Efficacy of Macrolide Immunomodulation in Severe Sepsis.

Efficacy of Macrolide Immunomodulation in Severe Sepsis

The purpose of this study is to determine whether macrolide treatment of patients with severe sepsis has an advantageous immunomodulatory and clinical effect compared to severe septic patients without macrolide therapy. Our main hypothesis is macrolide use in addition to standard therapy in severe septic patients has an advantageous immunomodulatory and clinical effect compared to patients with severe sepsis not treated with a macrolide.

Study Overview

• Status: Terminated
• Conditions: Systemic Inflammatory Response Syndrome
• Intervention / Treatment: Other: Azithromycin on admission - not enrolled in the RCT

Detailed Description

In recent studies, the significant effects of macrolide antibiotics (azithromycin) on immune response, unrelated to their anti-microbial properties, have been appreciated. Clinical trials of macrolides added to -lactams in bacteremic Streptococcus pneumoniae community-acquired pneumonia (CAP) have consistently demonstrated an absolute risk reduction in mortality of 15% in most populations. Several cytokines including tumor necrosis factor (TNF) interleukin (IL) -1 and IL-8 which are generally proinflammatory and IL-6 and IL-10, which tend to be anti-inflammatory have been associated with sepsis. TNF is a cytokine that for a number of reasons is thought to play a central role in the pathogenesis of sepsis and septic shock. TNF concentrations are increased during clinical and experimental sepsis and increasing concentrations and especially persistence of high concentrations of TNF during sepsis are associated with decreased survival. Therefore, our primary aim is to determine whether macrolide treatment of patients with severe sepsis has an advantageous immunomodulatory and clinical effect compared to severe septic patients without macrolide therapy. Our main hypothesis is macrolide use in addition to standard therapy in severe septic patients has an advantageous immunomodulatory and clinical effect compared to patients with severe sepsis not treated with a macrolide.

• Study Type: Interventional
• Enrollment (Anticipated): 100
• Phase: Phase 2

Contacts and Locations

Study Locations

• United States
  • Texas
    • San Antonio, Texas, United States, 78229
      • South Texas Health Care System, San Antonio, TX

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years and older (Adult, Older Adult)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

1. Subject, or legal representative, has given written informed consent.
2. 18 years of age or older.

3. SIRS is defined as two or more of:

   • Temperature > 38o C or < 36oC
   • Heart rate > 90 beats/min
   • Respiratory rate > 20 breaths/min or PaCO2< 32mmHg
   • White blood cell count > 12.000/mm3; < 4000/mm3; or > 10% immature (band) forms.
4. Presence of a suspected or proven infection. Patients with suspected infection must have evidence of an infection, such as white blood cells in a normally sterile body fluid, perforated viscus, chest x-ray consistent with pneumonia and associated with purulent sputum production, or a clinical syndrome associated with a high probability of infection (for example, purpura fulminans or ascending cholangitis).

5. Presence of one or more sepsis-associated organ failure. The onset of the first sepsis-associated organ failure must occur within the 48-hour period immediately preceding initiation of study drug infusion. A patient must have an organ failure attributable to the sepsis episode. The organ failure must be newly developed and not explained by underlying disease processes or by effects of concomitant therapy.

   • Cardiovascular: An arterial systolic blood pressure (SBP) of 90 mm Hg or a mean arterial pressure (MAP) 70 mm Hg for at least 1 hour despite adequate fluid resuscitation, adequate intravascular volume status, or the need for vasopressors to maintain SBP 90 mm Hg or MAP 70 mm Hg.
   • Renal: Average urine output <0.5 mL/kg/h for 1 hour despite adequate fluid resuscitation
   • Respiratory: Evidence of acute pulmonary dysfunction PaO2/FiO2 300 and, clinical exam or pulmonary capillary wedge pressure not suggestive of volume overload. If pneumonia is the suspected site of infection, the patient must have a PaO2/FiO2 200.
   • Hematology: Platelet count <80,000/mm3 or a 50% decrease in platelet count from the highest value recorded over the last 3 days.
   • Unexplained metabolic acidosis: Defined by (1) pH 7.30 or base deficit 5.0 mEq/L or (2) plasma lactate level >1.5 times the upper limit of normal.

Adequate fluid resuscitation or adequate intravascular volume is defined as either pulmonary arterial wedge pressure 12 mm Hg or central venous pressure 8 mm Hg. Vasopressors is defined as dopamine 5 g/kg/min or any dose of norepinephrine, epinephrine, or phenylephrine. Dobutamine is not considered a vasopressor.

Exclusion Criteria:

1. Macrolide therapy indicated for clinical condition. If after randomization, the treating physician determines that a macrolide is indicated and no other alternative antibiotic is appropriate, the patient will be excluded from the trial. However, if only one dose of azithromycin had been given and the treating physician decided to stop it, azithromycin might be administered.
2. Known allergy to macrolides.
3. Prolonged QT syndrome or on medications with increased risk of QT prolongation.
4. Pregnant or lactating.

Immunosuppression as defined by:

1. Chemotherapy within the last 30 days,
2. Leukemia or lymphoma which is not in remission,
3. Solid organ or bone marrow/stem cell transplant,
4. Human Immunodeficiency Virus infection with CD4 count < 200 cells/mm3,
5. Chronic corticosteroid use equivalent to > 10 mg prednisone per day,
6. Patient or family decision to limit ICU care.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Arm 1; Standard antibiotic therapy +Azithromycin 500 mg intravenously daily for 5 days	Other: Azithromycin on admission - not enrolled in the RCT; One dose of azithromycin prior to inclusion to the RCT; Other Names: Arm 3
No Intervention: Arm 2; Standard antibiotic therapy

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Change in cytokines expression	Between admission and day five of treatment

Secondary Outcome Measures

Outcome Measure	Time Frame
28-day mortality	28 days or discharge

Collaborators and Investigators

• Sponsor: VA Office of Research and Development
• Collaborators: National Heart, Lung, and Blood Institute (NHLBI); Northwestern University Feinberg School of Medicine
• Investigators: Principal Investigator: Marcos I Restrepo, MD BA MSc, South Texas Health Care System, San Antonio, TX

Publications and helpful links

General Publications

• Lopes Junior E, Leite HP, Pinho Franco MDC, Konstantyner T. Association of selenium status with endothelial activation during acute systemic inflammation in children. Clin Nutr ESPEN. 2022 Feb;47:367-374. doi: 10.1016/j.clnesp.2021.11.007. Epub 2021 Nov 14.

Study record dates

Study Major Dates

• Study Start (Actual): November 1, 2007
• Primary Completion (Actual): November 1, 2013
• Study Completion (Actual): November 1, 2013

Study Registration Dates

• First Submitted: June 27, 2008
• First Submitted That Met QC Criteria: July 1, 2008
• First Posted (Estimate): July 2, 2008

Study Record Updates

• Last Update Posted (Actual): April 21, 2017
• Last Update Submitted That Met QC Criteria: April 19, 2017
• Last Verified: April 1, 2017

More Information

Terms related to this study

• Additional Relevant MeSH Terms: Pathologic Processes; Infections; Inflammation; Shock; Sepsis; Systemic Inflammatory Response Syndrome; Anti-Infective Agents; Anti-Bacterial Agents; Azithromycin
• Other Study ID Numbers: VISN 17-001; 5K23HL096054-03 (U.S. NIH Grant/Contract); UHS#20151 (Other Identifier: UTHSCSA/South Texas Veterans Health Care System)