Polypharmacy and Potential Drug–Drug Interactions in Home-Dwelling Older People – A Cross-Sectional Study
Received 15 December 2020
Accepted for publication 16 February 2021
Published 9 March 2021 Volume 2021:14 Pages 589—597
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 3
Editor who approved publication: Dr Scott Fraser
Monica Hermann,1 Nina Carstens,2 Lars Kvinge,1 Astrid Fjell,1,3 Marianne Wennersberg,4 Kjersti Folleso,5 Knut Skaug,6 Ake Seiger,7 Berit Seiger Cronfalk,3,8 Anne-Marie Bostrom1,3,9
1Department of Health and Caring Sciences, Western Norway University of Applied Sciences, Stord, Norway; 2Hospital Pharmacies Enterprise, Western Norway, Bergen, Norway; 3Department of Neurobiology, Care Sciences and Society, Division of Nursing, Karolinska Institutet, Stockholm, Sweden; 4FOUSAM, Western Norway University of Applied Sciences, Haugesund, Norway; 5Bømlo Municipality, Hordaland, Norway; 6Department of Research and Innovation, Helse Fonna HF, Haugesund, Norway; 7Division of Clinical Geriatrics, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; 8Department of Health Care Sciences, Palliative Research Centre Ersta Sköndal Bräcke University College, Stockholm, Sweden; 9Theme Aging, Karolinska University Hospital, Huddinge, Sweden
Correspondence: Monica Hermann Tel + 47 53491477
Email [email protected]
Background: Risks associated with polypharmacy and drug–drug interactions represent a challenge in drug treatment, especially in older adults. The aim of the present study was to assess the use of prescription and non-prescription drugs and the frequency of potential drug–drug interactions in home-dwelling older individuals.
Methods: A cross-sectional study design was applied. Data were collected during preventive home visits among individuals aged ≥ 75 in three separate communities of Western Norway. A questionnaire, which was filled out by the individual, their next-of-kin, and the nurse performing the home visit was used for the collection of demographic and clinical data (age, sex, medication use, diagnoses, need of assistance with drug administration). Potential drug–drug interactions were identified electronically by IBM Micromedex Drug Interaction Checking. Point prevalence of potential drug–drug interactions and polypharmacy (≥ 5 drugs) were calculated. Binary logistic regression analyses were performed to assess factors potentially associated with polypharmacy or potential drug–drug interactions.
Results: Among the 233 individuals (mean age 78± 3 years, 46% male) included in the study, 43% used ≥ 5 drugs, 3.4% ≥ 10 drugs, while 4.3% used no drugs. In 54% of the 197 individuals using two or more drugs, at least one potential drug–drug interaction was detected. Low-dose aspirin and simvastatin were most frequently involved in potential drug–drug interactions. In total, 25% of the individuals reported current use of drugs sold over the counter of which more than 95% were analgesic drugs. Potential drug–drug interactions involving ibuprofen were identified in nine of 11 (82%) individuals using over-the-counter ibuprofen.
Conclusion: The study revealed a high prevalence of polypharmacy and potential drug–drug interactions with both prescription and non-prescription drugs in older home-dwelling individuals. Close monitoring of the patients at risk of drug–drug interactions, and increased awareness of the potential of over-the-counter drugs to cause drug–drug interactions, is needed.
