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囊性纤维化中心的过渡项目:团队成员的看法

Transition programs in cystic fibrosis centers: perceptions of team members.

作者信息

Flume Patrick A, Taylor Lloyd A, Anderson Deborah L, Gray Sue, Turner David

机构信息

Department of Medicine, Medical University of South Carolina, Charleston, South Carolina 29425, USA.

出版信息

Pediatr Pulmonol. 2004 Jan;37(1):4-7. doi: 10.1002/ppul.10391.

Abstract

We previously surveyed cystic fibrosis (CF) center directors and adult patients with CF to assess their perceptions regarding transition from a pediatric to an adult setting. An important finding in those studies was a lack of standard programs for transfer of young adults with CF from pediatric to adult care settings. Patients with CF typically receive care from clinics utilizing a multidisciplinary approach, suggesting that every member of the CF team can impact the transition process. Our purpose in this study was to gain an appreciation for various team members' perspectives on transition. An Internet survey was offered to all CF centers across the country to be completed by team members, excluding physicians. We received 291 completed surveys, nearly half completed by nurses, but our respondents included social workers, nutritionists, respiratory therapists, and a few team members with other training. Nearly half of the respondents work for both pediatric and adult teams. The majority of respondents (71.8%) reported that their adult patients receive care from an internist in a separate adult program, but nearly 20% reported that a pediatrician follows their adult patients. A minority thought that age (37.4% of respondents), marriage (16.2%), and pregnancy (27.1%) were criteria for transfer, though most (86.2%) suggested that patients should be transferred by age 21 years. Criteria precluding transfer included patient/family resistance (45%), disease severity (34%), and developmental delay (31.3%). It was uncommon (11.4%) for an introduction to the concept of transition at the time of diagnosis. Over one-half of patients did not meet the adult team until time of transfer. Team members' perceptions of patients' concerns were similar to what we had previously measured in physicians, again far greater than what we have measured in patients themselves. In many ways, what we have measured here in team members reflects what we have reported by physicians, demonstrating slow development of standard transition programs and an overestimate of patients' concerns regarding transition. These differences may impede the successful transition of patients into an adult program. It is clear from this study that team members have an interest in and opinions on transition, and are likely play a vital role in the transition process. Standard programs of transition should be developed, and team members should be engaged in that process.

摘要

我们之前对囊性纤维化(CF)中心主任和成年CF患者进行了调查,以评估他们对从儿科向成人医疗环境过渡的看法。这些研究中的一个重要发现是,缺乏将患有CF的年轻人从儿科护理环境转移到成人护理环境的标准项目。CF患者通常在采用多学科方法的诊所接受治疗,这表明CF团队的每个成员都可能影响过渡过程。我们进行这项研究的目的是了解团队各成员对过渡的看法。我们向全国所有CF中心提供了一项网络调查,由团队成员(不包括医生)完成。我们收到了291份完整的调查问卷,近一半是护士完成的,但我们的受访者还包括社会工作者、营养师、呼吸治疗师以及一些接受过其他培训的团队成员。近一半的受访者同时为儿科和成人团队工作。大多数受访者(71.8%)报告说,他们的成年患者在一个单独的成人项目中由内科医生提供治疗,但近20%的受访者报告说,他们的成年患者由儿科医生跟进。少数人认为年龄(37.4%的受访者)、婚姻状况(16.2%)和怀孕(27.1%)是转移的标准,不过大多数人(86.2%)建议患者应在21岁时转移。排除转移的标准包括患者/家属的抵触情绪(45%)、疾病严重程度(34%)和发育迟缓(31.3%)。在诊断时介绍过渡概念的情况并不常见(11.4%)。超过一半的患者在转移时才见到成人团队。团队成员对患者担忧的看法与我们之前在医生中测量的结果相似,再次远远超过我们在患者自身中测量的结果。在许多方面,我们在此处测量的团队成员的情况反映了我们在医生中报告的情况,表明标准过渡项目的发展缓慢,且对患者过渡担忧的估计过高。这些差异可能会阻碍患者成功过渡到成人项目。从这项研究中可以清楚地看出,团队成员对过渡感兴趣并持有相关意见,并且很可能在过渡过程中发挥至关重要的作用。应该制定标准的过渡项目,并且团队成员应该参与到这个过程中。

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