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Screen-and-treat strategies for albuminuria to prevent cardiovascular and renal disease: Cost-effectiveness of nationwide and targeted interventions based on analysis of cohort data from the Netherlands

Abstract Background: Albuminuria is a marker for renal and cardiovascular (CV) risk, allowing early diagnosis of subjects with elevated renal and CV risk. Objective: This study aimed to estimate the costeffectiveness and budget impact of various population-based screen-and-treat scenarios for elevat...

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Published in:Clinical therapeutics 2010-06, Vol.32 (6), p.1103-1121
Main Authors: Boersma, Cornelis, PhD, Gansevoort, Ron T., MD, PhD, Pechlivanoglou, Petros, MSc, Visser, Sipke T., MSc, van Toly, Flip F.J., MSc, de Jong-van den Berg, Lolkje T.W., PhD, de Jong, Paul E., MD, PhD, Postma, Maarten J., PhD
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cited_by cdi_FETCH-LOGICAL-c598t-2cd9bd46ee4d92e7e4b4bbfef4b987adaf05f2ba8180dd424e81fb6c3c27680b3
cites cdi_FETCH-LOGICAL-c598t-2cd9bd46ee4d92e7e4b4bbfef4b987adaf05f2ba8180dd424e81fb6c3c27680b3
container_end_page 1121
container_issue 6
container_start_page 1103
container_title Clinical therapeutics
container_volume 32
creator Boersma, Cornelis, PhD
Gansevoort, Ron T., MD, PhD
Pechlivanoglou, Petros, MSc
Visser, Sipke T., MSc
van Toly, Flip F.J., MSc
de Jong-van den Berg, Lolkje T.W., PhD
de Jong, Paul E., MD, PhD
Postma, Maarten J., PhD
description Abstract Background: Albuminuria is a marker for renal and cardiovascular (CV) risk, allowing early diagnosis of subjects with elevated renal and CV risk. Objective: This study aimed to estimate the costeffectiveness and budget impact of various population-based screen-and-treat scenarios for elevated albuminuria levels (ie, microalbuminuria) in the Netherlands. Methods: A multistate transition Markov model was developed to simulate the natural course of albuminuria-based disease progression to dialysis and occurrence of CV events. Several population-based strategies directed at screening for elevated albuminuria were evaluated. These strategies depended on urinary albumin concentration (UAC), urinary albumin excretion (UAE), and age. Transition probabilities were derived from the observational community-based Prevention of Renal and Vascular End Stage Disease (PREVEND) cohort study. Health care costs (in year-2008 euros) and life-years gained were calculated over an 8-year period. In the base-case analysis, we analyzed screening for and treatment of microalbuminuria. Screening for microal-buminuria involved prescreening for UAC ≥20 mg/L, followed by a confirmation test for UAE ≥30 mg/d. Other options based on combinations of albuminuria for UAC prescreening (no prescreening, and ≥10, ≥20, ≥100, and ≥200 mg/L) and UAE confirmation test (≥15, ≥30, and ≥300 mg/d) for treatment were investigated in scenario analyses. Furthermore, these various strategies based on UAC and UAE values were analyzed in different subgroups based on age (all ages, aged ≥50 years, and aged ≥60 years). Results: The PREVEND study included 8592 Dutch residents aged 28 to 75 years at the time of initial screening. Among a hypothetical cohort of 1000 subjects identified and treated in the base-case analysis, it was estimated (based on PREVEND follow-up data) that, in the screening/treatment and no-screening scenarios, 76 versus 124 CV events occurred, 16 versus 27 CV deaths, and 3 versus 5 dialysis cases, respectively. The per-person difference in net costs for screening was calculated at €926 (€2003 vs €1077), and prevention of CV deaths was estimated to gain 0.0421 discounted life-year per person. Correspondingly, the cost-effectiveness was estimated at €22,000 per life-year gained. In the base-case analysis, probabilistic sensitivity analysis indicated that the likelihood of cost-effectiveness of a screen-and-treat strategy was 54%, 90%, and 95% for a maximum acceptable cost-effective
doi_str_mv 10.1016/j.clinthera.2010.06.013
