Skip to content

Procalcitonin as a Marker of Antibiotic Therapy in Patients With Lower Respiratory Tract Infections

Procalcitonin as a Marker of Antibiotic Therapy in Patients With Lower Respiratory Tract Infections. Can Measurement of Procalcitonin Reduce the Use of Antibiotics?

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02171338
Enrollment
55
Registered
2014-06-24
Start date
2013-10-31
Completion date
2014-09-30
Last updated
2014-08-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Exacerbation of Chronic Obstructive Airways Disease, Pneumonia

Keywords

Procalcitonin, Antibiotic therapy, Lower respiratory tract diseases

Brief summary

The purpose of this study is to investigate weather or not the use of a procalcitonin(PCT)-based treatment in the daily clinical work could lower the consumption of antibiotics in patients with lower respiratory tract infections.

Detailed description

An increasing amount of antibiotics are being consumed and along with the increased resistance they carry along, they pose an increasing problem for the health sector. A method to decrease the use of antibiotics is highly desirable and of great importance in order to halt the spread of multi-resistant bacteria that is becoming an increasing problem in Denmark. Lower respiratory tract infections such as pneumonia and acute exacerbations of chronic obstructive pulmonary disease (AECOPD) are frequent reasons for patient contact in both the primary and secondary sectors. Identifying which patients that could benefit from treatment with antibiotics is a great challenge to the health sector. This is why patients often are treated with antibiotics if there is a mere suspicion of the above-mentioned disorders, even if they are not proved for certain. An increasing amount of data suggests that procalcitonin (PCT) could serve as a possible marker of respiratory tract infections caused by bacteria. Alongside the conventional clinical parameters, the level of PCT is regarded as a promising means to decide whether to treat with antibiotics and how long such a treatment should endure. When an infection is under control by the immune system of the individual or by treatment with antibiotics, the level of PCT will diminish by 50% on a daily basis. Accordingly, a decline in the PCT levels should indicate a favorable response to antibiotic treatment. Therefore there is a need to further investigate if the PCT levels can be used, in the everyday clinic, to diagnose patients with pneumonia or AECOPD caused by bacteria and if this could have an effect on the use of antibiotics, thus optimizing the treatment of the patients. The purpose of this research project is to compare the amount of antibiotics consumed using standard treatment and treatment based on the PCT levels of patients with lower respiratory tract infections, respectively. With the research at hand, a clarification of whether a measurement of PCT can serve as a diagnostic tool to distinguish between bacterial and non-bacterial infections in patients that are suspected of having pneumonia or AECOPD is desirable. In extension, this study wants to clarify if the PCT levels can indicate when a potential antibiotic treatment should be initiated and if the use of a PCT-based treatment in the daily clinical work could lower the consumption of antibiotics. The hypothesis is that PCT will be increased (≥0.25 µg/l and ≥0.10 µg/l for pneumonia and AECOPD respectively) in lower respiratory tract infections caused by bacteria, whereas PCT should only be slightly increased in non-bacterial lower respiratory tract infections if at all. It is expected that using a PCT-based treatment in lower respiratory tract infections could lower the consumption of antibiotics, while at the same time it should not prove a greater health risk to patients than by using a standard treatment.

Interventions

OTHERPCT-level

PCT-level is available to the treating doctor.

BEHAVIORALAntibiotic treatment based on PCT-level

PCT-level is available to the treating doctor and the decision whether or not to treat with antibiotic is based on the level of PCT. The type of antibiotic chosen to treat is based on the existing antibiotic treatment guidelines of Holbaek Hospital and includes the antibiotics listed above.

Sponsors

Region Sjælland
CollaboratorOTHER
Aase and Ejnar Danielsens Foundation
CollaboratorOTHER
Holbaek Sygehus
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Hospitalized in Holbæk Hospital * Clinical and paraclinical signs of pneumonia and/or AECOPD.

Exclusion criteria

* Unable to hand over written consent. * Terminal patients. * Patients with known abscess in the lungs and/or emphysema. * Patients who have received treatment with strong doses (\>5mg/day) of biotin (vitamin B7 og B8) within the last eight hours.

Design outcomes

Primary

MeasureTime frame
Days of antibiotic treatmentParticipants will be followed for the duration of hospital stay, an expected average of 2 weeks, and up to 2 weeks after discharge.

Secondary

MeasureTime frameDescription
Numbers of days admittedParticipants will be followed for the duration of hospital stay, an expected average of 2 weeks.Numbers of days admitted from the day og enrollment in the study to the day of discharge.

Other

MeasureTime frameDescription
Patients with low PCT-levelParticipants will be followed for the duration of hospital stay, an expected average of 2 weeks.Numbers of patients with a PCT-level ≤0,1 µm/L and ≤0,25 µm/L in AECOPD and pneumonia respectively who gets treated with antibiotics during their hospitalization.
Recurrence within 30 days after dischargeFrom 1 to 30 days after dischargeNumbers of patients with recurrence of AECOPD or pneumonia within 30 days after discharge.
Type of antibioticsParticipants will be followed for the duration of hospital stay, an expected average of 2 weeks, and up to 2 weeks after discharge.Antibiotics used to treat the enrolled patients (name, i.v. or p.o.)
Death and adverse events in the two treatment groupsParticipants will be followed for the duration of hospital stay, an expected average of 2 weeks, and up to 30 days after discharge.Death and adverse events in the two treatment groups meaning: * Death by any cause * Complications in connection with lower respiratory tract infections (empyema, abscess) * Severe complications from treatment with antibiotics (anaphylactic shock, rash) * Admission to intensive care unit * Readmission within 30 days

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026