damage from IJFT may limit improvements in visual acuity.
Tomographic fundus features in Pseudoxanthoma Elasticum Abdallah Ellabban
This study analyzed optical coherence tomography (OCT) scans of 52 eyes from 27 patients with pseudoxanthoma elasticum (PXE) and compared features between those with choroidal neovascularization (CNV) secondary to angioid streaks (AS) vs CNV secondary to age-related macular degeneration (AMD). Unique lesions were more common in PXE patients, including outer retinal tubulation (ORT) seen in 70.5% of eyes with CNV secondary to AS vs 34.1% of AMD eyes, and Bruch's membrane undulation seen in 70.8% vs 11.4% respectively. ORT appeared as round or ovoid structures beneath the outer plexiform layer.
A brief description of different methods (in use or proposed) of radiological assessment of X-linked ALD.
By Felice D'Arco Pediatric neuroradiology consultant Great Ormond Street Hospital London
This document summarizes recent developments in retinopathy of prematurity (ROP). It discusses that ROP cases are increasing in the US due to declining infant mortality. Imaging techniques now allow wide-angle retinal imaging. Telemedicine enables remote diagnosis of ROP. Anti-VEGF treatments show promise but require more research on dosage and side effects. Future areas of study include genetics, epigenetics, stem cells, and using artificial intelligence for remote image grading to manage increasing ROP cases.
This document discusses the use of multimodal imaging to diagnose and monitor MacTel-2, a progressive retinal disease. It describes how digital color fundus photography, multicolor scanning laser fundus photography, optical coherence tomography, and dye-based angiography can be combined to identify early disease features like loss of foveal autofluorescence and subtle retinal changes. Over time, imaging reveals complications such as subretinal neovascularization and macular holes. By concurrently assessing different retinal structures, multimodal imaging improves understanding, evaluation, and treatment of MacTel-2.
A Variety of Anatomical and Clinical Manifestations of Myelinated Retinal Ner...inventionjournals
Introduction: Myelinated Retinal Nerve Fibers (MRNF) represent a developmental anomaly that occurs in about 1% of the population. They appear as different in size, well demarcated white striated lesions along the retinal nerve fibers mainly in contiguity with the optic nerve head. The MRNF may be an isolated asymptomatic finding or associated with other ocular or systemic abnormalities, causing mild to significant visual loss. Purpose: To present a variety of anatomical and clinical manifestations of MRNF. Patients and methods: Between 2011 and 2016 nine patients (six children and three adults) with MRNF were admitted to the Eye clinic of the University Alexandrovska hospital in Sofia, Bulgaria. Full orthoptic and ophthalmologic examination was performed. Results: Eight patients had unilateral MRNF, seven with the left eye and one - with the right eye involved. Two of them had the triad of MRNF, axial myopia and amblyopia (Straatsma syndrome). One patient had bilateral MRNF and hyperopia („reverse” Straatsma syndrome). Two adult patients were asymptomatic. The rest had a substantial visual impairment because of anisometropia, strabismus or massive myelinated lesions. Conclusion: There is a great variety of anatomical and clinical manifestations of MRNF and their effect on the visual function depends on both organic and amblyogenic factors
Retinopathy of Prematurity, Pain Management, BIUMS, Dr Joobin Khadamy, 1st fe...Joobin Khadamy . MD
Retinopathy of Prematurity, Pain Management, BIUMS, Dr Joobin Khadamy, 1st feb 2018
It review current approach in management of pain during retinopathy of prematurity screening.
Irregular Astigmatism after DSAEK in case of Congenital Hereditary Endothelial Distrophy with Intrastromal Vacuolization - L. Avoni, L. Cappuccini, M. Busin
Gene therapy shows promise for treating previously incurable hereditary retinal degenerations like Leber Congenital Amaurosis (LCA). Clinical trials of gene therapy using an AAV2 vector carrying the RPE65 gene for LCA caused by RPE65 mutations demonstrated safety and modest efficacy. However, subfoveal injections carried some risk and provided no benefit, as patients with better foveal structure lost retinal thickness and acuity. While gene therapy is sufficiently safe and efficacious in the extrafoveal retina for LCA caused by RPE65 mutations, treating the fovea requires more research due to risks.
