首页> 外文期刊>Zeitschrift fur Gastroenterologie >Preference of patients with inflammatory bowel disease regarding information and shared decision-making: Results from a cross-sectional survey in germany [Zu welchen Themen wünschen Patientinnen und Patienten mit Morbus Crohn oder Colitis ulcerosa mehr Informationen und welche eigene Rolle bevorzugen sie bei medizinischen Behandlungsentscheidungen? Ergebnisse einer Betroffenenbefragung in Deutschland]
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Preference of patients with inflammatory bowel disease regarding information and shared decision-making: Results from a cross-sectional survey in germany [Zu welchen Themen wünschen Patientinnen und Patienten mit Morbus Crohn oder Colitis ulcerosa mehr Informationen und welche eigene Rolle bevorzugen sie bei medizinischen Behandlungsentscheidungen? Ergebnisse einer Betroffenenbefragung in Deutschland]

机译:炎症性肠病患者在信息和共享决策方面的偏爱:德国的一项横断面调查结果[克罗恩病或溃疡性结肠炎患者希望获得哪些信息,在医疗决策中他们希望扮演什么角色?对德国受影响者的调查结果]

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Background: Evidence-based and consented pathways for patients with inflammatory bowel diseases (IBD, Crohn's disease, ulcerative colitis) call for tailored education programmes to foster shared decision-making and patient self-management. Their preferences should be taken into account. Methods: In 2005 a cross-sectional postal questionnaire survey was conducted in different regions of Germany. Adult patients with ulcerative colitis (UC) or Crohn's disease (CD) were recruited from specialised gastroenterological practices, university outpatient clinics and the member registry of the relevant patient organisation DCCV. They returned a questionnaire including (inter)nationally established scales (e. g., HADS) as well as questions on their information needs, preferred information sources and their role in decision-making. Results: Data of 1056 responders could be analysed (65 % female; CD: 58 %; DCCV member: 71 %). The mean age of the patients was 42 (SD 12,8) years. Almost all patients wanted more information on "treatment alternativeso" (83 %), "causes of diseaseo" (80 %) and "what can I (still) do by myselfo" (79 %). 27 % of the patients asked for more information on 15 or more of overall 19 topics. The high information need was significantly associated with HADS potential depressive disorder (score > 8) and HADS probable anxiety disorder (score > 10). Most IBD patients (70 %) obviously regard their physicians as the most desirable source of information, 67 % prefer an active involvement in clinical decision-making. Conclusions: The data demonstrate high information needs of IBD patients and may serve in the planning of future educational programmes.
机译:背景:炎症性肠病(IBD,克罗恩病,溃疡性结肠炎)患者的循证途径和同意途径要求制定有针对性的教育计划,以促进共同的决策和患者自我管理。应该考虑他们的偏好。方法:2005年在德国不同地区进行了横断面邮政问卷调查。溃疡性结肠炎(UC)或克罗恩病(CD)的成年患者是从专门的胃肠病学实践,大学门诊和相关患者组织DCCV的成员注册表中招募的。他们返回了一份调查表,其中包括(国际)国家制定的量表(例如HADS)以及有关其信息需求,偏好的信息来源及其在决策中的作用的问题。结果:可以分析1056名应答者的数据(女性65%; CD:58%; DCCV成员:71%)。患者的平均年龄为42(SD 12,8)岁。几乎所有患者都希望获得有关“替代治疗”(83%),“病因”(80%)和“我自己还能做什么”(79%)的更多信息。 27%的患者要求获得有关19个主题中的15个或更多主题的更多信息。高度的信息需求与HADS潜在的抑郁症(得分> 8)和HADS可能的焦虑症(得分> 10)显着相关。显然,大多数IBD患者(70%)认为他们的医生是最理想的信息来源,67%的患者更愿意积极参与临床决策。结论:数据表明IBD患者对信息的需求很高,可能有助于未来教育计划的规划。

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