Jamieson Anne E, Fletcher Paula C, Schneider Margaret A
Department of Kinesiology & Physical Education, Wilfrid Laurier University, Waterloo, Ontario, Canada.
Clin Nurse Spec. 2007 May-Jun;21(3):152-60. doi: 10.1097/01.NUR.0000270015.97457.9c.
The overall objective of this investigation was to study the lived experience, in relation to diet, of women who have been diagnosed with Inflammatory Bowel Disease and/or Irritable Bowel Syndrome. This study specifically explored pre-illness and postdiagnosis dietary patterns of participants with an emphasis on the changes, if any, that participants had made to their diet.
This study took place on a university campus in southwestern Ontario, Canada. Eight women between the ages of 18 and 23 years were recruited. Participants completed a consent form, background questionnaire, and a 14-day food diary. Participant also engaged in one-on-one semistructured interviews that consisted of 8 open-ended questions aimed at gaining a thorough understanding of the lived experience of these women, with respect to their dietary practices.
The 3 major themes identified included: control; family and friend support; and adverse behaviors. The salient theme of control included the subthemes timing and awareness of surroundings, giving into temptations, and determination of diet. Determining one's diet, the subtheme that is addressed in this article, involved several key elements, including (1) the role of the physician(s), (2) experimentation, (3) seeking information, and (4) food modifications.
Diet was the primary behavioral factor manipulated by participants to manage their conditions. The determination of potential trigger foods/beverages, however, entailed an often frustrating process of trial and error, in which few of the women received assistance from primary healthcare professionals. As a result, many of the women sought dietary information from alternate sources, some of which may not provide reliable information. Through experimentation and, for some, the documentation of food intake and symptom production, all participants identified food/beverage items they believed to cause symptom development. Although similar items were identified by many, all participants had individual triggers and sensitivities.
本调查的总体目标是研究被诊断患有炎症性肠病和/或肠易激综合征的女性在饮食方面的生活经历。本研究特别探讨了参与者病前和确诊后的饮食模式,重点关注参与者在饮食方面所做的改变(如有)。
本研究在加拿大安大略省西南部的一所大学校园进行。招募了8名年龄在18至23岁之间的女性。参与者填写了同意书、背景问卷和一份为期14天的食物日记。参与者还参与了一对一的半结构化访谈,访谈包含8个开放式问题,旨在全面了解这些女性在饮食习惯方面的生活经历。
确定的3个主要主题包括:控制;家人和朋友的支持;以及不良行为。控制这一突出主题包括以下子主题:时间安排和对周围环境的意识、屈服于诱惑以及饮食的决定。本文所讨论的子主题——决定个人饮食,涉及几个关键要素,包括(1)医生的作用,(2)尝试,(3)寻求信息,以及(4)食物调整。
饮食是参与者用来控制自身病情的主要行为因素。然而,确定潜在的触发食物/饮料往往需要一个令人沮丧的反复试验过程,其中很少有女性得到初级医疗保健专业人员的帮助。因此,许多女性从其他渠道寻求饮食信息,其中一些渠道可能无法提供可靠信息。通过尝试,以及对一些人来说记录食物摄入和症状产生情况,所有参与者都确定了他们认为会导致症状出现的食物/饮料项目。尽管许多人确定了类似的项目,但所有参与者都有各自的触发因素和敏感点。