Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
1.
Chinese Journal of Infection Control ; (4): 647-649, 2017.
Artigo em Chinês | WPRIM | ID: wpr-613764

RESUMO

Objective To understand the pathogenic characteristics of intra-abdominal infection after appendecto-my in patients with appendicitis.Methods Clinical data of patients undergoing appendectomy in a hospital from January 2013 to December 2015 were analyzed retrospectively,pathogenic characteristics,treatment,and prognosis of patients with intra-abdominal infection were analyzed.Results A total of 431 patients undergoing appendectomy were investigated,38 (8.82%)developed intra-abdominal infection.36 strains of pathogenic bacteria were isolated, 34 (94.44%)of which were gram-negative bacteria,mainly Escherichiacoli(n=29,80.55%);2 (5.56%)strains were gram-positive bacteria,1 of which was Staphylococcusaureus,and the other was Enterococcusavium.The re-sistance rates of 29 strains of Escherichia coli to commonly used antimicrobial agents (amoxicillin,piperacillin,ti-carcillin,cefuroxime,ceftazidime,and cefalotin)were 72.41%-93.10%,none of strains were found to be resistant to piperacillin/tazobactam,meropenem,imipenem,and amikacin.Conclusion Escherichiacoli is the most common pathogen causing intra-abdominal infection after appendectomy and it has high resistance rates to most commonly used antimicrobial agents,piperacillin/tazobactam,amikacin,and carbapenems are recommended for treating intra-abdominal infection after appendectomy.

2.
Chinese Journal of Oncology ; (12): 508-511, 2015.
Artigo em Chinês | WPRIM | ID: wpr-286790

RESUMO

<p><b>OBJECTIVE</b>To explore the value of serum neuron-specific enolase (NSE) before treatment in predicting brain metastases and prognosis of advanced non-small cell lung cancer (NSCLC).</p><p><b>METHODS</b>A total of 128 hospitalized patients with advanced NSCLC from Jan 2012 to Mar 2012 were followed up, and their clinicopathological data, serum NSE, carcinoembryonic antigen, cytokeratin 21-1 (cyfra21-1) levels, albumin (ALB), white blood cell (WBC) before treatment were analyzed retrospectively to determine the factors affecting brain metastasis and prognosis of advanced NSCLC.</p><p><b>RESULTS</b>Among the 128 NSCLC patients, 90 cases were of adenocarcinoma, 30 cases were of squamous cell carcinoma, and 8 cases were of large cell carcinoma. The median levels of pre-treatment NSE, CEA and cyfra21-1 were 13.6 ng/ml, 7.8 ng/ml and 6.1 ng/ml, respectively. The average levels of ALB and WBC were (35.41 ± 5.60) g/L and (8.16 ± 2.53) × 10⁹/ml, respectively. Multi-variate logistic regression analysis showed that serum NSE before treatment was associated with brain metastasis of advanced NSCLC (P = 0.030). Pre-treatment NSE levels were (34.18 ± 28.48) ng/ml in 28 patients with brain metastasis and (13.87 ± 4.49) ng/ml in 98 patients without brain metastasis (P < 0.05). The median survival time were 3.5 months in patients with normal levels of NSE, and 10.7 months in patients with elevated levels of NSE pre-treatment (P < 0.05).</p><p><b>CONCLUSIONS</b>A higher pre-treatment level of NSE is closely correlated with brain metastasis of advanced NSCLC, and can be used as a predictor of brain metastases in advanced NSCLC. High pre-treatment levels of NSE indicate a poor prognosis in advanced NSCLC patients.</p>


Assuntos
Humanos , Adenocarcinoma , Sangue , Antígenos de Neoplasias , Sangue , Neoplasias Encefálicas , Antígeno Carcinoembrionário , Sangue , Carcinoma de Células Grandes , Sangue , Carcinoma Pulmonar de Células não Pequenas , Sangue , Carcinoma de Células Escamosas , Sangue , Queratina-19 , Sangue , Contagem de Leucócitos , Neoplasias Pulmonares , Sangue , Patologia , Fosfopiruvato Hidratase , Sangue , Prognóstico , Estudos Retrospectivos , Albumina Sérica
3.
Chinese Journal of Primary Medicine and Pharmacy ; (12): 667-669, 2013.
Artigo em Chinês | WPRIM | ID: wpr-431855

