Rinke Michael L, Mikat-Stevens Natalie, Saul Robert, Driscoll Amy, Healy Jill, Tarini Beth A
Department of Pediatrics, Children's Hospital at Montefiore, Bronx, New York.
Am J Med Genet A. 2014 Feb;164A(2):449-55. doi: 10.1002/ajmg.a.36339. Epub 2013 Nov 19.
Given the integral role primary care pediatricians (PCPs) play in caring for children with genetic conditions, we aimed to identify current practices of PCPs regarding genetic patients, their attitudes toward genetic medical care and their choices regarding family history taking. We conducted an on-line survey of a national convenience sample of PCPs associated with the American Academy of Pediatrics' Quality Improvement Innovation Networks. Eighty-eight respondents (29% response rate) were included in the analysis. Seventy-four (86%) reported ordering genetic based tests three or less times annually. Eleven (13%) strongly agreed that they discuss with patients the potential risks, benefits, and limitations of genetic tests. Forty-three (49%) agreed or strongly agreed that they feel competent in providing healthcare to patients related to genetics and genomics. Perceived competence was not associated with more recent training (P = 0.29), number of genetic tests ordered annually (P = 0.84) or mean number of weekly patient encounters (P = 0.15). 100% of participants stated that taking a family history is important. 27 (31%) agreed or strongly agreed that they gather a minimum of a three-generation family history. Forty-one of the 63 participants with an electronic health record (65%) reported their system was fair or poor in its ability to easily capture a three-generation family history. PCPs interested in quality improvement reported variation in care practices for children with genetic diseases and a majority did not feel competent to provide genetic related healthcare. Research should focus on improving the care and diagnosis of children with genetic disorders and enhanced integration of genetic medicine into routine primary preventative care.
鉴于初级保健儿科医生(PCP)在照顾患有遗传疾病的儿童方面发挥着不可或缺的作用,我们旨在确定PCP对遗传疾病患者的当前诊疗实践、他们对遗传医疗护理的态度以及他们在家族史采集方面的选择。我们对与美国儿科学会质量改进创新网络相关的全国便利样本PCP进行了在线调查。88名受访者(回复率29%)纳入分析。74人(86%)报告每年进行基于基因的检测三次或更少。11人(13%)强烈同意他们会与患者讨论基因检测的潜在风险、益处和局限性。43人(49%)同意或强烈同意他们觉得自己有能力为与遗传学和基因组学相关的患者提供医疗保健。感知到的能力与最近的培训(P = 0.29)、每年订购的基因检测数量(P = 0.84)或每周平均患者诊疗次数(P = 0.15)无关。100%的参与者表示采集家族史很重要。27人(31%)同意或强烈同意他们至少采集三代家族史。63名拥有电子健康记录的参与者中有41人(65%)报告他们的系统在轻松获取三代家族史方面能力一般或较差。对质量改进感兴趣的PCP报告了遗传疾病儿童护理实践的差异,并且大多数人觉得自己没有能力提供与遗传相关的医疗保健。研究应专注于改善遗传疾病儿童的护理和诊断,并加强将遗传医学融入常规初级预防保健。