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Delayed diagnosis of pulmonary tuberculosis with pleuritis due to ampicillin/sulbactam:A case report
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作者 Munechika Hara Toshitsugu Yashiro Yasuaki Yashiro 《World Journal of Clinical Cases》 2025年第19期72-77,共6页
BACKGROUND Tuberculosis(TB)remains a global health concern despite decreasing incidence.Delayed TB diagnosis can exacerbate patient outcomes and lead to broader public health issues such as mass infections.Differentia... BACKGROUND Tuberculosis(TB)remains a global health concern despite decreasing incidence.Delayed TB diagnosis can exacerbate patient outcomes and lead to broader public health issues such as mass infections.Differentiation between TB and bacterial pneumonia is often complicated by variable clinical and radiological manifestations of TB,leading to diagnostic delays.CASE SUMMARY An 89-year-old,Japanese male patient with a history of diabetes mellitus,hypertension,and hypothyroidism presented with right-sided chest pain.Based on the elevated inflammatory response,right pleural effusion,and infiltrating shadow in the lung field,the diagnosis of right pleurisy was made and the antibiotic,ampicillin/sulbactam,was administered.The patient’s condition,inflammatory reaction,and right pleural effusion temporarily improved.However,persistent low-grade fever and malaise prompted further evaluation,revealing repeated right pleural effusion and inflammatory response.A right thoracentesis was performed;the patient was diagnosed with tuberculous pleurisy as a result of exudative effusion with lymphocyte predominance,elevated adenosine deaminase levels,and positive Mycobacterium TB polymerase chain reaction test.Anti-TB treatment,including isoniazid,rifampicin,and ethambutol was initiated,leading to significant clinical improvement.The patient successfully completed a 12-month course of TB therapy without recurrence or deterioration.CONCLUSION There are cases of TB wherein temporary improvement apparently could be shown through treatment with antimicrobial agents other than anti-TB drugs,necessitating careful evaluation in atypical cases of bacterial pneumonia. 展开更多
关键词 Antibiotics Ampicillin/sulbactam PNEUMONIA Tuberculosis Tuberculous pleuritis Case report
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Construction of universal quantitative models for the determination of cefoperazone sodium/sulbactam sodium for injection from different manufacturers using near-infrared reflectance spectroscopy 被引量:4
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作者 逄焕欢 冯艳春 +1 位作者 张学博 胡昌勤 《Journal of Chinese Pharmaceutical Sciences》 CAS 2008年第1期22-29,共8页
To develop near-infrared (NIR) reflectance spectroscopic methods for the quantitative analysis of cefoperazone sodium/ sulbactam sodium from different manufacturers for injection powder medicaments. Various powders ... To develop near-infrared (NIR) reflectance spectroscopic methods for the quantitative analysis of cefoperazone sodium/ sulbactam sodium from different manufacturers for injection powder medicaments. Various powders of cefoperazone sodium/ sulbactam sodium were directly analyzed by non-destructive NIR reflectance spectroscopy using the spectrometer EQUINOX55. Two quantitative methods via integrating sphere (IS) and fiberoptic probe (FOP) models were explored from 6 batches of commercial samples and 42 batches of laboratory samples at a content ranging from 30% to 70% for cefoperazone and 60% to 20% for sulbactam. The root mean square errors of cross validation (RMSECV) and the root mean square errors of prediction (RMSEP) of IS were 1.79% and 2.85%, respectively, for cefoperazone sodium, and were 1.86% and 3.08%, respectively, for sulbactam sodium; and those of FOP were 2.93% and 2.92%, respectively, for cefoperazone sodium, and were 2.23% and 3.01%, respectively, for sulbactam sodium. Based on the ICH guidelines and Ref. 12, the quantitative models were then evaluated in terms of specificity, linearity, accuracy, precision, robustness and model transferability. The non-destructive quantitative NIR methods used in this study are applicable for rapid analysis of injectable powdered drugs from different manufacturers. 展开更多
