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Management of major trauma: changes required for improvement. 重大创伤的处理:改善所需的改变。
Pub Date : 1999-06-01 DOI: 10.1136/qshc.8.2.78
J Dyas, P Ayres, M Airey, J Connelly

Aims: To describe the views of key healthcare professionals on the changes they considered to be important in the reduction of major trauma mortality between 1988 and 1995 in Leeds.

Methods: Qualitative unstructured interviews with a purposive sample of 10 healthcare professionals deemed to be key personnel by an experienced consultant who had provided acute trauma care throughout the relevant period. Each interview was tape recorded and transcribed; each transcript was analysed for important themes by two independent researchers who then discussed their results to resolve any differences in interpretation.

Results: Three categories of change became evident: "policy", "infrastructure", and "philosophy of care". Each of these categories seemed to be equally important. Policy changes identified as important were the Royal College of Surgeons of England's report into trauma care (1988), the setting of standards for paramedic training, and the national audit of major trauma outcomes. Important infrastructure changes identified were training in advanced trauma life support, decreased ambulance response times, reorganisation towards "consultant led" hospital services, and an emphasis on quality monitoring. Changes in philosophy of care were increases in levels of teamwork, commitment, communication, and confidence. Together these facilitated an overall restructuring and refocusing of care.

Conclusions: No individual change is seen as dominant for improved care, but rather a strategic mixture of facilitating national and regional policy guidance, organisational restructuring, and congruent professional attitudes were integral components leading to the observed changes. Improving outcomes in other areas is likely to involve an integrated series of changes which must be managed as a total system.

目的:描述主要医疗保健专业人员对1988年至1995年间在减少利兹重大创伤死亡率方面的重要变化的看法。方法:定性非结构化访谈,目的样本为10名医疗保健专业人员,由一名经验丰富的顾问认为是关键人员,他们在相关期间提供急性创伤护理。每次采访都有录音和文字记录;每一份记录都由两位独立的研究人员分析了重要的主题,然后讨论了他们的结果,以解决解释上的任何差异。结果:“政策”、“基础设施”和“护理理念”这三个方面的变化变得明显。这些类别似乎都同样重要。被认为重要的政策变化包括1988年英国皇家外科医学院创伤护理报告、护理人员培训标准的制定以及主要创伤结果的国家审计。确定的重要基础设施变化是高级创伤生命支持培训、缩短救护车反应时间、向"顾问领导"的医院服务重组,以及强调质量监测。护理理念的变化是团队合作、承诺、沟通和信心水平的提高。这些因素共同促进了护理工作的全面重组和重新聚焦。结论:没有个人的改变被认为是改善护理的主导因素,而是促进国家和地区政策指导、组织重组和一致的专业态度的战略混合是导致观察到的变化的组成部分。改善其他领域的成果可能涉及一系列必须作为一个整体系统加以管理的综合变革。
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引用次数: 13
Day surgery in Scotland: patient satisfaction and outcomes. 苏格兰日间手术:患者满意度和结果。
Pub Date : 1999-06-01 DOI: 10.1136/qshc.8.2.86
J Bain, H Kelly, D Snadden, H Staines

Objective: To evaluate patients' views on the process and outcome of day surgery in Scotland, and to study patients' satisfaction with care in a range of specific procedures.

Design: Questionnaires completed by a census of day case surgery patients within a band of 25 procedures under the umbrella of five broad groups: (1) general surgery; (2) urology; (3) gynaecology; (4) orthopaedics; (5) ear, nose, and throat; ophthalmology.

Setting: 13 hospitals in six health board areas in Scotland.

Subjects: During the period 1995-6, 5069 day case patients were asked to complete a questionnaire within two weeks of their operation and discharge from hospital.

Main outcome measures: Arrangements before admission; immediate postoperative symptoms and complications; problems experienced after discharge; readmission after discharge.

Results: A response rate of 68% was obtained from 13 sites ranging from 43% to 82%. The overall satisfaction score was 85. A total of 894 patients (26%) experienced pain after surgery and 783 (23%) had relatively minor medical problems after discharge. In total, 265 (7.8%) patients were readmitted to hospital after discharge. Few notable differences existed between specialties or hospitals in terms of satisfaction scores, although notable pain was experienced more frequently in gynaecology and general surgery patients. Readmission was more common for urological procedures.

