Literature DB >> 24926708

National trends in hospitalizations for sickle cell disease in the United States following the FDA approval of hydroxyurea, 1998-2008.

Maureen M Okam1, Shimon Shaykevich, Benjamin L Ebert, Alan M Zaslavsky, John Z Ayanian.   

Abstract

BACKGROUND: Patients with sickle cell disease (SCD) can suffer frequent hospital admissions for painful vasoocclusive crises. Hydroxyurea was approved by the FDA in 1998 to decrease the morbidity of SCD, but nationwide hospitalizations for SCD in the United States since 1998 have not been evaluated. We hypothesized that the availability of hydroxyurea for SCD would be associated with a decrease in hospitalizations for SCD over time.
OBJECTIVE: To assess trends in hospitalization and length-of-stay in hospital for SCD in the United States, 1998 through 2008. RESEARCH
DESIGN: Retrospective cohort study of SCD-related hospital discharges in the Nationwide Inpatient Sample of US hospital discharges.
SUBJECTS: All discharges in the Nationwide Inpatient Sample associated with a principal diagnosis of SCD in blacks, 1998 through 2008. MEASURES: Trends in hospitalization rates and average length-of-stay in hospital for SCD.
RESULTS: We found 216 (95% confidence interval, 173.3-258.7) SCD-related hospitalizations per 100,000 US blacks in 1998 and 178.4 (95% confidence interval, 144.2-212.5) in 2008, but no consistent yearly decrease, 1998 through 2008 (P=0.30). Conversely, the length-of-stay in hospital in 1998 was 5.38 days and in 2008 was 5.18 days, an absolute change of 0.2 days and a downward trend that was statistically significant.
CONCLUSIONS: Between 1998 and 2008, there was not a steady decrease in hospitalization rates for the population of SCD in the United States. On the contrary, there was a decline in length-of-stay in hospital over this time. Hydroxyurea underuse is well documented. Efforts to increase hydroxyurea use may help to reduce hospitalization rates.

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Year:  2014        PMID: 24926708      PMCID: PMC4177169          DOI: 10.1097/MLR.0000000000000143

Source DB:  PubMed          Journal:  Med Care        ISSN: 0025-7079            Impact factor:   2.983


  38 in total

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Authors:  Courtney D Thornburg; Agustin Calatroni; Marilyn Telen; Alex R Kemper
Journal:  J Pediatr       Date:  2009-11-01       Impact factor: 4.406

3.  Tissue factor expression by endothelial cells in sickle cell anemia.

Authors:  A Solovey; L Gui; N S Key; R P Hebbel
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4.  Hydroxyurea therapy for sickle cell disease in community-based practices: a survey of Florida and North Carolina hematologists/oncologists.

Authors:  Marc S Zumberg; Suresh Reddy; Robert L Boyette; Robert J Schwartz; Thomas R Konrad; Richard Lottenberg
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5.  Hb F levels, longevity of homozygotes and clinical course of sickle cell anemia in Brazil.

Authors:  M H Hutz; F M Salzano; J Adams
Journal:  Am J Med Genet       Date:  1983-04

6.  Natural history of sickle cell anemia in Saudi Arabs. A study of 270 subjects.

Authors:  R P Perrine; M E Pembrey; P John; S Perrine; F Shoup
Journal:  Ann Intern Med       Date:  1978-01       Impact factor: 25.391

7.  Adherent leukocytes capture sickle erythrocytes in an in vitro flow model of vaso-occlusion.

Authors:  Eileen M Finnegan; Aslihan Turhan; David E Golan; Gilda A Barabino
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8.  The effect of prolonged administration of hydroxyurea on morbidity and mortality in adult patients with sickle cell syndromes: results of a 17-year, single-center trial (LaSHS).

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9.  Delay time of hemoglobin S polymerization prevents most cells from sickling in vivo.

Authors:  A Mozzarelli; J Hofrichter; W A Eaton
Journal:  Science       Date:  1987-07-31       Impact factor: 47.728

10.  Augmentation of fetal-hemoglobin production in anemic monkeys by hydroxyurea.

Authors:  N L Letvin; D C Linch; G P Beardsley; K W McIntyre; D G Nathan
Journal:  N Engl J Med       Date:  1984-04-05       Impact factor: 91.245

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Authors:  Manyoo A Agarwal; Mahek Shah; Brijesh Patel; Vikki G Nolan; Guy L Reed; Ronald J Oudiz; Gaurav Choudhary; Bradley A Maron
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6.  Patient-Reported Outcomes and Economic Burden of Adults with Sickle Cell Disease in the United States: A Systematic Review.

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7.  Hydroxyurea use in Children with Sickle Cell Disease: Do Severely Affected Patients Use It and Does It Impact Hospitalization Outcomes?

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8.  Opioid Use in Adults With Sickle Cell Disease Hospitalized During Vaso-Occlusive Crisis: A Systematic Review.

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9.  The accuracy of hospital ICD-9-CM codes for determining Sickle Cell Disease genotype.

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10.  Profile of crizanlizumab and its potential in the prevention of pain crises in sickle cell disease: evidence to date.

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