* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Use of levosimendan in the treatment of acute heart failure
Coronary artery disease wikipedia , lookup
Arrhythmogenic right ventricular dysplasia wikipedia , lookup
Remote ischemic conditioning wikipedia , lookup
Electrocardiography wikipedia , lookup
Cardiac contractility modulation wikipedia , lookup
Management of acute coronary syndrome wikipedia , lookup
Heart failure wikipedia , lookup
Antihypertensive drug wikipedia , lookup
Dextro-Transposition of the great arteries wikipedia , lookup
FACULTY OF M EDIC INE – U NIVERSITY OF P ORTO Department of Biostatistics and Medical Informatics Introdução à Medicina 2005/2006 Use of levosimendan in the treatment of acute heart failure Cristina Mendes, David Mota, Débora Monteiro, Diana Gomes [email protected] [email protected] [email protected] [email protected] Diana Martins Diana Rodrigues Diogo Garrido Diva Oliveira [email protected] [email protected] [email protected] [email protected] Ricardo Correia [email protected] Adviser: Dra. Filipa Almeida, [email protected], Class: 7 Abstract Introduction: Acute heart failure (AHF) is a condition that can result from any structural or functional cardiac disorder that impairs the ability of the heart to fill with or pump a sufficient amount of blood throughout the body. Usual treatments for AHF are inotropic agents. A new inotropic agent, levosimendan, was developed for the treatment of this disease. It has been shown to bring better haemodynamic function in patients with decompensated heart failure while maintaining arterial blood pressure. Aim: Estudar o efeito do levosimendan no tratamento da insufiência cardíaca aguda comparando-o com os tratamentos usuais (dobutamina e dopamina). Methods: A literature search covering PubMed and Cochrane medical databases was conducted to identify randomised controlled trials (RCT’s) about the effects of Levosimendan in the treatment of acute heart failure. The articles obtained in this search were submitted to an exclusion phase, followed by an inclusion phase. A total amount of 10 articles meeting the inclusion criteria were accepted and were statistically analyzed by a group of three reviewers. Results: Levosimendan was effective in the treatment of acute heart failure. From the total analyzed articles, 5 were found to report statistically significant results, from which 4 revealed a favorable effect of levosimendan in the treatment of AHF. Discussion: based on the available studies, levosimendan showed to be more advantageous than placebo concerning the number of survivors after 6 months of treatment, the variation of SV after 24 hours of infusion, a SV increase of 25% or more and favourable variation of BNP levels after 48 hours of treatment. Key-words: Heart Failure, Congestive; Cardiotonic Agents; Shock, Cardiogenic Introduction Acute Heart Failure (AHF) is a physiopathologic state, defined as the rapid onset of symptoms and signs secondary to abnormal cardiac function [12], in which the heart is prevented from pumping the required amount of blood to suppress the tissues’ metabolic needs [11]. It is usually a consequence of a severe anatomic or functional change, such as an acute myocardial infarction, a hypertensive crisis or an acute arrhythmia or even a decompensation of pre-existing chronic heart failure [13], commonly accompanied by a FACULTY OF M EDIC INE – U NIVERSITY OF P ORTO Department of Biostatistics and Medical Informatics Introdução à Medicina 2005/2006 sudden appearance of symptoms, such as fatigue, orthopnea, weakness, chest pain, increased BNP levels, among others, hence the “Acute” designation. Brain Natriuretic Peptides (BNP) are cardiac neurohormones that appear as a sistemic response to increases in ventricular wall tension, pressure overload and also ventricular volume expansion. Therefore, it is easy to understand that increased levels of serum BNP indicate overworking of ventricular muscle and/or some sort of cardiac disfunction, often associated with AHF. Patients with AHF have a very poor prognosis, being that in the largest randomized trial to date in patients hospitalized with decompensated heart failure, the 60-day mortality rate was 9.6% and the combined rate for mortality and re-hospitalization within 60 days was 35,2% [14]. Estimates of