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Subsequent fibrovascular tissue growth may partially or totally obscure their margins hair loss oil dutasteride 0.5 mg cheap. Patients with angioid streaks should be warned of the potential risk of choroidal rupture from even relatively mild eye trauma hair loss vitamins that work buy dutasteride 0.5mg otc. It usually occurs in healthy patients between the third and sixth decades of life hair loss cure home remedies generic dutasteride 0.5 mg with amex, and the scars are probably caused by an antecedent subclinical systemic infection with Histoplasma capsulatum hair loss cure 3 shoes buy 0.5 mg dutasteride with visa. If it extends inside the foveal avascular zone hair loss hormones purchase dutasteride online from canada, only 15% of eyes will retain 20/40 vision hair loss cure guide quality 0.5mg dutasteride. Intravitreal injections have additional risks in younger patients because their posterior vitreous has not detached, but intravitreal bevacizumab produces significant improvement in vision at 1 year. Surgical removal of subfoveal membranes has been disappointing, with stabilization of vision occurring only in those with preoperative visual acuity worse than 20/100. However, visual acuity remains 6/15 or less in 25% of cases, and recurrence occurs in 50%. The prognosis in atypical cases, such as unilateral disease or older presentation, is more guarded. Serpiginous Choroidopathy this is a rare, recurrent, and chronically progressive inflammatory disease of unknown cause. It presents with unilateral blurring of central vision, metamorphopsia, or scotoma, but usually, there is asymmetrical bilateral involvement. It characteristically involves the juxtapapillary retina and extends radially to involve the macula and peripheral retina. The natural history is variable and may correlate with the presence of disease in the fellow eye. Oral or systemic corticosteroid treatment or other immunosuppressants, such as infliximab, may be beneficial during active disease. Electroretinography is useful for diagnosis and monitoring disease progression and response to treatment. The macular lesions are subtle, reddish-brown, and best seen with a red-free light. The retinal lesions gradually regress in a matter of weeks, leaving only minor retinal pigment epithelial defects. Usually the disease is restricted to symmetrical macular involvement, but rarely there is associated spinocerebellar ataxia. In others, the fundoscopic changes are very striking when the patient is still asymptomatic. Visual acuity begins to 481 fall during the first or second decade of life and then may remain stable until the fifth or sixth decade but generally reduces to between 20/40 and 20/200 as the disease progresses. Fifty percent of patients have peripheral retinoschisis with peripheral visual field abnormalities. X-linked juvenile retinoschisis with typical superficial retinal cysts in the fovea. Enhanced S-cone syndrome showing typical disk-like pigmentation around the vascular arcades. Cone and Cone-Rod Dystrophies (Cone-Dominant Dystrophies) Cone and cone-rod dystrophies are relatively rare. Most cases are sporadic, but there may be autosomal dominant, autosomal recessive, or X-linked recessive inheritance. The hallmark is predominant involvement of cone photoreceptors, with presentation in early adulthood with impairment of central vision and color vision, and hemeralopia (intolerance to light). There may be optic disk pallor with no obvious macular changes, leading to misdiagnosis of optic nerve disease. Electroretinography shows marked loss of cone function and slight to moderate loss of rod function. About one-third of patients present in the first decade of life, one-third in the second decade of life, and one-third over 20 years of age. Initially, there is no 486 macular abnormality clinically, but subsequently, there develops a bronze metal appearance together with mid-peripheral retinal flecks, like those seen in fundus flavimaculatus. Once visual acuity has dropped to 20/40, it usually declines to 20/200 in 5 years. Patients with fundus flavimaculatus present later than patients with Stargardt disease. They have retinal flecks distributed over the whole of the posterior pole of each eye. Different phenotypes can be partly explained by different mutations of the same genes. Abnormal vitamin A metabolism including high level of vitamin A dimers may play a role in disease progression (eg, acceleration of accumulation of lipofuscin), and hence vitamin A supplementation should be avoided. Best Vitelliform Macular Dystrophy Best disease is an autosomal dominant disorder with variable penetrance and expressivity. Optical coherence tomography showing hyperreflective subretinal material in the fovea. It is the most common hereditary fundus dystrophy, with a reported prevalence of 1 in 5000. X-linked recessive is the least common but most severe form, with some affected individuals being totally blind by the third or fourth decade. Sporadic cases may have a more favorable prognosis, with retained central vision until the sixth decade or later. The hallmark symptoms of retinitis pigmentosa are night blindness (nyctalopia) and gradually progressive peripheral visual field loss as a result of increasing and coalescing ring scotomas. Although retinitis pigmentosa is a generalized photoreceptor disorder, in most cases, rod function is more severely affected, predominantly leading to poor scotopic vision. Retinitis pigmentosa with arteriolar narrowing and peripheral retinal pigment clumping. Other less common complications include open-angle glaucoma, keratoconus, posterior vitreous detachment, intermediate uveitis, and a Coats-like disease with peripheral retinal lipid deposition and exudative retinal detachment. Central visual impairment may be due to macular atrophy, epimacular membrane, or cystoid macular edema. No specific treatment is available, but regular follow-up may help provide support to patients. High-dose vitamin A has been reported to be marginally beneficial but can be toxic. Patients need to be advised to stop smoking and to avoid other retinotoxic drugs such as hydroxychloroquine, phenothiazine, and vigabatrin. There has been rapid progress in identification of mutations in retinitis pigmentosa. Patients should be referred to specialized centers for genetic counseling and selective mutation analysis. Genetic analysis is useful to identify female carriers in families with X-linked disease and to diagnose dominant disease. In recessive disease, specific features are needed for genetic analysis to be worthwhile. Patients have night blindness, but other parameters such as visual acuity, visual fields, and color vision are normal. Retinitis punctata albescens is the less common progressive variant of this dystrophy. Familial benign fleck retina syndrome is a very rare autosomal recessive disorder. Benign flecked retina syndrome with multiple diffuse yellow white lesions throughout the retina but sparing the fovea. It presents as a triad of severe visual impairment or blindness beginning in the first year of life, nystagmus, and generalized retinal dystrophy. The fundoscopic findings are variable; most patients show either a normal appearance or only subtle retinal pigment epithelial granularity and mild vessel attenuation. The division between these entities is unclear, and they are best classified on a genetic basis. Human clinical trials of gene therapy are ongoing in England and the United States. The incidence of this disorder is relatively high in Finland, and the ophthalmologic features are the most prominent manifestations of the disease. Patients initially present with myopia and then develop nyctalopia within the first decade of life, followed by progressive loss of peripheral visual field. Characteristic sharply demarcated circular areas of chorioretinal atrophy develop in the midperiphery of the fundus during the teenage years and become confluent with macular involvement late in the course of the disease. Reduction in dietary intake of arginine has been shown to slow progression of the disease. Other treatments include pyridoxine supplementation and supplemental dietary lysine. Spectral sensitivity studies have identified blue, green, and red cone photoreceptors. A minimal requirement for color (hue) discrimination is the presence of at least two kinds of cone photopigment (opsin), and normal color vision requires the presence of all three (trichromacy). Acquired color vision defects vary in type and severity, depending on the location and source of the ocular pathology, and frequently affect one eye more than the other. Congenital color vision defects are constant