Titlebook: Optical Coherence Tomography in Multiple Sclerosis; Clinical Application Axel Petzold Book 2016 Springer International Publishing Switzerla

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Clinical Use of OCT and MSON Mimics,ritis (ION), relapsing isolated optic neuritis (RION), chronic relapsing inflammatory optic neuropathy (CRION), and neuromyelitis optica optic neuritis (NMO-ON). The differential diagnosis also includes infectious, reactive, vascular, nutritional and toxic, compressive, systemic disease, ocular, her

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OCT and Early MS: Clinically Isolated Syndromes (CIS),lly susceptible host. The actual cause of MS is not known, and there is ongoing debate about whether this CNS disorder is predominantly an inflammatory versus a degenerative condition. The afferent visual pathway (AVP) is frequently involved in MS, such that 1 in every 5 affected individuals present

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,OCT in Relapsing–Remitting Multiple Sclerosis (RRMS),uantify and track axonal and neuronal degeneration operative as part of the disease process. Although RRMS is traditionally conceptualized as an inflammatory demyelinating disorder of the central nervous system, axonal and neuronal degeneration, which predominantly results from these processes, are

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Progressive Multiple Sclerosis (SP and PP MS),pses relapse-associated damage is unknown. Despite the high number of patients with progressive disease course, comparatively little is known about changes in the visual system of these patients. In this chapter we will review optical coherence tomography of retinal changes occurring in eyes from pa

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Drug Trials in Neuroprotection,MS) brain. Acute multiple sclerosis associated optic neuritis (MSON) resembles an acute lesion model in MS leading to acute retinal neurodegeneration. Acute MSON is clinically eloquent and technically amenable to be monitored by OCT and visual function tests. Acute MSON and OCT are good partners for

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Role of the OCT Reading Center,r treatment on retinal and neuronal structures. To ensure the most accurate data possible, it is essential that the OCT scans are of usable quality and that the values of interest are extracted in a precise, objective manner without regard to the study outcome or clinical status of the individual pa

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