Rapid Access Scheduler: A Web-Based System for Direct Provider Scheduling to Pediatric Neurology.

IF 2.3 Q3 CLINICAL NEUROLOGY
Neurology. Clinical practice Pub Date : 2024-02-01 Epub Date: 2023-12-27 DOI:10.1212/CPJ.0000000000200233
Trevor Slater, Jacob Zimmerli, Gary R Nelson, Joshua L Bonkowsky
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引用次数: 0

Abstract

Purpose of review: Access to pediatric neurology care is limited, and outpatient waits can exceed 6 months. The referral process is often complex and burdensome. Our objective was to trial a program for scheduling access to pediatric neurology, to be controlled and accessed directly by outside providers.

Recent findings: We developed a web-based automated system, "Rapid Access Scheduler" (RASr), for direct scheduling by outside providers. RASr is built around a calendar view that allows the provider to see and reserve an available slot at the time of care. Once a slot is reserved, the scheduling team contacts the family to finalize scheduling.

Summary: The RASr system is a novel approach for facilitating pediatric neurology patient access through direct scheduling by outside providers using a web-based portal. Advantages of this include control and responsibility by outside providers, easy visibility of availability, and opportunity to inform patients and families at their point-of-care.

Rapid Access Scheduler:基于网络的系统,可直接为小儿神经科提供医疗服务。
审查目的:获得儿科神经病学治疗的机会有限,门诊病人的等待时间可能超过 6 个月。转诊过程通常既复杂又繁琐。我们的目标是试行一种可由外部医疗服务提供者直接控制和访问的儿科神经病学就诊时间安排程序:我们开发了一个基于网络的自动化系统 "快速就诊调度程序"(RASr),供外部医疗服务提供者直接安排就诊时间。RASr 以日历视图为基础,允许医疗服务提供者查看并预约护理时间段。小结:RASr 系统是一种新颖的方法,可通过外部医疗服务提供者使用基于网络的门户直接安排时间,方便儿科神经病学患者就诊。其优点包括由外部医疗服务提供者进行控制和负责,易于查看可用性,并有机会在患者和家属就诊时通知他们。
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来源期刊
Neurology. Clinical practice
Neurology. Clinical practice CLINICAL NEUROLOGY-
CiteScore
4.00
自引率
0.00%
发文量
77
期刊介绍: Neurology® Genetics is an online open access journal publishing peer-reviewed reports in the field of neurogenetics. The journal publishes original articles in all areas of neurogenetics including rare and common genetic variations, genotype-phenotype correlations, outlier phenotypes as a result of mutations in known disease genes, and genetic variations with a putative link to diseases. Articles include studies reporting on genetic disease risk, pharmacogenomics, and results of gene-based clinical trials (viral, ASO, etc.). Genetically engineered model systems are not a primary focus of Neurology® Genetics, but studies using model systems for treatment trials, including well-powered studies reporting negative results, are welcome.
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