ORIGINAL RESEARCH article
Volume 13 - 2022 | https://doi.org/10.3389/fphar.2022.832994
Prescription Rates, Polypharmacy and Prescriber Variability in Swiss General Practice—A Cross-Sectional Database Study
- Institute of Primary Care, University of Zurich and University Hospital Zurich, Zurich, Switzerland
Purpose: The frequency of medication prescribing and polypharmacy has increased in recent years in different settings, including Swiss general practice. We aimed to describe patient age- and sex-specific rates of polypharmacy and of prescriptions of the most frequent medication classes, and to explore practitioner variability in prescribing.
Methods: Retrospective cross-sectional study based on anonymized electronic medical records data of 111 811 adult patients presenting to 116 Swiss general practitioners in 2019. We used mixed-effects regression analyses to assess the association of patient age and sex with polypharmacy (≥5 medications) and with the prescription of specific medication classes (second level of the Anatomical Therapeutic Chemical Classification System). Practitioner variability was quantified in terms of the random effects distributions.
Results: The prevalence of polypharmacy increased with age from 6.4% among patients aged 18–40 years to 19.7% (41–64 years), 45.3% (65–80 years), and 64.6% (81–92 years), and was higher in women than in men, particularly at younger ages. The most frequently prescribed medication classes were antiinflammatory and antirheumatic products (21.6% of patients), agents acting on the renin-angiotensin system (19.9%), analgesics (18.7%), and drugs for acid related disorders (18.3%). Men were more often prescribed agents targeting the cardiovascular system, whereas most other medications were more often prescribed to women. The highest practitioner variabilities were observed for vitamins, for antiinflammatory and antirheumatic products, and for mineral supplements.
Conclusion: Based on practitioner variability, prevalence, and risk potential, antiinflammatory drugs and polypharmacy in older patients appear to be the most pressing issues in current drug prescribing routines.
A global increase in life expectancy has been observed in recent decades (GBD 2017 Mortality Collaborators, 2018), resulting in an older and more chronically ill population (Barnett et al., 2012; Cao et al., 2020). This demographic change is inevitably accompanied by an increasing need for medical interventions such as medication prescribing. Accordingly, the prevalence of polypharmacy (i.e., concurrent prescription of five or more medications) has climbed to over 25% among the older population in many healthcare systems (Guthrie et al., 2015a; Midão et al., 2018; Khezrian et al., 2020). This phenomenon is concerning because incremental health benefits tend to decrease with each additional medication, while the risk of adverse effects increases and may even outweigh the expected benefits (Kongkaew et al., 2013; Donaldson et al., 2017; Insani et al., 2021). The risk associated with prescribing varies greatly among different medication classes, with some medications (e.g., vitamins) posing minimal risks and others (e.g., anti-inflammatory drugs) posing substantial risks (Singh and Triadafilopoulos, 1999; McGettigan and Henry, 2011).
Given the potential negative health consequences of excessive prescribing and, in particular, polypharmacy, unwarranted variability in prescribing is of particular concern. Prescribing variability is unwarranted when it depends on physician factors (i.e., recognition of an indication) rather than patient factors (i.e., the presence of an indication) (Wennberg, 2011). Practitioner variability can thus serve as an indicator of issues with indication quality and potential healthcare inequity, which are particularly problematic in publicly funded healthcare systems like the Swiss.
Large primary care databases have been used before for measuring prescription rates and general practitioner (GP) variability in prescribing, but analyses have generally been limited to specific medication classes (e.g., antibiotics or opioids) (Guthrie et al., 2015b; Haastrup et al., 2016; Coyle et al., 2019) or populations (e.g., older patients) (Aubert et al., 2016; Schnegg et al., 2020). Comprehensive assessments across all medication classes and patient demographics are needed to identify the specific medication classes contributing to polypharmacy and to develop targeted initiatives to improve prescribing practices.
Therefore, the aim of the present study was to comprehensively describe medication prescribing in Swiss general practice and, in particular, to present patient age- and sex-specific prescription rates as well as practitioner variability in polypharmacy and the most common medication classes.
