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Medicina Interna

versão impressa ISSN 0872-671X

Medicina Interna vol.30 no.2 Lisboa jun. 2023  Epub 01-Jul-2023

https://doi.org/10.24950/rspmi.1654 

CARTAS AO EDITOR/ LETTERS TO EDITOR

Methylene Blue and its Role in the Critically Ill Patient

O Azul de Metileno e o Seu Papel no Doente Crítico

Juan Santiago Serna - Trejos1  2  3  4  5 
http://orcid.org/0000-0002-3140-8995

Stefanya Geraldine Bermudez - Moyano5 
http://orcid.org/0000-0002-2259-6517

Jose Daniel Estacio - Diaz5 
http://orcid.org/0000-0002-5395-0283

1Department of Epidemiology, Universidad Libre, Cali, Colombia

2Department of Doctorate in Public Health, University of Cuauhtémoc, Aguascalientes, Mexico

3Institute of Health. Bogotá, Colombia

4Interdisciplinary Research Group in Epidemiology and Public Health, Cali, Colombia

5Hospital Universitario del Valle, Intensive Care Unit, Cali, Colombia


Mr. Editor:

Methylene blue is a versatile drug that is a powerful aid in different clinical contexts, especially in the context of critically ill patients, especially in states associated with profound vaso-dilatation such as distributive shock (septic shock). Historically, the use of methylene blue has been used as an antimalarial treatment, in the treatment of gonococcal infections, as well as in the treatment of methemoglobinemia (MetHB), although in this particular condition, the use of methylene blue is only used in selected cases of patients with respiratory symptoms associated with MetHB levels above 920%.1 It has been used as an antidote for cyanide poisoning, which makes the use of this type of compound relevant. These types of pharmacological aids are conditioned to their use, since, if used early and rationally, they constitute an improvement in the survival of patients. The versatility of the use of methylene blue allows it to be used in multiple medical conditions; its use in intensive care units is described below, especially in states of "shock" in the care of critically ill patients.2

The mechanism of action of methylene blue is given mainly in the inhibition of soluble guanylate cyclase, therefore it plays a role in the inhibition of nitric oxide (NO) formation, thus reversing the hypotension induced by endotoxins, it also has an antagonistic role in the hyporeactivity to vasoconstrictors. The doses of administration of the drug in shock conditions are usually indicated at 2 mg/kg as a bolus and then continued as an infusion at 0.25-1.2 mg/kg/hour.3,4The side effects described secondary to the use of methylene blue in the literature date initially from blue staining of the urine and skin, as well as the generation of symptoms associated with nausea, vomiting, and abdominal pain.5

Kirov et al conducted in 2001 the first study related to the use of methylene blue in the treatment of patients with septic shock, where it was found that the early use of methylene blue could reduce the requirement of vasopressors; the survival of the population in this study did not have sufficient statistical power to find differences in mortality.6 Another study by Juffermans et al aimed to evaluate the use of methylene blue in the treatment of patients with severe septic shock; multiple doses of methylene blue were used at a rate of 1-3-7 mg/kg during 20 minutes in 15 patients with the diagnosis, the use of methylene blue improved several variables in these patients such as cardiac index and mean pulmonary artery arterial pressure, decreased serum lactate and less oxygen requirement in patients under invasive mechanical ventilation.7

A recent study by Ibarra-Estrada et al aimed to evaluate methylene blue as an early adjuvant in patients with refractory septic shock in order to measure primary and secondary outcomes associated with vasopressor reduction during ICU stays. This study included 91 patients who were randomized and compared with 46 placebos. The primary outcome was that patients who used methylene blue had a shorter time of vasopressor use compared to the placebo group (69 h [IQR 59-83] vs 94 h [IQR 74-141]; p 0.001), as well as a decrease in the requirement for norepinephrine in the group that used methylene blue. Other important secondary outcomes were related to one day less vasopressor requirement at day 28 (p = 0.008), a shorter ICU stay by 1.5 days (p = 0.039), and a shorter hospital stay by 2.7 days (p = 0.027). Other results showed that the days of invasive mechanical ventilation and mortality were similar to those in the comparison group without obtaining statistical significance. The most important adverse effects were related to 93% of cases, which presented bluish-green urine coloration (93%), as an increase in MetHB saturation (2.9% [RIC 2.2-3.3] vs 0.5% [RIC 0.4-0.7]; p 0.001). Some serum markers, such as serum creatinine, bilirubins, and hepatic aminotransferases, did not show statistically significant changes versus the comparison group.8

