Literature DB >> 18768997

Use and prescribing patterns for erythropoiesis-stimulating agents in inpatient and outpatient hospital settings.

Jerry Siegel1, James Jorgenson, Philip E Johnson, Donald F Brophy, Thomas Comstock, Amy Feng, Paul Audhya.   

Abstract

PURPOSE: Erythropoiesis-stimulating agent (ESA) use in the outpatient and inpatient settings through pharmacist-conducted, hospital-based chart audits is examined and discussed.
METHODS: Data from four hospital chart audits conducted in 250 hospitals between October 2005 and July 2006 were pooled for analyses. Eligible hospitals were categorized by ESA sales volume, with approximately equal numbers randomly selected from each decile. The last five inpatients and outpatients within each specified month receiving either darbepoetin alfa or epoetin alfa were evaluated. Study variables by setting included ESA use, prescriber specialty, and dosage regimen.
RESULTS: The most common hospital locations of ESA administration were a cancer center in the outpatient setting (49%) and general medicine (57%) in the inpatient setting. ESA prescribers were most commonly hematologists and oncologists in the outpatient setting, and nephrologists were the most common prescribers in the inpatient setting. In the outpatient analysis, 2155 patients were prescribed darbepoetin alfa and 3106 were prescribed epoetin alfa. The predominant administration frequencies were every two weeks and once weekly for darbepoetin alfa, and once weekly for epoetin alfa. In the inpatient analysis, 1633 patients were prescribed darbepoetin alfa and 3231 were prescribed epoetin alfa. The predominant administration frequencies were once weekly for darbepoetin alfa and once weekly and three times weekly for epoetin alfa. Common uses for both ESAs were chemotherapy-induced anemia (outpatient setting) and anemia of end-stage renal disease with chronic dialysis (inpatient setting). There was considerable variability in ESA dosages and administration frequencies in both settings within all patient groups when analyzed by specified use.
CONCLUSION: ESA use differed between outpatient and inpatient settings in indication, frequency of administration, and specialty of the prescriber.

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Year:  2008        PMID: 18768997     DOI: 10.2146/ajhp070526

Source DB:  PubMed          Journal:  Am J Health Syst Pharm        ISSN: 1079-2082            Impact factor:   2.637


  5 in total

1.  Assessing the quality of prescribing and monitoring erythropoiesis-stimulating agents in the nursing home setting.

Authors:  An-Kwok I Wong; Scott B Stephens; Monica B Aspinall; Shyam Visweswaran; Joseph T Hanlon; Steven M Handler
Journal:  J Am Med Dir Assoc       Date:  2009-07       Impact factor: 4.669

2.  Uptake of evidence by physicians: De-adoption of erythropoiesis-stimulating agents after the TREAT trial.

Authors:  Khoa Vu; Jiani Zhou; Alexander Everhart; Nihar Desai; Jeph Herrin; Anupam B Jena; Joseph S Ross; Nilay D Shah; Pinar Karaca-Mandic
Journal:  BMC Nephrol       Date:  2021-08-21       Impact factor: 2.388

3.  Erythropoiesis-stimulating agent use among non-dialysis-dependent CKD patients before and after the trial to Reduce Cardiovascular Events With Aranesp Therapy (TREAT) using a large US health plan database.

Authors:  Mae Thamer; Yi Zhang; Onkar Kshirsagar; Dennis J Cotter; James S Kaufman
Journal:  Am J Kidney Dis       Date:  2014-07-08       Impact factor: 8.860

4.  Trends in anemia care in non-dialysis-dependent chronic kidney disease (CKD) patients in the United States (2006-2015).

Authors:  Haesuk Park; Xinyue Liu; Linda Henry; Jeffrey Harman; Edward A Ross
Journal:  BMC Nephrol       Date:  2018-11-09       Impact factor: 2.388

5.  Staff time and motion assessment for administration of erythropoiesis-stimulating agents: a two-phase pilot study in clinical oncology practices.

Authors:  John F Reitan; Arletta van Breda; Patricia K Corey-Lisle; Sanatan Shreay; Ze Cong; Jason Legg
Journal:  Clin Drug Investig       Date:  2013-05       Impact factor: 2.859

  5 in total

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