{"id":256444,"date":"2013-12-27T05:42:11","date_gmt":"2013-12-27T10:42:11","guid":{"rendered":"http:\/\/www.eugenesis.com\/ann-arbor-study-many-pediatricians-uncomfortable-providing-care-to-kids-with-genetic-conditions\/"},"modified":"2013-12-27T05:42:11","modified_gmt":"2013-12-27T10:42:11","slug":"ann-arbor-study-many-pediatricians-uncomfortable-providing-care-to-kids-with-genetic-conditions-2","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/ann-arbor-study-many-pediatricians-uncomfortable-providing-care-to-kids-with-genetic-conditions-2.php","title":{"rendered":"ANN ARBOR: Study: Many pediatricians uncomfortable providing care to kids with genetic conditions"},"content":{"rendered":"<p><p>ANN ARBOR  Many primary care pediatricians say they feel  uncomfortable providing health care to patients with genetic  disorders. Also, many do not consistently discuss all risks and  benefits of genetic tests with patients, according to research  published recently in the American Journal of Medical Genetics.  <\/p>\n<p>    Investigators from the University of Michigans C.S. Mott    Childrens Hospital and The Childrens Hospital at Montefiore    (CHAM) conducted a national survey of 88 physicians who are    part of the American Academy of Pediatrics Quality Improvement    Innovation Networks, assessing their comfort level ordering    genetic tests for their pediatric patients, their attitudes    toward genetic medical care and their choices regarding taking    family histories. The majority of those physicians reported    ordering few genetic tests (three or less times) per year,    excluding newborn screening which is federally mandated for all    newborns; few (13 percent) strongly agreed that they discussed    the potential risks, benefits, and limitations of genetic tests    with all their patients and only half felt competent in    providing healthcare to patients with genetic disorders.  <\/p>\n<p>    While genetics has historically been viewed as a discipline    focused on rare conditions, recent genomic advances have    highlighted that genetics has a role in common conditions    encountered in primary care medicine, said Dr. Beth Tarini,    senior author, assistant professor of pediatrics, Child Health    Evaluation & Research (CHEAR) Unit, Division of General    Pediatrics, University of Michigan and co-medical director of    the Genetics in Primary Care Institute (GPCI), a project of the    American Academy of Pediatrics. Unfortunately, most PCPs    have received insufficient education and training about    genetics, which has left them uncertain about their role in    providing genetics related care.  <\/p>\n<p>    The study found that 100 percent of study participants stated    that taking a family history is important, but less than    one-third stated that they gather a minimum of a    three-generation family history, a basic component of a genetic    medical evaluation. Previous studies have shown that using    family history and genetic information greatly improved    outcomes for patients so researchers encourage patients to know    their family history and share this with their providers in    order to optimize their health care.  <\/p>\n<p>    PCPs play an integral role in caring for children with genetic    conditions and it is vital that they feel comfortable    identifying issues and providing comprehensive care to suit    their patients unique needs, said Dr. Michael L. Rinke, lead    author and assistant medical director for quality, CHAM, and    assistant professor of pediatrics at Albert Einstein College of    Medicine of Yeshiva University. Thousands of children in the    U.S. are diagnosed with genetic disorders annually and in order    to optimize outcomes for these patients early identification    and medical intervention is essential.  <\/p>\n<p>    The researchers say that robust education, increased access to    resources, improved electronic health records systems to    document family histories and rigorous quality improvement    efforts are key to enhancing integration of genetic medicine    into routine primary preventative care.  <\/p>\n<p>    Tarini says that the national Genetics in Primary Care    Institute Quality Improvement Project hopes to identify    effective strategies so that physicians who are at the    forefront of diagnosing and managing patients with genetic    disorders feel confident and competent in their abilities to    provide care for these patients.  <\/p>\n<p>    Investigators from the University of Michigans C.S. Mott    Childrens Hospital and The Childrens Hospital at Montefiore    (CHAM) conducted a national survey of 88 physicians who are    part of the American Academy of Pediatrics Quality Improvement    Innovation Networks, assessing their comfort level ordering    genetic tests for their pediatric patients, their attitudes    toward genetic medical care and their choices regarding taking    family histories. The majority of those physicians reported    ordering few genetic tests (three or less times) per year,    excluding newborn screening which is federally mandated for all    newborns; few (13 percent) strongly agreed that they discussed    the potential risks, benefits, and limitations of genetic tests    with all their patients and only half felt competent in    providing healthcare to patients with genetic disorders.  <\/p>\n<p>    While genetics has historically been viewed as a discipline    focused on rare conditions, recent genomic advances have    highlighted that genetics has a role in common conditions    encountered in primary care medicine, said Dr. Beth Tarini,    senior author, assistant professor of pediatrics, Child Health    Evaluation & Research (CHEAR) Unit, Division of General    Pediatrics, University of Michigan and co-medical director of    the Genetics in Primary Care Institute (GPCI), a project of the    American Academy of Pediatrics. Unfortunately, most PCPs    have received insufficient education and training about    genetics, which has left them uncertain about their role in    providing genetics related care.  <\/p>\n<p>    The study found that 100 percent of study participants stated    that taking a family history is important, but less than    one-third stated that they gather a minimum of a    three-generation family history, a basic component of a genetic    medical evaluation. Previous studies have shown that using    family history and genetic information greatly improved    outcomes for patients so researchers encourage patients to know    their family history and share this with their providers in    order to optimize their health care.  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Go here to see the original:<\/p>\n<p><a target=\"_blank\" href=\"http:\/\/heritage.com\/articles\/2013\/12\/26\/ann_arbor_journal\/news\/doc52b1de1a46ef0118410453.txt\" title=\"ANN ARBOR: Study: Many pediatricians uncomfortable providing care to kids with genetic conditions\">ANN ARBOR: Study: Many pediatricians uncomfortable providing care to kids with genetic conditions<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> ANN ARBOR Many primary care pediatricians say they feel uncomfortable providing health care to patients with genetic disorders. Also, many do not consistently discuss all risks and benefits of genetic tests with patients, according to research published recently in the American Journal of Medical Genetics. Investigators from the University of Michigans C.S.  <a href=\"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/genetic-medicine\/ann-arbor-study-many-pediatricians-uncomfortable-providing-care-to-kids-with-genetic-conditions-2.php\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":57,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"limit_modified_date":"","last_modified_date":"","_lmt_disableupdate":"","_lmt_disable":"","footnotes":""},"categories":[5],"tags":[],"class_list":["post-256444","post","type-post","status-publish","format-standard","hentry","category-genetic-medicine"],"modified_by":null,"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/256444"}],"collection":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/users\/57"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/comments?post=256444"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/posts\/256444\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/media?parent=256444"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/categories?post=256444"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/futurist-transhuman-news-blog\/wp-json\/wp\/v2\/tags?post=256444"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}