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Monitoring plan Agents Intervening against Delirium in the Intensive Care Unit (AID ICU) A randomized, blinded, placebo controlled trial. The trials EudraCTnumber: 201700382915The monitoring plans
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How to fill out agents intervening against delirium

01
Identify patients at high risk for delirium, such as those with advanced age or preexisting cognitive impairment.
02
Use validated screening tools like the Confusion Assessment Method (CAM) to assess for delirium.
03
Implement non-pharmacological interventions first, such as reorientation, early mobilization, and ensuring adequate pain control.
04
Consider pharmacological interventions only if non-pharmacological measures are ineffective or insufficient.
05
Ensure proper dosing and avoid polypharmacy by reviewing and adjusting medications as needed.
06
Monitor the patient for adverse effects and adjust the treatment plan accordingly.
07
Collaborate with a multi-disciplinary team including physicians, nurses, and pharmacists to provide comprehensive care for patients with delirium.

Who needs agents intervening against delirium?

01
Patients in the hospital or long-term care settings who are at high risk for delirium.
02
Patients with underlying medical conditions or factors that increase their susceptibility to delirium.
03
Healthcare professionals who are responsible for the care of patients at risk for delirium.
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Agents intervening against delirium refer to medications, therapies, or interventions employed to prevent or treat delirium, a state of severe confusion and rapid changes in brain function.
Healthcare providers, including hospitals and clinics, are required to file agents intervening against delirium as part of their patient care documentation and regulatory compliance.
To fill out agents intervening against delirium, healthcare professionals should document the specific interventions used, the patient's response, and any relevant observations in the patient's medical record.
The purpose of agents intervening against delirium is to minimize the incidence and duration of delirium, improve patient outcomes, and promote recovery in individuals at risk.
Information that must be reported includes the type of intervention used, dosage, duration, patient assessments, and any adverse effects or complications.
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