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. 2015 Aug 13;2(3):249–259. doi: 10.1007/s40801-015-0035-4

Correlation of Incident Potentially Inappropriate Medication Prescriptions and Hospitalization: An Analysis Based on the PRISCUS List

Frank Henschel 1,✉, Marcus Redaelli 1,3, Martin Siegel 2, Stephanie Stock 1
PMCID: PMC4883217  PMID: 27747571

Abstract

Background

Multimorbidity and polypharmacy represent a major problem for elderly patients. Potentially inappropriate medication (PIM) use is highly prevalent among the elderly. PIMs are considered high-risk drugs and are suspected to be responsible for adverse drug events (ADEs) leading to hospitalization.

Objective

The objective of this study was to determine hospitalization rates related to selected ADEs in elderly patients with an incident prescription of a PIM as defined by the PRISCUS list. A second objective was to identify other factors independently associated with hospitalization.

Methods

We retrospectively analysed a full census of pharmaceutical claims, from one of the largest public sickness funds in Germany, for 647,073 patients aged ≥65 years in 2010, the year of publication of the PRISCUS list. Patients who received an incident PIM in 2010 were assigned to the intervention group. Propensity score matching was used to build a control group of patients at a comparable risk level who received an incident equivalent non-PIM. The risk of hospitalization due to PIM prescription was estimated via the odds ratio (OR). Risk factors were analysed via logistic regression models.

Results

The results showed significantly more ADEs in the PIM group. The OR for hospitalization was 1.54 [95 % confidence interval (CI) 1.23–1.93] for patients receiving any PIM compared with those who received a non-PIM. This trend remained stable [OR 1.46 (95 % CI 1.16–1.84)] after adjustment for relevant covariates in the logistic regression models showing ORs for each risk factor. Besides PIMs, common risk factors such as greater age, comorbidity and specific drug classes were significantly responsible for hospitalization.

Conclusion

PIMs (as defined by the PRISCUS list) are associated with high rates of ADEs associated with hospitalization. Our study suggests that PIM reduction may result in a lower risk of hospitalization in the elderly.

Key Points

Prescription of potentially inappropriate medication (PIM) leads to a significant increase in adverse drug events in the elderly.
Elderly patients taking PIMs are at increased risk of PIM-related hospitalization.
Other common risk factors for an increased risk of hospitalization are greater age, comorbidity and use of cardiovascular drugs.
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Introduction

Adverse drug events (ADEs) cause up to 6 % of all hospitalizations in industrialized countries [1–4]. In particular, frail elderly patients are at risk because of age-related physiological impairments, concomitant comorbidities and polypharmacy. Pharmacokinetic and pharmacodynamic alterations in the elderly may enhance sensitivity to specific drugs and make the elderly more vulnerable to ADEs [5].

Evidence-based guidelines mainly address single indications only and often recommend treatment with drug combinations. Therefore, multimorbidity results in multiple drug treatment, which often generates further medication via the so-called prescribing cascade phenomenon, meaning prescription of extra medications aimed at relieving the symptoms of unrecognized ADEs [6]. The lack of clinical trial data on the efficacy and safety of drugs in elderly patients contributes to this development [7, 8]. More than a quarter of hospital admissions in elderly patients that are due to ADEs are judged to have been preventable if more caution had been exercised in drug prescription [4, 9, 10]. One approach to reducing ADEs in the elderly is development of explicit recommendations for drugs to be avoided. The first structured approach is the Beers Criteria, which specify “potentially inappropriate medications” (PIMs) for patients aged ≥65 years. PIMs are defined as drugs whose risks outweigh their clinical benefits, particularly when there is a safer or more effective alternative drug available for the same condition [11].

To take into consideration country-specific characteristics, PIM lists have been developed in several countries (e.g. Canada [12], France [13], Ireland [14] and Sweden [15]). In Germany, the so-called PRISCUS list was published in 2010 [16]. It comprises drugs that should generally be avoided and names alternatives with a better benefit-to-risk ratio in the elderly. The PRISCUS list uses the four most important international PIM lists as a reference [12, 13, 17, 18]. More than 60 % of the drugs in the PRISCUS list can be found in one of these other lists, which include a common core set of medications [19]. Yet prescription of PIMs is still highly prevalent across health care systems [11, 20, 21], with an international median prevalence rate of 20.5 % in primary care [22]. For example, in Germany, one in four elderly patients receives at least one PIM as defined by the PRISCUS list (PRISCUS–PIM) [23, 24].

Although a significant association between prescription of PIMs and health outcomes is expected, clear evidence of causality is missing. Several systematic reviews have come to the conclusion that there is only weak evidence of an association between PIMs and adverse patient outcomes, and they have emphasized that further research is needed [11, 19, 25, 26]. The Cochrane Collaboration assessed the grade for the quality of evidence as being “very low” [27], but to conduct randomized controlled trials (as the clinical gold standard), with randomization of older patients to receive a potentially high-risk drug, would be inappropriate. Therefore, other study designs are necessary.

Many earlier studies had limitations with regard to their data and methods. Important confounders such as comorbidity and temporal relationships between PIM use and outcomes were not taken into account, the samples were small, or the samples did not represent the general population.

This retrospective cohort study investigated hospitalization rates related to PIM prescription in the elderly. Additionally, other factors independently associated with hospitalization in the elderly were analysed.

Methods

Data Source

We analysed a full census of all insured patients aged ≥65 years from one of the largest public sickness funds in Germany [Allgemeine Ortskrankenkasse (AOK) Rheinland-Hamburg], which insures 2.8 million people. It reflects a region of Germany of about 10 million people, including rural and urban areas, of whom approximately 30 % are insured by this statutory health insurance organization. The observation period was the year 2010 to ensure we had the latest data without major changes in prescribing behaviour after the PRISCUS list was published. The data were anonymized. The following characteristics of the insured persons were available for this study: age; sex; time insured; German modification of the International Classification of Diseases 10th edition (ICD-10GM) coded diagnoses for ambulatory care, hospital stay or long-stay nursing care; and ambulatory drug prescription.

