The Cincinnati Comprehensive Sickle Cell Center serves 185 children at the Children's Hospital Medical Center where the administrative core of the Center is located, and 190 adults at the University of Cincinnati Hospital. Integration of the two branches of the Center is facilitated by the proximity of the two hospitals. Four research projects draw upon the clinical resources for both the pediatric and adult patients with SCA: 1) a study relating intra- arterial sickling, red cells physiology and the regulation of fetal hemoglobin production to clinical severity; 2) a study of blood oxygenation and intra-arterial sickling during sleep; 3) a study of abnormalities of hemostatic mechanisms and endothelial integrity; 4) and patient compliance and ability to cope during transfer of care from childrens' to adults' program. Children only will be involved in an evaluation of nutrition and caloric needs and a study of the immune responses to pneumococcal antigens 3) or 4) Projects will employ recombinant DNA techniques to investigate the molecular mechanisms governing developmental regulation of the globin genes. Another project will entail introducing anti- sickling agents into red cells to affect therapy of the disease. A diagnostic program for newborns, that has been at the Center for twelve years, will be extended to the remainder of the state and affected children detected will be given prophylactic penicillin. Methodology will be established to assess the effectiveness of counseling, and patient and professional education in the Center.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Comprehensive Center (P60)
Project #
5P60HL015996-19
Application #
3108452
Study Section
Special Emphasis Panel (SRC (JB))
Project Start
1973-06-25
Project End
1993-03-31
Budget Start
1991-04-01
Budget End
1992-03-31
Support Year
19
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Cincinnati Children's Hospital Medical Center
Department
Type
DUNS #
071284913
City
Cincinnati
State
OH
Country
United States
Zip Code
45229
Graumlich, S E; Powers, S W; Byars, K C et al. (2001) Multidimensional assessment of pain in pediatric sickle cell disease. J Pediatr Psychol 26:203-14
Bellet, P S; Kalinyak, K A; Shukla, R et al. (1995) Incentive spirometry to prevent acute pulmonary complications in sickle cell diseases. N Engl J Med 333:699-703
Cotter, P D; Rucknagel, D L; Bishop, D F (1994) X-linked sideroblastic anemia: identification of the mutation in the erythroid-specific delta-aminolevulinate synthase gene (ALAS2) in the original family described by Cooley. Blood 84:3915-24
Johnson, K; Stastny, J F; Rucknagel, D L (1994) Fat embolism syndrome associated with asthma and sickle cell-beta(+)-thalassemia. Am J Hematol 46:354-7
Morris, C L; Rucknagel, D L; Joiner, C H (1993) Deoxygenation-induced changes in sickle cell-sickle cell adhesion. Blood 81:3138-45
Morris, C L; Gruppo, R A; Shukla, R et al. (1991) Influence of plasma and red cell factors on the rheologic properties of oxygenated sickle blood during clinical steady state. J Lab Clin Med 118:332-42
McConnell, M E; Daniels, S R; Lobel, J et al. (1989) Hemodynamic response to exercise in patients with sickle cell anemia. Pediatr Cardiol 10:141-4
Morris, C L; Rucknagel, D L; Shukla, R et al. (1989) Evaluation of the yield stress of normal blood as a function of fibrinogen concentration and hematocrit. Microvasc Res 37:323-38
Cyran, S E; James, F W; Daniels, S et al. (1988) Comparison of the cardiac output and stroke volume response to upright exercise in children with valvular and subvalvular aortic stenosis. J Am Coll Cardiol 11:651-8