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1.
Rev Neurol ; 44(7): 411-4, 2007.
Article in Spanish | MEDLINE | ID: mdl-17420967

ABSTRACT

INTRODUCTION: Apraxia of eyelid closure (AEC) is an infrequent disorder that is characterised by the inability to close the eyelids on command, although spontaneous blinking and reflex shutting of the eyes is preserved. Very few cases of unilateral AEC have been reported and no long-term follow-ups have been carried out. We report the case of a patient with unilateral AEC that was followed up over a 3-year period and also discuss the role played by the right hemisphere in this disorder. CASE REPORT" We examined the case of a 67-year-old right-handed male who was admitted because of a parietotemporal infarction with extension into the subcortex. A few days after the stroke the patient reported the inability to close his left eye on command, although he was still able to blink spontaneously and the blink and visual threat reflexes were preserved. This deficiency was associated to a dense hemiparesis on the left side and notable aprosodia affecting language. At 3 years' follow-up the AEC had not improved significantly. CONCLUSIONS: There are data to suggest that the right hemisphere is related to emotional perception and expressiveness, as well as the regulation of language prosody. Likewise, symbolic anthropology stresses the importance of winking as a gesture involved in non-verbal communication. These data suggest that AEC may be a consequence of a dysfunction of the role played by the right hemisphere in emotional expressiveness through gestures. The association with language aprosodia could support this hypothesis.


Subject(s)
Apraxias/etiology , Brain , Communication , Emotions , Eyelids , Gestures , Stroke , Aged , Brain/pathology , Brain/physiology , Humans , Male , Stroke/complications , Stroke/physiopathology
2.
Rev Neurol ; 43(7): 388-92, 2006.
Article in Spanish | MEDLINE | ID: mdl-17006856

ABSTRACT

INTRODUCTION: The system by which approval must be given by the primary care physician before a patient can visit a specialist is known as gatekeeping and is aimed at preventing the mistaken or simple referral of patients to the next stage of health care services. We present a study that compares the final diagnoses of 400 patients who used a direct access model of referral (DAM) with those of 400 patients referred by a primary care physician in a prior authorisation model (PAM). PATIENTS AND METHODS: We conducted a prospective analysis of two cohorts of patients who visited the same neurologist in a PAM system versus a DAM system. The 800 patients were evaluated following similar diagnostic criteria. The primary objective of the study was to compare the patients who were referred with a final diagnosis of 'non-neurological pathology' in the PAM and the DAM systems. Secondary aims consisted in conducting an analysis of the diagnoses by different pathologies between the two models. RESULTS: No significant differences were found between the referrals that were considered to be non-neurological in the PAM and the DAM systems (27.0% versus 26.3%; p = 0.48). A logistic regression model was performed with 'non-neurological pathology' as the dependent variable and age, sex and type of model (PAM or DAM) as the independent variables, similar results being obtained in both cases. CONCLUSIONS: Our data suggest that the role played by the primary care physician is not effective when it comes to preventing mistaken referrals to the neurologist in our area. A populational study would be needed to evaluate the rate at which resources are used and the spending on health care in the two models.


Subject(s)
Gatekeeping/standards , Nervous System Diseases/diagnosis , Neurology , Primary Health Care , Female , Humans , Male , Middle Aged , Prospective Studies , Spain
3.
Rev Neurol ; 34(3): 211-5, 2002.
Article in Spanish | MEDLINE | ID: mdl-12022067

ABSTRACT

OBJECTIVES: The homeostatic regulation of sleep is based on the model devised by Borb ly in 1982. During the sleep waking cycle there is an interaction between the natural tendency to sleep, which increase as the vigil is prolonged (S process) and the circadian variation (C process). In this study, we aimed to find how slow activity (0.5 4.5 Hz) during sleep (SWA), mainly registered in phases 3 and 4, may be an indicator of process S. PATIENTS AND METHODS: We compared two groups of persons: 10 with chronic sleep deprivation (CSD) (less than 6 hours of sleep/day) as compared with 10 persons who slept more than 6 hours per day, using spectral analysis of their delta activity during sleep. RESULTS: There was a predominance of delta activity in the group of persons with CSD as compared with the control group. CONCLUSIONS: An increase in SWA was accompanied by an increased tendency to sleep and may therefore be considered to be a marker for this. This marker allows conditions associated with hypersomnolence due to alteration of process S to be identified.


Subject(s)
Homeostasis/physiology , Sleep/physiology , Adult , Aged , Chronic Disease , Delta Rhythm , Disorders of Excessive Somnolence/etiology , Electroencephalography , Female , Humans , Male , Middle Aged , Severity of Illness Index , Sleep Deprivation/complications , Sleep Deprivation/diagnosis , Sleep, REM/physiology
4.
Rev Neurol ; 32(2): 123-6, 2001.
Article in Spanish | MEDLINE | ID: mdl-11299474