关键词 NIR diffuse reflectance spectroscopy Non-destructive determination Cefoperazone sodium/sulbactam sodium Injection powder medicament Validation Counterfeit medicine
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In vitro activity of moxifloxacin and piperacillin/sulbactam against pathogens of acute cholangitis 被引量:19
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作者 Andreas Weber Wolfgang Huber +5 位作者 Klaus Kamereck Philipp Winkle Petra Voland Hans Weidenbach Roland M Schmid Christian Prinz 《World Journal of Gastroenterology》 SCIE CAS CSCD 2008年第20期3174-3178,共5页
AIM:To analyze the in vitro activity of moxifloxacin and piperacillin/sulbactam against pathogens isolated from patients with acute cholangitis. METHODS: In this prospective study a total of 65 patients with acute c... AIM:To analyze the in vitro activity of moxifloxacin and piperacillin/sulbactam against pathogens isolated from patients with acute cholangitis. METHODS: In this prospective study a total of 65 patients with acute cholangitis due to biliary stone obstruction (n = 7), benign biliary stricture (n = 16), and malignant biliary stricture (n = 42) were investigated with regard to spectrum of bacterial infection and antibiotic resistance. Pathogens were isolated from bile cultures in all study patients. In 22 febrile patients, blood cultures were also obtained. In vitro activity of moxifloxacin and piperacillin/ sulbactam was determined by agar diffusion. RESULTS: Thirty-one out of 65 patients had positive bile and/or blood cultures. In 31 patients, 63 isolates with 17 different species were identified. The predominant strains were Enterococcus species (26/63), Ecoli (13/63) and Klebsiella species (8/63). A comparable in vitro activity of moxifloxacin and piperacillin/sulbactam was observed for E.coli and Klebsiella species. In contrast, Enterococcus species had higher resistances towards moxifloxacin. Overall bacteria showed antibiotic resistances in vitro of 34.9% for piperacillin/sulbactam and 36.5% for moxifioxacin.CONCLUSION: Enterococcus species, E.co/i and Klebsiella species were the most common bacteria isolated from bile and/or blood from patients with acute cholangitis. Overall, a mixed infection with several species was observed, and bacteria showed a comparable in vitro activity for piperacillin/sulbactam and moxifloxacin. 展开更多
关键词 CHOLANGITIS Acute cholangitis Endoscopy ANTIBIOTICS MOXIFLOXACIN PIPERACILLIN sulbactam Biliarystricture Resistance Bacterial pathogens
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Cefoperazone sodium/sulbactam sodium vs piperacillin sodium/tazobactam sodium for treatment of respiratory tract infection in elderly patients 被引量:17
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作者 Xiao-Xia Wang Cheng-Tai Ma +3 位作者 Yan-Xia Jiang Yun-Jie Ge Fa-Yun Liu Wen-Gang Xu 《World Journal of Clinical Cases》 SCIE 2021年第29期8694-8701,共8页
