The authors have declared that no competing interests exist.
Conceived and designed the experiments: DO SE AAH. Analyzed the data: DO SE AAH. Wrote the paper: DO. Carried out literature search: DO SE. Revised and improved manuscript: DO SE AAH SV SDV JCK.
Inappropriate medication prescription is a common cause of preventable adverse drug events among elderly persons in the primary care setting.
The aim of this systematic review is to quantify the extent of inappropriate prescription to elderly persons in the primary care setting.
We systematically searched Ovid-Medline and Ovid-EMBASE from 1950 and 1980 respectively to March 2012. Two independent reviewers screened and selected primary studies published in English that measured (in)appropriate medication prescription among elderly persons (>65 years) in the primary care setting. We extracted data sources, instruments for assessing medication prescription appropriateness, and the rate of inappropriate medication prescriptions. We grouped the reported individual medications according to the Anatomical Therapeutic and Chemical (ATC) classification and compared the median rate of inappropriate medication prescription and its range within each therapeutic class.
We included 19 studies, 14 of which used the Beers criteria as the instrument for assessing appropriateness of prescriptions. The median rate of inappropriate medication prescriptions (IMP) was 20.5% [IQR 18.1 to 25.6%.]. Medications with largest median rate of inappropriate medication prescriptions were propoxyphene 4.52(0.10–23.30)%, doxazosin 3.96 (0.32 15.70)%, diphenhydramine 3.30(0.02–4.40)% and amitriptiline 3.20 (0.05–20.5)% in a decreasing order of IMP rate. Available studies described unequal sets of medications and different measurement tools to estimate the overall prevalence of inappropriate prescription.
Approximately one in five prescriptions to elderly persons in primary care is inappropropriate despite the attention that has been directed to quality of prescription. Diphenhydramine and amitriptiline are the most common inappropriately prescribed medications with high risk adverse events while propoxyphene and doxazoxin are the most commonly prescribed medications with low risk adverse events. These medications are good candidates for being targeted for improvement e.g. by computerized clinical decision support.
The elderly population is increasing, resulting in a concomitant increase in chronic diseases and functional impairment
Adverse drug events are common in ambulatory care settings
Aparasu
The aim of this systematic review was to identify and summarize published studies on IMP in elderly in primary care in order to quantify its extent in elderly persons, and to identify medications for which interventions may be implemented to improve medication prescription quality.
We searched for relevant English articles using MeSH terms and keywords in title and abstract in the Ovid EMBASE (1980–8th March 2012), Ovid-Medline and Ovid Medline In-Process (1950 to 8th March 2012). The final literature search was performed on 8th March 2012.
The search included terms related to elderly or geriatric persons, medications, prescription, appropriate prescription, primary care, ambulatory care, general practice, office practice or outpatient care as shown in
Two reviewers independently screened the titles and abstracts of the retrieved articles. Inclusion was limited to studies that defined the elderly as persons of 65 years and older who received prescriptions in the primary care setting.
In this review, we only included papers that explicitly defined the setting of prescription as outpatient clinics, office practice, general practice and primary health care clinics. Studies that included institutionalized patients and community dwelling elderly without indicating the specific setting in which the prescriptions were prescribed were excluded. In addition, studies which did not report the clinical setting of the study were also excluded (see
Our analysis was limited to studies that reported IMP using drug-age criteria, which belong to the
To be included, studies must have also reported the rate of IMP for individual medications. This requirement allows for comparability of IMP rates of individual medication across different studies. Studies that reported rate of IMP after aggregating prescription by pharmacological classes, for example cardiovascular drugs, were excluded since it was impossible to find out which individual medications were included.
Discrepancies between the two reviewers were resolved by consensus involving a third reviewer.
The two reviewers extracted data from the selected articles on the following items: country; source of data used and instrument of assessing the appropriateness of medication prescription. Additional data extracted included the number of patients involved in each study and data on the rate of IMP. In the studies where more than one instrument was used to measure the rate of IMP, the rate estimated by the latest Beers criteria was used to compare studies. When repeated measurements were reported, we used the most recent rate of IMP. We calculated weighted rates of IMP for individual medications in studies that reported rates of IMP in males and females separately.
Discrepancies between these two reviewers were again resolved by consensus involving the third reviewer.
