Matias G. Lindholm
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Research Interests
Matias G. Lindholm has a total of 28 co-authors. Here are the top co-authors by number of shared publications:
Søren Boesgaard
Medical Department B, Division of Cardiology, Rigshospitalet, University Hospital of Copenhagen
2 shared publications- Alessandro Sionis
Cardiology Department, Hospital de la Santa Creu i Sant Pau, IIB-Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain; Centro de Investigación Biomédica en Red de Enfermedades Cardiovasculares (CIBERCV) , 28029 Madrid
1 shared publication - Alexandre Mebazaa
Intensive Care Department, Hôpital Lariboisière, Sorbone University , Paris
1 shared publication Anders Hejmdal
Department of Medicine, Division of Cardiology, University of Copenhagen, Denmark
1 shared publicationC. Torp-Pedersen
Medical Department B, Division of Cardiology, Rigshospitalet, University Hospital of Copenhagen
1 shared publication- Heli Tolppanen
Department of Cardiology, Heart and Lung Center (J. Pirinen, H.T., J.S.), Helsinki University Hospital and University of Helsinki, Finland
1 shared publication
Latest Publications
- Open Access
- 1 January 2017
- Published by Elsevier in Annals of Intensive Care
- Vol. 7 (1) , 1-10
Adrenomedullin: a marker of impaired hemodynamics, organ dysfunction, and poor prognosis in cardiogenic shock
- 1 January 2017
- Published by Elsevier in Annals of Intensive Care
- Vol. 7 (1) , 1-10
Open AccessAdrenomedullin: a marker of impaired hemodynamics, organ dysfunction, and poor prognosis in cardiogenic shock
- 1 July 2008
- Published by Oxford University Press (OUP) in European Journal of Heart Failure
- Vol. 10 (7) , 668-674
Percutaneous Coronary Intervention for Acute MI Does not Prevent In-Hospital Development of Cardiogenic Shock Compared to Fibrinolysis
Background: It has been speculated that invasive revascularization prevents development of cardiogenic shock. Data from randomised trials comparing angioplasty with fibrinolysis on the development of cardiogenic shock are lacking. Aims: To elucidate the effect of angioplasty on in-hospital development of cardiogenic shock compared to fibrinolysis. To evaluate whether mortality in patients who develop cardiogenic shock after treatment is dependent on revascularization strategy. Methods and results: DANAMI-2 randomly assigned 1572 STEMI patients to fibrinolysis (782 patients) or angioplasty (790 patients). Data on patients with in-hospital development of cardiogenic shock after randomisation were included. Of the 103 patients (6.6%) patients developing cardiogenic shock 57% were randomised to angioplasty with an unadjusted odds ratio of 1.39 (0.92–2.11, p=0.14). During the three year follow-up 58% of the total mortality was due to cardiogenic shock, and treatment strategy did not influence the risk associated with shock (hazard ratio of 1.05 (0.67–1.64) for angioplasty vs. fibrinolysis). Conclusions: Angioplasty does not prevent the in-hospital development of cardiogenic shock complicating acute MI compared to fibrinolysis. Cardiogenic shock is still the leading cause of death in patients hospitalised for acute MI. There was no difference in mortality, with regards to treatment strategy in patients developing cardiogenic shock after the initial treatment.
- 1 July 2008
- Published by Oxford University Press (OUP) in European Journal of Heart Failure
- Vol. 10 (7) , 668-674
Percutaneous Coronary Intervention for Acute MI Does not Prevent In-Hospital Development of Cardiogenic Shock Compared to Fibrinolysis
Background: It has been speculated that invasive revascularization prevents development of cardiogenic shock. Data from randomised trials comparing angioplasty with fibrinolysis on the development of cardiogenic shock are lacking. Aims: To elucidate the effect of angioplasty on in-hospital development of cardiogenic shock compared to fibrinolysis. To evaluate whether mortality in patients who develop cardiogenic shock after treatment is dependent on revascularization strategy. Methods and results: DANAMI-2 randomly assigned 1572 STEMI patients to fibrinolysis (782 patients) or angioplasty (790 patients). Data on patients with in-hospital development of cardiogenic shock after randomisation were included. Of the 103 patients (6.6%) patients developing cardiogenic shock 57% were randomised to angioplasty with an unadjusted odds ratio of 1.39 (0.92–2.11, p=0.14). During the three year follow-up 58% of the total mortality was due to cardiogenic shock, and treatment strategy did not influence the risk associated with shock (hazard ratio of 1.05 (0.67–1.64) for angioplasty vs. fibrinolysis). Conclusions: Angioplasty does not prevent the in-hospital development of cardiogenic shock complicating acute MI compared to fibrinolysis. Cardiogenic shock is still the leading cause of death in patients hospitalised for acute MI. There was no difference in mortality, with regards to treatment strategy in patients developing cardiogenic shock after the initial treatment.
