Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
Kathmandu Univ Med J (KUMJ) ; 21(82): 190-196, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-38628014

RESUMO

Background Headache disorders are among the most prevalent and disabling conditions worldwide. People, however, do not seek early advice in developing countries. Objective To study clinical profile of patients with headache and their existing knowledge, attitude, and practice regarding primary headaches. Method Descriptive cross-sectional study conducted among 196 patients. Patients were selected using purposive sampling technique fulfilling inclusion criteria. Patients were interviewed based on semi-structural headache questionnaire and data was collected from 4th October to 21st December 2021. Descriptive statistics was used for analysis and interpretation. Result Among 196 participants, 74% were females, 29.6% of patients were between (31 to 40) years of age. The majority were Hindu and belongs to province 3; 36.7% were homemakers, and 32.2% were literate. Migraine headache was the most common type with 14.3% reporting aura. Most reported headache within 1 to 5 years. The commonest triggers were sunlight 64.8%, crowd 54.7%, stress 39.8%, fasting state 31.7%, cold 26.3%. Almost 39% believed that headache could be a chronic neurologic disorder. Majority had knowledge of the causes, triggers, and the relieving factors. Fifty-five percent seek help of a doctor for first time, and the rest seek help of a pharmacist or self-medication. Only 19% tried to manage the headache triggers; 66.8% felt that lifestyle modification is the best treatment for headache comparing drugs. Conclusion Migraine headache was the commonest headache occurring at middle age group with sunlight being the most common trigger factor. Lifestyle modification was perceived to be the best for headache management.


Assuntos
Conhecimentos, Atitudes e Prática em Saúde , Transtornos de Enxaqueca , Pessoa de Meia-Idade , Feminino , Humanos , Masculino , Estudos Transversais , Cefaleia/terapia , Cefaleia/etiologia , Transtornos de Enxaqueca/etiologia , Inquéritos e Questionários
2.
Kathmandu Univ Med J (KUMJ) ; 13(49): 71-3, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26620753

RESUMO

BACKGROUND: Stroke is common neurological problems in Nepal. The common risk factors for stroke are age, hypertension, diabetes, dyslipidemia and atrial fibrillation. Vitamin D is an emerging risk factors for cardio-cerebrovascular disease. OBJECTIVE: This study is to find out Vitamin D and risk factors in stroke patient in Nepalese population. METHOD: We reviewed the record of 281 stroke patients, admitted to Neurology ward of College of Medical Sciences, Bharatpur, Nepal from 1st January to 31st December 2013. The records were analyzed on the basis of age, sex, hypertension (HTN), body mass index (BMI), smoking habits, hemoglobin(Hb), diabetes mellitus(DM), Lipid profile, Atrial fibrillation(AF) and vascular territory with clinical and radiological evidences. The vitamin D analysis was done all stroke patients. RESULT: Total patient were 281, with male 161 and age range from 18 - 87. Ischemic stroke was noted in 86.8% and hemorrhagic stroke was noted in 13.2% of patients. Middle cerebral artery (MCA) ischemia was noted in 51.5% of patients and anterior cerebral artery (ACA) ischemia was noted in 3% of patients. Multiple infarcts were noted in 12.90% of patients. About half of them were smoker, hypertension 47.40%, Diabetes mellitus 24.20% and 14.1% had atrial fibrillation. 174 (61.92%) of the stroke had less than sufficient Vitamin D. CONCLUSION: The common risk factors for stroke patients like smoking, hypertension, diabetes mellitus and atrial fibrillations are present in Nepalese population. The level of vitamin D was also low in stroke patients.


