Morten Schou
Copenhagen University Hospital
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Publication
Featured researches published by Morten Schou.
European Journal of Heart Failure | 2007
Morten Schou; Finn Gustafsson; Per H. Nielsen; Lene H. Madsen; Andreas Kjær; Per Hildebrandt
The usefulness of brain‐natriuretic‐peptide (BNP) and N‐terminal‐pro‐brain‐natriuretic‐peptide (NT‐proBNP) for monitoring of chronic heart failure (CHF) patients has been questioned because of high levels of unexplained variation.
European Journal of Heart Failure | 2017
Anders Jorsal; Caroline Kistorp; Pernille Holmager; Rasmus Stilling Tougaard; Roni Nielsen; Anja Hänselmann; Brian Nilsson; Jacob Eifer Møller; Jakob Hjort; Jon B. Rasmussen; Trine Welløv Boesgaard; Morten Schou; Lars Videbæk; Ida Gustafsson; Allan Flyvbjerg; Henrik Wiggers; Lise Tarnow
To determine the effect of the glucagon‐like peptide‐1 analogue liraglutide on left ventricular function in chronic heart failure patients with and without type 2 diabetes.
European Journal of Heart Failure | 2007
Pernille Corell; Finn Gustafsson; Morten Schou; John Markenvard; Tonny Nielsen; Per Hildebrandt
Atrial fibrillation (AF) is common in patients with heart failure (HF) due to left ventricular systolic dysfunction (LVSD), with conflicting prognostic data. The aim of our study was to assess the prevalence and incidence of AF in patients with HF and to determine the prognostic impact of baseline AF and the development of new onset AF.
European Journal of Heart Failure | 2011
Louise Balling; Morten Schou; Lars Videbæk; Per Hildebrandt; Henrik Wiggers; Finn Gustafsson
Hyponatraemia has been reported to be a potent predictor of poor outcome in patients hospitalized for heart failure (HF). The aim of the study was to determine the prevalence and prognostic significance of hyponatraemia in a large cohort of HF outpatients followed in clinics participating in the Danish Heart Failure Clinics Network.
European Heart Journal | 2013
Morten Schou; Finn Gustafsson; Lars Videbæk; Chr Tuxen; Niels Keller; Jens Handberg; Anne Sejr Knudsen; G. T. Espersen; John Markenvard; Kenneth Egstrup; Hans Ulriksen; Per Hildebrandt
BACKGROUND Outpatient follow-up in specialized heart failure clinics (HFCs) is recommended by current guidelines and implemented in most European countries, but the optimal duration of HFC programmes has not been established. Nor is it known whether all or only high-risk patients, e.g. identified by NT-proBNP, might benefit from an extended HFC follow-up. METHODS AND RESULTS In a multi-centre setting, we randomly assigned 921 clinically stable systolic heart failure (HF) outpatients on optimal medical therapy to undergo either an extended follow-up in the HFC (n = 461) or referral back to their general practitioner (GP) (n = 460). The primary composite endpoint was death or a cardiovascular admission. Secondary endpoints included mortality, an HF admission, quality of life, number of days admitted, and number of admissions. The median age of the patients was 69 years; 23% were females; the median left ventricular ejection fraction was 0.30; and the median NT-proBNP was 801 pg/mL; 89% were in NYHA class I-II. The median follow-up was 2.5 years. Time-to-event did not differ between groups (HFC vs. GP) (HR: 1.17, 95% CI: 0.95-1.45, P = 0.149). The two groups did not differ with respect to any of the secondary endpoints at the follow-up (P> 0.05 for all). In high-risk patients identified by NT-proBNP ≥1000 pg/mL, no benefit from HFC follow-up was found (P = 0.721). CONCLUSION Irrespective of the level of NT-proBNP stable HF patients on optimal medical therapy do not benefit from long-term follow-up in a specialized HFC in a publicly funded universal access healthcare system. Heart failure patients on optimal medical therapy with mild or moderate symptoms are safely managed by their personal GP. TRIAL REGISTRATION www.Centerwatch.com: 173491 (NorthStar).
Journal of Cardiac Failure | 2012
Louise Balling; Caroline Kistorp; Morten Schou; Michael Egstrup; Ida Gustafsson; Jens Peter Goetze; Per Hildebrandt; Finn Gustafsson
BACKGROUND Copeptin, a stable fragment of the vasopressin prohormone, has been shown to be a significant biomarker for morbidity and mortality in heart failure. The aims of this study were to evaluate the influence of plasma sodium on the prognostic significance of copeptin concentrations in heart failure outpatients and to determine whether increased copeptin concentrations predict future development of hyponatremia. METHODS AND RESULTS A total of 340 heart failure patients with left ventricular systolic dysfunction were followed for 55 months (median) in a Danish heart failure clinic. A baseline measurement of plasma copeptin, N-terminal pro-B-type natriuretic peptide (NT-proBNP), and sodium was performed, and the sodium concentrations were recorded during 3 months after the baseline visit in the heart failure clinic. Patients were divided into 3 groups according to copeptin tertiles. In multivariate Cox proportional hazard models adjusted for confounders, including plasma sodium, loop diuretic dose, and NT-proBNP, copeptin was a significant predictor of hospitalization or death (hazard ratio 1.4, 95% confidence interval 1.1-1.9; P < .019) but did not predict mortality independently from NT-proBNP. Additionally, copeptin concentrations did not predict future development of hyponatremia. CONCLUSIONS Plasma copeptin levels predict mortality in outpatients with chronic heart failure independently from clinical variables, plasma sodium, and loop diuretic doses. Furthermore, copeptin predicts the combined end point of hospitalization or death independently from NT-proBNP.