BACKGROUND Respiratory tract infections in the elderly are difficult to cure and can easily recur,thereby posing a great threat to patient prognosis and quality of life.AIM To investigate the therapeutic effects of di... BACKGROUND Respiratory tract infections in the elderly are difficult to cure and can easily recur,thereby posing a great threat to patient prognosis and quality of life.AIM To investigate the therapeutic effects of different antibiotics in elderly patients with respiratory tract infection.METHODS Seventy-four elderly patients with respiratory tract infection were randomly allocated to a study(n=37;treated with cefoperazone sodium/sulbactam sodium)or control(n=37;treated with piperacillin sodium/tazobactam sodium on the basis of routine symptomatic support)group.Both groups were treated for 7 d.Time to symptom relief(leukocyte recovery;body temperature recovery;cough and sputum disappearance;and rale disappearance time),treatment effect,and laboratory indexes[procalcitonin(PCT),C-reactive protein(CRP),white blood cell count(WBC),and neutrophil percentage(NE)]before and 7 d after treatment and the incidence of adverse reactions were assessed.RESULTS In the study group,the time to WBC normalization(6.79±2.09 d),time to body temperature normalization(4.15±1.08 d),time to disappearance of cough and sputum(6.19±1.56 d),and time to disappearance of rales(6.68±1.43 d)were shorter than those of the control group(8.89±2.32 d,5.81±1.33 d,8.77±2.11 d,and 8.69±2.12 d,respectively;P=0.000).Total effective rate was higher in the study group(94.59%vs 75.68%,P=0.022).Serum PCT(12.89±3.96μg/L),CRP(19.62±6.44 mg/L),WBC(20.61±6.38×10^(9)/L),and NE(86.14±7.21%)levels of the study group before treatment were similar to those of the control group(14.05±4.11μg/L,18.79±5.96 mg/L,21.21±5.59×10^(9)/L,and 84.39±6.95%,respectively)with no significant differences(P=0.220,0.567,0.668,and 0.291,respectively).After 7 d of treatment,serum PCT,CRP,WBC,and NE levels in the two groups were lower than those before treatment.Serum PCT(2.01±0.56μg/L),CRP(3.11±1.02 mg/L),WBC(5.10±1.83×10^(9)/L),and NE(56.35±7.17%)levels were lower in the study group than in the control group(3.29±0.64μg/L,5.67±1.23 mg/L,8.13±3.01×10^(9)/L,and 64.22±8.08%,respectively;P=0.000).There was no significant difference in the incidence of adverse reactions between the groups(7.50%vs 12.50%,P=0.708).CONCLUSION Piperacillin sodium/tazobactam sodium is superior to cefoperazone sodium/sulbactam sodium in the treatment of elderly patients with respiratory tract infection with a similar safety profile. 展开更多
关键词 Cefoperazone sodium sulbactam sodium Piperacillin sodium Tazobactam sodium Respiratory tract infection ELDERLY
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Sclerotherapy with Leuprolide and Cefoperazone Sulbactam in the Management of Ovarian Endometriomas under Ultrasound Guidance: A Novel Approach 被引量:1
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作者 Yazhini Selvaraj 《Advances in Sexual Medicine》 2022年第1期34-46,共13页
<span style="font-family:Verdana;">Endometriosis is an estrogen dependent gynecological disorder, which can occur throughout the reproductive age of women, causing chronic pelvic pain, substantial morb... <span style="font-family:Verdana;">Endometriosis is an estrogen dependent gynecological disorder, which can occur throughout the reproductive age of women, causing chronic pelvic pain, substantial morbidity, and impaired fertility. It is clinically defined as the presence of ectopic endometrium resulting in sustained inflammatory reaction. In India</span><span style="font-family:Verdana;">,</span><span style="font-family:Verdana;"> about 29,000,000 women suffer from endometriosis. Severe pelvic pain and recurrent endometriomas were observed even after surgery. We have conducted aspirations totally in 110 patients in which most of the patients were suffering from Stage III & Stage IV of endometriosis except for 7 patients for whom we have done as primary therapy for endometriomas. Among 110 </span><span style="font-family:Verdana;">patients</span><span style="font-family:;" "=""><span style="font-family:Verdana;">, 4 patients didn’t turn up for follow up after first