ECLIPS: An extended clinical laboratory information processing system

The clinical laboratory is regarded as a component of the medical care system extending from physician to laboratory staff and back to physician. From this concept a computer-based system of laboratory information is derived, emphasizing: (1) total laboratory responsibility for the test and its request, and (2) physician-oriented output reports.     

Survey of recognition and utilization of guidelines for the diagnosis and management of bronchial asthma in Japan

BACKGROUND: In Japan in 1993, the Japanese Society of Allergology (JSA) developed guidelines for diagnosis and management of asthma (JGL), which were based on the concept that asthma is a chronic inflammatory disorder of the airway. METHODS: This survey study was intended to investigate the recognition and utilization of JGL among physicians who had treated asthma. The survey comprised two methods: a quantitative mail survey and a qualitative door-to-door survey conducted by trained interviewers. RESULTS: In the mail survey, a total of 1028 physicians responded; 552 members of the JSA and 476 nonmembers. Ninety-four percent of JSA members were aware of adult asthma management guidelines, while 53% of nonmembers were aware of them. Although approximately half of the physicians, both members and nonmembers, found differences between the asthma management policies in JGL and their previous policies, most of them utilized JGL once they read it. In the qualitative door-to-door survey, 80-90% of physicians evaluated JGL as good after they read it. CONCLUSIONS: JGL was recognized and utilized by most JSA members, but only half of nonmember physicians were aware of JGL, although they utilized JGL after they read it. Further action to implement JGL among nonspecialist physicians is needed to improve management of asthma.     

Cytogenetic studies of bone marrow and extramedullary tissues and clinical course during metamorphosis of chronic myelocytic leukemia

Of 33 consecutive patients with chronic myelocytic leukemia, examined during metamorphosis, 82% showed chromosome abnormalities in addition to the Ph1. Aberrations most frequently encountered were +8 (39%), +22q - (30%), and i(17q) (18%). Translocations other than the Ph1 were observed in four cases and - Y clones in four cases. Discrepancies in the cytogenetic pattern between bone marrow and extramedullary tissues or blood were noted in a total of 15 patients. In six cases, transformation occurred in extramedullary organs at a time when it was not present in the marrow. In three cases the bone marrow transformation was preceded by a lymph node blastic infiltrate; in one case, by a skin infiltrate; and in one case, by a subdural blastoma. Clonal abnormalities additional to the Ph1 were identified in the tumor tissue from all these cases. Patients with primary extramedullary transformation tended to have a lower median age at onset of metamorphosis, shorter survival, and higher incidence of chromosome abnormalities than the cases without extramedullary involvement. Patients with only Ph1-positive cells and no other anomalies had a slightly longer duration of metamorphosis and longer total survival. Basophilia and thrombocytopenia were more marked in cases with i(17q) than in the rest of the series.     

催经止孕药Ru-486的临床药代动力学

应用高效液相色谱法(HPLC)研究了抗孕激素药,Ru-486的临床药代动力学。六名志愿受试者,一次口服Ru-486 50毫克后测得该药的药代动力学各项参数,血药半寿期t 1/2 33.0小时,一级消除速率常数Kel 0.021 hr~(-1),血药表观容积Vd 120.1 Liter,体内血药总廓清率Cl2.5 Liter/hr,药-时曲线下面积Auc 19825.1 ng/ml/hr。实验表明,服药后一小时血药浓度迅即达高峰,随后转入消除期,血浆药物浓度在消除相的头4～8小时消除较快,而后逐渐减慢,持续24小时,到48小时血药浓度已较低(0.15±0.07μg/ml)。     

Ten years of Pan-InfORM: modelling research for public health in Canada

Modelling and simulation methods can play an important role in guiding public health responses to infectious diseases and emerging health threats by projecting the plausible outcomes of decisions and interventions. The 2003 SARS epidemic marked a new chapter in disease modelling in Canada as it triggered a national discussion on the utility and uptake of modelling research in local and pandemic outbreaks. However, integration and application of model-based outcomes in public health requires knowledge translation and contextualization. We reviewed the history and performance of Pan-InfORM (Pandemic Influenza Outbreak Research Modelling), which created a national infrastructure in Canada with a mandate to develop innovative knowledge translation methodologies to inform policy makers through modelling frameworks that bridge the gaps between theory, policy, and practice. This review demonstrates the importance of a collaborative infrastructure as a “Community of Practice” to guide public health responses, especially in the context of emerging diseases with substantial uncertainty, such as the COVID-19 pandemic. Dedicated resources to modelling and knowledge translation activities can help create synergistic strategies at the global scale and optimize public health responses to protect at-risk populations and quell socioeconomic and health burden.     

