The use of corticosteroids in patients with severe community pneumonia, bacterial infection which kills lots of patients around the world, reduces the mortality of this infection. However, there are no studies with this type of drug regarding hospital-acquired pneumonia. This is the first multicenter randomized trial to test hydrocortisone plus standard therapy in critical care patients with nosocomial pneumonia. This intervention is inexpensive and may improve the outcome of those patients, besides having an acceptable side effects profile.
Introduction and Objectives: the use of corticosteroids in patients with severe community pneumonia reduces morbimortality. However, to our knowledge, there are no studies with steroids for patients in intensive care with nosocomial pneumonia, among which those with ventilator associated pneumonia, infections which carry a high mortality rate. The treatment for those diseases involves intensive care and antibiotics, but there is a need for inexpensive, adjuvant therapies which improve the outcome for those patients. Therefore, the objective of this study is to compare hydrocortisone versus placebo, both with standard therapy, in the outcome of critical care patients diagnosed with nosocomial pneumonia. Methods: multicenter randomized, open-label, controlled trial, with two parallel groups: hydrocortisone or placebo, associated with nosocomial pneumonia's standard treatment. Patients with viral or other etiologies of pneumonia are excluded, as well as corticosteroids chronical users, or patients with conditions which demand this type of therapy. Intravenous 100mg of hydrocortisone and normal saline (the placebo) are tested every eight hours for five days or until intensive care unit (ICU) discharge or until the patient dies. The sample is 180 patients, 90 in each group, in different ICUs in Brazil. The primary outcome is early clinical failure. The secondary outcomes are survival and mortality in both groups, need for intubation, mechanical ventilation, vasoactive drugs and dialysis, lengths of stay in the hospital and in the ICU, radiological progression and adverse events. Discussion, risks, and benefits: this is the first multicenter randomized trial to test hydrocortisone plus standard therapy in critical care patients with nosocomial pneumonia. This intervention is inexpensive and may improve the outcome of those patients, besides having an acceptable side effects profile. Weighing the benefits and risks of this study, as well as its strengths and potential weaknesses, it is believed that its realization is justified, in addition to bringing important advances in the field of intensive care.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
180
Corticosteroid
Normal saline only
Hospital do Servidor Publico Estadual
São Paulo, Sao Paulo SP, Brazil
RECRUITINGEarly Clinical Failure
Composite outcome: Death OR Respiratory worsening OR Cardiovascular worsening
Time frame: Between days 0 and 7 for death; between days 3 and 7 for respiratory or cardiovascular worsening
Survival
In the intensive care unit and in the hospital
Time frame: Days 7 and 28
Respiratory failure
Need for mechanical ventilation
Time frame: 7 days
Septic shock
Need for vasoactive drugs
Time frame: 7 days
Time of mechanical ventilation
Number of days patients require invasive ventilation support
Time frame: 7 days
Ventilator parameters (1)
Positive end expiratory pressure (PEEP)
Time frame: 7 days
Ventilator parameters (2)
Inspired oxygen fraction (FiO2)
Time frame: 7 days
Arterial blood gas analysis
Partial pressure of oxygen (PaO2)
Time frame: 7 days
Respiratory condition
Horowitz index for lung function (P/F ratio) - obtained from PaO2/FiO2
Time frame: 7 days
Time of vasoactive drugs use
Dosage and types of vasoactive drugs
Time frame: 7 days
Length of stay
In the Intensive Care Unit and in the hospital
Time frame: 28 days
Need for renal substitution therapy
Need for dialysis
Time frame: 7 days
Radiological worsening
Progression of image in the chest X-ray image
Time frame: 7 days
Adverse effects
psychosis, insomnia, hyperglycemia, hypernatremia, rhabdomyolysis, gastrointestinal bleeding and critical myopathy illness
Time frame: 7 days
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