Study Design, Setting, and Participants
We performed a retrospective cross-sectional study based on data from the large Swiss primary care database FIRE (FIRE is an acronym for Family Medicine ICPC Research using Electronic Medical Records) (Chmiel et al., 2011). Since the FIRE project started in 2009, over 700 individual GPs have voluntarily contributed anonymized clinical routine data from their electronic medical records to the FIRE database (>10% of all Swiss GPs (mfe Haus- und Kinderärzte Schweiz, 2020)). As of April 2021, the database holds over 11 million consultation records with administrative information, laboratory and vital signs measures as well as medication plans.
For this study, we included GPs of practices exporting medication data labelled with starting and stopping dates since at least the year 2018 and covering the full year 2019 (26.6% of FIRE practices in 2019). From included GPs, we considered all patients aged 18 years or older who had at least one consultation in the year 2019 (total number of considered patients: n = 112 934). We grouped patients of the same sex and age (in years) into sex × age strata and excluded all patients in strata of less than 100 patients (i.e., all patients aged >92 years, n = 1 123). This left 111 811 patients in 150 sex × age strata for analysis.
The local Ethics Committee of the Canton of Zurich waived approval for the present study because the FIRE project is outside the scope of the law on human research (BASEC-Nr. Req-2017–00797).
Database Query and Definitions
We extracted GP- and patient-level data from the database. From GPs, we used sex and year of birth. From patients, we used sex, year of birth, and the list of active medication prescriptions at their last consultation in 2019. We labeled medication prescriptions with the anatomical therapeutic chemical (ATC) classification system (WHOCC, 2020). The ATC classification system organizes active substances in a hierarchy with five different levels, according to the organ or system on which they act and their therapeutic, pharmacological, and chemical properties. We identified ATC codes of all recorded prescriptions, and excluded non-systemic medications, namely: 1) dermatologicals (ATC code D) except antifungals for systemic use (D01B), antipsoriatics for systemic use (D05B), and anti-acne preparations for systemic use (D10B); 2) drugs targeting sensory organs (S), i.e., ophthalmologicals and otologicals; 3) stomatological preparations (A01); 4) antiinflammatory preparations for topical use (M02AA); 5) throat preparations (R02); 6) agents for treatment of hemorrhoids and anal fissures for topical use (C05A); 7) decongestants and other nasal preparations for topical use (R01A); and 8) heparins or heparinoids for topical use (C05BA). Lastly, we excluded vaccines (J02) because of inconsistent data capturing.
For each patient, the medication count was defined as the number of distinct, active ATC codes (considering all five levels of the code), and polypharmacy was defined as a medication count ≥5. For the remaining analyses, prescriptions were aggregated on the second level of the ATC code, which represents therapeutic or pharmacological subgroups. We referred to the aggregated prescriptions as “(medication) classes”. We adopted the names of the classes as defined in the ATC classification system.
We used counts and proportions (n and %) or medians with interquartile ranges (IQRs) to describe the data. Prescription rates and polypharmacy rates per stratum (overall, sex-specific, age-specific, sex × age-specific) were calculated as proportions of patients with a prescription within a specific medication class or with polypharmacy, respectively. Sex × age-specific prescription rates of the different medication classes as well as sex-specific and age-specific rates of polypharmacy were presented graphically.
For statistical modelling, patient age was categorized into the groups 18–40 years, 41–64 years, 65–80 years, and 81–92 years. For each medication class separately, we built a mixed-effects logistic regression model of whether a patient had a matching prescription, with demographic patient variables as fixed effects (age groups and sex, with interaction terms) and random GP effects. An analogous model was built for the presence of polypharmacy. For the regression analyses, only GPs with at least 500 patients in 2019 were considered (n = 100 of total n = 116).
