Commission on Professional and Hospital Activities

  • 文章类型: Journal Article
    The Dutch Gynecological Oncology Audit (DGOA) was initiated in 2014 to serve as a nationwide audit, which registers the four most prevalent gynecological malignancies. This study presents the first results of clinical auditing for ovarian cancer in the Netherlands.
    The Dutch Gynecological Oncology Audit is facilitated by the Dutch Institute of Clinical Auditing (DICA) and run by a scientific committee. Items are collected through a web-based registration based on a set of predefined quality indicators. Results of quality indicators are shown, and benchmarked information is given back to the user. Data verification was done in 2016.
    Between January 01, 2014 and December 31, 2018, 6535 patients with ovarian cancer were registered. The case ascertainment was 98.3% in 2016. The number of patients with ovarian cancer who start therapy within 28 days decreased over time from 68.7% in 2014 to 62.7% in 2018 (p < 0.001). The percentage of patients with primary cytoreductive surgery decreased over time (57.8%-39.7%, P < 0.001). However, patients with complete primary cytoreductive surgery improved over time (53.5%-69.1%, P < 0.001). Other quality indicators did not significantly change over time.
    The Dutch Gynecological Oncology Audit provides valuable data on the quality of care on patients with ovarian cancer in the Netherlands. Data show variation between hospitals with regard to pre-determined quality indicators. Results of \'best practices\' will be shared with all participants of the clinical audit with the aim of improving quality of care nationwide.
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  • 文章类型: Journal Article
    To audit the young patients referred to the Hypertension Clinic at Groote Schuur Hospital that predominately serves the underprivileged communities of Cape Town.Folders of patients between the ages of 15 and 30 years over a 2 year period were reviewed. The data collected included demographic, clinical and laboratory data, investigations, causes of hypertension, and presence of hypertensive organ damage.Of the 110 patients reviewed, 61 (55.5%) were females, 22 (20%) Black African, and 88 (80%) of Mixed Ancestry. Eight (7.3%) were found to be normotensive, 16 (14.5%) had a secondary cause and 86 (78.2%) had essential hypertension. Thirty five (31.8%) were current or previous smokers, and 11 (10%) admitted to current or prior use of metamphetamines. A family history of hypertension in a first degree relative was present in 80 (72.7%) patients. Comorbidities present were diabetes in 7 (6.4%) patients, metabolic syndrome in 13 (11.8%), and obesity in 26 (23.6%), but 42.6% had a body mass index (BMI) <25 kg/m. Chronic kidney disease (CKD) was present in 29 (26.4%) patients and ECG left ventricular hypertrophy in 56 (50.9%). Overall organ damage was present in 72 (65.5%) patients.In this cohort of young hypertensives most patients had essential hypertension with a strong family history. Significant organ damage was identified. High risk behavior, including smoking and illicit drug use, and obesity were identified as contributing factors. Secondary causes were identified in 14.2%. These results suggest a targeted approach to the investigation of young hypertensives for secondary causes, and significant opportunities for lifestyle intervention.
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  • 文章类型: Journal Article
    Intensive medical care in companion animal clinics could pose a risk for the selection and dissemination of multidrug-resistant organisms (MDROs). Infection prevention and control (IPC) concepts are key measures to reduce the spread of MDROs, but data on IPC standards in companion animal clinics is sparse. The study assessed IPC standards in seven companion animal clinics and practices in Switzerland by structured IPC audits and combined results with environmental MDRO contamination and MDRO carriage of the personnel.
    IPC audits were held between August 2018 and January 2019. The observations in 34 IPC areas were scored based on predefined criteria (not fulfilled/partially fulfilled/fulfilled = score 0/1/2). Environmental swabs and nasal and stool samples from veterinary personnel were tested for methicillin-resistant (MR) staphylococci and macrococci and for colistin-resistant, extended-spectrum β-lactamase- and carbapenemase-producing (CP) Enterobacterales (CPE). Species was identified by MALDI-TOF MS, antimicrobial resistance determined by microdilution and β-lactam resistance gene detection, and genetic relatedness assessed by REP-/ERIC-PCR and multilocus sequence typing.
