Procalcitonin-guided Antibiotic Therapy During Severe Exacerbation of COPD Requiring Mechanical Ventilation: a Controlled Randomized Trial
| Registry | NCT03440060 |
|---|---|
| Status | Unknown |
| Phase | Not applicable |
| Study type | Interventional; randomized, parallel, masking: none, treatment |
| Enrollment | 100 (Estimated) |
| Sponsor | University Hospital, Mahdia (Other) |
| Conditions | Acute Exacerbation Copd |
| Interventions | procalcitonin (Diagnostic test) |
| Dates | start 2017-10-05, primary completion 2020-10-01 (estimated), completion 2020-12-31 (estimated), first posted 2018-02-20, last updated 2019-05-13 |
| Locations | 1 site in Tunisia |
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This study assess whether a procalcitonin guided antibiotic therapy can reduce significantly unnecessary antibiotic prescription during severe exacerbation of COPD requiring mechanical ventilation without compromising patients' outcome. The first group of patients will receive systematically empiric antibiotic therapy and the second group will receive antibiotics only if procalcitonin value is at or greater than 0.25 ng/ml.
Recently, procalcitonin gained interest as the most reliable biomarker in predicting bacterial origin in low respiratory tract infections and sepsis.
Procalcitonin was shown to be non-inferior to standard guidelines in guiding antibiotic therapy during COPD exacerbation, without worsening patients' outcomes, and with a significant reduction in antibiotic exposure.
Its use to guide antibiotic treatment during COPD exacerbation may be more challenging because of the frequent colonization of the airways in patients with COPD, and thus it needs further evaluation.
Additionally, until today, no interventional studies evaluating procalcitonin protocol have been conducted in ventilated COPD patients.
| Arm | Type | Interventions | Description |
|---|---|---|---|
| standard group | No intervention | participants receive systematically empiric antibiotic therapy on admission with amoxicillin- acid clavulanic or levofloxacin in case of allergy | |
| Procalcitonin group | Active comparator | Diagnostic Test: procalcitonin | participants receive antibiotics only if the procalcitonin value is at or greater than 0.25 ng/ml |
Sex: All, ages: 40 Years to any
Inclusion Criteria: * Patients > 40 years old who consent to the study protocol * COPD diagnosis based on GOLD guidelines Exclusion Criteria: * Patients who did not consent * Asthma * Malignancy * Immunocompromised * Survival for at least 1 year is unlikely * Patients already enrolled in this study
| Facility | City | Country | Status |
|---|---|---|---|
| Tilouche Nejla | Mahdia | Tunisia | Recruiting |