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减充血治疗对早期乳腺癌相关手臂淋巴水肿女性患者手臂多余体积及以患者为中心的结局的临床疗效:一项系统评价

Clinical effectiveness of decongestive treatments on excess arm volume and patient-centered outcomes in women with early breast cancer-related arm lymphedema: a systematic review.

作者信息

Jeffs Eunice, Ream Emma, Taylor Cath, Bick Debra

机构信息

Florence Nightingale Faculty of Nursing and Midwifery, King's College London, London, United Kingdom.

The Nottingham Centre for Evidence Based Healthcare: a Joanna Briggs Institute Centre of Excellence.

出版信息

JBI Database System Rev Implement Rep. 2018 Feb;16(2):453-506. doi: 10.11124/JBISRIR-2016-003185.

Abstract

OBJECTIVE

To identify the effect of decongestive lymphedema treatment on excess arm volume or patient-centered outcomes in women presenting within either 12 months or a mean nine months of developing arm lymphedema following breast cancer treatment.

INTRODUCTION

Lymphedema is a common consequence of breast cancer treatment requiring life-long treatment to reduce symptoms and prevent complications. Currently, evidence to inform the optimal decongestive lymphedema treatment package is lacking.

INCLUSION CRITERIA

The review included studies on women who received lymphedema treatment within either 12 months or a mean of nine months of developing unilateral breast cancer-related arm lymphedema. The intervention was any decongestive lymphedema treatment delivered with the purpose of reducing arm lymphedema, compared to another form of lymphedema treatment (whether self or practitioner-administered), placebo or no treatment. The clinical outcome was excess arm volume; patient-centered outcomes were health-related quality of life, arm heaviness, arm function, patient-perceived benefit and satisfaction with treatment. Experimental study designs were eligible, including randomized and non-randomized controlled trials, quasi-experimental, prospective and retrospective before and after studies were considered.

METHODS

A three-step search strategy was utilized to find published and unpublished studies. The search identified studies published from the inception of each database to July 6, 2016. Reference lists were scanned to identify further eligible studies. Studies were critically appraised using appropriate standardized critical appraisal instruments from the Joanna Briggs Institute. Details describing each study and treatment results regarding outcomes of interest were extracted from papers included in the review using appropriate standardized data extraction tools from the Joanna Briggs Institute. Due to heterogeneity in included studies, results for similar outcome measures were not pooled in statistical meta-analysis. A narrative and tabular format was used to synthesize results from identified and included studies.

RESULTS

Seven studies reporting results for outcomes of interest were critically appraised and included in the review: five randomized controlled trials and two descriptive (uncontrolled) studies. Reported outcomes included excess arm volume (five studies), health-related quality of life (three studies), arm heaviness (one study), arm function (two studies) and patient-perceived benefit (two studies). There was some evidence that decongestive treatments were effective for women presenting within either 12 months or a mean of nine months of developing breast cancer-related arm lymphedema, but the wide range of data prevented comparison of treatment findings which limited our ability to answer the review questions.

CONCLUSIONS

Weak evidence (grade B) for the impact of decongestive lymphedema treatment on women with early lymphedema (i.e. less than 12 months duration of BCRL symptoms) did not allow any conclusions to be drawn about the most effective treatment to be offered when these women first present for treatment. Findings provided no justification to support change to current practice.Future primary research needs to focus on the most effective treatment for women when they first present with lymphedema symptoms, e.g. treatment provided within 12 months of developing symptoms. Studies should be adequately powered and recruit women exclusively with less than 12 months duration of breast cancer-related lymphedema symptoms, provide longer follow-up to monitor treatment effect over time, with comparable treatment protocols, outcome measures and reporting methods.

摘要

目的

确定消肿性淋巴水肿治疗对乳腺癌治疗后12个月内或平均9个月内出现手臂淋巴水肿的女性手臂多余体积或以患者为中心的结局的影响。

引言

淋巴水肿是乳腺癌治疗的常见后果,需要终身治疗以减轻症状并预防并发症。目前,缺乏为最佳消肿性淋巴水肿治疗方案提供依据的证据。

纳入标准

该综述纳入了对在单侧乳腺癌相关手臂淋巴水肿发生后12个月内或平均9个月内接受淋巴水肿治疗的女性的研究。干预措施为任何旨在减轻手臂淋巴水肿的消肿性淋巴水肿治疗,与另一种淋巴水肿治疗形式(无论是自我管理还是由从业者管理)、安慰剂或不治疗进行比较。临床结局为手臂多余体积;以患者为中心的结局为与健康相关的生活质量、手臂沉重感、手臂功能、患者感知的益处以及对治疗的满意度。符合条件的实验性研究设计,包括随机和非随机对照试验、准实验、前瞻性和回顾性前后对照研究。

方法

采用三步检索策略查找已发表和未发表的研究。检索确定了从每个数据库建立到2016年7月6日发表的研究。扫描参考文献列表以识别更多符合条件的研究。使用乔安娜·布里格斯研究所的适当标准化批判性评价工具对研究进行严格评价。使用乔安娜·布里格斯研究所的适当标准化数据提取工具从综述中纳入的论文中提取描述每项研究的详细信息以及关于感兴趣结局的治疗结果。由于纳入研究的异质性,相似结局指标的结果未进行统计荟萃分析。采用叙述性和表格形式综合已识别和纳入研究的结果。

结果

七项报告了感兴趣结局结果的研究经过严格评价并纳入综述:五项随机对照试验和两项描述性(非对照)研究。报告的结局包括手臂多余体积(五项研究)、与健康相关的生活质量(三项研究)、手臂沉重感(一项研究)、手臂功能(两项研究)和患者感知的益处(两项研究)。有一些证据表明,消肿性治疗对在乳腺癌相关手臂淋巴水肿发生后12个月内或平均9个月内出现症状的女性有效,但广泛的数据范围妨碍了对治疗结果的比较,这限制了我们回答综述问题的能力。

结论

关于消肿性淋巴水肿治疗对早期淋巴水肿(即BCRL症状持续时间少于12个月)女性的影响的证据薄弱(B级),无法就这些女性首次就诊时应提供的最有效治疗得出任何结论。研究结果没有理由支持改变当前的做法。未来的初级研究需要关注女性首次出现淋巴水肿症状时的最有效治疗,例如在症状出现后12个月内提供治疗。研究应具备足够的样本量,专门招募乳腺癌相关淋巴水肿症状持续时间少于12个月的女性,提供更长时间的随访以监测治疗效果随时间的变化,采用可比的治疗方案、结局指标和报告方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c7f6/5828398/4042eb879532/jbisris-16-453-g001.jpg

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