    Of a maximum total IPC score of 68, the institutions reached a median (range) score of 33 (19-55). MDROs were detected in median (range) 8.2% (0-33.3%) of the sampling sites. Clinics with low IPC standards showed extensive environmental contamination, i.e. of intensive care units, consultation rooms and utensils. CPE were detected in two clinics; one of them showed extensive contamination with CP Klebsiella pneumoniae (ST11, blaOXA-48) and MR Staphylococcus pseudintermedius (ST551, mecA). Despite low IPC scores, environmental contamination with MDROs was low in primary opinion practices. Three employees were colonized with Escherichia coli ST131 (blaCTX-M-15, blaCTX-M-27, blaCTX-M-14). Two employees carried CP E. coli closely related to environmental (ST410, blaOXA-181) and patient-derived isolates (ST167, blaNDM-5). MR Staphylococcus aureus (ST225, mecA) and MR S. pseudintermedius (ST551, mecA) of the same sequence types and with similar resistance profiles were found in employees and the environment in two clinics.
    The study indicates that IPC standards in companion animal clinics are variable and that insufficient IPC standards could contribute to the evolution of MDROs which can be transferred between the environment and working personnel. The implementation of IPC concepts in companion animal clinics should urgently be promoted.
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    文章类型: Journal Article
    Aims The primary objective of this audit was to assess 30-day unplanned admission or readmission rates following day case tonsillectomy. Secondary objectives included assessing demographic characteristics of patients and surgical and anaesthetic techniques employed. Methods Retrospective chart review was performed. Results 34 tonsillectomies or adenotonsillectomies were performed for children aged between 5 and 17 years. A total of six patients (17.6%) were either admitted from the day ward or readmitted within 30 days. This was not statistically significantly greater than the maximum acceptable rate of 15% as recommended by ENT UK and the Royal College of Surgeons (95% confidence intervals 4.8% - 30.5%, p = 0.33). Of these admissions, one (2.9%) was due to nausea and inadequate oral intake, one (2.9%) was due to clinical concerns regarding sleep apnoea and four readmissions (11.8%) were due to bleeding. Anaesthesia techniques used varied considerably. Conclusion Further multidisciplinary co-operation and standardisation of care may help to improve this programme and reduce unplanned admission and readmission rates.
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  • 文章类型: Journal Article
    Objective.量化药学教职员工对委托专业活动(EPA)的重要性以及确定APPE准备程度应达到的预期委托水平的看法。方法。可信任的专业活动定义了新药学毕业生的核心技能和任务,并可以作为确定药学学生准备开始高级药学实践经验(APPE)的逻辑框架。向所有教职员工分发了五个问题的调查,工作人员,以及费里斯州立大学药学院的管理人员。受访者被要求对映射到12个EPAs的18个陈述进行评分,以了解每个陈述的重要性以及学生应达到的预期委托水平,以确定APPE的准备情况。阈值用于确定每个陈述的重要性和委托级别的共识。结果。在接受调查的44名教职员工中,28人(63.6%)回答。对18项声明中的16项(89%)的重要性水平达成了强烈共识,而两项声明显示中等共识(11%)。在委托级别上没有达成强烈共识。18份陈述中有7份(39%)表现出适度的委托共识,11份(61%)陈述几乎没有共识。结论。关于确定哪些EPA对于确定学生的APPE准备程度很重要,已达成了强烈共识;但是,在评估委托水平时,没有发现强烈的共识。缺乏关于委托的共识提出了几个问题,需要进一步研究和澄清,因为在整个学院继续实施EPA。
    Objective. To quantify pharmacy faculty members\' perceptions of the importance of entrustable professional activities (EPAs) and the expected level of entrustment that should be achieved to determine APPE readiness. Methods. Entrustable professional activities define the core skills and tasks expected of new pharmacy graduates and may serve as a logical framework for determining pharmacy student readiness to begin advanced pharmacy practice experiences (APPEs). A five-question survey was distributed to all faculty members, staff members, and administrators at Ferris State University College of Pharmacy. Respondents were asked to rate 18 statements mapped to 12 EPAs on the perceived importance of each statement and the expected level of entrustment students should achieve to determine readiness for APPEs. Thresholds were used to determine consensus for importance and level of entrustment for each statement. Results. Of the 44 faculty members surveyed, 28 (63.6%) responded. A strong consensus was reached on the level of importance for 16 of 18 statements (89%), while two statements demonstrated moderate consensus (11%). No strong consensus was identified on levels of entrustment. Seven (39%) of 18 statements demonstrated moderate entrustment consensus and 11 (61%) statements demonstrated little consensus. Conclusion. Strong consensus was identified regarding which EPAs are important to determine students\' APPE readiness; however, no strong consensus was found when evaluating levels of entrustment. Lack of consensus regarding entrustment raises several questions that require further study and clarification as the implementation of EPAs continues throughout the Academy.