RESUMO

Objective To explore the different changes of the adult cerebral blood flow with ages,different weight and gender,to summarize the changing characteristics of cerebral blood flow.Methods 360 cases of examination were divided into two groups according to gender,and were divided into five groups at different ages,and were divided into four groups according to body mass index,using TCD detector blood flow velocity.Results 196 cases of male physical examination,the mean cerebral blood flow was (969.37 ± 117.54)ml/min;the 164 females physical examination,the average cerebral blood flow was (987.76 ± 114.34)ml/min,there was no statistically significant difference (P > 0.05).Different ages cerebral blood flow velocity were different,20 to 29-year-old group and the 30 to 39-year-old group had no significant difference (P > 0.05) ;40 to 49-year-old group,50 to 59 years,60 to 69 years old > 70 age group significantly declined compoued with the first two groups,there was significant difference (P < 0.05) ;there were significant difference between the four groups (P < 0.05).Overweight and obese group were significantly lower than the light and the normal group,there was a statistically significant difference (P < 0.05).Conclusion TCDcan be a sensitive and accurate hemodynamic changes in the human brain,and is very important in the early diagnosis,prevention,treatment,and follow-up of cerebrovascular disease.

4.
Chinese Journal of Medical Genetics ; (6): 147-150, 2003.
Artigo em Chinês | WPRIM | ID: wpr-248474

RESUMO

<p><b>OBJECTIVE</b>To establish a high sensitive and specific method of interphase fluorescence in situ hybridization (IFISH) to detect the low-frequency human cells in human/goat xenogeneic models.</p><p><b>METHODS</b>Human-specific Y-chromosome satellite DNA CEPY and 17-chromosome satellite DNA p17H8 were used as probes for IFISH. The peripheral blood samples from 2 goats transplanted with human male hematopoietic stem cells (HSC), 1 normal negative goat and 1 normal man were analyzed. The actual FISH efficiency was confirmed by serial dilutions (1/100, 1/500 and 1/1000) of the cell mixture of normal man and normal negative goat. A set of signal scoring criteria was determined to guarantee the stability and reliability of the method.</p><p><b>RESULTS</b>Positive cell (human cell) frequencies were consistent with the established frequencies for the human/goat cell mixture. The average frequencies of positive cells were 98.60% (CEPY) and 100% (p17H8) for normal man, 0 for normal negative goat, 0.23% (CEPY) and 0.11% (p17H8) for human/goat xenogeneic models. The results demonstrated that low-frequency human cells (male cells confirmed by Y-chromosome probe) existed in human/goat xenogeneic models.</p><p><b>CONCLUSION</b>The IFISH developed in this study is of high sensitivity and specificity and can identify the actual frequency of human cells, which offers a direct, sensitive and specific approach to the detection of low-frequency human cells in human/goat xenogeneic models.</p>


Assuntos
Animais , Humanos , Cromossomos Humanos Par 17 , Genética , Cromossomos Humanos Y , Genética , Sondas de DNA , Cabras , Transplante de Células-Tronco Hematopoéticas , Células-Tronco Hematopoéticas , Biologia Celular , Metabolismo , Hibridização in Situ Fluorescente , Métodos , Interfase , Genética , Repetições de Microssatélites , Genética , Quimeras de Transplante , Sangue , Genética , Transplante Heterólogo
5.
Chinese Journal of Hematology ; (12): 634-637, 2002.
Artigo em Chinês | WPRIM | ID: wpr-261373

RESUMO

<p><b>OBJECTIVE</b>To identify the human hematopoietic stem cells from the human/goat xenogeneic model with molecular techniques.</p><p><b>METHODS</b>DNA and total RNA were extracted from 11 transplanted goat peripheral blood cells. Human CD(34), GPA and SRY genes were amplified with PCR in these samples, and CD(34), GPA mRNA transcripts were detected using RT-PCR in 5 and 6 goat peripheral blood cells, respectively. Southern blot analysis was performed in 8 goat DNAs to detect the human specific alpha-satellite sequence. Meanwhile FISH was also performed to detect the human cells in goat blood with a probe of human Y chromosome.</p><p><b>RESULTS</b>Human CD(34) and GPA genes could be detected with PCR in all the 11 goats, and SRY gene did in 5 goats transplanted with hematopoietic stem cells derived from male human babies. Southern blot showed that human specific alpha-satellite sequence was present in 8 goats. By RT-PCR, human CD(34) mRNA was detected in 5 experimental goats, GPA mRNA was found in the other 6 experimental goats and FISH assay showed that some peripheral blood cells of the human/goat xenogeneic model were positive.</p><p><b>CONCLUSION</b>Existence of human cells in the recipient goats was identified by molecular detection, which was feasible for the examination of human/goat xenogeneic models.</p>


Assuntos
Animais , Feminino , Humanos , Masculino , Antígenos CD34 , Genética , Southern Blotting , Genes sry , Genética , Glicoforinas , Genética , Cabras , Transplante de Células-Tronco Hematopoéticas , Métodos , Células-Tronco Hematopoéticas , Biologia Celular , Metabolismo , Hibridização in Situ Fluorescente , Reação em Cadeia da Polimerase , Quimeras de Transplante , Genética , Transplante Heterólogo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA