Related Experiment Video
Updated: Jun 24, 2026

Multiplex Therapeutic Drug Monitoring by Isotope-dilution HPLC-MS/MS of Antibiotics in Critical Illnesses
Published on: August 30, 2018
Tigecycline in the treatment of infections from multi-drug resistant gram-negative pathogens
Garyphallia Poulakou1, Flora V Kontopidou, Elisabeth Paramythiotou
14th Department of Internal Medicine, Athens University School of Medicine, ATTIKON University General Hospital of Athens, Athens, Greece.
Objective:
This observational retrospective study aims to present early experience with tigecycline (TIG) in the treatment of infections due to multi-drug resistant (MDR) microorganisms.
Methods:
Adult patients included, received TIG for >5 days either as monotherapy (M group) or as presumed active monotherapy (PAM group). In the PAM group, all co-administered antimicrobial(s) were resistant in vitro against the targeted pathogen(s) or had been clinically and microbiologically failing after >or=5 days of therapy despite in vitro susceptibility.
Results:
Forty-five patients (35 in ICU) were treated for 28 Acinetobacter baumannii and 23 Klebsiella pneumoniae infections [21 ventilator-associated and healthcare-acquired pneumonia (VAP/HCAP), 10 bloodstream infections (BSI) and 14 surgical infections (SI)]. Successful overall clinical outcome was 80%, i.e. 81.8% in M group, 78.3% in PAM group, 90.5% in VAP/HCAP, 80% in BSI, 64.3% in SI and 85% in the cases with septic shock. Superinfections from Enterobacteriaceae inherently resistant to tigecycline occurred in 31.8% of M and 13% of PAM group (p<0.001).
Conclusion:
TIG represents a promising option in infections from MDR pathogens, however, further clinical experience is required.
Insights
Tigecycline (TIG) shows promise for treating infections caused by multi-drug resistant (MDR) pathogens, with an 80% overall success rate. However, further clinical experience is needed, especially regarding superinfections.
Area of Science:
- Infectious Diseases
- Pharmacology
- Critical Care Medicine
Background:
- Multi-drug resistant (MDR) microorganisms pose a significant threat in healthcare settings.
- Tigecycline (TIG) is an antibiotic approved for complicated skin, intra-abdominal, and community-acquired pneumonia infections.
- Limited data exists on TIG's efficacy in treating diverse infections caused by MDR pathogens.
Purpose of the Study:
- To evaluate the early clinical experience with tigecycline (TIG) in treating infections caused by multi-drug resistant (MDR) microorganisms.
- To assess the clinical outcomes and safety of TIG in adult patients.
- To compare TIG's effectiveness as monotherapy versus presumed active monotherapy.
Main Methods:
- Retrospective observational study of adult patients receiving TIG for >5 days.
- Patients were categorized into monotherapy (M group) or presumed active monotherapy (PAM group).
- PAM group included cases where co-administered antimicrobials failed or were resistant in vitro.
Main Results:
- Forty-five patients, primarily in ICU, were treated for infections including Acinetobacter baumannii and Klebsiella pneumoniae.
- Overall clinical success rate was 80%, with higher rates in ventilator-associated/healthcare-acquired pneumonia (90.5%).
- Superinfections by tigecycline-resistant Enterobacteriaceae occurred more frequently in the M group (31.8%) than the PAM group (13%).
Conclusions:
- Tigecycline (TIG) demonstrates potential as a treatment option for infections caused by MDR pathogens.
- The study highlights the need for careful patient selection and monitoring for superinfections.
- Further clinical experience and research are warranted to fully establish TIG's role in managing MDR infections.
Related Concept Videos
Inhibitors of Bacterial DNA Synthesis
Inhibitors of Bacterial Protein Synthesis
Pulmonary Tuberculosis V
Latent tuberculosis infection occurs when TB bacteria are present in a person's body, but are not causing illness or symptoms. It is not contagious, and preventive treatment is crucial to avoid the progression...
Inhibitors of Gram-positive Cell Wall Synthesis
Mechanism of Antibiotic Resistance in MRSA
Clinical Significance of Antibiotic Resistance
