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1.
Zhonghua Jie He He Hu Xi Za Zhi ; 43(5): 427-430, 2020 May 12.
Artículo en Zh | MEDLINE | ID: mdl-32087623

RESUMEN

Objective: To raise awareness about 2019 novel coronavirus pneumonia (NCP) and reduce missed diagnosis rate and misdiagnosis rate by comparing the clinical characteristics between RNA positive and negative patients clinically diagnosed with NCP. Methods: From January 2020 to February 2020, 54 patients who were newly diagnosed with NCP in Wuhan Fourth Hospital were included in this study. RT-PCR method was used to measure the level of 2019-nCov RNA in pharyngeal swab samples of these patients. The patients were divided into RNA positive and negative group, and the differences of clinical, laboratory, and radiological characteristics were compared. Results: There were 31 RNA of 2019-nCov positive cases, and 23 negative cases. Common clinical symptoms of two groups were fever (80.64% vs. 86.96%) , chills (61.29% vs. 52.17%) , cough (80.64% vs. 95.65%) , fatigue (61.30% vs. 56.52%) , chest distress (77.42% vs.73.91%) . Some other symptoms were headache, myalgia, dyspnea, diarrhea, nausea and vomiting. The laboratory and radiological characteristics of two groups mainly were lymphopenia, increased erythrocyte sedimentation rate, increased C-reactive protein, increased lactate dehydrogenase, decreased oxygenation index, normal white blood cell count and bilateral chest CT involvement. There was no statistically significant difference in other clinical characteristics except for dyspnea between two groups. Conclusions: RNA positive and negative NCP patients shared similar clinical symptoms, while RNA positive NCP patients tended to have dyspnea. Therefore, we should improve the understanding of NCP to prevent missed diagnosis and misdiagnosis; In addition, more rapid and accurate NCP diagnostic approaches should be further developed.


Asunto(s)
Infecciones por Coronavirus , Pandemias , Neumonía Viral , ARN Viral , Betacoronavirus/aislamiento & purificación , COVID-19 , Prueba de COVID-19 , Técnicas de Laboratorio Clínico/normas , Infecciones por Coronavirus/diagnóstico , Infecciones por Coronavirus/patología , Errores Diagnósticos/estadística & datos numéricos , Humanos , Diagnóstico Erróneo/estadística & datos numéricos , Neumonía Viral/diagnóstico , Neumonía Viral/patología , ARN Viral/análisis , SARS-CoV-2
2.
Zhonghua Xin Xue Guan Bing Za Zhi ; 48(10): 842-847, 2020 Oct 24.
Artículo en Zh | MEDLINE | ID: mdl-33076621

RESUMEN

Objective: We aimed to explore the feasibility and perioperative safety of performing catheter ablation and left atrial appendage closure (LAAC) in a single (one-stop) session in patients with atrial fibrillation (AF). Methods: This study is an observational study. Consecutive AF patients who underwent the combined procedure of catheter ablation and LAAC with Watchman device of Xinhua Hospital in Shanghai between March 2017 and May 2019 were prospectively enrolled. Baseline, intra-and peri-procedural parameters were evaluated. Results: A total of 358 AF patients (189 males, (69.0±8.0) years) underwent the one-stop procedure. The CHA2DS2-VASc score was 3.2±1.5 and HAS-BLED score was 2.4±1.1, respectively in this patient cohort. Pulmonary vein isolation was achieved in all patients, while additional linear ablation was applied in 180 (50.3%) patients, yielding immediate success rate of 99.7%. Successful Watchman implantation was achieved in all patients. The perioperative serious adverse event occurred in 14 cases (3.9%). including 6 pericardial effusions (1.7%), 1 stroke (0.3%) and 5 vascular complications (1.4%), yielding procedure-related complication rate of 3.4%. In addition, 2 (0.6%) new-onset heart failures occurred postoperatively. There was no major bleeding or death during the perioperative period. Conclusions: Combined catheter ablation and LAAC can be successfully and safely performed in AF patients with high stroke risk. Follow-up data are needed to evaluate the outcome of this one-stop procedure.


Asunto(s)
Apéndice Atrial , Ablación por Catéter , Anciano , Apéndice Atrial/cirugía , China , Estudios de Factibilidad , Femenino , Humanos , Masculino , Persona de Mediana Edad , Resultado del Tratamiento
3.
Zhonghua Nei Ke Za Zhi ; 58(8): 560-565, 2019 Aug 01.
Artículo en Zh | MEDLINE | ID: mdl-31365976

