Age‐related treatment patterns in sickle cell disease patients and the associated sickle cell complications and healthcare costs1. Issue 5 (17th January 2013)
- Record Type:
- Journal Article
- Title:
- Age‐related treatment patterns in sickle cell disease patients and the associated sickle cell complications and healthcare costs1. Issue 5 (17th January 2013)
- Main Title:
- Age‐related treatment patterns in sickle cell disease patients and the associated sickle cell complications and healthcare costs1
- Authors:
- Blinder, Morey A.
Vekeman, Francis
Sasane, Medha
Trahey, Alex
Paley, Carole
Duh, Mei Sheng - Abstract:
- <abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="abs1-1" sec-type="section"> <title>Background</title> <p>This study explored the blood transfusion patterns, SCD complications, utilization of iron chelation therapies (ICT), healthcare resource use, and costs in pediatric, transitioning (18 years old) and adult patients with SCD.</p> </sec> <sec id="abs1-2" sec-type="section"> <title>Procedure</title> <p>Data from Florida (1998–2009), New Jersey (1996–2009), Missouri (1997–2010), Kansas (2001–2009), and Iowa (1998–2010) state Medicaid were used. Patients with ≥2 SCD diagnoses and ≥1 transfusion event were included. Rates of transfusion events, SCD complications, and proportion of eligible patients receiving ICT were calculated. ICT eligibility was defined as receiving ≥10 transfusions over lifetime. SCD complications included pain, pulmonary event, infection event, renal, cardiovascular, stroke, leg ulcers, and avascular necrosis. Regressions were used to assess risk factors for transfusion and identify the main drivers of costs.</p> </sec> <sec id="abs1-3" sec-type="section"> <title>Results</title> <p>The sample included 3, 208 patients. The transfusion rate increased from 1‐year‐old to a peak at 16 years old, then dropped until age 26 and remained stable thereafter. In contrast the frequency of diagnoses for SCD complications increased markedly after age 16. Post‐transition patients (≥18 years old) were significantly associated with fewer<abstract abstract-type="main" xml:lang="en"> <title>Abstract</title> <sec id="abs1-1" sec-type="section"> <title>Background</title> <p>This study explored the blood transfusion patterns, SCD complications, utilization of iron chelation therapies (ICT), healthcare resource use, and costs in pediatric, transitioning (18 years old) and adult patients with SCD.</p> </sec> <sec id="abs1-2" sec-type="section"> <title>Procedure</title> <p>Data from Florida (1998–2009), New Jersey (1996–2009), Missouri (1997–2010), Kansas (2001–2009), and Iowa (1998–2010) state Medicaid were used. Patients with ≥2 SCD diagnoses and ≥1 transfusion event were included. Rates of transfusion events, SCD complications, and proportion of eligible patients receiving ICT were calculated. ICT eligibility was defined as receiving ≥10 transfusions over lifetime. SCD complications included pain, pulmonary event, infection event, renal, cardiovascular, stroke, leg ulcers, and avascular necrosis. Regressions were used to assess risk factors for transfusion and identify the main drivers of costs.</p> </sec> <sec id="abs1-3" sec-type="section"> <title>Results</title> <p>The sample included 3, 208 patients. The transfusion rate increased from 1‐year‐old to a peak at 16 years old, then dropped until age 26 and remained stable thereafter. In contrast the frequency of diagnoses for SCD complications increased markedly after age 16. Post‐transition patients (≥18 years old) were significantly associated with fewer transfusions (odds ratio: 0.80, <italic>P</italic> = 0.002). Among eligible patients for ICT, there was no statistically significant difference in total cost between the ICT and no ICT groups (adjusted cost difference, $136, <italic>P</italic> = 0.114).</p> </sec> <sec id="abs1-4" sec-type="section"> <title>Conclusions</title> <p>Patients transitioning to adult care received less transfusions and hydroxyurea, less ICT when eligible for chelation therapy, had higher healthcare costs and suffered from more frequent SCD related complications than pediatric patients. These findings highlight the changes in treatment patterns corresponding to transition to adult care. Pediatr Blood Cancer 2013; 60: 828–835. © 2013 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Pediatric blood & cancer. Volume 60:Issue 5(2013:May)
- Journal:
- Pediatric blood & cancer
- Issue:
- Volume 60:Issue 5(2013:May)
- Issue Display:
- Volume 60, Issue 5 (2013)
- Year:
- 2013
- Volume:
- 60
- Issue:
- 5
- Issue Sort Value:
- 2013-0060-0005-0000
- Page Start:
- 828
- Page End:
- 835
- Publication Date:
- 2013-01-17
- Subjects:
- Tumors in children -- Periodicals
Blood -- Diseases -- Periodicals
Cancer in children -- Periodicals
618.92 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1545-5017 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pbc.24459 ↗
- Languages:
- English
- ISSNs:
- 1545-5009
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6417.533500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4160.xml