Procalcitonin Guided Antibiotic Therapy

NCT ID: NCT04240288

Last Updated: 2021-10-21

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: NA
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-09-30
• Study Completion Date: 2023-12-31

Brief Summary

The overuse of antibiotics is an enormous problem facing the healthcare system both in the United States and across the world. The investigators plan to test the hypothesis that using procalcitonin levels (blood test) to guide the length of antibiotic therapy in patients with complicated intra-abdominal infections leads to shorter antibiotic treatment courses.

Detailed Description

A 2019 Centers for Disease Control (CDC) report describes the rate of antibiotic resistance as alarmingly high and says clinicians must make efforts to lower the development of resistance through more discerning antibiotic use. Complicated intra-abdominal infections (CIAIs), defined as an infection that extends beyond the hollow viscus of origin and into the peritoneal space, are a common problem with a 9.2% mortality rate worldwide, a morbidity of 5-50% and a 21.5% risk of extra-abdominal infections. The basic principles for treatment of CIAIs include source control and appropriate antibiotic coverage; however, source control cannot always be achieved in CIAIs, i.e. diverticular or appendiceal abscesses. The STOP-IT trial concluded that shorter courses of antibiotics for CIAIs with source control are equivalent to the traditional longer courses with regard to recurrent infections and mortality, even in the setting of sepsis, but the optimal duration of antibiotic treatment is unknown for patients with CIAIs without source control. Due to lack of guidelines, these patients are routinely treated with long antibiotic courses. Given the association of prolonged antibiotic courses and increased rates of post-treatment infectious complications and antimicrobial resistance, the Infectious Disease Society of America and the Surgical Infection Society acknowledge that there is an urgent need to study the appropriate duration of antimicrobial therapy for CIAIs. The biomarker procalcitonin is expressed by human epithelial cells in response to bacterial infections, distinguishes true bacterial infection from Systemic Inflammatory Response Syndrome (SIRS) and has been used in studies to identify CIAIs.

Procalcitonin-guided antibiotic management has been shown to decrease the number of antibiotic days in respiratory infections and reduce mortality among medical and surgical Intensive Care Unit (ICU) populations (including those with CIAIs). However, there is little data evaluating its role in guiding antibiotic therapy specifically for CIAIs.

Conditions

Intra-Abdominal Infections

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Control Arm

Participants randomized to the control arm will be managed with the current standard of care including daily white blood cell count and vital sign documentation. The control group will also have daily procalcitonin levels drawn but the results will not be used to make decisions regarding antibiotic duration. Antibiotics will be given orally or intravenously at the discretion of the treating physician and will be given for a 10-day course, the current standard of care.

Group Type: OTHER

Standard of Care Antibiotic Treatment

Intervention Type: OTHER

Antibiotics will be administered based on standard of care treatment. The treating physicians will determine the treatment course.

Treatment Arm

These participants will be managed with procalcitonin-guided antibiotic therapy. An index procalcitonin will be drawn within 24 hours of admission followed by daily procalcitonin levels. Per standard of care, patients will have daily white blood cell counts drawn and regular vital sign documentation. Antibiotics will be given orally or intravenously at the discretion of the treating physician. Antibiotics in this arm will be stopped once the procalcitonin value drops to ≤80% of its index value or to \<0.5 ng/ml. Extension of antibiotics for more than 24 hours past this time will be documented.

Group Type: EXPERIMENTAL

Procalcitonin-guided antibiotic treatment

Intervention Type: OTHER

Antibiotics will be administered based on the procalcitonin lab results.

Interventions

Procalcitonin-guided antibiotic treatment

Antibiotics will be administered based on the procalcitonin lab results.

Intervention Type: OTHER

Standard of Care Antibiotic Treatment

Antibiotics will be administered based on standard of care treatment. The treating physicians will determine the treatment course.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• ≥ 18 years old
• Ability to give consent in English or Spanish
• Imaging proven intra-abdominal infection (CT, US, and/or MRI)

Exclusion Criteria

• Unable to give informed consent
• Patients enrolled in another trial
• Those having surgery for source control
• Patients with anastomotic leak
• Unable or unwilling to return or be contacted for clinical follow-up visits
• Currently incarcerated in a detention facility or in police custody
• Conditions with altered immune response or at risk for bacterial seeding
• Immunodeficiency (e.g., absolute neutrophil count <500/mm3, chronic immunosuppressive drugs, active chemotherapy or plans for chemotherapy in the following 30 days, or known AIDS [CD4 count <200 or AIDS-defining illness within the last year] assessed by patient history)
• Uncompensated liver failure
• Taking medication to treat active inflammatory bowel disease
• Malignancy, not in remission (ongoing chemotherapy patients excluded)
• Pregnant or expectation of becoming pregnant in the 30 days following baseline/screening
• Expected concurrent hemodialysis, peritoneal dialysis, or treatments using indwelling venous catheters
• Recent (within 90 days) placement of surgical implant (e.g., pacemaker, joint prosthesis, mechanical valve)
• Indwelling Left Ventricular Assist Device
• Patients with another infection (e.g., pneumonia, urinary tract infection) that requires treatment with another antibiotic

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Columbia University

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Katherine Fischkoff, MD

Role: PRINCIPAL_INVESTIGATOR

Columbia University

Other Identifiers

AAAS5105

Identifier Type: -

Identifier Source: org_study_id