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提供者视角下姑息治疗在左心发育不全综合征中的作用。

Provider perspective on the role of palliative care in hypoplastic left heart syndrome.

机构信息

School of Medicine, Oregon Health & Science University, Portland, OR, USA.

Bridges Palliative Care Program, Doernbecher Children's Hospital, Portland, OR, USA.

出版信息

Cardiol Young. 2020 Mar;30(3):377-382. doi: 10.1017/S1047951120000128.

Abstract

OBJECTIVE

Hypoplastic left heart syndrome is a single ventricle defect. While staged surgical palliative treatments have revolutionised care, patients with hypoplastic left heart syndrome continue to have significant morbidity and mortality. In 2017, the National Pediatric Cardiology Quality Improvement Collaborative recommended all single ventricle patients to receive a prenatal palliative care consult. This study aimed to elucidate provider perspectives on the implementation of prenatal palliative care consults for families expecting a child with hypoplastic left heart syndrome.

METHODS

An online survey was administered to obstetric and paediatric providers of relevant disciplines to assess their experience with palliative care involvement in hypoplastic left heart syndrome cases.

RESULTS

Nearly, all physicians (97%) and most registered nurses (79%) agreed that the initial palliative care consult for patients with hypoplastic left heart syndrome should occur during the prenatal period. Respondents also indicated that prenatal palliative care consults should also be offered in a variety of other CHD conditions. Participants believed positive aspects of this new referral protocol included an expanded support network for families, decreased family stress during the postnatal period, increased patient education about what to expect during the postnatal period, and continuity of care.

CONCLUSION

Multidisciplinary healthcare professionals believe that prenatal palliative care consults provide a variety of benefits for patients and families with hypoplastic left heart syndrome. Additional, multi-centre research is necessary to evaluate whether prenatal palliative care consults should become standard of care for families expecting a child with a single ventricle defect.

摘要

目的

左心发育不全综合征是一种单心室缺陷。虽然阶段性的外科姑息治疗已经彻底改变了治疗方法,但左心发育不全综合征患者仍有显著的发病率和死亡率。2017 年,国家儿科心脏病学质量改进合作组织建议所有单心室患者接受产前姑息治疗咨询。本研究旨在阐明提供者对为预期患有左心发育不全综合征的儿童的家庭实施产前姑息治疗咨询的看法。

方法

对相关学科的产科和儿科提供者进行了在线调查,以评估他们在左心发育不全综合征病例中参与姑息治疗的经验。

结果

几乎所有的医生(97%)和大多数注册护士(79%)都认为,左心发育不全综合征患者的初始姑息治疗咨询应在产前进行。受访者还表示,在各种其他 CHD 情况下也应提供产前姑息治疗咨询。参与者认为这一新的转介方案的积极方面包括为家庭提供更广泛的支持网络,减少产后期间的家庭压力,增加患者对产后期间预期的教育,以及连续性护理。

结论

多学科医疗保健专业人员认为,产前姑息治疗咨询为左心发育不全综合征患者及其家庭提供了多种益处。还需要进行更多的多中心研究,以评估产前姑息治疗咨询是否应成为期待患有单心室缺陷的儿童的家庭的标准护理。

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