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1.
Article | IMSEAR | ID: sea-217601

Résumé

Background: Anterior mediastinal tumors comprise only 3% of all chest tumours. They are often of diagnostic challenge to both clinicians and histopathologists owing to their wide variety of clinical presentations and diversity in histomorphological appearance respectively. Hence, there is a need for elaborated studies to make the pathologists and clinicians aware of their diversity. Aim and Objectives: The present study was aimed to evaluate the diverse spectrum of clinical presentations and histomorphological appearances of anterior mediastinal lesions. In addition, cytological and radiological interpretations were correlated with histological diagnosis to assess their comparative role in diagnosis. Materials and Methods: It was a descriptive observational cross-sectional study. Patients diagnosed with anterior mediastinal mass on chest computed tomography (CT) scan were included in this study. Demographic details including clinical presentations and radiological interpretations were recorded. Patients underwent both CT guided Fine needle aspiration cytology (FNAC) and needle core/excisional biopsy. Histological diagnosis was correlated with radiological and cytological interpretations. Results: Of 659 patients presented with chest tumours, 19 were detected as having anterior mediastinal mass on chest CT scan indicating the prevalence of 2.88%. The most common presenting symptom was respiratory distress (73.68%), followed by chest pain (36.84%), superior vena cava syndrome (26.32%) and Myasthenic features (5.26%). About 50% of malignant tumours occurred at the 2nd decade of life. Thymic epithelial neoplasms comprise the major tumour type in this study (52.63%) followed by germ cell tumors (15.79%) and lymphomas (10.53%). Cytology was found to be more effective compared to radiology in diagnosis. Conclusion: Anterior mediastinal tumors are extremely heterogeneous in clinical presentation and histomorphological appearance. CT-guided FNAC can play an important role in their diagnosis along with radiology and histology.

2.
Indian J Ophthalmol ; 2001 Mar; 49(1): 31-5
Article Dans Anglais | IMSEAR | ID: sea-70150

Résumé

PURPOSE: Postoperative astigmatism following intracapsular cataract extraction with or without anterior chamber intraocular lens implantation is reported as an outcome from a randomised controlled trial. METHODS: Five hundred and two of 1002 eyes randomised to intracapsular cataract extraction with anterior chamber intraocular lens (ICCE/AC IOL) and 417 of 998 eyes to intracapsular cataract extraction with aphakic spectacles (ICCE/AS) were seen for objective refraction one year after surgery. The prevalence and axis of astigmatism were evaluated using univariate analysis. Logistic regression was used to compare the postoperative astigmatism between the groups. RESULTS: Acceptable astigmatism (-0.5 to 0.0 DCyl) in the AC IOL group was found in 60 (12.0%) patients (95% CI 9.1%-14.9%) and in the aphakic spectacles group (AS) in 69 (16.5%) patients (95% CI 12.9%-20.1%), moderate astigmatism (-1.0 to-1.5 DCyl) was found in 153 (30.4%) patients (95% CI 26.4-34.6%) in ACIOL group and in 288 (69.1%) patients (95% CI 64.6%-73.6%) in AS group; and large astigmatism (-2.0 to - 8.0 D Cyl) was found in 289 (57.6%) patients (95% CI 53.1%-61.6%) in ACIOL group and in 60 (14.4%) patients (95% CI 11.0% 17.8%) in AS group. Large astigmatism was approximately four times more common in the ICCE/AC IOL group compared to ICCE/AS group. In both groups, most patients had "against-the-rule" astigmatism, 446 (88.8%) (95%CI 86.0%-91.6%) in AC IOL group and 348 (83.5%) (95%CI 79.9%-87.1%) in AS group. CONCLUSION: Astigmatism is common after intracapsular cataract extraction. Insertion of an anterior chamber IOL increases the risk of astigmatism.


Sujets)
Adolescent , Adulte , Pôle antérieur du bulbe oculaire , Astigmatisme/épidémiologie , Extraction de cataracte/effets indésirables , Enfant , Enfant d'âge préscolaire , Femelle , Études de suivi , Humains , Capsule du cristallin/chirurgie , Pose d'implant intraoculaire/effets indésirables , Mâle , Adulte d'âge moyen , Népal/épidémiologie , Complications postopératoires , Prévalence , Réfraction oculaire , Acuité visuelle
3.
Neurol India ; 2000 Jun; 48(2): 99-104
Article Dans Anglais | IMSEAR | ID: sea-121590

Résumé

Women in India are greatly discriminated against if they happen to have epilepsy. Engagements are often cancelled. The parents of epileptic girls have to give heavy dowry at the time of marriage, even if the boy is handicapped. As a result, many girls do not disclose their problem before marriage. They take the medicine secretly. Epilepsy may sometimes produce problems during pregnancy and delivery, otherwise epileptic women on anti epileptic drugs, can lead a normal married, professional and social life. The stigma of epilepsy should be done away with, as we enter the 21st century.