We calculated the median and ranges of the overall rates of IMP for all medications reported in a study. We compared the overall rates of IMP per country and source of data. For each study that assessed IMP with more than one instrument, we compared the incidences of IMP among them.
Subsequently, we grouped all individual medications reported in the studies into their Anatomical Therapeutic and Chemical (ATC) class. The ATC is a World Health Organisation (WHO) hierarchical standard for classifying medications based on the anatomical organ or system on which they act, the therapeutic group and chemical composition of the active ingredient
For each medication in a therapeutic class, we calculated the median and range its IMP rate among all studies reporting on it. Additionally, each medication was labelled as high risk (H) or low risk (L) for adverse events to allow analysis at the level of a medication’s adverse event risk profile. This risk categorization was derived from the Beers criteria that distinguish between IMP with potentially low and high severity of adverse outcomes
Out of 946 articles screened 19 met the inclusion criteria for detailed analysis.
No | Author | Year | Country | Data Source | No. Patients | Criteria | Overall IMP rate |
1 | Goltz |
2012 | Germany | Insurance data | 12513584 | Beers 2003 | 2.90 |
2 | Ghadimi |
2011 | Iran | Insurance data | 2041 | Beers 2003 | 30.0 |
3 | Zaveri |
2010 | India | Prospective data | 407 | Beers 2003 | 23.6 |
4 | Maio |
2010 | Italy | Others | 91741 | Modified Beers 2003 | 25.8 |
5 | Ryan |
2009 | Ireland | Practice data | 1329 | Beers 2003 | 18.3 |
6 | Lai |
2009 | Taiwan | Insurance data | 2133864 | Beers 2003 | 19.1 |
7 | Lin |
2008 | Taiwan | Insurance data | 5741 | Beers 2003 | 23.7 |
8 | Wilde |
2007 | UK | National health data | 162000 | Beers 2003 | 32.2 |
9 | Bierman |
2007 | USA | National health data | 965756 | Zhan | 15.6 |
10 | Maio |
2006 | USA | Prospective data | 100 | Beers 2003 | 25.0 |
11 | De Oliveira |
2006 | Portugal | Prospective data | 213 | Beers 2003 | 38.5 |
12 | Maio |
2006 | Italy | Insurance data | 849425 | Beers 2003 | 18.0 |
13 | Pugh |
2006 | USA | National health data | 1096361 | HEDIS HRME | 19.6 |
14 | Van der Hooft |
2005 | Holland | National health data | 25258 | Beers 2003 | 20.0 |
15 | Pugh |
2005 | USA | National health data | 1265434 | Others | 33.0 |
16 | Curtis |
2004 | USA | Insurance data | 765423 | Beers 1997 | 21.0 |
17 | Aparasu |
1999 | USA | National health data | NA | Beers 1997 | 4.45 |
18 | Straand |
1999 | Norway | Prospective data | 16874 | MRPS List | 13.5 |
19 | Aparasu |
1997 | USA | National Health data | NA | Beers 1991 | 5.04 |
Eight different tools were used to assess the IMP rates. Beers based criteria were used in 15 of 19 studies: one study used Beers 1991, 2 studies used its 1997 version (Beers 1997), 11 used its 2003 version, (Beers 2003) and one study used modifications of Beers 2003. Other instruments used for assessing medication prescription included: Zhan’s criteria (1 studies)
Four studies used more than one instrument for assessing the appropriateness of medication use. Two studies
Six of the 18 studies (33.3%) used health insurance data, while 4 (22.2%) used prospectively collected data. Six studies (33.3%) used national health surveys and databases, and one study (5.6%) used general practice data. One study did not explicitly report the data sources used.
The overall median rate of IMP among the elderly was 20.0% with an absolute range of 2.9 to 38.5% and interquartile range of 16.8 to 25.4%. In the seven studies from the United States of America, the median was 19.6% with a range from 4.5 to 33.3%. In the European Union the median rate of inappropriate prescription was 19.1% with a range of 2.9 to 38.5%.
Results for grouping prescriptions by the type of prescription quality assessment instrument were: for Beers 1997 the median IMP rate was 12.7% (range: 4.5 to 21.0%); for Beers 2003 the median was 23.6% (range: 2.9 to 38.5%); and for Zhan’s criteria, the only study reported a rate of IMP of 15.6%.