in type and severity throughout life and affect both eyes equally. The most common congenital color vision defect, red-green color deficiency, is a form of dichromacy, with only two out of three cone opsins functioning normally. It results from mutation in the gene encoding for either the red (protanopia) or green (deuteranopia) cone opsin. The third type of dichromacy, tritanopia, in which there is loss of blue-yellow discrimination due to defect in the blue cone opsin, is a rare autosomal dominant condition resulting from a mutation on chromosome 7. Although both leave the affected individual completely without color discrimination (achromatopsia), they are two quite separate entities. In the less common cone monochromacy (1 in 100,000), visual acuity is normal, but there is no hue discrimination. It is usually due to blue cone monochromacy, an X-linked recessive condition resulting from mutations in the genes encoding for both red and green cone opsins. In rod monochromacy (1 in 30,000), an autosomal recessive condition caused by mutations in genes encoding proteins of the photoreceptor cation channel or cone transducin, there 493 are no functioning cones, resulting in achromatic vision, low visual acuity, photophobia, and nystagmus. They may enlarge slowly but have little or no invasive potential and no metastatic capability. Hamartomas are congenital tumors composed of normal or near normal cells and tissues that occur normally at that anatomic site but are present in excess. Choristomas are congenital tumors composed of normal cells and tissue elements that do not occur normally at that anatomic site. It may be part of an inheritable syndrome, usually tuberous sclerosis, or a noninherited isolated entity. The retinal astrocytomas that occur in tuberous sclerosis frequently are multifocal and bilateral, whereas nonsyndromic retinal astrocytomas are almost exclusively unilateral and unifocal. Retinal astrocytomas usually become evident during the first or second 494 decade of life. Small lesions appear as ill-defined translucent spots in the inner retina (opalescent patches). Generally, no treatment is indicated unless substantial enlargement is documented. Rarely, a retinal astrocytoma of either the syndromic or isolated variety undergoes substantial progressive enlargement associated with malignant transformation. Solitary retinal astrocytoma just superior to fovea in an 11 year-old boy with tuberous sclerosis. Retinal Capillary Hemangioma (von Hippel tumor) Retinal capillary hemangioma is an acquired benign neoplasm of the retina that is composed of neural retinal cells transformed into poorly differentiated small cells with prominent nuclei and little cytoplasm. The tumor blood vessels tend to be leaky, resulting in progressive accumulation of 495 intraretinal edema and exudates and exudative subretinal fluid around the tumor. As the tumor enlarges, the exudative retinal detachment usually increases in extent and becomes associated with substantial vitreoretinal fibrosis resulting in tractional retinal detachment.

Once the maximum laser intensity was achieved hair loss 5 years dutasteride 0.5 mg cheap, the d d gram nds the match between the calculated and the mea analyzer was placed behind a pair of blank slides without the sured values of R and T hair loss in men zip wallet buy discount dutasteride 0.5 mg line, the optical properties of the sample sample between them hair loss 11 year old discount dutasteride american express. The analyzer was then rotated to d d are found; these values are then given as output of the pro maximize the light intensity so that the transmission axes of gram in terms of the two dimensionless quantities: a and excessive hair loss cure purchase genuine dutasteride, the polarizer and analyzer were parallel hair loss cure protein order dutasteride 0.5mg online. The blank slides were then replaced by the retinal tissue sample placed in between absorption coefcient a and scattering coefcient s us the polarizer and analyzer hair loss in men 80 generic dutasteride 0.5mg otc. The average scattering anisotropy coef cients for diseased retinal tissues are signicantly wave cient of retinal tissues was determined from the goniometric length dependent, whereas the total attenuation coefcients measurements on the healthy sample and was found to be for the healthy retinal tissues are less wavelength dependent. The diseased tissue paper is too narrow to observe the wavelength dependencies was assumed to be of the same makeup as the healthy tissue, of the healthy tissues. Hence the anisotropy for the dis reectance Rd and total diffuse transmittance Td used to eased tissue was assumed to be 0. The margin of errors of the centage differences between the values obtained from the ex measurements of Rd and Td are also given in Table 1. The absorption and scattering coefcients were then calculated from the values of a and and the thickness t of the sample. The absorption coefcient a, scattering co efcient s, total attenuation coefcient t= a+ s, pen etration depth 1/ t, albedo a, and optical depth for the retinal tissues are given in Table 1. This shows that our assumption of nearly single scattering phenomenon in our experimental measurements for g is valid only within the experimental un certainties. The total attenuation coefcients of the healthy and diseased tissues are plotted as a function of laser wave Fig. In both the healthy and diseased retinal tissues, smaller than in the healthy tissues. The higher polarization the scattering coefcients are found to be signicantly higher shifts in the diseased retinal tissues can be attributed to the than the absorption coefcients; the higher values of scatter structural changes due to neovascularization. This observation is supported by the results given in Note also that the diseased eyes have both higher absorption Table 1, which shows that the scattering coefcient of the and higher scattering. The increased number of localized diseased retinal tissue is much higher than that of the healthy neovascularizations in the diseased retinal tissues could be the tissue for each laser wavelength. Note, however, that even polarization shifts between the left and right eyes could be though it does not account for the light that could be lost at attributed to the physiological differences in the eyes. Fur could have signicant importance for practical applications ther details can be found in Ref. Variable pigmentation obviously complicates the laser diseased human retinal tissues are given in Table 3. The dosimetry for such treatment modes, because the amount of average polarization shifts and average intensities for the light delivered will have to be adjusted based on the amount healthy and neovascularized human retina are shown in Figs. The tissue polarization study also is of particular im Table 3 Comparison of the average polarization shift and average intensity I between the healthy and diseased retinal tissues for the human left and right eyes at 632. The authors would like to thank Elia Villazana for preparing the tissue samples used in this study and also acknowledge Felipe Salinas for taking the data. Jacques Or egon Medical Laser Center and Lihong Wang Texas A&M University for the use of the source code for the Monte Carlo model. Finally, note that the diseased retinal tis the optical properties of the skin with in vitro and in vivo applica sues possess the strong polarization characteristics. It classically leads to bilateral chronic granulomatous diffuse uveitis, and its extraocular manifestation can include sensorineural hearing loss, meningitis, and cutaneous fndings of vitiligo, poliosis (loss of hair pigment) and alopecia. It is an and frightening for these patients than their autoimmune disorder of melanocyte proteins back pain and stiffness, so that most of them that occurs in genetically susceptible individu will urgently seek ophthalmology consultation. Furthermore, they are also refer fndings of vitiligo, poliosis (loss of hair pigment) ring patients with many other forms of non and alopecia [4,5,10,11]. It is therefore necessary for the rheu fectious uveitis in Brazil [14], the second most matologists to be familiar with its clinical aspects, common cause in Saudi Arabia [10], and the pathogenesis and appropriate management. However, a subse strikes between the third and ffth decades of life, quent analysis of microsatellite polymorphisms although there are also rare reports of its occur in the tyrosinase gene family in 87 Japanese rence in children [16]. A systemic inflammatory response against autoantigens by molecular cascade follows, affecting the meninges, uveal mimicry. This allele often marked by a prodromal period suggestive