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1.
Chinese Journal of Dermatology ; (12): 16-19, 2022.
Artigo em Chinês | WPRIM | ID: wpr-933504

RESUMO

Objective:To compare efficacy and safety of 308-nm SQ light-emitting diode (LED) light versus 308-nm excimer light in the treatment of facial vitiligo.Methods:Patients with stable facial vitiligo were retrospectively collected from Department of Physical Therapy, Hospital of Dermatology, Chinese Academy of Medical Sciences from June 2018 to June 2020, who received treatment with 308-nm SQ LED light (LED group) or 308-nm excimer light (excimer light group). The treatment was performed once or twice a week, and patients who had received more than 8 sessions of treatment were included in the analysis of efficacy and safety. Statistical analysis was carried out by using chi-square test.Results:Totally, 68 patients with 90 lesions were enrolled into the LED group, including 36 males and 32 females, aged 25.01 ± 13.37 years; 20 patients with 28 lesions were enrolled into the excimer light group, including 13 males and 7 females, aged 27.15 ± 14.30 years. After 8 and 16 sessions of treatment, there was no significant difference in the response rate between the LED group (23.33%, 46.67%, respectively) and excimer light group (14.29%, 46.43%, χ2 = 1.05, < 0.001, respectively, both P > 0.05). During the treatment, 36 (52.94%) patients in the LED group developed persistent erythema, 17 (85%) in the excimer light group developed persistent erythema or blisters. The incidence of adverse reactions was significantly lower in the LED group than in the excimer light group ( χ2 = 16.43, P < 0.001) . Conclusion:Compared with the 308-nm excimer light, the 308-nm SQ LED light showed similar effect but higher safety for the treatment of facial vitiligo.

2.
China Pharmacy ; (12): 2890-2894, 2021.
Artigo em Chinês | WPRIM | ID: wpr-906657

RESUMO

OBJECTIVE:To investigate the effec ts of angiotensin receptor neprilysin inhibitor (ARNI)sacubitril valsartan sodium(SVS)on the short-term prognosis of patients with acute anterior myocardial infarction (AAMI)complicated with acute cardiac insufficiency. METHODS :A total of 80 patients with AAMI and Killip grade Ⅱ-Ⅳ of cardiac function ,who met the inclusion criteria ,were randomly divided into ARNI group and control group ,with 40 patients in each group. Both groups were given the same basic standardized drug treatment ,vital signs support treatment and percutaneous coronary intervention treatment at the same time. On this basis ,ARNI group was given SVS tablet orally ,with initial dose of 25 mg each time ,twice a day ; thereafter,gradually adjust the dose to 200 mg each time ,twice a day. Control group was given Enalapril maleate tablets orally , with an initial dose of 5 mg each time ,twice a day ;thereafter,gradually adjust the dose to 10 mg each time ,twice a day. Both groups took medicine for a long time ,and were followed up after 1,3 and 6 months of medication to the clinic. The levels of N-terminal pro-B-type natriuretic peptide (NT-proBNP), soluble growth stimulation expressed gene 2 protein (sST2) and echocardiography indexes were compared between 2 groups before and after medication. The 6-minute walking test (6MWT)and the incidence of cardiogenic readmission events were recorded in 2 groups after medication. RESULTS :Compared with before treatment,the indexes of the two groups were significantly improved at 1,3 and 6 months after treatment (P<0.05). Compared with control group ,the levels of NT-proBNP and sST 2 in ARNI group decreased significantly (P<0.05),the levels of left ventricular ejection fraction and 6MWT increased significantly(P<0.05),and the left ventricular end systolic diameter and left ventricular end diastolic diameter decreased significantly,after 3 and 6 months of treatm ent(P<0.05). However ,there was no significant difference in the velocity ratio of peak E to peak A ,pulmonary artery pressure ,right ventricular end diastolic diameter and the incidence of cardiogenic readmission events between 2 groups(P>0.05). CONCLUSIONS :For patients with AAMI complicated with acute cardiac insufficiency , compared with enalapril ,SVS can significantly improve the cardiac function (especially the left ventricular systolic function ), reduce the inflammatory reaction of cardiomyocytes ,protect cardiomyocytes ,so as to improve the short-term prognosis of patients.

3.
Journal of Medical Postgraduates ; (12)2003.
Artigo em Chinês | WPRIM | ID: wpr-585550

RESUMO

Objective: To observe the effect of valsartan and amlodipine on the reduction of blood pressure in aged hyperpietic patients,as well as on the improvement of left ventricular diastolic function,endothelium function and insuline resistence. Methods: We divided 40 cases of aged hypertension patients(1 to 2 grade) into Valsartan and Amlodipine groups at random,giving valsartan 80-160 mg or amlodipine 5-10 mg,respectively,for 12 weeks as a treating period.We measured the blood pressure twice a week,observed the differences of blood pressure and heart rate before and after the treatment,as well as the changes of insuline sensitivity,left ventricular diastolic function and endothelium vascular disatolic function. Results and Conclusion: Both valsartan and amlodipine can effectivly reduce the blood pressure of aged hypertension patients(l to 2 grade).They can also improve the diastolic function,insuline resistance and endothelium dependent vascular diastolic function.