Intrastromal corneal ring segments are devices used to correct mild to moderate myopia by flattening the cornea. They are inserted through a peripheral incision and come in various thicknesses to determine the degree of correction. Intrastromal corneal ring segments work by shortening the corneal cord length and producing flattening across the entire cornea. They are indicated for mild myopia up to -3.00 diopters with minimal astigmatism in patients over 21 with stable refraction, and can also be used to treat keratoconus and post-LASIK ectasia. Complications are generally rare and reversible.
This document discusses retinopathy of prematurity (ROP), including aggressive posterior ROP (AP-ROP). It provides details on:
1. The classification system for ROP which stages the disease based on location and severity. AP-ROP is noted as a rapidly progressive form of posterior ROP.
2. Treatment options for ROP including laser ablation therapy which destroys retinal tissue, and anti-VEGF therapy which aims to reduce abnormal blood vessel growth.
3. A case study on 10 preterm infants with AP-ROP who were treated with intravitreal ranibizumab injections followed by laser therapy, with results showing regression of ROP and no complications.
Case Review #8: 62 year old female with cervical spinal stenosisRobert Pashman
62 year old female with neck pain and left arm weakness. On MRI, the patient was found to have spinal stenosis. Dr. Pashman treated the patient with an Anterior Cervical Discecomy and fusion C4-/7.
Leber congenital amaurosis (LCA) is a rare inherited retinal disease present from birth that causes severe vision loss. It is caused by mutations in genes critical for the visual cycle, preventing the retina from responding normally to light. Diagnosis involves assessing lack of retinal response on electroretinogram and genetic testing to identify the specific mutation. While currently no treatment can restore lost vision, gene therapy targeting the RPE65 gene has been approved for LCA type 2 based on clinical trials demonstrating improved light sensitivity.
Pediatric cervical spine clearance: A review and understanding of the conceptsApollo Hospitals
Cervical spine injuries are uncommon in pediatric trauma
patients. Delayed or missed diagnosis is usually attributed to failure to suspect an injury to the cervical spine, or to inadequate cervical spine radiology and incorrect interpretation of radiographs. New imaging techniques have become available, but did not solve the problem, adding their own ‘baggage’, such as cost, availability, logistic difficulties, radiation dosage, lack of specificity and evidence of effectiveness or safety.
This document summarizes considerations for intraocular lens (IOL) power calculation in children. It discusses that children's eyes continue growing post-surgery, unlike adult eyes. This growth normally leads to increasing myopia. Studies show a myopic shift of several diopters on average after IOL implantation in young children, with the greatest shifts in infants. There is no consensus on the ideal postoperative refractive goal in children, though many surgeons aim for hyperopia in younger children and emmetropia or mild myopia in older children.
This study investigated the effect of under-correcting myopia on myopic progression by analyzing clinical refraction data from 275 visits of 76 myopic patients. The results showed a significant positive correlation between the degree of under-correction and myopic progression, with greater under-correction associated with greater progression. Myopic progression also correlated positively with the degree of myopia. However, progression did not correlate with age or gender. The findings suggest that under-correcting myopia may induce small increases in myopic progression compared to full correction.
This study evaluated the long-term safety and efficacy of Ferrara intrastromal corneal ring segments for keratoconus treatment. The records of 36 eyes of 30 patients who received ICRS from 1996-2002 were reviewed. At the 5-year follow-up, uncorrected and corrected visual acuity significantly improved, and keratometry and corneal thickness values significantly decreased. At the 10-year follow-up, these improvements were maintained without significant changes, demonstrating the long-term effectiveness and stability of ICRS for keratoconus. This is the longest reported follow-up of ICRS for keratoconus correction.
