Literature DB >> 19829150

Decision analysis of treatment strategies in children with severe sickle cell disease.

Sarah H O'Brien1, Jane S Hankins.   

Abstract

We designed a decision analysis model comparing 4 treatment strategies for severe sickle cell disease: no intervention, hydroxyurea (HU), chronic transfusion, or stem cell transplant (SCT). The treatment strategy associated with the highest average utility (quality of life) was SCT (0.85). Average utilities for no treatment, chronic transfusion, and HU were 0.68, 0.71, and 0.80, respectively. Our model was quite sensitive to quality-of-life estimates, indicating that a true comparison of HU and transplantation cannot occur until investigators directly measure the health-related quality of life in children with sickle cell disease during HU therapy and after SCT.

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Year:  2009        PMID: 19829150      PMCID: PMC4486015          DOI: 10.1097/MPH.0b013e3181b83cab

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  30 in total

1.  Myocardial iron loading in transfusion-dependent thalassemia and sickle cell disease.

Authors:  John C Wood; J Michael Tyszka; Susan Carson; Marvin D Nelson; Thomas D Coates
Journal:  Blood       Date:  2003-11-20       Impact factor: 22.113

2.  Hydroxyurea therapy for diverse pediatric populations with sickle cell disease.

Authors:  Z R Rogers
Journal:  Semin Hematol       Date:  1997-07       Impact factor: 3.851

3.  Bone marrow transplantation versus periodic prophylactic blood transfusion in sickle cell patients at high risk of ischemic stroke: a decision analysis.

Authors:  P J Nietert; M R Abboud; M D Silverstein; S M Jackson
Journal:  Blood       Date:  2000-05-15       Impact factor: 22.113

4.  Long-term hydroxyurea therapy for infants with sickle cell anemia: the HUSOFT extension study.

Authors:  Jane S Hankins; Russell E Ware; Zora R Rogers; Lynn W Wynn; Peter A Lane; J Paul Scott; Winfred C Wang
Journal:  Blood       Date:  2005-10-01       Impact factor: 22.113

5.  Impact of chronic transfusion on incidence of pain and acute chest syndrome during the Stroke Prevention Trial (STOP) in sickle-cell anemia.

Authors:  S T Miller; E Wright; M Abboud; B Berman; B Files; C D Scher; L Styles; R J Adams
Journal:  J Pediatr       Date:  2001-12       Impact factor: 4.406

6.  Severity of iron overload in patients with sickle cell disease receiving chronic red blood cell transfusion therapy.

Authors:  P Harmatz; E Butensky; K Quirolo; R Williams; L Ferrell; T Moyer; D Golden; L Neumayr; E Vichinsky
Journal:  Blood       Date:  2000-07-01       Impact factor: 22.113

7.  Chronic transfusion therapy for children with sickle cell disease and recurrent acute chest syndrome.

Authors:  Jane Hankins; Michael Jeng; Sylvia Harris; Chin-Shang Li; Tiebin Liu; Winfred Wang
Journal:  J Pediatr Hematol Oncol       Date:  2005-03       Impact factor: 1.289

8.  Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial.

Authors:  A Ferster; C Vermylen; G Cornu; M Buyse; F Corazza; C Devalck; P Fondu; M Toppet; E Sariban
Journal:  Blood       Date:  1996-09-15       Impact factor: 22.113

9.  Clinical and hematologic effects of hydroxyurea in children with sickle cell anemia.

Authors:  S Jayabose; O Tugal; C Sandoval; P Patel; D Puder; T Lin; P Visintainer
Journal:  J Pediatr       Date:  1996-10       Impact factor: 4.406

10.  Toward consistency in cost-utility analyses: using national measures to create condition-specific values.

Authors:  M R Gold; P Franks; K I McCoy; D G Fryback
Journal:  Med Care       Date:  1998-06       Impact factor: 2.983

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  4 in total

1.  Health-related quality of life (HRQL) in children with sickle cell disease and thalassemia following hematopoietic stem cell transplant (HSCT).

Authors:  Michael J Kelly; Brian W Pennarola; Angie Mae Rodday; Susan K Parsons
Journal:  Pediatr Blood Cancer       Date:  2011-12-19       Impact factor: 3.167

2.  The association between hydroxyurea treatment and pain intensity, analgesic use, and utilization in ambulatory sickle cell anemia patients.

Authors:  Wally R Smith; Samir K Ballas; William F McCarthy; Robert L Bauserman; Paul S Swerdlow; Martin H Steinberg; Myron A Waclawiw
Journal:  Pain Med       Date:  2011-04-11       Impact factor: 3.750

3.  Health State Utilities for Sickle Cell Disease: A Catalog Prepared From a Systematic Review.

Authors:  Boshen Jiao; Anirban Basu; Scott Ramsey; Joshua Roth; M A Bender; Dalyna Quach; Beth Devine
Journal:  Value Health       Date:  2021-09-04       Impact factor: 5.725

Review 4.  The Use of Cost-Effectiveness Analysis in Sickle Cell Disease: A Critical Review of the Literature.

Authors:  Boshen Jiao; Anirban Basu; Joshua Roth; M Bender; Ilsa Rovira; Traci Clemons; Dalyna Quach; Scott Ramsey; Beth Devine
Journal:  Pharmacoeconomics       Date:  2021-08-09       Impact factor: 4.981

  4 in total

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