Conclusion: Overall, patient satisfaction with day case surgery was high. Dissatisfaction was largely related to waiting times between admission, operation, and discharge. The amount of pain experienced also had a notable impact on the level of patient satisfaction. Day surgery is not without complications, with 26% of patients experiencing notable degrees of pain; 23% having minor medical problems after discharge; and 8% of respondents having to reattend hospital with problems relating to their original operations.

目的:评估患者对苏格兰日间手术过程和结果的看法,并研究患者对一系列具体手术的护理满意度。设计:问卷调查是通过对五大类25种手术的日间手术患者进行普查来完成的:(1)普通外科;(2)泌尿外科;(3)妇科;(4)骨科;(5)耳、鼻、喉;眼科。环境:苏格兰6个卫生局辖区的13家医院。对象:在1995- 1996年期间,5069例日间病例患者被要求在手术和出院后两周内完成一份问卷。主要观察指标:入院前安排;术后即刻症状和并发症;出院后遇到的问题;出院后再入院。结果:在43% ~ 82%的13个站点中,有效率为68%。总体满意度为85分。共有894名患者(26%)在手术后出现疼痛,783名患者(23%)在出院后出现相对较小的医疗问题。共有265例(7.8%)患者出院后再次住院。不同专科或医院在满意度评分方面几乎没有显著差异,尽管妇科和普外科患者更频繁地经历明显的疼痛。泌尿外科手术再入院更为常见。结论:总体而言,患者对日间手术的满意度较高。不满意主要与入院、手术和出院之间的等待时间有关。疼痛程度对患者满意度也有显著影响。日间手术并非没有并发症,26%的患者经历了明显程度的疼痛;23%的人在出院后有轻微的医疗问题;8%的受访者因与原来的手术有关的问题不得不再次住院。
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引用次数: 105
Some limits to evidence-based medicine: a case study from elective orthopaedics. 循证医学的一些限制:择期骨科的案例研究。
Pub Date : 1999-06-01 DOI: 10.1136/qshc.8.2.99
E Ferlie, M Wood, L Fitzgerald

There has been growing interest in recent years in the application of the principles of evidence-based medicine (EBM), although implementation is complex. Scientific, organisational, and behavioural factors all combine to shape clinical behaviour change. Case study based qualitative data are presented which illuminate such processes within one clinical setting (elective orthopaedics), drawn from a larger study. It is suggested that (1) there are alternative models of what constitutes "evidence" in use; (2) scientific knowledge is in part socially constructed; and (3) clinical professionals retain a monopoly of technical knowledge. The implication is that there may be severe obstacles to the rapid or broad implementation of EBM.

