outcome assessment (health care)

结果评估 (卫生保健)
  • 文章类型: Journal Article
    为了描述这些原则,process,以及针对手部和腕部状况创建国际健康结果测量联盟(ICHOM)标准集的结果。
    遵循ICHOM的标准化方法,一个由手外科医师组成的国际工作组,治疗师,研究人员聚集在一起开发一种基于证据的,以病人为中心,手和腕患者的标准结果测量。进行了多项系统评价,以支持我们选择手部和腕部疾病的结果领域和工具。在2018年3月至2020年3月之间举行了14次视频会议,并使用了修改后的Delphi流程。
    在5条测量轨道上达成共识:拇指,手指,手腕,神经,和严重的手部创伤痕迹,在适用特定分配标准的常规和扩展轨道之间有区别。标准集包含结果工具的选择和用于结果测量的预定时间点。此外,当存在多个条件时,我们开发了一个使用轨道的层次结构,我们选择了风险调整,案例混合变量。
    针对手部和腕部疾病的ICHOM标准的全球实施可以促进手部和腕部疾病患者的基于价值的医疗保健。
    针对手部和腕部疾病的ICHOM标准集可以实现临床决策,质量改进,以及治疗和医疗保健专业人员之间的比较。
    To describe the principles, process, and results of creating the International Consortium for Health Outcomes Measurement (ICHOM) standard set for hand and wrist conditions.
    Following the standardized methods of ICHOM, an international working group of hand surgeons, therapists, and researchers was assembled to develop an evidence-based, patient-centered, standard set of outcome measures for patients with hand and wrist conditions. Multiple systematic reviews were performed to support our choices of outcome domains and tools for hand and wrist conditions. Fourteen video conferences were held between March 2018 and March 2020, and a modified Delphi process was used.
    A consensus was reached on 5 measurement tracks: the thumb, finger, wrist, nerve, and severe hand trauma tracks, with a distinction between regular and extended tracks for which specific allocation criteria applied. The standard set contains a selection of outcome tools and predefined time points for outcome measurement. Additionally, we developed a hierarchy for using the tracks when there are multiple conditions, and we selected risk-adjustment, case-mix variables.
    The global implementation of the ICHOM standard set for hand and wrist conditions may facilitate value-based health care for patients with hand and wrist conditions.
    The ICHOM standard set for hand and wrist conditions can enable clinical decision making, quality improvement, and comparisons between treatments and health care professionals.
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  • 文章类型: Journal Article
    Chronic hepatitis B is an important health problem that can progress to cirrhosis and complications such as hepatocellular carcinoma. There is approximately 290 million of people with chronic hepatitis B virus (HBV) infection worldwide, however only 10% of patients are currently identified. Most part of Brazil is considered of low prevalence of HBV infection but there are some regions with higher frequency of carriers. Unfortunately, many infected patients are not yet identified nor evaluated for treatment. The Brazilian Society of Infectious Diseases (SBI) and the Brazilian Society of Hepatology worked together to elaborate a guideline for diagnosis and treatment of hepatitis B. The document includes information regarding the population to be tested, diagnostic tools, indications of treatment, therapeutic schemes and also how to handle HBV infection in specific situations (pregnancy, children, immunosuppression, etc). Delta infection is also part of the guideline, since it is an important infection in some parts of the country.
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  • 文章类型: Journal Article
    Objective  To develop standardized definitions for a list of indicators that represent significant events during pediatric transport, which were previously identified by a national Delphi study. Methods  We designed a three-phase consensus process that applied Delphi methodology to a combination of electronic questionnaires and a live consensus meeting. Results  Thirty-one pediatric transport experts evaluated a total of 59 indicators. Twenty-four indicators represented events or interventions that did not require definition. One indicator was removed from the list. Definitions for the remaining 34 indicators were developed. Conclusion  This standardized indicator list is intended for application to quality improvement and clinical research initiatives.
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  • 文章类型: Journal Article
    目的:确定青光眼专家认为最重要和最实用的一组青光眼手术结果指标。
    方法:一百零二位青光眼专家(英国和欧洲青光眼学会(UKEGS)的57位成员和欧洲青光眼学会(EGS)的45位成员)参加了在线Delphi练习。使用RAND/UCLA适当性方法分析每一轮的数据并生成分歧指数。
    结果:参与者就13个基线数据点和12个结果达成一致,这些数据点被认为是重要且实用的。对于眼内压(IOP),IOP从基线的百分比降低(术后前最后三个IOP读数)和低于指定目标的降低被认为是重要的。对于视野,全局视野指数的变化,例如,MD,和通过线性回归评估的进展发展被认为是重要的。从安全的角度来看,导致最小分辨率角度加倍的任何视觉损失,5dB或更多的视野损失或高级视野损失的发展(HodappParrishAnderson阶段4)被认为是重要的。强调了常规使用患者报告结果测量(PROM)的重要性。共识建议青光眼治疗的结果应在1年、5年和10年报告。
    结论:关于报告青光眼手术结果和结果测量间隔的最小数据集存在广泛共识。
    OBJECTIVE: To identify the key set of glaucoma surgery outcome measures considered most important and practical to collect by glaucoma specialists.
