Intravenous levosimendan treatment is cost-effective compared with dobutamine in severe low-output heart failure: an analysis based on the international LIDO trial

Background: Levosimendan, a novel calcium sensitiser, improves cardiac performance and symptoms without increasing oxygen consumption, and decreases the mortality of patients with low‐output heart failure. Aims: To estimate the cost‐effectiveness of intravenous treatment with levosimendan compared w...

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Veröffentlicht in:European journal of heart failure 2003-01, Vol.5 (1), p.101-108
Hauptverfasser: Cleland, J.G.F., Takala, A., Apajasalo, M., Zethraeus, N., Kobelt, G.
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container_end_page 108
container_issue 1
container_start_page 101
container_title European journal of heart failure
container_volume 5
creator Cleland, J.G.F.
Takala, A.
Apajasalo, M.
Zethraeus, N.
Kobelt, G.
description Background: Levosimendan, a novel calcium sensitiser, improves cardiac performance and symptoms without increasing oxygen consumption, and decreases the mortality of patients with low‐output heart failure. Aims: To estimate the cost‐effectiveness of intravenous treatment with levosimendan compared with dobutamine in patients with severe low‐output heart failure. Methods: This economic evaluation was based on a European clinical trial (LIDO), in which 203 patients with severe heart failure randomly received a 24 h infusion with either levosimendan or dobutamine. Survival and resource utilisation data were collected for 6 months; survival was extrapolated assuming a mean additional lifetime of 3 years based on data from the Cooperative North Scandinavian Enalapril Survival Study trial. Costs were based on study drug usage and hospitalisation in the 6‐month follow‐up. A sensitivity analysis on dosage of drug and duration of survival was performed. Results: The mean survival over 6 months was 157±52 days in the levosimendan group and 139±64 days in the dobutamine group (P
doi_str_mv 10.1016/S1388-9842(02)00246-5
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Aims: To estimate the cost‐effectiveness of intravenous treatment with levosimendan compared with dobutamine in patients with severe low‐output heart failure. Methods: This economic evaluation was based on a European clinical trial (LIDO), in which 203 patients with severe heart failure randomly received a 24 h infusion with either levosimendan or dobutamine. Survival and resource utilisation data were collected for 6 months; survival was extrapolated assuming a mean additional lifetime of 3 years based on data from the Cooperative North Scandinavian Enalapril Survival Study trial. Costs were based on study drug usage and hospitalisation in the 6‐month follow‐up. A sensitivity analysis on dosage of drug and duration of survival was performed. Results: The mean survival over 6 months was 157±52 days in the levosimendan group and 139±64 days in the dobutamine group (P&lt;0.01). When extrapolated up to 3 years, the gain in life expectancy was estimated at 0.35 years (discounted at 3%). Levosimendan increased the mean cost per patient by €1108, which was entirely due to the cost of the study drug. The incremental cost per life‐year saved (LYS) was €3205 at the European level; in the individual countries the cost per LYS ranged between €3091 and €3331. The result was robust in the sensitivity analysis. Conclusions: Although the patients in the levosimendan group were alive for more days and thus at risk of hospitalisation for longer, there was no increase in hospitalisation or hospitalisation costs with levosimendan treatment. The cost per LYS using levosimendan compares favourably with other cost‐effectiveness analyses in cardiology.</description><identifier>ISSN: 1388-9842</identifier><identifier>EISSN: 1879-0844</identifier><identifier>DOI: 10.1016/S1388-9842(02)00246-5</identifier><identifier>PMID: 12559222</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Aged ; Cardiac Output, Low - drug therapy ; Cardiac Output, Low - economics ; Cardiac Output, Low - epidemiology ; Cardiotonic Agents - economics ; Cardiotonic Agents - therapeutic use ; Cost-Benefit Analysis - economics ; cost-effectiveness ; dobutamine ; Dobutamine - economics ; Dobutamine - therapeutic use ; Double-Blind Method ; Europe - epidemiology ; Female ; Follow-Up Studies ; heart failure ; Heart Failure - drug therapy ; Heart Failure - economics ; Heart Failure - epidemiology ; Humans ; Hydrazones - economics ; Hydrazones - therapeutic use ; Infusions, Intravenous ; Length of Stay - economics ; levosimendan ; LIDO trial ; Life Expectancy ; Male ; Middle Aged ; Patient Admission - economics ; Pyridazines - economics ; Pyridazines - therapeutic use ; Randomized Controlled Trials as Topic ; Risk Factors ; Sensitivity and Specificity ; Severity of Illness Index ; Simendan ; Survival Analysis ; Treatment Outcome</subject><ispartof>European journal of heart failure, 2003-01, Vol.5 (1), p.101-108</ispartof><rights>Published on behalf of the European Society of Cardiology. 