aspiration. This pilot study conducted with 110 patients in Ponni Hospital and Fertility Research Centre, Madurai aimed to evaluate pregnancy outcome in 51 infertile patients, and to alleviate pelvic pain, to restore a healthy sexual life and to reduce the recurrence rate of Ovarian Endometriomas (OE) in 59 patients, who did not seek fertility, After using the newer sclerosing agent Leuprolide with Cefoperazone Sulbactam (LCS) under ultrasound guidance. This prospective pilot study resulted in a highly significant achievement in pregnancy where 41 patients conceived out of 51 patients (80.39%) only 6 are in ongoing treatment. Those who didn’t seek fertility were 59 of which 43 have </span><span style="font-family:Verdana;">completed family 1</span></span><span style="font-family:Verdana;">3</span><span style="font-family:Verdana;"> have one child</span><span style="font-family:Verdana;"> and 3 unmarried girls</span><span style="font-family:Verdana;">. 96.61% were relieved of pain and recurrence and restored healthy sexual life, 2 are in ongoing treatment. We have not encountered any adverse effects during this</span><span style="font-family:Verdana;"> treatment.</span> 展开更多
关键词 Ovarian Endometriomas (OE) Infertility (IF) Sclerosing Agent (SA) Leuprolide with Cefoperazone sulbactam (LCS) In Vitro Fertilization (IVF)
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Study on the Effect of Shuanghuanglian Powder Needle Combined with Cefoperazone and Sulbactam Sodium on Pseudomonas aeruginosa in Vitro 被引量:1
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作者 Jiming Li Meide Wei +5 位作者 Lili Wang Yanbo Wu Lu Kang Chunchun Su Fengli Yang Guosheng Su 《Advances in Microbiology》 CAS 2023年第5期223-236,共14页
Objective: To explore the antibacterial activity of combined use of Shuanghuanglian and cefoperazone sulbactam sodium on resistant strains of Pseudomonas aeruginosa. Methods: The Pseudomonas aeruginosa strains which w... Objective: To explore the antibacterial activity of combined use of Shuanghuanglian and cefoperazone sulbactam sodium on resistant strains of Pseudomonas aeruginosa. Methods: The Pseudomonas aeruginosa strains which were sensitive and resistant to cefoperazone sulbactam sodium were selected to prepare different test bacterial solutions respectively;The experimental liquid of Shuanghuanglian and Cefoperazone Sulbactam Sodium were prepared separately and set as different test groups and control groups;The Drug Sensitivity Tests of Shuanghuanglian and cefoperazone sulbactam sodium at different concentration gradients which were used alone or used in combination were carried out for different strains with sensitivity and resistance, And use standard entry as a reference control. Result: The results of drug sensitivity test of Shuanghuanglian combined with Cefoperazone-Sulbactam sodium against the resistant strains of Pseudomonas aeruginosa were compared with the results of drug sensitivity test of the two separately used, and the difference was statistically significant (P 〈 0.05) [The drug sensitivity test results of Shuanghuanglian and cefoperazone sulbactam sodium to Pseudomonas aeruginosa resistant strains were statistically significant compared with the drug sensitivity test results of Shuanghuanglian and Cefoperazone Sulbactam Sodium used separately (P 〈 0.05)];There was a dependence between strains and concentration in the effect of the combination of the two drugs. Conclusion: The combination of Shuanghuanglian and cefoperazone sulbactam sodium has synergistic antibacterial or bactericidal effect on Pseudomonas aeruginosa resistant strains. . 展开更多
关键词 Shuanghuanglian Cefoperazone-sulbactam Sodium Use in Combination Pseudomonas aeruginosa Drug Resistance BACTERIOSTASIS
