Effects of methylene blue on microcirculatory alterations following cardiac surgery: A prospective cohort study
Autor: | Matthias Jacquet-Lagrèze, Carole Maurin, Philippe Portran, Stéphane Junot, Rémi Schweizer, Bernard Allaouchiche, Jean-Luc Fellahi |
---|---|
Přispěvatelé: | Hôpital Louis Pradel [CHU - HCL], Hospices Civils de Lyon (HCL), Centre Hospitalier Lyon Sud [CHU - HCL] (CHLS), VetAgro Sup - Institut national d'enseignement supérieur et de recherche en alimentation, santé animale, sciences agronomiques et de l'environnement (VAS), Agressions Pulmonaires et Circulatoires dans le Sepsis - UR (APCSé), Cardiovasculaire, métabolisme, diabétologie et nutrition (CarMeN), Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Hospices Civils de Lyon (HCL)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), CarMeN, laboratoire |
Rok vydání: | 2021 |
Předmět: |
Adult
medicine.medical_specialty Mean arterial pressure [SDV]Life Sciences [q-bio] Cardiac index Hemodynamics Vascular occlusion law.invention Cohort Studies law Internal medicine medicine Cardiopulmonary bypass Humans Prospective Studies Vasoplegic syndrome Cardiac Surgical Procedures medicine.diagnostic_test business.industry Microcirculation medicine.disease Capillary refill Cardiac surgery [SDV] Life Sciences [q-bio] Methylene Blue Anesthesiology and Pain Medicine Cardiology medicine.symptom business |
Zdroj: | European Journal of Anaesthesiology European Journal of Anaesthesiology, Lippincott, Williams & Wilkins, 2022, 39 (4), pp.333-341. ⟨10.1097/eja.0000000000001611⟩ |
ISSN: | 1365-2346 0425-0389 0265-0215 |
DOI: | 10.1097/eja.0000000000001611⟩ |
Popis: | International audience; BACKGROUND: Methylene blue is used as rescue therapy to treat catecholamine-refractory vasoplegic syndrome after cardiac surgery. However, its microcirculatory effects remain poorly documented. OBJECTIVE: We aimed to study microcirculatory abnormalities in refractory vasoplegic syndrome following cardiac surgery with cardiopulmonary bypass and assess the effects of methylene blue. DESIGN: A prospective open-label cohort study. SETTING: 20-Bed ICU of a tertiary care hospital. PATIENTS: 25 Adult patients receiving 1.5 mg kg-1 of methylene blue intravenously for refractory vasoplegic syndrome (defined as norepinephrine requirement more than 0.5 μg kg-1 min-1) to maintain mean arterial pressure (MAP) more than 65 mmHg and cardiac index (CI) more than 2.0 l min-1 m-2. MAIN OUTCOME MEASURES: Complete haemodynamic set of measurements at baseline and 1 h after the administration of methylene blue. Sublingual microcirculation was investigated by sidestream dark field imaging to obtain microvascular flow index (MFI), total vessel density, perfused vessel density and heterogeneity index. Microvascular reactivity was assessed by peripheral near-infrared (IR) spectroscopy combined with a vascular occlusion test. We also performed a standardised measurement of capillary refill time. RESULTS: Despite normalised CI (2.6 [2.0 to 3.8] l min-1 m-2) and MAP (66 [55 to 76] mmHg), patients with refractory vasoplegic syndrome showed severe microcirculatory alterations (MFI \textless 2.6). After methylene blue infusion, MFI significantly increased from 2.0 [0.1 to 2.5] to 2.2 [0.2 to 2.8] (P = 0.008), as did total vessel density from 13.5 [8.3 to 18.5] to 14.9 [10.1 to 14.7] mm mm-2 (P = 0.02) and perfused vessel density density from 7.4 [0.1 to 11.5] to 9.1 [0 to 20.1] mm mm-2 (P = 0.02), but with wide individual variation. Microvascular reactivity assessed by tissue oxygen resaturation speed also increased from 0.5 [0.1 to 1.8] to 0.7 [0.1 to 2.7]% s-1 (P = 0.002). Capillary refill time remained unchanged throughout the study. CONCLUSION: In refractory vasoplegic syndrome following cardiac surgery, we found microcirculatory alterations despite normalised CI and MAP. The administration of methylene blue could improve microvascular perfusion and reactivity, and partially restore the loss of haemodynamic coherence. TRIAL REGISTRATION: ClinicalTrials.gov identifier: NCT04250389. |
Databáze: | OpenAIRE |
Externí odkaz: |