RESUMEN

Objectives: To evaluate the effectiveness and safety of peramivir trihydrate in patients with influenza. Methods: This was a randomized, double-blind, double-dummy, placebo and positive control, multicenter clinical trial, comparing peramivir trihydrate with oseltamivir and placebo. The inclusive criteria were 15-70 years old, onset within 48 h, positive rapid influenza antigen test, and febrile (>38℃) accompanied with at least two associated symptoms. The severe cases complicated with chronic pulmonary and cardiac diseases, malignancies, organ transplantation, hemodialysis, uncontrolled diabetes, immunocompromised status, pregnancy and coexistence of bacterium infections were excluded. All patients were randomized 2∶2∶1 to receive peramivir, oseltamivir and placebo respectively. The primary endpoint was the disease duration, the secondary endpoints included time to normal axillary temperature and normal living activities, viral response, and adverse effects. Results: Following informed consent, 133 patients were included in this study. Four patients were exclude due to missing medical records, not fitting inclusion or exclusion criteria and poor compliance. A total of 129 patients were finally analyzed, including 49 cases, 54 cases and 26 cases in peramivir group, oseltamivir group and placebo group. The median disease duration were 96 (76, 120) hours, 105 (90,124) hours, and 124 (104, 172) hours in three groups respectively (P>0.05) . The time to normal axillary temperature, normal living activities and viral response were not significantly different in three groups (P>0.05) . Conclusion: The value of antiviral therapy in patients with mild influenza needs to be further determined.


Asunto(s)
Antivirales/uso terapéutico , Ciclopentanos/uso terapéutico , Guanidinas/uso terapéutico , Gripe Humana/tratamiento farmacológico , Oseltamivir/uso terapéutico , Ácidos Carbocíclicos , Adolescente , Adulto , Anciano , Método Doble Ciego , Humanos , Gripe Humana/diagnóstico , Persona de Mediana Edad , Resultado del Tratamiento , Adulto Joven
4.
Zhonghua Liu Xing Bing Xue Za Zhi ; 10(5): 295-8, 1989 Oct.
Artículo en Zh | MEDLINE | ID: mdl-2611872

RESUMEN

A latex agglutination test was first used for the serological diagnosis of Brucellosis. Results of tested sera obtained from patients with a clinical diagnosis of Brucellosis and cows infected with Brucella showed that this test was specific and sensitive. Meantime the procedure of this test was easily and rapidly to perform. In addition, preparation of immuno-latex, the procedure of this test and some factors which affected the result of this test were also described in the paper.


Asunto(s)
Brucelosis Bovina/diagnóstico , Brucelosis/diagnóstico , Adolescente , Adulto , Anciano , Animales , Bovinos , Niño , Femenino , Humanos , Pruebas de Fijación de Látex , Masculino , Persona de Mediana Edad , Pruebas Serológicas
5.
Zhonghua Liu Xing Bing Xue Za Zhi ; 16(2): 92-4, 1995 Apr.
Artículo en Zh | MEDLINE | ID: mdl-7781055

RESUMEN

A carboxylated latex agglutination test was developed for detecting antibodies in sera from 372 human and animal brucellosis. Of which 94 sera from human was detected by ELISA. The latex was chemical-linked with B. melitensis 16M and extracted with 5% NaCl. Comparing with RBPT in detecting antibodies with brucellosis, the LAT was more stable and specific; the positive or negative results detected by LAT were consistent with those by SAT and ELISA. LAT may detect both IgG and IgM antibodies to Brucella in Human and animal. It is concluded that LAT is stable, specific, sensitive and practicable for the serodiagnosis of brucellosis.


Asunto(s)
Anticuerpos Antibacterianos/sangre , Brucelosis/diagnóstico , Animales , Brucella/inmunología , Brucelosis/veterinaria , Bovinos , Enfermedades de los Bovinos/diagnóstico , Humanos , Pruebas de Fijación de Látex , Ovinos , Enfermedades de las Ovejas/diagnóstico
6.
J Tongji Med Univ ; 15(1): 59-64, 1995.
Artículo en Alemán | MEDLINE | ID: mdl-7783268

RESUMEN

965 workers engaged in working tasks of work intensity grade 2, 3, 4 (based on Chinese National Standard) were investigated on the musculoskeletal disorders with a questionnaire. The lumbar vertebra of 136 randomly chosen workers were also radiologically examined. The result revealed that the prevalence of low-back disorders was 51.2% on average and it was obviously correlated with such factors as age, standing, previous back injury, education level, sport activity, work intensity, working posture, satisfaction with the tools as well as work condition and house work. Heavy work load and unneutral working posture were proved to be the main factors as revealed by the multifactor analysis and further supported by the findings of X-ray examination.


Asunto(s)
Enfermedades Musculoesqueléticas/epidemiología , Carga de Trabajo , Adulto , Dolor de Espalda/epidemiología , China/epidemiología , Femenino , Humanos , Vértebras Lumbares/diagnóstico por imagen , Masculino , Persona de Mediana Edad , Análisis Multivariante , Postura , Radiografía , Encuestas y Cuestionarios
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