Abstract:Aim The use of multiple medications is rising steadily among older individuals, but little is known about the impact of polypharmacy at a population level, both over time and across countries. Surveillance of polypharmacy is required to overcome these gaps. There currently exists no standard population indicator of polypharmacy. The objective of this survey was to query expert opinion on establishing a gold standard method for polypharmacy surveillance at the population level. Methodology We invited 71 experts… Show more
“…Our ndings provide guidance for the inclusion of other medication-related factors, including use of high risk medicines and inappropriate medication duplication when developing future polypharmacy tools and deprescribing guidelines. These results align with recent literature which has suggested to look beyond simply the number of medicines and incorporate the concept of the quality of prescribing by considering speci c types of medicines and inappropriate medication duplication to assess polypharmacy appropriateness [10,21,[28][29][30][31]. Additionally, these ndings provide guidance for identifying patients who may require a comprehensive review of their medicines such as a home medicines review (HMR) by a pharmacist [32].…”
Section: Discussionsupporting
confidence: 80%
“…Our ndings further con rm this process from the perspective of a large number and range of clinicians. Previous studies of clinical experts in geriatric medicine have found strong consensus regarding considering medicationrelated factors such as the use of high-risk medicines including benzodiazepines and antipsychotics as well as inappropriate duplication of medicines in addition to the medicines count for polypharmacy rationalisation [21,30,33]. Our ndings combined with previous literature provide guidance for pharmacists undertaking home medicines reviews in the community and nursing home settings and clinicians undertaking medication reviews in the hospital setting, to identify medicines commonly associated with harm and exploring the possibility of deprescribing them.…”
Background: Little is known about how clinicians assess polypharmacy in real-world practice. Objectives: To identify which medication-related factors influence clinicians’ ratings of polypharmacy, harm from medicines and deprescribing of medicines when presented with a patient’s list of medications and comorbidities.Setting: A novel website called What Is Polypharmacy Exactly (WIPE) was created with 50 de-identified real-world cases with varying numbers of comorbidities and medicines.Methods: Participants, consisting of physicians and pharmacists were asked to rate each case from zero (lowest) to 10 (highest) on three questions: i) degree of polypharmacy, ii) potential for medication-related harm and iii) potential to deprescribe medicines. Medication-related factors including medicines count, high-risk medicines, inappropriate duplication, drug-drug and drug-disease interactions were assessed. Multiple linear regression was used to determine which medication-related factors influenced median ratings for the three questions. Main outcome measures: The primary outcome measure was the median rating for the degree of polypharmacy for each case. Secondary outcome measures were the median rating for the potential for harm from medicines for each case and median rating for the potential to deprescribe medicines for each case. Results: Ninety-two clinicians were included in the study, comprising of 76.1% pharmacists (n=70) and 23.9% physicians (n=22). The comorbidity count (P=0.001), medicines count (P<0.001), inappropriate medication duplication (P=0.017), high-risk medicines (P=0.049), use of NSAIDs (P=0.032) and antihypertensives (P=0.040) were predictive of the perceived degree of polypharmacy. The comorbidity count (P<0.001), medicines count (P<0.001), inappropriate medication duplication (P=0.016) and high-risk medicines (P=0.036) were predictive of the recognised potential for medication-related harm. The medicines count (P<0.001), inappropriate medication duplication (P=0.017), benzodiazepine use (P=0.003) and antipsychotic use (P=0.039) were predictive of the recognised potential to deprescribe medicines. Conclusion: Whilst polypharmacy has traditionally been defined using the medicines count, our findings suggest that clinicians also consider other factors such as high-risk medicines and inappropriate medicines duplication to identify patients at risk of adverse outcomes. Future polypharmacy assessment tools should additionally include these factors.
“…Our ndings provide guidance for the inclusion of other medication-related factors, including use of high risk medicines and inappropriate medication duplication when developing future polypharmacy tools and deprescribing guidelines. These results align with recent literature which has suggested to look beyond simply the number of medicines and incorporate the concept of the quality of prescribing by considering speci c types of medicines and inappropriate medication duplication to assess polypharmacy appropriateness [10,21,[28][29][30][31]. Additionally, these ndings provide guidance for identifying patients who may require a comprehensive review of their medicines such as a home medicines review (HMR) by a pharmacist [32].…”
Section: Discussionsupporting
confidence: 80%
“…Our ndings further con rm this process from the perspective of a large number and range of clinicians. Previous studies of clinical experts in geriatric medicine have found strong consensus regarding considering medicationrelated factors such as the use of high-risk medicines including benzodiazepines and antipsychotics as well as inappropriate duplication of medicines in addition to the medicines count for polypharmacy rationalisation [21,30,33]. Our ndings combined with previous literature provide guidance for pharmacists undertaking home medicines reviews in the community and nursing home settings and clinicians undertaking medication reviews in the hospital setting, to identify medicines commonly associated with harm and exploring the possibility of deprescribing them.…”
Background: Little is known about how clinicians assess polypharmacy in real-world practice. Objectives: To identify which medication-related factors influence clinicians’ ratings of polypharmacy, harm from medicines and deprescribing of medicines when presented with a patient’s list of medications and comorbidities.Setting: A novel website called What Is Polypharmacy Exactly (WIPE) was created with 50 de-identified real-world cases with varying numbers of comorbidities and medicines.Methods: Participants, consisting of physicians and pharmacists were asked to rate each case from zero (lowest) to 10 (highest) on three questions: i) degree of polypharmacy, ii) potential for medication-related harm and iii) potential to deprescribe medicines. Medication-related factors including medicines count, high-risk medicines, inappropriate duplication, drug-drug and drug-disease interactions were assessed. Multiple linear regression was used to determine which medication-related factors influenced median ratings for the three questions. Main outcome measures: The primary outcome measure was the median rating for the degree of polypharmacy for each case. Secondary outcome measures were the median rating for the potential for harm from medicines for each case and median rating for the potential to deprescribe medicines for each case. Results: Ninety-two clinicians were included in the study, comprising of 76.1% pharmacists (n=70) and 23.9% physicians (n=22). The comorbidity count (P=0.001), medicines count (P<0.001), inappropriate medication duplication (P=0.017), high-risk medicines (P=0.049), use of NSAIDs (P=0.032) and antihypertensives (P=0.040) were predictive of the perceived degree of polypharmacy. The comorbidity count (P<0.001), medicines count (P<0.001), inappropriate medication duplication (P=0.016) and high-risk medicines (P=0.036) were predictive of the recognised potential for medication-related harm. The medicines count (P<0.001), inappropriate medication duplication (P=0.017), benzodiazepine use (P=0.003) and antipsychotic use (P=0.039) were predictive of the recognised potential to deprescribe medicines. Conclusion: Whilst polypharmacy has traditionally been defined using the medicines count, our findings suggest that clinicians also consider other factors such as high-risk medicines and inappropriate medicines duplication to identify patients at risk of adverse outcomes. Future polypharmacy assessment tools should additionally include these factors.