Keywords: drug–drug interactions, polypharmacy, home-dwelling, old people
Polypharmacy in older people is frequent, and recent data from the Norwegian Prescription Database has shown that 23% of the prescription drug users 65 years and older were prescribed 10 or more drugs in 2017.1 Polypharmacy in older people is a double-edged sword. Many drugs are crucial in the treatment of diseases, and relief of symptoms, in multimorbid older individuals. Concomitantly, polypharmacy is associated with increased risk of drug–drug interactions and adverse events leading to functional decline, hospital admission, and even death.2–4 Adverse events related to drug use are estimated to cause around 10% of hospital admissions in older people.2
Drug–drug interactions (DDIs) occur when the effect of a drug is affected by a concomitantly administered second drug. The result of drug–drug interactions can be either decreased effect of the affected drug or enhanced effect, and consequently increased risk of side-effects. The frequency of DDIs increases with increasing number of drugs.5 The reported frequencies of DDIs in observational studies vary between 15% and 70% depending on the characteristics of the study participants (age, morbidity), the setting, and assessment of potential DDIs.5–10
Through the last decades, increasing attention has been drawn towards improving drug prescription in older individuals. This has resulted in increased use of clinical decision support systems for prescribers, and increased use of structured medication reviews. In Norway, all inhabitants are assigned a regular general practitioner. The regular general practitioner is responsible for the coordination of the patients’ drug treatment and performing a medication review when needed in patients with polypharmacy.11 Both clinical decision support systems and systematic medication reviews have been shown to reduce negative health outcomes from multiple drug use by reducing potentially serious DDIs and adverse drug reactions.12,13
Despite the use of decision support systems and medication reviews, there is a risk of DDIs, especially for patients where multiple prescribers are involved in drug prescription.14 This is likely to be the case for home-dwellers, as they may visit other medical doctors such as different specialists, practitioners at the out-of-hours emergency primary health care or hospitals, in addition to their regular general practitioner. A Norwegian multicenter study from 2015 showed discrepancies in up to 80% of medication lists upon hospital admission, illustrating the challenge of information transfer.15 Since 2012 there have been ongoing national efforts to develop a common system for electronic patient records across levels of the health care sector in Norway, but full implementation is still years away.16 Therefore, the transfer of patient information between levels will remain a challenge for several years to come. Also, self-medication with over-the-counter (OTC) drugs is frequent in older people with a prevalence of around 40% in western countries.17,18 Previous studies have shown that common OTC drugs like aspirin and other non-steroid anti-inflammatory drugs (NSAIDs) are frequently involved in DDIs, and are also the drugs most commonly involved in DDIs leading to hospital admission.4,5,19 The use of OTC drugs, therefore, adds to the total risk of potential DDIs. This is a challenge in general practice, as self-medication with OTC drugs are often not recorded in electronic patient records.20 Also, most studies on the consequences of drug–drug interactions for hospitalization or visits to the emergency department are based on medical records, and OTC drugs are therefore often ignored when evaluating drug–drug interactions.19 On this basis, we aimed to assess the use of prescription and non-prescription drugs and the frequency of potential drug–drug interactions in a cross-sectional study with home interviews of older home-dwelling individuals.
Study Design and Data Collection
A cross-sectional study design with preventive home-visits in home-dwelling older individuals was applied.21 Older home-dwelling inhabitants of three different non-neighboring municipalities, one urban and two rural municipalities of different sizes, situated in Western Norway, were invited to receive a preventive home visit. The three municipalities were selected as they were starting up a preventive home visit program (ie, convenience sampling). The visits aimed to identify persons at risk of developing illness by addressing four focal areas; malnutrition, falls, cognitive impairment, and polypharmacy. The home visit program has previously been described in detail.21 Briefly, older home-dwellers able to communicate in Norwegian were eligible for inclusion. In the smaller community, all individuals 75 years of age and above were included in the preventive home visit program, while in the two larger communities only home-dwellers 77 years of age were invited to receive a preventive home visit. The individuals were identified by the Norwegian National Registry, contacted by telephone, and asked to participate in the study. Approximately 60% of the invited individuals agreed to participate.21 The preventive home visits were performed by specially trained nurses. The nurses collected data using a questionnaire, which consisted of a substantial number of questions and validated tests on cognitive function, balance/falls, nutrition, and polypharmacy, in addition to questions on demographics, lifestyle, and medical diagnoses.21 For the focal area polypharmacy, the individual’s age, sex, place of living (urban/rural), prescription and non-prescription drugs, medical diagnoses, and need for help with administration of medication were registered. Data on the use of prescription and non-prescription medication was collected during the home visit by a combination of sources; interview with participant and next-of-kin, visual inspection of medication after asking the participants to show the medication they were using, and written information in form of a medication list issued by the individuals’ general practitioner (available for 23% of the participants) or home care nursing service (11%).
Two of the authors screened for drug–drug interactions. IBM Micromedex® Drug Interaction Checking (electronic version) was selected as knowledge base to identify potential drug–drug interactions, based on previous reports on accuracy and comprehensiveness.22–24 In the presentation of the results, the term potential drug–drug interaction (pDDI) is used, as many drug–drug interactions are avoidable and manageable with dose adjustments and/or close clinical follow-up and we do not have data on the consequence of the pDDI in the individual patient. PDDIs were classified in accordance with the classification system of Micromedex as either; contraindicated, major (interaction may be life-threatening or require medical intervention to minimize or prevent adverse effects), or moderate (the interaction may result in exacerbation of the patient’s condition and/or require an alteration on therapy). The primary and secondary endpoints were point-prevalences of pDDIs and polypharmacy, respectively. Polypharmacy was defined as the use of five or more drugs.25 All participants were included in the analysis of point prevalence of polypharmacy, while only individuals using 2 or more drugs were included in the calculations of point-prevalence of pDDIs.