European Heart Journal | 2008
Jens Rosenberg; Morten Schou; Finn Gustafsson; Jørn Badskjær; Per Hildebrandt
AIMS Chronic heart failure (HF) is a common condition with a poor prognosis. As delayed diagnosis and treatment of HF patients in primary care can be detrimental, risk-stratified waiting lists for echocardiography might optimize resource utilization. We investigated whether a prognostic threshold level of the cardiac peptide, NT-proBNP, could be identified. METHODS AND RESULTS From 2003-2005, 5875 primary care patients with suspected HF (median age 73 years) had NT-proBNP analysed in the Copenhagen area. Eighteen percent died and 20% had a cardiovascular (CV) hospitalization (median follow-up time: 1127 and 1038 days, respectively). In Cox proportional hazards regression models regarding NT-proBNP levels, the fourth decile (range: 83-118 pg/mL) was associated with a 90% (95% CI: 30-190, P < 0.01) increased risk for CV hospitalization and the seventh decile (range: 229-363 pg/mL) was associated with an 80% (95% CI: 20-190, P = 0.01) increased mortality risk after adjustment for age, sex, previous hospitalization, CV diseases, and chronic diseases. CONCLUSION We identified prognostic threshold levels for mortality and CV hospitalization for NT-proBNP in primary care patients suspected of HF. Our results have the potential to be used to risk-stratify waiting lists for echocardiography.
European Journal of Heart Failure | 2011
Michael Egstrup; Morten Schou; Ida Gustafsson; Caroline Kistorp; Per Hildebrandt; Christian Tuxen
We evaluated the applicability and prognostic importance of oral glucose tolerance testing (OGTT) among outpatients with systolic heart failure (SHF).
International Journal of Cardiology | 2013
Helle Bosselmann; Michael Egstrup; Kasper Rossing; Ida Gustafsson; Finn Gustafsson; Niels Tonder; Caroline Kistorp; Jens Peter Goetze; Morten Schou
OBJECTIVE To assess whether the prognostic significance of cardiovascular (CV) biomarkers, is affected by renal dysfunction (RD) in systolic heart failure (HF). BACKGROUND It is unknown, whether the prognostic significance of CV biomarkers, such as N-terminal-pro-brain-natriuretic-peptide (NT-proBNP), high-sensitive troponin T (hsTNT), pro-atrial natriuretic peptide (proANP), copeptin and pro-adrenomedullin (proADM), is affected by renal function in HF. METHODS Clinical data and laboratory tests from 424 patients with systolic HF were collected prospectively. The patients were followed for 4.5 years (interquartile range: 2-7.7 years). CV biomarkers were analyzed on frozen plasma, and renal function was estimated by the Modification of Diet in Renal Disease (MDRD) formula. Cox proportional hazard models for mortality risk were constructed and tests for interaction between each CV biomarker and RD were performed. RESULTS Median age was 73 years (51-83), 29% were female, LVEF was 30% (13-45), 74% were NYHA classes I-II and estimated glomerular filtration rate (eGFR) was 68 ml/min/1.73 m(2) (18-157). A total of 252 patients died. All five biomarkers--log(NT-proBNP) (HR: 2.13, 95% CI: 1.57-2.87:, P<0.001), hsTNT (HR: 3.07, 95% CI: 1.90-4.96 P<0.001), proANP (HR: 1.02, 95% CI: 1.01-1.03, P<0.001), copeptin (HR: 1.02, 95% CI: 1.01-1.03, P=0.008) and proADM (HR: 2.37, 95% CI: 1.66-3.38, P<0.001)--were associated with mortality risk, but not affected by RD (P>0.05 for all interactions). CONCLUSION Established and new CV biomarkers are closely associated with renal function in HF. However, their prognostic significance is not affected by RD, and all CV biomarkers can be used for risk stratification independently of renal function.
European Journal of Heart Failure | 2007
Finn Gustafsson; Morten Schou; Lars Videbæk; Tonny Nielsen; Hans Ulriksen; John Markenvard; Tage Lysbo Svendsen; Henrik Ryde; Else Vigholt; Per Hildebrandt
Beta‐blockers (BBs) are a cornerstone in the treatment of chronic heart failure (HF), but several surveys have documented that many patients are not offered treatment or are not titrated to target doses. In part to address this problem, specialized, nurse‐led HF clinics have been initiated in many countries. However, little information is available to describe if such programs are successful in initiating and up‐titrating BBs in daily clinical practice.