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一项关于初级保健医生对罕见或复杂病症儿童与专科医生共同管理的偏好的调查。

A survey of the preferences of primary care physicians regarding the comanagement with specialists of children with rare or complex conditions.

作者信息

McClain Monica R, Cooley W Carl, Keirns Tracy, Smith Andrew

机构信息

1University of New Hampshire, Durham, NH, USA.

出版信息

Clin Pediatr (Phila). 2014 Jun;53(6):566-70. doi: 10.1177/0009922814528035. Epub 2014 Mar 25.

Abstract

OBJECTIVES

To assess primary care pediatric providers' comfort with co-managing patients with rare conditions.

METHODS

A survey was sent via an electronic link to pediatricians and family practitioners. Chi-square test of significance and Fisher's exact test were used for categorical variable comparisons and the Student's t test was used for continuous variable comparisons.

RESULTS

Most of the providers believed that care decisions are most frequently made by the specialist with consultation with the primary care clinician. The most common source of information is direct communication from the specialist. The most effective tool to increase clarity and comfort about provider roles was an active care plan identifying current care needs, who will act on the plan, and when the action should be completed.

CONCLUSIONS

Coordinated co-management in which caregiving roles are explicitly defined and tools are available for the timely exchange of information among all key participants warrants further study.

摘要

目的

评估初级保健儿科医疗服务提供者对共同管理罕见病患者的接受程度。

方法

通过电子链接向儿科医生和家庭医生发送调查问卷。采用卡方显著性检验和费舍尔精确检验进行分类变量比较,采用学生t检验进行连续变量比较。

结果

大多数医疗服务提供者认为,护理决策通常由专科医生在咨询初级保健临床医生后做出。最常见的信息来源是专科医生的直接沟通。提高对医疗服务提供者角色的清晰度和接受度的最有效工具是一份积极的护理计划,该计划明确当前的护理需求、谁将执行该计划以及何时应完成行动。

结论

明确界定护理角色并为所有关键参与者提供及时信息交流工具的协调共同管理值得进一步研究。

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