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Completed

NCT Number: NCT03452826

Combined Use of a Respiratory Broad Panel mPCR and Procalcitonin to Reduce Duration of Antibiotics Exposure in Patients With Severe Community-Acquired Pneumonia

To assess the effectiveness of a management strategy combining a broad panel respiratory mPCR and an algorithm of early antibiotic de-escalation and discontinuation based on both the mPCR results and the procalcitonin (intervention) in severe CAP, as compared to a conventional strategy (control).

A multicentre, parallel-group, open-label, randomized controlled trial. The primary assessment criterion est the number of antibiotic-free days at 28 days

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Hôpital BICHAT

Paris, 75018, France

About this study

Randomization is performed immediately after the inclusion.

  • In the intervention arm, a broad panel respiratory mPCR is performed on a lower respiratory tract sample (bronchoalveolar lavage fluid or tracheal aspirate, otherwise sputum), collected before the 12th hour following inclusion.
  • In both arms, an additional lower respiratory tract sample (bronchoalveolar lavage fluid or tracheal aspirate, otherwise sputum) is collected for biological studies and banking.
  • In the intervention arm, an algorithm of early antibiotic de-escalation and discontinuation is based on the early microbiological results, including the mPCR results, and the procalcitonin value. This algorithm is applied as soon as possible (before the 24th hour following inclusion if possible).
  • In the control arm, initial antibiotic therapy is maintained, according to guidelines.
  • In both arms, after 72 hours of antibiotic therapy, ICU physicians are advised to use procalcitonin (values and kinetics) to guide antibiotic therapy discontinuation, with a recommended total duration of 7 days, unless otherwise indicated.
  • In both arms, a switch to oral therapy is encouraged

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults (≥18 years) with CAP admitted to the ICU since 18 hours or less; the diagnosis of pneumonia includes two clinical criteria among a temperature > 37.8°C, tachypnea (respiratory rate > 25/min), chest pain, cough, expectoration, localized crackles, with or without signs of pleural effusion, pulse oximetry less than 92% while breathing room air, and a newly-appeared parenchymal infiltrate; the pneumonia is community-acquired if the time between hospital admission and ICU referral is below or equal to 48 hours.
  • Informed consent or emergency procedure.

Exclusion criteria

  • Pregnancy;
  • Congenital immunodeficiency;
  • HIV infection with the lymphocyte CD4 count below 200/mm3 or unknown in the last year;
  • Acute hematologic malignancy;
  • Neutropenia (<1 leucocyte/mL or < 0.5 neutrophil/mL);
  • Immunosuppressive drugs within the previous 30 days, including anti-cancer chemotherapy and anti-rejection drugs for organ/bone marrow transplant
  • Corticosteroids ≥ 20 mg/d of prednisone equivalent for more than 14 days;
  • chronic obstructive pulmonary disease (COPD) with previous history of colonization/infection with Pseudomonas aeruginosa;
  • Tracheostomy;
  • Diffuse bronchiectasis, cystic fibrosis;
  • Aspiration pneumonia;
  • Moribund patient or death expected from underlying disease during the current admission;
  • Patient deprived of liberty or under legal protection measure;
  • Participation in another interventional trial.

Treatment and study plan

Antibiotic therapy according to the result of mPCR (device)

Device
  • Phone call at D28 and D90, unless the patient is still hospitalized;
  • Collection of a respiratory tract sample (either distal, i.e. tracheal aspirate or bronchoalveolar lavage, or proximal, i.e. sputum) for broad panel respiratory mPCR in the intervention arm.
  • Collection of an additional respiratory tract sample for biological banking in both arms.

Other names: Antibiotic therapy to be adapted according to the result of mPCR (device)

Primary outcomes

  1. The effectiveness of a management combining a broad panel respiratory mPCR and an algorithm of early antibiotic de-escalation and discontinuation based on both the mPCR results and the procalcitonin in severe CAP, as compared to a conventional strategy

    Time frame: Day 28

    the number of antibiotic free days at D28, which corresponds to the number of days alive without any at Day 28.

Secondary outcomes

  1. Mortality at 28 (D28) and 90 days (D90);

    Time frame: Day 28 and day 90

    Mortality rate at D28 and D90

  2. Number of defined daily dose (DDD) per 100 patient days of broad- and narrow-spectrum antibiotics

    Time frame: Day 28

    Number of defined daily dose (DDD) per 100 patient days of broad- and narrow-spectrum antibiotics

  3. Antibiotics duration at D28

    Time frame: Day 28

    Antibiotics duration at D28

  4. Number of organ-failure free days (based on SOFA) at D28

    Time frame: Day 28

    Number of organ-failure free days (based on SOFA) at D28

  5. Incidence rates of bacterial superinfections at D28

    Time frame: Day 28

    Incidence rates of bacterial superinfections at D28

  6. Incidence rates of colonization/infection with multidrug resistant bacteria and Clostridium difficile infections at D28

    Time frame: Day 28

    Incidence rates of colonization/infection with multidrug resistant bacteria and Clostridium difficile infections at D28

  7. Incidence rates of relapse (same pathogen) or reinfection (another pathogen) at D28

    Time frame: Day 28

    Incidence rates of relapse (same pathogen) or reinfection (another pathogen) at D28

  8. Duration of ICU and hospital stay

    Time frame: Day 90

    Duration of ICU and hospital stay

  9. Cost of the total hospital admissions (including 90-day repeated admissions), ICU costs, cost of the microbiological diagnostic workup;

    Time frame: Day 90

    Cost of the total hospital admissions (including 90-day repeated admissions), ICU costs, cost of the microbiological diagnostic workup;

  10. Incremental / decremental cost effectiveness ratio in cost per treatment success (90-day composite of all-cause death and infection recurrence).

    Time frame: Day 90

    Incremental / decremental cost effectiveness ratio in cost per treatment success (90-day composite of all-cause death and infection recurrence).

  11. Sensitivity, specificity, and likelihood ratios of the broad panel mPCR Film Array for the diagnosis of pneumonia, taking the conventional microbiological tests as reference

    Time frame: Day 28

    Sensitivity, specificity, and likelihood ratios of the broad panel mPCR Film Array for the diagnosis of pneumonia, taking the conventional microbiological tests as reference

  12. Euroquol questionary (EQ-5D-3L)

    Time frame: Day 90

    Euroquol questionary (EQ-5D-3L)

  13. To assess the operational values of the broad panel mPCR Film Array for the diagnosis of ventilator associated pneumonia (in the intervention group only).

    Time frame: Day 28

    Sensitivity, specificity, and likelihood ratios of the broad panel mPCR Film Array for the diagnosis of ventilator associated pneumonia (in the intervention group only), taking the conventional microbiological tests as reference.

Sponsors and collaborators

Lead sponsor

Assistance Publique - Hôpitaux de Paris

Other

Registry information

Official study title

Combined Use of a Respiratory Broad Panel MULTIplex PCR and Procalcitonin to Reduce Antibiotics Exposure in Patients With Severe Community-Acquired Pneumonia: a Multicentre, Parallel-group, Open-label, Randomized Controlled Trial.

Acronym: MULTI-CAP

Important dates

Study start
2018
Primary completion
2022
Study completion
2023
First posted
Mar 2, 2018
Registry last updated
Oct 18, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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