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1.
目的 目的 观察氨氯地平和贝尼地平治疗原发性高血压的安全以及疗效.方法 选择原发性高血压患者56例,随机分为贝尼地平组26例,氨氯地平组30例.分别观察服药前和服药后(8周末)的血压变化及贝尼地平服药前、后的24 h.白昼、夜间的动态血压变化.结果 贝尼地平组服药8周后SBP和DBP下降(16.9±11.8)和(12.8±9.2)mmHg(P<0.01).氨氯地平组SBP和DBP下降(14.8±10.9)和(11.2±8.7)mmHg(P<0.01).动态血压资料分析示服用贝尼地平后24 h、白天、夜间平均收缩压/舒张压显著下降,收缩压和舒张压的谷峰比值分别为0.62和0.61.无严重不良反应.结论 贝尼地平是一种安全有效的抗高血压药.  相似文献   

2.
目的 应用动态血压监测(ABPM)的方法 ,评价盐酸贝尼地平和硝苯地平控释片对轻、中度高血压病的疗效.方法 选择原发性高血压患者118例随机分为盐酸贝尼地平组(n=56)和硝苯地平控释片组(n=62),分别给与盐酸贝尼地平、硝苯地平控释片治疗,疗程为8周,并于治疗前后进行动态血压监测(ABPM).结果 两药均能降低24h、白昼、夜间血压,但差异无统计学意义,仅硝苯地平控释片全日平均收缩压下降有统计学差异(P<0.05).硝苯地平控释片组服药后24 h舒张压的平滑指数(24hSID)、白天收缩压的平滑指数(dSIS)、夜间舒张压的平滑指数(nSID)较服药前有明显降低(P<0.05),贝尼地平组服药后24 hSID、nSID较服药前有明显降低(P<0.05),同时硝苯地平控释片组服药后24 h收缩压的平滑指数(24SID)、夜间收缩压的平滑指数(nSID)均较贝尼地平组明显降低(P<0.01).硝苯地平控释片组、贝尼地平组的收缩压晨峰服药后均较服药前减低(P<0.05).硝苯地平控释片组舒张压晨峰服药后较服药前减低(P<0.05),但两组间比较,差异无显著性.两药均无明显不良反应发生.结论 盐酸贝尼地平和硝苯地平控释片一样的能安全有效的降压.两者均能有效控制晨峰,具有满意的平滑指数.  相似文献   

3.
目的用动态血压监测(ABPM)的方法评价贝尼地平治疗原发性高血压的疗效。方法选择原发性高血压患者56例,随机分为贝尼地平组26例,厄贝沙坦组30例。分别观察服药前和服药后(8周末)的血压变化及贝尼地平服药前、后的24h,白昼、夜间的动态血压变化。结果贝尼地平组服药8周后SBP和DBP下降(16.9±11.8)和(12.8±9.2)mmHg(P〈0.01)。厄贝沙坦组SBP和DBP下降(14.8±10.9)和(11.2±8.7)mmHg(P〈0.01)。动态血压资料分析示服用贝尼地平后24h、白天、夜间平均收缩压/舒张压显著下降,收缩压和舒张压的谷峰比值分别为0.62和0.61。无严重不良反应。结论贝尼地平是一种安全有效的抗高血压药。  相似文献   

4.
目的:探讨氨氯地平治疗轻中度原发性高血压患者的谷峰比值和平滑指数.方法:对30例轻中度高血压患者,口服氨氯地平5mg,每天1次,疗程8周,于治疗前后进行24h动态血压监测并计算其谷峰比值和平滑指数.结果:治疗8周后,24h收缩压和24h舒张压、白昼收缩压和舒张压、夜间收缩压和舒张压与治疗前比较均有非常显著性差异(P<0.001),T/P为收缩压72%,舒张压71%.平滑指数为收缩压(1.12±0.59),舒张压(0.92±0.54).结论:氨氯地平有较高的T/P比值及良好的平滑指数.  相似文献   

5.
贝尼地平在原发性高血压患者中的应用   总被引:1,自引:0,他引:1  
目的:观察盐酸贝尼地平治疗原发性轻中度高血压患者的疗效、安全性.方法:采取随机双盲对照观察法,原发性轻中度高血压的患者经安慰剂治疗两周,血压符合入选标准者,随机分为二组.分别给予盐酸贝尼地平4mg每日1次或氨氯地平5mg每日1次,第2周末,如舒张压≥90mmHg则剂量加倍,继续治疗6周.观察贝尼地平降压疗效及安全性.结果:两组血压治疗后均显著下降,治疗前后均有显著差异(P<0.001),但二组之间无显著差异(P>0.05)不良反应在两组间无统计学差异.心率的改变两组治疗前后无统计学差异(P>0.05).结论:贝尼地平能有效降低轻中度原发性高血压患者的血压,疗效与氨氯地平组无统计学差异.具有较好安全性和耐受性.  相似文献   