http://igolenses.co.uk
After reading the outcomes of the LORIC, CRAYON and SMART studies, two US opticians then undertook their own investigation into whether Overnight Vision Correction (OVC) can slow down or halt the further development of short-sightedness once patients are fitted with overnight ortho-k corrective contact lenses. T
The Lancet - Human embryonic stem cell-derived retinal pigment epithelium in...John Redaelli
This summarizes the results of two clinical trials evaluating the safety and efficacy of transplanting human embryonic stem cell-derived retinal pigment epithelium (hESC-RPE) in patients with Stargardt's macular dystrophy or dry age-related macular degeneration. A total of 18 patients received subretinal injections of hESC-RPE in one eye. Over a median follow-up of 22 months, there were no safety issues identified and 72% of patients showed signs of graft survival. Visual acuity improved in some patients and quality of life measures increased, suggesting possible biological activity. The results provide initial evidence that hESC-derived cells can be safely transplanted and have potential for treating retinal diseases
This document summarizes the evidence from clinical trials on using orthokeratology (overnight vision correction treatment) to slow the progression of myopia in children. It discusses two key studies, the LORIC study from Hong Kong and the CRAYON study from the US, that found orthokeratology can slow further myopia progression. However, the author notes more research is still needed to provide stronger evidence and ensure the safety of overnight orthokeratology lens wear in children, as it may increase the risk of microbial keratitis. The review then examines two small pilot studies that also found orthokeratology appears to slow myopia progression in children compared to single vision spectacle wear, but controlled trials are still lacking.
Clinical study of fundal changes in high myopiaiosrjce
IOSR Journal of Dental and Medical Sciences is one of the speciality Journal in Dental Science and Medical Science published by International Organization of Scientific Research (IOSR). The Journal publishes papers of the highest scientific merit and widest possible scope work in all areas related to medical and dental science. The Journal welcome review articles, leading medical and clinical research articles, technical notes, case reports and others.
This document discusses myopia (nearsightedness), including its definition, causes, risk factors, prevalence, and interventions to reduce progression. It notes that myopia is highly prevalent worldwide and is influenced by both genetic and environmental factors like education level, time spent outdoors, and ambient lighting exposure. Current interventions discussed include increasing time outdoors, pharmacological options like atropine, and optical treatments, but there remains no definitive approach to halt progression.
This case report compares the long-term effects of 1-phase vs 2-phase orthodontic treatment in identical twin sisters with Class III malocclusions. Patient 1 received early orthodontic intervention as the first phase of a 2-phase treatment at age 9 to correct an anterior crossbite. Patient 2 did not receive early treatment and was managed with a 1-phase treatment approach starting at age 16. Facial and dental changes were recorded over 11 years through cephalometric analyses at 4 time points. The results showed that both patients achieved similar dentofacial outcomes in the retention phase, with Class I occlusions and satisfactory profiles, despite receiving different treatment approaches. The case report aimed to clarify the benefits of 1
This study investigated outcomes of cataract surgery with and without intraocular lens (IOL) implantation in children under 2 years old. It found that while IOLs were associated with better early vision for bilateral cataracts, they did not provide benefits for unilateral cataracts and increased risks of reoperations and complications. Younger age increased odds of both better vision and glaucoma. The study provides evidence that IOL use should be reconsidered for unilateral congenital cataracts in young children.
The IOSR Journal of Pharmacy (IOSRPHR) is an open access online & offline peer reviewed international journal, which publishes innovative research papers, reviews, mini-reviews, short communications and notes dealing with Pharmaceutical Sciences( Pharmaceutical Technology, Pharmaceutics, Biopharmaceutics, Pharmacokinetics, Pharmaceutical/Medicinal Chemistry, Computational Chemistry and Molecular Drug Design, Pharmacognosy & Phytochemistry, Pharmacology, Pharmaceutical Analysis, Pharmacy Practice, Clinical and Hospital Pharmacy, Cell Biology, Genomics and Proteomics, Pharmacogenomics, Bioinformatics and Biotechnology of Pharmaceutical Interest........more details on Aim & Scope).
All manuscripts are subject to rapid peer review. Those of high quality (not previously published and not under consideration for publication in another journal) will be published without delay.
This Journal publishes original research work that contributes significantly to further the scientific knowledge in pharmacy.
Human embryonic stem cell-derived retinal pigment epithelium in patients with age-related macular degeneration and Stargardt's macular dystrophy: follow-up of two open-label phase 1/2 studies
Published Online: 15 October 2014
Including Comment By, Anthony Atala
This study investigated the clinical course of patients with idiopathic vitreomacular adhesion (VMA) who were initially observed without treatment. 106 eyes of 81 patients with VMA were followed for an average of 23 months. Based on optical coherence tomography findings, VMA was graded as mild (Grade 1), moderate (Grade 2), or severe (Grade 3). Over the course of observation, spontaneous release of VMA occurred in 32% of eyes, while progression occurred in 16% and vitrectomy was required in 5% of eyes. Best corrected visual acuity remained stable on average. This study found that initial observation is generally a favorable approach for managing mild to moderate VMA.
