The Effects of Methylene Blue on Hemodynamic Parameters and Cytokine Levels in Refractory Septic Shock.
10.3904/kjim.2005.20.2.123
- Author:
Byung Kyu PARK
1
;
Tae Sun SHIM
;
Chae Man LIM
;
Sang Do LEE
;
Woo Sung KIM
;
Dong Soon KIM
;
Won Dong KIM
;
Younsuck KOH
Author Information
1. Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea. yskoh@amc.seoul.kr
- Publication Type:Original Article ; Comparative Study ; Research Support, Non-U.S. Gov't
- Keywords:
Septic shock;
Methylene blue;
Guanylate cyclase;
Hemodynamics;
NO;
Cytokines
- MeSH:
Anti-Infective Agents, Urinary/administration & dosage/*therapeutic use;
Blood Pressure/*drug effects/physiology;
Comparative Study;
Cytokines/*blood;
Enzyme-Linked Immunosorbent Assay;
Female;
Humans;
Infusions, Intravenous;
Male;
Methylene Blue/administration & dosage/*therapeutic use;
Middle Aged;
Pulmonary Circulation/drug effects/physiology;
Research Support, Non-U.S. Gov't;
Retrospective Studies;
Shock, Septic/blood/*drug therapy/physiopathology;
Treatment Outcome;
Vascular Resistance/*drug effects/physiology
- From:The Korean Journal of Internal Medicine
2005;20(2):123-128
- CountryRepublic of Korea
- Language:English
-
Abstract:
BACKGROUND: Endogenous nitric oxide (NO) induces the peripheral vasodilation via the activation of guanylate cyclase in patients with septic shock. The purpose of this study was to assess the acute effects of methylene blue (MB), which is an inhibitor of guanylate cyclase, on the hemodynamics and on the production of pro-inflammatory cytokines and nitric oxide (NO) in patients with refractory septic shock. METHODS: Twenty consecutive patients with refractory septic shock, which was defined as shock refractory to a dopamine infusion of more than 20 microgram/kg/min with the appropriate use of antibiotics and adequate volume replacement, received MB infusion of 1 mg/kg intravenously. The hemodynamic and respiratory variables were measured at baseline, 30, 60 and 120 min after an infusion of MB (1 mg/kg). The blood levels of NO, IL-1, IL-10 and TNF-alpha were measured at baseline, 30 and 120 min after MB infusion. RESULTS: The administration of MB induced an increase in the systemic vascular resistance (SVR) that resulted in an increase of the mean arterial pressure (MAP) in patients with refractory septic shock, and this was without a decrease in cardiac output. The administered MB induced an increase in pulmonary vascular resistance (PVR) that resulted in an increase of pulmonary arterial pressure (PAP), without any deterioration of gas exchange. However, the increases in SVR and PVR were not associated with the alteration of endogenous production of NO, IL-1, IL-10 and TNF-alpha. CONCLUSION: MB transiently elevated the MAP by increasing the SVR without altering the endogenous productions of NO, IL-1, IL-10 and TNF-alpha during the study period in patients with refractory septic shock.
