Effect of Day Optimizing Throughput (Dot) Knee Software Implementation on Magnetic Resonance Imaging Workflow Efficiency

PurposeAttempts by magnetic resonance (MR) manufacturers to help imaging centres improve patient throughput has led to the development of more automated acquisition. This software is capable of customizing individual scan alignment; potentially improving imaging efficiency and standardizing protocols. However, substantial investments are required to introduce such systems, potentially deterring their widespread application. This study assessed the implementation costs and reduction in examination durations for automated knee MR imaging (MRI) software.Materials and MethodsResearch activities were performed at a community-based academic centre on a 3-Tesla (3-T) system using Siemens' Day Optimizing Throughput (Dot) knee software. Examination acquisition times were extracted from the system before and after software implementation. Fiscal year 2012/13 finances were used to determine the average hourly cost of MRI utilization. Costs associated with automated software implementation were also calculated. Finally, the number of knee scans required to achieve a positive return on investment using the software was established.Results and DiscussionThe mean (standard deviation, sample size) pre- and post-Dot software scan times were 23.20 (4.18, n = 266) and 21.94 (4.51, n = 59) minutes, respectively, for a routine knee scan and 11.88 (1.60, n = 74) and 11.24 (1.51, n = 27) minutes, respectively, for a fast knee scan. The overall weighted average resulted in a 64-second time savings per automated knee examination. This negligible time savings would be extremely difficult to make use of clinically. Dot simplified 29 unique knee protocols to two, improving the consistency of knee examinations. Current Dot software is not compatible with all patients and therefore has limitations that are a concern among MR technologists.ConclusionAdoption of automated knee systems could assist in standardizing protocols; however, the cost of implementation and difficulty in modifying patient scheduling to reflect the minimal time savings would make a financial return unlikely to occur at small- and medium-sized institutions.     

汉语失写症的神经心理学研究及其意义

目的 探讨汉语失写症的神经心理语言学机制以及该研究对于汉语失写症病理行为的康复学意义。方法 采用汉语失语检查法和汉语失写检查法测试口语和书写能力，详细记录患者的书写、失写行为特征，区分言语障碍类型；运用计算机图像处理技术对病灶CT／MRI图像进行标准化、二维叠加、三维重建等处理，并与非失写对照组相减，显示不同失写类型病变的集中趋势。结果 左侧半球损害48例，其中失语30例，失写32例，后者中纯失写1例，失读并失写1例；右侧半球损害15例，其中失语失写3例。具体的资料分析表明：不同的失写类型有不同的病理行为特点。计算机图像处理结果显示：失语性失写病灶较集中的区域为左额顶叶深部白质。惰性失写主要集中在左外侧裂的前方、从额中下回向后部延伸。镜像书写则分散于左丘脑、基底节附近。结论 汉语失写症的病理行为特点与病损定位有密切的关系；双通道理论有可能符合汉语语言学机制；汉语失写症的神经心理学研究对汉语失写康复模式的制定有重要意义。     

Quality and standardization in blood component preparation with an automated blood processing technique

The use of automated blood processors in combination with bottom and top blood containers has been found to improve the standardization and quality of blood components. A study was performed to validate a new type of processor (Optipress® II) and compare its performance with a first generation processor (Optipress® I).
Primary separation on the Optipress II was investigated on 570 mL (± 10%) of anticoagulated blood in a nonpaired study. In addition, the quality of the products in routine production was compared between the results of the Optipress I and Optipress II. The whole blood units were kept overnight at room temperature (20 ± 2 °C). Separation was performed under conditions to obtain 55 mL buffy coats with a 50% haematocrit (ht). Platelet concentrate preparation was investigated in a paired study and compared to the routine manual method using PAS II additive solution. Parameters studied were volume, red cell, white cell and platelet counts, ht, haemoglobin (hb, total and free).
Primary separation was more efficient in the Optipress II because the platelet count was lower in the erythrocyte concentrates ( P  < 0.0001), platelets were lower in plasma ( P  < 0.0001) and platelet counts were higher in buffy coats ( P  < 0.0001). Buffy coat volume showed less variation (Optipress II VC = 4%, Optipress I VC = 7.4%). Secondary separation did not show differences between the Optipress II and manual method but was advantageous because of the automatic termination of the procedure.
Further improvement of standardization in blood component preparation is possible with an automated blood processor, leading to improvement of the quality of blood products for patient care.     

