Abstract

Background: Severe metformin-associated lactic acidosis (MALA) is a rare but potentially fatal side effect of metformin. The clinical presentation is often unspecific, thus hindering early recognition. We aimed to assess the prevalence of MALA in an intensive care unit (ICU) and describe the demographic and clinical characteristics according to patient outcome. Methods: We conducted a 13-year single-center retrospective study, including all patients admitted in ICU with a high anion-gap metabolic acidosis and hyperlactatemia secondary to therapeutic use of metformin, after excluding other medical causes of acidosis. Results: Twenty one patients were admitted in ICU due to severe MALA (less than 1% of all admissions) with an ICU mortality rate of 23.8% (N=5). The baseline clinical characteristics were similar in survivors and nonsurvivors, both with a high prevalence of cardiovascular comorbidities as well as frequent concomitant therapy with angiotensin-converting-enzyme inhibitors and diuretics. All patients were treated with continuous renal replacement therapy (CRRT) and other organ failure support. Normal acid-base balance was achieved in all survivors in the first 24 hours. At baseline, the clinical and laboratory features of nonsurvivors were undistinguishable from survivors. Conclusions: Severe MALA is a rare cause of admission in the ICU. Although early institution of supportive therapy, MALA can progress to severe multiple-organ failure, especially when diagnosis and CRRT are delayed. Clinicians should suspect of MALA in all diabetic patients taking metformin with unexplained high anion-gap metabolic acidosis and hyperlactatemia.

Highlights

  • In 1995, metformin was approved by Food and Drug Administration (FDA) to treat type 2 diabetes mellitus, with established results concerning mortality and morbidity, especially in overweight patients [1]

  • We aimed to assess the prevalence of metformin-associated lactic acidosis (MALA) in our Intensive Care Unit (ICU), describe the main demographic and clinical characteristics and identify factors associated with poor outcome

  • 3479 patients were admitted in the intensive care unit (ICU) and 21 had the diagnosis of MALA, representing 0.6% of total admissions

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Summary

Introduction

In 1995, metformin was approved by Food and Drug Administration (FDA) to treat type 2 diabetes mellitus, with established results concerning mortality and morbidity, especially in overweight patients [1]. As a direct consequence of the accumulation of these carboxylic precursors, previously reported in some in vitro studies, lactic acidosis is the most serious side effect of metformin [5]. The exact mechanism for lactic acid accumulation in diabetic patients taking metformin is not clear. Some authors advocate that metformin associated lactic acidosis (MALA) results from the inhibition of complex I in mitochondrial respiratory chain through the decrease of pyruvate dehydrogenase activity [7]. Other consequence of pyruvate dehydrogenase inhibition is the shift towards anaerobic metabolism of carboxylic precursors, increasing the conversion of pyruvate to lactate [8]. Severe metformin-associated lactic acidosis (MALA) is a rare but potentially fatal side effect of metformin. We aimed to assess the prevalence of MALA in an intensive care unit (ICU) and describe the demographic and clinical characteristics according to patient outcome

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