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

Primary Purpose

Pneumonia, Acute Exacerbation of Chronic Obstructive Airways Disease

Status
Unknown status
Phase
Phase 4
Locations
Denmark
Study Type
Interventional
Intervention
PCT-level
Antibiotic treatment based on PCT-level
Sponsored by
Holbaek Sygehus
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Pneumonia focused on measuring Procalcitonin, Antibiotic therapy, Lower respiratory tract diseases

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Holbæk Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

No Intervention

Arm Label

Antibiotic treatment based on PCT-level

Control

Arm Description

Information regarding the PCT-levels in the intervention group is available to the treating doctor and the test subjects are randomized for treatment based on the level of PCT (PCT algorithm). With a PCT ≥0.25 µg/l and ≥0.10 µg/l for pneumonia and AECOPD respectively antibiotic treatment is advised to be started.

Test subjects randomized for standard treatment (control group) are treated in accordance with the existing treatment guidelines of Holbaek Hospital. PCT-level will be measured but the treating doctor has no access to the result.

Outcomes

Primary Outcome Measures

Days of antibiotic treatment

Secondary Outcome Measures

Numbers of days admitted
Numbers of days admitted from the day og enrollment in the study to the day of discharge.

Full Information

First Posted
June 17, 2014
Last Updated
August 14, 2014
Sponsor
Holbaek Sygehus
Collaborators
Region Sjælland, Aase and Ejnar Danielsens Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT02171338
Brief Title
Procalcitonin as a Marker of Antibiotic Therapy in Patients With Lower Respiratory Tract Infections
Official Title
Procalcitonin as a Marker of Antibiotic Therapy in Patients With Lower Respiratory Tract Infections. Can Measurement of Procalcitonin Reduce the Use of Antibiotics?
Study Type
Interventional

2. Study Status

Record Verification Date
August 2014
Overall Recruitment Status
Unknown status
Study Start Date
October 2013 (undefined)
Primary Completion Date
August 2014 (Anticipated)
Study Completion Date
September 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Holbaek Sygehus
Collaborators
Region Sjælland, Aase and Ejnar Danielsens Foundation

4. Oversight

Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pneumonia, Acute Exacerbation of Chronic Obstructive Airways Disease
Keywords
Procalcitonin, Antibiotic therapy, Lower respiratory tract diseases

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
55 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Antibiotic treatment based on PCT-level
Arm Type
Other
Arm Description
Information regarding the PCT-levels in the intervention group is available to the treating doctor and the test subjects are randomized for treatment based on the level of PCT (PCT algorithm). With a PCT ≥0.25 µg/l and ≥0.10 µg/l for pneumonia and AECOPD respectively antibiotic treatment is advised to be started.
Arm Title
Control
Arm Type
No Intervention
Arm Description
Test subjects randomized for standard treatment (control group) are treated in accordance with the existing treatment guidelines of Holbaek Hospital. PCT-level will be measured but the treating doctor has no access to the result.
Intervention Type
Other
Intervention Name(s)
PCT-level
Intervention Description
PCT-level is available to the treating doctor.
Intervention Type
Behavioral
Intervention Name(s)
Antibiotic treatment based on PCT-level
Other Intervention Name(s)
Avelox®, Azithromycin, Benzylpenicillin, Bioclavid®, Cefuroxim, Ciprofloxacin, Clarithromycin, Piperacillin/Tazobactam, Primcillin, Vepicombin®, Zinacef®
Intervention Description
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.
Primary Outcome Measure Information:
Title
Days of antibiotic treatment
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 2 weeks, and up to 2 weeks after discharge.
Secondary Outcome Measure Information:
Title
Numbers of days admitted
Description
Numbers of days admitted from the day og enrollment in the study to the day of discharge.
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 2 weeks.
Other Pre-specified Outcome Measures:
Title
Patients with low PCT-level
Description
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.
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 2 weeks.
Title
Recurrence within 30 days after discharge
Description
Numbers of patients with recurrence of AECOPD or pneumonia within 30 days after discharge.
Time Frame
From 1 to 30 days after discharge
Title
Type of antibiotics
Description
Antibiotics used to treat the enrolled patients (name, i.v. or p.o.)
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 2 weeks, and up to 2 weeks after discharge.
Title
Death and adverse events in the two treatment groups
Description
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
Time Frame
Participants will be followed for the duration of hospital stay, an expected average of 2 weeks, and up to 30 days after discharge.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hans Ibsen, M.D., D.M.Sc
Organizational Affiliation
Holbaek Sygehus
Official's Role
Study Director
Facility Information:
Facility Name
Holbæk Hospital
City
Holbæk
ZIP/Postal Code
4300
Country
Denmark

12. IPD Sharing Statement

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

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