codes for amino acid substitutions in the anti of an acute viral infection. Hypersensitivity of the hair to target the infammatory cascade in these and scalp to touch is also not uncommon. They have hypothesized ment at this stage, although there may be some that this inability to self-regulate may in turn fare noted on examination owing to mild-to lead to the chronic, recurrent uveitis, which is moderate anterior uveitis simulating a non often the fnal stage of the disease. Tinnitus is the gle nucleotide polymorphisms in the gene that most common inner ear symptom, occurring in codes for cytotoxic T lymphocyte-associated approximately 40% of patients [41,43]. There may also be focal areas drome, as costimulation blockers have proven of alopecia. The frst Advancing to this stage portends poorer prog of these stages, the prodromal stage, typically nosis. Common signs of anterior granulomatous lasts days to weeks and precedes ocular involve involvement include large deposits, known as ment. This stage is suggestive of an acute viral mutton-fat keratic precipitates (Figure 2), on the illness or aseptic meningitis. Headache, nuchal endothelium of the cornea as well as whitish rigidity, nausea, low-grade fevers, photophobia, nodules in the stroma of the iris. The third criterion is that the ocular involve Also present are keratic precipitates with red ment has to be bilateral [36]. The hallmark of early involvement is signs and symptoms with the aid of ancillary diffuse choroiditis with either focal areas of testing. The frst three compo chronic and recurrent stages of the disease, he nents of the revised criteria are mandatory for or she must have a clinical history suspicious for diagnosis. The frst component specifes that those fndings mentioned previously in addition the patient should not have had any history of to bilateral ocular involvement manifested by penetrating ocular trauma or ocular surgery either chronic anterior uveitis or retinochoroidal (including nonpenetrating laser photocoagu degeneration. The fnal two criteria for diagnosis relate to extraocular manifestations of the disease. Occurrences of vitiligo, poliosis and alopecia are highly variable, and manifest in the chronic and recurrent stages of the disease [4,5]. Fulfllment of the frst three crite Reproduced with permission from Ana Elisa ria with either neurological/auditory involve Brito [45]. No clinical or laboratory evidence of another ocular disease Ancillary testing 4. Neurological/auditory fndings: meningismus, tinnitus or cerebrospinal A complete medical history and thorough physi fuid pleocytosis cal examination with special attention paid to 5. Finally, in the case of inner ear choroidal neovascularization, subretinal fbrosis involvement, the patient should be referred for and optic atrophy. In addition to the duration of audiologic testing with follow-up for evaluation disease and number of recurrences, older age of of progression. However, in the disease, neurosarcoidosis and multiple sclero last several years it has been demonstrated that sis [36,40,47]. With a greater understanding of the pathic, systemic infammatory disease caused pathogenesis of the disease and the infamma by an autoimmune T-cell reaction against pre tory cascade it is possible that therapies that sumed autoantigens in genetically susceptible selectively inhibit or modify these pathways will individuals. The disease Biologics comprise another branch of thera selectively involves melanocyte-containing pies that have led to improved outcomes in structures, and manifests itself with the dis many autoimmune diseases. The latter has already been employment, consultancies, honoraria, stock ownership or shown to be involved in the pathogenesis of such options, expert testimony, grants or patents received or systemic infammatory disease as infammatory pending, or royalties. However, such success hinges on early diagnosis and aggressive treatment that includes immunomodulatory therapy, and as a result ophthalmologists are increasingly referring such patients to rheumatologists for management of such therapy. BioDrugs, to 2007) has demonstrated the effcacy of management of infammatory eye diseases. Previous editions copyrighted 2011, 2007, 2003, 1990, 1984, 1978, 1970, 1964, 1959, 1954, 1948, 1942, 1938, 1936, 1934, 1930, 1926, 1923, 1918, 1912, 1907 No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopying, recording, or any information storage and retrieval system, without permission in writing from the Publisher. This book and the individual contributions contained in it are protected under copyright by the Publisher (other than as may be noted herein). As new research and experience broaden our understanding, changes in research methods, professional practices, or medical treat ment may become necessary. Practitioners and researchers must always rely on their own experience and knowledge in evalu ating and using any information, methods, compounds, or experiments described herein. In using such information or methods they should be mindful of their own safety and the safety of others, including parties for whom they have a professional responsibility. To the fullest extent of the law, neither the Publisher nor the authors, contributors, or editors, assume any liability for any injury and/or damage to persons or property as a matter of products liability, negligence or otherwise, or from any use or operation of any methods, products, instruc tions, or ideas contained in the material herein. Please consult full prescribing information before issuing prescription for any product mentioned in this publication. The Publisher Published by Elsevier, a division of Reed Elsevier India Private Limited Registered Office: 305, Rohit House, 3 Tolstoy Marg, New Delhi-110 001 Corporate Office: 14th Floor, Building No. This classic textbook your information spectrum as much as we did in preparing with its unique features provides a comprehensive com it for you. This Ramanjit Sihota 22nd Edition has been updated keeping in view the chang Radhika Tandon ing disease spectrum, practice patterns and advancements v this page intentionally left blank Preface to the Nineteenth Edition It was a privilege to update this classic textbook of ophthal enough to warrant an independent chapter. In all, three mology, which has educated many generations of medical new chapters have been added: Ocular Manifestations students and ophthalmologists. In view of the tremendous advances in the diagno ing and make the text more interesting. The rest of the avatars, serves as a basic text to establish the foundations book has been almost completely rewritten to incorporate of knowledge of ophthalmology for undergraduates and newer trends in classification, diagnosis and management. Genetics is an integral part of medicine today and a detailed description of the presently Ramanjit Sihota known genetic associations and their possible utility in the Radhika Tandon management of ocular diseases was considered important vii this page intentionally left blank Acknowledgements the authors remain deeply indebted to the faculty, residents Dr. Rajendra Prasad Centre for Ophthalmic Professor and Head Sciences, Chief of the Centre, and Director of All India Department of Ophthalmology Institute of Medical Sciences for the rich academic and Bharati Vidyapeeth Deemed University Medical College clinical milieu provided to nurture our work. Department of Ophthalmology We acknowledge and greatly appreciate the efforts and Pt. Medical College invaluable comments of our reviewers, we would especially Raipur like to thank the following: Dr. Chaitra Jayadev Consultant Pediatric Ophthalmologist Consultant, Vitreoretina Services Dr. Shroff Senior Consultant, Glaucoma Services Medical Director, Shroff Eye Centre Glaucoma Department and Research Director Past President, Vitreo Retinal Society of India Sankara Nethralaya, Chennai New Delhi Dr. Jaya Devendra Assistant Professor Associate Professor Gandhi Medical College Department of Ophthalmology Bhopal Rohilkhand Medical College and Hospital Bareilly Our special thanks to Dr. Niharika Pant, Professor, Department of Ophthalmology Veer Chandra Singh Garhwali Government Medical Sciences Padmashree Dr. Specialist Ophthalmologist Last but not the least, we would like to make an endear Uveitis and Ocular Immunology ing mention of our families who with their loyal forbearance New Medical Centre Specialty Hospital allowed us to spend our spare time and devote our attention Abu Dhabi to this work without which it would have been impossible to achieve. Rao Professor and Head Ramanjit Sihota Department of Ophthalmology Radhika Tandon Kasturba Medical College & Hospital Manipal Dr.