ABSTRACT

INTRODUCTION: The diagnosis of peripheral neuropathy is based on clinical and neurophysiological features. This study aims to establish the diagnostic validity of different symptoms and clinical signs, as well as its correlation with electroneurography (ENG), to determine its sensitivity (SE), specificity (SP), positive (PLR) and negative likelihood ratio (NLR) for every peripheral neuropathies type. PATIENTS AND METHODS: A sample of 108 patients with clinical suspicion of peripheral neuropathy (pain, paresthesias, loss of strength, areflexia) was studied. ENG (nerve conduction velocity and response amplitude values in 208 nerves [Median and Posterior Tibial]) was used to confirm the diagnosis, classifying the sample in axonal group (A), demyelinating (D) and normal (N). It was made descriptive statistics of this sample, studies of SE, SP, PLR and NLR of symptoms, and association (contingency tables [Chi square] and Odds Ratio) between symptoms and clinical features. RESULTS: The patients with paresthesias, loss of strength or pathologic reflexes have larger motor latency (p< 0.01). Those with paresthesias, areflexia or pain have fewer sensitive conduction velocity (p< 0.05). Symptoms's value for sensory damage's diagnosis is (SE= 0.92, SP= 0.48, PLR= 1.78, NLR= 0.14). For motor damage (SE= 0.72, SP= 0.68, PLR= 2.25, NLR= 0.41). For axonal damage (SE= 0.83, SP= 0.44, PLR= 1.49, NLR= 0.37). And for demyelinating damage (SE= 0.92, SP= 0.44, PLR= 1.66, NLR= 0.16). CONCLUSIONS: The symptoms's combination is much more sensitive and has fewer NLR than each isolated symptom in all neuropathic damage's types. Paresthesias's presence is more indicative of sensory damage and loss of strength of motor damage. Pain is the only symptom that can aim for axonal damage than demyelinating.


Subject(s)
Peripheral Nervous System Diseases/diagnosis , Peripheral Nervous System Diseases/physiopathology , Cross-Sectional Studies , Electrodiagnosis , Female , Humans , Male , Middle Aged , Prospective Studies , Sensitivity and Specificity
5.
Rev Neurol ; 28(9): 863-7, 1999.
Article in Spanish | MEDLINE | ID: mdl-10390748

ABSTRACT

INTRODUCTION: Spinal tumours in infancy are an infrequent oncological disorder. The clinical features, usually of insidious onset, are alterations in gait and a painful spine. OBJECTIVE: To analyze the different histological types of spinal tumours seen in infancy and their form of presentation in our series. PATIENTS AND METHODS: We reviewed the clinical histories of 48 patients with intraspinal tumours, aged under 15 years, whose reports of histological diagnosis had been sent to our centre. RESULTS: Of the patients studied, 17 were girls (35.4%) and 31 boys (64.6%) with an average age of 7.7 years. The histological diagnoses made most frequently were astrocytomas (22.9%) and lipomas (18.8%) followed by metastases (12.5%), ependymomas (8.3%) and Edwing's sarcoma (8.3%). The clinical features were present prior to diagnosis for between 1 and 6 months in 13 patients, and for less than one month in 9 patients. The presenting symptoms were alterations in gait and back pain in most patients. Exploratory tests were related to the involvement of long vias and second motor-neurone lesions. The main topographical findings were: in the axial plane the lesions were extradural (23 patients) and in the sagittal plane there was dorsal involvement (34 patients). CONCLUSIONS: Insidious, progressive alterations in gait together with continuous, nocturnal back pain are valuable data when a serious spinal disorder is to be suspected. Early diagnosis should be based on neuroimaging tests, essentially MR, in the patients in whom spinal cord involvement is considered.


Subject(s)
Astrocytoma/pathology , Ependymoma/pathology , Lipoma/pathology , Sarcoma/pathology , Spinal Neoplasms/pathology , Adolescent , Astrocytoma/complications , Back Pain/diagnosis , Back Pain/etiology , Child , Child, Preschool , Diagnosis, Differential , Ependymoma/complications , Female , Humans , Infant , Infant, Newborn , Lipoma/complications , Magnetic Resonance Imaging , Male , Movement Disorders/diagnosis , Movement Disorders/etiology , Retrospective Studies , Sarcoma/complications , Spinal Neoplasms/complications
6.
Rev Neurol ; 28(9): 883-4, 1999.
Article in Spanish | MEDLINE | ID: mdl-10390754

ABSTRACT

INTRODUCTION: Hypnic headache is a condition characterized by nocturnal episodes of headache which periodically waken the sleeping patient. They usually occur in persons over 55 years of age and are thought to be due to some type of disturbance of biological rhythm. CLINICAL CASE: A 70 year old woman, with no relevant past history, complained that during the previous 12-14 months she had been woken from sleep by episodes of headache. The headache was diffuse, non-pulsatile and very intense. The duration was variable, from 15 to 45 minutes and usually disappeared without requiring analgesics. The pain was not associated with autonomic or ocular disorders, nausea, vomitting or focal neurological signs. Both general and neurological examinations were completely normal. No alterations were seen on cranial CT. Treatment with lithium was started and there was marked improvement in the frequency of headaches. CONCLUSIONS: Hypnic headache is an unusual disorder characterized by episodes of holocranial, or rarely hemicranial, headache of moderate-severe intensity and periodic occurrence. Typically the headache wakes the patient whilst he is asleep ('alarm clock') and there are no autonomic or neurological alterations of any type associated with the episode. The condition usually affects persons over 55 years of age, and it has been related to changes in biological rhythms. This presumed alteration of biological pacemakers has been based on the periodicity of the episodes and the response to lithium.


Subject(s)
Brain/diagnostic imaging , Headache/classification , Headache/diagnosis , Aged , Enzyme Inhibitors/therapeutic use , Female , Headache/drug therapy , Humans , Lithium/therapeutic use , Severity of Illness Index , Tomography, X-Ray Computed
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