围手术期预防青少年焦虑的非药物干预:范围审查方案。

Marcia Pestana-Santos, Margarida Reis Santos, Daniela Cardoso, Lurdes Lomba
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引用次数: 3

摘要

目的:本综述的目的是绘制围手术期用于预防青少年焦虑的非药物干预的范围。有证据表明,80%的青少年报告在围手术期经历过明显的焦虑。建议在围手术期实施非药物干预措施,以帮助控制青少年手术相关的预期、分离和围手术期焦虑和恐惧。纳入标准:本综述将纳入针对10 - 19岁接受过外科手术的青少年的研究,无论手术类型如何,并参与了旨在预防围手术期焦虑的非药物干预。干预可以由任何保健专业人员提供。与非手术住院相关的非药物干预相关的研究将被排除在外。方法:方法学将遵循JBI的范围审查建议。将考虑任何已发表和未发表的信息来源。以英语、西班牙语和葡萄牙语发表的研究将包括在内,不受地理或文化的限制。将删除重复的内容,两名独立审稿人将根据纳入标准筛选摘要并评估选定研究的全文。研究选择的结果将在系统评价和荟萃分析的首选报告项目(PRISMA)流程图中显示,用于范围评价。数据综合将以叙述性摘要的形式提出,以提供对现有证据的描述。
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Non-pharmacological interventions used during the perioperative period to prevent anxiety in adolescents: a scoping review protocol.

Objective: The objective of this review is to map the range of non-pharmacological interventions used during the perioperative period to prevent anxiety in adolescents.

Introduction: Evidence shows that 80% of adolescents report having experienced significant anxiety in the perioperative period. Non-pharmacological interventions implemented in the perioperative period are recommended as a resource to help to control anticipatory, separation and perioperative anxiety and fear related to surgical procedures in adolescents.

Inclusion criteria: This review will consider studies that focus on adolescents aged 10 to 19 who have undergone a surgical procedure, regardless of the type of surgery, and participated in non-pharmacological interventions aimed to prevent anxiety in the perioperative period. The intervention may be provided by any healthcare professional. Studies related to non-pharmacological interventions associated with hospitalization in a non-surgical context will be excluded.

Methods: The methodology will follow the JBI recommendations for scoping reviews. Any published and unpublished sources of information will be considered. Studies published in English, Spanish and Portuguese will be included, with no geographical or cultural limitations. Duplicates will be removed and two independent reviewers will screen the abstracts and assess the full text of selected studies, based on the inclusion criteria. The results of study selection will be presented in a Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) flow diagram for scoping reviews. Data synthesis will be presented in a narrative summary to provide a description of the existing evidence.

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