Sujets)
Anticonvulsivants/effets indésirables , Épilepsie/traitement médicamenteux , Femelle , Humains , Inde/épidémiologie , Grossesse , Femmes
4.
Indian J Physiol Pharmacol ; 1998 Oct; 42(4): 555-8
Article Dans Anglais | IMSEAR | ID: sea-106448

Résumé

A randomized placebo controlled double-blind clinical trial of nimodipine was conducted in 31 patients of acute cerebral infarction. Nimodipine was administered in dosage of 120 mg/day for 28 days. Treatment was begun within 48 hours of ischemic stroke. Diagnosis was confirmed by computed tomographic (CT) scan. Similar number of patients (control) received placebo. Neurological assessment was done at the time of entry into the trial, and after 4 weeks, by using Mathew's scale. After four weeks of treatment with nimodipine or placebo, Mathew's scale score improved significantly (< 0.001) in both groups, but difference in mean score between two groups was insignificant (> 0.05). However, significant difference (< 0.05) was noted in relative change in neurological deficit (mean X-value) of two groups. The nimodipine group had higher value in scores on Mathew's scale. No adverse reaction, was observed in either group. The study suggests a beneficial a effect of nimodipine in acute cerebral ischaemia.


Sujets)
Adulte , Sujet âgé , Encéphalopathie ischémique/traitement médicamenteux , Inhibiteurs des canaux calciques/usage thérapeutique , Infarctus cérébral/traitement médicamenteux , Méthode en double aveugle , Femelle , Humains , Mâle , Adulte d'âge moyen , Tests neuropsychologiques , Nimodipine/usage thérapeutique
5.
Article Dans Anglais | IMSEAR | ID: sea-91945

Résumé

Study was conducted to compare the pharmacokinetic profile of conventional and slow-release carbamazepine formulations in Indian epileptic patients. Twenty consecutive untreated patients of partial seizures were randomly assigned to receive either conventional carbamazepine (200 mg thrice a day) or slow-release carbamazepine formulation (200 mg thrice a day), 10 patients in each group. The serum carbamazepine concentrations were measured on 10th day and 20th day of treatment. The blood samples were collected before the morning dose. In the conventional treatment group five patients experienced side effects as compared to two in the slow-release group. On 10th day mean serum carbamazepine levels were significantly higher in conventional group (8.27 +/- 1.39 micrograms/ml) in comparison to slow release group (4.28 +/- 3.89 micrograms/ml). The difference was statistically significant (p < 0.05). On 20th day carbamazepine levels fell significantly in conventional group only (8.27 +/- 1.39 micrograms/ml to 5.76 +/- 2.32 micrograms/ml, p < 0.05). At this stage the difference in mean carbamazepine levels of two groups became insignificant (p < 0.05). In conclusion, controlled release formulations provide more steady serum concentrations of carbamazepine along with better tolerability.


Sujets)
Adolescent , Adulte , Anticonvulsivants/administration et posologie , Carbamazépine/administration et posologie , Chimie pharmaceutique , Préparations à action retardée/administration et posologie , Épilepsie/diagnostic , Études d'évaluation comme sujet , Femelle , Études de suivi , Humains , Mâle , Probabilité , Sensibilité et spécificité , Résultat thérapeutique
7.
Article Dans Anglais | IMSEAR | ID: sea-95398

Résumé

Alprazolam was evaluated in the treatment of 62 patients of chronic tension type headache using a double blind cross over design with random allocation to drug or placebo. The duration of the trial was 4 months with a 2 week run in period and 2 week washout period separating two treatment periods of 4 weeks each. The patients were followed up for 4 weeks at the completion of the trial. 48 patients completed the trial. There was no significant difference in the overall response rate based in terms of percentage reduction in headache frequency per week, however a significant decrease in headache index was observed during treatment with alprazolam as compared to placebo (P < 0.05). The mean analgesic intake per week was also significantly lower during treatment with alprazolam as compared to the run in period. Side effects were seen in 16.67% patients. In none of the patients was it significant enough to require withdrawal from the study.


