A Case of Confusion in an Obese Patient Treated With Daptomycin: Neurotoxicity

Rova Malala Fandresena Randrianarisoa1, Olivia Raulin2, Anthony Merlin3

  • 1Internal Medicine, University Hospital Joseph Raseta Befelatanana, Antananarivo, MDG.

Cureus
|July 15, 2024
PubMed

Insights

Daptomycin (DAP) can cause rare neurotoxicity, like confusion, especially in obese patients with high drug levels. Stopping DAP treatment resolved the confusion, suggesting a link and the need for dose adjustments in specific populations.

Area of Science:

  • Pharmacology
  • Infectious Diseases
  • Neurology

Background:

  • Daptomycin (DAP) is a potent cyclic lipopeptide antibiotic effective against Gram-positive bacteria, including methicillin-resistant Staphylococcus aureus (MRSA).
  • Common adverse effects of DAP include myotoxicity (rhabdomyolysis), gastrointestinal issues, skin lesions, bleeding, and pulmonary complications.
  • Neurotoxicity is a rare but reported adverse reaction to DAP, with mechanisms not fully understood.

Observation:

  • A case report details a 73-year-old obese male patient treated with DAP (9 mg/kg) for MRSA bacteremia and associated infections.
  • The patient experienced confusion and spatial disorientation on the fifth day of DAP treatment, coinciding with very high serum DAP concentrations.
  • Neurological symptoms resolved completely upon discontinuation of DAP therapy.

Findings:

  • The observed confusion and spatial disorientation were consistent with Daptomycin-induced neurotoxicity.
  • High serum DAP concentrations in this obese patient likely contributed to the neurotoxic event.
  • The patient's obesity was identified as a potential predisposing factor for DAP-related neurotoxicity.

Implications:

  • This case highlights a potential association between Daptomycin and neurotoxicity, particularly confusion, in obese patients.
  • Clinicians should maintain a high index of suspicion for neurological adverse events during DAP therapy.
  • Dose reduction of Daptomycin in obese patients may be prudent to mitigate the risk of neurotoxicity.

Related Concept Videos

Desensitization and Tachyphylaxis01:20

Desensitization and Tachyphylaxis

Tachyphylaxis is described as a rapid decrease in response to a drug after repeated or continuous administration of the same drug dose. It is a phenomenon where the body becomes less responsive to a particular substance or intervention over time, requiring higher doses or stronger interventions to achieve the same effect. It results from adaptive changes in the body's receptors, signaling pathways, or physiological processes that occur in response to prolonged exposure to a stimulus.
1.6K
Directly Acting Muscle Relaxants: Dantrolene and Botulinum Toxin01:26

Directly Acting Muscle Relaxants: Dantrolene and Botulinum Toxin

Directly acting muscle relaxants like dantrolene and botulinum toxin (BoNT) have distinct mechanisms and applications. Dantrolene, a hydantoin derivative, acts on the ryanodine receptor (RYR1) in skeletal muscle cells. RYR1 are calcium channels present at the sarcoplasmic reticulum membrane. In response to excitation, they release calcium ions from the sarcoplasmic reticulum to the cytosol. Calcium promotes actin-myosin-mediated contraction of muscles.
The binding of dantrolene to the RYR1...
666
Local Anesthetics: Adverse Effects01:12

Local Anesthetics: Adverse Effects

While local anesthetics are generally safe and well-tolerated, they can occasionally cause adverse effects that vary in severity. Local anesthetics can induce toxicity at two distinct levels. They can either produce local effects through direct contact with the neural elements or be absorbed into the bloodstream from the injection site, leading to systemic effects.
Once absorbed into the systemic circulation, local anesthetics can affect the organs that depend on the functioning of sodium...
404
Factors Affecting Drug Response: Overview01:21

Factors Affecting Drug Response: Overview

When it comes to infants and young children, they are typically administered smaller doses of medication in comparison to adults. This is primarily because their organ functions still need to fully develop, meaning their bodies are not as efficient at metabolizing or eliminating drugs. Additionally, their blood-brain barrier is more permeable than in adults. As a result, high concentrations of drugs can easily penetrate the central nervous system (CNS), potentially leading to neurological...
2.0K
Drug Distribution: Tissue Binding01:21

Drug Distribution: Tissue Binding

Upon entering the systemic circulation, drugs can distribute into the interstitial and intracellular fluid of various tissue cells. This distribution is facilitated by the binding of drugs to different cellular components within tissues, which may lead to drug accumulation in specific areas. Drugs bound to tissue components serve as reservoirs that release free drugs back into the system, prolonging the drug's overall action. However, this accumulation can also result in local toxicity.
For...
2.6K
Drugs Affecting Neurotransmitter Synthesis01:29

Drugs Affecting Neurotransmitter Synthesis

Drugs affecting neurotransmitter synthesis can impact the adrenergic neuron and the synthesis of neurotransmitters. For example, α-methyltyrosine and carbidopa target specific enzymes involved in catecholamine synthesis. α-methyltyrosine inhibits the enzyme tyrosine hydroxylase, which converts tyrosine into dopamine. By blocking this enzyme, α-methyltyrosine reduces dopamine production and other catecholamines. Carbidopa, on the other hand, inhibits the enzyme dopa decarboxylase,...
1.3K