To explore practitioner variability in prescribing, we reported crude distributions of GP-specific prescription rates (again considering only GPs with at least 500 patients). Also, using the 5th and 95th percentiles of the fitted random effects distributions, we quantified the variability unexplained by covariates, both of prescribing the various medication classes and of polypharmacy, using the odds ratios ORlib/cons = exp (q0.95 - q0.05), which are interpreted as the odds ratio (OR) of prescribing the respective medication class or of polypharmacy, respectively, between a rather liberal prescriber (at the 95th percentile of the random effects distribution) and a rather conservative prescriber (at the 5th percentile of the random effects distribution) for a patient of the same sex and age group. We reported results for the 20 medication classes with the highest overall prescription rates in the main text (out of a total of 72 appearing in the database); the appendix expands results to all classes with overall prescription rates >1%. For statistical analysis and visualization we used the R software (R Core Team. R, 2019), Version 4.0.0. Significance was assumed for p-values < 0.005 (Benjamin et al., 2018); 99.5% confidence intervals (CIs) were reported.
Patient and GP Population
We analyzed 111 811 adult patients of 116 different GPs. Patients are described in Table 1, overall and by age group (for description of patients by sex, see Supplementary Table S1). Of GPs, 34.5% were female, the median GP age was 52 years (IQR 43–57), and GPs treated 923 patients (IQR 643–1 218) in median.
Medication Counts and Polypharmacy
Overall, 28.9% of patients were without medication, 47.2% were prescribed one to four medications, and 24.0% had polypharmacy. The median medication count was 2 (IQR 0–4) overall and 3 (IQR 2–6) among patients with at least one medication. Medication counts (Figure 1) and, as a consequence, the likelihood of having polypharmacy (Figure 2), increased with patient age (see Table 1 for crude numbers and Supplementary Table S2 for regression analyses). Male patients exhibited considerably lower rates of polypharmacy than female patients in all age groups except 65–80 years (age 18–40 years: OR = 0.49 [99.5% CI 0.43 to 0.55], age 41–64 years: OR = 0.78 [99.5% CI 0.73 to 0.84], age 81–92 years: OR = 0.82 [99.5% CI 0.72 to 0.94], Supplementary Table S2). The difference remained even after hormonal contraceptives were excluded (Figure 2).
FIGURE 1. Proportion of patients with the specified number of medications, depending on age. Each shaded region represents the overall percentage of patients with the respective number of medications.
FIGURE 2. Age-dependent polypharmacy rates, by sex. The dotted line represents the proportion of female patients with polypharmacy if hormonal contraceptives for systemic use are excluded.
The most often prescribed medication classes were antiinflammatory and antirheumatic products (prescribed for 21.6% of patients), agents acting on the renin-angiotensin system (19.9%), analgesics (18.7%), and drugs for acid related disorders (18.3%; see Supplementary Table S3 for all prescription rates >1%).
For the vast majority of medication classes, prescription rates significantly increased with age (Figure 3; Supplementary Table S2 for regression models). Exceptions were antihistamines, which showed a decrease with age, antianemic preparations, which decreased in female patients at middle ages before increasing again at older ages, and antiinflammatory and antirheumatic products as well as lipid modifying agents, which increased up to a certain age before decreasing.
FIGURE 3. Age-dependent prescription rates of different medication classes, by sex. The 20 most common medication classes (second level of the anatomical therapeutic chemical classification system) are displayed, ordered by decreasing overall prescription rate.
Prescription rates of all medication classes showed significant sex differences at certain ages (Figure 3 and Supplementary Table S2). Men were more often prescribed agents targeting the cardiovascular system (such as antihypertensive agents, antithrombotic agents, and lipid modifying agents), whereas most remaining classes were more often prescribed to women. Consistently significant and unidirectional prescription rate differences across all age groups appeared in antiinflammatory and antirheumatic products (female > male), analgesics (female > male), vitamins (female > male), lipid modifying agents (male > female), psychoanaleptics (female > male), mineral supplements (female > male), drugs for constipation (female > male), urologicals (male > female), and thyroid therapy (female > male). Some medication classes exhibited sex differences only in older ages (drugs for acid related disorders, drugs used in diabetes), while for others, sex differences existed at younger ages and diminished with age (drugs for obstructive airway disease, antianemic preparations, and antihistamines for systemic use).