高效液相色谱-荧光检测法测定血浆总同型半胱氨酸浓度

目的 :建立测定血浆总同型半胱氨酸的高效液相色谱 (HPLC) 荧光检测分析方法。方法 :用TCEP将血浆中各种形式的同型半胱氨酸 (Hcy)还原成总同型半胱氨酸 (tHcy) ,以光胺作内标 ,巯基特异性荧光衍生剂SBD F对Hcy ,胱胺等含巯基化合物进行柱前衍生 ,然后行HPLC 荧光检测。结果 :本方法所检测的Hcy浓度在 2 .5～ 16 0 μmol·L- 1 范围具有良好的线性关系 (r =0 .9975 ) ,Hcy最低检测限 0 .6 2 5 μmol·L- 1 ,批内变异小于 5 .5 % ,批间变异小于 9.0 % ,平均回收率 98.87%。结论 :本法简便、灵敏、精确、稳定     

现代中医药发展战略思考

建国几十年来，由于党和政府的大力提倡和扶持，中医药得到了很大发展，但相对于西医的发展势头仍显不足。尤其是近10多年来，由于现代科技及现代管理学的有力推动，西医获得了突飞猛进的发展，然而，中医却由于种种原因发展相对缓慢。在这各行各业竞相发展的现代社会，中医要生存，就蓝须发展，中医要发展，就妊须总揽全局，从战略高度克服中医药发展的各种不利因素，充分发挥各方面的有利条件。     

规范临床新技术、新项目管理的做法与体会

探讨安徽省立医院规范临床新技术、新项目管理的做法:一是明确新技术、新项目的管理范畴和管理部门;二是抓好申报与管理的三个环节;三是管理与激励并重,实现两个效益稳步增长.并结合三年来的实践谈自身体会.     

眼外伤临床统计规范探讨

眼外伤是我国眼科住院三大主要疾病之一，占眼科住院病人总数的１６￣３２％。每年发表临床统计文章百余篇，但由于统计资料不全面，标准不统一，降低了这部分劳动的价值。本文就眼外伤临床统计规范及某些问题进行讨论，强调规范化的重要意义。     

精子质量参数分析的标准化与质量控制的研究进展

精液分析是评价男性生育能力的最基本测试。最近几年,对精液分析标准化的迫切需求已引起男科学家的广泛重视。本文对精子质量参数———精子密度、活动率和形态学分析的标准化及质量控制进行了综述。精子密度分析的关键是计数池的标准化,因此Cell-VU计数池应该是最佳的选择;精子活动率和精子形态学的分析由于主观性太强,CASA系统可能是其标准化的最终选择。精液质量参数分析的质量控制主要是质量控制材料的选择,以及在男科学实验室实施EQC和IQC项目,而一些监测质量控制的图表和计算方法应被相应地建立。     

医用机动车辆装备标准化发展刍议

分析了我国医用机动车辆装备的技术特征、市场发展的前景，综述了军内外医用车辆研制的现状及标准与标准化发展概况．并对我国医用机动车辆技术标准体系进行了论证，提出了当前医用机动车辆装备标准少的解决方法和措施以及标准化组织建设等建议。     

Testing for skin sensitization according to the notification procedure for new chemicals: the Magnusson and Kligman test

The notification procedure for new chemicals in the European Union (called the Chemicals Act in Germany) requires a skin sensitization test when the amount of a new chemical produced exceeds 100 kg/year. The preferred test is that of Magnusson and Kligman; more than 90% of the tests submitted are performed with it. Though the Magnusson and Kligman test is described in the literature, and in the test guidelines of the European Union and of the OECD, discrepancies do occur in the performance of the test between test laboratories. In this paper, recommendations are given for standardized performance of the Magnusson and Kligman test.