Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 4 de 4
Filtrar
1.
Journal of Central South University(Medical Sciences) ; (12): 1096-1101, 2021.
Artículo en Inglés | WPRIM | ID: wpr-922589

RESUMEN

OBJECTIVES@#Vagus nerve stimulation (VNS) is a neuromodulative therapeutic technique for patients with drug-resistant epilepsy who are not suitable for resection or who have experienced a failed resection. This study aims to explore the efficacy and safety of VNS in patients with refractory epilepsy, and to analyze the influential factors for the efficacy.@*METHODS@#A retrospective review of clinical data were conducted for 35 patients, who were treated for refractory epilepsy through VNS surgery in the Department of Neurosurgery, Xiangya Hospital, Central South University from April 2016 to August 2019. All patients were analyzed in terms of the clinical and follow-up data.@*RESULTS@#After a mean follow-up of 26 months (6-47 months), outcome was as follows: 7 patients were MuHugh class I, 13 patients were MuHugh class II, 8 patients were MuHugh class III, and 7 patients were MuHugh class IV-V. The total efficacy rate in the short duration group was significantly higher than that in the long duration group (77.8% vs 50.0%, @*CONCLUSIONS@#VNS is a safe and effective option in treating patients with refractory epilepsy, especially for those with short duration.


Asunto(s)
Humanos , Epilepsia Refractaria/terapia , Imagen por Resonancia Magnética , Estudios Retrospectivos , Convulsiones , Resultado del Tratamiento , Estimulación del Nervio Vago
2.
Chinese Journal of Neonatology ; (6): 201-204, 2017.
Artículo en Chino | WPRIM | ID: wpr-610426

RESUMEN

Objective To study the clinical characteristics of neonatal pertussis.Method From January 2011 to December 2015,clinical data of newborns with pertussis treated in our hospital were retrospectively analyzed,including the general information,clinical manifestations,laboratory examinations,treatment and prognosis.Result A total of 68 newborns with pertussis were found during the study period,including 1 case in 2011,5 cases in 2012,1 case in 2013,18 cases in 2014 and 43 cases in 2015.The time needed for diagnosis was 7 to 35 days after onset of symptoms,and 80.9% (55/68) in 14 days.The predominant manifestation was paroxysmal cough (68 cases,100%).Other common symptoms included flushing in 45 cases (66.2%) and cyanosis with coughing in 40 cases (58.8%).The uncommon symptoms included whooping cough (20 cases,29.4%),wheezing (10 cases,14.7%),fever (3 cases,4.4%) and apnea with decreased heart rate during cough (2 cases,2.9%).12 patients (17.6%) had elevated peripheral white blood cells or lymphocytes.The clinical manifestations didn't disappear despite erythromycin therapy,and the whooping cough continued for 12 to 42 days during the course of disease.22 cases (32.4%) had complications,including pneumonia in 12 cases,myocardial damage in 10 cases,heart failure in 2 cases,respiratory failure in 1 case,atrial tachycardia in 1 case and lung consolidation in 1 case.Conclusion Neonatal pertussis is not uncommon and has a tendency to increase year by year,and it's challenging for early diagnosis.The patients who have a whooping cough without fever should be considered of pertussis until otherwise ruled out.Leukocyte and lymphocyte count are of little value in the diagnosis of this disease.

3.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery ; (24): 874-877, 2015.
Artículo en Chino | WPRIM | ID: wpr-747891

RESUMEN

OBJECTIVE@#To summarize and analyze the clinical characteristics of Mondini dysplasia with cerebrospinal fluid leakage, as well as preliminarily investigate the genetic mechanism of the disease.@*METHOD@#The clinical data of 2 patients diagnosed as Mondini dysplasia with cerebrospinal fluid leakage treated in our hospital were analyzed. Blood samples of these two patients were obtained to extract DNA. We screened DNA samples for gene SLC26A4 mutations by using polymerase chain reaction and direct sequencing. The sequencing results were analyzed in DNASTAR software.@*RESULT@#Both patients came to our hospital because of recurrent meningitis, and the fistula were both located in vestibular window. Patients were cured one-time after surgical closure of the leakages with temporalis + temporalis fascia + temporalis through the mastoid approach. No pathogenic mutations of gene SLC26A4 with exome sequencing were found.@*CONCLUSION@#Mondini dysplasia with cerebrospinal fluid leakage should be considered in patients with recurrent meningitis and hearing disorder. Temporal bone HRCT is helpful to the diagnosis. Surgical closure is an effective therapeutic method and may prevent recurrent meningitis. The molecular mechanism of simple Mondini dysplasia needs further study.


Asunto(s)
Humanos , Pérdida de Líquido Cefalorraquídeo , Cóclea , Patología , Fístula , Patología , Hiperplasia , Genética , Proteínas de Transporte de Membrana , Genética , Meningitis , Mutación , Transportadores de Sulfato
4.
Journal of Clinical Otorhinolaryngology Head and Neck Surgery ; (24): 1850-1852, 2015.
Artículo en Chino | WPRIM | ID: wpr-746912

RESUMEN

OBJECTIVE@#Aimed to analyse the clinical features of the patients with sphenoid sinus mucocele, achieve earlier diagnosis and more timely intervention and decrease the occurrence of misdiagnoses.@*METHOD@#A retrospective study was first conducted in patients with sphenoid sinus mucoele treated in Xiangya hospital from Jan 2000 to Jan 2015. Then literature reports on this disease were collected and analyzed from China National Knowledge Infrastructure (CNKI) and Wan Fang database.@*RESULT@#We collected 82 patients with sphenoid sinus mucocele treated in Xiangya hospital. There were 52 patients presented with headache, 31 patients presented with visual impairment, 10 patients presented with cranial nerve palsy, 2 patients presented with exophthalmos, 15 patients presented with nasal symptoms, and 5 patients with no obvious symptoms. There was no significant difference for symptoms distribution between male and female patients (P > 0.05). Among 45 patients with headache as first symptom and 10 patients with ethmoid sinus mucocele, there were 18 patients and 8 patients subsequently suffering from visual impairment, respectively. We also collected 161 patients in literature except for enrolling, the 82 patients treated in Xiangya hospital, and found that headache was the most common symptom, followed by visual impairment, in the two independent cohorts.@*CONCLUSION@#To the best of our knowledge, this is the study of maximum sample for sphenoid sinus mucocele in China. Headache and visual impairment are the most common symptoms for sphenoid sinus mucocele. Surgical treatment should be early performed when the desease accompanied with headache or ethmoid sinus mucocele, to avoid other complications such as visual impairment and even blindness.


Asunto(s)
Femenino , Humanos , Masculino , China , Enfermedades de los Nervios Craneales , Bases de Datos Factuales , Errores Diagnósticos , Senos Etmoidales , Exoftalmia , Cefalea , Mucocele , Diagnóstico , Patología , Enfermedades de los Senos Paranasales , Estudios Retrospectivos , Seno Esfenoidal , Patología , Trastornos de la Visión
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA