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Edited by
Richard Pinder, Imperial College of Science, Technology and Medicine, London,Christopher-James Harvey, Imperial College of Science, Technology and Medicine, London,Ellen Fallows, British Society of Lifestyle Medicine
Deprescribing is the practice of stopping or reducing the dose of medicines that may be causing more harm than benefit to patients. Deprescribing can help prevent overprescribing, which can lead to adverse effects, unnecessary costs, or lack of efficacy. By deprescribing, patients can avoid medication-related problems, simplify their medication regimen, and enhance their wellbeing with non-pharmacological interventions. However, deprescribing is not without risks. Patients may experience withdrawal symptoms or recurrence of their original condition, which require careful monitoring and support. Deprescribing also faces several barriers, such as limited time and resources for clinicians, lack of clear guidelines, and patient reluctance or attachment to their medicines. To overcome these challenges, deprescribing should be based on a strong clinician–patient relationship, a gradual and individualised process, a multidisciplinary team approach, and a shared decision making model. Deprescribing can also be guided by various frameworks that help clinicians review, assess, prioritise, and follow-up on patients’ medications. There are tools that help identify potentially inappropriate or unnecessary medications and provide recommendations for deprescribing.
Describe and validate the CHROME (CHemical Restraints avOidance MEthodology) criteria.
Design:
Observational prospective longitudinal study.
Setting:
Single nursing home in Las Palmas de Gran Canaria, Spain.
Participants:
288 residents; mean age: 81.6 (SD 10.6). 77.4% had dementia.
Intervention:
Multicomponent training and consultancy program to eliminate physical and chemical restraints and promote overall quality care. Clinicians were trained in stringent diagnostic criteria of neuropsychiatric syndromes and adequate psychotropic prescription.
Measurements:
Psychotropic prescription (primary study target), neuropsychiatric syndromes, physical restraints, falls, and emergency room visits were semi-annually collected from December 2015 to December 2017. Results are presented for all residents and for those who had dementia and participated in the five study waves (completer analysis, n=107).
Results:
For the study completers, atypical neuroleptic prescription dropped from 42.7% to 18.7%, long half-life benzodiazepines dropped from 25.2% to 6.5%, and hypnotic medications from 47.7% to 12.1% (p<0.0005). Any kind of fall evolved from 67.3 to 32.7 (number of falls by 100 residents per year). Physicians’ diagnostic confidence increased, while the frequency of diagnoses of neuropsychiatric syndromes decreased (p<0.0005).
Conclusions:
Implementing the CHROME criteria reduced the prescription of the most dangerous medications in institutionalized people with dementia. Two independent audits found no physical or chemical restraint and confirmed prescription quality of psychotropic drugs. Adequate diagnosis and independent audits appear to be the keys to help and motivate professionals to optimize and reduce the use of psychotropic medication. The CHROME criteria unify, in a single compendium, neuropsychiatric diagnostic criteria, prescription guidelines, independent audit methodology, and minimum legal standards. These criteria can be easily adapted to other countries.
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