Lactobacillus GG in the Prophylaxis of Ventilator Associated Pneumonia

Creighton University125 enrolled

Overview

This study utilizes lactobacillus, or probiotics, delivered twice daily to the mouth and stomach, via feeding tube, in effort to determine whether the oral administration of a naturally occurring Lactobacillus species reduces the incidence of ventilator associated pneumonia therefore reducing intensive care unit(ICU)complications.

The long-term objective of this research is to determine the utility of altering the oral and gastric bacterial flora in mechanically ventilated patients in order to reduce intensive care unit (ICU)complications. Specifically, our goal is to determine whether the oral administration of a naturally occurring Lactobacillus species reduces the incidence of ventilator associated pneumonia (VAP). ICU admission is commonly accompanied by overgrowth of the natural gastrointestinal (GI) and oropharyngeal flor by pathogenic organisms. Patients requiring endotracheal intubation are predisposed to developing VAP, presumably via micro-aspiration of the altered oropharyngeal flora. By reducing VAP rates, we hope to improve ICU outcomes, minimize ICU expenses, and most importantly, decrease morbidity and mortality.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

TRIPLE

Enrollment

125

Conditions

Pneumonia Ventilator Associated Pneumonia

Interventions

Lactobacillus GGDIETARY_SUPPLEMENT

Every 12 hours, the contents of a single capsule containing Lactobacillus GG will be suspended in 3 ml of water-soluble jelly. The suspension will be applied to the oropharyngeal mucosa via sterile syringe. The contents of a second capsule will be suspended in 10 ml of sterile water and pushed through the NG tub followed by 10 mL of air to ensure complete administration.

placeboDIETARY_SUPPLEMENT

Every 12 hours, the contents of a single identical placebo capsule containing the inert plant carbohydrate inulin will be suspended in 3 ml of water-soluble jelly. This suspension will be applied to the oropharyngeal mucosa via sterile syringe. The contents of a second placebo capsule will be suspended in 10 ml of sterile water and pushed through eh NG tube followed by 10 mL of air to ensure complete administration

Eligibility

Sex: ALLMin age: 19 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Admission to the medical, surgical, or cardiac ICU * Age 19 years or greater (the age of majority in the state of Nebraska) * Anticipated need for \>72 hours of endotracheal intubation * Initial intubation during hospitalization * Approval of the attending physician responsible for the patient's care * Informed surrogate consent within 24 hours of intubation Exclusion Criteria: * Pregnancy * Pharmacologic immunosuppression (\>10mg prednisone daily or equivalent for at least 14 days) * Native immunosuppression: 1)known HIV disease or AIDS, 2)history of malignancy, 3)multiple organ system failure * History of prosthetic or bioprosthetic cardiac valve placement * History of prosthetic vascular graft placement * Cardiac trauma * History of rheumatic fever, endocarditis, congenital cardia abnormality, or acquired cardia abnormality * Gastroesophageal surgery or perforation associated with current admission * Intestinal surgery or perforation associated with current admission * Significant oropharyngeal mucosal injury * Placement of a tracheostomy

Locations (1)

Creighton University Medical Center

Omaha, Nebraska, United States

Outcomes

Primary Outcomes

To determine whether patients given oral Lactobacillus GG will have a smaller increase in the density of pathogenic bacterial in cultures from oral swabs, nasogastric aspirates, and minimally invasive bronchoalveolar lavage samples.

Time frame: daily while intubated

Secondary Outcomes

To assess whether administration of Lactobacillus GG to intubated patients reduces clinically diagnosed VAP,reduces microbiologically diagnosed VAP, affects mortality and duration of mechanical ventilation, and total antibiotic consumption.

Time frame: daily while intubated

Data from ClinicalTrials.gov

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