Houwink Elisa J F, Muijtjens Arno M M, van Teeffelen Sarah R, Henneman Lidewij, Rethans Jan Joost, Jacobi Florijn, van der Jagt Liesbeth, Stirbu Irina, van Luijk Scheltus J, Stumpel Connie T R M, Meijers-Heijboer Hanne E, van der Vleuten Cees, Cornel Martina C, Dinant Geert Jan
Department of Clinical Genetics, Section Community Genetics, EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, The Netherlands; School for Public Health and Primary Care, Department of Family Medicine, Maastricht University, Maastricht, The Netherlands.
Department of Educational Development and Research, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands.
PLoS One. 2015 Apr 2;10(4):e0122648. doi: 10.1371/journal.pone.0122648. eCollection 2015.
General practitioners (GPs) are increasingly called upon to identify patients at risk for hereditary cancers, and their genetic competencies need to be enhanced. This article gives an overview of a research project on how to build effective educational modules on genetics, assessed by randomized controlled trials (RCTs), reflecting the prioritized educational needs of primary care physicians. It also reports on an ongoing study to investigate long-term increase in genetic consultation skills (1-year follow-up) and interest in and satisfaction with a supportive website on genetics among GPs. Three oncogenetics modules were developed: an online Continuing Professional Development (G-eCPD) module, a live genetic CPD module, and a "GP and genetics" website (huisartsengenetica.nl) providing further genetics information applicable in daily practice. Three assessments to evaluate the effectiveness (1-year follow-up) of the oncogenetic modules were designed: 1.An online questionnaire on self-reported genetic competencies and changes in referral behaviour, 2.Referral rates from GPs to clinical genetics centres and 3.Satisfaction questionnaire and visitor count analytics of supportive genetics website. The setting was Primary care in the Netherlands and three groups of study participants were included in the reported studies:. Assessment 1. 168 GPs responded to an email invitation and were randomly assigned to an intervention or control group, evaluating the G-eCPD module (n = 80) or the live module (n = 88). Assessment 2. Referral rates by GPs were requested from the clinical genetics centres, in the northern and southern parts of the Netherlands (Amsterdam and Maastricht), for the two years before (2010 [n = 2510] and 2011 [n = 2940]) and the year after (2012 [n = 2875]) launch of the oncogenetics CPD modules and the website. Assessment 3. Participants of the website evaluation were all recruited online. When they visited the website during the month of February 2013, a pop-up invitation came up. Of the 1350 unique visitors that month, only 38 completed the online questionnaire. Main outcomes measure showed long-term (self-reported) genetic consultation skills (i.e. increased genetics awareness and referrals to clinical genetics centres) among GPs who participated in the oncogenetic training course, and interest in and satisfaction with the supportive website. 42 GPs (52%) who previously participated in the G-eCPD evaluation study and 50 GPs (57%) who participated in the live training programme responded to the online questionnaire on long-term effects of educational outcome. Previous RCTs showed that the genetics CPD modules achieved sustained improvement of oncogenetic knowledge and consultation skills (3-months follow-up). Participants of these RCTs reported being more aware of genetic problems long term; this was reported by 29 GPs (69%) and 46 GPs (92%) participating in the G-eCPD and live module evaluation studies, respectively (Chisquare test, p<0.005). One year later, 68% of the respondents attending the live training reported that they more frequently referred patients to the clinical genetics centres, compared to 29% of those who attended the online oncogenetics training (Chisquare test, p<0.0005). However, the clinical genetics centres reported no significant change in referral numbers one year after the training. Website visitor numbers increased, as did satisfaction, reflected in a 7.7 and 8.1 (out of 10) global rating of the website (by G-eCPD and live module participants, respectively). The page most often consulted was "family tree drawing". Self-perceived genetic consultation skills increased long-term and GPs were interested in and satisfied with the supportive website. Further studies are necessary to see whether the oncogenetics CPD modules result in more efficient referral. The results presented suggest we have provided a flexible and effective framework to meet the need for effective educational programmes for non-geneticist healthcare providers, enabling improvement of genetic medical care.
全科医生(GPs)越来越多地被要求识别有遗传性癌症风险的患者,他们的遗传能力需要得到提高。本文概述了一个研究项目,该项目旨在构建关于遗传学的有效教育模块,并通过随机对照试验(RCTs)进行评估,以反映初级保健医生的优先教育需求。它还报告了一项正在进行的研究,该研究旨在调查全科医生遗传咨询技能的长期提高情况(1年随访)以及他们对遗传学支持网站的兴趣和满意度。开发了三个肿瘤遗传学模块:一个在线继续职业发展(G-eCPD)模块、一个现场遗传继续职业发展模块和一个“全科医生与遗传学”网站(huisartsengenetica.nl),该网站提供适用于日常实践的进一步遗传学信息。设计了三项评估来评估肿瘤遗传学模块的有效性(1年随访):1.一份关于自我报告的遗传能力和转诊行为变化的在线问卷;2.全科医生向临床遗传学中心的转诊率;3.支持性遗传学网站的满意度问卷和访客计数分析。研究背景是荷兰的初级保健,报告的研究包括三组研究参与者:评估1。168名全科医生回复了电子邮件邀请,并被随机分配到干预组或对照组,分别评估G-eCPD模块(n = 80)或现场模块(n = 88)。评估2。要求荷兰北部和南部(阿姆斯特丹和马斯特里赫特)的临床遗传学中心提供全科医生在肿瘤遗传学继续职业发展模块和网站推出前两年(2010年[n = 2510]和2011年[n = 2940])以及推出后一年(2012年[n = 2875])的转诊率。评估3。网站评估的参与者均通过在线招募。当他们在2013年2月访问该网站时,会弹出邀请。当月的1350名独立访客中,只有38人完成了在线问卷。主要结果指标显示,参加肿瘤遗传学培训课程的全科医生具有长期(自我报告)的遗传咨询技能(即提高了遗传学意识并转诊至临床遗传学中心),以及对支持性网站的兴趣和满意度。42名曾参与G-eCPD评估研究的全科医生(52%)和50名参与现场培训计划的全科医生(57%)回复了关于教育成果长期影响的在线问卷。先前的随机对照试验表明,遗传学继续职业发展模块实现了肿瘤遗传学知识和咨询技能的持续提高(3个月随访)。这些随机对照试验的参与者报告称,长期来看对遗传问题的认识有所提高;参与G-eCPD和现场模块评估研究的分别有29名全科医生(69%)和46名全科医生(92%)报告了这一点(卡方检验,p<0.005)。一年后,参加现场培训的受访者中有68%报告称他们更频繁地将患者转诊至临床遗传学中心,而参加在线肿瘤遗传学培训的受访者中这一比例为29%(卡方检验,p<0.0005)。然而,临床遗传学中心报告称培训一年后转诊人数没有显著变化。网站访客数量增加,满意度也有所提高,网站的总体评分为7.7分和8.1分(满分10分)(分别由G-eCPD和现场模块参与者给出)。最常被访问的页面是“绘制家族树”。全科医生自我感知的遗传咨询技能长期提高,并且对支持性网站感兴趣且满意。有必要进行进一步研究,以确定肿瘤遗传学继续职业发展模块是否能带来更有效的转诊。所呈现的结果表明,我们提供了一个灵活有效的框架,以满足非遗传学家医疗保健提供者对有效教育计划的需求,从而改善遗传医疗服务。