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Objective: This study aimed to estimate the costeffectiveness and budget impact of various population-based screen-and-treat scenarios for elevated albuminuria levels (ie, microalbuminuria) in the Netherlands. Methods: A multistate transition Markov model was developed to simulate the natural course of albuminuria-based disease progression to dialysis and occurrence of CV events. Several population-based strategies directed at screening for elevated albuminuria were evaluated. These strategies depended on urinary albumin concentration (UAC), urinary albumin excretion (UAE), and age. Transition probabilities were derived from the observational community-based Prevention of Renal and Vascular End Stage Disease (PREVEND) cohort study. Health care costs (in year-2008 euros) and life-years gained were calculated over an 8-year period. In the base-case analysis, we analyzed screening for and treatment of microalbuminuria. Screening for microal-buminuria involved prescreening for UAC ≥20 mg/L, followed by a confirmation test for UAE ≥30 mg/d. Other options based on combinations of albuminuria for UAC prescreening (no prescreening, and ≥10, ≥20, ≥100, and ≥200 mg/L) and UAE confirmation test (≥15, ≥30, and ≥300 mg/d) for treatment were investigated in scenario analyses. Furthermore, these various strategies based on UAC and UAE values were analyzed in different subgroups based on age (all ages, aged ≥50 years, and aged ≥60 years). Results: The PREVEND study included 8592 Dutch residents aged 28 to 75 years at the time of initial screening. Among a hypothetical cohort of 1000 subjects identified and treated in the base-case analysis, it was estimated (based on PREVEND follow-up data) that, in the screening/treatment and no-screening scenarios, 76 versus 124 CV events occurred, 16 versus 27 CV deaths, and 3 versus 5 dialysis cases, respectively. The per-person difference in net costs for screening was calculated at €926 (€2003 vs €1077), and prevention of CV deaths was estimated to gain 0.0421 discounted life-year per person. Correspondingly, the cost-effectiveness was estimated at €22,000 per life-year gained. In the base-case analysis, probabilistic sensitivity analysis indicated that the likelihood of cost-effectiveness of a screen-and-treat strategy was 54%, 90%, and 95% for a maximum acceptable cost-effectiveness threshold of €20,000, €50,000, and €80,000 per life-year gained, respectively. Higher albuminuria thresholds for screening and start of treatment further improved the cost-effectiveness but reduced the overall health gains achieved. Limiting screening to those subjects aged ≥50 and ≥60 years resulted in more favorable cost-effectiveness compared with population-based screening without age restriction. Conclusions: Our analyses suggest the potentially favorable cost-effectiveness of population-based screening for albuminuria in the general Dutch population. The results offer health care decision-makers new tools for considering actual implementation of such screening.</description><identifier>ISSN: 0149-2918</identifier><identifier>EISSN: 1879-114X</identifier><identifier>DOI: 10.1016/j.clinthera.2010.06.013</identifier><identifier>PMID: 20637965</identifier><language>eng</language><publisher>Bridgewater, NJ: EM Inc USA</publisher><subject>Adult ; Age Factors ; Aged ; Albuminuria - diagnosis ; Albuminuria - economics ; Biological and medical sciences ; Biomarkers - analysis ; Cardiovascular Agents - economics ; Cardiovascular Agents - therapeutic use ; Cardiovascular disease ; Cardiovascular Diseases - economics ; Cardiovascular Diseases - prevention &amp; control ; Chronic illnesses ; Cohort Studies ; Cost analysis ; Cost-Benefit Analysis ; cost-effectiveness ; Diabetes ; Disease prevention ; Early Diagnosis ; Epidemiology ; Expected values ; Female ; Humans ; Hypertension ; Internal Medicine ; Kidney diseases ; Kidney Diseases - economics ; Kidney Diseases - prevention &amp; control ; Male ; Markov Chains ; Mass Screening - economics ; Medical Education ; Medical sciences ; microalbuminuria ; Middle Aged ; Mortality ; Nephrology ; Nephrology. Urinary tract diseases ; Netherlands ; Pharmacoeconomics ; Pharmacology. Drug treatments ; Pharmacy ; Public health ; renal disease ; Risk factors ; screening ; Urinary system involvement in other diseases. Miscellaneous ; Urinary tract. Prostate gland</subject><ispartof>Clinical therapeutics, 2010-06, Vol.32 (6), p.1103-1121</ispartof><rights>Excerpta Medica Inc.</rights><rights>2010 Excerpta Medica Inc.