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Efficacy Analysis of Tigecycline-based Therapy and Polymyxin B-based Therapy in ICU Infection

C

Central South University

Status

Unknown

Conditions

Tigecycline
Polymyxin B
Intensive Care Unit

Study type

Observational

Funder types

Other

Identifiers

NCT04970537
202105202

Details and patient eligibility

About

The gender, age, ICU diagnosis, basic diseases, antibiotic treatment plan, physiological indicators, duration of hospital stay, length of stay in ICU, hospitalization cost, prognosis and other discharge information of patients receiving tigecycline or polymyxin B admitted to the ICU of four provincial-level Grade A hospitals in Changsha, Hunan Province ,China from 2017 to 2021 were included.

To analyze the therapeutic effect of tigecycline-based or polymyxin B-based antibiotic regimens and their effect on the prognosis of patients, and to conduct subgroup analysis.

Full description

The gender, age, ICU diagnosis, basic diseases, antibiotic treatment plan, physiological indicators, duration of hospital stay, length of stay in ICU, hospitalization cost, prognosis and other discharge information of patients receiving tigecycline or polymyxin B admitted to the ICU of four provincial-level Grade A hospitals in Changsha, Hunan Province ,China from 2017 to 2021 were included. The four hospitals included the 1st-3th XiangYa Hospitals and Hunan Provincial People's Hospital. Organize the data.Patients with a course of treatment < 4 days and shedding were excluded.To analyze the therapeutic effect of tigecycline-based or polymyxin B-based antibiotic regimens and their effect on the prognosis of patients, and to conduct subgroup analysis. The chi-square test was used for the counting data, and the Mann-Whitney U test or Kruskal-Wallis H test was used for the measurement data. The significance value was adjusted by Bonferroni correction method for multiple tests, and the P was tested on both sides,P>0.05.

Enrollment

800 estimated patients

Sex

All

Ages

18 to 95 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • ICU patients receiving tigecycline or polymyxin B treatment;
  • Age 14-95, gender unlimited;
  • there are clear infections and strains;
  • The patient and/or his/her family agree to sign the informed consent voluntarily.

Exclusion criteria

  • Patients with treatment of less than 4 days;
  • patients with abscission;
  • Pregnant patients;
  • Patients with age < 14 years or > 95 years.

Trial contacts and locations

1

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Central trial contact

Shuangping Zhao

Data sourced from clinicaltrials.gov

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