Department of Pediatrics, McMaster University, Hamilton, Ontario, Canada.
Queen's University, 99 University Avenue, Kingston, Ontario, K7L 3N6, Canada.
BMC Med Educ. 2019 Jun 11;19(1):195. doi: 10.1186/s12909-019-1622-y.
The rapid expansion of genetic knowledge, and the implications for healthcare has resulted in an increased role for Primary Care Providers (PCPs) to incorporate genetics into their daily practice. The objective of this study was to explore the self-identified needs, including educational needs, of both urban and rural Primary Care Providers (PCPs) in order to provide genetic care to their patients.
Using a qualitative grounded theory approach, ten key informant interviews, and one urban and two rural PCP focus groups (FGs) (n = 19) were conducted. All PCPs practiced in Southeastern Ontario. Data was analyzed using a constant comparative method and thematic design. The data reported here represent a subset of a larger study.
Participants reported that PCPs have a responsibility to ensure patients receive genetic care. However, specific roles and responsibilities for that care were poorly defined. PCPs identified a need for further education and resources to enable them to provide care for individuals with genetic conditions. Based on the findings, a progressive stepped model that bridges primary and specialty genetic care was developed; the model ranged from PCPs identifying patients with genetic conditions that they could manage alone, to patients who they could manage with informal or electronic consultation to those who clearly required specialist referral.
PCPs identified a need to integrate genetics into primary care practice but they perceived barriers including a lack of knowledge and confidence, access to timely formal and informal consultation and clearly defined roles for themselves and specialists. To address gaps in PCP confidence in providing genetic care, interventions that are directed at accessible just-in-time support and consultation have the potential to empower PCPs to manage patients' genetic conditions. Specific attention to content, timing, and accessibility of educational interventions is critical to address the needs of both urban and rural PCPs. A progressive framework for bridging primary to specialty care through a 'stepped' model for providing continuing medical education, and genetic care can was developed and can be used to guide future design and delivery of educational interventions and resources.
遗传知识的快速扩展及其对医疗保健的影响,使得初级保健提供者(PCP)在日常实践中融入遗传学的角色不断增加。本研究的目的是探索城市和农村初级保健提供者(PCP)自我认同的需求,包括教育需求,以便为他们的患者提供遗传护理。
采用定性扎根理论方法,对 10 名关键知情人进行访谈,并对 1 个城市和 2 个农村 PCP 焦点小组(FG)(n=19)进行了访谈。所有 PCP 均在安大略省东南部执业。使用恒定比较方法和主题设计对数据进行分析。本报告的数据代表了一项更大研究的一个子集。
参与者报告说,PCP 有责任确保患者获得遗传护理。然而,这种护理的具体角色和责任尚未明确界定。PCP 认为需要进一步的教育和资源,使他们能够为患有遗传疾病的人提供护理。根据研究结果,开发了一种将初级保健和专科遗传护理联系起来的渐进式分步模型;该模型范围从 PCP 确定他们可以单独管理的具有遗传条件的患者,到他们可以通过非正式或电子咨询管理的患者,到那些显然需要专家转诊的患者。
PCP 确定需要将遗传学纳入初级保健实践,但他们认为存在障碍,包括知识和信心不足、及时获得正式和非正式咨询的机会有限以及为自己和专家明确角色。为了解决 PCP 在提供遗传护理方面信心不足的问题,针对即时支持和咨询的可访问干预措施有可能使 PCP 能够管理患者的遗传疾病。教育干预措施的内容、时间和可及性的具体关注对于满足城市和农村 PCP 的需求至关重要。通过提供继续医学教育和遗传护理的“分步”模型,建立了一种从初级保健到专科保健的渐进式框架,可以用来指导未来的教育干预措施和资源的设计和交付。