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c598t-2cd9bd46ee4d92e7e4b4bbfef4b987adaf05f2ba8180dd424e81fb6c3c27680b3</citedby><cites>FETCH-LOGICAL-c598t-2cd9bd46ee4d92e7e4b4bbfef4b987adaf05f2ba8180dd424e81fb6c3c27680b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=23019075$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20637965$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boersma, Cornelis, PhD</creatorcontrib><creatorcontrib>Gansevoort, Ron T., MD, PhD</creatorcontrib><creatorcontrib>Pechlivanoglou, Petros, MSc</creatorcontrib><creatorcontrib>Visser, Sipke T., MSc</creatorcontrib><creatorcontrib>van Toly, Flip F.J., MSc</creatorcontrib><creatorcontrib>de Jong-van den Berg, Lolkje T.W., PhD</creatorcontrib><creatorcontrib>de Jong, Paul E., MD, PhD</creatorcontrib><creatorcontrib>Postma, Maarten J., PhD</creatorcontrib><creatorcontrib>Prevention of Renal and Vascular End Stage Disease Study Group</creatorcontrib><title>Screen-and-treat strategies for albuminuria to prevent cardiovascular and renal disease: Cost-effectiveness of nationwide and targeted interventions based on analysis of cohort data from the Netherlands</title><title>Clinical therapeutics</title><addtitle>Clin Ther</addtitle><description>Abstract Background: Albuminuria is a marker for renal and cardiovascular (CV) risk, allowing early diagnosis of subjects with elevated renal and CV risk. Objective: This study aimed to estimate the costeffectiveness and budget impact of various population-based screen-and-treat scenarios for elevated albuminuria levels (ie, microalbuminuria) in the Netherlands. Methods: A multistate transition Markov model was developed to simulate the natural course of albuminuria-based disease progression to dialysis and occurrence of CV events. Several population-based strategies directed at screening for elevated albuminuria were evaluated. These strategies depended on urinary albumin concentration (UAC), urinary albumin excretion (UAE), and age. Transition probabilities were derived from the observational community-based Prevention of Renal and Vascular End Stage Disease (PREVEND) cohort study. Health care costs (in year-2008 euros) and life-years gained were calculated over an 8-year period. In the base-case analysis, we analyzed screening for and treatment of microalbuminuria. Screening for microal-buminuria involved prescreening for UAC ≥20 mg/L, followed by a confirmation test for UAE ≥30 mg/d. Other options based on combinations of albuminuria for UAC prescreening (no prescreening, and ≥10, ≥20, ≥100, and ≥200 mg/L) and UAE confirmation test (≥15, ≥30, and ≥300 mg/d) for treatment were investigated in scenario analyses. Furthermore, these various strategies based on UAC and UAE values were analyzed in different subgroups based on age (all ages, aged ≥50 years, and aged ≥60 years). Results: The PREVEND study included 8592 Dutch residents aged 28 to 75 years at the time of initial screening. Among a hypothetical cohort of 1000 subjects identified and treated in the base-case analysis, it was estimated (based on PREVEND follow-up data) that, in the screening/treatment and no-screening scenarios, 76 versus 124 CV events occurred, 16 versus 27 CV deaths, and 3 versus 5 dialysis cases, respectively. The per-person difference in net costs for screening was calculated at €926 (€2003 vs €1077), and prevention of CV deaths was estimated to gain 0.0421 discounted life-year per person. Correspondingly, the cost-effectiveness was estimated at €22,000 per life-year gained. In the base-case analysis, probabilistic sensitivity analysis indicated that the likelihood of cost-effectiveness of a screen-and-treat strategy was 54%, 90%, and 95% for a maximum acceptable cost-effectiveness threshold of €20,000, €50,000, and €80,000 per life-year gained, respectively. Higher albuminuria thresholds for screening and start of treatment further improved the cost-effectiveness but reduced the overall health gains achieved. Limiting screening to those subjects aged ≥50 and ≥60 years resulted in more favorable cost-effectiveness compared with population-based screening without age restriction. Conclusions: Our analyses suggest the potentially favorable cost-effectiveness of population-based screening for albuminuria in the general Dutch population. The results offer health care decision-makers new tools for considering actual implementation of such screening.