Sujets)
Adulte , Alprazolam/effets indésirables , Maladie chronique , Études croisées , Méthode en double aveugle , Femelle , Études de suivi , Humains , Hypnotiques et sédatifs/effets indésirables , Mâle , Céphalée de tension/traitement médicamenteux , Résultat thérapeutique
8.
Article Dans Anglais | IMSEAR | ID: sea-89328

Résumé

A double blind placebo controlled trial was conducted in 55 patients of acute ischaemic stroke. Twenty one and twenty six patients were randomly allotted in group A and group B respectively. In group A, the patients received 40 mg Ginkgo biloba extract at 6 hourly intervals along with routine management. The placebo tablets were dispensed in the tablet form of same size, shape and colour and were given in the same way. After the patients were subjected to computerized tomographic (CT) scan to confirm acute ischaemic infarction, they were assessed on Mathew's scale and reassessed, at 2 weeks and 4 weeks of drug/placebo administration. Both groups showed significant improvement in Mathew's scale score after 2 weeks and 4 weeks. The difference in degree of change was negligible (p > 0.05) in either group. Estimation of relative changes of neurological deficit based on baseline values also showed negligible (p > 0.05) difference. A trial of Ginkgo biloba extract within 6 hours of stroke in a larger dose and in larger sample could be beneficial clinically in patients of cerebral ischaemic infarct, and needs further study. The usefulness of the plant extract has been demonstrated clinically and experimentally in more than 40 trials of chronic cerebral ischaemia, done elsewhere. This was not evident in our study as our study group was different (more than 48 hours after stroke). There appears to be no contraindication or adverse effect of this medication (Ginkgo biloba) in acute ischaemic stroke.


Sujets)
Encéphalopathie ischémique/traitement médicamenteux , Méthode en double aveugle , Femelle , Piégeurs de radicaux libres/usage thérapeutique , Ginkgo biloba , Humains , Mâle , Adulte d'âge moyen , Projets pilotes , Extraits de plantes/usage thérapeutique , Facteurs temps , Résultat thérapeutique
9.
Article Dans Anglais | IMSEAR | ID: sea-91279

Résumé

Nifedipine was evaluated in the prophylaxis of 28 patients each of migraine and tension headache using a double blind cross over design with random allocation to drug or placebo group. The duration of the trial was 3 months with a 2 week run-in period and 2 week wash-oat period separating two treatment periods of 4 weeks each. A satisfactory response was obtained in 71.4% of migraineurs (p < 0.001) and 28.6% of patients with tension headache (p = N.S). Minor side effects were observed in 5 patients. Nifedipine is a useful agent for the management of migraine as it reduces frequency and severity of pain but the drug cannot be recommended for tension headache.


Sujets)
Adulte , Inhibiteurs des canaux calciques/effets indésirables , Études croisées , Méthode en double aveugle , Calendrier d'administration des médicaments , Femelle , Humains , Mâle , Migraines/prévention et contrôle , Nifédipine/effets indésirables , Céphalée de tension/prévention et contrôle , Facteurs temps
12.
Indian J Physiol Pharmacol ; 1995 Apr; 39(2): 149-53
Article Dans Anglais | IMSEAR | ID: sea-107174

Résumé

Study was conducted on 34 middle aged (35-52 years) diabetics of either sex to compare autonomic function in patients having and not having symptoms of dysautonomia. Fifteen age/sex matched healthy non-diabetic volunteers were control. No symptom of autonomic insufficiency was present in 19 (55.8%) while 15 (43%) diabetics had dysfunction in form of episodic syncope, vertigo, and palpitation, all on postural change. Tests of autonomic functions were restricted to evaluation of salivation, lacrimation, sweating, pilomotor response, reflex erythema and blood pressure changes with valsalva, posture and cold pressor. SSR was elicited using 5 stimuli on programmed Neuropack II and IV model machine. In asymptomatic diabetics, tests of autonomic functions were normal and comparable to controls but SSR was not recordable in 8 (42%). In remaining 11 (58%) asymptomatic diabetics, it was recordable. In 15 subjects who had symptoms of autonomic dysfunction, 6 (40%) had positive test of autonomic function but SSR was normal in only 5 (34%) and not recordable in 10 (66%) subjects. We conclude that SSR can be used as a easy, sensitive and probably early indicator of autonomic functions.


Sujets)
Adulte , Maladies du système nerveux autonome/diagnostic , Diabète de type 2/diagnostic , Neuropathies diabétiques/diagnostic , Femelle , Humains , Mâle , Adulte d'âge moyen , Peau/physiopathologie , Système nerveux sympathique/physiopathologie
13.
Article Dans Anglais | IMSEAR | ID: sea-91611

Résumé

30 healthy elderly males (mean age 77.4 +/- 4.3 yrs) were subjects in this study. Equal number of young males (mean age 22 +/- 3.5 years) and middle aged subjects (mean age 46 +/- 3.2 years) served as control. P300 wave was estimated using a Neuropack 4 model of Nihon Kohden EMG machine. We observed a significantly increased latency, poorly defined and non reproducible P300 wave in 90% old subjects while in young the latency was in normal limits and the wave was well defined and reproducible. We presume P300 could serve as a future potential marker of the neurophysiological basis of aging.