“…However, polypharmacy is challenging to address. There is a lack of clarity concerning what is the appropriate treatment of multi-morbidity, and what is overprescription with potentially harmful outcomes [17]. Clinicians often lack direction in this area, as guidelines generally focus on one or a cluster of disorders rather than polypharmacy specifically [49].…”
Section: Discussionmentioning
confidence: 99%
“…This entails documenting changes in the prevalence of dispensation, as well as clinical prescription patterns—including the source of prescription, treatment duration, and use of other central nervous system (CNS) drugs. CNS polypharmacy is of particular importance, as the safety and efficacy of combining psychotropic drug classes are not well established [17], with adverse effects including cumulative toxicity and drug interactions [18]. A US population-based study found that psychotropic polypharmacy of two drugs was associated with a 17% higher average number of side effects, while polypharmacy with three or more drugs was associated with a 38% higher average number, compared with monopharmacy [19].…”
This study examines trends in antidepressant drug dispensations among young people aged 0–24 years in Sweden during the period 2006–2013, as well as prescription patterns and central nervous system (CNS) polypharmacy with antidepressants. Using linkage of Swedish national registers, we identified all Swedish residents aged 0–24 years that collected at least one antidepressant prescription (here defined as antidepressant users) between 1 January 2006 and 31 December 2013 (
n
= 174,237), and categorized them as children (0–11 years), adolescents (12–17 years), and young adults (18–24 years). Prevalence of antidepressant dispensation rose from 1.4 to 2.1% between 2006 and 2013, with the greatest relative increase in adolescents [by 97.8% in males (from 0.6 to 1.3%) and by 86.3% in females (from 1.1 to 2.1%)]. Most individuals across age categories were prescribed selective serotonin reuptake inhibitors, received their prescriptions from psychiatric specialist care, and had treatment periods of over 12 months. Prevalence of CNS polypharmacy (dispensation of other CNS drug classes in addition to antidepressants) increased across age categories, with an overall increase in prevalence from 52.4% in 2006 to 62.1% in 2013. Children experienced the largest increase in polypharmacy of three or more psychotropic drug classes (4.4–10.1%). Anxiolytics, hypnotics, and sedatives comprised the most common additional CNS drug class among persons who were prescribed antidepressants. These findings show that the dispensation of antidepressants among the young is prevalent and growing in Sweden. The substantial degree of CNS polypharmacy in young patients receiving antidepressants requires careful monitoring and further research into potential benefits and harms.
Electronic supplementary material
The online version of this article (10.1007/s00787-018-01269-2) contains supplementary material, which is available to authorized users.
“…As both adult ADHD and the aforementioned comorbid disorders feature a chronic, long-lasting course, it may result in long treatment periods with simultaneous use of multiple medications. Although use of multiple medications has been associated with increased risks of adverse drug events, including nonadherence, cumulative toxicity, and drug–drug interactions ( Sarkar, 2017 ; Sirois et al, 2016 ), very little is known about comedication and polypharmacy patterns associated with ADHD medication. Moreover, there is limited information on how to address comedication in treatment guidelines for ADHD ( National Institute for Health and Care Excellence [NICE], 2018 ; Swedish National Board of Health and Welfare [Swedish: Socialstyrelsen], 2014 ; Wolraich et al, 2019 ).…”
Objective: Evidence regarding comedication among individuals with ADHD is lacking, especially in adults. This study investigated comedication and polypharmacy with ADHD medications in adults. Method: We identified adults dispensed with ADHD medications during 2013 in Sweden and matched them to controls. Logistic regression was used to calculate odds ratios (ORs) of receiving other medications. Results: Individuals receiving ADHD medications had higher risk of receiving any major classes of somatic medications (ORs ranged from 4.1, 95% confidence interval [CI] = [4.0, 4.3], to 7.4, 95% CI = [6.5, 8.5] across age groups). They were more likely to receive respiratory system, alimentary tract and metabolic system, and cardiovascular system medications. In addition, they had higher risk of receiving any other psychotropic medications. The proportion of polypharmacy with five or more medication classes increased from 10.1% to 60.4% from 18 to 64 years. Conclusion: Comedication was more common in adults receiving ADHD medications. Potential benefits and harms of comedication and polypharmacy require further research. (J. of Att. Dis. XXXX; XX[ X] XX-XX)
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.