Antiarrhythmic Drug Adverse Reaction, Anticholinergic Adverse Reaction, Anticholinergic Syndrome, Antiparkinsonism Drugs Causing Adverse Effects in Therapeutic Use, Antispasmodic Adverse Reaction, Psychotropic Agents Causing Adverse Effects in Therapeutic Use
Conditions
Keywords
anticholinergic burden, daily living activities, geriatrics
Brief summary
The anticholinergic burden was calculated based on the medications that the patients had used for more than 10 days. Short-term medications used by patients were not evaluated. Among all the medications used by the patients, those with anticholinergic effects were scored according to the scale, and the total anticholinergic burden was calculated by adding them up. Those who had no anticholinergic score were considered to have no anticholinergic burden. The study cohort will be stratified into two cohorts, distinguished by the presence or absence of anticholinergic burden. To evaluate the impact of anticholinergic burden on daily living activities and instrumental ADL, the groups will be compared with respect to hand grip strength and walking speed.In this study, the anticholinergic burden will be calculated based on medications used by the patients for more than 10 days, excluding short-term medications. Each medication with anticholinergic effects will be assigned a score according to a scale, and the total anticholinergic burden will be determined by summing up the scores. Patients without any anticholinergic score will be classified as having no anticholinergic burden. The study cohort will be divided into two groups based on the presence or absence of anticholinergic burden. To assess the impact of anticholinergic burden on daily living activities (ADLs) and instrumental ADLs, the groups will be compared in terms of hand grip strength and walking speed.
Interventions
None listed
Sponsors
Izmir Ataturk Training and Research Hospital
Study design
Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Being over 65 years old * Patients without a diagnosis of dementia and with MMSE\>24 * Patients who can communicate (without hearing or visual problems) * Those who give written consent to participate in the study
Exclusion criteria
* Patients with a diagnosis of dementia at their initial visit, * Bedridden patients (those with visual impairments) * Patients with walking difficulties (due to pain, prostheses, visual problems, etc.), vitamin D deficiency (10) (20ng/dl\>) or those who use assistive devices (walker, cane, etc.) or those with sequelae of cerebrovascular events or hip fractures. * Patients with a diagnosis of delirium, * Those who underwent major surgery in the last 6 months, * Those who experienced cardiac or cerebrovascular events during the follow-up period, * Patients with infectious diseases, * Those who did not sign or withdrew their consent form.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The Barthel Index for Activities of Daily Living (ADL) | 24 hours | ADL was evaluated on a scale of 100 points according to the patients' ability to feed themselves, bathe, perform personal hygiene, dress and undress, control bowel and bladder, use the toilet independently, use a wheelchair, mobility status, and ability to climb stairs. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| The Lawton-Brody Instrumental Activities of Daily Living (IADL) | 24 hours | IADL consisted of eight sections, including the ability to use a telephone, shop, prepare meals, clean the house, do laundry, take medication, travel, and manage finances, and was evaluated on a scale of 17 points. Low scores were considered an indicator of dependence. |
| Walking speed | 2 minute | For walking speed, the time to walk a 4.5-meter distance was measured. |
| Hand grip strength | 1 minute | Hand grip strength of the dominant hand was measured twice with a Jamar dynamometer while sitting with the elbow flexed at 90 degrees, and the highest value was recorded |
Contacts
Primary ContactHasan Oztin, MD
Outcome results
None listed