4.
Chinese Journal of Interventional Cardiology ; (4)1996.
Artigo em Chinês | WPRIM | ID: wpr-582291

RESUMO

Objective To evaluate the immediate results and the 6 month angiographic restenosis rate after repeat percutaneous intervention for in stent restenosis (ISR) Methods The acute and 6 month follow up outcomes of 156 patients with ISR who were treated by repeat PTCA or stenting were analyzed in this retrospective study Quantitative coronary angiography analyses (QCA) were performed before and after repeat intervention for in stent restenosis and on a average 6 month coronary angiogram to assess the recurrent restenosis rate Results All the patients were treated successfully Balloon angioplasty was performed in 134 patients (85 9%) and repeat stenting in 22 patients (14 1%) The six month follow up coronary angiogram showed the recurrent restenosis rate was 24 3% The recurrent restenosis rate was higher in 40 diffuse ISR lesions than that in 96 focal ISR lesions: 45% vs 18%, P75% was also the risk factor of recurrent restenosis Conclusion For the most patients with ISR, repeat PTCA or intracoronary stenting seems to be an effective and safe method The overall restenosis rate after repeat intervention for ISR is the same as that of initial intracoronary stenting

5.
Chinese Journal of Interventional Cardiology ; (4)1996.
Artigo em Chinês | WPRIM | ID: wpr-591027

RESUMO

Objective To analyze the effect and safety of cerebral protection filter in carotid artery and stenting(CAS) for the treatment of severe symptomatic carotid artery stenosis.Methods Elective CAS with the use of cerebral protection filters were undergone in 26 consecutive patients with severe carotid artery stenosis.The filter devices were advanced through lesions and opened distal to the lesions followed by CAS.The incidence of cerebral ischemic events and the debris collected in the filters were observed and analyzed.Results In all the patients,it was feasible and successful to position the filters devices in the internal carotid artery.After the filter devices were positioned,CAS were performed successfully in all the 26 patients.Thrombus or plague debris were found in 14 out of 26 retrieved filters(54%).There was no death or symptomatic cerebral thromboembolic event during the CAS procedure.Asymptomatic cerebral embolization lesions were detected in 3 patients by the means of diffusion-weighted magnetic resonance imaging after 1-6 days of the CAS.No major cerebral or cardiovascular ischemic events were recorded in all patients during their follow up period of 6-12 months.Conclusion Carotid artery stenting is an effective microinvasive therapy for severe carotid artery stenosis which effect and safety can be enhanced with the use of cerebral protection filter.

6.
Journal of Clinical Neurology ; (6)1993.
Artigo em Chinês | WPRIM | ID: wpr-586784

RESUMO

Objective To observe the effectiveness and safety of endovascular stent assisted angioplasty for symptomatic intracranial arteriostenosis.Methods 4 patients with symptomatic intracranial arteriostenosis were treated with endovascular angioplasty using balloon expandable stents. Therapeutic effects were evaluated by clinical manifestations, digital subtraction angiography (DSA) and transcranial Dopple (TCD) before and after the operation. Follow up was made for 7~10 months.Results Technical success was achieved in all patients, with no complication of cerebral embolism and hemorrhage except one of transient seizure during operation. Angiographic results immediately after stenting suggested that the residual postoperation stenosis was 8%(0%~17%), with significant reduction from preoperation stenosis of 75%(70%~80.7%). No recurrent TIA and stroke occurred and no restenosis was found with serial TCD in all 4 patients during follow up of 7~10 months.Conclusions Endovascular stenting is a safe and effective therapeutic tool for symptomatic intracranial arteriostenosis.

7.
Journal of Clinical Neurology ; (6)1992.
Artigo em Chinês | WPRIM | ID: wpr-588475

RESUMO

Objective To investigate the effectivety and safety of carotid angioplasty and stenting (CAS) with cerebral protection fitler for elder and high risk patients with symptomatic carotid stenosis.Methods 25 patients with symptomatic carotid stenosis over 60 years old at high risk were treated with CAS. Results The procedures were technically successful in all patients. All the degrees of stenosis after CAS were less than 20%. Clinical symptoms disappeared. Heart rate and blood pressure were decreased differently in 24 cases.None of them experienced serious clinical complications. Conclusion CAS with cerebral protection fitler are safe and effective in treatment of elder and high risk of patients with symptomatic carotid stenosis.

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