新生儿食管闭锁-气管食管瘘的症状负担经验:一项美国焦点小组研究。

IF 3.5 2区 医学 Q2 GENETICS & HEREDITY
Michaela Dellenmark-Blom, John Bennett, Rosella Micalizzi, Lianne Cole, Kaylee Woods, Lauren Cardoni, Leah Frain, Abdimajid Mohamed, Jessica Yasuda, Peter Ngo, Anke Widenmann, Graham Slater, Benjamin Zendejas
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引用次数: 0

摘要

背景:出生时患有食管闭锁-气管食管瘘(EA-TEF)的儿童可能会出现气消化疾病,影响他们的生活质量,并可能持续到成年。减轻他们的症状负担需要彻底了解儿童在生命早期的症状经历。我们的目的是探讨父母在患有EA-TEF的孩子出生后最初几年的空气消化症状负担的经历。这一探索还旨在帮助确定是否需要对症状负担进行疾病特异性测量。方法:采用5个标准化焦点小组(FGs),对22名在美国某三级儿科外科中心治疗的6个月~ 7岁EA-TEF患儿的家长进行调查,探讨患儿的症状体验。对FGs进行录音、转录、内容分析,以了解所表达的症状,以及所述的频率、严重程度和与儿童痛苦的关系。结果:22位家长对其孩子的气消化症状经历进行了450次独特陈述。呼吸道症状(n = 170份陈述,n = 21名家长)包括以下独特的症状表达:呼吸困难(n = 21),呼吸声(n = 6),咳嗽(n = 17),粘液问题(n = 22),容易发生频繁或严重的呼吸道感染(n = 20)和身体能力/力量下降(n = 8)。消化系统症状(181份陈述,n = 21名家长)包括胃酸反流/胃灼热(n = 7)、打嗝(n = 1)、恶心(n = 2)、胃酸反流/食物上涌(n = 10)、胃病(n = 4)、吞咽困难(n = 24)和呕吐/呕吐(n = 6)。呼吸道和消化道症状经历的描述包括症状频率、严重程度和儿童窘迫的变化。此外,喂养困难(99份陈述,n = 22名家长)包括儿童拒食(n = 8)、需要调整用餐时间(n = 7)、选择性/限制性进食(n = 14)和喂食时的不安/压力(n = 10)。大多数家长(n = 20,91%)描述他们的孩子有症状经历,涵盖所有三类(呼吸和消化症状,喂养困难)。结论:出生时患有EA-TEF的幼儿存在显著的症状负担,除了喂养困难外,还可以反映为呼吸和消化症状频率、严重程度和窘迫等维度的总结性复合。这支持了对症状负担进行疾病特异性测量的必要性,该测量由直接从父母描述中获得的内容和措辞指导,以帮助建立其内容效度。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Experiences of symptom burden among young children born with esophageal atresia-tracheoesophageal fistula: a US focus group study.

Experiences of symptom burden among young children born with esophageal atresia-tracheoesophageal fistula: a US focus group study.

Experiences of symptom burden among young children born with esophageal atresia-tracheoesophageal fistula: a US focus group study.

Experiences of symptom burden among young children born with esophageal atresia-tracheoesophageal fistula: a US focus group study.

Background: Children born with esophageal atresia-tracheoesophageal fistula (EA-TEF) can suffer from aerodigestive morbidity that impairs their quality of life and can persist into adulthood. Ameliorating their symptom burden requires a thorough understanding of the symptom experiences that children have early in life. We aimed to explore parents' experiences of their children's aerodigestive symptom burden during the first years of life after being born with EA-TEF. This exploration also aimed to help determine whether a disease-specific measurement of symptom burden is needed.

Method: Five standardized focus groups (FGs) with 22 parents of children with EA-TEF aged 6 months-7 years treated at a US tertiary pediatric surgical center were used to explore the children's symptom experiences. The FGs were audio-recorded, transcribed, content analyzed into what symptoms were expressed, together with their stated frequency, severity and relation to child distress.

Results: Twenty-two parents made 450 unique statements about their children's aerodigestive symptom experiences. The respiratory symptoms (n = 170 statements, n = 21 parents) included the following unique symptom expressions; Breathing difficulties (n = 21), Breathing sounds (n = 6), Cough (n = 17), Mucus problems (n = 22), Prone to frequent or severe respiratory infections (n = 20) and Reduced physical capacity/strength (n = 8). The digestive symptoms (181 statements, n = 21 parents) encompassed symptom expressions of Acid reflux/heartburn (n = 7), Hiccups (n = 1), Nausea (n = 2), Reflux/food coming up (n = 10), Stomach problems (n = 4), Swallowing difficulties (n = 24) and Vomiting/throw-up (n = 6). The descriptions of respiratory and digestive symptom experiences included a variation of symptom frequency, severity and child distress. Furthermore, feeding difficulties (99 statements, n = 22 parents) included the children's Food refusal (n = 8), Need for mealtime adjustment (n = 7), Selective/restrictive eating (n = 14) and Upset/stress with feeds (n = 10). Most parents (n = 20, 91%) described that their children had symptom experiences that spanned all three categories (respiratory and digestive symptoms, feeding difficulties).

Conclusions: Young children born with EA-TEF experience a significant symptom burden that can be reflected as a summative composite of the dimensions respiratory and digestive symptom frequency, severity and distress, in addition to feeding difficulties. This supports the need for a disease-specific measurement of symptom burden that is guided by the content and wording obtained directly from the parents' descriptions to help establish its content validity.

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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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