IOL POWER CALCULATION IN CHILDREN-Dr.Preetiilal.pptxdrPreetiilal
This document discusses intraocular lens (IOL) power calculation in children. It begins by outlining normal eye development in children and the myopic shift that occurs. It then discusses important considerations for IOL power calculation including accurate measurement of axial length and keratometry, choosing an appropriate IOL formula, determining the target postoperative refraction based on age, and making intraoperative adjustments if needed. Tables provide estimated axial length and keratometry values by age and examples of IOL powers to achieve emmetropia or a desired refraction to minimize myopic shift. The document emphasizes that IOL power calculation in growing children requires a multifaceted approach to determine the optimal lens power.
- Studies show that lowering IOP reduces risk of glaucoma progression and maintaining a steady IOP level over time is important. IOP fluctuation is associated with progressive visual field loss and is a stronger predictor of progression than mean IOP. Higher IOP fluctuation during office hours and over 24 hours is seen in glaucoma patients compared to normal subjects.
- Educating patients about their condition and treatment through tools like perimetry, OCT/GDx imaging can help improve compliance which is important for minimizing IOP fluctuations and risk of further optic nerve damage. Compliance is better with once or twice daily dosing compared to multiple medications or more frequent dosing.
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Myopic shift and preoperative axial length after congenital cataract surgery (ARVO Meeting 2018)
1. PREOPERATIVE AXIAL LENGTH AND MYOPIC SHIFT AFTER CONGENITAL
CATARACT SURGERY WITH PRIMARY INTRAOCULAR LENS IMPLANTATION
Diego A. Valera Cornejo MD1 , Abel Flores Boza 2
1 Vista Clinic 2 National Institute of Ophthalmology of Peru
The authors declare no financial or conflicting interests. No research funding was received for this study
INTRODUCTION
PURPOSE
There was no relationship between the initial axial length and the myopic shift in
all patients.
Unilateral cataracts had a greater myopic shift over 3 years.
In bilateral cataracts, a tendency to greater myopic shift with smaller axial
lengths was found; hence, this variable should be investigated more in this
group.
METHODS
RESULTS
CONCLUSION
Table 1.- Baseline characteristics (n=76)
Table 3 .- Mean myopic shift (diopters) in children with pseudophakia and bilateral cataracts (n=63)
Figure 2 Mean myopic shift in children with pseudophakia according to time after
surgery.
Baseline characteristic are summary in table 1. The mean myopic shift at 3 years
in all patients was 3.6 D (SD: 2.3 D), in group 1 was 3.2 D (SD: 3.3) and in group 2
was 3.9 D (SD: 3.2) (p=0.359) (Table 2) . In bilateral cataracts, this shift was 2.6 D
(SD: 2.0) and 3.4 D (SD: 1.8), respectively, in each group (p=0.098) (Table 3).
The mean follow-up time in bilateral cataracts was 38.9 months (SD: 12.9
months) with a mean myopic shift of 3.0 D, and 43.6 months (SD: 19.2 months)
in unilateral cataracts with a mean myopic shift of 6.3 D (p=0.001) (Table 2). In
this type of cataract, a greater myopic shift was observed in both groups (6.7 D
[SD: 6.7] and 6.1 D [SD: 6.3], p=0.882).
In the regression analysis, no relationship between the myopic shift and the
initial axial length was found in all the patients (R2=0.03; p=0.13), but a tendency
to show a negative correlation was seen (Figure 1).
The myopic shift had a tendency to have a direct relationship with the time after
the surgery being 1.95 D (at 1–2 years), 3.46 D (at 2–3 years) and 3.84 D (at 3
years) (Figure 2).
1. Rahi JS, Dezateux C; British Congenital Cataract Interest Group. Measuring and interpreting the incidence of congenital ocular
anomalies: lessons from a national study of congenital cataract in the UK. Invest Ophthalmol Vis Sci. 2001;42(7):1444–1448.