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The Study of Effect of Commercial Baicalin Combined with Cefoperazone Sulbactam Sodium on Pseudomonas aeruginosa in Vitro
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作者 Jiming Li Meide Wei +5 位作者 Linghong Wang Yanbo Wu Lu Kang Yan Tang Huan Zhao Yubiao Sun 《Natural Science》 2022年第3期117-124,共8页
Objective: To investigate the antibacterial effect of baicalin combined with cefoperazone-sulbactam sodium on drug-resistant strains of Pseudomonas aeruginosa. Method: Pseudomonas aeruginosa strains that are sensitive... Objective: To investigate the antibacterial effect of baicalin combined with cefoperazone-sulbactam sodium on drug-resistant strains of Pseudomonas aeruginosa. Method: Pseudomonas aeruginosa strains that are sensitive and resistant to cefoperazone-sulbactam sodium were selected to prepare different test bacterial solutions respectively;The test solutions of baicalin and cefoperazone sulbactam sodium were prepared respectively, and different test groups and control groups were set up;The drug sensitivity tests of different concentration gradients of baicalin and cefoperazone sulbactam sodium used alone and in combination were carried out for different sensitive and drug-resistant strains, and the standard strains were used as parallel control. Result: The drug susceptibility test results of the combined use of baicalin and cefoperazone-sulbactam against Pseudomonas aeruginosa drug-resistant strains were compared with the drug susceptibility results of the two used separately, and the difference was statistically significant (P Pseudomonas aeruginosa. 展开更多
关键词 BAICALIN Cefoperazone-sulbactam Sodium Combined Use Pseudomonas aeruginosa Drug Resistance ANTIBACTERIAL
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Clinical Effect and Safety of Western Medicine Cefoperazone Sodium and Sulbactam Sodium
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作者 XU Xia HU Yudi +1 位作者 HE Yu WEI Jing 《外文科技期刊数据库(文摘版)医药卫生》 2021年第9期017-019,共5页
Objective: to investigate the clinical value of western medicine cefoperazone sodium sulbactam sodium. Methods: the clinical data of patients with inflammation in our hospital were randomly selected, a total of 50 cas... Objective: to investigate the clinical value of western medicine cefoperazone sodium sulbactam sodium. Methods: the clinical data of patients with inflammation in our hospital were randomly selected, a total of 50 cases were divided into a group of 25 cases on average, the control group was treated with ceftazidime, and the observation group was treated with cefoperazone sodium and sulbactam sodium, and the treatment results were analyzed and compared. Results: there was no difference in inflammatory cytokines between the two groups before treatment (P > 0.05). After treatment, the total effective rate of 96% was significantly higher and the level of inflammatory factors was significantly lower in the observation group (P < 0.05). Compared with the treatment period, the incidence of adverse reactions in the control group was higher, the mean time of fever abatement and the time of cough disappearance were longer (P < 0.05). Conclusion: in clinical practice, cefoperazone sodium and sulbactam sodium has good final effect. After medication, it can not only reduce the level of inflammatory factors in patients, improve the prognosis of patients, but also have fewer adverse reactions and good therapeutic effect. Therefore, it can be widely used in clinical treatment. 展开更多
关键词 cefoperazone sodium and sulbactam sodium SECURITY clinical effect western medicine drugs
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Comparison of the Clinical Efficacy of Cefoperazone Sulbactam and Ceftazidime in the Treatment of Complicated Urinary Tract Infections
