Encouraging patient participation in general practice consultations: Effect on consultation length and content,patient satisfaction and health

Abstract

Following the evidence from earlier research that one-to-one interventions can increase the patient's contribution to the consultation, this paper reports the results from a randomised control trial which assessed the effects of a leaflet designed to enhance patient participation in consultations. A random sample of patients (aged 16 to 74) waiting to see a general practitioner were given either an intervention leaflet, which encouraged the patient to take an active role in the consultation, or a control leaflet which gave dietary advice. The effects of the intervention were assessed by measuring length of consultation, number of questions asked by the patient, patient satisfaction score, doctor's feelings about the consultation, the change in patients' health in the 4 weeks following the consultation (measured by the SF-36 Health Survey) and the number of patient visits to a GP in the following year. The results showed that patients in the intervention group had significantly longer consultations than those in the control group and tended to ask more questions but there was no significant effect on patient satisfaction. The doctor tended to feel that he had a better understanding of patients in the intervention group. Overall there was no significant effect on SF-36 scores but, for patients under the age of 40, and for those in higher social classes the scores of patients in the intervention group improved to a significantly greater degree than did those for the control group. The intervention did not have any effect on the number of GP visits made by patients in the subsequent year. The study results show that a relatively simple leaflet can have an impact on patients' behaviour during the consultation, even though there were no effects on patient satisfaction with the consultation or in the number of GP visits in the following year.     

中美教学医院门诊病历管理对比研究

通过文献检索、走访调研并结合笔者对美国教学医院门诊病历管理的实地考察,本文对中美两国教学医院人员对门诊病历管理的认识理念、门诊病历管理的方式、病历的规范设计以及门诊病历的质量控制等方面进行了对比研究。显示我国教学医院在门诊病历管理方面与发达国家存在着差距。从提高临床医疗和医学教学质量、有利于患者疾病的诊治和培养当代优秀...     

提高儿科研究生医患沟通能力的探讨

提高医患沟通能力,是建立良好的医患关系,构建和谐社会的必然要求。儿科医患沟通具有其特殊性,其面对的是病患儿及众多的家长,因此,在临床学习中强化医患沟通意识、掌握沟通技巧对儿科研究生尤显重要,本文就如何提高儿科研究生医患沟通能力进行探讨。     

What Makes Crohn's Disease Patients Difficult to Manage? The Role of Psychosocial Factors

Most GI clinicians face the problem of a small group Crohn's Disease (CD) patients who function poorly and consume inordinate amounts of service with poor outcome. This study examines the hypothesis that psychosocial factors differentiate the CD patients who function poorly from the typical CD patient. A prototypal sample of CD patients with problems functioning, more typical CD patients (not selected for having problems in functioning), and healthy controls each completed a battery of validated psychosocial measures of disease-specific quality of life, coping skills, social support and life stress, perceived medical symptoms and life history factors. Chart data on hospital admissions, ER, GI, Surgeon, and GP visits were also collected. The CD patients with problems functioning reported more symptoms (GI and non-GI) and had many more ER, GI, and GP visits than the typical group. Psychologically, those with problems functioning had poorer quality of life and were more likely to cope using emotional discharge and support seeking. They experienced significantly more stress and reported a more chaotic family history. No differences on an experimental method of information processing biases were found between the CD groups, however. These results indicated that patients with problems functioning, selected by GI staff because they were best-case examples of functional difficulties, shared little with a matched group of typical CD patients. These patients likely require psychological as well as medical intervention to best manage their illness.     

Informed Consent

Summary

This article focuses on informed consent and the components to be reviewed with clients in the first session or as early as possible thereafter. Recent changes that give patients greater autonomy in the treatment process are also presented. The process of obtaining informed consent or informed refusal places a new responsibility on the practitioner. Informed consent as it pertains to clinical practice, supervision and training, and psychological research is also discussed.     

外科疾病的发热

发热是临床上的一种常见症状,引起发热的原因很多,只有找到发热的原因才能做出正确的处理。启动临床思维必须掌握充分的临床资料,然后进行周密的鉴别诊断思维程序,首先排除引起发热的其他科疾病,再考虑外科原因。感染是外科发热最主要的原因,如果是手术病人,特别应该想到和手术有关的各种感染问题。思维惯性、思维顺性和思维惰性的误导是误诊的思维原因。     

生命回顾疗法介入晚期癌症患者死亡恐惧的实践探索

聚焦晚期癌症患者死亡恐惧,分析比较生命回顾疗法的实际应用。基于临床服务案例,医务社工发现晚期癌症患者的死亡恐惧主要受躯体症状、疾病归因、家庭支持和心性支持四方面影响。医务社工通过运用生命回顾疗法对晚期癌症患者进行干预,依托建立早期良好专业关系、正视死亡恐惧、回顾重要生命事件、强化/修复重要关系、增强自我认同五大策略,赋予患者生命新的价值和希望,实现生命意义的整合,有效缓解个体死亡恐惧,改善末期生命质量。

     

患者参与医患共同决策的思考

医患共同决策克服了传统医疗决策模式的固有弊端,实现了“家长式决策模式”与“知情式决策模式”的有机结合,有利于做出最适合患者的医疗决策。然而,部分患者盲从医者权威、缺乏必要医学知识以及医患互信基础薄弱等现实问题,制约了患者对医疗决策的参与,阻碍了医患共同决策的推进。作为医疗决策的主体,患者有效参与能够促成医患双方相互理解、促进医患决策落实、纠正医患决策失误。破解医患共同决策实践难题,要将提升患者参与能力置于首位,开展面向社会公众的医学常识教育、发挥社会支持系统的正向作用、培育医患互信的现实基础。

     

右侧基底节损伤遗忘症患者的知觉性启动效应与语义性启动效应的分离与定位

采用偏好、自由联想、字根补笔和字辨认等４项任务观察一例单纯性右侧基底节损伤遗忘症患者和两组正常对照的启动效应。结果发现：（１）该患者知觉性启动效应障碍、而语义性启动效应正常。认为知觉性启动效应的神经学基础可能在基底节。（２）该患者知觉性启动效应与语义性启动效应分离。认为神经组织的损伤可导致不同形式启动效应的分解,提出内隐记忆或启动效应的不同形式可能存在不同的神经学基础。