For polypharmacy, practitioner variability in terms of ORlib/cons was 4.4, meaning that patients of a given sex and age had 4.4 higher odds of having polypharmacy if they were treated by a liberal prescriber compared to a conservative prescriber. Among the medication classes, the highest practitioner variability was observed for vitamins (ORlib/cons = 8.8), followed by antiinflammatory and antirheumatic products (ORlib/cons = 5.6) and mineral supplements (ORlib/cons = 5.0). Lowest variability was observed for antithrombotic agents and thyroid therapy (both ORlib/cons = 2.0), followed by psychoanaleptics and urologicals (both ORlib/cons = 2.2). The crude practitioner variabilities of the medication classes (boxplots) along with the ORlib/cons are shown in Figure 4.
FIGURE 4. Practitioner variability in medication class prescribing (GPs: n = 100). Boxplots of the crude among-GP distributions of prescription rates, and the unexplained variability in terms of ORlib/cons, for the 20 most common medication classes (second level of the anatomical therapeutic chemical classification system) ordered by overall prescription rate. Prescription rates were calculated for each GP as the percentage of their patients who had a prescription within the respective medication class; ORlib/cons represents the OR between a liberal prescriber (95th percentile of the random effects distribution) and a conservative prescriber (5th percentile). Abbreviations: GP, general practitioner; OR, odds ratio.
Comprehensive displays of medication prescribing are scarce. Our study, designed to fill this gap, confirms patient age and sex differences in prescribing of specific medication classes and polypharmacy and reveals considerable practitioner variability in prescribing. In addition to providing epidemiologic insight, our findings uncover medication classes with high prescription rates and practitioner variability, thereby highlighting potential for improvement.
Overall, we found a polypharmacy prevalence of about 24% in the adult Swiss general practice population, increasing with age from 6% in patients aged 18–40 years to 65% in patients aged 81–92 years. Assessments of polypharmacy in younger individuals are scarce. In this context, our polypharmacy prevalence of 20% in patients aged 41–64 years, consistent with findings from Scotland (Guthrie et al., 2015a), raises concerns that polypharmacy may be an important but underappreciated issue in this age group. For older patients, our findings are in line with those of two recent Swiss studies conducted in similar settings but with fewer GPs and patients (polypharmacy prevalence of 37% in a sample aged 75–80 years and of 60% in a sample aged over 75 years, respectively) (Aubert et al., 2016; Schnegg et al., 2020), as well as with general practice prescribing data from Scotland (Guthrie et al., 2015a). Moreover, two Swiss studies with a population-based sampling strategy and presumably less morbid patients than in our general practice-based study found lower polypharmacy rates compared to our results, as would be expected (Castioni et al., 2017; Schneider et al., 2019). With regard to prescription rates of specific medication classes, we found highest rates for pain and inflammation medication, medication for cardiovascular risk management, and medications to regulate gastric acidity. These prescription rates are highly concordant with those found in similar national (Schnegg et al., 2020; Muheim et al., 2021) and international (Guthrie et al., 2015a) studies.
Our study provides relevant insights into the relationship between prescription rates and patient demographics. For age, we found a positive association with prescription rates for most medications, which we expected given the accumulation of chronic diseases with age. However, prescription rates of lipid modifying agents decreased markedly beyond 80 years of age in both sexes. This finding might be the result of many GPs’ willingness to de-prescribe these medications for patients in primary prevention of cardiovascular diseases (Jungo et al., 2021). Similarly, the prescription rates of antiinflammatory and antirheumatic products decreased in the older. It is quite plausible that this is also partly due to de-prescribing, as there is a broad consensus that these drugs are potentially inappropriate for older patients (Holt et al., 2010; Panel et al., 2019). In this context, it is worth noting that we found high rates of analgesics in the oldest age group. One might thus hypothesize that antiinflammatory drugs are replaced by analgesics (mostly paracetamol) in the old, especially considering that pain was the most frequent complaint in a study of old, multimorbid patients in Swiss general practice (Neuner-Jehle et al., 2017). On another note, however, the age-dependent increase in the prescription rates of diuretics also in the very old population is of particular concern, given their association with preventable hospitalizations (Howard et al., 2007).
Regarding sex differences, we found a higher rate of polypharmacy in women, consistent with the literature (Guthrie et al., 2015a; Schnegg et al., 2020). The difference was more pronounced at younger ages, and interestingly, hormonal contraceptives did not relevantly contribute to the difference. The most decisive drivers of the differing rates in the younger population seemed to be higher prescription rates of vitamins, mineral supplements, and antianemic preparations in female patients. Physiological reasons may explain the higher prescription rates of vitamins for women (i.e., folic acid for the prevention of embryonal neural tube defects during reproductive age, or vitamin D to prevent osteoporosis at advanced age). For mineral supplements, the sex difference at older ages may also be partly explained by physiology (i.e., with calcium supplementation for the prevention of osteoporosis), but this explanation does not readily apply to younger patients. For antianemic preparations, prescription rates are higher among women only during reproductive age, which is quite plausibly explained by iron deficiency caused by menstrual blood loss (Benson et al., 2021). Contrary, a higher prescription rate among male patients was observed for cardiovascular medications. While this finding is highly consistent with reports from other studies (Schnegg et al., 2020; Zhao et al., 2020), the higher intrinsic cardiovascular risk of male patients may not be the only explanation, as female patients have been found to receive less intensive cardiovascular care than men even when at similar risk (Rachamin et al., 2020a, 2020b, 2021).
Variability in prescribing can partly be explained by the GPs’ patient populations (case mix). However, it can also hint at (in)appropriateness because some of the variability may be due to medication over- (or under-)use, and the risk of prescribing potentially inappropriate medications is higher among physicians with a more liberal attitude towards prescribing. (Martinez et al., 2021). Hence, several studies have investigated practitioner variability in polypharmacy: A study from Swedish general practice found that the prevalence of polypharmacy varied by a factor of six among all GPs, whereas studies from Germany and the Netherlands found factors of 3.6 and 2.4, respectively (Bjerrum et al., 1999; Grimmsmann and Himmel, 2009; Sinnige et al., 2016). These numbers are, however, sensitive to outliers and therefore of limited informative value. We quelled the influence of outliers by introducing the ORlib/cons, which represents the central 90% of GPs. Our result of an ORlib/cons of 4.4 for polypharmacy is therefore a more conservative measure but still illustrates a large practitioner variability, suggesting that there may be much room for improvements in quality of care and potential cost savings.
Medication classes with both high overall prescription rates as well as high ORlib/cons are arguably of particular relevance and include vitamins, mineral supplements, antiinflammatory and antirheumatic products, antianemic preparations, and antihistamins for systemic use. The highest practitioner variability was found for vitamins which is—to our best knowledge—a novel finding. The high practitioner variability in vitamin prescribing is however in line with the high practitioner variability in vitamin testing observed both in Switzerland and internationally (Schumacher et al., 2020; O'Sullivan et al., 2018). Moreover, inappropriate prescribing of vitamins has been documented before, and in Switzerland specifically, a potential overuse of antianemic preparations has been suspected (Silverstein et al., 2019; Biétry et al., 2017; Meier et al., 2019). Interestingly, vitamins, mineral supplements, and antianemic preparations were also among those medications which were more often prescribed to (especially young) female patients. For antiinflammatory and antirheumatic products, high practitioner variability in prescribing has been acknowledged before, and is most relevant because of the well-known associated risks (Hawkey et al., 1997; Dreischulte et al., 2012). Furthermore, a medication class for which variability and potential overuse have often been investigated, due to their contribution to the emerging threat of multiresistant germs, are antibacterials. A recent Italian primary care-based study which investigated prescribing of a set of six frequently prescribed medications found the largest variability in antibiotics (Russo et al., 2020). In our study, antibiotics had a rather low prevalence (and are therefore not described in the main text), but practitioner variability in prescribing antibacterial medication was considerable (ORlib/cons = 4.9, Supplementary Table S2). In contrast, low practitioner variability was found in thyroid medications, antithrombotics, renin-angiotensin antagonists, beta blockers, and antidiabetic drugs. This consistent prescription behavior by GPs is reassuring especially in antithrombotic medication which convey high bleeding risks and require adherence to evidence-based treatment guidelines (Hutten et al., 1999).