近年来,人们对循证医学(EBM)原则的应用越来越感兴趣,尽管实施起来很复杂。科学、组织和行为因素共同影响临床行为的改变。案例研究基于定性数据提出,阐明了这样的过程在一个临床设置(选择性骨科),从一个更大的研究绘制。本文建议:(1)存在可供选择的构成“证据”的模型;(2)科学知识部分是社会建构的;(3)临床专业人员保持对技术知识的垄断。这意味着,快速或广泛实施循证医学可能存在严重障碍。
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引用次数: 93
Clinician education: a key to implementing asthma guidelines? 临床医生教育:实施哮喘指南的关键?
Pub Date : 1999-06-01 DOI: 10.1136/qshc.8.2.73
C Griffiths, G Feder
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引用次数: 4
Antimicrobial prophylaxis in colorectal surgery. 结直肠手术中的抗菌预防。
Pub Date : 1999-06-01 DOI: 10.1136/qshc.8.2.132
A M Glenny, F Song
volume 4,no 5,which is an update of a system-atic review of randomised controlled trials(RCTs) examining the eVectiveness of diVer-ent antimicrobial regimens used for the preven-tion of surgical wound infection in patientsundergoing colorectal surgery. Details of thereview’s methodology are publishedelsewhere.
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引用次数: 21
A model for continuous quality improvement in small scale practices. 一个小规模实践中持续质量改进的模型。
Pub Date : 1999-03-01 DOI: 10.1136/qshc.8.1.43
H Geboers, R Grol, W van den Bosch, H van den Hoogen, H Mokkink, P van Montfort, H Oltheten
During the past decade new models for quality improvement in health care were developed based on experiences in industry. These models became known as total quality management or continuous quality improvement and are now widely and successfully used in larger healthcare organisations. In general practice several tools are used to improve care, such as vocational training, continuous medical education, peer review, audit, and guideline development. Although valuable, these tools usually focus more on improving professional performance than on comprehensive care provision delivered by teams. Little is known about the use of continuous quality improvement in small scale general practice. The question is whether it is possible to translate the principles of continuous quality improvement into a model for quality improvement for general practice. Simply adopting the strategies of continuous quality improvement used in hospitals or larger organisations may fail because of the specific characteristics of general practice. Most of these practices have, for example, a hierarchical structure in which the general practitioner (GP) is not only the manager but also is often the owner. In many countries general practices have a small staV who lack the time for quality improvement activities. The aim of this article is to reflect on the applicability of continuous quality improvement in small scale practices. Firstly, the characteristics of general practice will be discussed. Secondly, the essential elements of continuous quality improvement are presented by giving a short review of previous publications. Finally, these elements are translated into a framework of practical possibilities for quality improvement in general practice, which results in a model for quality improvement that may be feasible and applicable in small scale general practice. Examples from a study on quality management in general practice done in the Netherlands are used to illustrate the model. 17
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引用次数: 36
Empowering patients using computer based health support systems. 使用基于计算机的健康支持系统为患者赋权。
Pub Date : 1999-03-01 DOI: 10.1136/qshc.8.1.49
D H Gustafson, F M McTavish, E Boberg, B H Owens, C Sherbeck, M Wise, S Pingree, R P Hawkins
With the increased pressure to contain healthcare costs, it is critical to find more eVective ways of providing information, emotional support, decision making, and behaviour change assistance for patients. In the United States, a doctor spends approximately 18 minutes in face to face contact with the patient during each clinic appointment. 1 During morning hospital rounds, physicians spend on average just over four minutes in the patient’s room. 2 It has been proposed that ideal physician communication with patients with breast cancer should be tailored to patients’ needs or coping styles to reduce their distress. 3 However, in an environment of continued pressure to reduce healthcare costs, it is virtually impossible for doctors to give patients adequate information or even direct them to appropriate support resources. If costs are to be reduced while at the same time improving patient support we must find new ways to help patients to cope with their disease, make necessary decisions, and gain emotional support. Computer systems can help to fill this void. A key problem encountered by people facing a health crisis is that they are often given information when they are least able to take it in, such as at the time of diagnosis. SiminoV and others have concluded that nearly all studies point to serious gaps in patient recall and understanding of the information they are given. 34
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引用次数: 84
Patient centred assessment of quality of life for patients with four common conditions. 以患者为中心的四种常见疾病患者生活质量评估。
Pub Date : 1999-03-01 DOI: 10.1136/qshc.8.1.22
D A Ruta, A M Garratt, I T Russell

Objectives: To assess the reliability, validity, and responsiveness of a new quality of life measure, the patient generated index (PGI) of quality of life, in patients with four common clinical conditions.

Design: Prospective one year follow up study.

Setting: Outpatient departments and four general practices in Grampian, Scotland.

Subjects: 1746 patients consulting a general practitioner in one of four practices, or referred to outpatients from all Grampian practices over a four month period, with low back pain, menorrhagia, suspected peptic ulcer, and varicose veins.

Main outcome measures: Postal questionnaire including the PGI, SF-36 health survey, and clinically derived condition specific measures of disease severity.

Results: Test-retest reliability was satisfactory for group comparisons (intraclass correlation coefficient 0.65). Validity was confirmed by the observed association of the PGI with the SF-36, condition specific instruments, and sociodemographic variables. For low back pain, the PGI and the SF-36 pain scale were found to be most responsive to clinical change. For patients with menorrhagia and suspected peptic ulcer, only the condition specific instruments detected larger changes than the PGI.

