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Perspectives about cyclic vomiting syndrome: Adult explanatory models.

机译:关于周期性呕吐综合征的观点:成人解释模型。

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摘要

Purpose: This study explored (a) CVS-related health experiences, (b) impact on relationships, employment, education, and leisure time as well as (c) responses to CVS-related treatments.;Background: Cyclic vomiting syndrome is a chronic gastrointestinal tract disorder affecting 3% to 14% of patients experiencing unexplained nausea and vomiting who were referred to health centers in the United States. Patients experience frequent cycles of severe nausea, vomiting, and abdominal pain placing them at risk for life-threatening health complications. These incapacitating episodes impact social, emotional, and physical health, however minimal research has focused on descriptions of illness perception, life impact, and response to treatment.;Methods: Purposive sampling was used in this phenomenological study to recruit 16 adults, 21 years or older with a diagnosis of CVS for more than one year. Data were collected electronically via Survey MonkeyRTM. Type-written data was analyzed using content analysis and constant comparison techniques. Demographic data, also collected electronically, was described using Excel.;Results: All 16 participants were Caucasian. Eleven were female and five were male. Participants ranged in age from 22 to 59 years at the time of the study. Six participants were classified as having pediatric-onset CVS and 10 were classified as having adult-onset CVS. Seven global themes emerged from the data: (a) perceived causes of cyclic vomiting syndrome, (b) triggers for CVS episodes, (c) onset of illness and symptoms of CVS, (d) understanding the chronic course of CVS, (e) impact on day-to-day life, (f) lack of health care provider knowledge, and (g) responses to CVS-related treatments. Participants discussed limited understanding of illness etiology. However, they revealed understanding CVS as a chronic and cyclic illness. Emphasis was placed on triggers for CVS, life impact, lack of health care provider knowledge leading to diagnostic delay, avoidance of care, and inappropriate treatment. Prophylactic, abortive, and self-management was discussed. Discussions of emotional impact highlight the need for multidisciplinary care to insure that physical as well as mental health issues are considered and addressed. Findings present the need for increased CVS awareness and education to improve health care, access, and quality of care.
机译:目的:本研究探讨了(a)与CVS相关的健康经历,(b)对人际关系,就业,教育和休闲时间的影响,以及(c)对与CVS相关的治疗的反应。;背景:循环呕吐综合征是一种慢性疾病胃肠道疾病影响到美国医疗中心的3%至14%的无法解释的恶心和呕吐患者。患者会经历频繁的恶心,呕吐和腹痛循环,使他们面临危及生命的健康并发症的风险。这些无行为能力的发作会影响社会,情感和身体健康,但是很少有研究集中在描述疾病的感知,生活影响和对治疗的反应上。方法:该现象学研究采用目的抽样,招募了16岁,21岁或16岁的成年人年长者诊断为CVS超过一年。通过Survey MonkeyRTM以电子方式收集数据。使用内容分析和常量比较技术分析了打字数据。使用Excel描述了也以电子方式收集的人口统计数据。结果:所有16位参与者均为白种人。女11人,男5人。在研究时,参与者的年龄从22岁到59岁不等。六名参与者被分类为患儿CVS,十名参与者被分类为患有成人CVS。从数据中发现了七个全球性主题:(a)周期性呕吐综合征的感知原因,(b)CVS发作的触发因素,(c)CVS的发病和症状发作,(d)了解CVS的慢性病程,(e)对日常生活的影响,(f)缺乏医疗保健提供者的知识,以及(g)对与CVS相关的治疗的反应。与会者讨论了对疾病病因的有限理解。但是,他们透露出将CVS理解为一种慢性和周期性疾病。重点放在引发CVS,影响生活,缺乏医疗保健提供者知识,导致诊断延迟,避免护理和不适当治疗等方面。讨论了预防,流产和自我管理。关于情感影响的讨论强调需要多学科的护理,以确保考虑并解决身体和心理健康问题。研究结果表明,需要提高CVS意识和教育水平,以改善医疗保健,获得机会和护理质量。

著录项

  • 作者

    Jensen, Ashley Dee Ann Rew.;

  • 作者单位

    University of Arkansas for Medical Sciences.;

  • 授予单位 University of Arkansas for Medical Sciences.;
  • 学科 Nursing.;Behavioral psychology.
  • 学位 Ph.D.
  • 年度 2014
  • 页码 115 p.
  • 总页数 115
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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