Strengths and Limitations
Strengths of this study lie in the comprehensiveness of medication classes assessed and of the population included, which together provide a large and detailed picture of medication prescribing activity in Swiss general practice. Moreover, we excluded topical medication in order to increase the relevance of our findings regarding polypharmacy. The data presented in this article is valuable for researchers as well as for policy makers and may help to inform assumptions, make comparisons, and set policy priorities. A limitation of this study are the unknown and potentially varying morbidities of the GPs’ patient populations, which made it impossible to more precisely judge the appropriateness of prescribed medications. In addition, due to the cross-sectional design of our study, we could not follow up prescription dynamics and were therefore unable to distinguish between cautious prescribing and secondary de-prescribing. Moreover, since we analyzed patients at their last visits to their GPs in 2019, we measured prescriptions immediately following a medical consultation and our results are therefore bound to an episode of care which may not be fully representative for a full patient year and may have overestimated prescription rates. This limitation would primarily affect drugs prescribed for acute indications, such as analgesics and antiinflammatory and antirheumatic products. Analyzing data from last encounters in 2019 also caused an overrepresentation of the winter season and may have biased prescription rates for medication targeting seasonal illnesses, e.g., antibiotics (Hawes et al., 2018). Lastly, we did not consider prescribed medication doses, which is also a limitation for judging adequacy of prescriptions.
Based on practitioner variability, prevalence and conveyed risks, the targets with the highest potential for subsequent initiatives to improve medication prescribing in Swiss general practice are antiinflammatory medications and polypharmacy in old and very old patients.
Data Availability Statement
The datasets presented in this article are not readily available because of institutional restrictions. Requests to access the datasets should be directed to email@example.com.
Ethical review and approval was not required for the study on human participants in accordance with the local legislation and institutional requirements. Written informed consent for participation was not required for this study in accordance with the national legislation and the institutional requirements.
YR: Conceptualization, Methodology, Formal analysis, Visualization, Writing—original draft, Writing—review and editing. LJ: Methodology, Writing—review and editing. RM: Data curation, Writing—review and editing. TG: Methodology, Writing—review and editing. OS: Resources, Writing—review and editing. JMB: Writing—review and editing. SM: Conceptualization, Writing—original draft, Writing—review and editing, Supervision.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
We thank the FIRE study group of general practitioners for contributing data to the study.
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2022.832994/full#supplementary-material
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Keywords: drug prescriptions, polypharmacy, clinical practice variation, demographic aging, sex differences, primary care, Switzerland
Citation: Rachamin Y, Jäger L, Meier R, Grischott T, Senn O, Burgstaller JM and Markun S (2022) Prescription Rates, Polypharmacy and Prescriber Variability in Swiss General Practice—A Cross-Sectional Database Study. Front. Pharmacol. 13:832994. doi: 10.3389/fphar.2022.832994
Received: 10 December 2021; Accepted: 05 January 2022;
Published: 14 February 2022.
Edited by:Daniela C. Moga, University of Kentucky, United States
Reviewed by:Frank Moriarty, Royal College of Surgeons in Ireland, Ireland
Andrea L. Schaffer, University of New South Wales, Australia
Copyright © 2022 Rachamin, Jäger, Meier, Grischott, Senn, Burgstaller and Markun. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Yael Rachamin, firstname.lastname@example.org