</description><subject>Adult</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Albuminuria - diagnosis</subject><subject>Albuminuria - economics</subject><subject>Biological and medical sciences</subject><subject>Biomarkers - analysis</subject><subject>Cardiovascular Agents - economics</subject><subject>Cardiovascular Agents - therapeutic use</subject><subject>Cardiovascular disease</subject><subject>Cardiovascular Diseases - economics</subject><subject>Cardiovascular Diseases - prevention &amp; control</subject><subject>Chronic illnesses</subject><subject>Cohort Studies</subject><subject>Cost analysis</subject><subject>Cost-Benefit Analysis</subject><subject>cost-effectiveness</subject><subject>Diabetes</subject><subject>Disease prevention</subject><subject>Early Diagnosis</subject><subject>Epidemiology</subject><subject>Expected values</subject><subject>Female</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Internal Medicine</subject><subject>Kidney diseases</subject><subject>Kidney Diseases - economics</subject><subject>Kidney Diseases - prevention &amp; control</subject><subject>Male</subject><subject>Markov Chains</subject><subject>Mass Screening - economics</subject><subject>Medical Education</subject><subject>Medical sciences</subject><subject>microalbuminuria</subject><subject>Middle Aged</subject><subject>Mortality</subject><subject>Nephrology</subject><subject>Nephrology. Urinary tract diseases</subject><subject>Netherlands</subject><subject>Pharmacoeconomics</subject><subject>Pharmacology. Drug treatments</subject><subject>Pharmacy</subject><subject>Public health</subject><subject>renal disease</subject><subject>Risk factors</subject><subject>screening</subject><subject>Urinary system involvement in other diseases. Miscellaneous</subject><subject>Urinary tract. 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Urinary tract diseases</topic><topic>Netherlands</topic><topic>Pharmacoeconomics</topic><topic>Pharmacology. Drug treatments</topic><topic>Pharmacy</topic><topic>Public health</topic><topic>renal disease</topic><topic>Risk factors</topic><topic>screening</topic><topic>Urinary system involvement in other diseases. Miscellaneous</topic><topic>Urinary tract. Prostate gland</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boersma, Cornelis, PhD</creatorcontrib><creatorcontrib>Gansevoort, Ron T., MD, PhD</creatorcontrib><creatorcontrib>Pechlivanoglou, Petros, MSc</creatorcontrib><creatorcontrib>Visser, Sipke T., MSc</creatorcontrib><creatorcontrib>van Toly, Flip F.J., MSc</creatorcontrib><creatorcontrib>de Jong-van den Berg, Lolkje T.W., PhD</creatorcontrib><creatorcontrib>de Jong, Paul E., MD, PhD</creatorcontrib><creatorcontrib>Postma, Maarten J., PhD</creatorcontrib><creatorcontrib>Prevention of Renal and Vascular End Stage Disease Study Group</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>ProQuest Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Healthcare Administration Database (Alumni)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Database (Alumni Edition)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Healthcare Administration Database (Proquest)</collection><collection>Medical Database</collection><collection>ProQuest research library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Research Library (Corporate)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boersma, Cornelis, PhD</au><au>Gansevoort, Ron T., MD, PhD</au><au>Pechlivanoglou, Petros, MSc</au><au>Visser, Sipke T., MSc</au><au>van Toly, Flip F.J., MSc</au><au>de Jong-van den Berg, Lolkje T.W., PhD</au><au>de Jong, Paul E., MD, PhD</au><au>Postma, Maarten J., PhD</au><aucorp>Prevention of Renal and Vascular End Stage Disease Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Screen-and-treat strategies for albuminuria to prevent cardiovascular and renal disease: Cost-effectiveness of nationwide and targeted interventions based on analysis of cohort data from the Netherlands</atitle><jtitle>Clinical therapeutics</jtitle><addtitle>Clin Ther</addtitle><date>2010-06-01</date><risdate>2010</risdate><volume>32</volume><issue>6</issue><spage>1103</spage><epage>1121</epage><pages>1103-1121</pages><issn>0149-2918</issn><eissn>1879-114X</eissn><abstract>Abstract Background: Albuminuria is a marker for renal and cardiovascular (CV) risk, allowing early diagnosis of subjects with elevated renal and CV risk. Objective: This study aimed to estimate the costeffectiveness and budget impact of various population-based screen-and-treat scenarios for elevated albuminuria levels (ie, microalbuminuria) in the Netherlands. Methods: A multistate transition Markov model was developed