IMP rates markedly varied across and within individual therapeutic medication classes as shown in
Beers 1991 | Beers 1997 | Beers 2003 | HD | MB | MR | OT | ZN | |||||||||||||||
MEDICATIONS | N | Aparasu |
Curtis |
Aparasu |
Goltz |
Ghadimi |
Zaveri |
Ryan |
Lai |
Lin |
Wilde |
Maio |
De Oliveira |
Maio |
Van der Hooft |
Pugh |
Maio |
Straand |
Pugh |
Bier-man |
Med | Range (LL- UL) |
|
||||||||||||||||||||||
Indomethacin |
|
7.0 | 6.5 | 3.86 | 0.40 | 6.2 | 6.5 | 0.2 | 0.55 | 0.9 | 3.9 | 0.5 | 1 | 0.2 | 1.4 | 2.04 | 1.40 | 0.20–7.00 | ||||
Ketorolac |
|
2.2 | 0 | 20.5 | 0.2 | 0.5 | 2.3 | 1.35 | 0.00–20.5 | |||||||||||||
Meperidine |
|
0.01 | 0.1 | 0.04 | 0.1 | 0.1 | 0.09 | 0.10 | 0.01–0.10 | |||||||||||||
Naproxen |
|
0.45 | 0.1 | 0.63 | 13 | 0.9 | 0.63 | 0.10–13.0 | ||||||||||||||
Pentazocine |
|
0.96 | 0.44 | 0.01 | 0.01 | 0.1 | 0 | 0 | 0.04 | 0.1 | 0.02 | 0.03 | 0.00–0.96 | |||||||||
Piroxicam |
|
0.12 | 2.3 | 1.21 | 0.12–2.30 | |||||||||||||||||
Propoxyphene |
|
23.3 | 23.3 | 0.57 | 9.37 | 0.1 | 4.52 | 0.3 | 4.1 | 4.81 | 4.52 | 0.10–23.3 | ||||||||||
|
||||||||||||||||||||||
Amiodarone |
|
0.08 | 0.1 | 0.05 | 0.67 | 1.9 | 10.9 | 1.2 | 4 | 6.1 | 12.6 | 0.7 | 1.20 | 0.05–12.6 | ||||||||
Digoxin |
|
3 | 0.01 | 2.8 | 21.1 | 3.4 | 3.10 | 0.01–21.1 | ||||||||||||||
Disopyramide |
|
0.01 | 0.05 | 0.4 | 0.1 | 0.1 | 0.05 | 0.08 | 0.01–0.40 | |||||||||||||
|
||||||||||||||||||||||
Belladona alkaloids |
|
0.03 | 0.05 | 0 | 0.5 | 0.3 | 0 | 0.1 | 0.02 | 0.04 | 0.00–0.50 | |||||||||||
Chlorpheniramine |
|
0.7 | 1.09 | 0.07 | 0.7 | 1.21 | 0.1 | 2.11 | 1.8 | 2.26 | 1.09 | 0.07–2.26 | ||||||||||
Clidinium |
|
3.1 | 3.10 | 3.01–3.10 | ||||||||||||||||||
Cyproheptadine |
|
0.01 | 0.4 | 0.02 | 0.1 | 0.3 | 0.2 | 0.31 | 0.20 | 0.01–0.40 | ||||||||||||
Dicyclomine |
|
4.2 | 0.5 | 0.74 | 13 | 0.51 | 0.4 | 0.49 | 0.51 | 0.40–13.0 | ||||||||||||
Diphenhydramine |
|
0.03 | 4.4 | 0.5 | 0.02 | 3.52 | 3.3 | 3.8 | 3.30 | 0.02–4.40 | ||||||||||||
Hydroxyzine |
|
6.9 | 0.08 | 2.0 | 0.07 | 0.51 | 4 | 0.9 | 0.3 | 3.2 | 2.7 | 3.43 | 2.00 | 0.07–6.90 | ||||||||
Hyoscamine |
|
0.1 | 0.1 | 0.15 | 0.10 | 0.10–0.15 | ||||||||||||||||
Oxybutinin |
|
6.8 | 0.09 | 1.2 | 0.52 | 0.6 | 0.96 | 8.0 | 0.7 | 1.6 | 2.39 | 0.96 | 0.09–6.80 | |||||||||
Propantheline |
|
0 | 0.1 | 0.05 | 0.05 | 0.00–0.10 | ||||||||||||||||
Promethazine |
|
0.24 | 0.8 | 0.9 | 0.71 | 0.2 | 0.71 | 0.71 | 0.20–0.90 | |||||||||||||
|
||||||||||||||||||||||
Dipyridamole |
|
18.6 | 12.56 | 0.7 | 0.1 | 36.1 | 0.24 | 1.4 | 0.6 | 0 | 0.58 | 0.65 | 0.00–36.1 | |||||||||