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Aims: To estimate the cost‐effectiveness of intravenous treatment with levosimendan compared with dobutamine in patients with severe low‐output heart failure. Methods: This economic evaluation was based on a European clinical trial (LIDO), in which 203 patients with severe heart failure randomly received a 24 h infusion with either levosimendan or dobutamine. Survival and resource utilisation data were collected for 6 months; survival was extrapolated assuming a mean additional lifetime of 3 years based on data from the Cooperative North Scandinavian Enalapril Survival Study trial. Costs were based on study drug usage and hospitalisation in the 6‐month follow‐up. A sensitivity analysis on dosage of drug and duration of survival was performed. Results: The mean survival over 6 months was 157±52 days in the levosimendan group and 139±64 days in the dobutamine group (P&lt;0.01). When extrapolated up to 3 years, the gain in life expectancy was estimated at 0.35 years (discounted at 3%). Levosimendan increased the mean cost per patient by €1108, which was entirely due to the cost of the study drug. The incremental cost per life‐year saved (LYS) was €3205 at the European level; in the individual countries the cost per LYS ranged between €3091 and €3331. The result was robust in the sensitivity analysis. Conclusions: Although the patients in the levosimendan group were alive for more days and thus at risk of hospitalisation for longer, there was no increase in hospitalisation or hospitalisation costs with levosimendan treatment. 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Aims: To estimate the cost‐effectiveness of intravenous treatment with levosimendan compared with dobutamine in patients with severe low‐output heart failure. Methods: This economic evaluation was based on a European clinical trial (LIDO), in which 203 patients with severe heart failure randomly received a 24 h infusion with either levosimendan or dobutamine. Survival and resource utilisation data were collected for 6 months; survival was extrapolated assuming a mean additional lifetime of 3 years based on data from the Cooperative North Scandinavian Enalapril Survival Study trial. Costs were based on study drug usage and hospitalisation in the 6‐month follow‐up. A sensitivity analysis on dosage of drug and duration of survival was performed. Results: The mean survival over 6 months was 157±52 days in the levosimendan group and 139±64 days in the dobutamine group (P&lt;0.01). When extrapolated up to 3 years, the gain in life expectancy was estimated at 0.35 years (discounted at 3%). Levosimendan increased the mean cost per patient by €1108, which was entirely due to the cost of the study drug. The incremental cost per life‐year saved (LYS) was €3205 at the European level; in the individual countries the cost per LYS ranged between €3091 and €3331. The result was robust in the sensitivity analysis. Conclusions: Although the patients in the levosimendan group were alive for more days and thus at risk of hospitalisation for longer, there was no increase in hospitalisation or hospitalisation costs with levosimendan treatment. The cost per LYS using levosimendan compares favourably with other cost‐effectiveness analyses in cardiology.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>12559222</pmid><doi>10.1016/S1388-9842(02)00246-5</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Cardiac Output, Low - drug therapy
Cardiac Output, Low - economics
Cardiac Output, Low - epidemiology
Cardiotonic Agents - economics
Cardiotonic Agents - therapeutic use
Cost-Benefit Analysis - economics
cost-effectiveness
dobutamine
Dobutamine - economics
Dobutamine - therapeutic use
Double-Blind Method
Europe - epidemiology
Female
Follow-Up Studies
heart failure
Heart Failure - drug therapy
Heart Failure - economics
Heart Failure - epidemiology
Humans
Hydrazones - economics
Hydrazones - therapeutic use
Infusions, Intravenous
Length of Stay - economics
levosimendan
LIDO trial
Life Expectancy
Male
Middle Aged
Patient Admission - economics
Pyridazines - economics
Pyridazines - therapeutic use
Randomized Controlled Trials as Topic
Risk Factors
Sensitivity and Specificity
Severity of Illness Index
Simendan
Survival Analysis
Treatment Outcome
title Intravenous levosimendan treatment is cost-effective compared with dobutamine in severe low-output heart failure: an analysis based on the international LIDO trial
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