- 30 April 2007
- Published by Elsevier in Journal of Cardiac Failure
- Vol. 13 (3) , 184-188
B-Type Natriuretic Peptide and its Molecular Precursor in Myocardial Infarction Complicated by Cardiogenic Shock
- 30 April 2007
- Published by Elsevier in Journal of Cardiac Failure
- Vol. 13 (3) , 184-188
B-Type Natriuretic Peptide and its Molecular Precursor in Myocardial Infarction Complicated by Cardiogenic Shock
- 1 August 2005
- Published by Oxford University Press (OUP) in European Journal of Heart Failure
- Vol. 7 (5) , 834-839
Diabetes Mellitus and Cardiogenic Shock in Acute Myocardial Infarction
Aims: Cardiogenic shock is the leading cause of in-hospital mortality after acute myocardial infarction (MI). This study investigates the importance of age and preexisting diabetes mellitus on the incidence and prognosis of cardiogenic shock in a large group of consecutive patients with MI. Methods and results: Baseline characteristics and in-hospital complications to the infarction were prospectively recorded in 6676 patients with MI. Ten-year mortality was collected. Diabetes was present in 10.8% of the total population. A total of 443 developed cardiogenic shock with an incidence of 6.2% among nondiabetics and 10.6% among diabetics. Age, wall motion index, reinfarction, and the absence of thrombolytic treatment were significant independent predictors of mortality in patients with cardiogenic shock. Intriguingly, diabetes was not a significant predictor for short- and long-term mortality in this population. The 30-day and 5-year mortality rate was equally poor in both diabetic and nondiabetic patients with cardiogenic shock (diabetics: 30-day 63%, 5-year 91%; nondiabetics: 30-day 62%, 5-year 86%; p>0.05). Conclusions: Cardiogenic shock develops approximately twice as often among diabetics as among nondiabetic patients with acute MI. The prognosis of diabetics with cardiogenic shock is similar to the prognosis of nondiabetic patients with cardiogenic shock.
- 1 August 2005
- Published by Oxford University Press (OUP) in European Journal of Heart Failure
- Vol. 7 (5) , 834-839
Diabetes Mellitus and Cardiogenic Shock in Acute Myocardial Infarction
Aims: Cardiogenic shock is the leading cause of in-hospital mortality after acute myocardial infarction (MI). This study investigates the importance of age and preexisting diabetes mellitus on the incidence and prognosis of cardiogenic shock in a large group of consecutive patients with MI. Methods and results: Baseline characteristics and in-hospital complications to the infarction were prospectively recorded in 6676 patients with MI. Ten-year mortality was collected. Diabetes was present in 10.8% of the total population. A total of 443 developed cardiogenic shock with an incidence of 6.2% among nondiabetics and 10.6% among diabetics. Age, wall motion index, reinfarction, and the absence of thrombolytic treatment were significant independent predictors of mortality in patients with cardiogenic shock. Intriguingly, diabetes was not a significant predictor for short- and long-term mortality in this population. The 30-day and 5-year mortality rate was equally poor in both diabetic and nondiabetic patients with cardiogenic shock (diabetics: 30-day 63%, 5-year 91%; nondiabetics: 30-day 62%, 5-year 86%; p>0.05). Conclusions: Cardiogenic shock develops approximately twice as often among diabetics as among nondiabetic patients with acute MI. The prognosis of diabetics with cardiogenic shock is similar to the prognosis of nondiabetic patients with cardiogenic shock.