Ticlopidine |
|
0.03 | 2.6 | 1.2 | 8 | 18.3 | 0.4 | 0.51 | 0.86 | 0.03–18.3 | ||||||||||||
|
||||||||||||||||||||||
Amitriptiline |
|
20.5 | 16.3 | 10.46 | 0.25 | 1.0 | 0.05 | 1.12 | 1.7 | 3.8 | 4.5 | 1.4 | 6.7 | 2 | 6.2 | 0.7 | 2.6 | 3.98 | 2.60 | 0.05–16.3 | ||
Doxepin |
|
3.1 | 0.8 | 0.3 | 0.12 | 0.1 | 0.6 | 0.84 | 0.60 | 0.10–3.10 | ||||||||||||
Fluoxetine |
|
1.6 | 1.5 | 1.8 | 1.49 | 17 | 2.3 | 0.4 | 1.60 | 0.40–17.0 | ||||||||||||
|
||||||||||||||||||||||
Clonidine |
|
0.06 | 0.05 | 0.07 | 0.15 | 8 | 9.5 | 0.1 | 0.9 | 0.12 | 0.05–9.5 | |||||||||||
Doxazosin |
|
0.32 | 6.47 | 15.7 | 3.91 | 4 | 23 | 0.5 | 3.96 | 0.32–15.7 | ||||||||||||
Guanethidine |
|
0.1 | 0 | 0.05 | 0.00–0.10 | |||||||||||||||||
Methyldopa |
|
0.07 | 1.4 | 0.07 | 0.2 | 0.2 | 0.5 | 0.1 | 0.6 | 1.23 | 0.1 | 0.1 | 0.20 | 0.07–1.40 | ||||||||
Nifedipine |
|
0.19 | 0.7 | 0.15 | 12.9 | 6 | 0.22 | 1.9 | 0.1 | 0.1 | 0.20 | 0.10–12.90 | ||||||||||
Reserpine |
|
0 | 0.1 | 0.06 | 0.06 | 0.00–0.10 | ||||||||||||||||
|
||||||||||||||||||||||
Carisoprodol |
|
0.50 | 3.6 | 1.49 | 0 | 0.2 | 0.1 | 0.16 | 0.20 | 0.00–3.60 | ||||||||||||
Chlorzoxazone |
|
6.1 | 0.1 | 0.2 | 0.20 | 0.10–6.10 | ||||||||||||||||
Cyclobenzaprine |
|
2.7 | 9.7 | 1.95 | 1.91 | 1.2 | 2 | 1.95 | 1.20–9.70 | |||||||||||||
Metaxalone |
|
0 | 0.1 | 0 | 0.05 | 0.00–0.10 | ||||||||||||||||
Methocarbamol |
|
1.0 | 0.42 | 0.01 | 4.0 | 0.7 | 2.21 | 1.6 | 2.41 | 1.30 | 0.01–4.00 | |||||||||||
Orphenadrine |
|
1.8 | 0.99 | 0.01 | 3.1 | 0.05 | 1.6 | 0.1 | 0 | 0.7 | 0.70 | 0.00–3.10 | ||||||||||
|
||||||||||||||||||||||
Alprazolam |
|
0 | 0.1 | 0.05 | 0.00–0.10 | |||||||||||||||||
Chlorazepate |
|
0.01 | 0.02 | 3.8 | 0.4 | 0.21 | 0.01–3.80 | |||||||||||||||
Chlordiazepoxide |
|
6.0 | 2.4 | 8.7 | 0.07 | 3.0 | 0.3 | 1.6 | 0.24 | 0.9 | 0.2 | 0.4 | 0.4 | 0.44 | 0.44 | 0.07–8.70 | ||||||
Diazepam |
|
11.6 | 10.6 | 30.05 | 0.43 | 1.6 | 0.05 | 2.7 | 21.3 | 2 | 2.74 | 13 | 11.7 | 2.8 | 1.5 | 1.2 | 1.57 | 2.74 | 0.05–30.0 | |||
Flurazepam |
|
2.7 | 1.26 | 0.01 | 0.1 | 0.7 | 0.05 | 0.5 | 0.1 | 0.1 | 0.06 | 0.10 | 0.01–2.70 | |||||||||
lorazepam |
|
0.1 | 0.82 | 0.2 | 0.1 | 0.15 | 0.10–0.82 | |||||||||||||||
Meprobamate |
|
3.5 | 0.93 | 0.1 | 0.1 | 0.1 | 0 | 0.1 | 0.01 | 0.10 | 0.00–3.50 | |||||||||||
Oxazepam |
|
0 | 0.1 | 0.05 | 0.00–0.10 | |||||||||||||||||
Temazepam |
|
0.6 | 0.74 | 4 | 1 | 0.74 | 0.60–4.00 | |||||||||||||||
Triazolam |
|
0.22 | 0 | 0.1 | 0.10 | 0.00–0.22 |
N: Number of studies.
