OBJECTIVES: To describe real-world use of tigecycline in cIAIs patients. METHODS: A retrospective, observational study enrolled cIAIs patients hospitalized in The First Affiliated Hospital, Sun Yat-sen University from January 1, 2013 to June 30, 2017 was conducted. Patients’ data were collected and matched based on age, gender, and Acute Physiologic Assessment and Chronic Health Evaluation II (APACHE II) score according to receiving first-line, later-line, or no tigecycline during hospitalization. RESULTS: Data were collected for 52 patients. 82.6% were male. Mean age was 57.8 years and APACHE II score was 14.8. The incidence of both extended-spectrum beta-lactamase producing and carbapenem-resistant pathogens was high on initial culture; however, few patients received first-line tigecycline. No significant difference in mortality rate was identified among first-line, later-line and no tigecycline users. Of surviving patients, shorter hospital length of stay was observed for patients receiving first- vs later-line or no tigecycline, respectively. ICU length-of-stay was shorter in patients receiving first- vs later-line or no tigecycline. CONCLUSIONS: First-line tigecycline use was rare in our surgical intensive care unit. Resistant organisms were commonly cultured from initial specimens. Although these results are limited by small patient numbers and single center, our results suggest that early tigecycline use may have significant benefits with similar mortality. Further research is warranted to demonstrate the values of early tigecycline use in cIAIs patients.
Intra-abdominal infections have a high incidence and are often associated with poor prognosis [
The conditions of critically ill patients are complex, and most of them have used a variety of anti-infective drugs in the early stage. As a result, it is very difficult to choose antibiotics after being transferred to ICU [
We performed a retrospective analysis of hospitalization data obtained from the surgical intensive care unit of The First Affiliated Hospital, Sun Yat-sen University.
Patients
All patients hospitalized in our surgical ICU from January 1, 2013 to June 30, 2017 were screened. The inclusion criteria are: 1) diagnosed with cIAIs; 2) ≥18 years old. The exclusion criteria include: 1) tigecycline administration is not for abdominal infections; 2) severe infection in other parts of the body; 3) existence of immunodeficiency (e.g. HIV); 4) history of alcohol abuse; 5) no drug susceptibility results, or no culture specimens obtained within one week after using antibiotics. Patients were categorized into the case group if they received tigecycline within 24 hours of confirmed pathogen test results. Those who did not receive tigecycline during this time period were categorized into the control group. Matched controls were selected based on age, gender, the Acute Physiologic Assessment and Chronic Health Evaluation II (APACHE II) score, lab results, and previously used antibiotics. First-line TGC users were those who received TGC as the first antibiotic during hospitalization. Later-line TGC users were those who received TGC after prior antibiotic administration. All patients were followed up to discharge or death, which came first.
Descriptive analyses were conducted on patient baseline characteristics. Clinical and economic outcomes were compared between the treatment groups. Antibiotic use prior to TGC administration was assessed among patients treated with later-line TGC therapy and confirmed carbapenem-resistant or extended spectrum beta-lactamase (ESBL)-producing organisms.
Data from 52 patients were collected. 82.6% of the patients were male, with the mean age of 57.8 years and the mean APACHE II 14.8. Despite matching patients receiving TGC to those not receiving TGC therapy on APACHE II score, the score was lower in patients not receiving TGC vs those receiving TGC. Patients not receiving TGC may not be comparable to patients receiving TGC due to their underlying conditions. Therefore, comparisons between the TGC and no TGC treatment groups were not performed. APACHE II scores were similar in patients receiving first- vs later-line TGC. The incidence of both carbapenem-resistant pathogens and ESBL-producing organisms was high on the initial abdominal culture; however, few patients received first-line TGC (
Among TGC users, no statistically significant differences were found in mortality. Of surviving patients, shorter hospital length of stay was observed for patients who received first- vs later-line TGC therapy. Of survivors admitted to the ICU, length of ICU stay was shorter in patients receiving first- vs later-line TGC, but with no statistical significance. No statistically significant difference was found in antibiotic costs between patients receiving first- and later-line TGC therapy.
| No TGC | First-line TGC | Second-line TGC | P value | ||
|---|---|---|---|---|---|
| Age | 61.7 ± 9.68 | 55.4 ± 16.4 | 51.2 ± 17.0 | 0.066 | |
| Gender | Male | 25 | 10 | 8 | 0.222 |
| Female | 3 | 2 | 4 | ||
| APACHE-II | 13.7 ± 5.7 | 15.8 ± 8.6 | 17.4 ± 4.9 | 0.348 | |
| Bacteria | Gram-Negative | 19 | 10 | 6 | 0.219 |
| Gram-Positive | 9 | 2 | 6 | ||
| ESBL (N) | 15 | 6 | 1 | 0.069 | |
| Carbapenem-resistant (N) | 4 | 2 | 2 | 0.821 |
Among patients with carbapenem-resistant infections, imipenem, teicoplanin, and meropenem were the most frequently used antibiotics before initiation of TGC therapy. Among patients with ESBL infections, imipenem was the most frequently used antibiotics before initiation of TGC therapy.
Since the pathogenic bacteria of early complicated intra-abdominal cavity infections are mostly Enterobacteriaceae, such as Escherichia coli, Klebsiella pneumoniae, Enterobacter cloacae, etc., the sensitivity rate of carbapenems to Enterobacteriaceae was almost 100% in early years; therefore, carbapenem antibiotics have always been the most effective antibiotics for the treatment of severe cIAIs. However, in recent years, bacteria resistant to carbapenem antibiotics in local areas have gradually shown an increasing trend, and the related mortality rate has also been climbing [
There are many reasons for the increase in drug resistance, and some studies suggest that overexposure may be one of the important factors. A prospective study in Greece showed that frequent use of carbapenems and polymyxins and a longer treatment course were factors influencing carbapenem antibiotic resistance, and polymyxins was an independent risk factor for multiple drug resistance (Multidrug-resistant, MDR) [
Tigecycline belongs to a new type of glycylcycline antibacterial drug. Its mechanism is similar to that of tetracycline antibiotics. After administration, it can bind to bacterial 30S ribosomes to prevent transfer RNA from entering, thereby effectively inhibits peptides chain formation, interrupts bacterial structure and makes it difficult for bacteria to perform certain functions, which ultimately exerts antibacterial effect and inhibits bacterial reproduction. Tigecycline has a strong binding ability to ribosomes. After injection, about 22% of the drug will be excreted in the urine, with an average elimination half-life of 27 h. The antibacterial spectrum is very broad, mainly including Acinetobacter baumannii,Escherichia coli,Enterobacter cloacae,Klebsiella oxytoca,Aeromonas hydrophila,Citrobacter klebsiella,andKlebsiella pneumoniae. These pathogens are highly sensitive to Tigecycline and have obvious therapeutic effects.
For critically ill patients with sepsis and septic shock in surgical ICU, tigecycline treatment can significantly reduce the mortality rate [
Our study results are limited by small patient numbers and data from single hospital, but our results suggest that early TGC use may have significant economic benefits with similar mortality. Additional research is warranted to further demonstrate the value of early TGC therapy in patients hospitalized with cIAIs in China.
The authors declare no conflicts of interest regarding the publication of this paper.
Nie, Y., Pei, F., Wang, L.H., Si, X. and Guan, X.D. (2021) Tigecycline Use in Surgical Intensive Care Unit for the Treatment of Complicated Intra-Abdominal Infections: A Real-World Study. International Journal of Clinical Medicine, 12, 1-6. https://doi.org/10.4236/ijcm.2021.121001