the risk of death or re-hospitalizations within 60 days of admission vary from 30 to 60% depending on the population studied. [15, 16] The goals of common treatments are to improve symptoms and to stabilize the hemodynamic condition, turning to several drugs that can be used for such purpose, as for instance: diuretics, vasodilators, inotropic agents (such as dobutamine or dopamine, who mimic the actions of the nervous sympathetic system), vasopressor agents (such as epinephrine or norepinephrine) or phosphodiesterase inhibitors [17]. Levosimendan, that is an inotropic agent, is on the top of the list of the leading drugs in the treatment of this pathology. It appears to be an alternative treatment to AHF [18] because it works as a calcium-sensitizer, which is able to enhance cellular responsiveness to Ca2+ without increasing calcium’s intracellular concentration, improving myocardial contractility (inotropic agent) without altering the heart muscle cells’ natural physiologic conditions. It does so by increasing Troponin C’s affinity to Ca2+ and helping to maintain its original conformation. It is also a vasodilator, by activating ATP-dependent potassium channels that cause an increased diameter of blood vessels throughout the body. The other inotropic therapies appear to be associated with higher mid/long term mortality rate and conditions such as arrhythmias and disturbed oxygen balance on the heart. Recently some studies have been published about the efficacy and safety of levosimendan in the treatment of AHF. FACULTY OF M EDIC INE – U NIVERSITY OF P ORTO Department of Biostatistics and Medical Informatics Introdução à Medicina 2005/2006 Methods The bibliographic research was performed in PubMed and Cochrane’s databases, from the earliest achievable date until that day. The query to search Pubmed was defined as: (("Heart Failure, Congestive"[MeSH] OR "Shock, Cardiogenic"[MeSH] OR heart failure OR cardiac insufficiency) AND (levosimendan OR calcium sensitizer) AND (placebo OR “Dopamine”[MeSH] OR Dopamine OR Dobutamine OR "Dobutamine"[MeSH] OR inotropic OR "Epinephrine"[MeSH] OR Epinephrine OR norepinephrine OR adrenaline OR noradrenaline OR "Norepinephrine"[MeSH] OR "Cardiotonic Agents"[MeSH] OR "Phosphodiesterase Inhibitors"[MeSH] OR "Natriuretic Peptide, Brain"[MeSH] OR “Atrial Natriuretic Factor”[MeSH])) NOT Review. Another query was also defined to search Cochrane’s database: ("Heart Failure" OR "Cardiogenic Shock" OR “acute heart failure” OR “acute cardiac insufficiency”) AND (levosimendan OR “calcium sensitizer”) AND (placebo OR Dopamine OR Dobutamine OR inotropic OR Epinephrine OR Norepinephrine OR Cardiotonic OR “Phosphodiesterase Inhibitors”). As much as 115 articles in Pubmed and 39 articles in Cochrane were found. After searching, the exclusion criteria were established. In the exclusion process, done by three reviewers, articles were considered relevant when presented in English, Portuguese, Spanish and French and mentioned levosimendan, directly or indirectly (through other designation such as calcium sensitizer) and did not approach its effects on the heart and/or cardiac tissue. The searched articles should also be either a randomized clinical trial or an observational longitudinal study. Upon tracing, 84 articles from PubMed and 21 articles from Cochrane were excluded. In the following stage another group of three reviewers defined the inclusion criteria which highlighted the articles that were directly related to the reviews’ main subject and compared the therapeutical effects of levosimendan with those of other standard treatments, tested on a minimum of 5 human individuals. With the approval of the majority of the reviewers, 8 articles were included from PubMed and 10 articles from Cochrane, of which 8 were repeated when crossed with PubMed’s results. FACULTY OF M EDIC INE – U NIVERSITY OF P ORTO Department of Biostatistics and Medical Informatics Introdução à Medicina 2005/2006 In the end, a pool of 10 different articles was available for data extraction, having selected and obtained the most relevant results from each individual article, bearing in mind the project’s objective, and registering them with the help of SPSS. Results Article number Measured parameter Compares Levosimendan to: Difference of survivors after 6 Dobutamine