HD: Health Plan Employer Data and Information Set (HEDIS) criteria.
MB: Modified beers 2003.
MR: More & Romsdal Prescription Study (MRPS) list.
OT: Other unspecified criteria.
ZN: Zhan’s Criteria.
ATC: World Health Organisation’s Anatomic Therapeutic and Chemical Classification.
Med: Median.
LL: Lower limit.
UL: Upper limit.
The four most commonly inappropriately prescribed medications were, in a decreasing order of IMP rate, were propoxyphene 4.52(0.10–23.30)%, doxazosin 3.96 (0.32–15.70)%, diphenhydramine 3.30(0.02–4.40)% and amitriptiline 3.20 (0.05–20.5)%.
Within the class of analgesic/NSAIDS, propoxyphene, which is a low risk analgesic medication, had the highest IMP median of 4.52% with range of 0.10 to 23.30%, while meperidine and pentozacine, which are high risk medications, had the lowest median of 0.1% and 0.03% (with range of 0.01 to 0.10% and of 0.00 to 0.44%, respectively).
Dysopyramide had the lowest median rate of IMP 0.08(0.01–0.4)% among the antiarrhythmic medications while the digoxin was the most inappropropriately prescribed antiarrhythmic medication 3.10(0.01–21.1)%. Disopyramide is classified as a high risk medication while digoxin in a low risk medication.
Diphenhydramine was the most inappropriately prescribed anticholinergic medication 3.30(0.02 4.40)% while belladonna alkaloids were the least inappropriate prescribed anticholinergic 0.04(0.0–0.50)%. Both diphenhydramine and belladonna alkaloids are high risk anticholinergic medications.
IMP was reported for two anticlotting medication as follows dipyridamole 0.65(0.00–36.1)% and ticlopidine 0.86 (0.03–18.3)%. Dipyridamole is a low risk medication while toclopidine is a high risk anticlotting agent.
Doxepin was the least inappropriately 0.6(0.10–3.1) % prescribed antidepressant medication while amitryptiline 3.2(0.05–20.5)% was the most inappropriately prescribed. Both antidepressants are high risk medications.
The median rate of IMP among the antihypertensive medication was lowest with guanethidine, 0.05 (0.00–0.1)%. Doxazosin 3.96 (0.32–15.7) % was reported to be the most inappropriately prescribed antihypertensive medication. Guanethidine is a high risk antihypertensive medication while doxazosin is a low risk medication.
Among the muscle relaxants, metaxalone 0.05(0.00–0.1)% had the lowest IMP rates while cyclobenzaprine 1.95 (1.20–9.7)% had the highest. Both muscle relaxants are high risk medications.
Diazepam 2.74 (0.05 30.05)% had the highest rates of IMP while alprazolam 0.05 (0.00–0.10)% and oxazepam 0.05 (0.00–0.10)% had the lowest rate of IMP among the sedative hypnotic medications. All sedative hypnotics investigated are considered to be high-risk medications.
In spite of increasing attention to the quality of medication prescription among elderly persons presenting to the primary care setting, there are still high overall rates of inappropriate medication prescription in primary care. This review found that one in five (20.0%) prescriptions to elderly persons is inappropropriate with marked variation of rates of IMP within individual therapeutic classes.