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Fluorescein angiography montage shows several anomalies: Capillary anomalies related to the presence of collateral circulation in the temporal part of the macula hair loss in men hair buy dutasteride in india. There are also multiple capillary anomalies in the vicinity of the vein whose walls are highly hyperfuorescent in the lower part of the macula hair loss cure pgd2 purchase 0.5 mg dutasteride otc. The examination allows clear visualization of the ischemic areas and anomalies related to the disappearance of capillary networks in the vicinity of the vein and in the lower part of the macula hair loss using wen products trusted 0.5mg dutasteride. The examination shows hair loss cure queentet order generic dutasteride online, in the vicinity of the inferior temporal artery hair loss treatment usa generic dutasteride 0.5mg free shipping, a small preretinal choroidal neovascularization hair loss cure in 2016 order dutasteride line. The scan passing through the superfcial retina (A) clearly shows the ischemic area and the preretinal choroidal neovascularization. The choroidal neovascularization is better analyzed in front of the retinal plane (B), which confrms the preretinal location of the neovascularization. However, there are a few microaneurysms that are better visualized on the corresponding fuorescein angiography (A). The image comparison shows that the preretinal neovascularization develops at the retina surface but also extends in front of it, along the posterior vitreous cortex into the vitreous cavity. The color photo shows micro-hemorrhages but does not allow visualization of the capillary impairment. Fluorescein angiography shows macular capillary impairment 1 2 in ischemic diabetic maculopathy. Color photo (3) and fuorescein angiography (4) in 2011: the fuorescein angiography follow-up allows assessing the loss of macular capillaries over time. The capillary changes are much more important in the deep retina where the deep capillary plexus has almost disappeared. However, they are commonly accompanied, at one stage or another in their evolution, by a localized disappearance of the retinal pigment epithelium, i. C the scan passing through the choriocapillaris shows an almost complete disappearance of the choriocapillaris. D the scan passing through the choroid shows a normal choroidal vascular network. On fundus autofuorescence (2), there are the pseudo-drusen and the presence of paracentral dark areas corresponding to the atrophy. Indeed at the atrophic areas, abnormal choroidal vascular networks are visualized. This should not be mistaken for choroidal neovascularization, it simply corresponds to a window defect allowing visualizing abnormal choroid networks. Color photo (1) and fundus autofuorescence image (2) show areas of retinal pigment epithelium atrophic, with better visualization on fundus autofuorescence. Note the difuse and nonhomogeneous hyperautofuorescence of the fundus outside the atrophy areas. Note an early central hyperfuorescence with late dye leakage (yellow arrows) was poorly identifable due to the staining of many atrophy areas. The image is very dark in the late phase (4), due to a choroidal silence outside the atrophy. This allows clear visualization of large choroidal vessels for the scans passing through the choroid (B). However, the scan passing through the retinal pigment epithelium (A) shows a neovascular network corresponding to active new vessels (red circle). Fundus autofuorescence image (2): the vitelliform deposit appears highly hyperautofuorescent. However, there is some hypoautofuorescence in the upper part of the vitelliform deposit. B the scan theoretically passing through the deep retina actually passes through the vitelliform deposit. C the scan passing through the choroid is disrupted probably because the subretinal vitelliform deposit blocks the signal. However, the presence of choroidal neovascularization may be ruled out (no network fow). Color photo (1) and red-free image (2) shows retinal pigment epithelium disturbances, drusen and vitelliform deposits. Angiographic sequence: There is a difuse nonhomogeneous fuorescence that could be related either to the staining of deposits or to the presence of associated occult neovascularization. Fundus autofuorescence image (2) shows macular pigment disturbances associated with a temporal atrophic area. B the scan passing through the deep retina is also relatively undisrupted and shows no signifcant diference between the atrophic area and the remaining portion of the fundus. C and D However, the deeper scans passing through the retinal pigment epithelium (C) or the choroid (D) show discontinuous areas corresponding to areas of localized disappearance of the choriocapillaris. However, most often the choriocapillaris appears nonhomogeneous, making choroidal vessels visible that should not be mistaken with choroidal new vessels. Fundus autofuorescence image (2): Interpapillo-macular retinal pigment epithelium disturbances. There is mainly a leaking point (red arrow) appearing from the intermediate phases of the sequence (5) flling a serous retinal detachment (6). C the scan pass beneath the retinal pigment epithelium confrms the avascular appearance of the pigment epithelium detachment. Some retinal pigment epithelium disturbances are seen on fundus autofuorescence (2). After treatment, the laser scar results in a highly localized dark image (red arrow). Note also small hyperautofuorescent spots that could correspond to photoreceptor debris, which shows the chronic appearance of a serous retinal detachment. In contrast, the B-scan (6) passing through the macula confrms the presence of areas of retinal pigment epithelium elevation associated with a serous retinal detachment. This appearance could correspond to an abnormal visibility of some vessels in the choroid. The red-free flter image (2) was discreetly decentered to better visualize the exudates developed in the nasal part of the fundus. C the scan passing through the superfcial capillary plexus shows the angioma over which the vascular network is superimposed. There are dilations on the wall of the large vessels as well as at the capillaries. The horizontal B-scan passing through the macula (5) shows a serous retinal detachment associated with an intraretinal edema. There is an excellent correlation between both examinations to locate some, but not all, capillary dilations. It is surrounded by a hyperautofuorescent area that