Assuntos
Ataque Isquêmico Transitório/sangue , Ataque Isquêmico Transitório/epidemiologia , Acidente Vascular Cerebral/sangue , Acidente Vascular Cerebral/epidemiologia , Vitamina D/sangue , Adulto , Idoso , Fibrilação Atrial/epidemiologia , Biomarcadores/sangue , Comorbidade , Diabetes Mellitus Tipo 2/epidemiologia , Dislipidemias/complicações , Feminino , Humanos , Hipertensão/epidemiologia , Masculino , Pessoa de Meia-Idade , Nepal/epidemiologia , Fatores de Risco , Fumar/epidemiologia , Adulto Jovem
3.
Kathmandu Univ Med J (KUMJ) ; 11(44): 342-3, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24899334

RESUMO

With the advancement of neuroradiology, clinical localization followed by radiology, had made neurology more interesting. Vertical gage palsy as presentation cerebrovascular disease is not so common. Vertical gaze palsy usually localizes the lesion to dorsal mid brain. A 56 years male patient presented with sudden onset vertigo, diplopia, transient loss of consciousness and sways toward right side while walking. Clinical examination showed vertical gaze palsy with skew deviation along with swaying towards rt. during walk. MRI brain showed - infarct involving dorsal midbrain at superior colliculus level and medial thalamus.


Assuntos
Transtornos da Motilidade Ocular/diagnóstico , Transtornos da Motilidade Ocular/fisiopatologia , Humanos , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade
4.
Kathmandu Univ Med J (KUMJ) ; 10(38): 96-9, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-23132486

RESUMO

Three cases of acute intermittent porphyria are reported. While in first case severe pain in abdomen with intermittent exacerbation was the only presentation, the second patient presented as accelerated hypertension and acute abdominal crises in whom the clinical course was characterized by development of deep coma due to inappropriate secretion of antidiuretic hormone before she made complete recovery. The third patient, initially manifested as acute encephalitic syndrome. After initial improvement, she developed features of acute intermittent porphyria i.e. acute abdomen, neuropsychiatric symptoms, and rapidly progressing acute motor neuropathy leading to respiratory and bulbar paralysis. In addition, she developed severe and fluctuating dysautonomia leading to cardiac arrest and fatal termination. The importance of early diagnosis, recognition of autonomic disturbances, prompt treatment and counseling for avoidance of precipitating factors is stressed.


Assuntos
Síndrome de Secreção Inadequada de HAD/etiologia , Porfirias/complicações , Disautonomias Primárias/etiologia , Doença Aguda , Adolescente , Adulto , Feminino , Humanos , Porfirias/terapia , Adulto Jovem
5.
Kathmandu Univ Med J (KUMJ) ; 10(37): 91-3, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22971872

RESUMO

With the advances in neurogenetics association of epilepsy and intellectual disability with chromosomal abnormalities are being increasingly recognized. While onset of seizures with mental retardation at an early age indicate chromosomal abnormality, combination of characteristics facial dysmorphism and congenital abnormalities gives a clue of a particular syndrome. In addition MRI findings may help in confirming the diagnosis. A nine years old boy is presented where early onset seizure, mental retardation, delayed development of speech, presence of facial dysmorphism,, umbilical hernia and undescended testes suggested possibility of chromosomal 6q deletion disorder. Important deletion disorders are discussed and importance of clinical examination is stressed.


Assuntos
Anormalidades Congênitas/epidemiologia , Convulsões/complicações , Anormalidades Múltiplas/diagnóstico , Anormalidades Múltiplas/genética , Criança , Deleção Cromossômica , Transtornos Cromossômicos , Cromossomos Humanos Par 6 , Anormalidades Congênitas/diagnóstico , Anormalidades Congênitas/genética , Anormalidades Craniofaciais , Criptorquidismo/complicações , Criptorquidismo/diagnóstico , Criptorquidismo/genética , Fácies , Hérnia Umbilical/complicações , Hérnia Umbilical/diagnóstico , Hérnia Umbilical/genética , Humanos , Deficiência Intelectual/complicações , Deficiência Intelectual/genética , Masculino , Atrofia Muscular/complicações , Atrofia Muscular/diagnóstico , Atrofia Muscular/genética , Convulsões/diagnóstico , Convulsões/genética
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...