Impact of Intravenous Fluid Challenge Infusion Time on Macrocirculation and Endothelial Glycocalyx in Surgical and Critically Ill Patients
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, randomizované kontrolované studie
PubMed
30519590
PubMed Central
PMC6241356
DOI
10.1155/2018/8925345
Knihovny.cz E-zdroje
- MeSH
- endotel účinky léků patofyziologie MeSH
- glykokalyx účinky léků patologie MeSH
- hemodynamika účinky léků MeSH
- intravenózní infuze metody MeSH
- kohortové studie MeSH
- krevní tlak MeSH
- kritický stav terapie MeSH
- lidé středního věku MeSH
- lidé MeSH
- prospektivní studie MeSH
- senioři MeSH
- septický šok patofyziologie terapie MeSH
- tekutinová terapie metody MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- randomizované kontrolované studie MeSH
(i) Purpose. The fluid challenge (FC) is a well-established test of preload reserve. Only limited data exist in regard to the FC efficacy based on infusion time. Slow administration may be associated with lack of effect based on fluid redistribution and external conditions changes. On the contrary, fast administration may lead to brisk fluid overload and damage to the endothelium and endothelial glycocalyx (EG). The aim of this trial was to compare the FC infusion time on its hemodynamic effects and EG. (ii) Methods. Prospective randomized single-center trial of fast (5-10 minutes) versus slow (20-30 minutes) administration of 500ml balanced crystalloid FC in spinal surgery (cohort OR) and septic shock (cohort SEP) patients. Hemodynamic response was assessed using standard monitoring and blood flow measurements; damage to EG was assessed using the perfused boundary region (PBR) via intravital microscopy monitoring in the sublingual region within relevant time points ranging up to 120 minutes. (iii) Results. Overall, 66 FCs in 50 surgical and 16 septic patients were assessed. Fluid administration was associated with increase of PBR in general (1.9 (1.8-2.1) vs. 2.0 (1.8-2.2); p= 0.008). These changes were transient in OR cohort whereas they were long-lasting in septic fluid responders. The rate of fluid responsiveness after fast versus slow administration was comparable in global population (15 (47%) vs. 17 (50%); p=0.801) as well as in both cohorts. (iv) Conclusions. Fluid challenge administration was associated with increased PBR (and presumable EG volume changes) which normalized within the next 60 minutes in surgical patients but remained impeded in septic fluid responders. The fluid responsiveness rate after fast and slow FC was comparable, but fast administration tended to induce higher, though transient, response in blood pressure.
Biomedical Center Faculty of Medicine in Plzen Charles University Plzen Czech Republic
Dpt of Anesthesiology and Intensive Care Medicine University Hospital in Plzen Plzen Czech Republic
Faculty of Medicine in Hradec Kralove Charles University Hradec Kralove Czech Republic
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Benes J. Cumulative Fluid Balance: The Dark Side of the Fluid. Critical Care Medicine. 2016;44(10):1945–1946. doi: 10.1097/CCM.0000000000001919. PubMed DOI
Marik P., Bellomo R. A rational approach to fluid therapy in sepsis. British Journal of Anaesthesia. 2016;116(3):339–349. doi: 10.1093/bja/aev349. PubMed DOI
Cecconi M., Hofer C., Teboul J.-L., et al. Fluid challenges in intensive care: the FENICE study: a global inception cohort study. Intensive Care Medicine. 2015;41(9):1529–1537. doi: 10.1007/s00134-015-3850-x. PubMed DOI PMC
Aya H. D., Ster I. C., Fletcher N., Grounds R. M., Rhodes A., Cecconi M. Pharmacodynamic analysis of a fluid challenge. Critical Care Medicine. 2016;44(5):880–891. doi: 10.1097/CCM.0000000000001517. PubMed DOI
Aya H. D., Rhodes A., Chis Ster I., Fletcher N., Grounds R. M., Cecconi M. Hemodynamic effect of different doses of fluids for a fluid challenge: A quasi-randomized controlled study. Critical Care Medicine. 2017;45(2):e161–e168. doi: 10.1097/CCM.0000000000002067. PubMed DOI
Hahn R. G., Lyons G. The half-life of infusion fluids. European Journal of Anaesthesiology. 2016;33(7):475–482. doi: 10.1097/EJA.0000000000000436. PubMed DOI PMC
Biais M., De Courson H., Lanchon R., et al. Mini-fluid Challenge of 100 ml of Crystalloid Predicts Fluid Responsiveness in the Operating Room. Anesthesiology. 2017;127(3):450–456. doi: 10.1097/ALN.0000000000001753. PubMed DOI
Chappell D., Bruegger D., Potzel J., et al. Hypervolemia increases release of atrial natriuretic peptide and shedding of the endothelial glycocalyx. Critical Care. 2014;18(5, article 538) doi: 10.1186/s13054-014-0538-5. PubMed DOI PMC
