2.Utilizing a Previous Silicone Band Track in Recurred Retinal Detachment
Journal of the Korean Ophthalmological Society 2019;60(7):696-700
PURPOSE: We report a case of utilizing a previous silicone band track in the reoperation of scleral encircling. CASE SUMMARY: An 8-year-old male presented with rhegmatogenous retinal detachment in the right eye. Five days after this diagnosis, he received scleral buckling surgery and cryopexy to seal the retinal tear. One month after surgery, a fundus examination showed subretinal fluid at the inferior site of the scleral buckle. He underwent scleral encircling surgery and a cryopexy procedure. The patient has had an uneventful postoperative course, and the retina has remained attached over a follow-up period of 9 months. However, exotropia and hypotropia developed in the right eye. Diagnosis of restrictive strabismus due to tissue adhesion around the silicone band was made. The encircling band was therefore removed and laser photocoagulation was performed 360° around the retina. Twenty-four hours after surgery, a fundus examination showed subretinal fluid. He received 360° scleral encircling surgery not using the 360° conjunctival peritomy. After confirming a previous encircling tract using #0-0 polydioxanone as a guide, #5-0 Nylon was tied to the end of the guide and inserted through the encircling tract with the end sutured with the silicone band. The silicone band was inserted into the encircling tract by pulling the #5-0 Nylon as a guide. Ophthalmoscopy revealed an attached retina with indentation of the scleral buckle at 360°. CONCLUSIONS: For reoperation in patients who previously underwent scleral encircling surgery, using the previous scleral encircling tract may be effective in cases with conjunctival and tissue adhesion.
Child
;
Diagnosis
;
Exotropia
;
Follow-Up Studies
;
Humans
;
Light Coagulation
;
Male
;
Nylons
;
Ophthalmoscopy
;
Polydioxanone
;
Reoperation
;
Retina
;
Retinal Detachment
;
Retinal Perforations
;
Retinaldehyde
;
Scleral Buckling
;
Silicon
;
Silicones
;
Strabismus
;
Subretinal Fluid
;
Tissue Adhesions
3.Medical Litigations Associated with Cataract Surgery in Korea.
Ji Yoon KWAK ; Kyu Ryong CHOI ; Roo Min JUN ; Kyung Eun HAN
Journal of Korean Medical Science 2018;33(27):e180-
BACKGROUND: To analyze the results of court rulings about medical litigations related to cataract surgery in Korea. METHODS: We collected 50 anonymized judgements regarding cataract surgery between 2000 and 2016 and analyzed the reasons for the medical litigations, the court rulings, the reasons for compensation, and the amount claimed and finally awarded. RESULTS: Forty-eight litigations (96%) resulted from errors in treatment, and the reasons were as follows: endophthalmitis, dissatisfaction of visual outcome or ocular discomfort, bullous keratopathy or corneal opacity, retinal detachment, glaucoma or vitreous hemorrhage due to the progression of an underlying diabetic retinopathy, and others in order. Two litigations (4%) arose due to errors in diagnosis. Among the 50 final cases, 21 litigations (42%) were decided in favor of the plaintiff, and 29 litigations (58%) were decided against the plaintiff and dismissed. Ten cases awarded damages to the plaintiffs because of a violation of duty of care, and 11 cases awarded damages due to a violation of informed consent. When comparing cases with errors in diagnosis to cases with errors in treatment, there was no significant difference in the relative risk of a defendant's verdict (P = 0.503). The total amount of awarded damages was KRW 439,124,496 (USD 399,204), and the average amount was KRW 20,910,690 (USD 19,010). CONCLUSION: Nearly half of the cases were decided in favor of the plaintiff due to the violation of informed consent. This study's results will be helpful in understanding the results of medical litigations regarding cataract surgery and reducing future lawsuits.
Anonyms and Pseudonyms
;
Awards and Prizes
;
Cataract*
;
Compensation and Redress
;
Corneal Opacity
;
Diabetic Retinopathy
;
Diagnosis
;
Endophthalmitis
;
Glaucoma
;
Informed Consent
;
Jurisprudence*
;
Korea*
;
Ophthalmology
;
Retinal Detachment
;
Vitreous Hemorrhage
4.Trends of Pars Plana Vitrectomy Rates in South Korea: A Nationwide Cohort Study.
