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针对囊性纤维化患者及其家庭的心理干预措施。

Psychological interventions for individuals with cystic fibrosis and their families.

作者信息

Goldbeck Lutz, Fidika Astrid, Herle Marion, Quittner Alexandra L

机构信息

Dptm. Child and Adolescent Psychiatry/Psychotherapy, University Clinic Ulm, Steinhoevelstr. 5, Ulm, Baden-Württemberg, Germany, D-89075.

出版信息

Cochrane Database Syst Rev. 2014 Jun 18;2014(6):CD003148. doi: 10.1002/14651858.CD003148.pub3.

Abstract

BACKGROUND

With increasing survival estimates for individuals with cystic fibrosis, long-term management has become an important focus. Psychological interventions are largely concerned with adherence to treatment, emotional and social adaptation and health-related quality of life. We are unaware of any relevant systematic reviews.

OBJECTIVES

To determine whether psychological interventions for people with cystic fibrosis provide significant psychosocial and physical benefits in addition to standard medical care.

SEARCH METHODS

Studies were identified from two Cochrane trials registers (Cystic Fibrosis and Genetic Disorders Group; Depression, Anxiety and Neurosis Group), Ovid MEDLINE and PsychINFO; unpublished trials were located through professional networks and Listserves. Most recent search of the Cystic Fibrosis and Genetic Disorders Group's register: 19 December 2013.Most recent search of the Depression, Anxiety and Neurosis Group's register: 12 November 2013.

SELECTION CRITERIA

Randomised controlled studies of a broad range of psychological interventions evaluating subjective and objective health outcomes, such as quality of life or pulmonary function, in individuals of all ages with cystic fibrosis and their immediate family. We were interested in psychological interventions, including psychological methods within the scope of psychotherapeutic or psychosomatic mechanism of action (e.g. cognitive behavioural, cognitive, family systems or systemic, psycho-dynamic, or other, e.g. supportive, relaxation, or biofeedback), which were aimed at improving psychological and psychosocial outcomes (e.g. quality of life, levels of stress or distress, psychopathology, etc.), adaptation to disease management and physiological outcomes.

DATA COLLECTION AND ANALYSIS

Three authors were involved in selecting the eligible studies and two of these authors assessed their risk of bias.

MAIN RESULTS

The review includes 16 studies (eight new studies included in this update) representing data from 556 participants. Studies are diverse in their design and their methods. They cover interventions with generic approaches, as well as interventions developed specifically to target disease-specific symptoms and problems in people with cystic fibrosis. These include cognitive behavioural interventions to improve adherence to nutrition or psychosocial adjustment, cognitive interventions to improve adherence or those associated with decision making in lung transplantation, a community-based support intervention and other interventions, such as self-hypnosis, respiratory muscle biofeedback, music therapy, dance and movement therapy, and a tele-medicine intervention to support patients awaiting transplantation.A substantial proportion of outcomes relate to adherence, changes in physical status or other specific treatment concerns during the chronic phase of the disease.There is some evidence that behavioural interventions targeting nutrition and growth in children (4 to 12 years) with cystic fibrosis are effective in the short term. Evidence was found that providing a structured decision-making tool for patients considering lung transplantation improves patients' knowledge of and expectations about the transplant, and reduces decisional conflict in the short term. One study about training in biofeedback-assisted breathing demonstrated some evidence that it improved some lung function measurements. Currently there is insufficient evidence for interventions aimed at other aspects of the disease process.

AUTHORS' CONCLUSIONS: Currently, insufficient evidence exists on psychological interventions or approaches to support people with cystic fibrosis and their caregivers, although some of the studies were promising. Due to the heterogeneity between studies, more of each type of intervention are needed to support preliminary evidence. Multicentre studies, with consequent funding implications, are needed to increase the sample size of these studies and enhance the statistical power and precision to detect important findings. In addition, multicentre studies could improve the generalisation of results by minimizing centre or therapist effects. Psychological interventions should be targeted to illness-specific symptoms or behaviours to demonstrate efficacy.

摘要

背景

随着囊性纤维化患者生存预估的增加,长期管理已成为重要关注点。心理干预主要涉及治疗依从性、情绪和社会适应以及健康相关生活质量。我们未发现任何相关的系统评价。

目的

确定针对囊性纤维化患者的心理干预除标准医疗护理外是否能带来显著的心理社会和身体益处。

检索方法

从两个Cochrane试验注册库(囊性纤维化和遗传疾病组;抑郁、焦虑和神经症组)、Ovid MEDLINE和PsychINFO中识别研究;通过专业网络和邮件列表找到未发表的试验。囊性纤维化和遗传疾病组注册库的最新检索时间:2013年12月19日。抑郁、焦虑和神经症组注册库的最新检索时间:2013年11月12日。

选择标准

对广泛心理干预进行的随机对照研究,评估所有年龄段囊性纤维化患者及其直系亲属的主观和客观健康结局,如生活质量或肺功能。我们感兴趣的心理干预包括心理治疗或心身作用机制范围内的心理方法(如认知行为、认知、家庭系统或系统、心理动力或其他,如支持性、放松或生物反馈),其旨在改善心理和心理社会结局(如生活质量、压力或痛苦水平、精神病理学等)、适应疾病管理和生理结局。

数据收集与分析

三位作者参与选择符合条件的研究,其中两位作者评估其偏倚风险。

主要结果

该评价纳入16项研究(本次更新纳入8项新研究),代表556名参与者的数据。研究在设计和方法上各不相同。它们涵盖通用方法的干预,以及专门针对囊性纤维化患者特定疾病症状和问题开发的干预。这些包括改善营养依从性或心理社会适应的认知行为干预、改善依从性或与肺移植决策相关的认知干预、基于社区的支持干预以及其他干预,如自我催眠、呼吸肌生物反馈、音乐治疗、舞蹈和运动治疗,以及支持等待移植患者的远程医疗干预。相当一部分结局与疾病慢性期的依从性、身体状况变化或其他特定治疗问题相关。有证据表明,针对4至12岁囊性纤维化儿童营养和生长的行为干预在短期内有效。有证据表明,为考虑肺移植的患者提供结构化决策工具可提高患者对移植的了解和期望,并在短期内减少决策冲突。一项关于生物反馈辅助呼吸训练的研究有证据表明其改善了一些肺功能指标。目前,针对疾病过程其他方面的干预证据不足。

作者结论

目前,关于支持囊性纤维化患者及其护理人员的心理干预或方法的证据不足,尽管一些研究很有前景。由于研究之间的异质性,需要更多每种类型的干预来支持初步证据。需要多中心研究(这会带来资金方面的影响)来增加这些研究的样本量,并提高检测重要发现的统计效力和精度。此外,多中心研究可通过最小化中心或治疗师效应来提高结果的普遍性。心理干预应针对特定疾病症状或行为以证明其有效性。

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