Fever, infection
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: For inclusion of patients in this study will be established the following criteria: be over 18 years; body temperature 38.3 ° C; to consent to participate in the survey or have authorized their participation by signing the Statement of responsibility Consent
Exclusion criteria
Exclusion criteria: Exclusion criteria are: patient or guardian does not agree to sign the Instrument of Consent; patients with severe heart disease, traumatic brain injury, malignant hyperthermia, pregnant women, which has a history of adverse reactions following the use of physical methods (hot or cold) in the reduction of body temperature and do not tolerate treatment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Verify the effectiveness of the use of compress associated with antipyretic for the treatment of adult patients admitted to intensive care unit with a fever. The compresses are applied to the axillary and inguinal regions. The patient's temperature is measured every 10 minutes for a period of 4 hours, this period will also be observed the time that the patient's body temperature took to reach the smaller value 38.3C. | — |
Secondary
| Measure | Time frame |
|---|---|
| Verify the effectiveness of using cold compress associated with antipyretic for the treatment of adult patients admitted to intensive care unit with a fever. The measurements and parameters used to assess this outcome is the same as described for the primary outcome.;Verify the effectiveness of using a warm compress associated with antipyretic for the treatment of adult patients admitted to intensive care unit with a fever. The measurements and parameters used to assess this outcome is the same as described for the primary outcome. | — |
Countries
Brazil
Contacts
Hospital Municipal Odilon Behrens;Escola de Enfermagem Universidade Federal de Minas Gerais