Sujets)
Stimulation acoustique , Adulte , Sujet âgé , Sujet âgé de 80 ans ou plus , Vieillissement/physiologie , Électromyographie/instrumentation , Potentiels évoqués cognitifs P300/physiologie , Humains , Mâle , Adulte d'âge moyen , Neurophysiologie , Temps de réaction/physiologie , Reproductibilité des résultats , Traitement du signal assisté par ordinateur
14.
Indian J Physiol Pharmacol ; 1994 Oct; 38(4): 277-80
Article Dans Anglais | IMSEAR | ID: sea-106383

Résumé

Sixty-two subjects in age range of 25-50 years consuming more than 300 ml of alcohol daily, and an equal number of age matched non-alcoholic volunteers serving as control were tested. Their clinical and neurological evaluation, including electrophysiology was carried out. Their cognitive functions were measured using the modified WAIS system. In alcoholics there was a significant impairment of cognition, especially in orientation, attention and immediate recall. Their P300 wave was grossly abnormal as compared with the controls. Other electrophysiological investigations (EEG, NCV, EMG, BAER, VER) were normal. It is concluded that cognition may be grossly impaired in chronic alcoholics, which may not manifest clinically but is observed only after formal testing.


Sujets)
Adulte , Consommation d'alcool , Alcoolisme/physiopathologie , Cognition/effets des médicaments et des substances chimiques , Électrocardiographie , Éthanol/pharmacologie , Potentiels évoqués auditifs/effets des médicaments et des substances chimiques , Humains , , Mâle , Adulte d'âge moyen , Neurophysiologie , Échelles d'évaluation en psychiatrie , Essais contrôlés randomisés comme sujet
15.
J Indian Med Assoc ; 1993 Mar; 91(3): 53-4
Article Dans Anglais | IMSEAR | ID: sea-100510

Résumé

Thirty-eight patients of generalised tonic-clonic seizures of epileptics in the age group of 15-30 years were included in this study. Of these 20 were started sodium valproate afresh and 18 already taking it for more than one year prior to inclusion. Serum amylase and serum valproic acid levels were measured in all of them, initially and at every 3 months interval for 9 months. Though no clinical evidence was present, there was significant increase in serum amylase levels in both the groups which has no correlation with dose or serum valproic acid levels.


Sujets)
Adolescent , Adulte , Amylases/sang , Grand mal épileptique/traitement médicamenteux , Femelle , Humains , Mâle , Facteurs temps , Acide valproïque/sang
18.
Article Dans Anglais | IMSEAR | ID: sea-93115

Résumé

We report a case of herpes zoster oticus with involvement of the mandibular division of the trigeminal nerve and loss of taste sensation in the anterior two third of the tongue. Infranuclear facial palsy and sensorineural deafness were also present.


Sujets)
Atteintes des nerfs crâniens/étiologie , Surdité/étiologie , Paralysie faciale/étiologie , Femelle , Zona auriculaire/complications , Humains , Adulte d'âge moyen , Troubles du goût/étiologie , Nerf trijumeau
19.
Article Dans Anglais | IMSEAR | ID: sea-19343

Résumé

In an attempt to ascertain the role of aluminium in sporadic motor neuron disease (MND), trace metals were estimated in blood, plasma and cerebrospinal fluid (CSF) of 38 patients of sporadic MND and 30 controls by direct current plasma emission spectrophotometry. CSF aluminium levels (20.76 +/- 4.38 micrograms/dl) were significantly higher (P less than 0.05) in those patients of MND who presented as progressive bulbar palsy (PBP) as compared to the other subtypes of MND (amyotrophic lateral sclerosis = 7.71 +/- 2.01 micrograms/dl; progressive muscular atrophy = 10.01 +/- 2.41 micrograms/dl) and controls (11.63 +/- 2.82 micrograms/dl). Aluminium may be important in the etiopathogenesis of a subgroup of sporadic MND.


Sujets)
Adolescent , Adulte , Sujet âgé , Aluminium/sang , Femelle , Humains , Mâle , Adulte d'âge moyen , Motoneurones , Maladies neuromusculaires/sang
20.
Indian J Med Sci ; 1989 Apr; 43(4): 89-91
Article Dans Anglais | IMSEAR | ID: sea-69055

Résumé

Seven male silver jewellery workers aged between 25 to 70 years complained of acute abdominal colic, sweet metallic taste, constipation and anorexia. Clinical, hematological examinations and urinalysis confirmed lead poisoning. Oral therapy with D-Penicillamine for seven days led to significant improvement in patients.


Sujets)
Adulte , Sujet âgé , Humains , Inde , Intoxication par le plomb/diagnostic , Mâle , Métallurgie , Adulte d'âge moyen , Maladies professionnelles/diagnostic , Pénicillamine/usage thérapeutique , Argent
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