Conclusions: It is possible to develop a patient generated index of quality of life that not only assesses the extent to which patients' expectations are matched by reality but also satisfies criteria of reliability and responsiveness to change. Further work is required to make the PGI more acceptable and meaningful to patients, but it is believed that it offers an exciting new approach to the evaluation of medical care.

目的:评估一种新的生活质量测量方法——患者生活质量生成指数(PGI)在四种常见临床疾病患者中的信度、效度和反应性。设计:前瞻性1年随访研究。设置:门诊部门和四个一般做法在格兰扁,苏格兰。研究对象:1746名患者在四个月的时间里,在四个诊所中的一个咨询全科医生,或转介到所有格兰pian诊所的门诊病人,患有腰痛,月经出血,疑似消化性溃疡和静脉曲张。主要结果测量:邮寄问卷包括PGI, SF-36健康调查,和临床衍生的疾病严重程度的具体措施。结果:组间比较重测信度满意(类内相关系数0.65)。通过观察到PGI与SF-36、特定条件工具和社会人口变量之间的关联,证实了有效性。对于腰痛,PGI和SF-36疼痛量表被发现对临床变化最敏感。对于月经过多和疑似消化性溃疡的患者,只有特定条件的仪器检测到比PGI更大的变化。结论:有可能开发一个患者生成的生活质量指标,不仅评估患者期望与现实的匹配程度,而且满足可靠性和对变化的反应性标准。进一步的工作需要使PGI更容易被患者接受和有意义,但相信它提供了一个令人兴奋的评估医疗服务的新方法。
{"title":"Patient centred assessment of quality of life for patients with four common conditions.","authors":"D A Ruta,&nbsp;A M Garratt,&nbsp;I T Russell","doi":"10.1136/qshc.8.1.22","DOIUrl":"https://doi.org/10.1136/qshc.8.1.22","url":null,"abstract":"<p><strong>Objectives: </strong>To assess the reliability, validity, and responsiveness of a new quality of life measure, the patient generated index (PGI) of quality of life, in patients with four common clinical conditions.</p><p><strong>Design: </strong>Prospective one year follow up study.</p><p><strong>Setting: </strong>Outpatient departments and four general practices in Grampian, Scotland.</p><p><strong>Subjects: </strong>1746 patients consulting a general practitioner in one of four practices, or referred to outpatients from all Grampian practices over a four month period, with low back pain, menorrhagia, suspected peptic ulcer, and varicose veins.</p><p><strong>Main outcome measures: </strong>Postal questionnaire including the PGI, SF-36 health survey, and clinically derived condition specific measures of disease severity.</p><p><strong>Results: </strong>Test-retest reliability was satisfactory for group comparisons (intraclass correlation coefficient 0.65). Validity was confirmed by the observed association of the PGI with the SF-36, condition specific instruments, and sociodemographic variables. For low back pain, the PGI and the SF-36 pain scale were found to be most responsive to clinical change. For patients with menorrhagia and suspected peptic ulcer, only the condition specific instruments detected larger changes than the PGI.</p><p><strong>Conclusions: </strong>It is possible to develop a patient generated index of quality of life that not only assesses the extent to which patients' expectations are matched by reality but also satisfies criteria of reliability and responsiveness to change. Further work is required to make the PGI more acceptable and meaningful to patients, but it is believed that it offers an exciting new approach to the evaluation of medical care.</p>","PeriodicalId":20773,"journal":{"name":"Quality in health care : QHC","volume":"8 1","pages":"22-9"},"PeriodicalIF":0.0,"publicationDate":"1999-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1136/qshc.8.1.22","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"21417977","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 124
Unmet care demands as perceived by stroke patients: deficits in health care? 脑卒中患者未满足的护理需求:医疗保健的缺陷?
Pub Date : 1999-03-01 DOI: 10.1136/qshc.8.1.30
W J op Reimer, R J Scholte de Haan, P T Rijnders, M Limburg, G A van den Bos