6.
目的 观察不同降压药物联合应用对老年高血压患者血压变异性(BPV)的影响。 方法 选择2015年1月—2016年1月宜兴市人民医院就诊的老年原发性高血压患者128例,将其按照随机数字法分为A、B两组,每组64例,A组给予氨氯地平和培哚普利;B组给予培哚普利和氢氯噻嗪;服药前及服药8周后均采用无创便携式动态血压监测仪监测24 h动态血压(动态收缩压及动态舒张压),以测量值变异系数(CV)作为BPV的指标。 结果 服药8周后A组24 h平均收缩压(24hSBP)、白天平均收缩压(dSBP)、夜间平均收缩压(nSBP)、24 h平均收缩压变异系数(24hSCV)、白天平均收缩压变异系数(dSCV)、夜间平均收缩压变异系数(nSCV)均显著性低于B组(均P<0.05),但服药8周后2组24 h平均舒张压(24hDBP)、白天平均舒张压(dDBP)、夜间平均舒张压(nDBP)相比差异无统计学意义(均P>0.05),A组24 h平均舒张压变异系数(24hDCV)、白天平均舒张压变异系数(dDCV)、夜间平均舒张压变异系数(nDCV)显著低于B组(均P<0.05)。服药8周后2组相比,A组一氧化氮水平显著高于B组,而内皮素水平显著低于B组(均P<0.05)。 结论 氨氯地平联合培哚普利和氢氯噻嗪联合培哚普利均能有效降低老年原发性高血压患者血压变异性,但氨氯地平联合培哚普利效果更为明显。   相似文献   

7.
目的:应用动态血压监测进行轻、中度原发性高血压患者每日口服盐酸贝尼地平2~4mg的持续性降压疗效研究。方法:20例轻、中度原发性高血压患者经安慰剂1片/d洗脱2周,若诊室舒张压95~109mmHg且24h平均舒张压≥85mmHg,患者接受贝尼地平2mg/d治疗,如舒张压90mmHg或下降>20 mmHg,则维持原剂量不变,否则递增剂量至4mg/d,治疗8周后进行动态血压监测。另选36例治疗8周且降压有效的患者继续维持原剂量治疗24周。结果:20例患者贝尼地平2~4mg/d治疗后动态血压监测表明,24h动态收缩压/舒张压均值由135.67±6.52/87.30±5.81mmHg降至126.24±7.34/83.35±5.59mmHg,24h、日间和夜间治疗前后差异显著(P<0.01和P<0.05)。36例患者治疗24周,诊室收缩压/舒张压由153.06±13.09/98.89±3.65mmHg降低至133.27±12.70/83.69±6.0mmHg(P<0.01),降压总有效率为88.9%。贝尼地平片主要不良反应有轻度头痛、心慌、浮肿、瘙痒等。结论:每日口服贝尼地平2~4mg可持久、平稳地降低轻、中度原发性高血压患者的血压水平。  相似文献   

8.
目的:探讨老老年高血压患者颈动脉病变与血压变异的关系。方法:将入选的64名老老年原发性高血压患者依据颈动脉超声检查结果分为颈动脉病变组和无颈动脉病变组,行24 h动态血压检查,分析两组间全天24 h收缩压变异、24 h舒张压变异、白昼收缩压变异、白昼舒张压变异、夜间收缩压变异、夜间舒张压变异的差异。结果:颈动脉病变组24 h收缩压变异、24 h舒张压变异、白昼收缩压变异、夜间收缩压变异、夜间舒张压变异明显高于无颈动脉病变组(14.09±2.67 vs 8.88±1.19,12.42±3.08 vs 10.22±2.80,11.71±3.20 vs 8.44±1.80,11.40±10.70 vs 6.82±2.65,10.52±3.50 vs 8.29±2.62;P<0.01或P<0.05)。结论:老老年高血压患者的颈动脉病变与血压变异密切相关。  相似文献   

