Methylene Blue in Septic Shock: A Systematic Review and Meta-Analysis

Author:

Fernando Shannon M.12ORCID,Tran Alexandre234,Soliman Karim15,Flynn Barbara1,Oommen Thomas1,Wenzhe Li6,Adhikari Neill K.J.,Kanji Salmaan23,Seely Andrew J.E.234,Fox-Robichaud Alison E.7,Wax Randy S.15,Cook Deborah J.78,Lamontagne François910,Rochwerg Bram78

Affiliation:

1. Department of Critical Care, Lakeridge Health Corporation, Oshawa, ON, Canada.

2. Clinical Epidemiology Program, Ottawa Hospital Research Institute, Ottawa, ON, Canada.

3. Division of Critical Care, Department of Medicine, University of Ottawa, Ottawa, ON, Canada.

4. Department of Surgery, University of Ottawa, Ottawa, ON, Canada.

5. Department of Critical Care Medicine, Queen’s University, Kingston, ON, Canada.

6. Department of Critical Care Medicine, First Affiliated Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.

7. Department of Medicine, Division of Critical Care, McMaster University, Hamilton, ON, Canada.

8. Department of Health Research Methods, Evidence, and Impact, McMaster University, Hamilton, ON, Canada.

9. Department of Medicine, Université de Sherbrooke, Sherbrooke, QC, Canada.

10. Centre de Recherche du CHU de Sherbrooke, Sherbrooke, QC, Canada.

Abstract

OBJECTIVES: Although clinicians may use methylene blue (MB) in refractory septic shock, the effect of MB on patient-important outcomes remains uncertain. We conducted a systematic review and meta-analysis to investigate the benefits and harms of MB administration in patients with septic shock. DATA SOURCES: We searched six databases (including PubMed, Embase, and Medline) from inception to January 10, 2024. STUDY SELECTION: We included randomized clinical trials (RCTs) of critically ill adults comparing MB with placebo or usual care without MB administration. DATA EXTRACTION: Two reviewers performed screening, full-text review, and data extraction. We pooled data using a random-effects model, assessed the risk of bias using the modified Cochrane tool, and used Grading of Recommendations Assessment, Development, and Evaluation to rate certainty of effect estimates. DATA SYNTHESIS: We included six RCTs (302 patients). Compared with placebo or no MB administration, MB may reduce short-term mortality (RR [risk ratio] 0.66 [95% CI, 0.47–0.94], low certainty) and hospital length of stay (mean difference [MD] –2.1 d [95% CI, –1.4 to –2.8], low certainty). MB may also reduce duration of vasopressors (MD –31.1 hr [95% CI, –16.5 to –45.6], low certainty), and increase mean arterial pressure at 6 hours (MD 10.2 mm Hg [95% CI, 6.1–14.2], low certainty) compared with no MB administration. The effect of MB on serum methemoglobin concentration was uncertain (MD 0.9% [95% CI, –0.2% to 2.0%], very low certainty). We did not find any differences in adverse events. CONCLUSIONS: Among critically ill adults with septic shock, based on low-certainty evidence, MB may reduce short-term mortality, duration of vasopressors, and hospital length of stay, with no evidence of increased adverse events. Rigorous randomized trials evaluating the efficacy of MB in septic shock are needed. REGISTRATION: Center for Open Science (https://osf.io/hpy4j).

Funder

Lakeridge Health Foundation

Publisher

Ovid Technologies (Wolters Kluwer Health)

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