|Trends in the Treatment of Anemia Using Recombinant Human Erythropoietin in Patients with HIV Infection.|
|Jump to Full Text|
|PMID: 22253666 Owner: NLM Status: PubMed-not-MEDLINE|
|BACKGROUND: Treating anemia with erythropoietin (EPO) to hemoglobin (Hb) endpoints >11 g/dL may increase risk of serious adverse cardiovascular events.
METHODS: We used medical records data (1996-2003 from the Adolescent Spectrum of HIV Disease Project [ASD] and 1996-2006 from the HIV Outpatient Study [HOPS]) to describe EPO prescription patterns for mildly, moderately, or severely anemic HIV-infected patients. We calculated proportions prescribed EPO and treated to Hb>12 g/dL, and tested for trends over time. We calculated median hemoglobin at first EPO prescription, and described temporal changes using linear regression.
RESULTS: Among 37,395 patients in ASD and 7,005 patients in HOPS, EPO prescription increased over time for moderately anemic patients; for patients with severe anemia, EPO prescription increased only among ASD patients. Hb at EPO prescription decreased over time in ASD patients (median=8.5 g/dL), but not in HOPS patients (median 9.5 g/dL). Percentage of EPO-treated patients with post-treatment Hb>12 g/dL was 18.3% in ASD and stable, and was 56.7% in HOPS and increased over time (p = 0.03).
CONCLUSIONS: Through 2006, EPO prescription increased over time for patients with moderate or severe anemia. Many patients treated with EPO had post-treatment Hb>12 g/dL. Based on 2011 FDA recommendations, changes in previous prescription practices will be needed.
|Patrick S Sullivan; Debra L Hanson; James T Richardson; John T Brooks|
Related Documents :
|12891206 - Safety of abciximab in patients with chronic renal insufficiency who are undergoing per...
23627576 - The costs of warfarin underuse and nonadherence in patients with atrial fibrillation: a...
25115486 - X-linked adrenoleukodystrophy: pathogenesis and treatment.
23296416 - Carotid stenting in asymptomatic patients: how to identify patients without symptoms an...
16750306 - Reasons patients present to the emergency department might change during epidemics and ...
24118626 - Ifnl3 (il28b) polymorphism does not predict long-term response to interferon therapy in...
|Type: Journal Article Date: 2011-12-29|
|Title: The open AIDS journal Volume: 5 ISSN: 1874-6136 ISO Abbreviation: Open AIDS J Publication Date: 2011|
|Created Date: 2012-01-18 Completed Date: 2012-08-23 Revised Date: 2013-05-29|
Medline Journal Info:
|Nlm Unique ID: 101480215 Medline TA: Open AIDS J Country: Netherlands|
|Languages: eng Pagination: 113-8 Citation Subset: -|
|Centers for Disease Control and Prevention, Atlanta, Georgia, USA.|
|APA/MLA Format Download EndNote Download BibTex|
Journal ID (nlm-ta): Open AIDS J
Journal ID (publisher-id): TOAIDJ
Publisher: Bentham Open
© Sullivan et al.; Licensee Bentham Open.
Received Day: 4 Month: 9 Year: 2010
Revision Received Day: 31 Month: 3 Year: 2011
Accepted Day: 6 Month: 10 Year: 2011
Electronic publication date: Day: 29 Month: 12 Year: 2011
collection publication date: Year: 2011
Volume: 5First Page: 113 Last Page: 118
PubMed Id: 22253666
Publisher Id: TOAIDJ-5-113
|Trends in the Treatment of Anemia Using Recombinant Human Erythropoietin in Patients with HIV Infection|
|Patrick S Sullivan*12|
|Debra L Hanson1|
|James T Richardson3|
|John T Brooks1||Author Comment: for the Adult/Adolescent Spectrum of HIV Disease (ASD) and HIV Outpatient Study (HOPS) Investigators
1Centers for Disease Control and Prevention, Atlanta, Georgia, USA
2Department of Epidemiology, Rollins School of Public Health, Atlanta Georgia
3Cerner Corporation, Vienna, Virginia, USA
|*Address correspondence to this author at the Rollins School of Public Health, Emory Universtiy, 1518 Clifton Road NE, 4th Floor, Atlanta GA, 30322, USA; Tel: 404-727-2038; Fax: 866-311-8234; E-mail: Patrick.email@example.com
Anemia has long been recognized as highly prevalent among untreated patients with HIV infection [1-3]; prevalence of anemia among AIDS patients before HAART is as high as 90% . Anemia has been consistently associated in observational studies with shorter survival [1-3], and prescription of recombinant human erythropoietin (EPO, an erythropoesis stimulating agent, or ESA) has been associated with improved survival in some , but not all , studies of HIV-infected, anemic patients. Procrit®, an EPO formulation, has a label indication for treatment of AZT-associated anemia in patients with HIV infection .
