Ireland
--:--IST
Active, not recruiting Observational

Characteristics of Patients in the ICU With Palliative Care Consults in a Tertiary University Hospital

NCT06984471 · tracked via the Priya Life Science Switzerland tracker
Phase
Observational
Started
2025-05-01
Last updated
2026-06-17

Condition(s) studied

Palliative Care Referral

Investigational drug(s) / intervention(s)

Palliative care consult

Palliative care consult: A palliative care (PC) consult involves a specialized palliative care team to provide symptom management, psychosocial support, and assistance with goals-of-care discussions for patients with serious or life-limiting illnesses.

Study summary

The aim of this retrospective observational single-center cohort study is to investigate the factors associated with palliative care (PC) referral, examine intensive care unit (ICU) involvement before, during, or after the referral, and evaluate patient outcomes such as mortality, hospital and ICU length of stay, discharge destination, functional status, symptom management, and the content of PC consultation reports.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adult patients (i.e., patients ≥18 years of age) * Palliative care consult either before, during or after a ICU stay at the University Hospital Basel between 2019 and until the end of 2024 Exclusion Criteria: * Patients younger than 18 years * Patients with documented refusal to use data

Primary outcome measure(s)

  • Patient demographics — 2019-2024
    Demographic information (e.g. age, sex) is collected.
  • Acute prehospital management data — 2019-2024
    Data from acute prehospital management, as documented in emergency medical services (EMS) treatment protocols, is collected. The collected data elements are aggregated to describe the overall EMS response.
  • Duration of intensive care unit stay — 2019-2024
    The length of intensive care unit (ICU) stay is recorded.
  • Duration of hospital stay — 2019-2024
    The length of the total hospital stay is recorded.
  • Discharge destination — 2019-2024
    The destination at discharge is recorded.
  • Date of palliative care consult — 2019-2024
    The specific date of palliative care consult is documented.
  • Reason for palliative care consult — 2019-2024
    The documented reason for palliative care consult is analyzed.
  • Place of palliative care consult — 2019-2024
    The specific place of palliative care consult is documented.
  • Number of visits by the palliative care team — 2019-2024
    The number of visits by the palliative care team is analyzed.
  • Additional features of the palliative care consult — 2019-2024
    Assessment of additional features related to the palliative care consult (changes in management, referral for psychiatric or psychological evaluation, treatment recommendations, etc.) documented in the medical records or consult report. These features are aggregated to characterize the scope, complexity, and potential impact of the palliative care consultation on the patient's overall treatment and care trajectory.
  • Comprehensive assessment of the neurological status based on validated clinical assessment — 2019-2024
    Neurological status during ICU stay is assessed using available data in the patient register from validated neurological assessments. These may include the Richmond Agitation-Sedation Scale (RASS), Sedation-Agitation Scale (SAS), Glasgow Coma Scale (GCS), Intensive Care Delirium Screening Checklist (ICDSC), or Status Epilepticus Severity Score (STESS). The specific tool used, as well as the scale of the score and meaning behind the score, depends on routine clinical practice and available documentation in the register. If multiple scores are available for a patient, they will be aggregated to provide a comprehensive assessment of neurological status. This outcome will be reported as a descriptive summary, synthesizing findings across tools, rather than as a single quantitative score.
  • Comprehensive assessment of critical illness severity based on standardized scoring systems — 2019-2024
    Disease severity during ICU stay is assessed using standardized scoring systems, including the Acute Physiology and Chronic Health Evaluation II (APACHE II), Simplified Acute Physiology Score II (SAPS II), and Sequential Organ Failure Assessment (SOFA), depending on data availability in the patient register. The specific scoring system applied, as well as the scale and interpretation of the score, varies based on routine clinical practice and available documentation. Where multiple severity scores are available, they will be synthesized to provide a descriptive summary of overall illness severity rather than a single quantitative score.
  • Charlson Comorbidity Index — 2019-2024
    The Charlson Comorbidity Index (CCI) is calculated based on pre-existing comorbidities and additional diagnoses. The CCI predicts the ten-year mortality for a patient who may have a range of comorbid conditions. It assigns weighted scores (from 0 to maximal 6) to 17 comorbid conditions (e.g., heart disease, diabetes, cancer), resulting in a total score ranging from 0 to 33, if the patient had the most severe form of each of the 17 conditions.
  • Laboratory parameters — 2019-2024
    Routine laboratory value for e.g. C-Reactive Protein (CRP), albumin, Lactate Dehydrogenase (LDH), Creatine Kinase (CK), procalcitonin, white blood cell levels, creatinine, liver enzymes, blood gas analyses, metabolic data, etc. is collected. The specific parameters recorded may vary depending on the laboratory assessments documented in the patient register. All values will be reported using their respective units of measurement.These parameters are aggregated to support an overall clinical interpretation rather than a single numerical value. This approach reflects standard clinical practice, where multiple lab values are considered together to assess a patient's condition.
  • Complications associated with palliative Care consult — 2019-2024
    The complications occurring during or after the palliative care consultation are recorded, including inadequate symptom control, dissatisfaction expressed by the patient or relatives, cardiac arrest, unplanned emergency transfers to the ICU, and poor functional outcomes.
  • Glasgow Outcome Score — 2019-2024
    The Glasgow Outcome Score (GOS) is calculated based on the assessment of key clinical outcomes such as inhospital mortality, survival, survival with neurofunctional alteration, return to premorbid neurological function, and hospital readmission to determine the patient outcome. The GOS ranges from 1 (death) to 5 (good recovery).
  • Therapeutic intervention — 2019-2024
    The therapeutic intervention is documented, including information on duration, dosage and number of treatment medication, number of neuroleptic, sedative and analgesic drugs, invasive procedures, such as intubation, mechanical, ventilation, vasopressors, installation of central lines, nutrition, etc.
  • Vital signs — 2019-2024
    Vital signs are analyzed based on the data available in the patient register. These may include blood pressure, heart rate, respiratory rate, oxygen saturation, body temperature, level of consciousness, etc. The specific parameters recorded depend on the clinical documentation available. All values will be reported using their respective units of measurement. These values are aggregated to support an overall clinical assessment rather than a single numerical score. This reflects standard practice, where multiple vital signs are interpreted together to evaluate a patient's condition.
  • Fluid balance data — 2019-2024
    Fluid balance data, including the administration of fluids such as blood products, crystalloids, and enteral/parenteral nutrition, are documented. These components are aggregated to represent overall fluid input for each patient.
  • Assessment of diagnostic procedure — 2019-2024
    The diagnostic procedures performed during intensive care-whether invasive (e.g., lumbar puncture, central line placement) or non-invasive (e.g., radiologic imaging, ultrasound)-are systematically documented. Additionally, if physical restraints are used to ensure patient safety or procedural success, their usage are also recorded.

Trial sites (1)

FacilityCityRegionStatus
University Hospital Basel, Clinic for Intensive Care Medicine Basel Switzerland
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06984471 on ClinicalTrials.gov ↗ ← All trials in Switzerland