9.
目的 探讨依那普利、左旋氨氯地平时辰化服用治疗高血压病的疗效.方法 61例高血压病患者随机分为两组,A组(时辰化服药组)32例,依那普利10mg于清晨6:00时、左旋氨氯地平2.5mg于中午12:00时服用.B组(常规化服药组)29例,依那普利、左旋氨氯地平均于上午8:00时服用,剂量用A组.采用无创袖带式动态血压监测系统Spacelab 90217-1 B于服药前及1周、3周后进行24 h每半小时测血压一次.结果 A、B两组服药后3周末与服药前比较,A组治疗后24h平均收缩压(24hMSBP)/舒张压(24hMDBP)、白昼平均收缩压(dMSBP)/舒张压(dMDBP),夜间平均收缩压(nMSBP)/舒张压(nMDBP),白昼血压负荷(dLBp)/夜间血压负荷(nLBp)、平均动脉压(MAP)、血压晨蜂(MBPS)较前均显著下降(P<0.01);B组治疗3周末以上各指标较服药前也有明显下降(P<0.05),但是下降程度较小;服药治疗3周末A组与B组比较,以上各指标A组较B组下降明显(P<0.05);服药治疗3周末,A组24 h血压变异小,T/P高,B组24 h血压变异大,T/P低.结论 依那普利、左旋氨氯地平按时辰化服用可平稳、有效控制24 h血压,能最大限度降低血压波动和保护靶器官功能.  相似文献   

10.
目的探讨依那普利、左旋氨氯地平时辰化服用治疗高血压病的疗效。方法61例高血压病患者随机分为两组,A组(时辰化服药组)32例,依那普利10mg于清晨6:00时、左旋氨氯地平2.5mg于中午12:00时服用。B组(常规化服药组)29例,依那普利、左旋氨氯地平均于上午8:00时服用,剂量用A组。采用无创袖带式动态血压监测系统Spacelab 90217-1B于服药前及1周、3周后进行24h每半小时测血压一次。结果A、B两组服药后3周末与服药前比较,A组治疗后24h平均收缩压(24hMSBP)/舒张压(24hMDBP)、白昼平均收缩压(dMSBP)/舒张压(dMDBP)、夜间平均收缩压(nMSBP)/舒张压(nMDBP)﹑白昼血压负荷(dLBp)/夜间血压负荷(nLBp)、平均动脉压(MAP)、血压晨峰(MBPS)较前均显著下降(P&lt;0.01);B组治疗3周末以上各指标较服药前也有明显下降(P&lt;0.05),但是下降程度较小;服药治疗3周末A组与B组比较,以上各指标A组较B组下降明显(P&lt;0.05);服药治疗3周末,A组24h血压变异小,T/P高,B组24h血压变异大,T/P低。结论依那普利、左旋氨氯地平按时辰化服用可...  相似文献   

11.
Objective: To evaluatel the value of D-dimers in patients with acute aortic dissection (AAD). Methods: This study consisted of 16 patients with AAD and 27 non-AAD patients. Serum D-dimets were measured by Sta-Liatest D-DI immunoturbidimetric assay. Results: D-dimer level was higher (P < 0.001) in patients with AAD(7.91 ± 5.52 μg/ml) than that in non- AAD group(1.57±1.24 μg/ml). D-dimer was positive (>0.4 μg/ml) in all patients with AAD and in 10 control group patients (37%). Among patients with acute AAD, D-dimers tended to be higher in Stanford A than in Stanford B (8.67 ± 4.31 μg/ml vs. 3.24±1.27 μg/ml, P <0.01). D-dimer values tended to be higher in more extended disease(3.84 ± 1.65 μg/ml, 8.57 ± 3.58 μg/ml and 11.87 ± 5.69 μg/ml in thoracic aorta, thoracic and abdominal aorta, thoracic and abdominal aorta and iliacal arteries, respectively, P < 0.05 for both 8.57 ± 3.58 and 11.87 ± 5.69 vs. 3.84 ± 1.65 ). Including the control group into the analysis, we found a sensitivity of 100%, a negative predictive value of 100%, and a specificity of 66% and a positive predictive value of 64% for D-dimer in diagnosis of AAD in our patients with suspected AAD. Conclusion: D-dimer was elevated in patients with AAD. A negative D-dimer test result could be useful in excluding AAD.  相似文献   