could correspond to a leakage area. Fluorescein angiography confrms the presence of a nonhomogeneous fuorescence remote from the tumor. The fundus autofuorescence image (2) shows a central, dark nonhomogeneous image associated with a lower hyper-autofuorescence that could indicate a chronic serous retinal detachment. The late phase of the indocyanine green angiography (4) shows a central dark image, corresponding to the nevus. The B-scan pass at this level (6) confrms the presence of a serous retinal detachment. In the present case, B-scan ultrasonography has found a simple nevus complicated by leakages without signs of malignancy. On fundus autofuorescence (2), there are signifcant retinal pigment epithelium disturbances resulting in a very dark image. On the B-scan (8) passing through the macula, the deep retina appears hyper-refective. The scans passing through the choroid (B) show a localized disappearance of the choroidal circulation and choriocapillaris. Blue refectance image (2): the greyish oval is very suggestive of the diagnosis of macular telangiectasia type 2. Quantitative optical coherence tomography angiography of choroidal neovascularization in age-related macular degeneration. Spectral Domain Optical Coherence tomography angiography of choroidal neovascularization. Choroidal neovascularization analyzed on ultrahigh-speed swept-source optical coherence tomography angiography compared to spectral-domain optical coherence tomography angiography. Type 2 neovscularization secondary to age-related macular degeneration imaged by optical coherence tomography angiography. Optical coherence tomography angiography of asymptomatic neovascularization in intermediate age-related macular degeneration. Detection of non-exudative choroidal neovascularization in age-related macular degeneration with optical coherence tomography angiography. Optical coherence tomography angiography of type 1 neovascularization in age-related macular degeneration. Optical coherence tomography angiography characteristics of polypoidal choroidal vasculopathy. Optical coherence tomography angiography of idiopathic polypoidal choroidal vasculopathy. Optical coherence tomography angiography of polypoidal choroidal vasculopathy and polypoidal choroidal neovascularization. Optical coherence tomography angiography features of subretinal fbrosis in age related macular degeneration. Highlight shows a perfused vascular network within the fbrosis associated with changes in outer retinal layers and choriocapillaris in contact with fbrosis. Optical coherence tomography angiography shows signs of vascular abnormalization with antiangiogenic therapy for choroidal neovascularization. Shows vascular rearrangement under antiangiogenic treatment but there is an absence of normalization. Longitudinal optical coherence tomography angiography study of type 2 naive choroidal neovascularization early response after treatment. Characterizing the efect of anti-vascular endothelial growth factor therapy on treatment-naive choroidal neovascularization using optical coherence tomography angiography. Optical coherence tomography angiography reveals mature, tangled vascular networks in eyes with neovascular age-related macular degeneration showing resistance to geographic atrophy. Optical coherence tomography angiography of choroidal neovascularization secondary to pathologic myopia. Retinal and choroidal vasculature in birdshot chorioretinopathy analyzed using spectral domain optical coherence tomography angiography. Edema and ischemia Diabetic retinopathy and diabetic macular edema Ishibazawa A, Nagaoka T, Takahashi A, et al. Optical coherence tomography angiography in diabetic retinopathy: a prospective pilot study. Capillary plexus anomalies in diabetic retinopathy on optical coherence tomography angiography. Evaluation of preretinal neovascularization in proliferative diabetic retinopathy using optical coherence tomography angiography. Distinguishing diabetic macular edema from capillary nonperfusion using optical coherence tomography angiography. Automated quantifcation of capillary non-perfusion using optical coherence tomography angiography in diabetic retinopathy. Enlargement of foveal avascular zone in diabetic eyes evaluated by en face optical coherence tomography angiography. Optical coherence tomography angiography of the foveal avascular zone in diabetic retinopathy. This study stresses the disorganization of the vasculature surrounding the central avascular zone with the presence of more pronounced disturbances at the deep capillary plexus. Optical coherence tomography angiography in retinal vein occlusion: evaluation of superfcial and deep capillary plexa. En-face optical coherence tomography angiography of neovascularization elsewhere in hemicentral retinal vein occlusion. Optical coherence tomography angiography in retinal vascular diseases and choroidal neovascularization. Microvascular abnormalities on optical coherence tomography angiography in macular edema associated with branch retinal vein occlusion. Capillary network anomalies in branch retinal vein occlusion on optical coherence tomography angiography. Optical coherence tomography angiography shows deep capillary plexus hypo perfusion in incomplete central retinal artery occlusion. Optical coherence tomography angiography of a choroidal neovascularization in adult-onset foveomacular vitelliform dystrophy: pearls and pitfalls. Optical coherence tomography angiography in adult-onset foveomacular vitelliform dystrophy. Chronic central serous chorioretinopathy imaged by optical coherence tomographic angiography. Vascularization of irregular retinal pigment epithelial detachments in chronic central serous chorioretinopathy evaluated with oct angiography. Optical coherence tomography angiography of shallow irregular pigment epithelial detachments in pachychoroid spectrum disease. Association of choroidal neovascularization and central serous chorioretinopathy with optical coherence tomography angiography. Outer retina capillary invasion and ellipsoid zone loss in macular telangiectasia type 2 imaged by optical coherence tomography angiography. Characteristics and quantifcation of vascular changes in macular telangiectasia type 2 on optical coherence tomography angiography. Wide-feld imaging of retinal vasculature using optical coherence tomography-based microangiography provided by motion tracking. Professor Bruno Lumbroso, for his perspicacity, his communicative enthusiasm and the kindness of his welcome.