In a randomized controlled clinical trial conducted by Aguilar Arzapalo et al, where 60 individuals were divided into two groups respectively, within which were critically ill, with differ-ent stages of septic shock and/or vasodilated shock, the administration of methylene blue was monitored, and monitored in one of the two groups. The results obtained in the group to which it was administered were associated with methylene blue being effective as an adjuvant in the treatment of individuals with septic, vasodilated or distributive shock. Shock time, as well as vasopressor consumption, is significantly reduced with the use of methylene blue. An important advance in lactate clearance and improvement in central venous saturation was also demonstrated, a significantly better result with the use of methylene blue, and mortality was reduced, being lower with the use of methylene blue at 28 days after hospital discharge.9

Although there is little scientific evidence or lack of randomized clinical trials on the use of methylene blue, alternative uses have been shown, such as in the treatment of anaphylaxis; a study conducted by Moreia Rodriguez et al employed the use of this pharmacological agent in a series of cases, mainly in bronchospasm. Although the authors do not explain the mechanisms directly involved in the use of this drug due to the low evidence of its use, they propose a synergy mechanism with the previous use of adrenaline, especially as first-line treatment in this type of conditions.10

Given the above, several annotations arise concerning the use of methylene blue in the intensive care unit. Initially, it could be considered or its use could be considered as a secondary alternative to the use of the vasopressor of choice described throughout the available literature as norepinephrine, even in the initial stages of septic shock; however, it is necessary to explore the literature with more evidence and which is more conclusive for the aforementioned. Methylene blue will have to be used according to the clinical conditions of each patient, individualizing each case, considering each comorbidity or patient's condition, according to the criteria of the intensivist or specialist if considered relevant; however, it should be noted that its efficacy is linked to early onset of the same.

As a commentary, in Colombia, especially in the health centre of the present authors, we use methylene blue in refractory septic shock when adjuvant therapy with norepinephrine and vasopressin is not effective in controlling hypotension despite the parallel medical management established with antibiotics and steroids, sometimes requiring renal replacement therapy, among others. We do not have a study on their use in our institution in a standardized way; however, their use promises encouraging horizons.

REFERENCES

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Suporte Financeiro: O presente trabalho não foi suportado por nenhum subsidio o bolsa ou bolsa.

Proveniência e Revisão por Pares: Não comissionado; revisão externa por pares.

Financial Support: This work has not received any contribution grant or scholarship.

Provenance and Peer Review: Not commissioned; externally peer reviewed.

© Autor (es) (ou seu (s) empregador (es)) e Revista SPMI 2023. Re-utilização permitida de acordo com CC BY. Nenhuma reutilização co-mercial. © Author(s) (or their employer(s)) and SPMI Journal 2023. Re-use per-mitted under CC BY. No commercial re-use.

Received: February 22, 2023; Accepted: May 09, 2023

Correspondence / Correspondência: Juan Santiago Serna - Trejos - juansantiagosernatrejos@gmail.com Department of Epidemiology, Universidad Libre, Cali, Colombia Cra. 109 #22 -00, Cañasgordas, Cali, Valle del Cauca Postal Code:760008

Declaração de Contribuição JSST, SGBM, JDED - Concepção da ideia, pesquisa bibliográfica, redação e aprovação final do manuscrito. Todos os autores aprovaram a versão final a ser submetida. Contributorship Statement JSST, SGBM, JDED - Idea conception, literature search, writing and final approval of the manuscript. All authors approved the final draft.

Conflitos de Interesse: Os autores declaram não possuir conflitos de interesse.

Conflicts of Interest: The authors have no conflicts of interest to declare.

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