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作者 LUOHaiping 《外文科技期刊数据库(文摘版)医药卫生》 2022年第10期088-092,共5页
Objective: to compare and analyze the clinical efficacy of cefoperazone sulbactam and ceftazidime in the treatment of complicated urinary tract infections and to provide a theoretical basis for the clinical drug treat... Objective: to compare and analyze the clinical efficacy of cefoperazone sulbactam and ceftazidime in the treatment of complicated urinary tract infections and to provide a theoretical basis for the clinical drug treatment of diseases. Methods: a retrospective study of 140 patients with complicated urinary tract infections admitted to the urology department of Hu’nan Provincial Peoples Hospital from January 2017 to December 2017: cefoperazone sulbactam group (71 patients, 1.0g / bid, 2 g/d) and (69 patients, 1.5g / bid, 3g / d), and PCT, CRP. Results: more cefoperazone subactam (70 / 71,94.29%) than ceftazidime (60 / 69,84.29%) were significant (P < 0.05). A total of 19 strains were detected in the cefoperazone and sulbactam group and 33 strains in the ceftazidime group, with a significant difference in the degree of bacterial clearance in the ceftazidim group (P < 0.05). Between groups, found that the bacterial clearance rate was higher in cefoperazone sulbactam group (84.21%) than in ceftazidime group (72.73%). Plasma PCT, CRP content were decreased compared to before treatment, and the difference between the groups was significant (P < 0.05). After treatment comparison, plasma PCT(0.21±0.15ng/m L) and CRP (0.68±5.24mg/L) content in cefoperazone sulbactam group were lower than those in ceftazidime group (0.87±0.32ng/m L), (20.49±6.81mg/L), and both differences were significant (P < 0.05). The cefoperazone sulbactam group (2.73 ± 0.95 days) and the treatment cost (1078.90 ± 375.44 yuan) were less than the ceftazidime group (6.97 ± 2.25 days) and (1141.69 ± 368.55 yuan), all statistically significant (P < 0.05). The incidence of adverse reactions between cefoperazone and sulbactam (1.40%) and ceftazidime (2.89%) was not significantly different (P > 0.05), and no serious adverse drug reactions occurred. Conclusion: cefoperazone subactam has better efficacy than ceftazidime for complicated urinary tract infections, mainly in bacterial clearance, course control and treatment cost. Patients with cefoperazone subactatan treatment also have better inflammatory status control. 展开更多
关键词 cefoperazone sulbactam CEFTAZIDIME complicated urinary tract infection
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麻杏石甘汤联合常规西医治疗老年肺部感染临床研究
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作者 闫云 范风江 +3 位作者 赵璟 史晶心 左远航 吴金海 《河南中医》 2026年第1期46-50,共5页
目的:观察麻杏石甘汤联合常规西医治疗老年肺部感染的临床疗效。方法:选择2024年1月至2025年1月在南阳市第一人民医院就诊的老年肺部感染患者40例,随机分为对照组和研究组,每组各20例,对照组采用常规西医治疗,研究组在常规西医治疗基础... 目的:观察麻杏石甘汤联合常规西医治疗老年肺部感染的临床疗效。方法:选择2024年1月至2025年1月在南阳市第一人民医院就诊的老年肺部感染患者40例,随机分为对照组和研究组,每组各20例,对照组采用常规西医治疗,研究组在常规西医治疗基础上采用麻杏石甘汤治疗。两组均治疗7 d,观察两组患者的临床疗效、呼吸机使用时间、住院时间及治疗前后炎症因子水平、中医证候评分、生活质量评分等。结果:对照组有效率为65.00%,研究组有效率为95.00%,两组有效率比较,差异有统计学意义(P<0.05)。研究组呼吸机使用时间、住院时间较对照组明显缩短(P<0.05)。两组患者治疗后,降钙素原(procalcitonin,PCT)、C反应蛋白(C-reactive protein,CRP)、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)水平明显降低,且研究组低于对照组(P<0.05);喘息、肺部啰音、气短、咳嗽评分明显降低,且研究组低于对照组(P<0.05);生活质量评分明显升高,且研究组高于对照组(P<0.05)。结论:麻杏石甘汤联合常规西医治疗老年肺部感染,可改善患者症状,降低炎症因子水平,缩短呼吸机使用时间和住院时间,提高患者生活质量。 展开更多
关键词 老年肺部感染 麻杏石甘汤 盐酸氨溴索注射液 头孢哌酮钠舒巴坦钠 《伤寒论》 张仲景
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头孢哌酮-舒巴坦相关凝血障碍危险因素分析及列线图模型构建
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作者 欧汝静 卢美怡 +6 位作者 罗骞 王腾华 王莉 曾洁 罗良 梁志明 江惠珍 《中国感染与化疗杂志》 北大核心 2026年第1期1-7,共7页
