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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05400707
Other study ID # PB_2016-02667; am22Bingisser
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 15, 2024
Est. completion date May 27, 2024

Study information

Verified date April 2024
Source University Hospital, Basel, Switzerland
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is to evaluate a tool capable of improved risk prediction regarding the 30-day mortality. The primary objective of this study is hospitalization, ICU-admission, morbidity and mortality in correlation with external validation of International Early Warning Score (IEWS) and decision-making processes regarding diagnosis, treatment and disposition in the ED.


Description:

Most emergency departments (EDs) perform an initial risk stratification of patients, called triage. Triage defines the process of systematically grouping patients according to their treatment priority on the base of algorithms in an environment with scarce health care resources. To this date no gold standard in triage risk stratification has been established. Most of the existing triage systems rely on the measurement of vital signs and a list of chief complaints. All of these systems have their shortcomings, especially in nonspecific ED presentations and in older patients. The primary objective of this study is hospitalization, ICU-admission, morbidity and mortality in correlation with external validation of International Early Warning Score (IEWS) and decision-making processes regarding diagnosis, treatment and disposition in the ED. In this national single centre, prospective, consecutive, observational all-comers study patients entering the ED undergo triage and will be verbally informed about the study. First, each patient's vital signs (respiratory rate, oxygen saturation, heart rate, blood pressure, temperature) are measured and pain is rated on a scale of 0 to 10. In addition, the patient's level of consciousness is assessed using the AVPUC scale (alert, new confusion, verbal, pain, unresponsive, new confusion). Patients are asked to rate their own mobility between stable walking without aids or limited mobility with aids (walking aid, wheelchair, lying down). In addition, the patient's mobility is observed by the triage staff. The probability that the patient will be admitted as an inpatient is then assessed. A Clinical Frailty Scale (CFS) is also completed for patients over 65. After triage, patients are transferred to the treatment unit. Patients in need of immediate therapy, such as analgesia, will receive therapy before start of the interview. Patients will then be approached by a member of the study personnel and will be asked "which symptoms are you experiencing at the moment?". The question will be repeated 3 times, Answers will be recorded by ticking boxes in the CRF for a predefined list of 37 symptoms. Then, patients will be asked "which of the symptoms you reported is most important to you?". Patients are asked for their opinion on whether they should be discharged home after emergency treatment or whether they should stay in the hospital. Patients over the age of 65 are asked the following: "generally asked: what matters most to you at the moment?" and "why is that important for you?". Then, the attending senior physicians are asked how injured/ill they rate the patients on a scale from 0 (not ill/injured) to 10 (very ill/injured). The senior physicians are asked questions about decision-making in the emergency department. With regard to diagnostics, they are asked what type of diagnostic decision is involved (simple or complex decision), whether there was time pressure when making the diagnostic decision and which factors formed the basis for their diagnostic decision (list of 14 factors, numbered according to importance if applicable). Regarding therapy, respondents were also asked what type of therapeutic decision was involved (simple or complex decision), whether there was time pressure in making the therapeutic decision, and which factors formed the basis for their therapeutic decision (list of 14 factors, numbered according to importance if applicable). Then the disposition of the patient (ambulatory or hospitalized) is defined. For ambulant patients, senior physicians are asked which factors formed the basis for their ambulant disposition (list of 9 factors, numbered according to importance if applicable). For hospitalized patients, the senior physicians are asked which factors were the basis for their inpatient disposition (list of 17 factors, numbered according to importance if applicable). Finally, the attending physicians are asked who made the disposition decision. Follow-up to assess 30-day and 1-year mortality rate and date of death will start one year after the end of the inclusion period.


Recruitment information / eligibility

Status Completed
Enrollment 6467
Est. completion date May 27, 2024
Est. primary completion date May 27, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Patients presenting to the ED of the University Hospital Basel over a timecourse of 9 weeks from 15.04.2024 to 27.05.2024 Exclusion Criteria: - Obstetric, ophthalmologic, and paediatric patients will not be included - unwillingness to participate - insufficient ability to communicate with the study personnel.

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Assessment of vital signs
heart rate, blood pressure, body temperature, respiration rate, peripheral capillary haemoglobin oxygen saturation)
Assessment of patient mobility at presentation
Patients are asked how they assess their own mobility: - Stable walking without aids or limited mobility with aids (walking aid, wheelchair, lying down).
Assessment of level of consciousness by AVPUC scale
Assessment of level of consciousness by AVPUC scale (alert, new confusion, verbal, pain, unresponsive, new confusion)
Assessment of symptoms patients presenting when admitted to ED
Questionnaire with a predefined list of 37 symptoms
Assessment of what matters most in patients of 65 years and older
Patients over the age of 65 are asked the following: "generally asked: what matters most to you at the moment?" and "why is that important for you?".
Assessment of Decision-making in senior physicians
Questionnaire consisting of 10 questions about the decision-making processes in the emergency department and the factors that form the basis of their decisions regarding the diagnosis, treatment, and disposition of the patient.
Pain Numeric Rating Scale (NRS)
The NRS is a segmented numeric version of the visual analog scale (VAS) in which a respondent selects a whole number (0-10 integers) that best reflects the intensity of his/her pain ('0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme (e.g. "pain as bad as you can imagine"))
Clinical Frailty Scale (CFS)
The CFS is a commonly used score to assess frailty. It was developed within the Canadian Study of Health and Aging and consists of a 9-level ordinal scale ranging from very fit (score 1) to living with very severe frailty (score 8), and score 9 reserved for those who are terminally ill.

Locations

Country Name City State
Switzerland Department of Emergency Medicine, University Hospital Basel Basel

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Basel, Switzerland

Country where clinical trial is conducted

Switzerland, 

Outcome

Type Measure Description Time frame Safety issue
Primary 30-day mortality 30-day mortality is defined as death within 30 days of the day of presentation to the ED within 30 days of the day of presentation to the ED
Secondary Number of hospitalizations Hospitalization is defined as the direct admission from the ED to any hospital in-patient department with a stay of over 24 hours at baseline (= day of presentation to the ED)
Secondary Number of ICU-admissions ICU-admission is defined as any direct admission to the ICU of the University Hospital of Basel at baseline (= day of presentation to the ED)
Secondary Death rate (In-hospital mortality) In-hospital mortality is defined as death occurring during presentation to the ED and hospital discharge from day of presentation to the ED to day of hospital discharge (assessed within 365 days of the day of presentation to the ED)
Secondary 1-year mortality 1-year mortality is defined as death within 1 year of the day of presentation to the ED within 1 year of the day of presentation to the ED
Secondary Number of institutionalisations Institutionalisation is defined as no time spent at home during 365 days following presentation within 1 year of the day of presentation to the ED
Secondary Morbidity Acute Morbidity defined as framework of fourteen rationales: administration of antibiotics, virostatics, antifungals, immunosuppressives, diuretics, anticoagulants, antihypertensives, and procoagulants; the need for invasive interventions, or prolonged monitoring; new neurological deficits, or seizures; fractures, or self-harm within 1 year of the day of presentation to the ED
See also
  Status Clinical Trial Phase
Completed NCT03892551 - Triage - Symptoms and Other Predictors in an All-comer Emergency Department Population; (EKBB 236/13)