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首页> 外文期刊>European journal of cancer care >Cancer patients' opinions concerning post-treatment follow-up.
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Cancer patients' opinions concerning post-treatment follow-up.

机译:癌症患者对治疗后随访的意见。

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摘要

Cancer is one of the most serious and widespread diseases known. Statistics show that of about 4 million Norwegians, every third person will be afflicted by some form of cancer during one's lifetime. Around 20,000 Norwegians receive this diagnosis yearly. People who have cancer often indicate that they feel neglected after they have received the diagnosis and perhaps hospital treatment. This article describes a survey in which a questionnaire was employed to map the services and post-treatment care offered by county health services to cancer patients. The form was sent to 199 persons between the age of 18 and 70, all of whom had been diagnosed with cancer from 6 months to 3 years earlier. The questionnaire was addressed directly to the patients, and distributed by mail. Both the Regional Medical Ethics Committee and the Information Protection Agency gave their approval with respect to how the patients and control group were selected, and to the general procedures used in the project. Eighty-six questionnaires were filled out and returned, giving a response rate of 43%. Of those who returned the form, 44 were women and 42 were men. Their average age was 57 years. The majority of those who responded to the questionnaire had been diagnosed for cancer at least 2 years earlier. Of the responding patients, 49 persons said that they had been declared cured, 25 answered that they were still ill and 12 did not reply to this question. The survey results indicate that few services or training programmes had been offered to the patients after their treatment was completed. This conclusion is corroborated by a questionnaire filled out by doctors and administrative leaders in the home-nursing programme as part of the same project. The cancer patients had not been clearly informed whether they should contact the hospital or the health services in their home county if they needed assistance. The patients also expressed a desire for better information and a more systematic post-treatment programme, as well as clear guidelines delineating the specific areas of responsibility assigned to hospitals and the local public health services.
机译:癌症是已知的最严重和最普遍的疾病之一。统计数据显示,约有400万挪威人,一生中三分之一的人会遭受某种形式的癌症困扰。每年约有20,000挪威人接受此诊断。患有癌症的人通常表示接受诊断甚至住院治疗后会被忽略。本文介绍了一项调查,其中使用了调查表来绘制县卫生服务机构为癌症患者提供的服务和治疗后护理的地图。该表格已发送给18至70岁之间的199人,这些人在6个月至3年前被诊断出患有癌症。问卷直接发给患者,并通过邮件分发。区域医学伦理委员会和信息保护局都在如何选择患者和对照组以及项目中使用的一般程序方面给予了批准。填写并返回了86份问卷,答复率为43%。退回表格的人中,女性为44人,男性为42人。他们的平均年龄是57岁。回答问卷的大多数人至少在2年之前被诊断出患有癌症。在有反应的患者中,有49人说他们已经被宣布治愈,有25人回答说他们仍然生病,还有12人未回答这个问题。调查结果表明,在患者完成治疗后几乎没有为他们提供任何服务或培训计划。作为该项目的一部分,由家庭护理计划中的医生和行政领导填写的调查问卷证实了这一结论。没有明确告知癌症患者是否需要帮助,是否应该联系医院或家乡的医疗机构。患者还希望获得更好的信息和更系统的后处理方案,以及明确的指导方针,以明确分配给医院和当地公共卫生服务的具体责任领域。

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