Cogulu Ozgur, Ozkinay Ferda, Akin Haluk, Onay Huseyin, Karaca Emin, Durmaz Asude Alpman, Durmaz Burak, Aykut Ayca, Pariltay Erhan, Kirbiyik Ozgur, Gunduz Cumhur, Ozkinay Cihangir
Department of Medical Genetics, Ege University, Bornova, Izmir, Turkey.
J Genet Couns. 2011 Jun;20(3):287-93. doi: 10.1007/s10897-010-9342-9. Epub 2011 Jan 8.
A limited numbers of published studies evaluate the referral reasons for genetic counseling services in the literature. These studies are focused on prenatal genetic counseling services, in particular, prenatal diagnosis. In order to provide the most effective and helpful genetic counseling services, genetics professionals need adequate knowledge about the profile of individuals referred for these services. In addition, physicians need increased awareness of the nature of genetic issues in order to make appropriate referrals. This study was intended to provide a descriptive analysis of the referral reasons of patients that received genetic counseling at a genetics center in Izmir, Turkey during an 11-year period. A total of 8965 records generated between 1998 and 2008 from one genetic center (which consists of The Department of Medical Genetics and Division of Pediatric Genetics) were evaluated retrospectively. Of these, 6,258 involved referrals for prenatal reasons, and 2,707 involved referrals for postnatal reasons. Both prenatal and postnatal records were further classified into more specific categories of referral reasons. The most common reason for genetic counseling among the prenatal patients was advanced maternal age (42.0%), followed by high risk results on prenatal biochemical screening tests such as second trimester double test [(serum concentration of alphafetoprotein (AFP), beta-human chorionic gonadotropin (beta-HCG)], triple test (serum concentration of AFP, beta-HCG, oestriol) and integrated test (26.5%). The most common indications for postnatal patients were recurrent miscarriages (28.2%) and infertility (19.7%). A significant increase in number of specific categories of referrals for genetic counseling was observed for the last 3 years after the establishment of the Medical Genetics Department. These data provide useful information about the frequency of referrals to the genetics department, and the feasibility of genetic services. Organization of genetic services and systematic procedures for genetic counseling and genetic testing may improve the public's awareness of genetics and ensure a high standard of patient care.
文献中仅有少数已发表的研究评估了遗传咨询服务的转诊原因。这些研究主要聚焦于产前遗传咨询服务,尤其是产前诊断。为了提供最有效且有益的遗传咨询服务,遗传学专业人员需要充分了解转诊接受这些服务的个体情况。此外,医生需要增强对遗传问题本质的认识,以便进行恰当的转诊。本研究旨在对在土耳其伊兹密尔一家遗传中心接受遗传咨询的患者在11年期间的转诊原因进行描述性分析。回顾性评估了1998年至2008年期间来自一个遗传中心(包括医学遗传学系和儿科遗传学部门)的总共8965份记录。其中,6258份涉及产前转诊原因,2707份涉及产后转诊原因。产前和产后记录进一步被分类为更具体的转诊原因类别。产前患者进行遗传咨询的最常见原因是产妇年龄偏大(42.0%),其次是产前生化筛查试验结果高危,如孕中期二联试验[甲胎蛋白(AFP)、β-人绒毛膜促性腺激素(β-HCG)血清浓度]、三联试验(AFP、β-HCG、雌三醇血清浓度)和整合试验(26.5%)。产后患者最常见的指征是反复流产(28.2%)和不孕(19.7%)。医学遗传学系成立后的最后3年,遗传咨询特定转诊类别的数量显著增加。这些数据提供了关于转诊至遗传科的频率以及遗传服务可行性的有用信息。遗传服务的组织以及遗传咨询和基因检测的系统程序可能会提高公众对遗传学的认识,并确保高标准的患者护理。