2. Plager DA, Lynn MJ, Buckley EG, Wilson ME, Lambert SR; Infant Aphakia Treatment Study Group. Complications in the first 5
years following cataract surgery in infants with and without intraocular lens implantation in the Infant Aphakia Treatment
Study. Am J Ophthalmol. 2014;158(5):892–898
3. Flitcroft DI, Knight-Nanan D, Bowell R, Lanigan B, O’Keefe M. Intraocular lenses in children: changes in axial length, corneal
curvature, and refraction. Br J Ophthalmol. 1999;83(3):265–269.
4. Tartarella MB, Carani JCE, Scarpi MJ. The change in axial length in the pseudophakic eye compared to the unoperated fellow
eye in children with bilateral cataracts. J AAPOS. 2014;18(2):173–177
5. Hussin HM, Markham R. Changes in axial length growth after congenital cataract surgery and intraocular lens implantation in
children younger than 5 years. J Cataract Refract Surg. 2009;35(7):1223–1228.
6. Lambert SR, Lynn MJ, DuBois LG, et al. Axial elongation following cataract surgery during the first year of life in the infant
Aphakia Treatment Study. Invest Ophthalmol Vis Sci. 2012;53(12):7539–7545.
7. Crouch ER, Crouch ER, Pressman SH. Prospective analysis of pediatric pseudophakia: myopic shift and postoperative
outcomes. J AAPOS. 2002;6(5):277–282.
We performed an analytical retrospective cohort study. Patients who underwent
congenital cataract surgery with intraocular lens implantation in the pediatric
ophthalmology service at the National Institute of Ophthalmology of Perú in the period
of 2007 to 2011.
We included patients younger than 4 years of age who underwent cataract surgery with
primary IOL implantation, primary posterior capsulorhexis and anterior vitrectomy.
Patients who had cataracts of another etiology or other associated ocular pathology
were excluded.
The population was divided into 2 groups: patients with an axial length of >21.5 (group
1) and patients with an axial length of ≤21.5 mm (group 2). The mean myopic shift was
estimated to be 2.5 D (standard deviation [SD]: 2) and 3.8 D (SD: 2) in group 1 and
group 2, respectively. With this, a sample size of 76 patients was estimated, with a
power of 80%, a 95% confidence interval and a 5% error. The sample was randomly
selected (probabilistic sampling), and the sample unit was the operated eyes of
congenital cataract.
10 to 38% of blindness in children is caused by congenital cataract 1. Cataract
aspiration with primary intraocular lens (IOL) implantation and primary posterior
capsulorhexis with anterior vitrectomy has been the choice of surgical procedure since
quite some time now in patients who are less than 2 years. However, the age at which
IOL needs to be implanted is still debatable especially due to its complications 2.
How the presence of cataract, surgical removal, and insertion of an IOL
(pseudophakia) may affect the ocular growth and his subsequent refractive change is
poorly understood 3. Factors such as time of surgery, aphakia, pseudophakia, laterality,
visual deprivation and axial length have been reported to influence axial growth and
visual prognosis 4. Many studies show much variability on how axial growth behaves in
pseudophakic children after surgery 4-7.
An expected myopic shift (-2.00 a -6 .00D) 5,6, its seen due to increased axial growth
during the first 3 years of life 7. However, the factors that are related to this refractive
change have not been evaluated in detail.
We anticipate a large myopic shift (because the pseudophakic eye of a young child
stills grows), and it is recommended the selection of an intraocular lens power that
results in a large hyperopic error in the immediate postoperative period. For which the
child will need to wear spectacles, but there is no consensus on how hyperopic the IOL
must be. It would be useful to determine which factors are related to greater myopic
shift and which IOL power to choose, that could bring the child closer to emetropia in
adulthood.
Our purpose was to evaluate if there is any relationship between pre operative axial
length and myopic shift after congenital cataract extraction and primary IOL
implantation.
A the secondary endpoint was to identify other possible factors that could be
associated with greater myopic shift.
REFERENCES
Figure 1 Relationship between axial length and average myopic shift in children with
pseudophakia (n=76).
Table 2.- Relationship between axial length and others factors associated with average myopic shift
(diopters) in children with pseudophakia (n=76)
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Presentation
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