目的筛选头孢哌酮-舒巴坦相关凝血障碍的独立危险因素,并构建列线图预测模型。方法回顾性收集2017年7月至2023年12月广州医科大学附属第五医院694例接受头孢哌酮-舒巴坦(2∶1)治疗的患者资料,分为凝血正常组和凝血异常组,经单因素分析... 目的筛选头孢哌酮-舒巴坦相关凝血障碍的独立危险因素,并构建列线图预测模型。方法回顾性收集2017年7月至2023年12月广州医科大学附属第五医院694例接受头孢哌酮-舒巴坦(2∶1)治疗的患者资料,分为凝血正常组和凝血异常组,经单因素分析及多因素logistic回归分析筛选独立危险因素,基于独立危险因素构建列线图模型,采用受试者工作特征(ROC)曲线和校准曲线、Hosmer-Lemeshow拟合优度检验评估模型的预测效能。结果694例患者中,156例发生凝血异常,发生率为22.48%。单因素分析显示,年龄、年龄分组、高血压、糖尿病、脑血管疾病、肾功能、肝功能、饮食情况、营养评分、血清白蛋白、血肌酐在两组间差异有统计学意义(P<0.05)。多因素logistic回归分析显示,肾功能、肝功能、营养评分、禁食是头孢哌酮-舒巴坦相关凝血障碍的独立危险因素。基于独立危险因素,构建列线图模型,其内部验证显示ROC曲线的曲线下面积AUC=0.728(95%CI:0.685~0.771),Hosmer-Lemeshow拟合优度检验的χ2=11.987(P=0.101),提示模型区分度及校准度良好。结论肾功能、肝功能、营养评分及禁食是头孢哌酮-舒巴坦相关凝血障碍的独立危险因素,列线图模型可直观地预测用药风险,为临床监护提供参考。 展开更多
关键词 头孢哌酮-舒巴坦 列线图 LOGISTIC回归 凝血障碍
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基于AHM-TOPSIS法建立头孢哌酮钠舒巴坦钠药物利用评价及应用结果分析
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作者 谢祥威 黄碧青 +1 位作者 黄松清 张宏亮 《临床合理用药》 2026年第4期29-34,共6页
目的基于属性层次模型(AHM)赋权的逼近理想解排序法(TOPSIS)建立头孢哌酮钠舒巴坦钠药物利用评价及应用结果分析。方法制订头孢哌酮钠舒巴坦钠药物利用评价细则,按照此评价细则,利用加权TOPSIS法评价某三甲医院2023年第一季度使用头孢... 目的基于属性层次模型(AHM)赋权的逼近理想解排序法(TOPSIS)建立头孢哌酮钠舒巴坦钠药物利用评价及应用结果分析。方法制订头孢哌酮钠舒巴坦钠药物利用评价细则,按照此评价细则,利用加权TOPSIS法评价某三甲医院2023年第一季度使用头孢哌酮钠舒巴坦钠的出院病历50份。结果50份病历评价结果中相对接近度>60%的有12份(占比24.00%),50%~60%的有30份(占比60.00%),40%~50%的有8份(占比16.00%)。结论基于加权的TOPSIS法可用于头孢哌酮钠舒巴坦钠的药物利用评价。 展开更多
关键词 头孢哌酮钠舒巴坦钠 药物利用评价 属性层次模型 逼近理想解排序法
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多黏菌素B分别联合替加环素头孢哌酮钠舒巴坦钠治疗碳青霉烯类耐药鲍曼不动杆菌肺部感染的有效性安全性和经济性
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作者 郭兴 车虹昱 +1 位作者 李林 杨蕊 《中国药物与临床》 2026年第3期137-146,共10页
目的比较多黏菌素B(PMB)联合替加环素(TC)与PMB联合头孢哌酮钠舒巴坦钠(CPZ/SBT)静脉给药治疗碳青霉烯类耐药鲍曼不动杆菌(CRAB)肺部感染患者的有效性、安全性和经济性。方法采用回顾性队列分析方法,纳入CRAB肺部感染且接受PMB+TC或PMB+... 目的比较多黏菌素B(PMB)联合替加环素(TC)与PMB联合头孢哌酮钠舒巴坦钠(CPZ/SBT)静脉给药治疗碳青霉烯类耐药鲍曼不动杆菌(CRAB)肺部感染患者的有效性、安全性和经济性。方法采用回顾性队列分析方法,纳入CRAB肺部感染且接受PMB+TC或PMB+CPZ/SBT静脉给药治疗的患者。根据联合给药方案不同分为PMB+TC组(29例)和PMB+CPZ/SBT组(48例),比较2组患者的有效性(住院病死率、放弃治疗率、住院死亡合并放弃治疗率、临床有效率和住院时间)、安全性(肾功能异常、肝功能异常以及血液系统异常)和经济性(抗菌药物费用和住院总费用)。采用单因素分析和多因素Logistic回归分析有效性与安全性的影响因素。结果2组患者的有效性差异无统计学意义(P>0.05);安全性除纤维蛋白原降低(P=0.036)外,其他因素差异均无统计学意义(P>0.05);PMB+CPZ/SBT组的抗菌药物费用更低(P<0.01),但2组的住院总费用比较差异无统计学意义。多因素Logistic回归分析显示,合并透析状态(OR=12.459,P=0.006)、休克(OR=4.399,P=0.027)以及联合免疫抑制剂(OR=3.577,P=0.041)与住院死亡合并放弃治疗独立相关(P<0.05);合并高血压病(OR=6.529,P=0.008)、大肠埃希菌感染(OR=4.045,P=0.030)与肾功能异常独立相关(P<0.05);合并肝功能不全(OR=4.324,P=0.027)、PMB用药时间(OR=1.118,P=0.045)与肝功能异常独立相关(P<0.05)。结论PMB+TC组和PMB+CPZ/SBT组治疗CRAB肺部感染时疗效相当,PMB+TC组与纤维蛋白原降低的更高风险相关,而PMB+CPZ/SBT组具有更优的安全性与经济性,可优先考虑该方案;此外,合并透析状态、休克和联合免疫抑制剂是预后不良的独立危险因素,提示此类患者需采取更积极的综合治疗策略,合并高血压病、大肠埃希菌感染的高风险人群,需加强肾功能监测,合并肝功能不全者则需警惕肝功能异常。 展开更多
关键词 多黏菌素B 替加环素 头孢哌酮钠舒巴坦钠 碳青霉烯类耐药鲍曼不动杆菌 肺部感染
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头孢哌酮钠舒巴坦钠结合人免疫球蛋白治疗新生儿感染性肺炎的效果
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作者 刘辉 杨小鑫 朱红勇 《中国医学创新》 2026年第2期40-44,共5页
目的:探讨头孢哌酮钠舒巴坦钠结合人免疫球蛋白治疗新生儿感染性肺炎的效果。方法:回顾性选择2022年7月—2024年8月瑞金市人民医院收治的102例新生儿感染性肺炎患儿,根据治疗方案不同分为对照组(头孢哌酮钠舒巴坦钠)、观察组(头孢哌酮... 目的:探讨头孢哌酮钠舒巴坦钠结合人免疫球蛋白治疗新生儿感染性肺炎的效果。方法:回顾性选择2022年7月—2024年8月瑞金市人民医院收治的102例新生儿感染性肺炎患儿,根据治疗方案不同分为对照组(头孢哌酮钠舒巴坦钠)、观察组(头孢哌酮钠舒巴坦钠联合人免疫球蛋白),各51例。持续治疗7 d。比较两组的治疗效果、炎症因子[CRP、降钙素原(PCT)、调节性T细胞(Treg)与辅助性T细胞17(Th17)]、免疫功能与不良反应发生情况。结果:治疗后,观察组治疗总有效率高于对照组,Treg水平高于对照组,CRP、PCT与Th17水平均低于对照组(P<0.05)。两组不良反应发生率比较,差异无统计学意义(P>0.05)。结论:头孢哌酮钠舒巴坦钠结合人免疫球蛋白可以提高新生儿感染性肺炎的疗效,保护免疫功能,降低炎症水平且安全性良好。 展开更多
关键词 头孢哌酮钠舒巴坦钠 人免疫球蛋白 新生儿 感染性肺炎
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头孢哌酮舒巴坦钠联合小剂量甲泼尼龙治疗儿童重症肺炎的临床疗效及安全性
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作者 王君 蔡听听 《浙江医学》 2026年第4期410-413,共4页
目的探讨头孢哌酮舒巴坦钠联合小剂量甲泼尼龙治疗儿童重症肺炎的临床疗效及安全性。方法回顾性选取2022年1月至2024年11月台州市中心医院(台州学院附属医院)收治的102例重症肺炎患儿,其中接受头孢哌酮舒巴坦钠治疗51例(对照组),头孢哌... 目的探讨头孢哌酮舒巴坦钠联合小剂量甲泼尼龙治疗儿童重症肺炎的临床疗效及安全性。方法回顾性选取2022年1月至2024年11月台州市中心医院(台州学院附属医院)收治的102例重症肺炎患儿,其中接受头孢哌酮舒巴坦钠治疗51例(对照组),头孢哌酮舒巴坦钠联合小剂量甲泼尼龙治疗51例(观察组)。比较两组患儿临床疗效、临床症状消失时间、炎症指标水平及不良事件发生率。结果观察组临床有效率高于对照组(P<0.05);治疗后,观察组临床症状消失时间短于对照组,C反应蛋白、降钙素原、中性粒细胞百分比水平均低于对照组(均P<0.05);两组不良事件发生率比较,差异无统计学意义(P>0.05)。结论头孢哌酮舒巴坦钠联合小剂量甲泼尼龙能够有效减轻重症肺炎患儿机体炎症反应,缓解临床症状,缩短治疗周期,且安全性良好,具有临床推广价值。 展开更多