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  • 文章类型: Clinical Trial Protocol
    背景:目前2型糖尿病(T2D)的治疗模式通常涉及使用多种药物来降低葡萄糖水平,以期减少长期并发症。然而,这种治疗不一定解决疾病的潜在病理生理学,很少有患者达到部分,完成,或诊断后T2D的缓解时间延长。最近,根据临床试验报告通过靶向饮食方法缓解T2D的结果,强调了营养的治疗潜力。在限制碳水化合物和/或引起快速体重减轻的此类干预措施的初始阶段,低血糖对患者存在显著风险.因此,我们假设提供非常低的碳水化合物,通过社区药房提供低热量的治疗性营养将是一种创新策略,可以促进糖化血红蛋白(A1C)的降低,同时安全地减少T2D中降糖药物的使用.
    方法:一项基于社区的随机对照试验,本质上是务实的,将进行平行组设计(N=200)。参与者将有平等的机会被随机分配给药剂师领导,治疗性碳水化合物限制(Pharm-TCR)饮食或基于指南的常规治疗(TAU)。Pharm-TCR涉及12周非常低的碳水化合物,由药剂师和生活方式教练领导的卡路里限制商业饮食计划,药剂师与参与者的家庭医生合作负责管理药物。主要纳入标准是T2D的诊断,目前接受降糖药物治疗,年龄30-75岁,体重指数≥30。主要结果是使用降糖药物的二元测量。次要结果包括A1C,人体测量学和临床血液标记。
    结论:如果服用降糖药物的T2D患者遵循非常低的碳水化合物饮食,则存在固有风险。这项随机对照试验旨在确定参与社区药剂师是否是一种安全有效的方法来提供治疗性碳水化合物限制并减少/消除T2D患者对降糖药物的需要。
    背景:ClinicalTrials.gov,NCT03181165。2017年6月8日注册
    BACKGROUND: The current treatment paradigm for type 2 diabetes mellitus (T2D) typically involves use of multiple medications to lower glucose levels in hope of reducing long-term complications. However, such treatment does not necessarily address the underlying pathophysiology of the disease and very few patients achieve partial, complete, or prolonged remission of T2D after diagnosis. The therapeutic potential of nutrition has been highlighted recently based on results of clinical trials reporting remission of T2D with targeted dietary approaches. During the initial phase of such interventions that restrict carbohydrates and/or induce rapid weight loss, hypoglycemia presents a notable risk to patients. We therefore hypothesized that delivering very low-carbohydrate, low-calorie therapeutic nutrition through community pharmacies would be an innovative strategy to facilitate lowering of glycated hemoglobin (A1C) while safely reducing the use of glucose-lowering medications in T2D.
    METHODS: A community-based randomized controlled trial that is pragmatic in nature, following a parallel-group design will be conducted (N = 200). Participants will have an equal chance of being randomized to either a pharmacist-led, therapeutic carbohydrate restricted (Pharm-TCR) diet or guideline-based treatment as usual (TAU). Pharm-TCR involves a 12-week very low carbohydrate, calorie-restricted commercial diet plan led by pharmacists and lifestyle coaches with pharmacists responsible for managing medications in collaboration with the participants\' family physicians. Main inclusion criteria are diagnosis of T2D, currently treated with glucose-lowering medications, age 30-75 years, and body mass index ≥ 30. The primary outcome is a binary measure of use of glucose-lowering medication. Secondary outcomes include A1C, anthropometrics and clinical blood markers.
    CONCLUSIONS: There are inherent risks involved if patients with T2D who take glucose-lowering medications follow very low carbohydrate diets. This randomized controlled trial aims to determine whether engaging community pharmacists is a safe and effective way to deliver therapeutic carbohydrate restriction and reduce/eliminate the need for glucose-lowering medications in people with T2D.
    BACKGROUND: ClinicalTrials.gov, NCT03181165. Registered on 8 June 2017.
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  • 文章类型: Journal Article
    It is widely agreed that children\'s services should use participation-focused practice, but that implementation is challenging. This paper describes a method for using audit and feedback, an evidence-based knowledge translation strategy, to support implementation of participation-focused practice in front-line services, to identify barriers to implementation, and to enable international benchmarking of implementation and barriers.
