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Gatekeeper role of gastroenterologists and surgeons in recognising and discussing familial colorectal cancer

机译:肠胃科医生和外科医生在识别和讨论家族性结直肠癌中的关守作用

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This study aimed to gain insight into the gatekeeper role of surgeons and gastroenterologists (including residents) during a first consultation at a tertiary gastrointestinal centre regarding referral for genetic counselling, and to test the feasibility of a checklist for indications for referral. Consecutive patients were invited before and after introduction of a checklist, to complete a questionnaire assessing their perception of discussing cancer genetic topics. Initial consultations were audiotaped to assess the quality of this discussion by gastroenterologists and surgeons. Data on completeness of the checklist and referral were collected from medical files. No significant differences were found between the Before and After group regarding patients' reports of discussing cancer in the family (77 %, n = 34 vs 89 %, n = 33, p = 0.16). In 28 % (n = 10) of the audiotaped consultations family history was adequately discussed, in 58 % (n = 21) it was considered inadequate and in 14 % (n = 5) of consultations it was not discussed at all. A checklist was present in 53 % (n = 27) of the medical files. Of these, 5 (19 %) were incomplete. Gastroenterologists and surgeons (in training) have difficulty in fulfilling their gatekeeper role of recognizing patients at familial risk for CRC. Although they often discuss familial cancer during the initial consultation, their exploration seems insufficient to reveal indications for referral for genetic counselling. Therefore, healthcare professionals should not only understand genetics and the importance of cancer family history, but also be effective in the communication of this subject to enable more adequate referral of patients for genetic counselling.
机译:这项研究的目的是在第三级胃肠道中心就遗传咨询转诊进行首次咨询时,了解外科医生和胃肠病学家(包括居民)的看门人角色,并检验转诊指征清单的可行性。在引入检查表之前和之后邀请连续患者完成一份问卷,以评估他们对讨论癌症遗传主题的看法。胃肠病学家和外科医生对最初的咨询进行了录音,以评估讨论的质量。清单和转诊完整性的数据是从医疗档案中收集的。在患者家庭中讨论癌症的报告之间,前后组之间没有发现显着差异(77%,n = 34对89%,n = 33,p = 0.16)。在有音频录音的咨询中有28%(n = 10)进行了充分的讨论,在58%(n = 21)的咨询中被认为是不充分的,在有14%(n = 5)的咨询中根本没有讨论。 53%(n = 27)的医疗文件中存在检查清单。其中,5个(19%)不完整。胃肠病学家和外科医生(正在培训中)难以履行其看门人的角色,以识别患有家族性CRC风险的患者。尽管他们经常在初诊期间讨论家族性癌症,但他们的探索似乎不足以揭示转介遗传咨询的迹象。因此,医疗保健专业人员不仅应了解遗传学和癌症家族史的重要性,而且还应有效地沟通这一主题,以使患者能够更充分地接受遗传咨询。

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