关键词 儿童重症肺炎 头孢哌酮舒巴坦钠 甲泼尼龙 疗效
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舒巴坦-度洛巴坦和依拉环素在耐碳青霉烯类鲍曼不动杆菌中的药物敏感性分析
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作者 聂正超 鲁怀伟 戴媛媛 《安徽医学》 2026年第1期4-8,共5页
目的研究舒巴坦-度洛巴坦(SUD)和依拉环素(ERV)对临床分离的耐碳青霉烯类鲍曼不动杆菌(CRAB)的体外抗菌活性,为临床治疗CRAB提供参考。方法收集2025年1~6月中国科学技术大学附属第一医院(安徽省立医院)临床分离的非重复CRAB 120株,使用V... 目的研究舒巴坦-度洛巴坦(SUD)和依拉环素(ERV)对临床分离的耐碳青霉烯类鲍曼不动杆菌(CRAB)的体外抗菌活性,为临床治疗CRAB提供参考。方法收集2025年1~6月中国科学技术大学附属第一医院(安徽省立医院)临床分离的非重复CRAB 120株,使用VITEK MS微生物质谱仪和VITEK2 Compact微生物药敏分析仪对分离的菌株进行鉴定和药敏试验。纸片扩散法测定CRAB对SUD和ERV的药物敏感性。采用全基因组测序技术分析CRAB对SUD的耐药机制。结果CRAB对β-内酰胺类药物、环丙沙星、左旋氧氟沙星、妥布霉素、复方磺胺甲恶唑和多西环素耐药率较高,对米诺环素、替加环素和多粘菌素的耐药率较低。CRAB对SUD和ERV的敏感性较好,120株CRAB仅有5株对SUD耐药,耐药率为4.2%,所有CRAB均对ERV敏感。测序结果显示对SUD耐药的5株CRAB,有2株菌产生金属酶NDM-1,另外3株菌存在PBP3位点突变。结论SUD和ERV对CRAB均表现出良好的体外抗菌活性,为CRAB感染治疗提供了新的用药选择,临床可以根据药敏结果合理选用。 展开更多
关键词 舒巴坦-度洛巴坦 依拉环素 耐碳青霉烯类鲍曼不动杆菌 药物敏感性
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头孢哌酮舒巴坦钠联合盐酸氨溴索治疗支气管扩张合并感染患者的效果
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作者 代花花 燕艳艳 梁予峰 《中国民康医学》 2026年第2期29-32,共4页
目的:观察头孢哌酮舒巴坦钠联合盐酸氨溴索治疗支气管扩张合并感染患者的效果。方法:选取2020年1月至2024年4月该院收治的98例支气管扩张合并感染患者进行前瞻性研究,按照信封法将其分为研究组和对照组各49例。对照组采用盐酸氨溴索治疗... 目的:观察头孢哌酮舒巴坦钠联合盐酸氨溴索治疗支气管扩张合并感染患者的效果。方法:选取2020年1月至2024年4月该院收治的98例支气管扩张合并感染患者进行前瞻性研究,按照信封法将其分为研究组和对照组各49例。对照组采用盐酸氨溴索治疗,研究组在对照组基础上联合头孢哌酮钠舒巴坦钠治疗,比较两组临床疗效,临床症状(咳嗽、发热、肺啰音)消失时间,治疗前后肺功能指标[第1秒用力呼气容积(FEV_(1))、用力肺活量(FVC)、每分钟最大通气量(MVV)、呼气峰值流速(PEF)]水平、日排痰量、动脉血气指标[动脉血氧饱和度(SaO_(2))、动脉血氧分压(PaO_(2))、氧合指数(OI)]水平、炎性指标[白细胞计数(WBC)、C反应蛋白(CRP)、降钙素原(PCT)]水平,以及不良反应发生率。结果:研究组治疗总有效率为91.84%(45/49),高于对照组的73.47%(36/49),差异有统计学意义(P<0.05);研究组咳嗽、发热、肺啰音等症状消失时间均短于对照组,差异有统计学意义(P<0.05);治疗后,两组FEV_(1)、FVC、MVV、PEF水平均高于治疗前,且研究组高于对照组,两组日排痰量均少于治疗前,且研究组少于对照组,差异有统计学意义(P<0.05);治疗后,两组SaO_(2)、OI、PaO_(2)水平均高于治疗前,且研究组高于对照组,差异有统计学意义(P<0.05);治疗后,两组CRP、PCT、WBC水平均低于治疗前,且研究组低于对照组,差异有统计学意义(P<0.05);两组不良反应发生率比较,差异无统计学意义(P>0.05)。结论:头孢哌酮舒巴坦钠联合盐酸氨溴索治疗支气管扩张合并感染患者可提高治疗总有效率、肺功能指标水平和动脉血气指标水平,缩短临床症状消失时间,以及降低日排痰量和炎性指标水平,效果优于单纯盐酸氨溴索治疗。 展开更多
关键词 头孢哌酮舒巴坦钠 盐酸氨溴索 支气管扩张 感染 肺功能 血气指标
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哌拉西林他唑巴坦与头孢哌酮钠舒巴坦钠治疗社区获得性肺炎的效果对比及炎性因子水平的影响
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作者 周彤 《首都食品与医药》 2026年第1期57-59,共3页
目的研究哌拉西林他唑巴坦与头孢哌酮钠舒巴坦钠治疗社区获得性肺炎患者的临床效果以及炎性因子水平的缓解作用对比。方法选择我院在2023年6月-2024年5月期间收治的100例社区获得性肺炎患者,按照随机数表法分组,对照组(n=50)通过哌拉西... 目的研究哌拉西林他唑巴坦与头孢哌酮钠舒巴坦钠治疗社区获得性肺炎患者的临床效果以及炎性因子水平的缓解作用对比。方法选择我院在2023年6月-2024年5月期间收治的100例社区获得性肺炎患者,按照随机数表法分组,对照组(n=50)通过哌拉西林他唑巴坦进行治疗,观察组(n=50)通过头孢哌酮钠舒巴坦钠进行治疗,比较两组治疗前后临床症状评分、治疗前后炎症因子水平、治疗前后肺功能指标、治疗前后血气分析指标及临床症状消失时间。结果治疗后,观察组临床症状评分与对照组对比,无明显差异(P>0.05);治疗后,观察组炎症因子水平与对照组对比,无明显差异(P>0.05);治疗后,观察组肺功能指标与对照组对比,无明显差异(P>0.05);治疗后,观察组血气分析指标与对照组对比,无明显差异(P>0.05);观察组临床症状消失时间与对照组对比,无明显差异(P>0.05)。结论社区获得性肺炎患者通过头孢哌酮钠舒巴坦钠治疗,其临床疗效、炎症因子的缓解作用与哌拉西林他唑巴坦相似,均能够起到良好的治疗效果,故临床中可以根据实际情况合理选择哌拉西林他唑巴坦或头孢哌酮钠舒巴坦钠进行治疗。 展开更多
关键词 哌拉西林他唑巴坦 头孢哌酮钠舒巴坦钠 社区获得性肺炎 炎性因子 临床症状
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清金化痰汤联合头孢哌酮钠舒巴坦钠治疗慢性支气管炎痰热壅肺证患者的效果
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作者 李宗富 《中国民康医学》 2026年第1期103-105,109,共4页
目的:观察清金化痰汤联合头孢哌酮钠舒巴坦钠治疗慢性支气管炎(CB)痰热壅肺证患者的效果。方法:选取2022—2023年该院收治的86例CB痰热壅肺证患者进行前瞻性研究,采用随机数字表法将其分为对照组和观察组各43例。对照组予以头孢哌酮钠... 目的:观察清金化痰汤联合头孢哌酮钠舒巴坦钠治疗慢性支气管炎(CB)痰热壅肺证患者的效果。方法:选取2022—2023年该院收治的86例CB痰热壅肺证患者进行前瞻性研究,采用随机数字表法将其分为对照组和观察组各43例。对照组予以头孢哌酮钠舒巴坦钠治疗,观察组在对照组基础上联合清金化痰汤治疗。比较两组临床疗效,治疗前后中医证候积分(咳嗽气促、痰多黄稠、口干烦躁、小便短赤、大便秘结)、血气分析指标[动脉血氧分压(PaO_(2))、动脉血二氧化碳分压(PaCO_(2))]水平,以及不良反应发生率。结果:观察组治疗总有效率为95.35%(41/43),高于对照组的81.40%(35/43),差异有统计学意义(P<0.05);治疗后,两组咳嗽气促、痰多黄稠、口干烦躁、小便短赤、大便秘结等中医证候积分均低于治疗前,且观察组低于对照组,差异有统计学意义(P<0.05);治疗后,两组PaO_(2)水平均高于治疗前,且观察组高于对照组,两组PaCO_(2)水平均低于治疗前,且观察组低于对照组,差异有统计学意义(P<0.05);两组不良反应发生率比较,差异无统计学意义(P>0.05)。结论:清金化痰汤联合头孢哌酮钠舒巴坦钠治疗CB痰热壅肺证患者可提高治疗总有效率,改善血气分析指标水平,降低中医证候积分,效果优于单纯头孢哌酮钠舒巴坦钠治疗。 展开更多
关键词 清金化痰汤 头孢哌酮钠舒巴坦钠 慢性支气管炎 痰热壅肺证 中医证候积分 血气分析 不良反应
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