Joo Yeon KIM ; Tyler Hyungtaek RIM ; Sung Soo KIM
Korean Journal of Ophthalmology 2017;31(5):446-451
PURPOSE: To assess the trends in pars plana vitrectomy surgery rates and factors affecting rate change between 2002 and 2013 in South Korea. METHODS: Data from National Health Insurance Service-National Sample Cohort 2002–2013, which represents 1,025,340 samples with a sampling rate of 2.2% from the total eligible Korean population, was analyzed. RESULTS: A total of 3,816 vitrectomy procedures were performed (male, 2,010; female, 1,806) from 2002 to 2013. Annual rates of vitrectomy increased from 15.1 (in 2002) to 49.4 (in 2013) per 100,000 individuals, and this trend was prominent in those aged 60 years or older. As for the anesthetic method, vitrectomy under local anesthesia increased more prominently than vitrectomy under general anesthesia. The most common diagnoses associated with vitrectomy were diabetic retinopathy, retinal detachment, epiretinal membrane, and macular hole. CONCLUSIONS: The average annual rate of vitrectomy surgery was 31.5 per 100,000 between 2002 and 2013, and the rate has steadily increased.
Anesthesia, General
;
Anesthesia, Local
;
Cohort Studies*
;
Diabetic Retinopathy
;
Diagnosis
;
Epiretinal Membrane
;
Female
;
Humans
;
Incidence
;
Korea*
;
Methods
;
National Health Programs
;
Republic of Korea
;
Retinal Detachment
;
Retinal Perforations
;
Vitrectomy*
5.Clinical Features of Pregnancy-associated Retinal and Choroidal Diseases Causing Acute Visual Disturbance.
Young Joo PARK ; Kyu Hyung PARK ; Se Joon WOO
Korean Journal of Ophthalmology 2017;31(4):320-327
PURPOSE: To report clinical features of patients with retinal and choroidal diseases presenting with acute visual disturbance during pregnancy. METHODS: In this retrospective case series, patients who developed acute visual loss during pregnancy (including puerperium) and visited a tertiary hospital from July 2007 to June 2015, were recruited by searching electronic medical records. Patients were categorized according to the cause of visual loss. Clinical features and required diagnostic modalities were analyzed in the retinal and choroidal disease group. RESULTS: Acute visual loss occurred in 147 patients; 49 (38.9%) were classified into the retinal and choroidal group. The diagnoses included central serous chorioretinopathy (22.4%), hypertensive retinopathy with or without pre-eclampsia (22.4%), retinal tear with or without retinal detachment (18.4%), diabetic retinopathy progression (10.2%), Vogt-Koyanagi-Harada disease (4.1%), retinal artery occlusion (4.1%), multiple evanescent white dot syndrome (4.1%), and others (14.3%). Visual symptoms first appeared at gestational age 25.9 ± 10.3 weeks. The initial best-corrected visual acuity (BCVA) was 0.27 ± 0.39 logarithm of the minimum angle of resolution (logMAR); the final BCVA after delivery improved to 0.13 ± 0.35 logMAR. Serious visual deterioration (BCVA worth than 20 / 200) developed in two patients. Differential diagnoses were established with characteristic fundus and spectral-domain optical coherence tomography findings in all cases. CONCLUSIONS: In pregnant women with acute visual loss, retinal and choroidal diseases are common and could be vision threatening. Physicians should be aware of pregnancy-associated retinal and choroidal diseases and their clinical features. The differential diagnosis can be established with non-invasive techniques.
Central Serous Chorioretinopathy
;
Choroid Diseases*
;
Choroid*
;
Diabetic Retinopathy
;
Diagnosis
;
Diagnosis, Differential
;
Electronic Health Records
;
Female
;
Gestational Age
;
Humans
;
Hypertensive Retinopathy
;
Pre-Eclampsia
;
Pregnancy
;
Pregnant Women
;
Retinal Artery Occlusion
;
Retinal Detachment
;
Retinal Diseases
;
Retinal Perforations
;
Retinaldehyde*
;
Retrospective Studies
;
Tertiary Care Centers
;
Tomography, Optical Coherence
;
Uveomeningoencephalitic Syndrome
;
Visual Acuity
6.Clinical Features and Surgical Outcomes of Primary Rhegmatogenous Retinal Detachment according to Age.
Gye Jung KIM ; Min Chul SHIN ; Ho Sik HWANG ; So Young HAN ; Bum Joo CHO
Journal of the Korean Ophthalmological Society 2017;58(1):56-61
PURPOSE: To investigate the clinical features and surgical outcomes of rhegmatogenous retinal detachment (RRD) requiring surgery according to age. METHODS: Medical records of patients who underwent surgery for primary RRD between January 2008 and March 2016 were reviewed retrospectively. Patients were classified into two groups according to age at diagnosis: the under-40 group and the over-40 group. The two groups were compared in terms of demographic features, ocular manifestation, operating methods, primary anatomical success rate, and visual outcome. RESULTS: One hundred and forty-four eyes from 144 patients were included. Mean subject age was 48.6 ± 16.9 years old. The under-40 group involved 42 eyes from 42 patients, and the over-40 group included 102 eyes from 102 patients. Symptom duration was shorter in the under-40 group compared to the over-40 group (7.6 ± 10.7 days vs. 14.5 ± 24.4 days; p = 0.029). Proliferative vitreoretinopathy (PVR) occurred more frequently in the under-40 group (40.0% vs. 17.4%, p = 0.007) than in the over-40 group. The anatomical success rate of primary surgery was significantly different between the two groups; 78.6% in the under-40 group and 91.2% in the over-40 group (p = 0.038). Preoperative PVR increased the rate of anatomical failure (40.0% vs. 6.2%, p < 0.001). The visual outcomes were not significantly different between the two groups. CONCLUSIONS: RRD is combined with PVR more frequently in young patients than in old patients, which increases the failure rate of primary re-attachment surgery.
