Marjut Varpula

Dr. Marjut Varpula


Research Focus & Metrics

Academic Career Length

22Years (2005-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 June 2005 in Intensive Care Medicine
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Journal Article
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MVMarjut Varpula
Marjut Varpula
MTMinna Tallgren
Minna Tallgren
KSKatri Saukkonen
Katri Saukkonen
LVLiisa-Maria Voipio-Pulkki
Liisa-Maria Voipio-Pulkki
VPVille Pettilä
Ville Pettilä

4 July 2016 in Critical Care
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Journal Article
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FIfor the CardShock study investigators
for the CardShock study investigators
TTTuukka Tarvasmäki
Tuukka Tarvasmäki
JLJohan Lassus
Johan Lassus
MVMarjut Varpula
Marjut Varpula
ASAlessandro Sionis
Alessandro Sionis
VHVeli-Pekka Harjola
Veli-Pekka Harjola
Vasopressors and inotropes remain a cornerstone in stabilization of the severely impaired hemodynamics and cardiac output in cardiogenic shock (CS). The aim of this study was to analyze current real-life use of these medications, and their impact on outcome and on changes in cardiac and renal biomarkers over time in CS. The multinational CardShock study prospectively enrolled 219 patients with CS. The use of vasopressors and inotropes was analyzed in relation to the primary outcome, i.e., 90-day mortality, with propensity score methods in 216 patients with follow-up data available. Changes in cardiac and renal biomarkers over time until 96 hours from baseline were analyzed with linear mixed modeling. Patients were 67 (SD 12) years old, 26 % were women, and 28 % had been resuscitated from cardiac arrest prior to inclusion. On average, systolic blood pressure was 78 (14) and mean arterial pressure 57 (11) mmHg at detection of shock. 90-day mortality was 41 %. Vasopressors and/or inotropes were administered to 94 % of patients and initiated principally within the first 24 hours. Noradrenaline and adrenaline were given to 75 % and 21 % of patients, and 30 % received several vasopressors. In multivariable logistic regression, only adrenaline (21 %) was independently associated with increased 90-day mortality (OR 5.2, 95 % CI 1.88, 14.7, p = 0.002). The result was independent of prior cardiac arrest (39 % of patients treated with adrenaline), and the association remained in propensity-score-adjusted analysis among vasopressor-treated patients (OR 3.0, 95 % CI 1.3, 7.2, p = 0.013); this was further confirmed by propensity-score-matched analysis. Adrenaline was also associated, independent of prior cardiac arrest, with marked worsening of cardiac and renal biomarkers during the first days. Dobutamine and levosimendan were the most commonly used inotropes (49 % and 24 %). There were no differences in mortality, whether noradrenaline was combined with dobutamine or levosimendan. Among vasopressors and inotropes, adrenaline was independently associated with 90-day mortality in CS. Moreover, adrenaline use was associated with marked worsening in cardiac and renal biomarkers. The combined use of noradrenaline with either dobutamine or levosimendan appeared prognostically similar.

7 July 2006 in Intensive Care Medicine
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MVMarjut Varpula
Marjut Varpula
SKSari Karlsson
Sari Karlsson
EREsko Ruokonen
Esko Ruokonen
VPVille Pettilä
Ville Pettilä

1 May 2007 in Critical Care Medicine
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Journal Article
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MVMarjut Varpula
Marjut Varpula
KPKari Pulkki
Kari Pulkki
SKSari Karlsson
Sari Karlsson
EREsko Ruokonen
Esko Ruokonen
VPVille Pettilä
Ville Pettilä
The aim of this study was to evaluate the predictive value of N-terminal pro-brain natriuretic peptide (NT-proBNP) on mortality in a large, unselected patient population with severe sepsis and septic shock. Prospective observational cohort study about incidence and prognosis of sepsis in 24 intensive care units in Finland (the FINNSEPSIS study). A total of 254 patients with severe sepsis or septic shock. After informed consent, the blood tests for NT-proBNP analyses were drawn on the day of admission and 72 hrs thereafter. Patients' demographic data were collected, and intensive care unit and hospital mortality and basic hemodynamic and laboratory data were recorded daily. NT-proBNP levels at admission were significantly higher in hospital nonsurvivors (median, 7908 pg/mL) compared with survivors (median, 3479 pg/mL; p = .002), and the difference remained after 72 hrs (p = .002). The receiver operating characteristic curves of admission and 72-hr NT-proBNP levels for hospital mortality resulted in area under the curve values of 0.631 (95% confidence interval, 0.549-0.712; p = .002) and 0.648 (95% confidence interval, 0.554-0.741; p = .002), respectively. In logistic regression analyses, NT-proBNP values at 72 hrs after inclusion and Simplified Acute Physiology Score for the first 24 hrs were independent predictors of hospital mortality. Pulmonary artery occlusion pressure (p < .001), plasma creatinine clearance (p = .001), platelet count (p = .03), and positive blood culture (p = .04) had an independent effect on first-day NT-proBNP values, whereas after 72 hrs, only plasma creatinine clearance (p < .001) was significant in linear regression analysis. NT-proBNP values are frequently increased in severe sepsis and septic shock. Values are significantly higher in nonsurvivors than survivors. NT-proBNP on day 3 in the intensive care unit is an independent prognostic marker of mortality in severe sepsis.

18 October 2007 in Acta Anaesthesiologica Scandinavica
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Journal Article
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MVMarjut Varpula
Marjut Varpula
SKS. Karlsson
S. Karlsson
IPI. Parviainen
I. Parviainen
ERE. Ruokonen
E. Ruokonen
VPV. Pettilä
V. Pettilä
FGFinnsepsis Study Group
Finnsepsis Study Group

19 December 2006 in Intensive Care Medicine
Verified
Journal Article
Closed access
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MVMarjut Varpula
Marjut Varpula
SKSari Karlsson
Sari Karlsson
EREsko Ruokonen
Esko Ruokonen
VPVille Pettilä
Ville Pettilä