12.
Objective: To set up a simple and reliable rat model of combined liver-kidney transplantation. Methods: SD rats served as both donors and recipients. 4℃ sodium lactate Ringer's was infused from portal veins to donated livers,and from abdominal aorta to donated kidneys, respectively. Anastomosis of the portal vein and the inferior vena cava (IVC) inferior to the right kidney between the graft and the recipient was performed by a double cuff method, then the superior hepatic vena cava with suture. A patch of donated renal artery was anastomosed to the recipient abdominal aorta. The urethra and bile duct were reconstructed with a simple inside bracket. Results: Among 65 cases of combined liver-kidney transplantation, the success rate in the late 40 cases was 77.5%. The function of the grafted liver and kidney remained normal. Conclusion: This rat model of combined liver-kidney transplantation can be established in common laboratory conditions with high success rate and meet the needs of renal transplantation experiment.  相似文献   

13.
Objective To observe blood pressure change with age in salt-sensitive teenagers whose salt sensitivity were determined by repeated testing.Methods Salt sensitivity was determined through intravenous infusion of normal saline combined with volume-depletion by oral diuretic furosemide in 55 teenagers. After five years, salt sensitivity was re-examined and subject blood pressure was followed up. Blood pressure changes in salt-sensitive teenagers were compared to that of non-salt sensitive teenagers over five years.Results After 5 years, the repetition rate of salt sensitivity determined by intravenous saline loading is 92.7%. In teenagers with salt sensitivity on the baseline, both the systolic blood pressure increments and increment rates were much higher than non-salt sensitive teenagers (12.7±12.1 mmHg vs. 2.8±5.2 mmHg, P< 0.01; 12.2%± 12.0% vs. 2.5% ±4.4%, P< 0.001,respectively). There was a similar trend for diastolic blood pressure (8.4 ± 6.4 mmHg vs. 3.7 ± 6.4 mmHg, P = 0.052; 13.2% ±10.6 % vs. 6.8%± 10.1%, P = 0.053, respectively).Conclusions Salt sensitivity determined by intravenous saline loading showed good reproducibility. Blood pressure increments with age were much higher in salt-sensitive teenagers than non-salt sensitive teenagers, especially in terms of systolic blood pressure.  相似文献   

14.
目的:评价使用安心颗粒对急诊经皮冠状动脉介入术(PPCI)术后生活质量的影响.方法:将160例接受PPCI的急性ST段抬高型心肌梗死患者随机分为安心颗粒组(术前顿服安心颗粒8.8g,术后安心颗粒4.4 g/次,每日2次)和对照组(仅接受基础药物治疗).所有患者均服用阿司匹林、氯吡格雷和阿托伐他汀.分别在入院时、出院前1d、出院后180 d时,应用心肌梗死多维度量表(MIDAS)、中文版SF-36评价量表对患者生活质量评分.并观察术后30 d以内的出血并发症、血小板减少症发生情况.结果:入院时和出院前1d,两组患者的心肌梗死MIDAS、SF-36量表评分比较无差异(P>0.05);出院后180 d时,与对照组比较,安心颗粒组MIDAS、SF-36评分明显减低(P<0.05);组内与入院时比较,两组出院前1d、出院后180 d时,MIDAS、SF-36评分均降低(P<0.05).两组患者在随访期间均无大量出血、少量出血、重度和极重度血小板减少症发生,安心颗粒组有4例、对照组有7例发生不明显出血(P>0.05).两组发生轻度血小板减少症的患者数比较无差异(P>0.05).结论:PPCI使用安心颗粒,能改善急性ST段抬高型心肌梗死患者的生活质量,且不增加出血风险.  相似文献   

15.
Objective:To investigate the influences of urapidil and nicardipine on rabbit sinus function,atrio-ventricular node function and hemodynamics.Methods:Thirty-two Angora's rabbits were selected and randomly divided into four groups.U1 group:urapidil 0.25 mg/kg;U2 group:urapidil 0.5 mg/kg;N1 group:nicardipine 10 μg/kg;N2 group:nicardipine 20 μg/kg.All these medicine were administrated within 30 seconds.Measurements were taken before and after the administration of urapidil or nicardipine for the following data:mean blood pressure(MAP),heart rate(HR),sino-atrial conduction time(SACT),maximal sinoatrial recovery time(SNRTmax)corrected sinus node recovery time(CSNRT),index of sinus node recovery time(SNRTI),Wenckebach A-V conduction frequency (WB),and P-R interval.Results:Significant MAP and HR changes were identified in all of the four groups before and after administration of both urapidil and nicardipine.No significant changes could be found in the rest of the parameters.Intergroup analysis showed that SACT and CSNRT of N1 and N2 groups were shorter than those of the U2 group(P<0.01);the MAP decreased(P<0.01)and the HR increased drastically(P<0.01).Conclusions:Neither urapidil(0.25 mg/kg,0.5 mg/kg)nor nicardipine(10μg/kg,20μg/kg)has any significant influence on rabbit sinus function or rabbit atrio-ventricular node function.Nicardipine could be a better choice than urapidil for parafunctional sinus node patients.  相似文献   