The study sample was described in terms of demographics (age, sex, place of living (urban/rural), diagnoses, need for help with medicine administration), polypharmacy and drug–drug interactions using mean and standard deviation for continuous variables and frequencies and percentages for categorical variables. Binary logistic regression analyses were used to assess factors potentially associated with polypharmacy, and drug–drug interactions. Age, sex, place of living (urban/rural), “need help with medicines” (yes/no) and clinical diagnose were investigated as potential covariates in the analysis of polypharmacy. In the analysis of pDDIs, the total number of medications was also included as a potential covariate. The category “need help with medicines” included individuals that received help with administration of medicines from their next-of-kins or home care nurses. Diagnose categories were collapsed to reduce the number of independent variables and increase the frequency of positive outcomes in each category. Diagnose categories with less than 10% positive outcomes (ie, less than persons with the disease) were not included in the regression models. The included diagnose categories were as follows: diabetes, cardiovascular disease (hypertension, hyperlipidemia, heart failure, coronary heart disease), lung disease (chronic obstructive pulmonary disease and asthma), cancer, musculoskeletal disorders (osteoporosis, arthritis). Preliminary analyses were performed to ensure that the variables were not subjected to multicollinearity. The ratio of cases to variables in the logistic regression analysis was above 20. As there were no variables with a positive response rate of less than 10%, the sample size was considered sufficient for this analysis. A p-value <0.05 was considered a statistically significant difference. SPSS version 27 (IBM Corporation, Armonk, NY, USA) was used for statistical analyses.
In total, data from 233 home-dwellers were included, 109 from the urban community and 124 from the rural communities. The mean age of the participants was 78±3 years and 46% were male. Hypertension and hyperlipidemia were the two most common diagnoses, affecting 52% and 43% of the individuals, respectively (Table 1).
Table 1 Socio-Demographic Characteristics of Study Participants (n=233)
The median number of drugs was 4 (range 0–15) and polypharmacy was registered for 102 individuals (43%). Eight individuals (3.4%) used 10 or more drugs while 10 (4.3%) individuals did not use any drugs (Table 2). Diabetes diagnose (P=0.021), cardiovascular disease (P<0.001), and “need help with medicines” (P=0.022) were positively associated with polypharmacy (Table 3). Age, sex, place of living, and the diagnoses of cancer, lung disease, and musculoskeletal disease were not significantly associated with polypharmacy.
Table 2 Polypharmacy and Potential Drug–Drug Interactions in 233 Older Home-Dwellers
Table 3 Sociodemographic and Clinical Variables Associated with Polypharmacy and Potential Drug–Drug Interactions
Potential Drug–Drug Interactions
In total, 197 individuals used two or more drugs. Among these individuals, 302 pDDIs were identified, affecting 107 (54%) of the individuals. A total number of 132 pDDIs were classified as major pDDIs and these affected 80 (41%) of the individuals (Table 2). Two of the patients, using 10 and 14 different drugs, respectively, were each exposed to six major pDDIs. The total number of drugs was associated with both being exposed to a least one pDDI and at least one major pDDI (P<0.001, Table 3). Also, cardiovascular disease was positively associated with being exposed to a pDDI (P=0.023). Age, sex, place of living, need of help with medicines, and the diagnoses of diabetes, lung disease, musculoskeletal disease, and cancer were not significantly associated with pDDIs.
One individual used a contraindicated combination (isosorbide mononitrate and sildenafil). Among the 132 identified major pDDIs, the drugs most frequently involved were low-dose aspirin (47 times) and simvastatin (32 times) (Table 4). Simvastatin in combination with a calcium channel blocker, amlodipine (17 individuals), verapamil (3 individuals), and diltiazem (1 individual) was the most common pDDI. For aspirin, the most common pDDI was combination with a diuretic (hydrochlorothiazide or loop-diuretic, n=16). Also, aspirin in combination with other drugs affecting platelet function or coagulation; NSAID (6 individuals), warfarin (1 individual), and clopidogrel (1 individual) was frequently observed. Buprenorphine was the drug most frequently involved in pDDIs considering the number of users, with eight pDDIs in only four individuals (Table 4).
