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1.
Chinese Journal of Cardiology ; (12): 467-471, 2020.
Article de Chinois | WPRIM (Pacifique Occidental) | ID: wpr-941065

RÉSUMÉ

Objective: To identify the characteristics including clinical features and pulmonary computed tomography (CT) features of heart failure and COVID-19. Methods: This study was a retrospective study. A total of 7 patients with heart failure and 12 patients with COVID-19 in the Second Xiangya Hospital of Central South University between December 1, 2019 and February 15, 2020 were enrolled. The baseline clinical and imaging features of the two groups were statistically analyzed. Results: There was no significant difference in age and sex between the two groups(both P>0.05), but the incidence of epidemiological contact history, fever or respiratory symptoms in the COVID-19 group was significantly higher than that in the heart failure group (12/12 vs. 0, P<0.001; 12/12 vs. 4/7, P=0.013). While the proportion of cardiovascular diseases and impaired cardiac function was significantly less than that of the heart failure group(2/12 vs.7/7, P<0.001;0 vs.7/7, P<0.001). For imaging features, both groups had ground-glass opacity and thickening of interlobular septum, but the ratio of central and gradient distribution was higher in patients with heart failure than that in patients with COVID-19 (4/7 vs. 1/12, P=0.04). In heart failure group, the ratio of the expansion of pulmonary veins was also higher (3/7 vs. 0,P=0.013), and the lung lesions can be significantly improved after effective anti-heart failure treatment. Besides, there were more cases with rounded morphology in COVID-19 group(9/12 vs. 2/7, P=0.048). Conclusions: More patients with COVID-19 have epidemiological history and fever or respiratory symptoms. There are significant differences in chest CT features, such as enlargement of pulmonary veins, lesions distribution and morphology between heart failure and COVID-19.


Sujet(s)
Humains , Betacoronavirus , COVID-19 , Infections à coronavirus/imagerie diagnostique , Défaillance cardiaque/étiologie , Pandémies , Pneumopathie virale/imagerie diagnostique , Études rétrospectives , SARS-CoV-2 , Tomodensitométrie
2.
Ai Zheng ; 28(12): 1324-7, 2009 Dec.
Article de Chinois | MEDLINE | ID: mdl-19958629

RÉSUMÉ

BACKGROUND AND OBJECTIVE: p53 gene is one of cancer suppressor genes and its mutation and deletion induces almost all human cancers. This study was to evaluate the clinical efficacy and toxicity of recombinant human Ad-p53 injection (rAd-p53) combined with cisplatin in treatment of malignant pleural effusion induced by lung cancer. METHODS: A total of 35 cases of malignant pleural effusion were randomly divided into the combined group (n=17) and the single-agent group (n=18). On the basis of systemic treatment (vinorelbine 25 mg/m2, Days 1-8, every 3 weeks), the combined group were given intracavitary administration of rAd-p53 (1x1012 VP) and cisplatin (40 mg/m2) once a week for 4 weeks. The single-agent group were given the same intracavitary administration as the combined group but without rAd-p53 therapy. RESULTS: The total effective rates in the combined group and the single-agent group were 82.35% and 50.00% (P<0.05), respectively. The total modification rates in the combined group and the single-agent group were 64.70% and 33.33% (P<0.05), respectively. The toxicities in the two groups were fever, stethalgia, nausea/vomiting and leukopenia. The toxic reaction in combined group was mainly self-limited fever (P<0.05), which disappeared automatically after 36 h. CONCLUSIONS: rAd-p53 and cisplatin is safe and effective for malignant pleural effusion induced by lung cancer. It is worthy of application in clinical treatment.


Sujet(s)
Cisplatine/usage thérapeutique , Thérapie génétique , Tumeurs du poumon/thérapie , Épanchement pleural malin/thérapie , Protéine p53 suppresseur de tumeur/usage thérapeutique , Adénocarcinome/thérapie , Adénovirus humains/génétique , Adulte , Sujet âgé , Antinéoplasiques/effets indésirables , Antinéoplasiques/usage thérapeutique , Carcinome épidermoïde/thérapie , Cisplatine/effets indésirables , Association thérapeutique , Femelle , Fièvre/étiologie , Gènes p53 , Thérapie génétique/effets indésirables , Humains , Leucopénie/étiologie , Mâle , Adulte d'âge moyen , Nausée/étiologie , Qualité de vie , Protéines recombinantes/effets indésirables , Protéines recombinantes/usage thérapeutique , Protéine p53 suppresseur de tumeur/effets indésirables , Protéine p53 suppresseur de tumeur/génétique
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