Abstract

The present review will cover the mechanisms of release and the potential pathophysiological role of different natriuretic peptides in critically ill patients. By focusing on the cardiovascular system, possible implications of natriuretic peptides for diagnosis and treatment will be presented. In critical illness such as sepsis, trauma or major surgery, systemic hypotension and an intrinsic myocardial dysfunction occur. Impairment of the cardiovascular system contributes to poor prognosis in severe human sepsis. Natriuretic peptides have emerged as valuable marker substances to detect left ventricular dysfunction in congestive heart failure of different origins. Increased plasma levels of circulating natriuretic peptides, atrial natriuretic peptide, N-terminal pro-atrial natriuretic peptide, brain natriuretic peptide and its N-terminal moiety N-terminal pro-brain natriuretic peptide have also been found in critically ill patients. All of these peptides have been reported to reflect left ventricular dysfunction in these patients. The increased wall stress of the cardiac atria and ventricles is followed by the release of these natriuretic peptides. Furthermore, the release of atrial natriuretic peptide and brain natriuretic peptide might be triggered by members of the IL-6-related family and endotoxin in the critically ill. Apart from the vasoactive actions of circulating natriuretic peptides and their broad effects on the renal system, anti-ischemic properties and immunological functions have been reported for atrial natriuretic peptide. The early onset and rapid reversibility of left ventricular impairment in patients with good prognosis associated with a remarkably augmented plasma concentration of circulating natriuretic peptides suggest a possible role of these hormones in the monitoring of therapy success and the estimation of prognosis in the critically ill.

Highlights

  • Critical illness, such as sepsis, trauma and major surgery, is accompanied by an activation of the immune system and mediator cells; that is, macrophages elaborating soluble inflammatory products such as cytokines and vasoactive compounds

  • There might be a considerable overlap of patients with increased brain natriuretic peptide (BNP) due to acute respiratory distress syndrome (ARDS) and patients with primary symptomatic congestive heart failure, where BNP levels have to reach more than 500 pg/ml to ensure the diagnosis with a probability greater than 95% [92]

  • These findings suggest that these peptides might reflect myocardial dysfunction as described in congestive heart failure in septic shock as well

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Summary

Introduction

Critical illness, such as sepsis, trauma and major surgery, is accompanied by an activation of the immune system and mediator cells; that is, macrophages elaborating soluble inflammatory products such as cytokines and vasoactive compounds. In support of this concept, elevated values reported for ANP [86], N-terminal proANP [87], BNP [88] and NT-proBNP [93] in patients with acute lung injury and/or sepsis are well in the range found in patients with severe heart failure These data suggest at least for BNP a limited value of intermediate BNP values for the discrimination of primary pulmonary disease (i.e. ARDS) or cardiac disease. A negative relationship between heart function indices and elevated plasma levels of ANP [116], N-terminal pro-ANP [87] and, recently, for BNP [117] and NT-proBNP [93] has been reported in human septic shock These findings suggest that these peptides might reflect myocardial dysfunction as described in congestive heart failure in septic shock as well. It has been suspected that increased concentrations of CNP might contribute to venous pooling by vasodilative action on the vein in septic shock [123]

Conclusion
Bone RC
Bone R
Findings
11. Parillo JE
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