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头孢哌酮钠舒巴坦钠和阿奇霉素联用治疗社区获得性肺炎38例 被引量:2
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作者 翟穗燕 《内科》 2007年第4期550-551,共2页
目的探讨头孢哌酮钠舒巴坦钠和阿奇霉素联合治疗社区获得性肺炎的临床疗效。方法72例社区获得性肺炎患者,治疗组38例,采用阿奇霉素和头孢哌酮钠舒巴坦钠联合治疗。对照组34例,采用头孢哌酮钠舒巴坦钠治疗。两组疗程均为7~14d。观察治... 目的探讨头孢哌酮钠舒巴坦钠和阿奇霉素联合治疗社区获得性肺炎的临床疗效。方法72例社区获得性肺炎患者,治疗组38例,采用阿奇霉素和头孢哌酮钠舒巴坦钠联合治疗。对照组34例,采用头孢哌酮钠舒巴坦钠治疗。两组疗程均为7~14d。观察治疗前后的症状、体征等临床疗效和细菌学疗效。结果治疗组和对照组的临床总有效率分别为92.11%和73.53%,P<0.05;细菌清除率分别为89.66%和66.67%,P<0.05。结论头孢哌酮钠舒巴坦钠和阿奇霉素联合治疗社区获得性肺炎疗效高,安全性好,无明显副作用,值得临床推广应用。 展开更多
关键词 孢哌酮钠舒巴坦钠 阿奇霉素 联合用药 社区获得性肺炎
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头孢哌钠酮舒巴坦钠与盐酸左氧氟沙星联合对支气管扩张患者疗效及血清炎性因子的影响
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作者 王仅仅 《黑龙江医药科学》 2024年第5期153-155,159,共4页
目的:探讨支气管扩张患者联合应用头孢哌钠酮舒巴坦钠与盐酸左氧氟沙星对其疗效及血清炎性因子(CRP、白细胞介素-6)的影响。方法:选取河南宏力医院2022年10月至2023年10月收治的86例支气管扩张患者为研究对象,根据随机数字表法分别纳入... 目的:探讨支气管扩张患者联合应用头孢哌钠酮舒巴坦钠与盐酸左氧氟沙星对其疗效及血清炎性因子(CRP、白细胞介素-6)的影响。方法:选取河南宏力医院2022年10月至2023年10月收治的86例支气管扩张患者为研究对象,根据随机数字表法分别纳入盐酸左氧氟沙星治疗的患者为对照组43例和基于对照组接受头孢哌钠酮舒巴坦钠治疗的患者为研究组43例。比较两组临床疗效,探讨不同分组患者临床症状改善情况,对比治疗前后不同分组患者的炎性因子及肺功能相关指标水平差异统计治疗期间用药不良反应的发生情况。结果:与对照组相比,研究组临床治疗总有效率93.02%显著更高,临床症状消失时长显著更短(P<0.05),降钙素原(procalcitonin, PCT)、白细胞介素-6(interleukin-6,IL-6)、C反应蛋白(C-reactive protein, CRP)、红细胞沉降率(erythrocyte sedimentation rate, ESR)等炎性因子水平显著更低,用力肺活量(forced vital capacity, FVC)、第1秒用力呼气容积(forced expiratory volume in one second, FEV1)、FEV1占预计值百分比值(forced expiratory volume in one second predicted, FEV1%)、FEV1与FVC的百分比值(forced expiratory volume in one second/forced vital capacity, FEV1/FVC)等肺功能相关指标水平显著更高(P<0.05);较之治疗前,治疗后两组PCT、IL-6、CRP、ESR等炎症因子水平显著更低(P<0.05),FVC、FEV1、FEV1%、FEV1/FVC等肺功能相关指标水平显著更高(P<0.05)。且研究组治疗期间用药不良反应发生率13.96%与对照组11.64%比较无统计学意义(P>0.05)。结论:支气管扩张患者采取头孢哌钠酮舒巴坦钠与盐酸左氧氟沙星联合用药方案,临床疗效显著,不仅可有效缩短其临床症状消失时间,在降低患者机体内炎症因子水平、改善其肺功能方面也具有明显积极作用,且并不会增加用药不良反应发生风险,安全性良好。 展开更多
关键词 孢哌舒巴坦 盐酸左氧氟沙星 支气管扩张 疗效 血清炎性因子
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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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