Zobrazeno 1 - 10
of 76
pro vyhledávání: '"Jane S Hankins"'
Autor:
Patrícia Moura, Emilia Matos do Nascimento, Delaine Fidlarczyk, Nickhill Bhakta, Jane Duran, Roberto Barbosa, Clarisse Lopes de Castro Lobo, Thais Oliveira Figueiredo, Jane S. Hankins
Publikováno v:
BMC Health Services Research, Vol 22, Iss 1, Pp 1-11 (2022)
BMC Health Services Research
BMC Health Services Research
Background: The costs associated with the treatment of sickle cell disease (SCD) are understudied in low and middle-income countries (LMIC), where resources are scarcer and policy decisions about resource allocation rely on detailed cost data. Few st
Publikováno v:
JAMA health forum. 2(10)
Importance Although considered a rare disease with fewer than 200 000 cases annually in the US, sickle cell disease (SCD) is the most common and clinically significant inherited blood disorder in the US and worldwide. Despite the relatively high prev
Autor:
Grace Champlin, Winfred C. Wang, Jeremie H. Estepp, Andrew M. Heitzer, Robert F. Davis, Kenneth I. Ataga, Jane S. Hankins, Curtis L. Owens, Guolian Kang, Scott N. Hwang, Allison A. King, Lisa M. Jacola, Juan Ding, Justin Newman
Publikováno v:
Exp Biol Med (Maywood)
Silent cerebral infarcts and arteriopathy are common and progressive in individuals with sickle cell anemia. However, most data describing brain lesions in sickle cell anemia are cross-sectional or derive from pediatric cohorts with short follow-up.
Autor:
Rhiannon R. Penkert, Melissa Azul, Robert E. Sealy, Bart G. Jones, Jola Dowdy, Randall T. Hayden, Li Tang, A. Catharine Ross, Jane S. Hankins, Julia L. Hurwitz
Publikováno v:
Nutrients; Volume 14; Issue 16; Pages: 3415
Human parvovirus B19 causes life-threatening anemia due to transient red cell aplasia (TRCA) in individuals with sickle cell disease (SCD). Children with SCD experiencing profound anemia during TRCA often require red blood cell transfusions and hospi
Autor:
Jason F. Goldberg, Vijaya M. Joshi, Rhiannon R. Penkert, Jane S. Hankins, Amber M Yates, Kenneth I. Ataga, Parul Rai, Victoria I Okhomina, Guolian Kang
Publikováno v:
Blood Adv
Elevated tricuspid regurgitant velocity (TRV) ≥2.5 m/s is a predictor of disease severity in adults and children with sickle cell anemia (SCA), but how disease-modifying therapies (DMTs) affect this biomarker is incompletely understood. We investig
Autor:
Mary Eapen, Ruta Brazauskas, Damiano Rondelli, Barbara Cappelli, Courtney D. Fitzhugh, Julie Kanter, Hai-Lin Wang, Jane S. Hankins, Julie A. Panepinto, John E. Wagner, Shalini Shenoy, Mark C. Walters, Eliane Gluckman, Graziana Maria Scigliuolo, John F. Tisdale, Joerg J Meerpohl, Annalisa Ruggeri
Publikováno v:
Blood
We developed a risk score to predict event-free survival (EFS) after allogeneic hematopoietic cell transplantation for sickle cell disease. The study population (n = 1425) was randomly split into training (n = 1070) and validation (n = 355) cohorts.
Autor:
Jeffrey D. Lebensburger, Kenneth I. Ataga, Guolian Kang, Rima S. Zahr, Jane S. Hankins, Winfred C. Wang, Jeremie H. Estepp, Jeffrey Gossett
Publikováno v:
Haematologica
Autor:
Patricia Adams-Graves, Adetola A. Kassim, Marsha Treadwell, Michael R. DeBaun, Robert M. Cronin, Jeannie Byrd, Manshu Yang, Karen Kalinyak, Jane S. Hankins, Alexis A. Thompson, Brandi Pernell
Publikováno v:
Hematology (Amsterdam, Netherlands), vol 25, iss 1
Hematology
Hematology
Objective: To test the hypothesis that caregivers' or adult participants' low ratings of provider communication are associated with more hospital admissions among adults and children with sickle cell disease (SCD), respectively. Secondarily, we deter
Autor:
Vikki G. Nolan, Matthew P. Smeltzer, Jane S. Hankins, Lisa M. Klesges, William O. Cooper, Joacy G. Mathias, Sherif M Badawy
Publikováno v:
JAMA Network Open
During transition from pediatrics to adult health care, young adults with sickle cell disease (SCD) face increased risk of severe morbidities and premature mortality.1 Sickle cell disease complications can be mitigated with hydroxyurea use.2 However,
Autor:
Vijaya M. Joshi, Tisha Mentnech, Nicholas S Whipple, Ronak J. Naik, Mary M McFarland, Jane S. Hankins, Vikki G. Nolan
Publikováno v:
Pediatr Blood Cancer
Cardiac disease is the primary cause of death in sickle cell disease (SCD). Cardiac abnormalities begin in childhood and progress throughout life. Right and left ventricular (RV, LV) myocardial strain are early markers of systolic dysfunction but are