Cerny V., Astapenko D., Brettner F., et al. Targeting the endothelial glycocalyx in acute critical illness as a challenge for clinical and laboratory medicine. Critical Reviews in Clinical Laboratory Sciences. 2017;54(5):343–357. doi: 10.1080/10408363.2017.1379943. PubMed DOI
Woodcock T. E., Woodcock T. M. Revised Starling equation and the glycocalyx model of transvascular fluid exchange: an improved paradigm for prescribing intravenous fluid therapy. British Journal of Anaesthesia. 2012;108(3):384–394. doi: 10.1093/bja/aer515. PubMed DOI
Tatara T. Context-sensitive fluid therapy in critical illness. Journal of Intensive Care. 2016;4(1) doi: 10.1186/s40560-016-0150-7. PubMed DOI PMC
Lee D. H., Dane M. J., van den Berg B. M., et al. Deeper Penetration of Erythrocytes into the Endothelial Glycocalyx Is Associated with Impaired Microvascular Perfusion. PLoS ONE. 2014;9(5):p. e96477. doi: 10.1371/journal.pone.0096477. PubMed DOI PMC
Vlahu C. A., Lemkes B. A., Struijk D. G., Koopman M. G., Krediet R. T., Vink H. Damage of the endothelial glycocalyx in dialysis patients. Journal of the American Society of Nephrology. 2012;23(11):1900–1908. doi: 10.1681/ASN.2011121181. PubMed DOI PMC
Rovas A., Lukasz A., Vink H., et al. Bedside analysis of the sublingual microvascular glycocalyx in the emergency room and intensive care unit – the GlycoNurse study. Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine . 2018;26(1) doi: 10.1186/s13049-018-0483-4. PubMed DOI PMC
Puskarich M. A., Cornelius D. C., Tharp J., Nandi U., Jones A. E. Plasma syndecan-1 levels identify a cohort of patients with severe sepsis at high risk for intubation after large-volume intravenous fluid resuscitation. Journal of Critical Care. 2016;36:125–129. doi: 10.1016/j.jcrc.2016.06.027. PubMed DOI PMC
Powell M. F., Mathru M., Brandon A., Patel R., Frölich M. A. Corrigendum to “Assessment of endothelial glycocalyx disruption in term parturients receiving a fluid bolus before spinal anesthesia: a prospective observational study” (International Journal of Obstetric Anesthesia (2014) 23 (330–334)(S0959289X14000843)(10.1016/j.ijoa.2014.06.001)) International Journal of Obstetric Anesthesia. 2016;28:p. 100. doi: 10.1016/j.ijoa.2016.07.002. PubMed DOI
Zeng Y., Tarbell J. M., Vinci M. C. The Adaptive Remodeling of Endothelial Glycocalyx in Response to Fluid Shear Stress. PLoS ONE. 2014;9(1):p. e86249. doi: 10.1371/journal.pone.0086249. PubMed DOI PMC
Belavić M., Sotošek Tokmadžić V., Fišić E., et al. The effect of various doses of infusion solutions on the endothelial glycocalyx layer in laparoscopic cholecystectomy patients. Minerva Anestesiologica. 2018;84(9) doi: 10.23736/S0375-9393.18.12150-X. PubMed DOI
Anand D., Ray S., Srivastava L. M., Bhargava S. Evolution of serum hyaluronan and syndecan levels in prognosis of sepsis patients. Clinical Biochemistry. 2016;49(10-11):768–776. doi: 10.1016/j.clinbiochem.2016.02.014. PubMed DOI
Murphy L. S., Wickersham N., McNeil J. B., et al. Endothelial glycocalyx degradation is more severe in patients with non-pulmonary sepsis compared to pulmonary sepsis and associates with risk of ARDS and other organ dysfunction. Annals of Intensive Care. 2017;7(1) doi: 10.1186/s13613-017-0325-y. PubMed DOI PMC
Gorshkov A. Y., Klimushina M. V., Boytsov S. A., Kots A. Y., Gumanova N. G. Increase in perfused boundary region of endothelial glycocalyx is associated with higher prevalence of ischemic heart disease and lesions of microcirculation and vascular wall. Microcirculation. 2018;25(4):p. e12454. doi: 10.1111/micc.12454. PubMed DOI
Vincent J.-L., Weil M. H. Fluid challenge revisited. Critical Care Medicine. 2006;34(5):1333–1337. doi: 10.1097/01.CCM.0000214677.76535.A5. PubMed DOI
Toscani L., Aya H. D., Antonakaki D., et al. What is the impact of the fluid challenge technique on diagnosis of fluid responsiveness? A systematic review and meta-analysis. Critical Care. 2017;21(1) doi: 10.1186/s13054-017-1796-9. PubMed DOI PMC
Messina A., Longhini F., Coppo C., et al. Use of the Fluid Challenge in Critically Ill Adult Patients. Anesthesia & Analgesia. 2017;125(5):1532–1543. doi: 10.1213/ANE.0000000000002103. PubMed DOI
Hahn R. G. Why are crystalloid and colloid fluid requirements similar during surgery and intensive care? European Journal of Anaesthesiology. 2013;30(9):515–518. doi: 10.1097/EJA.0b013e328362a5a9. PubMed DOI
Ukor I. F., Hilton A. K., Bailey M. J., Bellomo R. The haemodynamic effects of bolus versus slower infusion of intravenous crystalloid in healthy volunteers. Journal of Critical Care. 2017;41:254–259. doi: 10.1016/j.jcrc.2017.05.036. PubMed DOI