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父母对婴儿高级别膀胱输尿管反流治疗和结局的体验——VUR 管理拼图的一部分?

Parents' experiences of treatment and outcomes in high-grade vesicoureteral reflux in infants - One piece in the puzzle of VUR management?

机构信息

The Peadiatric Uronephrologic Center at the Department of Pediatric Surgery, Queen Silvia Children's Hospital, Gothenburg, Sweden; Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Sweden.

The Peadiatric Uronephrologic Center at the Department of Pediatric Surgery, Queen Silvia Children's Hospital, Gothenburg, Sweden; Department of Pediatrics, Institute of Clinical Sciences, Sahlgrenska Academy, University of Gothenburg, Sweden.

出版信息

J Pediatr Urol. 2024 Oct;20(5):939-947. doi: 10.1016/j.jpurol.2024.05.020. Epub 2024 May 31.

DOI:10.1016/j.jpurol.2024.05.020
PMID:38876891
Abstract

INTRODUCTION

Countless papers have been published regarding the management and clinical outcome of vesicoureteral reflux (VUR), still no active treatment has been proven superior to another, regarding preserving renal function. When considering comparable treatment alternatives, qualitative research is needed to understand the parents' perspectives and preferences.

OBJECTIVE

This study aims to describe the parents' experiences of infant high-grade VUR (hVUR) regarding continuous antibiotic prophylaxis (CAP), surgical intervention (SI), urinary tract infection (UTI) and renal damage.

MATERIALS AND METHODS

We performed four randomized, semi-structured focus groups (FG) with 19 parents to 15 children (aged 1,5-6 years). All children had been diagnosed with hVUR at <8 months of age and treated with CAP (all groups) and SI (two groups). Discussions were recorded, transcribed and analysed to content. The sample size for the FGs was based on category saturation, which was confirmed through comparison analysis in multiple FGs.

RESULTS

The FGs generated 2,897 parent-reported experiences, of which this study reports on 1,123, sorted into the abovementioned four themes and underlying categories. Negative experiences regarding CAP, such as stress regarding the daily intake and worries about long-term use and side effects, were abundant, whereas positive experiences were few. The experiences regarding SI were negatively affected by inadequate information and postoperative difficulties and positively by empathy, accurate information and adequate preparations. The increased risk of UTIs were described as a constant emotional stress causing restricted social activities, frequent visits to the hospital and challenges regarding urine-sampling. There was a common awareness of renal damage, but few experiences reflected any actual worry.

DISCUSSION

The daily struggle with medications and monitoring for symptoms, concerns of future antibiotic resistance and a parental preference of SI have been documented in previous studies. FG methodology effectively collects data from several participants during the same occasion, the goal being to generate discussions that enable researchers to see the world from the participants' perspective. Since the management of infants with hVUR is still under debate, qualitative research can remind of valuable patient and parent perspectives.

CONCLUSION

This study shows that CAP and the risk of UTI have non-negligible, everyday impact on family life, while renal damage seems of secondary importance. The concerns of surgical treatment are related to an isolated occasion, which can be optimized with proper care and improved preoperative preparations. Awareness of parents' experiences and preferences is helpful when managing children with hVUR.

摘要

简介

关于治疗和管理膀胱输尿管反流(VUR)的临床结果,已有不计其数的文献发表,但至今仍未找到一种治疗方法能在保护肾功能方面优于其他方法。在考虑类似的治疗选择时,需要进行定性研究以了解父母的观点和偏好。

目的

本研究旨在描述父母对婴儿高级别 VUR(hVUR)的经验,包括持续抗生素预防(CAP)、手术干预(SI)、尿路感染(UTI)和肾损伤。

材料和方法

我们对 19 名父母和 15 名年龄在 1.5-6 岁的儿童进行了 4 次随机半结构化焦点小组(FG)。所有儿童均在 8 个月龄以下被诊断为 hVUR,并接受 CAP(所有组)和 SI(两组)治疗。记录讨论内容并进行转录和分析。FG 的样本量基于类别饱和,通过在多个 FG 中进行比较分析来确认。

结果

FG 共生成 2897 个父母报告的经验,本研究报告了其中的 1123 个,分为上述四个主题和潜在类别。关于 CAP 的负面经验,如对日常摄入量的压力以及对长期使用和副作用的担忧,非常丰富,而正面经验却很少。关于 SI 的经验受到信息不足和术后困难的负面影响,而受到同理心、准确信息和充分准备的正面影响。UTI 风险增加被描述为持续的情绪压力,导致社交活动受限、频繁去医院就诊以及尿液采样方面的挑战。父母普遍意识到肾损伤,但很少有经验反映出实际的担忧。

讨论

在以前的研究中,已经记录了父母每天与药物抗争以及监测症状、对未来抗生素耐药性的担忧,以及对 SI 的偏好。FG 方法可以在同一时间从多个参与者收集数据,目的是进行讨论,使研究人员能够从参与者的角度看待世界。由于婴儿 hVUR 的管理仍存在争议,定性研究可以提醒人们注意有价值的患者和家长观点。

结论

本研究表明,CAP 和 UTI 的风险对家庭生活有不可忽视的日常影响,而肾损伤似乎次之。对手术治疗的担忧与孤立的事件有关,可以通过适当的护理和改进术前准备来优化。了解父母的经验和偏好有助于管理婴儿 hVUR。

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