Key result
Medication regimen complexity varied widely among patients with the same number of medications, though MRCI score was strongly associated with medication count (Spearman r = 0.91, p < 0.01).
Why the study?
Complex medication regimens may be especially risky and burdensome for people with MCI or dementia, and automating the Medication Regimen Complexity Index could help identify those who would benefit from deprescribing.
Cross-Sectional (n=3,976)
Yes
Effect estimate: Spearman r = 0.91
p-value: p=<0.01
Automated calculation of the Medication Regimen Complexity Index (MRCI) using electronic medical records is feasible and highlights that dosing frequency is the primary driver of regimen complexity in older adults with MCI or dementia.
Beyond medication count, complex medication regimens may be especially risky and burdensome for people with dementia or mild cognitive impairment (MCI) and their caregivers. The Medication Regimen Complexity Index (MRCI), which incorporates dosage form, frequency, and additional directions,1, 2 may be a useful tool to identify people with dementia or MCI who would benefit from deprescribing. This study sought to automate MRCI calculation in a large, real-world database of people with MCI or dementia and to examine contributions of specific MRCI components to overall complexity. This was a cross-sectional study using existing medical record data from seven Minnesota counties in the Rochester Epidemiology Project (REP) medical records-linkage sytem,3 which captures information from healthcare provided to 90% of the residents of the region.4 We searched REP electronic indexes to identify residents aged ≥65 with incident MCI or dementia from January 1, 2015 through December 31, 2017 (Supplementary Table S3). We searched the REP for outpatient medication prescriptions and self-reported medications for individuals in the 30 days before and after their dementia diagnosis. The MRCI is a sum of three weighted subscores: form/route (Part A), frequency (Part B), and additional instructions (Part C).1 Information on form, route, and frequency was obtained from electronic prescription information. We examined the free-text and frequency fields for text patterns corresponding to Part C (e.g., "crush," "meal," and "bedtime").5 Decision rules were created for cases not clearly addressed in the MRCI instructions (Supplement). Two geriatricians (ARG, SN) refined the algorithm by searching for text patterns that had not been accounted for in earlier steps and to adjudicate discrepancies. We calculated MRCI scores first as a sum of the weighted scores for Part A and Part B only, and second as a sum of the weighted scores for all three parts.6 Higher scores indicated greater complexity. Patient characteristics were summarized and tested using chi-square tests. MRCI scores were summarized with median (interquartile range [IQR]); differences were tested using the Kruskal–Wallis test. Correlations were summarized with Spearman correlation coefficients. The cohort consisted of 3976 people and 29,059 linked medication records (Supplementary Tables S1 and S2). Among people with ≥1 medication, two central nervous system-active medications—opioids and antidepressants—together comprised 8% of medication prescriptions (Supplementary Table S2). Median MRCI scores across demographic/clinical characteristics are in Table 1. The median MRCI score was 12 (IQR: 5–25) calculated using Parts A and B and 14 (IQR: 6–29) calculated using all three parts. The biggest contributor to MRCI score was dosing frequency (Part B). Medication count was associated with MRCI score (Spearman r = 0.91, p < 0.01; Supplementary Figure S2). There was wide variation in MRCI scores among patients with the same number of medications (Figure 1). Frequency was the biggest contributor to medication regimen complexity in this cohort of patients with MCI or dementia, similar to studies in non-dementia populations.5 MRCI scores varied widely among patients with the same number of medications and may more accurately capture patients' and caregivers' lived experience than medication count. Complex medication regimens may increase the risk of poor health outcomes.7 The steps we undertook to calculate the MRCI could be used to identify people with MCI and dementia who may be most likely to benefit from deprescribing. Opioids and antidepressants were among the top 10 most common medication classes in our cohort. Reducing the use of central nervous system-active medications may be important to reducing complexity for this population, as use of such medications is common among people living with dementia and associated with numerous adverse health outcomes.8 To implement the MRCI for pragmatic deprescribing trials, it would need to be automated for use within electronic medical records in real time. Part C was difficult to automate because of the wide variety of ways in which special administration instructions can be expressed, requiring coder discretion. We found that calculating the MRCI score using only Parts A and B was comparable to incorporating the Part C subscore in terms of identifying patients with high versus low complexity.6 The MRCI may prove to be more useful than number of medications for identifying patients with MCI or dementia who are most likely to benefit from deprescribing interventions. Addressing high medication regimen complexity—for example, by eliminating medications that are taken multiple times per day or have complicated administration instructions—could reduce self-care demands, prevent institutionalization and lessen caregiver strain.9 A limitation of this research is that misclassification of medication use is possible. In conclusion, this study characterized medication regimen complexity among people with MCI or dementia. Future studies should assess the impact of reducing MRCI scores on clinical outcomes, including adverse events and patient- or caregiver-reported measures of treatment burden. Conception and design of study (all), analysis (Ruoxiang Jiang and Susan A. Weston), and interpretation of data (all), drafting manuscript (Ariel R. Green), revising manuscript (all), and final approval of version to be published (all). There are no relevant conflicts of interest. The funding sources had no role in the study concept and design, methods, subject recruitment, data collection, analysis, and preparation of paper. This project was supported by a grant from the National Institute on Aging (NIA AG 052425). In addition, this study used the resources of the Rochester Epidemiology Project (REP) medical records-linkage system, which is supported by the NIA (AG 058738), the Mayo Clinic Research Committee, and fees paid annually by REP users. Dr. Ariel Green acknowledges funding from the NIA (K23 AG054742; R01 AG077011) and NIA Impact Collaboratory (U54AG063546). Dr. Stephanie Nothelle acknowledges funding from the Grants for Early Medical/Surgical Specialists Transitioning to Aging Research (GEMSSTAR) (R03AG060170), her K23 (K23AG072037), both from the National Institute on Aging. The content of this article is solely the responsibility of the authors and does not represent the official views of the National Institutes of Health (NIH) or the Mayo Clinic. Supplementary Table S1. Characteristics of MCI/dementia patients with no medications vs ≥1 medication. Supplementary Table S2. Clinical characteristics of patients with MCI/dementia and ≥1 medication. Supplementary Table S3. ICD-9/10 codes used to identify patients with MCI and dementia decision rules for MRCI scoring. Supplementary Figure S1. Study flow diagram. Supplementary Figure S2. Association of medication count with MRCI score. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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Green et al. (2024) conducted a cross-sectional in incident mild cognitive impairment or dementia (n=3,976). Medication regimen complexity was evaluated on Association of medication count with MRCI score (Spearman r = 0.91, p=<0.01). Medication regimen complexity varied widely among patients with the same number of medications, though MRCI score was strongly associated with medication count (Spearman r = 0.91, p < 0.01).
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