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Navigational Note: Periodontal disease Gingival recession or Moderate gingival recession Spontaneous bleeding; severe gingivitis; limited bleeding on or gingivitis; multiple sites of bone loss with or without probing; mild local bone loss bleeding on probing; tooth loss; osteonecrosis of moderate bone loss maxilla or mandible Definition:A disorder in the gingival tissue around the teeth hair loss cure 2015 histogen discount 0.5mg dutasteride overnight delivery. Navigational Note: Rectal fissure Asymptomatic Symptomatic Invasive intervention indicated Definition:A disorder characterized by a tear in the lining of the rectum hair loss and stress order dutasteride on line. Navigational Note: Rectal fistula Asymptomatic Symptomatic hair loss heart medication purchase dutasteride 0.5 mg with mastercard, invasive Invasive intervention Life-threatening Death intervention not indicated indicated consequences; urgent intervention indicated Definition:A disorder characterized by an abnormal communication between the rectum and another organ or anatomic site hair loss nexplanon buy 0.5mg dutasteride visa. Navigational Note: Rectal hemorrhage Mild symptoms; intervention Moderate symptoms; Transfusion indicated; Life-threatening Death not indicated intervention indicated invasive intervention consequences; urgent indicated; hospitalization intervention indicated Definition:A disorder characterized by bleeding from the rectal wall and discharged from the anus hair loss cure jm dutasteride 0.5mg lowest price. Navigational Note: Rectal perforation Invasive intervention not Invasive intervention Life-threatening Death indicated indicated consequences; urgent operative intervention indicated Definition:A disorder characterized by a rupture in the rectal wall hair loss natural treatment purchase dutasteride cheap online. Navigational Note: Salivary duct inflammation Slightly thickened saliva; Thick, ropy, sticky saliva; Acute salivary gland necrosis; Life-threatening Death slightly altered taste. Navigational Note: Salivary gland fistula Asymptomatic Symptomatic, invasive Invasive intervention Life-threatening Death intervention not indicated indicated consequences; urgent intervention indicated Definition:A disorder characterized by an abnormal communication between a salivary gland and another organ or anatomic site. Navigational Note: Small intestinal perforation Invasive intervention not Invasive intervention Life-threatening Death indicated indicated consequences; urgent operative intervention indicated Definition:A disorder characterized by a rupture in the small intestine wall. Navigational Note: Tooth discoloration Surface stains Definition:A disorder characterized by a change in tooth hue or tint. Navigational Note:Also report Investigations: Neutrophil count decreased Upper gastrointestinal Mild symptoms; intervention Moderate symptoms; Transfusion indicated; Life-threatening Death hemorrhage not indicated intervention indicated invasive intervention consequences; urgent indicated; hospitalization intervention indicated Definition:A disorder characterized by bleeding from the upper gastrointestinal tract (oral cavity, pharynx, esophagus, and stomach). Navigational Note: Visceral arterial ischemia Brief (<24 hrs) episode of Prolonged (>=24 hrs) or Life-threatening Death ischemia managed medically recurring symptoms and/or consequences; evidence of and without permanent invasive intervention end organ damage; urgent deficit indicated operative intervention indicated Definition:A disorder characterized by a decrease in blood supply due to narrowing or blockage of a visceral (mesenteric) artery. Navigational Note: Death neonatal Neonatal loss of life Definition:Newborn death occurring during the first 28 days after birth. Navigational Note:Synonym: Flu, Influenza Gait disturbance Mild change in gait. Navigational Note: Infusion site extravasation Painless edema Erythema with associated Ulceration or necrosis; severe Life-threatening Death symptoms. Signs and symptoms may include induration, erythema, swelling, burning sensation and marked discomfort at the infusion site. Navigational Note: Injection site reaction Tenderness with or without Pain; lipodystrophy; edema; Ulceration or necrosis; severe Life-threatening Death associated symptoms. Navigational Note: Neck edema Asymptomatic localized neck Moderate neck edema; slight Generalized neck edema. Vaccination site Local lymph node Localized ulceration; lymphadenopathy enlargement generalized lymph node enlargement Definition:A disorder characterized by lymph node enlargement after vaccination. Navigational Note: Biliary fistula Symptomatic, invasive Invasive intervention Life-threatening Death intervention not indicated indicated consequences; urgent intervention indicated Definition:A disorder characterized by an abnormal communication between the bile ducts and another organ or anatomic site. Navigational Note: Budd-Chiari syndrome Medical management Severe or medically significant Life-threatening Death indicated but not immediately life consequences; moderate to threatening; hospitalization or severe encephalopathy; coma prolongation of existing hospitalization indicated; asterixis; mild encephalopathy Definition:A disorder characterized by occlusion of the hepatic veins and typically presents with abdominal pain, ascites and hepatomegaly. Navigational Note: Cholecystitis Symptomatic; medical Severe symptoms; invasive Life-threatening Death intervention indicated intervention indicated consequences; urgent operative intervention indicated Definition:A disorder characterized by inflammation involving the gallbladder. Navigational Note: Gallbladder fistula Asymptomatic Symptomatic, invasive Invasive intervention Life-threatening Death intervention not indicated indicated consequences; urgent intervention indicated Definition:A disorder characterized by an abnormal communication between the gallbladder and another organ or anatomic site. Navigational Note: Gallbladder necrosis Life-threatening Death consequences; urgent invasive intervention indicated Definition:A disorder characterized by a necrotic process occurring in the gallbladder. Navigational Note: Gallbladder perforation Life-threatening Death consequences; urgent intervention indicated Definition:A disorder characterized by a rupture in the gallbladder wall. Navigational Note: Hepatic hemorrhage Mild symptoms; intervention Moderate symptoms; Transfusion indicated; Life-threatening Death not indicated intervention indicated invasive intervention consequences; urgent indicated; hospitalization intervention indicated Definition:A disorder characterized by bleeding from the liver. Navigational Note: Hepatic necrosis Life-threatening Death consequences; urgent invasive intervention indicated Definition:A disorder characterized by a necrotic process occurring in the hepatic parenchyma. Navigational Note: Perforation bile duct Invasive intervention Life-threatening Death indicated consequences; urgent operative intervention indicated Definition:A disorder characterized by a rupture in the wall of the extrahepatic or intrahepatic bile duct. Navigational Note: Portal hypertension Decreased portal vein flow Reversal/retrograde portal Life-threatening Death vein flow; associated with consequences; urgent varices and/or ascites intervention indicated Definition:A disorder characterized by an increase in blood pressure in the portal venous system. Navigational Note: Portal vein thrombosis Intervention not indicated Medical intervention Life-threatening Death indicated consequences; urgent intervention indicated Definition:A disorder characterized by the formation of a thrombus (blood clot) in the portal vein. Navigational Note: Sinusoidal obstruction Blood bilirubin 2-5 mg/dL; Blood bilirubin >5 mg/dL; Life-threatening Death syndrome minor interventions required coagulation modifier indicated consequences. Navigational Note:If related to infusion, use Injury, poisoning and procedural complications: Infusion related reaction. Anaphylaxis Symptomatic bronchospasm, Life-threatening Death with or without urticaria; consequences; urgent parenteral intervention intervention indicated indicated; allergy-related edema/angioedema; hypotension Definition:A disorder characterized by an acute inflammatory reaction resulting