The FDA has issued “black box” warnings in November 2006, and in November 2007 , warning of increased risk of thromboembolic events and progression of certain cancers associated with ESA prescription, particularly when ESAs were prescribed to treat to final hemoglobin concentrations (Hb) near physiological levels. Both warnings recommended that patients should not be treated with ESA to hemoglobin levels > 12 g/dL. In June 2011, an even more conservative recommendation was issued by FDA, recommending that ESAs should not be used to increase Hb to concentrations > 11 g/dL .
Because Hb endpoint guidelines for treatment of anemia in patients with HIV infection had been based on expert opinion prior to the black box warnings, and because data on EPO prescription patterns in patients with HIV infection have not been reported, the extent to which historical EPO prescription practices of HIV care providers have been in line with the 2007 or 2011 FDA recommendations is unclear, and it is not known if revision of prescription patterns is needed in light of the FDA black box warnings. We sought to describe EPO prescription practices for patients with HIV infection and anemia in the United States from 1996-2006, using data from two large observational cohorts.
We used data from the Adult and Adolescent Spectrum of HIV Disease Cohort, which collected data on over 60,000 patients in care for HIV infection in over 100 US clinics in 11 US cities from 1990-2004; and the HIV Outpatient Study, which has collected data on over 8,500 patients in care for HIV infection in 12 clinics in 10 US cities from 1992-present. The basic methodology and study sites for these cohorts have been previously described [8-10]. Both cohorts were reviewed and approved by the Institutional Review Board of the Centers for Disease Control and Prevention, and participating study sites. In the case of ASD, a waiver of informed consent was approved by the institutional review board. In the case of HOPS, written informed consent was obtained from all patient participants. In both cohorts, information was collected on hemoglobin measurements, and on prescription of ESAs. In the ASD study, data were collected by retrospective chart review in 6-month abstraction periods; in HOPS, data were collected prospectively at the time of each patient encounter.
To provide context for our analyses of EPO prescription, we assessed the annual prevalence of anemia (defined as at least one Hb < 12 g/dL in women, or < 14g/dL in men) among all patients in whom hemoglobin was measured from 1996-2003 for ASD and from 1996-2006 for HOPS. We tested for trend in prevalence of anemia over these years in each dataset using the Cochran-Armitage test .
For patients with anemia, we classified the baseline anemia status as mild (men: 10 g/dL ≤ Hb < 14; women: 10≤ Hb < 12), moderate (8 ≤ Hb < 10), or severe (Hb < 8); according to the National Cancer Institute definitions for severity of anemia, with the mild anemia definition modified to account for different reference ranges by sex . For each severity classification, and for each cohort, we calculated the proportion of anemic patients prescribed EPO by year. We tested for trends in prevalence of treatment over years (1996-2003 for ASD, 1996-2003 and 1996-2006 for HOPS) using the Cochran-Armitage test.
For patients treated with EPO, we calculated the median hemoglobin concentration last measured before treatment, and the median hemoglobin concentration last measured during EPO treatment among patients with follow-up after the initial treatment, by year and cohort. The hemoglobin concentration at the end of therapy was defined as the last measured hemoglobin before the date EPO was discontinued for HOPS patients, and as the hemoglobin in the last abstraction interval during which EPO was prescribed for ASD patients with subsequent follow-up. We tested for linear trend in the hemoglobin concentrations at the end of EPO prescription by least-squares regression, with hemoglobin as the dependent variable and year as the independent variable. We also calculated the proportions of patients who had Hb > 12 g/dL at the end of their course of EPO therapy, by year and cohort. We tested for trend in these proportions using the Cochran-Armitage test.
