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Monitoring of antibiotic treatment of patients with suspected sepsis using the biomarker Procalcitonin

Procalcitonin-guided Antibioticotherapy in critical patients with suspected Sepsis in a university hospital

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-99h7tc
Enrollment
Unknown
Registered
2020-05-26
Start date
2019-09-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Sepsis

Interventions

A prospective study was carried out divided into two quarters (Group A and Group B). In group A, the control group and in group B, the group undergoing therapy guided by Procalcitonin. A comparative s
Other
N04.590.874.500

Sponsors

Universidade Federal de Sergipe
Lead Sponsor
Hospital Universitário de Lagarto
Collaborator

Eligibility

Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Patients with suspected sepsis; hospitalized in critical areas (yellow, red clinic and ICU); Older than 18 years; Not pregnant.

Exclusion criteria

Exclusion criteria: Pregnancy discovered during collection; infections requiring prolonged antibiotic therapy, such as endocarditis, liver or brain abscess, deep abscess, mediastinitis and osteomyelitis; severe infection caused by viruses, parasites, fungi or mycobacteria; negative cultures (blood, urine, tracheal aspirate, or bronchoalveolar lavage) in patients with suspected sepsis, severe sepsis or septic shock.

Design outcomes

Primary

MeasureTime frame
It is expected to reduce the days of treatment with antibiotics and also to reduce the days of hospitalization between two groups, procalcitonin and control. Using the PRORATA method of the study by Bóuadma (2010), a large and complex study carried out in intensive care units. According to the procalcitonin serum level protocol, if the concentration is less than 0.25 µg / L, we suggest if you stop antibiotics; if less than or equal to 0.25 and less than 0.5 µg / L or greater than or equal to 80% of peak decrease, it is suggested to stop antibiotics encouraged; if it is greater than or equal to 0.5 µg / L or less than 80% of the peak decrease, continued stimulated antibiotics are suggested; and, if it is greater than or equal to 0.5 µg / L, increasing the peak, it is suggested to change antibiotics. Through this method, it was found that procalcitonin reduced exposure to antibiotics by 23%, but that it did not have a significant effect on mortality outcomes at the time.

Secondary

MeasureTime frame
It is expected to assess the economic impact during the first and second quarter of the study, as well as the study Deliberato et al. (2013), the total amount spent on antibiotic therapy in both groups will be used, plus the amounts spent on procalcitonin dosages (in the procalcitonin group only) and divided by the number of patients included in each group.

Countries

Brazil

Contacts

Public ContactPhydel Carvalho

Universidade Federal de Sergipe

phydel_ppc@yahoo.com.br+5577981163210

Outcome results

None listed

Source: REBEC (via WHO ICTRP)