from the release of histamine and histamine-like substances from mast cells, causing a hypersensitivity immune response. Clinically, it presents with breathing difficulty, dizziness, hypotension, cyanosis and loss of consciousness and may lead to death. It occurs approximately six to twenty-one days following the administration of the foreign antigen. Navigational Note: Appendicitis perforated Medical intervention Life-threatening Death indicated; operative consequences; urgent intervention indicated intervention indicated Definition:A disorder characterized by acute inflammation to the vermiform appendix caused by a pathogenic agent with gangrenous changes resulting in the rupture of the appendiceal wall. Navigational Note: Bacteremia Blood culture positive with no signs or symptoms Definition:A disorder characterized by the presence of bacteria in the blood stream. Navigational Note: Endophthalmitis Local intervention indicated Systemic intervention; Best corrected visual acuity of hospitalization indicated 20/200 or worse in the affected eye Definition:A disorder characterized by an infectious process involving the internal structures of the eye. Navigational Note: Fungemia Moderate symptoms; medical Severe or medically significant intervention indicated but not immediately life threatening; hospitalization or prolongation of existing hospitalization indicated Definition:A disorder characterized by the presence of fungus in the blood stream. Navigational Note: Hepatitis viral Asymptomatic, intervention Moderate symptoms; medical Symptomatic liver Life-threatening Death not indicated intervention indicated dysfunction; fibrosis by consequences; severe biopsy; compensated decompensated liver function cirrhosis; hospitalization or. Navigational Note:For symptoms and no intervention, consider Respiratory, thoracic and mediastinal disorders: Sore throat or Hoarseness. Navigational Note: Myelitis Asymptomatic; mild signs Moderate weakness or Severe weakness or sensory Life-threatening Death. Unlike acne, this rash does not present with whiteheads or blackheads, and can be symptomatic, with itchy or tender lesions. Navigational Note:Synonym: Boil Rhinitis infective Localized; local intervention indicated Definition:A disorder characterized by an infectious process involving the nasal mucosal. Navigational Note: Viremia Moderate symptoms; medical Severe or medically significant intervention indicated but not immediately life threatening; hospitalization or prolongation of existing hospitalization indicated Definition:A disorder characterized by the presence of a virus in the blood stream. Symptoms include marked discomfort, swelling and difficulty moving the affected leg and foot. Navigational Note: Biliary anastomotic leak Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage of bile due to breakdown of a biliary anastomosis (surgical connection of two separate anatomic structures). Navigational Note: Bladder anastomotic leak Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage of urine due to breakdown of a bladder anastomosis (surgical connection of two separate anatomic structures). Navigational Note: Bruising Localized or in a dependent Generalized area Definition:A finding of injury of the soft tissues or bone characterized by leakage of blood into surrounding tissues. Navigational Note: Dermatitis radiation Faint erythema or dry Moderate to brisk erythema; Moist desquamation in areas Life-threatening Death desquamation patchy moist desquamation, other than skin folds and consequences; skin necrosis mostly confined to skin folds creases; bleeding induced by or ulceration of full thickness and creases; moderate edema minor trauma or abrasion dermis; spontaneous bleeding from involved site; skin graft indicated Definition:A finding of cutaneous inflammatory reaction occurring as a result of exposure to biologically effective levels of ionizing radiation. Navigational Note: Fall Minor with no resultant Symptomatic; noninvasive Hospitalization indicated; injuries; intervention not intervention indicated invasive intervention indicated indicated Definition:A finding of sudden movement downward, usually resulting in injury. Navigational Note: Fallopian tube anastomotic Asymptomatic; clinical or Symptomatic; medical Severe symptoms; invasive Life-threatening Death leak diagnostic observations only; intervention indicated intervention indicated consequences; urgent intervention not indicated operative intervention indicated Definition:A finding of leakage due to breakdown of a fallopian tube anastomosis (surgical connection of two separate anatomic structures). Navigational Note:Prior to using this term consider specific fracture areas: Injury, poisoning and procedural complications: Ankle fracture, Hip fracture, Spinal fracture, or Wrist fracture Gastric anastomotic leak Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage due to breakdown of a gastric anastomosis (surgical connection of two separate anatomic structures). Navigational Note: Gastrointestinal anastomotic Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death leak finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage due to breakdown of a gastrointestinal anastomosis (surgical connection of two separate anatomic structures). Navigational Note: Gastrointestinal stoma Superficial necrosis; Severe symptoms; Life-threatening Death necrosis intervention not indicated hospitalization indicated; consequences; urgent elective operative intervention indicated intervention indicated Definition:A disorder characterized by a necrotic process occurring in the gastrointestinal tract stoma. Navigational Note: Infusion related reaction Mild transient reaction; Therapy or infusion Prolonged. Navigational Note: Intestinal stoma leak Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage of contents from an intestinal stoma (surgically created opening on the surface of the body). Navigational Note: Intestinal stoma site bleeding Minimal bleeding identified Moderate bleeding; medical Transfusion indicated; Life-threatening Death on clinical exam; intervention intervention indicated invasive intervention consequences; urgent not indicated indicated intervention indicated Definition:A disorder characterized by bleeding from the intestinal stoma. Navigational Note: Intraoperative hemorrhage Postoperative invasive Life-threatening Death intervention indicated; consequences; urgent hospitalization intervention indicated Definition:A finding of uncontrolled bleeding during a surgical procedure. Navigational Note: Kidney anastomotic leak Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage of urine due to breakdown of a kidney anastomosis (surgical connection of two separate anatomic structures). Navigational Note: Large intestinal anastomotic Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death leak finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage due to breakdown of an anastomosis (surgical connection of two separate anatomic structures) in the large intestine. Navigational Note: Pharyngeal anastomotic leak Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage due to breakdown of a pharyngeal anastomosis (surgical connection of two separate anatomic structures). Navigational Note: Postoperative thoracic Extubated within 24 72 hrs Extubated >72 hrs Life-threatening airway Death procedure complication postoperatively postoperatively, but before compromise; urgent tracheostomy indicated intervention indicated. Navigational Note: Prolapse of urostomy Asymptomatic; clinical or Local care or maintenance; Dysfunctional stoma; elective Life-threatening Death diagnostic observations only; minor revision indicated operative intervention or consequences; urgent intervention not indicated major stomal revision intervention indicated indicated Definition:A finding of displacement of the urostomy. Navigational Note: Rectal anastomotic leak Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage due to breakdown of a rectal anastomosis (surgical connection of two separate anatomic structures). Navigational Note: Seroma Asymptomatic; clinical or Symptomatic; simple Symptomatic, elective diagnostic observations only; aspiration indicated invasive intervention intervention not indicated indicated Definition:A finding of tumor-like collection of serum in the tissues. Navigational Note: Small intestinal