In the ASD cohort, a total of 37,395 patients contributed 119,906 person-years [PY] of follow time. In the HOPS cohort, 7,005 patients contributed 28,597 PY of follow time. The characteristics of patients observed in the two cohorts differed with respect to race, age, sex, and HIV acquisition mode (Table 1). The overall prevalence of any anemia decreased significantly over time in both cohorts (Fig. 1). For ASD patients, prevalence decreased from 58.5% in 1996 to 52.6% in 2003. For HOPS patients, prevalence decreased from 57.7% in 1996 to 37.5% in 2006.
Three primary findings emerged from the analysis of prevalence of prescription of EPO over time. First, prescription of EPO was consistently higher for patients with progressively severe anemia (Fig. 2A-C). For patients with mild anemia (Fig. 2A), prevalence of EPO prescription was lowest (all year-cohort-specific prevalences were < 4%). For patients with moderate anemia (Fig. 2B), year-cohort-specific prevalences of EPO prescription ranged from 2.3%-26%. For patients with severe anemia (Fig. 2C), year-cohort-specific prevalences of EPO prescription ranged from 7.1%-50%.
Second, the prescription of EPO was higher in HOPS patients than in ASD patients. For EPO prescription for patients with mild anemia, HOPS year-specific prevalences ranged from 1.1% to 3.7%; for ASD, year-specific prevalences ranged from 0.1% -0.8%. For EPO prescription for patients with moderate anemia, HOPS year-specific prevalences ranged from 9.6% to 26.2%; for ASD, year-specific prevalences ranged from 2.3% -6.8%. For EPO prescription for patients with severe anemia, HOPS year-specific prevalences ranged from 31.3% to 50.0%; for ASD, year-specific prevalences ranged from 7.1% -20.5%.
Third, EPO prescription increased over time for most cohort-severity specific analyses. EPO prescription increased for mildly anemic patients in HOPS, but only when the entire period from 1996-2006 was considered; when restricting the analysis to the period 1996-2003, no significant trend was observed (Fig. 2A). EPO prescription increased for moderately anemic patients in both cohorts (Fig. 2B). EPO prescription increased for severely anemic patients in ASD, but not for severely anemic patients in HOPS (Fig. 2C).
There was no trend in hemoglobin concentrations at initial EPO prescription in HOPS. In the ASD cohort, the median hemoglobin at first EPO prescription was 9.6 g/dL in 1996 and 8.4 g/dL in 2003, which was a significant decrease over time (Fig. 3). Pre-treatment hemoglobin concentrations in HOPS were higher than in ASD, with year-specific medians ranging from 8.9 g/dL to 10.9 g/dL, but did not change over time. Median post-treatment hemoglobin concentrations were higher in HOPS (range 11.8 g/dL to 13.6 g/dL) than in ASD (range 10 g/dL to 12 g/dL), but hemoglobin concentration at end of prescription did not change over time in either cohort (Fig. 3).
The proportion of anemic patients prescribed EPO who had hemoglobin concentrations > 12 g/dL at the end of their EPO prescription was higher in HOPS (year-specific range, 53%-71%) than ASD (range, 9%-26%). The proportion of patients ending therapy with hemoglobin concentrations > 12 g/dL increased among patients in HOPS from 1996-2006, but did not change among patients in ASD or HOPS from 1996-2003 (Fig. 4).
Our data indicate that the EPO prescription practices in diverse US HIV care settings from 1996-2006 were inconsistent with 2007 and 2011 FDA recommendations for duration of ESA therapy; thus, HIV care providers should consider that their earlier EPO prescribing practices may require change in light of FDA black box warnings and recent recommendations about ESAs. According to our data, from 9% to 71% of anemic, HIV-infected patients who received EPO in the several years before the new warnings were issued were treated to hemoglobin concentrations above the currently recommended thresholds. While these patterns of prescription were not inappropriate at the time of our observations, they indicate the need for changes from earlier prescribing practices. To our knowledge, these data are the first detailed published data on EPO prescription practices for anemic patients with HIV infection.
