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Procalcitonin-guided Antibiotic Therapy During Severe Exacerbation of COPD

NCT03440060 — Not applicable, Unknown, 100 participants, University Hospital, Mahdia

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Procalcitonin-guided Antibiotic Therapy During Severe Exacerbation of COPD Requiring Mechanical Ventilation: a Controlled Randomized Trial

RegistryNCT03440060
StatusUnknown
PhaseNot applicable
Study typeInterventional; randomized, parallel, masking: none, treatment
Enrollment100 (Estimated)
SponsorUniversity Hospital, Mahdia (Other)
ConditionsAcute Exacerbation Copd
Interventionsprocalcitonin (Diagnostic test)
Datesstart 2017-10-05, primary completion 2020-10-01 (estimated), completion 2020-12-31 (estimated), first posted 2018-02-20, last updated 2019-05-13
Locations1 site in Tunisia

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-Summary

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.

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+Detailed description

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.

+Arms and interventions

ArmTypeInterventionsDescription
standard groupNo interventionparticipants receive systematically empiric antibiotic therapy on admission with amoxicillin- acid clavulanic or levofloxacin in case of allergy
Procalcitonin groupActive comparatorDiagnostic Test: procalcitoninparticipants receive antibiotics only if the procalcitonin value is at or greater than 0.25 ng/ml
  • procalcitonin (Diagnostic test): procalcitonin value will be obtained within 24 hours after ICU admission in both groups and will be taken into account in the procalcitonin group only

+Outcome measures

Primary outcomes

  • time to recovery [28 days]: defined by resolution of symptoms ( cough, sputum purulence and respiratory rate less than 25 breath per minute) and NIV withdrawal (normal pH for 24 consecutive hours after stopping NIV), for patients with home NIV investigators retain stabilization after returning to the same number of hours of NIV before current exacerbation and pH normalization for 24 consecutive hours

Secondary outcomes

  • Antibiotic exposure at day 90 [90 days]: number of days the patient received antibiotics for any infection within 90 days from the day of admission
  • Hospital readmission for another exacerbation at day 90 [90 days]: another readmission for another episode of COPD exacerbation within 90 days after a first discharge
  • NIV failure [28 days]: clinical deterioration requiring invasive ventilation or death
  • ICU length of say (days) [90 days]: number of days spent in the ICU during the index exacerbation
  • Hospital length of stay (days) [90 days]: number of days spent in hospital during the index exacerbation
  • ICU mortality [28 days]

+Eligibility

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

+Locations (1)

FacilityCityCountryStatus
Tilouche NejlaMahdiaTunisiaRecruiting

+Publications

  • Mathioudakis AG, Chatzimavridou-Grigoriadou V, Corlateanu A, Vestbo J. Procalcitonin to guide antibiotic administration in COPD exacerbations: a meta-analysis. Eur Respir Rev. 2017 Jan 31;26(143):160073. doi: 10.1183/16000617.0073-2016. Print 2017 Jan. PMID 28143877
  • Results publication: Christ-Crain M, Jaccard-Stolz D, Bingisser R, Gencay MM, Huber PR, Tamm M, Muller B. Effect of procalcitonin-guided treatment on antibiotic use and outcome in lower respiratory tract infections: cluster-randomised, single-blinded intervention trial. Lancet. 2004 Feb 21;363(9409):600-7. doi: 10.1016/S0140-6736(04)15591-8. PMID 14987884
  • Results publication: Schuetz P, Christ-Crain M, Thomann R, Falconnier C, Wolbers M, Widmer I, Neidert S, Fricker T, Blum C, Schild U, Regez K, Schoenenberger R, Henzen C, Bregenzer T, Hoess C, Krause M, Bucher HC, Zimmerli W, Mueller B; ProHOSP Study Group. Effect of procalcitonin-based guidelines vs standard guidelines on antibiotic use in lower respiratory tract infections: the ProHOSP randomized controlled trial. JAMA. 2009 Sep 9;302(10):1059-66. doi: 10.1001/jama.2009.1297. PMID 19738090

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