Diagnosis
;
Humans
;
Medical Records
;
Retinal Detachment*
;
Retinaldehyde*
;
Retrospective Studies
;
Scleral Buckling
;
Vitrectomy
;
Vitreoretinopathy, Proliferative
7.Is massive proteinuria associated with maternal and fetal morbidities in preeclampsia?.
Mi Jung KIM ; Young Nam KIM ; Eun Jung JUNG ; Hye Ree JANG ; Jung Mi BYUN ; Dae Hoon JEONG ; Moon Su SUNG ; Kyung Bok LEE ; Ki Tae KIM
Obstetrics & Gynecology Science 2017;60(3):260-265
OBJECTIVE: The aim of this study was to investigate whether massive proteinuria in preeclampsia is associated with maternal and fetal complications. METHODS: We retrospectively analyzed the clinical records of 233 patients who were diagnosed with preeclampsia. We divided the preeclamptic patients into three groups based on the amount of proteinuria: massive (≥5 g/24 hr), moderate (2 to 5 g/24 hr) and mild (<2 g/24 hr) proteinuria group. We analyzed the clinical characteristics and maternal and neonatal complications among three groups. RESULTS: Gestational age at diagnosis and delivery were lower in women with massive and moderate proteinuria group than women with mild proteinuria group (31.5±3.1 vs. 32.3±3.6 vs. 34.0±3.5 weeks, P<0.001 for gestational weeks at diagnosis; 34.6±3.6 vs. 35.1±4.1 vs. 36.9±4.0 weeks, P=0.001 for gestational age at delivery). In maternal complications, the incidences of pleural effusion and retinal detachment were significantly different among three groups (29.9% vs. 22.4% vs. 9.0%, P=0.004 for pleural effusion; 11.5% vs. 3.0% vs. 1.3%, P=0.009 for retinal detachment). Creatinine levels were higher and albumin levels were lower in the massive proteinuria group than in the moderate and mild groups. However, other maternal and neonatal complications were not significantly different among three groups. CONCLUSION: Massive proteinuria might be associated with renal albumin excretion-related morbidity, such as pleural effusion, retinal detachment, and low serum albumin levels. Furthermore, it was associated with early-onset preeclampsia and early delivery.
Creatinine
;
Diagnosis
;
Female
;
Gestational Age
;
Humans
;
Incidence
;
Pleural Effusion
;
Pre-Eclampsia*
;
Pregnancy Complications
;
Proteinuria*
;
Retinal Detachment
;
Retinaldehyde
;
Retrospective Studies
;
Serum Albumin
8.A Case Report of Takayasu's Arteritis with Traction Retinal Detachment.
Ga In LEE ; Kunho BAE ; Jong Min KIM ; Se Woong KANG
Journal of the Korean Ophthalmological Society 2017;58(5):600-605
PURPOSE: To report a rare case of traction retinal detachment and retinal ischemia in inactive Takayasu's arteritis at ophthalmologic clinic. CASE SUMMARY: A 23-year-old woman presented with a floater, photophobia, and visual loss in her right eye one week prior to visit. She had no other systemic disease, such as diabetes mellitus or hypertension, or previous ophthalmic abnormalities except for a tumor in the adrenal gland. We found bilateral retinal ischemia and traction retinal detachment in the right eye on fundus examination without iris neovascularization. Pars plana vitrectomy, traction removal, endolaser treatment, and intravitreal bevacizumab injection were performed. Steroid eye drops and steroid systemic administration relieved the inflammation. On carotid doppler sonography, we found severe stenosis and thickness of the inner layer in both carotid arteries. We diagnosed the patient with an inactive phase of Takayasu's arteritis, which was conclusively correlated with the clinical features. Vascular anastomosis surgery along with follow-up was proposed by both the cardiology and vascular surgery departments. CONCLUSIONS: When a young patient presents with traction retinal detachment and retinal ischemia, Takayasu's arteritis should be considered for differential diagnosis and a systemic work-up should be performed as soon as possible.