    METHODS: One hundred two glaucoma specialists (57 members of the UK and Eire Glaucoma Society (UKEGS) and 45 members of the European Glaucoma society (EGS)) took part in an Online Delphi exercise. The RAND/UCLA appropriateness method was used analyse data from each round and generate a disagreement index.
    RESULTS: Participants agreed on 13 baseline data points and 12 outcomes that were considered important and practical to collect. For intraocular pressure (IOP) percentage reduction in IOP from baseline (last three IOP readings pre-op) and reduction below a specified target were considered important. For visual fields, change in a global visual field index, e.g. MD, and development of progression as assessed by linear regression were considered important. From a safety perspective, any visual loss resulting in a doubling of the minimal angle of resolution, loss of 5 dB or more of visual field or development of advanced field loss (Hodapp Parrish Anderson Stage 4) was considered important. The importance of routinely using patient reported outcome measures (PROMs) was highlighted. Consensus suggested that outcomes of glaucoma treatments should be reported at 1, 5 and 10 years.
    CONCLUSIONS: There was broad consensus on a minimum dataset for reporting the outcomes of glaucoma surgery and outcome measurement intervals.
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  • 文章类型: Journal Article
    Parkinson\'s disease (PD) is a progressive neurodegenerative condition that is expected to double in prevalence due to demographic shifts. Value-based healthcare is a proposed strategy to improve outcomes and decrease costs. To move towards an actual value-based health care system, condition-specific outcomes that are meaningful to patients are essential.
    Propose a global consensus standard set of outcome measures for PD.
    Established methods for outcome measure development were applied, as outlined and used previously by the International Consortium for Health Outcomes Measurement (ICHOM). An international group, representing both patients and experts from the fields of neurology, psychiatry, nursing, and existing outcome measurement efforts, was convened. The group participated in six teleconferences over a six-month period, reviewed existing data and practices, and ultimately proposed a standard set of measures by which patients should be tracked, and how often data should be collected.
    The standard set applies to all cases of idiopathic PD, and includes assessments of motor and non-motor symptoms, ability to work, PD-related health status, and hospital admissions. Baseline demographic and clinical variables are included to enable case mix adjustment.
    The Standard Set is now ready for use and pilot testing in the clinical setting. Ultimately, we believe that using the set of outcomes proposed here will allow clinicians and scientists across the world to document, report, and compare PD-related outcomes in a standardized fashion. Such international benchmarks will improve our understanding of the disease course and allow for identification of \'best practices\', ultimately leading to better informed treatment decisions.
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  • 文章类型: Journal Article
    Parkinson disease (PD) is associated with a clinical course of variable duration, severity, and a combination of motor and non-motor features. Recent PD research has focused primarily on etiology rather than clinical progression and long-term outcomes. For the PD patient, caregivers, and clinicians, information on expected clinical progression and long-term outcomes is of great importance. Today, it remains largely unknown what factors influence long-term clinical progression and outcomes in PD; recent data indicate that the factors that increase the risk to develop PD differ, at least partly, from those that accelerate clinical progression and lead to worse outcomes. Prospective studies will be required to identify factors that influence progression and outcome. We suggest that data for such studies is collected during routine office visits in order to guarantee high external validity of such research. We report here the results of a consensus meeting of international movement disorder experts from the Genetic Epidemiology of Parkinson\'s Disease (GEO-PD) consortium, who convened to define which long-term outcomes are of interest to patients, caregivers and clinicians, and what is presently known about environmental or genetic factors influencing clinical progression or long-term outcomes in PD. We propose a panel of rating scales that collects a significant amount of phenotypic information, can be performed in the routine office visit and allows international standardization. Research into the progression and long-term outcomes of PD aims at providing individual prognostic information early, adapting treatment choices, and taking specific measures to provide care optimized to the individual patient\'s needs.
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  • 文章类型: Comparative Study
    BACKGROUND: Performance metrics currently focus on the measurement of the application of guideline-indicated medications without considering the appropriate dosing of these drugs.