Table 4 Drug Most Frequently Involved in the 132 Major Potential Drug–Drug Interactions (pDDIs) in Older Home-Dwelling Older People Using ≥2 Drugs (n=197)
In total, 61 (26%) of the individuals reported current use of OTC medication. In 95% of the observations, the OTC drug was a pain reliever, mainly paracetamol which was used by 55 (90%) of the OTC users. Nine of the 11 individuals (82%) using ibuprofen were exposed to at least one potential drug–drug interaction involving ibuprofen. In seven of the nine individuals (56%) with a pDDI involving ibuprofen, the interaction was classified as major. The major pDDIs involving ibuprofen were interactions with aspirin or amitriptyline causing an increased risk of bleeding (n=3) and interactions with thiazide diuretics resulting in loss of diuretic effect (n=2).
The results of this study demonstrate that almost half of the older home-dwelling individuals use five or more drugs. Few other studies have described the prevalence of polypharmacy in a sample of home-dwellers not restricted to diagnosis or morbidity. However, the results are comparable to three recently published studies.6,7,26 Santos et al6 and Novaes et al7 found prevalences of polypharmacy from 26% to 45% in home-dwelling older individuals in Brazil, while Wauters et al26 observed a prevalence of approximately 60% in slightly older individuals (mean age 84) in Belgium. There are several challenges associated with polypharmacy, the main one being drug–drug interactions and risk of adverse events.2–5 In agreement with previous findings, a strong association between the number of drugs and drug–drug interaction was also observed in the present study.5 Recently, polypharmacy has also been shown to be associated with under-prescribing, and it is speculated that this might be a result of fear of causing harm to the patient through drug–drug interactions and adverse events.27
Overall, in the present study pDDIs were detected in 54% of home-dwelling older individuals using two or more drugs. This was higher than previous findings in similar age groups and settings.6,7 Cardiovascular disease was the most common diagnosis in this population and having a cardiovascular diagnose was positively associated with both polypharmacy and pDDIs. This was in agreement with the finding that drugs used to treat cardiovascular disease were most frequently involved in major pDDIs, with simvastatin and aspirin being the two most frequent. For simvastatin, the most commonly observed combination was with the calcium channel blocker amlodipine. Concomitant use of these two drugs may lead to increased systemic exposure of simvastatin due to inhibition of CYP3A4 by amlodipine and consequently increased risk of myopathy and rhabdomyolysis.28 The risk of rhabdomyolysis is dose-related, and doses of 20 mg or lower of simvastatin are recommended when used concomitantly with amlodipine.29,30 The risk of rhabdomyolysis is elevated in older individuals, and there have been several case reports on serious rhabdomyolysis in older individuals where simvastatin has been used in combination with a CYP3A4 inhibitor.31–33 In the present study, more than 95% of statin users were using simvastatin. The high use of simvastatin compared with other statins relates to a decision made by the Norwegian Medicines Agency in 2005 that simvastatin should be the preferred statin to reduce costs for the society.34 After 2014, the prescription of statins has not been subjected to restrictions, but many patients have nevertheless continued using simvastatin. The large number of major pDDIs involving simvastatin observed in this study is therefore probably not only a result of the drug–drug interaction potential of simvastatin compared with other statins but also the large use of this drug in the population.
For aspirin, a common major pDDI was combination with drugs causing an additive risk of bleeding. In the present study, both prescribed and OTC NSAIDs are registered, but even so, the reported frequency of the combination of aspirin and an NSAID is lower than previously reported data from the Swedish prescription registry in people ≥75 years.5 However, in total, 58% of the 81 individuals in the present study using antithrombotic treatment (warfarin, aspirin, clopidogrel, or dabigatran) were exposed to a major pDDI. This is similar to the recent finding by Schneider et al, where potentially severe or contraindicated interactions were detected in 58% of outpatients ≥60 years on antithrombotic therapy.35 The high frequencies of major pDDIs in patients on antithrombotic therapy calls for a continuous close monitoring of these patients.
