VAP - Ventilator Associated Pneumonia
Conditions
Brief summary
Statins with their powerful anti-inflammatory, immunomodulatory, and antioxidant properties make them candidate members to be used in the management of sepsis and different types of infections including pneumonia. This study aims to determine whether adjunctive statin therapy decreased day- 28 mortality among ICU patients with ventilator-associated pneumonia (VAP) & number of ventilator-free days (after successful weaning) between day 1 and both day 28.
Detailed description
This prospective randomized control-controlled triple blind study was conducted on above 18 years who had received mechanical ventilation in the ICU for at least 2 days. All included cases were subjected to: * Demographic data, * Physiological variables * Simplified Acute Physiology Score II at admission and radiologic score (Weinberg et al., 1984). * Antibiotics used, and relevant diagnostic and therapeutic interventions in the ICU. * The Sequential Organ Failure Assessment (SOFA) score and Clinical Pulmonary Infection Score (CPIS) were calculated on the day of enrolment (day 1) and then on days 3, 7, and 14. Patients were monitored daily for evidence of infection. * The duration of mechanical ventilation, length of ICU stay, and length of hospital stay were recorded. * The occurrence of myocardial ischemia or infarction was assessed until day 28. Serum levels of creatine kinase, ALT, and AST were measured. Patients were randomly allocated to simvastatin (60 mg) or control given via a nasogastric tube or orally from study inclusion to ICU discharge, death, or day 28, whichever occurred first. Simvastatin or control were started on the same day as antibiotic therapy for suspected VAP. The simvastatin dosage was halved in patients with renal failure (creatinine clearance \<30 mL/min). A computer-generated random- number table was prepared by statisticians to assign patients in blocks of 4 to receive either simvastatin or control. Block size was unknown to the investigators, who was enrolled the patients and then called the statistics department to obtain the randomization and treatment numbers after checking the inclusion and non-inclusion criteria Outcome The primary outcome was the day-28 mortality rate. Secondary outcomes were ICU mortality rates; number of days outside the ICU between day 1 and day 28; and number of ventilator-free days (after successful weaning) between day 1 and both day 28. Successful weaning was defined as spontaneous breathing for at least 48 hours after disconnection of the ventilator.
Interventions
DRUGSimvastatin
simvastatin 60 mg tab
Sponsors
Ain Shams University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Caregiver, Investigator)
Masking description
Block size was unknown to the investigators, who was enrolled the patients and then called the statistics department to obtain the randomization and treatment numbers after checking the inclusion and non-inclusion criteria.
Intervention model description
Patients were randomly allocated to simvastatin (60 mg) or control given via a nasogastric tube or orally from study inclusion to ICU discharge, death, or day 28, whichever occurred first. Simvastatin or control were started on the same day as antibiotic therapy for suspected VAP. The simvastatin dosage was halved in patients with renal failure (creatinine clearance \<30 mL/min). A computer-generated random- number table was prepared by statisticians to assign patients in blocks of 4 to receive either simvastatin or control. Block size was unknown to the investigators, who was enrolled the patients and then called the statistics department to obtain the randomization and treatment numbers after checking the inclusion and non-inclusion criteria.
Eligibility
Sex/Gender
ALL
Age
29 Years to 71 Years
Healthy volunteers
No
Inclusion criteria
* Patients who suspected to had VAP defined as a modified Clinical Pulmonary Infection Score (CPIS) of at least 5 and if they underwent quantitative bacteriological cultures of bronchoalveolar lavage (BAL) fluid, a protected telescopic catheter (PTC), or an endotracheal aspirate. The modified CPIS is based on body temperature, blood leukocyte count, amount and appearance of tracheal secretions, ratio of partial pressure of oxygen (PaO2) to fraction of inspired oxygen, acute respiratory distress syndrome (ARDS), and infiltrates on chest radiography. The total can range from 1 to 10 points (Luna et al., 2003). * Patients were included only for the first episode of suspected VAP.
Exclusion criteria
* o Statin therapy at intubation * Previous VAP episode during the same hospitalization * Known pregnancy * Immunodepression with bone marrow aplasia * Imminent death (Simplified Acute Physiology Score II of 75 or greater, calculated over the last 6 hours) * Treatment limitation decisions * Nothing-by-mouth order and no nasogastric tube, continuous gastric aspiration * Known chronic intestinal malabsorption * Known simvastatin hypersensitivity * Acute hepatic failure * Use of CYP3A4 inhibitors or cyclosporine * Creatine kinase level greater than 5 times the upper limit of normal * Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) levels greater than 3 times the upper limit of normal
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The primary outcome was the day-28 mortality rate. | 28 day | asses effect of statin on mortality in ventilator associated pneumonia patient |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| number of days outside the ICU between day 1 and day 28 | between day 1 and day 28 | the number of days patients who have improved spent outside the icu between day 1 and day 28 |
| ICU mortality rates | between day 1 and day 28 | rate of mortality of patients with ventilator associated pneumonia between simvastatin group and control group in intensive care unit |
| number of ventilator-free days (after successful weaning) between day 1 and both day 28. | between day 1 and day 28 | number of days patient of the two group spent without ventilator in the intensive care unit between day 1 and day 28 after successful weaning. Successful weaning was defined as spontaneous breathing for at least 48 hours after disconnection of the ventilator. |
Countries
Egypt
Outcome results
None listed