anastomotic Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death leak finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage due to breakdown of an anastomosis (surgical connection of two separate anatomic structures) in the small bowel. Navigational Note: Spermatic cord anastomotic Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death leak finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage due to breakdown of a spermatic cord anastomosis (surgical connection of two separate anatomic structures). Navigational Note: Stomal ulcer Asymptomatic; clinical or Symptomatic; medical Severe symptoms; elective diagnostic observations only; intervention indicated operative intervention intervention not indicated indicated Definition:A disorder characterized by a circumscribed, erosive lesion on the jejunal mucosal surface close to the anastomosis site following a gastroenterostomy procedure. Navigational Note: Tracheal hemorrhage Mild symptoms; intervention Moderate symptoms; Transfusion indicated; Life-threatening Death not indicated intervention indicated invasive intervention consequences; urgent indicated; hospitalization intervention indicated Definition:A disorder characterized by bleeding from the trachea. Navigational Note: Tracheostomy site bleeding Minimal bleeding identified Moderate bleeding; medical Transfusion indicated; Life-threatening Death on clinical exam; intervention intervention indicated invasive intervention consequences; urgent not indicated indicated intervention indicated Definition:A disorder characterized by bleeding from the tracheostomy site. Navigational Note: Urethral anastomotic leak Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage due to breakdown of a urethral anastomosis (surgical connection of two separate anatomic structures). Navigational Note: Urostomy leak Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage of contents from a urostomy. Navigational Note: Urostomy obstruction Asymptomatic; clinical or Symptomatic; dilation or Altered organ function. Navigational Note: Urostomy site bleeding Minimal bleeding identified Moderate bleeding; medical Transfusion indicated; Life-threatening Death on clinical exam; intervention intervention indicated invasive intervention consequences; urgent not indicated indicated intervention indicated Definition:A disorder characterized by bleeding from the urostomy site. Navigational Note: Uterine perforation Invasive intervention not Invasive intervention Life-threatening Death indicated indicated consequences; urgent intervention indicated Definition:A disorder characterized by a rupture in the uterine wall. Navigational Note:For systemic vaccination complications, consider Immune system disorders: Allergic reaction or Anaphylaxis. Vaginal anastomotic leak Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage due to breakdown of a vaginal anastomosis (surgical connection of two separate anatomic structures). Navigational Note: Vas deferens anastomotic leak Asymptomatic diagnostic Symptomatic; medical Severe symptoms; invasive Life-threatening Death finding; intervention not intervention indicated intervention indicated consequences; urgent indicated operative intervention indicated Definition:A finding of leakage due to breakdown of a vas deferens anastomosis (surgical connection of two separate anatomic structures). Navigational Note: Wound complication Observation only; topical Bedside local care indicated Operative intervention Life-threatening Death intervention indicated indicated consequences Definition:A finding of development of a new problem at the site of an existing wound. Navigational Note:Prior to using this term consider Injury, poisoning and procedural complications: Wound dehiscence or Infections and infestations: Wound infection Wound dehiscence Incisional separation, Incisional separation, local Fascial disruption or Life-threatening Death intervention not indicated care. Navigational Note:Also consider Hepatobiliary disorders: Hepatic failure Blood antidiuretic hormone Asymptomatic; clinical or Symptomatic; medical Hospitalization indicated abnormal diagnostic observations only; intervention indicated intervention not indicated Definition:A finding based on laboratory test results that indicate abnormal levels of antidiuretic hormone in the blood specimen. Navigational Note:Also consider Hepatobiliary disorders: Hepatic failure Blood corticotrophin Asymptomatic; clinical or Symptomatic; medical Hospitalization indicated decreased diagnostic observations only; intervention indicated intervention not indicated Definition:A finding based on laboratory test results that indicate an decrease in levels of corticotrophin in a blood specimen. Cardiac troponin T increased Levels above the upper limit Levels consistent with of normal and below the level myocardial infarction as of myocardial infarction as defined by the manufacturer defined by the manufacturer Definition:A finding based on laboratory test results that indicate increased levels of cardiac troponin T in a biological specimen. Navigational Note:Also consider Cardiac disorders: Heart failure or Cardiac disorders: Myocardial infarction. Navigational Note:Also consider Cardiac disorders: Left ventricular systolic dysfunction. Report Cardiac disorders: Left ventricular systolic dysfunction if same grade event. Navigational Note: Hemoglobin increased Increase in >0 2 g/dL Increase in >2 4 g/dL Increase in >4 g/dL Definition:A finding based on laboratory test results that indicate increased levels of hemoglobin above normal. Navigational Note: Lymphocyte count increased >4000/mm3 20,000/mm3 >20,000/mm3 Definition:A finding based on laboratory test results that indicate an abnormal increase in the number of lymphocytes in the blood, effusions or bone marrow. Navigational Note:If intervention initiated or symptomatic, report as Endocrine disorders: Hypothyroidism. Urine output decreased Adult:Oliguria (<80 ml in 8 Adult:Anuria (<240 ml in 24 hr); hr); Infants:< 0. Navigational Note:Also consider Investigations: Forced Expiratory Volume; Respiratory, thoracic and mediastinal disorders: Respiratory failure or Dyspnea Weight gain 5 <10% from baseline 10 <20% from baseline >=20% from baseline Definition:A finding characterized by an unexpected or abnormal increase in overall body weight; for pediatrics, greater than the baseline growth curve. Navigational Note:Do not use Metabolism and nutrition disorders: Obesity, this term is being retired. Navigational Note: Glucose intolerance Asymptomatic; clinical or Symptomatic; dietary Severe symptoms; insulin Life-threatening Death diagnostic observations only; modification or oral agent indicated consequences; urgent intervention not indicated indicated intervention indicated Definition:A disorder characterized by an inability to properly metabolize glucose. Navigational Note: Hyperlipidemia Requiring diet changes Requiring pharmaceutical Hospitalization; pancreatitis Life-threatening intervention consequences Definition:A disorder characterized by laboratory test results that indicate an elevation in the concentration of lipids in blood. Navigational Note: Hyperphosphatemia Laboratory finding only and Noninvasive intervention Severe or medically significant Life-threatening Death intervention not indicated indicated but not immediately life consequences; urgent threatening; hospitalization or intervention indicated. Navigational Note: Iron overload Moderate symptoms; Severe symptoms; Life-threatening Death intervention not indicated intervention indicated consequences; urgent intervention indicated Definition:A disorder characterized by accumulation of iron in the tissues. Navigational Note:Use term Investigations: Weight gain Tumor lysis syndrome Present Life-threatening Death consequences; urgent intervention indicated Definition:A disorder characterized by metabolic abnormalities that result from a spontaneous or therapy-related cytolysis of tumor cells. Navigational Note: Joint range of motion Mild restriction of rotation or Rotation <60 degrees to right Ankylosed/fused over decreased cervical spine flexion between 60 70 or left; <60 degrees of flexion multiple segments with no C degrees spine rotation Definition:A disorder characterized by a decrease in flexibility of a cervical spine joint.

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