Recommendations on practice strategies and treatment guidelines for use of EPO in patients with anemia and HIV infection were not definitive during the period covered by our report. The label indication for Procrit® in HIV-infected patients was and still is for AZT-related anemia, but research reports  and clinical HIV treatment guidelines  have broadly recommended consideration of EPO therapy for anemia without identified cause, even when patients are not prescribed AZT. Most anemia in HIV-infected persons in the United States is probably attributable to the anemia of HIV infection (anemia of chronic disease) , especially as prescriptions of AZT have decreased in recent years.
Previous recommendations for EPO treatment of anemia have been motivated by a large number of published reports describing the association of anemia and shorter survival (reviewed in 2002 ), and by information about quality of life and its relationship to anemia . In 2000, an expert panel concluded that the target hemoglobin for EPO therapy was 12 g/dL for men and 11 g/dL for women , but that EPO treatment should be discontinued only if hemoglobin concentration rose to > 13 g/dL during EPO therapy [14, 17]. Thus, for the many patients in our analysis who were treated to hemoglobin concentrations up to 13 g/dL, the EPO prescription practice may have been within recommended practice standards as documented by published treatment recommendations and published expert opinion.
Several new pieces of information have led to a reconsideration of EPO prescription practices, both from the regulatory point of view and based on meta-analytic data about survival and erythropoietin treatment. In 2006, trials of EPO in patients with chronic kidney disease [18, 19] demonstrated no improvement of cardiovascular outcomes, and, in one trial, a higher risk for a composite negative study endpoint (e.g., death or cardiac event). In 2007, preliminary data from an unpublished randomized trial of an ESA in spinal surgery patients found a higher incidence of deep venous thrombosis among EPO-treated patients , and several studies reported to FDA have suggested that ESA prescription may be associated with progression of certain cancers, including breast cancer, cervical cancer, and head and neck tumors [20, 21]. Further, a 2007 meta-analysis of data on anemia, survival, and EPO therapy for patients with HIV suggested that treatment with EPO did not improve survival . We did not assess in our analysis endpoints, such as thrombotic events or cancer progression, that are potentially EPO-related, and to the best of our knowledge, there are not data directly demonstrating increased risk for these events associated with EPO prescription in HIV-infected patients.
In other disease conditions, there has been evidence of more aggressive treatment of anemia with ESA in the past 15 years. In a cohort of renal dialysis patients with anemia followed through the United States Renal Data System (USRDS), in 2005 57% of patients were treated with an ESA to hemoglobin concentrations > 13 g/dL; from 1994-2005, mean weekly ESA dose in incident dialysis patients doubled, and the mean monthly hemoglobin concentrations of all patients in care increased by nearly 20% . The increased use of ESA therapy for anemia in renal dialysis patients even caught the attention of the popular press; the New York Times reported that mean dosages of EPO prescribed in the United States were much higher than prescribed doses in other countries, characterizing the US prescribing practices as aggressive . We found that, among patients in our cohorts, the prevalence of EPO prescription was as high as among patients in the USRDS report, and that increases in EPO prescription were mostly observed among patients with moderate or severe anemia. The proportions of anemic HOPS patients treated to hemoglobin concentrations > 12 g/dL from 2003-2006 ranged from 53-71%, similar to the USRDS findings of “overshoot”, suggesting that prescription patterns in the two groups may be similar.
There were consistent differences between HOPS and ASD patients in our outcomes of EPO prescription, and hemoglobin concentrations at treatment initiation and discontinuation. Generally, patients in the ASD cohort were prescribed less EPO, were prescribed EPO at more advanced stages of anemia, and were treated with EPO to lower ending hemoglobin concentrations. Although both ASD and HOPS include a variety of public and private treatment facilities, the facilities included in the ASD cohort are more inclusive of public treatment facilities than are the HOPS treatment settings, and it is likely that some of the differences in EPO prescription between the two cohorts reflect differences in insurance status between patients in the two cohorts. Because the ASD cohort did not collect complete information about insurance status, we could not address this possibility directly.