The overall prevalence of inappropriate prescription showed wide variations between 2.9 and 38.5%. Several factors may contribute to this variation. Different countries use different sets of medications due to registration issues. There is hence no universal list of medications and criteria for assessing the overall medication use by older patients. Even within the United States inappropriate medication use markedly differed, suggesting that there some systematic differences between practices may exist. The differences in the quality of prescribing across geographical regions have recently been highlighted
Consistent with our review, the review of Aparasu
Unlike the three reviews described above, our study compared the rate of IMP within therapeutic classes of medication. The patterns of inappropriate prescriptions vary considerably within therapeutic classes. Some medications with high risk for adverse events such as diazepam and nifedipine have high prevalence of inappropriate prescription compared to other medications in their respective therapeutic classes. Prescription of high-risk medication exposes the elderly to frequent and severe adverse drug events. Alternative low risk medications should be prescribed when available. There is therefore a need to move towards interventions that can improve the quality of medication prescriptions among the elderly in primary care such as employing clinical decision support systems (CDSS). These systems can provide alerts during prescription based on medication prescription guidelines such as the Beers criteria. Good alert design which focuses on the relevant information to the physician can improve the effectiveness of these systems
This review included various list based criteria for the measurement of IMP which are comparable to each other given that they report individual medications. Modifications that were made in the various versions of the Beers criteria involved inclusion and exclusion of individual medications on the list of medications inappropriate for elderly patients. It was therefore possible for us to compare the rates of IMP for individual medications between studies even if they used different versions of the Beers criteria. However, the overall rate of IMP was not comparable between studies that used different versions of the Beers criteria or other instruments to measure the rates of IMP.
We regard classification of medications as unconditionally appropriate for elderly patients over 65 years as suggested by the Beers criteria to be an over simplification of real clinical practice. Some medications such digoxin or doxazocin may still be used safely in patients who are older than 65 depending on their clinical conditions. Improvements in the definition of inappropriate medication prescription have been made based on drug-disease combination in the elderly.
Twelve studies (12 of 19) relied on secondary analysis of existing database sources such as National Health Service databases, general practice and insurance databases, which were developed for other purposes. Although previous studies have shown that insurance databases do not necessarily have high quality clinical notes documentation, they do generally have high quality of medication documentation due to their use for reimbursement purposes
A strength of our study is the analysis of medication prescription appropriateness within therapeutic classes based on an international standard. This classification mitigates the difficulty in comparing inappropriate medication prescription measures originating from studies with different sets of medication that is influenced by the availability of medications and local prescription practices. This analysis is useful to policy makers and clinicians when making choices between medications from the same therapeutic class. We also compared IMP in studies which utilised multiple instruments to measure quality of prescription.
We used extensive search criteria to capture the different ways inappropriate prescription and elderly are referred to in the published literature. Nevertheless our study maybe limited by publication bias of studies on inappropriate medication prescription. In addition, some of the excluded articles may be relevant but due to uncertainty about or lack of reporting about the setting of the prescription, they have been excluded.
Furthermore, our study was limited by the heterogeneity of the included studies. The number of patients included in the studies varied widely, which makes it difficult to estimate the overall prevalence of IMP. Heterogeneity in reporting of the rates of IMP limited our ability to completely compare rates of IMP for individual medication in all studies. Some studies reported fewer drugs than others. We believe that unavailability of some medications in some countries may have resulted in the differences in the sets of medications which were reported.
Although our study was limited to quantifying the extent of IMP among elderly patients, it would be important to understand the factors that predispose these patients to IMP. In addition, understanding the relationship between IMP and the incidence of adverse events to the patients will provide better guidance to the prescribing physician. Demonstration of the relationship between IMP and adverse events require the validation of the tools used to define IMP in the first place.
Future studies that investigate therapeutic intents and choices of medication among physicians may help further understanding of their prescribing behaviour. This may particularly aid in understanding how choices can be presented to physicians in primary care. Such studies can result in improvement strategies by computerized decision support.
Despite intensified efforts to scrutinize and improve the quality of medication prescription among elderly persons in the primary care setting, inappropriate medication prescriptions are still common. Approximately one in five prescriptions to elderly persons is inappropropriate. Diphenhydramine and amitriptiline are the most common inappropriately prescribed medications with high risk adverse events. These medications are good candidates for being targeted for improvement e.g. by computerized clinical decision support. Focused and systematic interventions are needed to improve the quality of medication prescription in this patient group.
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