months of treatment. Difference of 2 survivors after 6 Placebo months of treatment. Comparative increase 3 Placebo in HR. Difference of SV 4a variation after 24 Placebo hours of infusion. Difference of SV 4b variation after 24 Dobutamine hours of infusion. Difference of subjects whose 5 stroke volume Placebo increased 25% or more after treatment. Difference of disease progression (death or 6 rehospitalization) 5 Placebo months after treatment. Difference of BNP levels variation after 7 Dobutamine 48 hours of treatment. Difference of SV 8 variation after 6 Placebo hours of infusion. Difference of HR 9 variation after 24 Placebo hours of treatment. Difference of HR 10 variation after 12 Dobutamine hours of treatment. Table 1. Results extracted from analyzed articles. 1 n (comparison) Result Favorable to Statistically Significant (p<0,05) 103 100 11% Levosimendan n/a 103 102 5,2% Levosimendan Yes 4 4 7% Placebo Yes 23 20 21,47 % Levosimendan Yes 23 20 5,96% Levosimendan No 98 48 52% Levosimendan Yes 17 17 18% Levosimendan n/a 15 14 25,41 % Levosimendan Yes 98 48 30,95 % Levosimendan n/a 15 15 1,05% Levosimendan No 7 8 2,52% Levosimendan No n (levosimendan) FACULTY OF M EDIC INE – U NIVERSITY OF P ORTO Department of Biostatistics and Medical Informatics Introdução à Medicina 2005/2006 Discussion This study shows that levosimendan presents a favorable effect on patients with acute heart failure (AHF) in mosto f the evaluated paramenters. Acording to article [2], 6 months after treatment, levosimendan leads to a larger number of survivors when compared to placebo, demonstrating an improved treatment efficiency. In article 3, however, placebo was found to have an advantage in the heart’s rate variation, being that it’s reported increase by the use of levosimendan is not adequate for AHF patients who need to stabilize heart rate at lower values. In article [4], levosimendan is compared to placebo and dobutamine, although only the first comparison (levosimendan vs placebo) is statistically significant. A larger variation of SV after 24 hours of infusion was verified in levosimendan’s results. This haemodynamic effect is a favourable consequence of this new drug’s administration in the treatment of AHF, as it reveals an improvement in cardiac function. Article [5] also evaluates SV variation, detailing a percentage of patients that showed an increase of 25% or more in SV, where once again levosimendan was found to be more effective than placebo. Finally, article [7] shows a comparison of levosimendan to dobutamine, where levosimendan was found to cause a larger decrease of BNP levels, which is also considered a positive result seeing that BNP is secreted by the heart’s ventricles in response to excessive stretching of myocytes (heart muscle cells), and therefore elevated BNP levels in the blood can be used to diagnose AHF. Other articles focused on this study (1, 4b, 6, 8, 9, 10) are not discussed here, given the fact that they do not provide statistically significant results. It is also important to point out that the results from this study might not be strictly rigorous, given some methodologic limitations inherent to either its design or execution, such as the limited number of participants in some clinical trials, the unavailability of some articles found on the searched databases, inclusion and exclusion criteria that might not be the most appropriate and the possibility of human error during the inclusion, exclusion and/or article analysis. FACULTY OF M EDIC INE – U NIVERSITY OF P ORTO Department of Biostatistics and Medical Informatics Introdução à Medicina 2005/2006 Conclusion: The studies show levosimendan to be an effective drug in the treatment of acute heart failure (AHF). The parameters evidenced in table 1 and discussed above demonstrate its advantageous effect compared to dobutamine, in one of the cases, and to placebo, in other three. Levosimendan is therefore an innovating inotropic agent that can become a promising, if not leading treatment to AHF. A possible exception to this statement is the heart rate increase upon use of levosimendan verified in the article [3], which is not recommended in such cases, as AHF patients tend to require stabilization at lower heart rates, but, as discussed above, further research in this matter might be of interest