This proposal constitutes the University of Utah Health Sciences Center's application for membership with the NICHD Stillbirth Research Network. The University of Utah Health Sciences Center has several unique strengths, which render it an ideal center for the network. These attributes include: L Research Productivity in Multicenter Collaborative Studies: The MFM (Maternal- Fetal Medicine) division has made substantial contributions to over 20 multicenter clinical trials during the past five years, including many with the NICHD/MFMU. Further, over 12,000 subjects from Utah were enrolled in the recently completed FASTER trial, thereby, accounting for almost 32% of subjects nationwide. H. Perinatal Autopsy: Dr. John M. Opitz is one of the leading authorities in the world on perinatal autopsy. The team also features expertise in neuropathology and placental pathology. III. Recurrent Pregnancy Loss: The University of Utah Health Sciences Center enjoys international recognition as a center of excellence for clinical care and research on pregnancy loss. The Reproductive Immunology Laboratory is renowned for antiphospholipid antibody testing, and has been a referral center for several multicenter trials. IV. Reproductive and Medical Genetics: Utah's distinct population has attracted numerous world-class geneticists to the University. State of the art molecular and clinical genetic capabilities will be made available to the network through several Laboratories. V. University / Community Synergy: MFM subspecialists in Utah enjoy a unique clinical and research partnership that crosses competing health care systems, thereby affording universal access to patients for clinical research. VI. University/Utah Department of Health Collaboration: An ongoing 25-year continuum of clinical and research collaboration characterize the relationship between the University and the Utah Department of Health. VII. Proven Enrollment Strategy: The """"""""Champion"""""""" system has resulted in close to 100% ascertainment for the Utah Birth Defect Network. This system will be adapted for the Stillbirth Network.
Freedman, Alexa A; Kipling, Lauren M; Labgold, Katie et al. (2018) Comparison of diameter-based and image-based measures of surface area from gross placental pathology for use in epidemiologic studies. Placenta 69:82-85 |
Angley, Meghan; Thorsten, Vanessa R; Drews-Botsch, Carolyn et al. (2018) Association of participation in a supplemental nutrition program with stillbirth by race, ethnicity, and maternal characteristics. BMC Pregnancy Childbirth 18:306 |
Gibbins, Karen J; Reddy, Uma M; Saade, George R et al. (2018) Smith-Lemli-Opitz Mutations in Unexplained Stillbirths. Am J Perinatol 35:936-939 |
Page, Jessica M; Thorsten, Vanessa; Reddy, Uma M et al. (2018) Potentially Preventable Stillbirth in a Diverse U.S. Cohort. Obstet Gynecol 131:336-343 |
Freedman, Alexa A; Cammack, Alison L; Temple, Jeff R et al. (2017) Maternal exposure to childhood maltreatment and risk of stillbirth. Ann Epidemiol 27:459-465.e2 |
Boyle, Annelee; Preslar, Jessica P; Hogue, Carol J R et al. (2017) Route of Delivery in Women With Stillbirth: Results From the Stillbirth Collaborative Research Network. Obstet Gynecol 129:693-698 |
Christiansen-Lindquist, Lauren; Silver, Robert M; Parker, Corette B et al. (2017) Fetal death certificate data quality: a tale of two U.S. counties. Ann Epidemiol 27:466-471.e2 |
Boyle, Annelee; Preslar, Jessica P; Hogue, Carol J R et al. (2017) Route of Delivery in Women With Stillbirth: Results From the Stillbirth Collaborative Research Network. Obstet Gynecol : |
Silver, Robert M; Saade, George R; Thorsten, Vanessa et al. (2016) Factor V Leiden, prothrombin G20210A, and methylene tetrahydrofolate reductase mutations and stillbirth: the Stillbirth Collaborative Research Network. Am J Obstet Gynecol 215:468.e1-468.e17 |
Gibbins, Karen J; Silver, Robert M; Pinar, Halit et al. (2016) Stillbirth, hypertensive disorders of pregnancy, and placental pathology. Placenta 43:61-8 |
Showing the most recent 10 out of 30 publications