OBJECTIVES: To describe unmet care demands as perceived by stroke patients and to identify sociodemographic and health characteristics associated with these unmet demands to investigate the appropriateness of health care. SETTING: Sample of patients who participated in a multicentre study (23 hospitals) on quality of care in The Netherlands. PATIENTS: Non-institutionalised patients who had been admitted to hospital because of stroke. Patients were interviewed six months (n = 382) and five years (n = 224) after stroke. DESIGN: Six months after stroke data were collected on: (a) sociodemographic characteristics in terms of age, sex, living arrangement, educational level, and regional level of urbanisation; (b) health characteristics in terms of cognitive function, disability, emotional distress, and general health perception; (c) utilisation of professional care; and (d) unmet care demands as perceived by patients. Data on utilisation of care and unmet demands were also collected five years after stroke. Data were collected from June 1991 until December 1996. RESULTS: The percentage of unmet care demands was highest at six months after stroke (n = 120, 31%). Multiple logistic regression analyses showed that disabled patients were more likely to be unmet demanders for therapy, (I)ADL care and aids (range odds ratio (OR) = 3.5 to 7.9) than to be no demanders, whereas emotionally distressed patients were more likely to be unmet demanders for psychosocial support (OR = 3.8). When comparing unmet demanders with care users only for (instrumental) activities of daily living (I)ADL care differences were found: men (OR = 3.8), disabled patients (OR = 3.0), and emotionally distressed patients (OR = 6.5) were more likely to be users. CONCLUSIONS: Patients who perceived an unmet care demand do appear genuinely to have an unmet care need as supported by assessment of their health status: (a) types of unmet care demands correspond with types of health problems and (b) unmet demanders were in general unhealthier than no demanders and more comparable with care users for health characteristics. IMPLICATIONS: To improve an equitable distribution of healthcare services, guidelines for indicating and allocating health care have to be developed and should be based on scientific evidence and consensus meetings including professionals' and patients' perspectives.
目的:描述脑卒中患者未满足的护理需求,并确定与这些未满足需求相关的社会人口统计学和健康特征,以调查医疗保健的适宜性。背景:参加荷兰一项关于护理质量的多中心研究(23家医院)的患者样本。病人:因中风而入院的非住院病人。患者在脑卒中后6个月(n = 382)和5年(n = 224)接受访谈。设计:中风后6个月收集以下数据:(a)年龄、性别、生活安排、教育水平和地区城市化水平方面的社会人口特征;(b)在认知功能、残疾、情绪困扰和一般健康感知方面的健康特征;(c)利用专业护理;(d)患者认为未满足的护理需求。还收集了中风后5年护理利用和未满足需求的数据。数据是从1991年6月至1996年12月收集的。结果:未满足护理需求的百分比在脑卒中后6个月最高(n = 120, 31%)。多元logistic回归分析显示,残疾患者更有可能成为治疗、(I)ADL护理和艾滋病的未满足需求者(范围优势比(OR) = 3.5至7.9),而情绪困扰患者更有可能成为心理社会支持的未满足需求者(OR = 3.8)。当比较未被满足的需求者与仅为(工具性)日常生活活动(I)的护理使用者时,发现ADL护理差异:男性(OR = 3.8),残疾患者(OR = 3.0)和情绪困扰患者(OR = 6.5)更有可能成为使用者。结论:感知到未满足的护理需求的患者确实表现出真正存在未满足的护理需求,这一点得到了对其健康状况评估的支持:(a)未满足的护理需求类型与健康问题类型相对应;(b)未满足的需求者总体上比无需求者更不健康,在健康特征上与护理使用者更具可比性。影响:为了改善卫生保健服务的公平分配,必须制定指示和分配卫生保健的准则,并应以科学证据和协商一致会议为基础,包括专业人员和患者的观点。
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引用次数: 44
Patient education in the year 2000: tailored decision support, empowerment, and mutual aid. 2000年的患者教育:量身定制的决策支持、授权和互助。
Pub Date : 1999-03-01 DOI: 10.1136/qshc.8.1.5
A M O'Connor
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引用次数: 1
期刊
Quality in health care : QHC
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