    Best-practice guidelines for using audit and feedback were followed. For audit, participation-focused practice was specified as clinicians\' three observable behaviours: (a) targets participation outcomes; (b) involves child/parent in setting participation outcomes; and (c) measures progress towards participation outcomes. For barrier identification, the Theoretical Domains Framework Questionnaire (TDFQ) of known implementation barriers was used. A cycle of audit and barrier identification was piloted in three services (n = 25 clinicians) in a large U.K. healthcare trust. From each clinician, up to five randomly sampled case note sets were audited (total n = 122), and the clinicians were invited to complete the TDFQ. For feedback, data on the behaviours and barriers were shared visually and verbally with managers and clinicians to inform action planning.
    A Method for using Audit and feedback for Participation implementation (MAPi) was developed. The MAPi audit template captured clinicians\' practices: Clinicians targeted participation in 37/122 (30.3%) of the sampled cases; involved child/parent in 16/122 (13.1%); and measured progress in 24/122 (19.7%). Barriers identified from the TDFQ and fed back to managers and clinicians included clinicians\' skills in participation-focused behaviours (median = 3.00-5.00, interquartile range [IQR] = 2.25-6.00), social processes (median = 4.00, IQR = 3.00-5.00), and behavioural regulation (median = 4.00-5.00, IQR = 3.00-6.00).
    MAPi provides a practical, off-the-shelf method for front-line services to investigate and support their implementation of participation-focused practice. Furthermore, as a shared, consistent template, MAPi provides a method for generating cumulative and comparable, across-services evidence about levels and trends of implementation and about enduring barriers to implementation, to inform future implementation strategies.
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  • 文章类型: Journal Article
    目标:确定为什么在Cortrak指导下,未检测到的管错位可能与所使用的痕迹解释系统有关。
    方法:从2010年到2017年,我们从英国获得了8条Cortrak痕迹中的7条,这些痕迹未发现错位,患者接受了饲料。七人受到严重伤害。每个错位都由三个系统解释:屏幕位置,制造商指导和胃肠(GI)弯曲。
    方法:国家和地方记录。
    方法:识别错位的能力。
    结果:后来被确定为错位的痕迹,当它们完全或部分地与GI位置相区分时:a)与历史记录中绘制的GI屏幕区域重叠(57-71%)或b)符合制造商指导标准或与接收器错位或异常解剖结构混淆并达到左下象限(14-71%)。相反,所有肺部错位均使用胃肠弯曲系统被确定为不安全.所有三个系统均未能检测到腹膜内迹线。医疗中心存储的痕迹不一致。
    结论:Trace文件存储应由相关卫生授权机构授权并可访问,以改善安全性研究。仅靠屏幕位置和制造商的指导无法始终如一地将安全的形状与不安全的痕迹区分开。胃肠道弯曲解释似乎更安全,但需要在更大的研究中进行测试。
    OBJECTIVE: Determine why Cortrak-guided, undetected tube misplacement may occur in relation to the system of trace interpretation used.
    METHODS: From 2010 to 2017 we obtained seven of the eight Cortrak traces from the United Kingdom where misplacement was undetected and the patient received feed. Seven suffered serious harm. Each misplacement was interpreted by three systems: screen position, manufacturer guidance and gastrointestinal (GI) flexures.
    METHODS: National and local records.
    METHODS: Ability to identify misplacement.
    RESULTS: Traces that were later identified as misplacements, could not be differentiated from GI position when they wholly or partially: a) overlapped with the GI screen area plotted from historical records (57-71%) or b) met both manufacturer guidance criteria or were confused with receiver misplacement or unusual anatomy and reached the lower left quadrant (14-71%). Conversely, all lung misplacements were identified as unsafe using the GI flexure system. All three systems failed to detect the intra-peritoneal trace. Traces were inconsistently stored by healthcare centres.
    CONCLUSIONS: Trace file storage should be mandated by and accessible to relevant health authorisation bodies to improve safety research. Screen position alone and manufacturer guidance fail to consistently differentiate the shape of safe from unsafe traces. GI flexure interpretation appears safer but requires testing in larger studies.