    RESULTS: We studied 39 291 patients from the Can Rapid Risk Stratification of Unstable Angina Patients Suppress Adverse Outcomes with Early Implementation of the ACC/AHA Guidelines (CRUSADE) registry with non-ST-segment elevation acute coronary syndromes. We evaluated hospital variability in the composite use of American College of Cardiology/American Heart Association guideline-recommended therapies (adherence) and the proportion of treated patients with the recommended dose of heparins or a glycoprotein IIb/IIIa antagonist (safety), and its association with risk-adjusted in-hospital mortality and bleeding. The rates of composite guideline adherence (median, 85%; 25th, 75th percentile, 82, 88) and antithrombotic dosing safety (median, 53%; 25th, 75th percentile, 45%, 60%) varied among hospitals. Correlation between hospital composite adherence and safety metrics was significant but low (r=0.16, P=0.008). Risk-adjusted in-hospital mortality was inversely related to both guideline adherence (odds ratio-10% increment, 0.80; 95% confidence interval, 0.67-0.94) and safety metrics (odds ratio-10% increment, 0.90; 95% confidence interval, 0.83-0.98). Safety was inversely related to major bleeding (adjusted odds ratio-10% increment, 0.93; 95% confidence interval, 0.87-0.98). In comparison with hospitals with low adherence and safety (≤median performance) metrics, those with mixed performance metrics (high adherence and low safety, low adherence and high safety) had intermediate risk-adjusted mortality rates, whereas hospitals with above-average performance on both metrics (>median performance) had a trend for lowest risk adjusted mortality rates (odds ratio 0.83; 95% confidence interval, 0.68-1.01). Hospitals with high safety had lower bleeding rates in comparison to those with low safety.
    CONCLUSIONS: Guideline adherence and dosing safety appeared to provide independent and complementary information on hospital bleeding and mortality, supporting the need for broader metrics of quality that should include measures of both guideline-based care and safety.
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  • 文章类型: Journal Article
    目的:以前尚未在国家层面对院内卒中的护理质量进行分析。这项研究比较了患者的特征,质量的过程措施,在国家队列中,院内卒中与社区发作卒中的结果。
    方法:我们从2006年1月至2012年4月对美国心脏协会的GetWithTheGuidelines-Stroke(GWTG-Stroke)数据库进行了一项回顾性队列研究,使用来自1280家报告≥1例住院卒中的研究中心的数据。患者特征,合并症,药物,护理措施的质量,分析了21349例院内缺血性卒中与928885例社区发作缺血性卒中相比的结局.
    结果:住院卒中患者有更多的血栓栓塞危险因素,包括心房颤动,人工心脏瓣膜,颈动脉狭窄,心力衰竭(P<0.0001),并且经历了更严重的卒中(美国国立卫生研究院卒中评分中位数9.0对4.0;P<0.0001)。使用GWTG-中风成就测量,住院卒中患者接受无缺陷护理的比例较低(60.8%vs82.0%;P<0.0001).在考虑了患者和医院的特点之后,住院卒中患者出院回家的可能性较小(调整后比值比0.37;95%置信区间[0.35-0.39])或出院时能够独立行走(调整后比值比0.42;95%置信区间[0.39-0.45]).住院卒中患者的住院死亡率较高(校正比值比2.72;95%置信区间[2.57-2.88])。
    结论:与社区型缺血性卒中相比,住院中风患者经历了更严重的中风,对基于过程的质量措施的依从性较低,结果更糟。这些发现表明,对于住院中风患者,有针对性的质量改进工作是一个重要的机会。
    OBJECTIVE: Analysis of quality of care for in-hospital stroke has not been previously performed at the national level. This study compares patient characteristics, process measures of quality, and outcomes for in-hospital strokes with those for community-onset strokes in a national cohort.
    METHODS: We performed a retrospective cohort study of the Get With The Guidelines-Stroke (GWTG-Stroke) database of The American Heart Association from January 2006 to April 2012, using data from 1280 sites that reported ≥1 in-hospital stroke. Patient characteristics, comorbid illnesses, medications, quality of care measures, and outcomes were analyzed for 21 349 in-hospital ischemic strokes compared with 928 885 community-onset ischemic strokes.
    RESULTS: Patients with in-hospital stroke had more thromboembolic risk factors, including atrial fibrillation, prosthetic heart valves, carotid stenosis, and heart failure (P<0.0001), and experienced more severe strokes (median National Institutes of Health Stroke Score 9.0 versus 4.0; P<0.0001). Using GWTG-Stroke achievement measures, the proportion of patients with defect-free care was lower for in-hospital strokes (60.8% versus 82.0%; P<0.0001). After accounting for patient and hospital characteristics, patients with in-hospital strokes were less likely to be discharged home (adjusted odds ratio 0.37; 95% confidence intervals [0.35-0.39]) or be able to ambulate independently at discharge (adjusted odds ratio 0.42; 95% confidence intervals [0.39-0.45]). In-hospital mortality was higher for in-hospital stroke (adjusted odds ratio 2.72; 95% confidence intervals [2.57-2.88]).
    CONCLUSIONS: Compared with community-onset ischemic stroke, patients with in-hospital stroke experienced more severe strokes, received lower adherence to process-based quality measures, and had worse outcomes. These findings suggest there is an important opportunity for targeted quality improvement efforts for patients with in-hospital stroke.
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