小儿神经外科过渡护理评估:对患者和家长的单中心分析和调查。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC ACS Applied Electronic Materials Pub Date : 2024-08-01 DOI:10.3171/2024.5.FOCUS24232
Isabel Fernandes Arroteia, Florian Ebel, Maria Licci, Raphael Guzman, Jehuda Soleman
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引用次数: 0

摘要

目的:小儿神经外科的过渡护理对患者及其家长来说具有挑战性。与成人相比,神经系统受影响患者的特殊需求以及影响小儿神经外科患者的病症的独特性使得一个全面、有序的过渡过程对患者的健康和确保护理的连续性至关重要。目前,人们对患者在这方面的偏好和意见知之甚少。本研究旨在评估患者和家长对转院过程的期望和看法:作者回顾性地确定了在小儿神经外科接受手术的 16 至 30 岁患者。这些患者被分为两组:即将过渡的患者和已经过渡的患者。在后一组中确定了过渡模式。我们联系了符合条件的患者家长进行电话调查,并在可能的情况下纳入患者本人。调查使用了全国青少年健康促进联盟(National Alliance to Advance Adolescent Health)制定的 "学会过渡"(Got Transition)问卷的修订版:共纳入 34 名患者,并对患者及其家长进行了 44 次电话调查。采用了三种过渡模式,其中 7 名患者(41.2%)采用了持续照顾者模式,9 名患者(52.9%)采用了共同照顾者模式,1 名患者(5.9%)采用了专门诊所模式。在采用持续护理模式和专科门诊模式过渡的患者中,患者和家长的满意度最高:结论:儿童的神经外科病情与成人有很大不同,这给过渡护理带来了独特的挑战。持续护理模式已被证明能提供连续性护理,并能提高患者和家长的满意度。然而,家长和患者对过渡性护理的看法存在差异,家长通常更关注和需要详细信息。要减轻家庭和医疗机构的护理负担,实施结构合理、个性化的过渡流程至关重要。
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Assessment of transitional care in pediatric neurosurgery: a single-center analysis and survey of patients and parents.

Objective: Transitional care in pediatric neurosurgery is challenging for patients and their parents. The specific needs of neurologically affected patients and the unique characteristics of the pathologies affecting pediatric neurosurgical patients compared with adults make a comprehensive, well-organized transition process essential for patient well-being and ensuring continuity of care. Little is known about patients' preferences and opinions on this topic. This study aimed to assess the patients' and parents' expectations and perceptions of the transition process.

Methods: The authors retrospectively identified patients aged 16 to 30 years who underwent surgery in their pediatric neurosurgical department. The patients were divided into two groups: those about to transition and those who had already transitioned. Transition models were identified within the latter group. Parents of eligible patients were contacted for a telephone survey, and the patients themselves were included when possible. A modified version of the established Got Transition questionnaire from the National Alliance to Advance Adolescent Health was used.

Results: Thirty-four patients were included, and 44 telephone surveys were conducted with the patients and their parents. Three transition models were applied, with 7 patients (41.2%) transitioned using the continued caregiver model, 9 patients (52.9%) using the shared caregiver model, and 1 patient (5.9%) using the specialized clinic model. Patient and parent satisfaction was highest among the patients transitioned using the continued caregiver and specialized clinic models.

Conclusions: Neurosurgical conditions in children differ significantly from those in adults, creating unique transitional care challenges. The continuing caregiver model has been shown to provide continuity of care and high patient and parent satisfaction. However, there are differences in the perspectives of parents and patients regarding transitional care, with parents typically expressing greater concern and need for detailed information. Implementing a well-structured and individualized transition process is essential to reduce the caregiving burden on families and healthcare institutions.

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567
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