to simulate the natural course of albuminuria-based disease progression to dialysis and occurrence of CV events. Several population-based strategies directed at screening for elevated albuminuria were evaluated. These strategies depended on urinary albumin concentration (UAC), urinary albumin excretion (UAE), and age. Transition probabilities were derived from the observational community-based Prevention of Renal and Vascular End Stage Disease (PREVEND) cohort study. Health care costs (in year-2008 euros) and life-years gained were calculated over an 8-year period. In the base-case analysis, we analyzed screening for and treatment of microalbuminuria. Screening for microal-buminuria involved prescreening for UAC ≥20 mg/L, followed by a confirmation test for UAE ≥30 mg/d. Other options based on combinations of albuminuria for UAC prescreening (no prescreening, and ≥10, ≥20, ≥100, and ≥200 mg/L) and UAE confirmation test (≥15, ≥30, and ≥300 mg/d) for treatment were investigated in scenario analyses. Furthermore, these various strategies based on UAC and UAE values were analyzed in different subgroups based on age (all ages, aged ≥50 years, and aged ≥60 years). Results: The PREVEND study included 8592 Dutch residents aged 28 to 75 years at the time of initial screening. Among a hypothetical cohort of 1000 subjects identified and treated in the base-case analysis, it was estimated (based on PREVEND follow-up data) that, in the screening/treatment and no-screening scenarios, 76 versus 124 CV events occurred, 16 versus 27 CV deaths, and 3 versus 5 dialysis cases, respectively. The per-person difference in net costs for screening was calculated at €926 (€2003 vs €1077), and prevention of CV deaths was estimated to gain 0.0421 discounted life-year per person. Correspondingly, the cost-effectiveness was estimated at €22,000 per life-year gained. In the base-case analysis, probabilistic sensitivity analysis indicated that the likelihood of cost-effectiveness of a screen-and-treat strategy was 54%, 90%, and 95% for a maximum acceptable cost-effectiveness threshold of €20,000, €50,000, and €80,000 per life-year gained, respectively. Higher albuminuria thresholds for screening and start of treatment further improved the cost-effectiveness but reduced the overall health gains achieved. Limiting screening to those subjects aged ≥50 and ≥60 years resulted in more favorable cost-effectiveness compared with population-based screening without age restriction. Conclusions: Our analyses suggest the potentially favorable cost-effectiveness of population-based screening for albuminuria in the general Dutch population. The results offer health care decision-makers new tools for considering actual implementation of such screening.</abstract><cop>Bridgewater, NJ</cop><pub>EM Inc USA</pub><pmid>20637965</pmid><doi>10.1016/j.clinthera.2010.06.013</doi><tpages>19</tpages><oa>free_for_read</oa></addata></record>
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identifier ISSN: 0149-2918
ispartof Clinical therapeutics, 2010-06, Vol.32 (6), p.1103-1121
issn 0149-2918
1879-114X
language eng
recordid cdi_proquest_miscellaneous_733596183
source ScienceDirect Journals
subjects Adult
Age Factors
Aged
Albuminuria - diagnosis
Albuminuria - economics
Biological and medical sciences
Biomarkers - analysis
Cardiovascular Agents - economics
Cardiovascular Agents - therapeutic use
Cardiovascular disease
Cardiovascular Diseases - economics
Cardiovascular Diseases - prevention & control
Chronic illnesses
Cohort Studies
Cost analysis
Cost-Benefit Analysis
cost-effectiveness
Diabetes
Disease prevention
Early Diagnosis
Epidemiology
Expected values
Female
Humans
Hypertension
Internal Medicine
Kidney diseases
Kidney Diseases - economics
Kidney Diseases - prevention & control
Male
Markov Chains
Mass Screening - economics
Medical Education
Medical sciences
microalbuminuria
Middle Aged
Mortality
Nephrology
Nephrology. Urinary tract diseases
Netherlands
Pharmacoeconomics
Pharmacology. Drug treatments
Pharmacy
Public health
renal disease
Risk factors
screening
Urinary system involvement in other diseases. Miscellaneous
Urinary tract. Prostate gland
title Screen-and-treat strategies for albuminuria to prevent cardiovascular and renal disease: Cost-effectiveness of nationwide and targeted interventions based on analysis of cohort data from the Netherlands
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