Adrenal Glands
;
Bevacizumab
;
Cardiology
;
Carotid Arteries
;
Constriction, Pathologic
;
Diabetes Mellitus
;
Diagnosis, Differential
;
Female
;
Follow-Up Studies
;
Humans
;
Hypertension
;
Inflammation
;
Iris
;
Ischemia
;
Ophthalmic Solutions
;
Photophobia
;
Retinal Detachment*
;
Retinaldehyde*
;
Takayasu Arteritis*
;
Traction*
;
Vitrectomy
;
Young Adult
9.Systemic Steroid Therapy for Serous Retinal Detachment Caused by Excessive Endolaser during Diabetic Retinopathy Surgery.
Ji Soo SHIN ; Chung Hwan KIM ; Young Suk CHANG ; Young Hoon LEE
Journal of the Korean Ophthalmological Society 2016;57(6):1004-1011
PURPOSE: To report cases of macular serous retinal detachment caused by excessive intraoperative endolaser in patients with diabetic vitreous hemorrhage. Macular serous retinal detachment was improved by systemic steroid therapy. CASE SUMMARY: A 64-year-old male (case 1) and a 67-year-old female (case 2) treated with vitrectomy and endolaser (case 1, 3,184 shots; case 2, 1,734 shots) because of diabetic vitreous hemorrhage visited our out-patient clinic with blurred vision. Best corrected visual acuity (BCVA) in case 1 was hand motion and 0.03 in case 2. Fundus examination and optical coherence tomography (OCT) revealed extensive subretinal fluid accumulation of the posterior pole. With the diagnosis of macular serous retinal detachment caused by excessive intraoperative endoaser, oral steroid (40 mg/qd, 5 days) was administered and then later reduced in case 1. In case 2, we administered intravenous high-dose steroid (250 mg/qid, 3 days). After systemic steroid therapy, BCVA was improved to 20/30 in case 1 and 20/40 in case 2 and OCT showed the subretinal fluid was resolved. CONCLUSIONS: During diabetic retinopathy surgery, excessive endolaser induced macular serous retinal detachment and systemic steroid therapy was necessary in diabetic patients. Thus, physicians should be well acquainted with this complication.
Aged
;
Diabetic Retinopathy*
;
Diagnosis
;
Female
;
Hand
;
Humans
;
Male
;
Middle Aged
;
Outpatients
;
Retinal Detachment*
;
Retinaldehyde*
;
Subretinal Fluid
;
Tomography, Optical Coherence
;
Visual Acuity
;
Vitrectomy
;
Vitreous Hemorrhage
10.Diagnosis of Severe Protein C Deficiency Confirmed by Presence of Rare PROC Gene Mutation.
Myung Seop LIM ; Jung Eun SHIN ; Soon Min LEE ; Ho Sun EUN ; Min Soo PARK ; Kook In PARK ; Ran NAMGUNG ; Kyung A LEE ; Jin Sung LEE
Neonatal Medicine 2016;23(4):233-237
Protein C (PROC) deficiency is caused by mutations in the PROC gene on chromosome 2q14.3. Patients with PROC deficiency typically present distinguished purpura, intracerebral and intravascular coagulopathy, and ophthalmologic complications. Here, we report a rare severe form of PROC deficiency resulting from a compound heterozygosity in PROC. The patient was a 5-day-old female neonate born at 39 weeks of gestation with a birth weight of 2,960 g. She was transferred to our hospital with running a fever at 38.5℃ and with dark red patches on her feet. At admission, a complete blood count showed no specific findings, but levels of PROC and protein S were abnormally low (1% and 68%, respectively). Magnetic resonance imaging revealed intracerebral hemorrhaging and parenchymal damage with dysplasia of the brain. Ophthalmologic examination revealed vitreous hemorrhaging with retinal detachment. Genetic testing revealed a missense mutation (Arg211Trp) and a frameshift mutation (Gly239Serfs*8) in PROC, inherited from the father and mother, respectively. The patient recovered from purpura after undergoing ventriculoperitoneal shunting and treatment with fresh frozen plasma, warfarin sodium, and PROC concentrate. This is the first report of severe neonatal PROC deficiency with purpura fulminans, vitreous hemorrhage, and intracerebral hemorrhage confirmed via PROC genetic testing, which identified a rare compound heterozygosity of PROC.
Birth Weight
;
Blood Cell Count
;
Brain
;
Cerebral Hemorrhage
;
Diagnosis*
;
Fathers
;
Female
;
Fever
;
Foot
;
Frameshift Mutation
;
Genetic Testing
;
Humans
;
Infant, Newborn
;
Magnetic Resonance Imaging
;
Mothers
;
Mutation, Missense
;
Plasma
;
Pregnancy
;
Protein C Deficiency*
;
Protein C*
;
Protein S
;
Purpura
;
Purpura Fulminans
;
Retinal Detachment
;
Running
;
Ventriculoperitoneal Shunt
;
Vitreous Hemorrhage
;
Warfarin

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