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  • 文章类型: Journal Article
    背景:2011年发布了巴西宫颈癌筛查指南。目的是验证这一时期筛查指标的变化。
    方法:一项审计研究,其样本是坎皮纳斯市公共卫生系统从2010年到2016年进行的所有筛查测试。变量是绝对测试数字,过量测试,间隔和结果,按年龄。趋势分析使用Cochran-Armitage×2和线性回归。
    结果:在2010年进行了62,925项测试,在2016年进行了43,523项测试,趋势降低(P=0.001)。多年来,超额测试高于50%,呈下降趋势(P<0.001)。在此期间,对25岁以下女性进行的测试范围为20.2%至15.4%(P<0.001),而在25-64岁年龄段,75.1%~80.2%(P<0.001)。2010年最频繁的间隔是年度(47.5%),2016年是两年一次(34.7%)。有一个趋势,在第一次进行的测试的比例减少和那些与每年的间隔(P<0.001),以及间隔等于或大于每两年一次的测试增加的趋势(P<0.001)。我们观察到LSIL和HSIL-CIN2结果降低的趋势(分别为P=0.04和P=0.001),HSIL-CIN3结果呈增加趋势(P=0.02)。
    结论:超出推荐范围的宫颈癌筛查试验的比例显示,这一时期显著减少。这表明将坎皮纳斯的宫颈癌筛查与推荐的标准对齐的趋势。
    BACKGROUND: A Brazilian guideline on cervical cancer screening was released in 2011. The objective was to verify changes in screening indicators around this period.
    METHODS: An audit study which sample was all screening tests performed by the public health system of Campinas city from 2010 to 2016. Variables were absolute tests numbers, excess tests, intervals and results, by age. For trend analysis was used Cochran-Armitage × 2 and linear regression.
    RESULTS: Were carried out 62,925 tests in 2010 and 43,523 tests in 2016, a tendency at a reduction (P = 0.001). Excess tests were higher than 50% over the years, with a tendency at a reduction (P < 0.001). Tests performed on women under 25 ranged from 20.2 to 15.4% in the period (P < 0.001), while in the 25-64 years age-group, it ranged from 75.1 to 80.2% (P < 0.001). In 2010 the most frequent interval was annual (47.5%) and in 2016 biennial (34.7%). There was a tendency at a reduction in the proportion of tests performed at the first time and those with an annual interval (P < 0.001), and also a tendency at an increase in tests with intervals equal to or greater than biannual (P < 0.001). We observed a tendency at a reduction in LSIL and HSIL-CIN2 results (P = 0.04 and P = 0.001, respectively), and a tendency at an increase in HSIL-CIN3 result (P = 0.02).
    CONCLUSIONS: The proportion of cervical cancer screening tests performed out of the recommendation showed a significant reduction in the period. This indicates a tendency to align cervical cancer screening in Campinas with the standards recommended.
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  • 文章类型: Comparative Study
    BACKGROUND: The Parker Mobility Score has proven to be a valid and reliable measurement of hip fracture patient mobility. For hip fracture registries the Fracture Mobility Score is advised and used, although this score has never been validated. This study aims to validate the Fracture Mobility Score against the Parker Mobility Score.
    METHODS: The Dutch Hip Fracture Audit uses the Fracture Mobility Score (categorical scale). For the purpose of this study, five hospitals registered both the Fracture Mobility Score and the Parker Mobility Score (0-9 scale) for every admitted hip fracture patient in 2018. The Spearman correlation between the two scores was calculated. To test whether the correlation coefficient remained stable among different patient subgroups, analyses were stratified according to baseline patient characteristics.
    RESULTS: In total 1,201 hip fracture patients were included. The Spearman correlation between the Fracture Mobility Score and Parker Mobility Score was strong: 0.73 (p = < 0.001). Stratified for gender, age, ASA score, dementia, Index of Activities of Daily Living (KATZ-6 ADL score), living situation and nutritional status, the correlation coefficient varied between 0.40-0.84. For patients aged 90 and over and having an ASA score of III-IV who suffered from dementia, had a KATZ-6 ADL score of 1-6, lived in an institution and/or were malnourished, the correlation was moderate.
    CONCLUSIONS: The Fracture Mobility Score is overall strongly correlated with the Parker Mobility Score and can be considered as a valid score to measure hip fracture patient mobility. This may encourage other hip fracture audits to also use the Fracture Mobility Score, which would increase the uniformity of mobility score results among national hip fracture audits and decrease the overall registration load.
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