跳至主要内容
临床试验/NCT06984471
NCT06984471进行中(未招募)不适用

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

University Hospital, Basel, Switzerland1 个研究点 分布在 1 个国家目标入组 532 人开始时间: 2025年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
532
试验地点
1
主要终点
Patient demographics

研究概览

简要总结

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.

详细描述

Palliative care (PC) in the intensive care unit (ICU) can improve care for critically ill patients by supporting decision-making, managing symptoms, and planning for end-of-life care. Early referral to PC has been linked to more do-not-resuscitate and do-not-intubate decisions, fewer ICU procedures, and more transfers to hospice care. However, PC is still underused in many ICUs, partly because doctors often overestimate patient survival. Most referral guidelines are based on older patients or those with serious conditions, which may not apply to younger or potentially recovering patients.

Existing studies mostly focus on survival or length of stay, with limited information on symptoms, functional recovery, or patient comfort. Some research suggests that PC needs are often not well met in the ICU.

This retrospective single-center cohort study aims to better understand when and why ICU patients are referred to PC, how their care changes, and what outcomes follow. It will also examine symptom management, functional outcomes, and recommendations made by the PC team.

The results of this study may help improve the timing and use of PC in the ICU to better support patient needs.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Retrospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •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

排除标准

  • •Patients younger than 18 years
  • •Patients with documented refusal to use data

研究组 & 干预措施

Before ICU stay

Adult patients with a PC consult before an ICU stay at the University Hospital Basel between 2019 and until the end of 2024.

干预措施: Palliative care consult (Other)

During ICU stay

Adult patients with a PC consult during an ICU stay at the University Hospital Basel between 2019 and until the end of 2024.

干预措施: Palliative care consult (Other)

After ICU stay

Adult patients with a PC consult after an ICU stay at the University Hospital Basel between 2019 and until the end of 2024.

干预措施: Palliative care consult (Other)

结局指标

主要结局

Patient demographics

时间窗: 2019-2024

Demographic information (e.g. age, sex) is collected.

Acute prehospital management data

时间窗: 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

时间窗: 2019-2024

The length of intensive care unit (ICU) stay is recorded.

Duration of hospital stay

时间窗: 2019-2024

The length of the total hospital stay is recorded.

Discharge destination

时间窗: 2019-2024

The destination at discharge is recorded.

Date of palliative care consult

时间窗: 2019-2024

The specific date of palliative care consult is documented.

Reason for palliative care consult

时间窗: 2019-2024

The documented reason for palliative care consult is analyzed.

Place of palliative care consult

时间窗: 2019-2024

The specific place of palliative care consult is documented.

Number of visits by the palliative care team

时间窗: 2019-2024

The number of visits by the palliative care team is analyzed.

Therapeutic intervention

时间窗: 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.

Fluid balance data

时间窗: 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.

Additional features of the palliative care consult

时间窗: 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.

Complications associated with palliative Care consult

时间窗: 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

时间窗: 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).

Assessment of diagnostic procedure

时间窗: 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.

Comprehensive assessment of the neurological status based on validated clinical assessment

时间窗: 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

时间窗: 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

时间窗: 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

时间窗: 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.

Vital signs

时间窗: 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.

次要结局

未报告次要终点

研究者

发起方
University Hospital, Basel, Switzerland
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验