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临床试验/CTRI/2021/12/038480
CTRI/2021/12/038480尚未招募不适用

Estimation of the incidence and microbial profile of ventilator associated pneumonia in a tertiary care centre and its implication in health care system.

Dr Sandeep Dey1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年12月12日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
100
试验地点
1
主要终点
Incidence of ventilator associated pneumonia (VAP)

研究概览

简要总结

A cross sectional observational study will be carried out in the Intensive Care Units (Covid and Non Covid) of Jorhat Medical College and Hospital, Jorhat. All patients enrolled in the study will be followed daily for the development of signs and symptoms of VAP 48 hours after intubation and mechanical ventilation. Various clinical, physiological, microbiological and radiographic parameters, as described by Johanson et al., will be accessed giving them numerical values, which when scored can predict the presence or absence of VAP. In a case of new onset sepsis, tracheal aspirate will be collected using sterile mucus extractor and as par CDC guidelines for collection of tracheal aspirate sample.. Attempt to exclude other sources of infection will be made by focused physical examination and relevant investigations including urine culture, blood culture, imaging studies etc. depending upon the clinical profile of the patient. . If no other apparent source of infection will be found, then VAP will be suspected and lung protective ventilation as par ARDS net protocol will be started to prevent the development of ARDS. All samples will be processed in the department of microbiology for the growth of organisms by conventional methods. All isolates will be subjected to antimicrobial sensitivity testing using disk diffusion method Following CLSI guidelines

研究设计

研究类型
Observational

入排标准

年龄范围
18.00 Year(s) 至 80.00 Year(s)(—)
性别
All

入选标准

  • Patients more than 18 years where consent was obtained from responsible attendant/guardian.
  • Patient mechanically ventilated for at least more than 48 hours.

排除标准

  • Patients less than 18 years or where no consent was obtained.
  • Intubation done outside our ICU set up.
  • Patients with some other definite source of infection.
  • 4.Immune compromised states.
  • Patients with low GCS and were on NIV support prior to being referred to our set up.

结局指标

主要结局

Incidence of ventilator associated pneumonia (VAP)

时间窗: 48 hours after mechanical ventilation and after 6 months.

次要结局

  • To identify the microbial etiology of VAP(After 6 months)

研究者

发起方
Dr Sandeep Dey
申办方类型
Other [Principal investigator]

研究点 (1)

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