Critical Illness, Hematological Diseases
Conditions
Brief summary
Multicenter, observational and prospective study.
Detailed description
The data collection period will include 6 consecutive months, starting from the date of acceptance or conformity of the CEIC. Or, until an adequate sample size is reached that guarantees the statistical relevance of said analysis. All patients will subsequently be followed up 3 months after discharge from the ICU.
Interventions
There is no intervention in the study.
Sponsors
Study design
Eligibility
Inclusion criteria
* Adults * Solid organ tumor or hematological malignancy,
Exclusion criteria
-under 18 years old
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hospital mortality. | During the 6 months of the study. |