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儿童癌症幸存者长期随访护理的影响:一项系统综述。

The impact of long-term follow-up care for childhood cancer survivors: A systematic review.

作者信息

Signorelli Christina, Wakefield Claire E, Fardell Joanna E, Wallace W Hamish B, Robertson Eden G, McLoone Jordana K, Cohn Richard J

机构信息

Discipline of Paediatrics, School of Women's and Children's Health, UNSW Australia, Kensington, NSW, Australia; Kids Cancer Centre, Sydney Children's Hospital, NSW, Randwick, Australia.

Discipline of Paediatrics, School of Women's and Children's Health, UNSW Australia, Kensington, NSW, Australia; Kids Cancer Centre, Sydney Children's Hospital, NSW, Randwick, Australia.

出版信息

Crit Rev Oncol Hematol. 2017 Jun;114:131-138. doi: 10.1016/j.critrevonc.2017.04.007. Epub 2017 Apr 13.

Abstract

OBJECTIVES

Childhood cancer survivors are at risk of developing late treatment-related complications. In response, many hospitals worldwide have established follow-up clinics to monitor survivors as they age. However, there is limited evidence of the efficacy of these clinics in meeting the lifelong healthcare needs of survivors. In this review we collated evidence of the measurable impact of engagement in specialized survivorship care, on survivors' medical and psychosocial outcomes.

DESIGN

We conducted a systematic review according to PRISMA guidelines, and assessed the quality of included studies using 'QualSyst'.

DATA SOURCES

We screened 641 abstracts in Medline, Embase and CINAHL, yielding 9 eligible articles (N=5135 survivors).

ELIGIBILITY CRITERIA FOR SELECTING STUDIES

Articles were eligible if: participants were diagnosed with cancer prior to the age of 21; participants were classified as 'survivors' of childhood or adolescent cancer, usually defined as 5 years from diagnosis or 2 years from the end of treatment; studies evaluated the impact of engagement in long term follow-up (LTFU) care on medical, psychosocial or other outcomes in pediatric cancer survivors.

RESULTS

One article evaluated primary care physician-led follow-up and the remainder evaluated specialized survivorship clinics. Survivors attending follow-up care tended to demonstrate higher knowledge about their treatment and diagnosis (n=2), and had more accurate late effects risk perception (n=3). Attendees also engaged in increased more regular surveillance, had fewer emergency department visits/hospitalizations (n=1), and more late effects detected (n=3), than non-attendees.

CONCLUSIONS

There is a dearth of literature systematically evaluating the medical and psychosocial impact of follow-up care. Research suggests however, survivors engaged in follow-up care have better health and educational outcomes, highlighting the need for lifelong survivorship care and ongoing late effects education for survivors. Recalling survivors who become disengaged with follow-up care is also valuable, as their risk of treatment-related complications rises with age. Further systematic evaluation is urgently needed.

摘要

目的

儿童癌症幸存者有发生晚期治疗相关并发症的风险。作为应对措施,全球许多医院都设立了随访诊所,以便在幸存者成长过程中对其进行监测。然而,关于这些诊所满足幸存者终身医疗保健需求的效果,证据有限。在本综述中,我们整理了参与专门的幸存者护理对幸存者的医疗和心理社会结局产生可衡量影响的证据。

设计

我们根据PRISMA指南进行了系统综述,并使用“QualSyst”评估纳入研究的质量。

数据来源

我们在Medline、Embase和CINAHL中筛选了641篇摘要,得到9篇符合条件的文章(N = 5135名幸存者)。

选择研究的资格标准

如果文章符合以下条件则 eligible:参与者在21岁之前被诊断出患有癌症;参与者被归类为儿童或青少年癌症的“幸存者”,通常定义为自诊断起5年或自治疗结束起2年;研究评估了参与长期随访(LTFU)护理对儿科癌症幸存者的医疗、心理社会或其他结局的影响。

结果

一篇文章评估了由初级保健医生主导的随访,其余文章评估了专门的幸存者诊所。接受随访护理的幸存者往往对自己的治疗和诊断有更高的认知(n = 2),对晚期效应风险的认知更准确(n = 3)。与未参与者相比,参与者还进行了更定期的监测,急诊就诊/住院次数更少(n = 1),发现的晚期效应更多(n = 3)。

结论

系统评估随访护理的医疗和心理社会影响的文献匮乏。然而,研究表明,参与随访护理的幸存者有更好的健康和教育结局,这凸显了为幸存者提供终身幸存者护理和持续的晚期效应教育的必要性。召回与随访护理脱节的幸存者也很有价值,因为他们与治疗相关并发症的风险会随着年龄增长而上升。迫切需要进一步的系统评估。

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