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1.
Zh Nevrol Psikhiatr Im S S Korsakova ; 124(5. Vyp. 2): 87-92, 2024.
Artículo en Ruso | MEDLINE | ID: mdl-38934671

RESUMEN

OBJECTIVE: To determine the prevalence of insomnia and the effectiveness of its treatment in patients with a painful form of diabetic polyneuropathy (DPN). MATERIAL AND METHODS: Fifty patients with the painful form of DPN were randomly divided into 2 groups: the standard therapy group (ST) and the extended therapy group (ET). In the ST group, a single lesson on sleep hygiene was conducted, in the ET group there were 3-4 face-to-face individual sessions for the treatment of insomnia for two weeks. Both groups were interviewed at the time of hospitalization, after 3 and 6 months. The severity of polyneuropathy and the nature of neuropathic pain were assessed using the Neuropathic Neuropathy Impairment Score in the Lower Limbs (NIS-LL) and the Neuropathy Total Symptom Score - 9 (NTSS-9); the intensity of pain was assessed using a Visual Analog Scale (VAS). Sleep disorders were analyzed using the Pittsburgh Sleep Quality Index (PSQI) and the Insomnia Severity Index (ISI). RESULTS: Sleep disorders of varying severity were observed in 82% of patients in the initial survey. In both groups, improvement in sleep quality was noted during treatment, but significantly better results were in the ET group, the ISI score after 6 months was 7.15±2.08 for the ST group and 3.07±2.49 for the ET group (p<0.0001). In the ST group, there was no significant decrease in the intensity of pain and the severity of polyneuropathy in dynamics. In the ET group, a significant decrease in NTSS-9 and VAS scores was found during the initial survey and after 6 months (p<0.0001). The intensity of pain also significantly decreased in the ET group compared with the ST group (p<0.0001) at the end of follow-up, which indicates the importance of sleep normalization in the treatment of neuropathic pain. CONCLUSION: Most patients with the painful form of DPN have insomnia. Treatment of insomnia has shown its effectiveness as part of a multimodal approach to the managing of neuropathic pain in DPN and improving the quality of life of patients.


Asunto(s)
Neuropatías Diabéticas , Neuralgia , Índice de Severidad de la Enfermedad , Trastornos del Inicio y del Mantenimiento del Sueño , Humanos , Neuropatías Diabéticas/complicaciones , Masculino , Femenino , Trastornos del Inicio y del Mantenimiento del Sueño/etiología , Persona de Mediana Edad , Neuralgia/etiología , Anciano , Dimensión del Dolor , Adulto , Resultado del Tratamiento , Calidad del Sueño
2.
Ter Arkh ; 93(11): 1375-1380, 2021 Nov 15.
Artículo en Ruso | MEDLINE | ID: mdl-36286662

RESUMEN

Acute disseminated encephalomyelitis (AEM) and acute transverse myelitis (OPM) are autoimmune demyelinating diseases of the central nervous system. Two clinical observations of AEM and OPM developed after suffering acute coronavirus infection (SARS-CoV-2) are presented. Differential diagnosis was carried out with multiple sclerosis, encephalitis of an infectious nature, compressive myelopathy, and opticomyelitis. Both observations show an almost complete recovery of lost functions. The pathogenetic mechanisms of the development of AEM and OPM in patients with coronavirus infection are discussed. The onset of central nervous system dysimmune lesion in the context of coronavirus infection makes it necessary to monitor the clinical situation with the involvement of a neurologist for timely diagnosis and determination of therapeutic tactics that can reduce the degree of disability of patients.


Asunto(s)
COVID-19 , Encefalomielitis Aguda Diseminada , Mielitis Transversa , Enfermedades del Sistema Nervioso , Humanos , COVID-19/complicaciones , COVID-19/diagnóstico , Encefalomielitis Aguda Diseminada/diagnóstico , Encefalomielitis Aguda Diseminada/etiología , Encefalomielitis Aguda Diseminada/tratamiento farmacológico , Mielitis Transversa/diagnóstico , Mielitis Transversa/etiología , Mielitis Transversa/tratamiento farmacológico , SARS-CoV-2
3.
Vestn Oftalmol ; 136(5. Vyp. 2): 155-162, 2020.
Artículo en Ruso | MEDLINE | ID: mdl-33063958

