| Literature DB >> 31064365 |
Christine Gulla1, Elisabeth Flo1,2, Reidun L S Kjome3, Bettina S Husebo1.
Abstract
BACKGROUND: Multimorbid patients in nursing homes are prescribed long lists of medication, often without sufficient clinical evaluations beforehand. This results in poor clinical effects of the prescribed medication and significant side-effects, especially in patients with impaired cognition. The aim of this paper is to describe the process, content and implementation of a clinical medication review encompassing clinical testing and collegial support to prescribers.Entities:
Keywords: Behavioral and psychological symptoms of dementia; Implementation; Medication review; Needs assessment; Neuropsychiatric symptoms; Nursing homes; Symptom assessment
Mesh:
Year: 2019 PMID: 31064365 PMCID: PMC6505068 DOI: 10.1186/s12877-019-1139-6
Source DB: PubMed Journal: BMC Geriatr ISSN: 1471-2318 Impact factor: 3.921
Fig. 1The medication review process: 1: Researchers educated nursing home staff (“COSMOS ambassadors”), physicians, and nursing home leaders in safe use of drugs and the medication review intervention. 2: The COSMOS ambassadors used the lessons from the education to train the other staff in their units. 3: The researchers trained the nursing home staff in assessing the patients’ pain, neuropsychiatric symptoms, cognition, daily function, and quality of life. 4: Multidisciplinary medication reviews with the researchers, nurses, and nursing home physician were performed in each unit. The researcher gave collegial mentoring for the other participants. The results from the clinical assessments were used in evaluation of the prescriptions for each patient. 5: After two months, the nursing home staff was gathered for a midway evaluation to discuss promotors and barriers towards the implementation among themselves and with the researchers. 6: During the whole study period, the researchers regularly called the COSMOS ambassadors to follow up on the implementation. The researchers gave advice on how to overcome barriers, and collected practical tips from the COSMOS ambassadors that could be spread to other units
Instruments used in assessment of patient prior to medication review
| Short name | Range | Interpretation |
|---|---|---|
| Cognition | ||
| MMSE | 0–30 | The patient is asked 30 questions, scored correct (1) or wrong (0). Lower scores indicates lower cognitive function [ |
| FASTa | 1–7 | Staging cognitive function, normal to severe dementia [ |
| Neuropsychiatric symptoms | ||
| NPI-NHa | 0–144 | 12 individual items: delusions, hallucination, agitation, depression, anxiety, euphoria, apathy, disinhibition, irritability, aberrant motor behaviour, night-time behaviour, and eating disturbances. Each item is scored by frequency (“absent” to “daily”; 0–4), and intensity for the patient (“mild” to “severe”; 1–3) these scores are multiplied to a sum score of 0–12 for each item and summed to give a total score [ |
| CMAIa | 29–203 | 29 items with agitated behaviors (scored by frequency: “never” to “multiple times an hour”; 1–7) [ |
| CSDDa | 0–38 | 19 items on depressive behaviour (“absent” to “severe”; 0–2) [ |
| Pain | ||
| MOBID-2a | 0–10 | Pain intensity during five standardized, guided movements, and five domains related to internal organs, head and skin during the last week, each item is scored 0 to 10 (“no pain” to “worst imaginable pain”). A total pain score is based on the worst pain experienced. A score of ≥3 signifies a need for pain treatment [ |
| Activities of daily living | ||
| PSMSa | 0–30 | 6 items of toileting, feeding, dressing, grooming, physical ambulation, and showering are scored whether the patient are able to do the activity or unable (0–5), higher scores indicate more dependency [ |
| Quality of life | ||
| QUALIDa | 11–55 | 11 items on patient behaviour rated on severeness; 1 to 5. Lower score indicates higher quality of life [ |
aProxy-rated instrument. CMAI Cohen-Mansfield Agitation Inventory, CSDD Cornell Scale for Depression in Dementia, FAST Functional Assessment Staging, MMSE Mini Mental State Examination, MOBID 2 Mobilization-Observation-Behaviour-Intensity-Dementia 2 Pain Scale, NPI-NH Neuropsychiatric Inventory- nursing home version, QUALID quality of life in late-stage dementia
Responsibilities for the participants concerning the medication reviews
| Participant | Responsibilities |
|---|---|
| Physician | Order relevant blood tests before the medication review. Already existing blood test results could be used if they were not older than two weeks. Medical decision-making, including choice of drug and dose. |
| Nurse | Prior to the meeting use |
| Researchers | Plan the meeting and compile the results from the baseline assessment of the patients on a spreadsheet. Guide the interprofessional team through the medication review. Provide collegial mentoring and updated knowledge. Give general information on the physician’s prescribing practice, such as average number of regular and on demand prescriptions, in comparison to national numbers |
Experience, education and workload in health professionals in the intervention group
| Nursing home units in nursing home, N | 36 units in 18 NH | |
|---|---|---|
| Staffing, number of patients per nursing staffa (range) | Daytime | 3.2 (1.6–4.0) |
| Evening | 4.7 (2.3–6.0) | |
| Nighttime | 13.0 (4.0–30.3) | |
|
| 73 (2.0) | |
| Registered nurses, N (%) | 44 (61%) | |
| Licensed practical nurses, N (%) | 9 (12%) | |
| Unknown education | 19 (27%) | |
|
| 21 | |
| Age in years, mean (SD) | 48 (12.9) | |
| Female, N (%) | 8 (38%) | |
| Mean number of patients in the study, per physician, mean (range) | 22 (8–28) | |
| Minutes per patient per week, mean (range) | 20 (8–42) | |
aNursing staff: Registered nurses, licensed practical nurses, and uneducated staff
N Number, NH nursing homes, SD Standard deviation
Feedback by patient logs
| Whole period ( | ||||||
|---|---|---|---|---|---|---|
| Yes | No | Not applicable; don’t know | ||||
| Question in patient logs | N | % | N | % | N | % |
| Had at least one medication review | 220 | 92% | 16 | 7% | 3 | 1% |
| Indication on each drug | 200 | 83% | 36 | 15% | 4 | 2% |
| Informed patient and/or relative about change | 204 | 85% | 9 | 4% | 26 | 11% |
| Reinstated drug after pause | 72 | 30% | 141 | 59% | 27 | 11% |
| Documented change in patient health | 184 | 77% | 20 | 8% | 34 | 14% |
The answers in the patient logs were coded accordingly: If there were one or more “yes” in the 16 weeks of registration, the answer was coded yes. If there were one or more “no”, and no entries answered “yes”, we coded it as no. If there were one or more not applicable/don’t know, and no entries with yes or no, we coded it as not applicable/don’t know. The table includes only patients with at least one entry (57 excluded). Due to missing data, the numbers do not add up to 240
Barriers and promotors for good implementation
| Barriers | Promoters |
|---|---|
| New and difficult clinical instruments | Engagement |
| Lack of competence | Arena for learning |
| Practical challenges with changing drug regimes | Introducing a colleague to discuss difficult decisions with |
| Poor knowledge about electronic patient records | The intervention was perceived as important and relevant |
| Lack of time | Improved communication |
| Ethical dilemmas | Pleased relatives |