as the study that indicated this had a somewhat small participant number. Acknowledgments We would like to thank Dr. Filipa Almeida, our teacher for Medical Informatics on the subject of “Introduction to Medicine – IM” and our project orientor, for all her help and guidance throughout the entire project. References [1] J.G.F. Cleland, A. Takala, M. Apajasal, N. Zethraeus, G. Kobelt. Intravenous levosimendan treatment is cost-effective compared with dobutamine in severe lowoutput heart failure: an analysis based on the international LIDO trial. Eur J Heart Fail. 2003 Jan;5(1):101-8. [2] V. S. Moiseyev, P. Poder, N. Andrejevs, M. Y. Ruda, A. P. Golikov, L. B. Lazebnik, e tal. Safety and efficacy of a novel calcium sensitizer, levosimendan, in patients with left ventricular failure due to an acute myocardial infarction. Eur Heart J. 2002 Sep;23(18):1422-32. [3] Heikki Ukkonen, Markku Saraste, Juha Akkila, Juhani Knuuti, Meri Karanko, Hidehiro Iida, et al. Myocardial efficiency during levosimendan infusion in congestive heart failure. Clin Pharmacol Ther. 2000 Nov;68(5):522-31. FACULTY OF M EDIC INE – U NIVERSITY OF P ORTO Department of Biostatistics and Medical Informatics Introdução à Medicina 2005/2006 [4] Markku S. Nieminen, Juha Akkila, Gerd Hasenfuss, Franz X. Kleber, Lasse A. Lehtonen, Veselin Mitrovic, et al. Hemodynamic and Neurohumoral Effects of Continuous Infusion of Levosimendanin Patients With Congestive Heart Failure. J Am Coll Cardiol. 2000 Nov 15;36(6):1903-12. [5] Mara T. Slawsky, Wilson S. Colucci, Stephen S. Gottlieb, Barry H. Greenberg, Ernest Haeusslein, Joshua Hare. Acute Hemodynamic and Clinical Effects of Levosimendan in Patients With Severe Heart Failure. Circulation. 2000 Oct 31;102(18):2222-7. [6] John T. Parissis, Fotios Panou, Dimitrios Farmakis, Stamatis Adamopoulos, Gerasimos Filippatos, Ioannis Paraskevaidis, e al. Effects of Levosimendan on Markers of Left Ventricular Diastolic Function and Neurohormonal Activation in Patients With Advanced Heart Failure. Am J Cardiol. 2005 Aug 1;96(3):423-6 [7] Catherine Avgeropoulou, Ioanna Andreadou, Sophia Markantonis-Kyroudis, Maritina Demopoulou, Platon Missovoulos, Aris Androulakis, et al. The Ca2+-sensitizer levosimendan improves oxidative damage, BNP and pro-inflammatory cytokine levels in patients with advanced decompensated heart failure in comparison to dobutamine. Eur J Heart Fail. 2005 Aug;7(5):882-7. [8] Matti Kivikko, Lasse Lehtonen, PhD; Wilson S. Colucci. Sustained Hemodynamic Effects of Intravenous Levosimendan. Circulation. 2003 Jan 7;107(1):81-6. [9] Ha Kasikcioglu, Z Tartan1, E Okmen, E Kasikcioglu and N Cam. Effects of Levosimendan on Left Ventricular Functional Remodelling and Exercise Intolerance: a Tissue Doppler Study. J Int Med Res. 2005 Jul-Aug;33(4):397-405. [10] Ferenc Folláth, Susanna Hinkka, Detlef Jager, Hanjorg Just, Veselin Mitrovic, Julius Gy. Papp, et al. Dose-Ranging and Safety with Intravenous Levosimendan in Low-Output Heart Failure: Experience in Three Pilot Studies and Outline of the Levosimendan Infusion Versus Dobutamine (LIDO) Trial. Am J Cardiol. 1999, 83(12):21-25 [11] Braunwald, et al . A textbook of Cardiovascular Medicine. Elsevier Saunders, 7th Ed, 509-539 FACULTY OF M EDIC INE – U NIVERSITY OF P ORTO Department of Biostatistics and Medical Informatics Introdução à Medicina 2005/2006 [12] Felker G et al. The problem of decompensated heart failure: nomenclature, classification and risk stratification. Am Heart L 2003; 145: S18-25 [13] Swedberg K et al. Guidelines for the diagnosis and treatment of chronic heart failure. Eur Heart J 2005; 45: 123-200 [14] Cleland J el al. The Euroheart failure survey program. Eur Heart J 2003; 24: 442463 [15] McAlister f et al. A systematic review of randomized trials of disease management programs in heart failure. Am J Med 2001; 110: 378-384 [16] Rich M et al. A multidisciplinary intervention to prevent the readmission of elderly patients with congestive heart failure. N Engl J Med 1995; 333:1190-1195 [17] Nieminen M et al. Guidelines on the diagnosis and treatment of acute heart failure. Eur Heart J 2005; 44: 567-610 [18] F Follath, et al . Efficacy and safety of intravenous levosimendan compared with dobutamine in severe low-output heart failure (the LIDO study): a randomised doubleblind trial. Lancet 2002;