RESUMEN

Laser corneal confocal microscopy (CCM) is a method of objective visualization of thin corneal nerve fibers (CNF), the structure of which changes in patients with diabetes mellitus (DM). PURPOSE: To conduct comparative analysis of the results of CNF assessment using CCM and other known neurological instrumental techniques as well as evaluate their applicability to the early diagnosis of diabetic polyneuropathy (DPN). MATERIAL AND METHODS: We examined a total of 46 patients (85 eyes) with type 1 DM and either subclinical (24 patients), or clinical-stage DPN (22 patients) and 50 patients (87 eyes) with type 2 DM (subclinical DPN in 27 patients and clinical-stage DPN in 23 patients). The control group consisted of 34 healthy volunteers (68 eyes). All patients underwent standard ophthalmological examination, CCM with nerve tortuosity assessment (including calculation of coefficients of CNF orientation anisotropy, KΔL, and symmetry, Ksym) and interocular asymmetry, electroneuromyography (ENMG), and quantitative sensory testing (QST). RESULTS: Analysis of the CCM results revealed a reliable decrease in the average KΔL values in patients with type 1 and type 2 DM compared with the control group. In the group of patients with type 1 DM and subclinical DPN, correlations were revealed between the CNF tortuosity coefficients and a number of ENMG parameters, such as the M-response amplitude of the peroneal nerve (r=0.73, p≤0.02), M-response amplitude of the tibial nerve (r=0.58, p≤0.01), residual latency (r= -0.62, p≤0.05), and peroneal nerve conduction velocity (r=0.57, p≤0.01). Ksym values correlated with the warm sensitivity threshold (r=0.6, p≤0.008). Among patients with type 2 DM and subclinical DPN, the KΔL coefficient correlated with the peroneal nerve conduction velocity (r=0.46, p≤0.02), M-response amplitude of the tibial nerve (r=0.6, p≤0.04), and residual latency of the peroneal nerve (r=-0.56, p≤0.05). CONCLUSION: The state of thin corneal nerves correlates with functional changes in the peripheral nerves. Pathological changes in CNF in patients with DM can be detected at an early (subclinical) stage of DPN using laser CCM and a program for corneal nerve tortuosity analysis.


Asunto(s)
Diabetes Mellitus , Neuropatías Diabéticas , Córnea/diagnóstico por imagen , Neuropatías Diabéticas/diagnóstico , Diagnóstico Precoz , Humanos , Microscopía Confocal , Fibras Nerviosas
4.
Artículo en Ruso | MEDLINE | ID: mdl-29863704

RESUMEN

Diabetic polyneuropathy is the most often complication of diabetes mellitus. However, patients with diabetes may have other neuropathies, which need to be recognized and treated. Chronic nnflammatory demyelinating polyneuropathy is the most common non-diabetic polyneuropathy in patients with diabetes. The article discusses the classification, clinical features of diabetic and nondiabetic polyneuropathies, modern methods of diagnosis and approaches to treatment.


Asunto(s)
Neuropatías Diabéticas , Polineuropatías , Humanos
5.
Artículo en Ruso | MEDLINE | ID: mdl-26171485

RESUMEN

In this article, the authors consider the characteristics of pathogenesis and clinical picture of peripheral nervous system lesions in elderly patients. Current approaches to pathogenetic and symptomatic treatment of polyneuropathy in elderly patients are analyzed. The authors suggest complex treatment approaches using antiepileptic drugs, group B vitamins, alpha-lipoic acid.


Asunto(s)
Polineuropatías , Anciano , Anticonvulsivantes/uso terapéutico , Humanos , Persona de Mediana Edad , Polineuropatías/diagnóstico , Polineuropatías/tratamiento farmacológico , Polineuropatías/fisiopatología , Ácido Tióctico/uso terapéutico , Complejo Vitamínico B/uso terapéutico
7.
Klin Med (Mosk) ; 87(11): 67-71, 2009.
Artículo en Ruso | MEDLINE | ID: mdl-20143571

RESUMEN

A case of familial transthyretin amyloidosis with TTR Cys 114 gene polymorphism is described (first in Russia and third in the world). The clinical picture of the proband was dominated by symptoms of autonomous polyneuropathy (orthostatic hypotension, erectile dysfunction, diarrhea, tachycardia, foot dyshydrosis) and of somatic nerve lesions (dumbness, impaired surface and deep sensitivity in the limbs). The patient presented with vitreous body opacity, disturbed eye movements, lateralized sensory symptoms, and difficulty of speech (baryphonia). Electromyographic quantitative autonomous testing and measurement of evoked sympathetic skin potentials confirmed affection of peripheral nerves. Heart ultrasound revealed restrictive amyloid cardiopathy. Histological analysis showed amyloid deposition in the intestines and sural nerve. The proband, his daughter, brother (monozygous twin), and brother's daughter had mutant TTR Cys 114 gene. The brother also had amyloid deposits in the absence of clinical signs of the disease. Analysis of familial medical history demonstrated autosomal dominant inheritance of this mutation in 4 generations. Its possible origin and clinical features of the disease are discussed.


Asunto(s)
Amiloidosis Familiar/genética , ADN/genética , Predisposición Genética a la Enfermedad , Mutación , Polimorfismo Genético , Prealbúmina/genética , Amiloidosis Familiar/sangre , Marcadores Genéticos , Humanos , Masculino , Persona de Mediana Edad , Prealbúmina/metabolismo
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