无呼吸道症状肺癌35例临床分析

目的：探讨完全无症状或无呼吸道症状肺癌的早期诊断。方法：随机抽取1995年2月至2001年3月经临床及病理诊断为肺癌的380例,其中“无症状”肺癌35例进行分析。结果：由于“无症状”肺癌的异位内分泌等作用,致使患者表现为神经科,骨科,皮肤科,消化科,内分泌科学等多学科病变。结论：为了提高“无症状”肺癌的早期确诊率,及早行胸片,CT片,支行镜等相关检查相当重要,定期体检对于早期发现肺癌有重要的意义。     

0．75％罗哌卡因硬膜外麻醉用于妇产科手术的临床观察

目的 观察０．７５％罗哌卡因硬膜外用于妇产科手术的临床效果、方法 选择７２例ＡＳＡＩ－Ⅱ级妇产科手术随机分为两组．Ｉ组为０．７５％罗哌卡因组（３６例）Ⅱ组为０．５％布比卡因组（３６例）,两组均取腰１－２行硬膜外穿刺,观察两组的感觉阻滞、运动阻滞、镇痛效果及对循环呼吸的影响和不良反应,结果 两组感觉阻滞达Ｔ８的时间。切皮时ＶＡＳ评分、运动恢复时间有显著性差异（Ｐ＜０．０５）,不良反应中寒颤的发生率Ⅰ组明显比Ⅱ组少（Ｐ＜０．０５）,结论０．７５％罗哌卡因具有起效时间快,镇痛效果好,运动阻滞恢复早,对循环呼吸的影响小,神经毒性低的临床特点。     

细胞因子在清肝化瘀汤治疗慢性粒细胞性白血病中的研究

目的观察中药清肝化瘀汤治疗慢性粒细胞性白血病(慢性期)的疗效,并探讨细胞因子水平变化的意义。方法收集45例慢性粒细胞性白血病慢性期患者(治疗组),用清肝化瘀汤治疗,观察患者的临床疗效、细胞因子水平。另用20名正常人作为对照(对照组)。结果治疗组完全缓解率40％,部分缓解率46.7％,总有效率86.7％。治疗组细胞因子水平中白介素2、可溶性白介素2受体、肿瘤坏死因子a治疗前后有显著差异(P<0.05);干扰素γ水平变化无显著差异。且与正常对照组比较无显著差异(P>0.05)。结论清肝化瘀汤有清热泻肝解毒、活血化瘀消癥的功效,研究结果显示,该药对慢性粒细胞性白血病慢性期(肝热血瘀型)疗效确切,其作用机理可能与改善细胞因子水平有关。     

A systematic review of reporting quality for anaesthetic interventions in randomised controlled trials

Interventions from randomised controlled trials can only be replicated if they are reported in sufficient detail. The results of trials can only be confidently interpreted if the delivery of the intervention was systematic and the protocol adhered to. We systematically reviewed trials of anaesthetic interventions published in 12 journals from January 2016 to September 2019. We assessed the detail with which interventions were reported, using the Consolidated Standards of Reporting Trials statement for non-pharmacological treatments. We analysed 162 interventions reported by 78 trials in 18,675 participants. Detail sufficiently precise to replicate the intervention was reported for 111 (69%) interventions. Intervention standardisation was reported for 135 (83%) out of the 162 interventions, and protocol adherence was reported for 20 (12%) interventions. Sixty (77%) out of the 78 trials reported the administrative context in which interventions were delivered and 36 (46%) trials detailed the expertise of the practitioners. We conclude that bespoke reporting tools should be developed for anaesthetic interventions and interventions in other areas such as critical care.