Adverse drug reactions due to prolonged antibiotic therapy for malignant external otitis

Renata Shichmanter1, Edward B Miller, Zvi Landau

  • 1Department of Internal Medicine “D”, Kaplan Medical Center, P.O.B. 1, Rehovot 76001, Israel.

Insights

Malignant external otitis (MEO) treatment with beta-lactam antibiotics frequently causes adverse drug reactions (ADR). Ciprofloxacin showed no ADR, suggesting it may be a safer alternative for MEO patients.

Area of Science:

  • Infectious Diseases
  • Otolaryngology
  • Pharmacology

Background:

  • Malignant external otitis (MEO) is a severe infection necessitating extended antibiotic treatment.
  • Adverse drug reactions (ADR) are common with long-term antibiotic use, potentially hindering MEO treatment efficacy.

Purpose of the Study:

  • To identify and categorize the frequency and types of ADR in MEO patients.
  • To inform strategies for improving MEO treatment outcomes by understanding ADR patterns.

Main Methods:

  • Retrospective review of 21 MEO patients treated over a decade.
  • Analysis of demographic, clinical, and laboratory data to assess ADR occurrence.

Main Results:

  • Overall ADR rate was 26.8% (6 out of 21 patients).
  • No ADRs were observed in 15 patients treated with ciprofloxacin.
  • Six of nine patients on beta-lactam antibiotics experienced ADRs, including urticaria, elevated transaminases, and neutropenia.

Conclusions:

  • Prolonged MEO treatment with beta-lactam antibiotics is associated with a higher incidence of ADR.
  • Careful monitoring is crucial for MEO patients receiving beta-lactam therapy.
  • Ciprofloxacin appears to be a potentially safer alternative with fewer ADRs in MEO treatment.

Related Concept Videos

Mechanism of Antibiotic Resistance in MRSA01:25

Mechanism of Antibiotic Resistance in MRSA

Antibiotic resistance in bacteria arises when microorganisms evolve the ability to withstand drugs designed to kill them or inhibit their growth, rendering once-effective treatments useless. This phenomenon, driven by genetic change and selection under antibiotic exposure, poses a profound threat to modern medicine. Mechanisms include drug-inactivating enzymes (e.g., β-lactamases), efflux pumps that eject antibiotics, mutations altering antibiotic targets, decreased drug uptake, and acquisition...
Clinical Significance of Antibiotic Resistance01:25

Clinical Significance of Antibiotic Resistance

Methicillin-resistant Staphylococcus aureus (MRSA) presents a critical public health threat, arising from its capacity to resist β-lactam antibiotics due to acquisition of the mecA gene within the staphylococcal cassette chromosome mec (SCCmec). This gene encodes penicillin-binding protein 2a (PBP2a), which impairs binding efficacy of methicillin and other β-lactams. MRSA has evolved into distinct clonal lineages impacting humans and animals alike, reinforcing its significance within the One...
Inhibitors of Bacterial Protein Synthesis01:25

Inhibitors of Bacterial Protein Synthesis

Aminoglycosides constitute a highly potent class of bactericidal antibiotics that exert their antimicrobial effects by targeting the bacterial ribosome, specifically disrupting protein synthesis. These polycationic molecules consist of amino-modified sugars linked via glycosidic bonds to an aminocyclitol core such as 2-deoxystreptamine or streptamine. Their strong positive charges facilitate tight binding to the negatively charged phosphate backbone of ribosomal RNA (rRNA), primarily at the 16S...
Inhibitors of Bacterial DNA Synthesis01:28

Inhibitors of Bacterial DNA Synthesis

Bacterial pathogens depend on precise and efficient DNA replication to sustain infection. Two type II topoisomerases—DNA gyrase and topoisomerase IV—are critical to this process, as they resolve DNA supercoiling and unlink chromosomes during replication. Fluoroquinolones, synthetic derivatives of quinolones, exploit this mechanism by stabilizing the transient DNA–enzyme cleavage complex, preventing strand religation, and causing lethal double-strand breaks. These antibiotics are selectively...
Combined Effects of Drugs: Synergism01:27

Combined Effects of Drugs: Synergism

Synergism is a useful mechanism where combining two or more drugs is more effective than each constituent used alone. Such combinations are also called supra-additive interactions. The drugs collectively enhance the final therapeutic effect by acting on different targets. Another advantage is that the low dose of each constituent drug is sufficient to achieve the desired effect. This helps reduce the duration of therapy and lower the adverse effects of these drugs.
Such synergistic combinations...
Development of Antibiotic Resistance01:30

Development of Antibiotic Resistance

Antibiotic resistance is a major public health concern that arises when bacteria evolve mechanisms to withstand the effects of antibiotic treatments. This resistance can be intrinsic, acquired through genetic mutations, or transferred between bacteria via horizontal gene transfer. The development of antibiotic resistance poses significant challenges in treating bacterial infections and necessitates ongoing research to develop new therapeutic strategies.Intrinsic resistance occurs when bacterial...