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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03408028
Other study ID # CHUB- status code
Secondary ID
Status Completed
Phase N/A
First received January 17, 2018
Last updated January 17, 2018
Start date April 1, 2017
Est. completion date October 1, 2017

Study information

Verified date January 2018
Source Brugmann University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The diagnostic and therapeutic progresses, associated with modifications in lifestyle and socio-cultural level of populations, have led to a remarkable increase in life expectancy. At the same time, the increasing medicalization of the individual has eroded the traditional boundaries between health and illness, normal and pathological state. This leads to the patient losing his sense of ownership of his own death. If most patients died at home before the Second World War, 75% of the population dies in hospital or institution at the present date.

Most hospitals and care institutions have developed codes, in multidisciplinary internal consultation, to address the interruption or lack of implementation of treatments that make no sense from a medical point of vue. This avoids therapeutic relentlessness.The code in place within the CHU Brugmann is:

- code A: no therapeutic restriction

- code B: not to be resuscitated

- code C: not to be intensively treated (no escalation in therapeutic treatments)

- code D: best palliative care (progressive de-escalation in therapeutic treatments).

These codes are established in consultation with the patient or his legal representative and are re-evaluated in a multidisciplinary way every week.

Planning a care path and therefore establishing a therapeutic code is particularly important for people with cognitive impairment and dementia because the progressive loss of cognitive abilities complicates the process of decision making.

A large part of the admissions are made via the emergency department. For these patients, no therapeutic plan has been established beforehand. However, the perception of the functional and cognitive status of the patient directly influences the intensity of care provided. Cognitive disorders are a risk factor for the exclusion of access to palliative care for the elderly patient.

The objectives of this study are:

- To establish a record of the therapeutic limitation codes in an acute cognitive geriatric unit

- To correlate the therapeutic limitation code with the comorbidities of the patients


Recruitment information / eligibility

Status Completed
Enrollment 310
Est. completion date October 1, 2017
Est. primary completion date October 1, 2017
Accepts healthy volunteers
Gender All
Age group 65 Years and older
Eligibility Inclusion Criteria:

Elderly patients with cognitive impairment admitted in the geriatric unit 83 within the CHU Brugmann between 01-01-2016 and 31-12-2016.

Exclusion Criteria:

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Medical File consultation
Medical File consultation

Locations

Country Name City State
Belgium CHU Brugmann Brussels

Sponsors (1)

Lead Sponsor Collaborator
Murielle Surquin

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Therapeutic code Therapeutic code From 01-01-2016 till 31-12-2016
Primary Cumulative Illness Rating Scale for Geriatrics This scoring system measures the chronic medical illness ("morbidity") burden while taking into consideration the severity of chronic diseases in 14 items representing individual body systems. The cumulative final score can theoretically vary from 0 to 56. From 01-01-2016 till 31-12-2016
Secondary Age Age From 01-01-2016 till 31-12-2016
Secondary Sex Sex From 01-01-2016 till 31-12-2016
Secondary Ethnicity Ethnicity From 01-01-2016 till 31-12-2016
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