16.
Objective:To investigate the gene expression of osteoprotegerin(OPG) and osteoclast differentiation factor(ODF) in the bone tissue of patients with hip fracture due to osteoporosis. Methods:OPGmRNA and ODFmRNA in the bone tissue in 50 cases of osteoporosis sufferers(over 50 years old) with hip fracture(Observer Group) and 30 cases of hip facture sufferers with no osteoporosis(Control group) were analyzed with the Semi-Quantitative RT-PCR method. Results:The mRNA expressed of ODF, OPG were both high in the patients with hip fracture. In the control group, the expression of OPG mRNA was observed, while the expression of ODF mRNA was very slight. Conclusion:Aged patients contained all signals including OPG, ODF that are essential for inducing osteoclastogenesis and promoting bone resorption.  相似文献   

17.
Objective:To investigate the clinical features, pathological characteristics and immunophenotype of solid-pseudopapillary tumor of the pancreas(SPTP). Methods:Nine surgically treated cases of SPTP were retrospectively reviewed. Hematoxylin and Eosin(HE) staining and immunohistochemical staining were used to analyze all cases, and the general clinical data was collected. Results:Six patients were asymptomatic except for a palpable mass. Two patients complained of vague-epigastric pain. One patient appeared jaundice. The tumor was encapsulated and solid tissues alternately with cystic tissues. Histologically, the histological structure of solid portion was pseudopapillary with a fibrovascular core. Tumor cells were uniform and medium-sized which were arranged in sheets ets or nests or pseudopapillary patterns. Immunohistochemical studies demonstrated that SPTP proved positive in vimentin(9/9 cases), AAT(9/9 cases), NSE(9/9 cases), ACT(7/9 cases), CK20(2/9 cases), CgA(1/9 cases), S-100(3/gcases), PR(4/gcases), Syn(3/9 cases) and CD56(5/9cases), negative in CEA and ER. Conclusion:SPTP is a tumor predominantly occurring in young women frequently without special symptoms. This tumor has various characteristical histological patterns with different immunophenotype.  相似文献   

18.
Objective:To probe into the influence of changes of ovarian hormones on the pathogenesis of the specific sub-type premenstrual syndrome(PMS)and reveal partial microcosmic mechanisms of adverse flow of liver-qi.Methods:Estradiol(E2)and progesterone(P)levels in serum were determined at different phases of menstrual cycle by radioimmunoassay.Results:In the group of PMS with adverse flow of liver-qi.the secretive peak value Of E2 and P at the follicular phase significantly decreased,and the secretive peak value at the luteal phase did not come into being.Conclusions:Low E2 and P secretive peak at the follicular phase and absence of secretive peak at the luteal phase is one of the microcosmic mechanisms of PMS with adverse flow of liver-qi.One of the pathophysiologic mechanisms of specific sub-type PMS is probably the continuous low level of E2and P.  相似文献   

19.
Real-time three-dimensional echocardiography (RT3DE)is a new ultrasound technique that enables dynamic threedimensional visualization and quantification of the heart in real time. Investigation of feasibility and methodology of RT3DE in determining left ventricular (LV) and right ventricular (RV) volumes, RT3DE was performed in 35 normal adults using Philips SONOS 7500 system with a 2-4 MHz matrix array transducer. The 60°×60° "pyramid" volume database was obtained and analyzed on a TomTec echo workstation. Both LV and RV volumes were calculated with four 3DE methods (i.e. apical 2, 4, 8, and 16-plane) through manually tracing ventricular endocardial borders in end diastole and end systole. Stroke volumes were then calculated. LV volume was also measured by 2DE Simpson's rule using GE VIVID 7 ultrasound machine.  相似文献   

20.
Increasing maternal age is the only etiological factor unequivocally linked to Down's syndrome in humans. The occurrence rate of newborns with Down's syndrome is about 1/220 in women over 35 years old. However, the occurrence rate in embryos fertilized in vitro, of the elder woman is unclear. Using FISH we screened the number of chromosome 21 in preimplanted embryos of 5 elderly women (average age, 38.4 years) to study the feasibility and necessity of screening trisomy 21 in embryos in patients over 35 years old at the in vitro fertilization (IVF) center.  相似文献   

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