{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,23]],"date-time":"2026-10-23T12:15:13Z","timestamp":1792757713335,"version":"4.5.0"},"reference-count":15,"publisher":"Wiley","issue":"2","license":[{"start":{"date-parts":[[2012,8,18]],"date-time":"2012-08-18T00:00:00Z","timestamp":1345248000000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Journal of Genetic Counseling"],"published-print":{"date-parts":[[2013,4]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>Our objective was to describe: 1) physicians\u2019 knowledge of whether genetic counseling is provided to parents of newborns with sickle cell trait (SCT) or who are cystic fibrosis carriers (CFC), and 2) the prevalence of genetic counseling provided by primary care physicians. We conducted a cross\u2010sectional descriptive survey of 600 randomly\u2010sampled Michigan\u2010based pediatricians and family physicians, assessing physician knowledge of where and whether genetic counseling is received by parents whose newborns are carriers. Chi\u2010squared testing determined associations between genetic counseling location and physician demographic characteristics. Our response rate was 62 %: 298 (84 %) provided infant well care (183 pediatricians, 115 family physicians). Most respondents were non\u2010Hispanic White (65 %). Virtually all physicians believed parents whose newborns are carriers of either SCT or CFC should receive some genetic counseling (from the physician and\/or another source), yet 20 % reported that parents of newborns with SCT did not receive counseling. Parents of infants with CFC received more counseling overall (92 % vs. 80 %; <jats:italic>p<\/jats:italic>\u2009&lt;\u20090.01) and were counseled more frequently by genetic counselors or specialty centers than parents of newborns with SCT (85 % vs. 60 %; <jats:italic>p<\/jats:italic>\u2009&lt;\u20090.01). Although physicians agreed that parents whose newborns are carriers should receive genetic counseling, fewer parents of newborns with SCT than with CFC received counseling from any source. This finding strongly suggests the need for further education and investigation of this apparent health disparity.<\/jats:p>","DOI":"10.1007\/s10897-012-9537-3","type":"journal-article","created":{"date-parts":[[2012,8,17]],"date-time":"2012-08-17T15:11:42Z","timestamp":1345216302000},"page":"218-225","source":"Crossref","is-referenced-by-count":10,"title":["Who Counsels Parents of Newborns Who Are Carriers of Sickle Cell Anemia or Cystic Fibrosis?"],"prefix":"10.1002","volume":"22","author":[{"given":"Kathryn L.","family":"Moseley","sequence":"first","affiliation":[{"name":"Department of Pediatrics and Communicable Diseases, Child Health Evaluation and Research Unit, Division of General Pediatrics, Mott Children's Hospital University of Michigan 300 N. Ingalls St. 6D21 Ann Arbor MI 48109 USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Samya Z.","family":"Nasr","sequence":"additional","affiliation":[{"name":"Department of Pediatrics and Communicable Diseases, Cystic Fibrosis Center, Division of Pediatric Pulmonology, Mott Children's Hospital University of Michigan Ann Arbor MI USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jane L.","family":"Schuette","sequence":"additional","affiliation":[{"name":"Division of Pediatric Genetics, Department of Pediatrics and Communicable Diseases, Mott Children's Hospital University of Michigan Ann Arbor MI USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrew D.","family":"Campbell","sequence":"additional","affiliation":[{"name":"Department of Pediatrics and Communicable Diseases, Pediatric Comprehensive Sickle Cell Program, Division of Pediatric Hematology\/Oncology, Mott Children's Hospital University of Michigan Ann Arbor MI USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2012,8,18]]},"reference":[{"key":"e_1_2_7_2_1","unstructured":"American College of Medical Genetics(2006).Newborn Screening ACT Sheet: Sickle Cell Carrier (Trait) (Hb AS)."},{"key":"e_1_2_7_3_1","unstructured":"American College of Medical Genetics. (2010).Newborn screening ACT sheet: [Elevated IRT +\/\u2010 DNA] Cystic Fibrosis."},{"key":"e_1_2_7_4_1","unstructured":"American Medical Association. (2012).Physician data resources: Physician masterfile.http:\/\/www.ama\u2010assn.org\/ama\/pub\/about\u2010ama\/physician\u2010data\u2010resources\/physician\u2010masterfile.page. Accessed March 13 2012."},{"issue":"13","key":"e_1_2_7_5_1","first-page":"1","article-title":"Newborn screening for cystic fibrosis:evaluation of benefits and risks and recommendations for state newborn screening programs","volume":"53","author":"Centers for Disease Control and Prevention","year":"2004","journal-title":"MMWR"},{"key":"e_1_2_7_6_1","doi-asserted-by":"publisher","DOI":"10.1056\/NEJM198709243171301"},{"key":"e_1_2_7_7_1","doi-asserted-by":"publisher","DOI":"10.1542\/peds.2006-1639"},{"key":"e_1_2_7_8_1","first-page":"2","volume-title":"Michigan Newborn Screening Follow\u2010Up Brief","author":"Kleyn M.","year":"2009"},{"key":"e_1_2_7_9_1","volume-title":"Sickle cell disease in Michigan in newborn screening follow\u2010up program","author":"Kleyn M.","year":"2009"},{"key":"e_1_2_7_10_1","doi-asserted-by":"publisher","DOI":"10.1002\/ppul.21318"},{"issue":"5","key":"e_1_2_7_11_1","first-page":"541","article-title":"Exercise\u2010induced death in sickle cell trait: role of aging, training, and deconditioning","volume":"28","author":"Le Gallais D.","year":"1996","journal-title":"Med Sci Sports Exerc"},{"issue":"3","key":"e_1_2_7_12_1","first-page":"300","article-title":"Sickle cell trait and sudden death\u2010bringing it home","volume":"99","author":"Mitchell B. L.","year":"2007","journal-title":"J Natl Med Assoc"},{"key":"e_1_2_7_13_1","unstructured":"National Collegiate Athletic Association. (2010).NCAA football rules committee 2009\u20132010 Point of Emphasis.http:\/\/www.ncaa.org\/wps\/portal\/ncaahome?WCM_GLOBAL_CONTEXT=\/ncaa\/ncaa\/academics+and+athletes\/personal+welfare\/health+and+safety\/football+point+of+emphasis+sickle+cell+trait. Accessed July 28 2010."},{"key":"e_1_2_7_14_1","unstructured":"National Institutes of Health; National Heart Lung and Blood Institute. (2002).The Management of Sickle Cell Disease(4ed.)."},{"key":"e_1_2_7_15_1","unstructured":"National Newborn Screening and Genetics Resource Center. (2010).National newborn screening status report.http:\/\/genes\u2010r\u2010us.uthscsa.edu\/nbsdisorders.htm. Accessed May 27 2010."},{"key":"e_1_2_7_16_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.amjmed.2008.12.020"}],"container-title":["Journal of Genetic Counseling"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/pdf\/10.1007\/s10897-012-9537-3","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,9,15]],"date-time":"2023-09-15T20:37:29Z","timestamp":1694810249000},"score":1,"resource":{"primary":{"URL":"https:\/\/onlinelibrary.wiley.com\/doi\/10.1007\/s10897-012-9537-3"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,8,18]]},"references-count":15,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2013,4]]}},"alternative-id":["10.1007\/s10897-012-9537-3"],"URL":"https:\/\/doi.org\/10.1007\/s10897-012-9537-3","archive":["Portico"],"relation":{},"ISSN":["1059-7700","1573-3599"],"issn-type":[{"value":"1059-7700","type":"print"},{"value":"1573-3599","type":"electronic"}],"subject":[],"published":{"date-parts":[[2012,8,18]]}}}