A striking observation in this study was the high prevalence of major pDDIs in patients using buprenorphine. In two of the four individuals using buprenorphine, eight major pDDIs involving buprenorphine were detected. However, these were multimorbid patients using 14 and 8 prescription drugs, respectively. Although the risk of DDIs is known to increase with an increasing number of drugs, the high number of major pDDIs per user involving buprenorphine warrants a close follow-up of patients using this drug.5
A common feature of many of the pDDIs observed in this study is that a potentially harmful clinical outcome may theoretically be limited by dose adjustments of the affected drug and/or increased monitoring of the patients. No information on the prescribers was collected in this study, and consequently, information on precautions like dose adjustments or close follow-up of the patients was not available. However, the relatively high prevalence of major pDDIs might indicate that medication reviews should be performed more frequently. Currently, in Norway, a legal regulation calls for yearly medication reviews in patients where the regular general practitioner finds it necessary, but data on how often this is performed in practice is not available. Also, it is known from previous research that medication records are incomplete or contain errors in more than half of the cases in both primary and secondary health care, which complicates the work with identifying pDDIs.36,37
Nine of the 11 individuals using OTC ibuprofen, used it in combination with a prescription drug resulting in a pDDIs causing increased risk of bleeding (aspirin, tricyclic antidepressants) or affecting renal function (diuretics). Although the risk of GI bleeding has not been studied specifically for OTC NSAIDs, there is a large body of evidence showing that GI bleedings associated with NSAID use increases with increasing age and use of multiple NSAIDs, including low dose aspirin.38 The fact that 82% of the older individuals that used ibuprofen also used an interacting prescription drug, could be due to unawareness of the potentially harmful effects of OTC analgesics. Previous studies have shown that there is a general misperception among older adults that OTC drugs are too weak to cause any harm39 and that the awareness of pDDIs is higher in younger compared with older individuals.40 Safe use of OTC drugs is complicated by the fact that, typically, the regular general practitioner is not informed about the patients’ use of OTC drugs as these are generally not registered in the electronic patient records, and therefore the risk of prescribing an interacting drug increases.20 Improved labeling of OTC analgesics, as suggested by Roumie and co-workers, could potentially reduce the use of OTC NSAIDs in patients at risk, or may lead to patients informing the regular general practitioner about their OTC drug use.39 Also, for patients receiving home care services or preventive home visits, information about the patients’ use of OTC drugs could be communicated to the regular general practitioner by the nurse performing the visit.41
A limitation to the present study is the relatively limited variance in age among the included participants, which might explain the lack of association between age and polypharmacy observed in this study. The study is strengthened by the fact that information on drug use is based on more than one source of information. In addition to medication lists from the general practitioner or home care service where this was available, information on drug use was also collected through interviews with the patients themselves and their next-of-kin and visual inspection of actual medication in use. This increases the possibility of getting more complete information as it is known from previous research that medication lists frequently contain errors.36 Unfortunately, the general practitioners were not contacted and data on possible precautions (dose adjustments, closer follow-up) and clinical outcome of the pDDI are therefore lacking. Information on clinical outcome would have strengthened the study further. The response rate was around 60% and the main reason given for declining participation was no need for a preventive home visit. Unfortunately, characteristics of the individuals who declined participation were not collected and, thus, a possible selection bias cannot be ruled out.21 It is possible that the presented data represent individuals with a higher disease burden and drug use than the general population in this region. However, health status in terms of self-rated health in the participants was comparable to other large-scale European epidemiological studies, indicating a representative sample.42–44
This study revealed a high prevalence of polypharmacy and pDDIs with both prescription and non-prescription drugs in older home-dwelling individuals. Close monitoring of the patients at risk of pDDIs, increased awareness of the potential of OTC drugs to cause DDIs, and good communication between the general practitioner and patient is needed, to reduce the risk related to pDDI.
DDI, drug–drug interaction; NSAID, non-steroid anti-inflammatory drug; OTC, over the counter; pDDI, potential drug–drug interaction.
Data Sharing Statement
The dataset is available from the corresponding author upon a reasonable request.
Ethics Approval and Informed Consent
The study was approved by the Norwegian Data Protection Services (no. 26328 and 44970). Informed consent was obtained from all individuals included in the study. The study was conducted in accordance with the Declaration of Helsinki.
The contributions of Karen Johanne Vae and Dag-Helge Rønnevik are greatly acknowledged.
ÅS and BSC initiated and designed the project with contributions from NC, LK, and MW. BSC was responsible for the development of the data collection tool with contributions from NC, LK, AF, MW, KF, KS, ÅS. AF collected data (performed home visits). KF trained and advised nurses that performed home visits. All authors contributed to data analysis, drafting or revising the article, have agreed on the journal to which the article will be submitted, gave final approval of the version to be published, and agree to be accountable for all aspects of the work.
The planning and conduct of the study, as well as manuscript preparation, was done without external funding.
None of the authors has any conflicts of interest or competing interests to declare.
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