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Cardiac dysfunction in critical illness
- Source :
- Current Opinion in Anaesthesiology. 31:158-164
- Publication Year :
- 2018
- Publisher :
- Ovid Technologies (Wolters Kluwer Health), 2018.
-
Abstract
- Sepsis and septic shock are prevalent conditions that are likely to increase in prevalence in the future. Given the high mortality and morbidity associated with sepsis and sepsis-induced cardiac dysfunction, we must continue to make advances in knowledge of the complex physiologic interactions and how we may target specific mediators for potential therapeutic options in the future.Multiple biomarkers have been discovered, which when assayed in sepsis-induced cardiomyopathy predict morbidity and mortality. With increased sensitivity of echocardiography, we can diagnose subclinical cardiac dysfunction, which may have future implications for slowing or preventing progressive dysfunction.Sepsis-induced cardiomyopathy is the result of complicated interactions between the pathogen, the body's response to infection, and iatrogenic injury. Interplay between inflammatory, metabolic, and adrenergic systems results in direct and indirect myocardial injury leading to decreases in both systolic and diastolic cardiac function. As the interactions are further elucidated with additional research into other proteins and mediators, new treatment options can be researched. VIDEO ABSTRACT.
- Subjects :
- medicine.medical_specialty
business.industry
Septic shock
Critical Illness
High mortality
MEDLINE
030208 emergency & critical care medicine
030204 cardiovascular system & hematology
medicine.disease
Cardiac dysfunction
Sepsis
Intensive Care Units
03 medical and health sciences
0302 clinical medicine
Anesthesiology and Pain Medicine
Echocardiography
Critical illness
Prevalence
medicine
Humans
Cardiomyopathies
business
Intensive care medicine
Biomarkers
Subjects
Details
- ISSN :
- 09527907
- Volume :
- 31
- Database :
- OpenAIRE
- Journal :
- Current Opinion in Anaesthesiology
- Accession number :
- edsair.doi.dedup.....9399741cdfc6fb4a845a4a75cb4687f8
- Full Text :
- https://doi.org/10.1097/aco.0000000000000572