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德国先天性心脏病患者的转变:一项全国性患者调查结果

Transition in Patients with Congenital Heart Disease in Germany: Results of a Nationwide Patient Survey.

作者信息

Helm Paul C, Kaemmerer Harald, Breithardt Günter, Sticker Elisabeth J, Keuchen Roland, Neidenbach Rhoia, Diller Gerhard-Paul, Tutarel Oktay, Bauer Ulrike M M

机构信息

National Register for Congenital Heart Defects, Berlin, Germany.

DZHK (German Centre for Cardiovascular Research), Berlin, Germany.

出版信息

Front Pediatr. 2017 May 19;5:115. doi: 10.3389/fped.2017.00115. eCollection 2017.

Abstract

BACKGROUND

A growing number of adults with congenital heart disease (ACHD) pose a particular challenge for health care systems across the world. Upon turning into 18 years, under the German national health care system, ACHD patients are required to switch from a pediatric to an adult cardiologist or an ACHD-certified provider. To date, reliable data investigating the treatment situation of ACHD patients in Germany are not available.

MATERIALS AND METHODS

An online survey was conducted in collaboration with patient organizations to address the life situation and the conditions of health care provision for ACHD patients in Germany. ACHD patients were recruited from the database of the National Register for Congenital Heart Defects (NRCHD) and informed about the survey email, websites, and social networks. A total of 1,828 ACHD patients (1,051 females) participated in this study. The mean age was 31.7 ± 11.7 years. Participants were surveyed about treating physicians and the institution mainly involved in the treatment of their CHD. In addition, participants were asked questions to assess the level of trust toward their treating physician and their familiarity with the term "ACHD-certified provider."

RESULTS

Among the surveyed patients, 25.4% stated that they attended a specific ACHD clinic at a heart center regularly, 32.7% were treated in a private practice setting by a pediatric cardiologist, 32.4% in a private practice (adult) cardiology setting, and 9.5% were treated by an "other physician." Only 24.4% of the male and 29.7% of the female ACHD patients were familiar with the term "ACHD-certified provider."

CONCLUSION

The transfer from pediatric cardiology to ACHD care requires further attention as many adult patients have not transferred to certified ACHD providers. The question of whether ACHD patients in Germany are offered consistent and adequate care should also be investigated in more detail. The answers regarding the ACHD certification are particularly disappointing and indicative of a large information gap and inadequate education in clinical practice.

摘要

背景

越来越多的先天性心脏病成年患者(ACHD)给全球医疗保健系统带来了特殊挑战。在德国国家医疗保健系统下,ACHD患者年满18岁后,需要从儿科心脏病专家转为成人心脏病专家或获得ACHD认证的医疗服务提供者。迄今为止,尚无可靠数据调查德国ACHD患者的治疗情况。

材料与方法

与患者组织合作开展了一项在线调查,以了解德国ACHD患者的生活状况和医疗保健条件。从先天性心脏病国家登记册(NRCHD)数据库中招募ACHD患者,并通过电子邮件、网站和社交网络告知他们该调查。共有1828名ACHD患者(1051名女性)参与了本研究。平均年龄为31.7±11.7岁。参与者接受了关于治疗医生以及主要参与其CHD治疗的机构的调查。此外,还向参与者提问以评估他们对治疗医生的信任程度以及他们对“ACHD认证医疗服务提供者”这一术语的熟悉程度。

结果

在接受调查的患者中,25.4%表示他们定期前往心脏中心的特定ACHD诊所就诊,32.7%在私人诊所由儿科心脏病专家治疗,32.4%在私人诊所(成人)心脏病科治疗,9.5%由“其他医生”治疗。只有24.4%的男性和29.7%的女性ACHD患者熟悉“ACHD认证医疗服务提供者”这一术语。

结论

由于许多成年患者尚未转至获得认证的ACHD医疗服务提供者处,从儿科心脏病学向ACHD护理的过渡需要进一步关注。德国ACHD患者是否获得一致且充分的护理这一问题也应进行更详细的调查。关于ACHD认证的回答尤其令人失望,表明存在很大的信息差距以及临床实践中教育不足的问题。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a88a/5437851/de2a3333f8dd/fped-05-00115-g001.jpg

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