Literature DB >> 4008590

Cooperative Study of Sickle Cell Disease: Demographic and socioeconomic characteristics of patients and families with sickle cell disease.

M D Farber, M Koshy, T R Kinney.   

Abstract

Socioeconomic data on 3538 black patients enrolled in the Cooperative Study of Sickle Cell Disease (CSSCD) from 1979 to 1981 are summarized and compared with the U.S. black population (USBP) where appropriate. The following contrasts between the patients and families with Sickle Cell Disease (SCD) and the USBP were found: family structure differed, with fewer two-parent families (40 vs 54%) and more single female heads-of-household (53 vs 42%) within the SCD population; of those employed, twice as many of the SCD patients of both sexes worked in white collar positions; a higher percentage of patients were unemployed and disabled; and male SCD patients had a lower median personal income than USBP males. Several similarities were also noted: the percentage of high school graduates was 71% for SCD patients and 75% for the USBP; female heads-of-household employed full time earned approximately the same salary as USBP females. These data will help health professionals who counsel SCD patients and their families.

Entities:  

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Year:  1985        PMID: 4008590     DOI: 10.1016/0021-9681(85)90033-5

Source DB:  PubMed          Journal:  J Chronic Dis        ISSN: 0021-9681


  29 in total

Review 1.  Environmental determinants of severity in sickle cell disease.

Authors:  Sanjay Tewari; Valentine Brousse; Frédéric B Piel; Stephan Menzel; David C Rees
Journal:  Haematologica       Date:  2015-09       Impact factor: 9.941

2.  Hospital utilization patterns and costs for adult sickle cell patients in Illinois.

Authors:  K Woods; T Karrison; M Koshy; A Patel; P Friedmann; C Cassel
Journal:  Public Health Rep       Date:  1997 Jan-Feb       Impact factor: 2.792

3.  Similar burden of type 2 diabetes among adult patients with sickle cell disease relative to African Americans in the U.S. population: a six-year population-based cohort analysis.

Authors:  Jifang Zhou; Jin Han; Edith A Nutescu; William L Galanter; Surrey M Walton; Victor R Gordeuk; Santosh L Saraf; Gregory S Calip
Journal:  Br J Haematol       Date:  2019-02-03       Impact factor: 6.998

4.  An erythroid enhancer of BCL11A subject to genetic variation determines fetal hemoglobin level.

Authors:  Daniel E Bauer; Sophia C Kamran; Samuel Lessard; Jian Xu; Yuko Fujiwara; Carrie Lin; Zhen Shao; Matthew C Canver; Elenoe C Smith; Luca Pinello; Peter J Sabo; Jeff Vierstra; Richard A Voit; Guo-Cheng Yuan; Matthew H Porteus; John A Stamatoyannopoulos; Guillaume Lettre; Stuart H Orkin
Journal:  Science       Date:  2013-10-11       Impact factor: 47.728

5.  Influence of single parenthood on cardiopulmonary function in pediatric patients with sickle cell anemia.

Authors:  Xu Zhang; Kiarri N Kershaw; Caterina P Minniti; Andrew Campbell; Sohail R Rana; Deepika S Darbari; Lori Luchtman-Jones; Craig Sable; Niti Dham; Gregory Ensing; Manuel Arteta; James G Taylor; Lewis L Hsu; Sergei Nekhai; Victor R Gordeuk
Journal:  Blood Adv       Date:  2020-07-28

6.  Daily Opioid Use Fluctuates as a Function of Pain, Catastrophizing, and Affect in Patients With Sickle Cell Disease: An Electronic Daily Diary Analysis.

Authors:  Patrick H Finan; C Patrick Carroll; Gyasi Moscou-Jackson; Marc O Martel; Claudia M Campbell; Alex Pressman; Joshua M Smyth; Jean-Michel Tremblay; Sophie M Lanzkron; Jennifer A Haythornthwaite
Journal:  J Pain       Date:  2017-09-21       Impact factor: 5.820

Review 7.  The search for genetic modifiers of disease severity in the β-hemoglobinopathies.

Authors:  Guillaume Lettre
Journal:  Cold Spring Harb Perspect Med       Date:  2012-10-01       Impact factor: 6.915

8.  DNA polymorphisms at the BCL11A, HBS1L-MYB, and beta-globin loci associate with fetal hemoglobin levels and pain crises in sickle cell disease.

Authors:  Guillaume Lettre; Vijay G Sankaran; Marcos André C Bezerra; Aderson S Araújo; Manuela Uda; Serena Sanna; Antonio Cao; David Schlessinger; Fernando F Costa; Joel N Hirschhorn; Stuart H Orkin
Journal:  Proc Natl Acad Sci U S A       Date:  2008-07-30       Impact factor: 11.205

9.  Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients.

Authors:  Geneviève Galarneau; Sean Coady; Melanie E Garrett; Neal Jeffries; Mona Puggal; Dina Paltoo; Karen Soldano; Antonio Guasch; Allison E Ashley-Koch; Marilyn J Telen; Abdullah Kutlar; Guillaume Lettre; George J Papanicolaou
Journal:  Blood       Date:  2013-05-29       Impact factor: 22.113

10.  A pilot study of parent education intervention improves early childhood development among toddlers with sickle cell disease.

Authors:  Melanie E Fields; Catherine Hoyt-Drazen; Regina Abel; Mark J Rodeghier; Janet M Yarboi; Bruce E Compas; Allison A King
Journal:  Pediatr Blood Cancer       Date:  2016-08-11       Impact factor: 3.167

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