Our analysis is subject to several limitations. First, despite the large number of diverse clinical settings included in the ASD and HOPS cohorts, the facilities and their patients are not representative of all patients in care for HIV infection in the United States. Also, because our studies were observational, we did not specify when hemoglobin measurements were taken, and the times from the hemoglobin measurements to initiation or discontinuation of EPO prescription were variable. In the ASD cohort, EPO prescription was documented only as occurring within a 6-month interval and in some cases only one hemoglobin measurement may have been recorded per 6 month interval in ASD; this led to less analytic precision than in the HOPS analysis, for which precise dates and length of prescription were abstracted. It is possible that other underlying indications for EPO therapy, such as chronic renal disease, may have increased in the ASD and HOPS patient populations over time, and we did not account for this in our analysis. Also, our datasets did not have additional data, such as MCV, serum EPO concentrations, and other measurements of iron that would have allowed us to classify the likely causes of anemia, so we could not stratify our analysis by etiology of anemia. We also did not analyze data on sequelae or patient well-being as it related to ESA dosing. Finally, our analyses did not span the period in 2006-2007 when the original FDA black box warnings were issued, so we cannot evaluate whether prescription patterns have changed since that time.
Our study documents that from 1996-2006, HIV care providers treated anemia, especially moderate and severe anemia, aggressively with EPO. These changes occurred during a period of time when multiple lines of evidence suggested that managing anemia more aggressively bore clinical consideration, and during which anemic patients (not necessarily HIV-infected) in renal dialysis were treated for anemia with increasing aggressiveness. However, these data taken together with our current understanding of the risks associated with treatment of anemia to hemoglobin concentrations > 11 g/dL in other populations suggest that the EPO prescription patterns of HIV care providers should be substantially more conservative than they were in our historical analysis. Future analyses of observational clinical databases (either cohort or representative cross sectional surveys ) may be helpful in documenting changes in EPO prescription practices following the FDA warnings in 2006 and 2007, and the revised FDA recommendations for dosing in 2011.
Melanie Thompson and Ericka Sinclair (AIDS Research Consortium of Atlanta); David Cohn, Arthur Davidson, and Cornelius Rietmeijer (Denver Department of Health and Hospitals); Jane Turner and Amy Wohl (Los Angeles County Department of Health Services, Los Angeles); Anne Morse, Stephanie Broyles, and C. Lynn Besch (Louisiana Department of Health, Baton Rouge); Eve Mokotoff and Linda Wotring (Michigan Department of Community Health, Detroit); Judy Sackoff and Marie Antoinette Bernard (New York City Department of Health); Jose Otero, Robert Hunter, and Maria de los Angeles Gomez (University Central del Caribe, Bayamon); Sandra Miranda (Puerto Rico Department of Health, San Juan); Susan Buskin, Elizabeth Tesh Barash, and Sharon Hopkins (Public Health–Seattle & King County, Seattle); Sylvia Odem (Texas Department of Health, Austin); Philip Keiser (Parkland Hospital, Dallas); and Kaye Reynolds and Wes McNeely (Department of Health and Human Services, Houston).
The findings and conclusions in this report are those of the authors and do not necessarily represent the views of the Centers for Disease Control and Prevention.
|1.||Moore RD. Human immunodeficiency virus infection, anemia, and survivalClin Infect DisYear: 199929144910433563|
|2.||Sullivan PS,Hanson DL,Chu SY,Jones JL,Ward JW. Epidemiology of anemia in human immunodeficiency virus (HIV)-infected persons: results from the multistate adult and adolescent spectrum of HIV disease surveillance projectBloodYear: 199891130189414298|
|3.||Mocroft A,Kirk O,Barton SE,et al. Anaemia is an independent predictive marker for clinical prognosis in HIV-infected patients from across Europe. EuroSIDA study groupAIDSYear: 19991389435010371175|
|4.||Buskin SE,Sullivan PS. Anemia and its treatment and outcomes in persons infected with human immunodeficiency virusTransfusionYear: 2004446 8263215157246|
|5.||Ortho Biotech. Package insert for Procrit (Epoetin alfa). Available at: http://www.procrit.com/sites/default/files/shared/OBI/PI/ProcritBooklet.pdf#page=1|
|6.||Food and Drug Administration, 2008. Communication about an Ongoing Safety Review: Erythropoiesis-Stimulating Agents (ESAs) Epoetin alfa (marketed as Procrit, Epogen) Darbepoetin alfa (marketed as Aranesp) [internet report]. Available at: https: //www.accessdata.fda.gov/scripts/medwatch/medwatch-online.htmlast accessed October 5, 2011|
|7.||Food and Drug Adminsitration. Modified dosing recommendations to improve the safe use of Erythropoiesis-Stimulating Agents (ESAs) in chronic kidney disease [online recommendation]. 2011. Modified dosing recommendations to improve the safe use of Erythropoiesis-Stimulating Agents (ESAs) in chronic kidney disease [online recommendation] 2011. Available at: http://www.fda.gov/Drugs/DrugSafety/ucm259639. htmlast accessed October 5, 2011|
|8.||Moorman AC,Holmberg SD,Marlowe SI,et al. Changing conditions and treatments in a dynamic cohort of ambulatory HIV patients: the HIV outpatient study (HOPS)Annals EpidemiolYear: 19999634957|
|9.||Farizo KM,Buehler JW,Chamberland ME,et al. Spectrum of disease in persons with human immunodeficiency virus infection in the United StatesJ Am Med AssocYear: 199226713 1798805|
|10.||Palella FJ,Delaney KM,Moorman AC,et al. Declining morbidity and mortality among patients with advanced human immunodefici-ency virus infectionN Engl J MedYear: 199833813 853609516219|
|11.||Agresti Categorical data analysisYear: 1990New YorkJohn Wiley and Sons|
|12.||Groopman JE,Itri LM. Chemotherapy-induced anemia in adults: incidence and treatmentJ Nat Cancer InstYear: 19999119 16163410511589|
|13.||Balfour HH. Recombinant human erythropoietin for treatment of anemia in person with AIDS not receiving zidovudineInt J Antimicrob AgentsYear: 199783 1899218611800|
|14.||Bartlett JG,Gallant JE,Bartlett JGBartlett JG. Hematologic complications: anemiaMedical Management of HIV InfectionsYear: 2005-2006Baltimore MDJohns Hopkins Medicine Health Publishing Group2002|
|15.||Sullivan P. Associations of anemia, treatments for anemia, and survival in patients with human immunodeficiency virus infectionJ Infect DisYear: 2002185Suppl 2S1384212001035|
|16.||Abrams DI,Steinhart C,Frascino R. Epoetin alfa therapy for anaemia in HIV-infected patients: impact on quality of lifeInt J STD AIDSYear: 20001110 6596511057937|
|17.||Volberding P. Consensus statement: anemia in HIV infection--current trends, treatment options, and practice strategies Anemia in HIV Working GroupClin TherYear: 2000229 10042011048901|
|18.||Singh AK,Szczech L,Tang KL,et al. Correction of anemia with epoetin alfa in chronic kidney diseaseN Engl J MedYear: 200635520 20859817108343|
|19.||Drueke TB,Locatelli F,Clyne N,et al. Normalization of hemoglobin level in patients with chronic kidney disease and anemiaN Engl J MedYear: 200635520 20718417108342|
|20.||Food and Drug Adminsitration. Information for healthcare professionals: Erythropoiesis stimulating agents [online report]. 2008. Available at: https: //www.accessdata.fda.gov/scripts/medwatch/medwatch-online.htmYear: 2011last accessed October 5, 2011|
|21.||Henke M,Laszig R,Rube C,et al. Erythropoietin to treat head and neck cancer patients with anaemia undergoing radiotherapy: randomised, double-blind, placebo-controlled trialLancetYear: 2003362939212556014575968|
|22.||Marti-Carvajal AJ,Sola I. Treatment for anemia in people with AIDSCochrane Database Syst RevYear: 20071 CD004776.|
|23.||U.S. Renal Data System, USRDS 2007 Annual Data Report: Atlas of Chronic Kidney Disease and End-Stage Renal Disease in the United States, National Institutes of Health, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MDYear: 2007|
|24.||Berenson A. Doctors reap millions for anemia drugsNew York TimesYear: 2007Month: 5 Day: 9|
|25.||McNaghten AD,Wolfe MI,Onorato IM,et al. Improving behavioral and clinical HIV/AIDS surveillance in the United States: the rationale for developing a population-based approachPLoS OneYear: 200726e55017579722|
Keywords: Keywords HIV, anemia, erythropoietin..
Previous Document: Time-dependent cortical activation in voluntary muscle contraction.
Next Document: Readiness in HIV Treatment Adherence: A Matter of Confidence. An Exploratory Study.