Potentially Inappropriate Medications According to the PRISCUS List

Identification of PIM prescriptions was based on the PRISCUS list [16], which includes 18 therapeutic groups and 83 drugs. It specifies drugs to avoid; drugs to avoid, depending on the prescribed dose (nine drugs); and drugs with an arbitrary formulation (two drugs). For these 11 drugs, we used the central pharmaceutical number, which categorizes medications exactly into name, dose and size, to distinguish PIMs and non-PIMs. The daily defined dose was not assessed, since some medications are taken only for a limited period of time and we could not assess whether the patient took the medication, split it or took more than the normal dosage. An incident non-PIM was defined as a drug from the equivalent 18 medication groups (see Fig. 1) defined via Anatomical Therapeutic Chemical Classification System (ATC) coding (e.g. ATC codes N06A = antidepressants and N02 = analgesics). This restriction was done to exclude cases such as use of new toxic oncological drugs in the non-PIM group. Examples of non-PIMs for the indication “cardiovascular diseases” are bisoprolol or amlodipine, whereas acetyldigoxin and doxazosin are cardiovascular drugs included in the PRISCUS list.

Fig. 1.

Fig. 1

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Patient flow: selection of the final study population. a-/typical typical and atypical, PIM potentially inappropriate medication

Study Population

This retrospective cohort study was based on claims data from 647,073 insured patients aged ≥65 years.

Insured patients with PIM prescriptions were identified via the ATC. Those included in the study were all patients with at least one incident PIM prescription during the study year. Incident drug prescription was defined as prescription of a PIM during the study period AND either no PIM prescription or a non-PIM equivalent prescription within 6 months prior to the study period (the second half of 2009). Patients receiving a PIM or a non-PIM equivalent within 6 months preceding the study period or receiving simultaneous PIM and non-PIM prescriptions were excluded from the study. The time frame of 6 months was chosen to ensure that the drug was fully eliminated and to ensure reversal of any effect of tolerance. Matching variables were age, sex, drug classes, comorbidity and hospitalization in the preceding quarter, as well as insulin and phenprocoumon prescription. We included phenprocoumon (the European equivalent of warfarin) and insulin because these drugs and digoxin (a PIM) have been held responsible for many hospitalizations in previous studies [28]. The maximum tolerance for matching was 0.001, based on linear predictions from a logistic regression. Figure 1 describes the selection of the final study population.

Assessment of Hospitalization Risk Associated with PIM Prescribing

To ensure a temporal relationship between hospital admission and PIM prescription, hospitalization within 30 days after the first prescription of a new PIM was the main outcome variable [29, 30]. The 30-day observation period was chosen to ensure a temporal relationship to the dispensing, as drugs often lead to adverse reactions shortly after their first application [29, 30]. We based the length of this time period on a set of prior studies (e.g. Singh et al. [31] and Lau et al. [32]) to ensure that the temporal relationship was maintained in the analyses. Choosing a shorter time period might have led to underestimation of the potential adverse effects, as some long-term effects may occur only after a longer period of time. Likewise, choice of a longer time period would have incurred a risk of overestimation of potential adverse effects, as ADEs usually occur within the first weeks of drug intake [33, 34]. We performed some sensitivity analyses using a 5-day period and a 90-day period. The results changed only marginally when the time lag was altered, suggesting that the method was fairly robust.

Hospital admission was counted as ADE related if the main diagnosis responsible for the admission was potentially related to ADEs, as proposed and validated by Stausberg et al. The diagnoses suggested by Stausberg have shown good results in representing plausible adverse events linked to drugs [35–37]. Under real-life conditions, detection of ADEs in elderly patients suffering from comorbidities and taking several drugs is complicated. Likewise, in our retrospective study, it was not possible to delineate a causal association between the hospitalization and the newly dispensed drug.

Statistical Analysis

Propensity score matching (PSM) was used to build a risk-adjusted control group from administrative data. PSM mimics randomization for observed variables. Propensity scores for matching are obtained through logistic regression analysis weighing covariates for the risk of hospitalization. In addition, the risk of PIM prescription and each covariate (e.g. drug classes responsible for hospital admissions due to ADEs) were estimated using logistic regression (Table 2). Independent variables were age, sex, number of drugs, classes of drugs, comorbidity and hospitalization within 3 months preceding the study period, as well as insulin or phenprocoumon dispensing during the same time. The Charlson comorbidity index (CCI) was used to adjust for comorbid conditions/burden of disease [38]. To verify this ICD-10 diagnoses, both outpatient and inpatient data were used for the CCI. Standard errors were computed using the robust Huber–White sandwich estimator. All analyses were performed using Stata 10.1 software.

Table 2.

Results of the logistic regression model describing the factors for each covariate associated with hospitalization

OR (95 % CI) P value
First PIM 1.46 (1.16–1.84) <0.001
Age group
 65–69 years 1 (reference)
 70–74 years 1.34 (0.90–1.99) 0.145
 75–79 years 1.83 (1.23–2.70) 0.003
 80–84 years 2.15 (1.45–3.20) <0.001
 85–89 years 2.18 (1.38–3.45) <0.001
 90–94 years 2.02 (1.09–3.75) 0.026
 95+ years 2.47 (1.08–5.65) 0.032
Sex
 Female 1.00 (reference)
 Male 0.80 (0.63–1.01) 0.058
Charlson Comorbidity Index score
 0 1.00 (reference)
 1 2.49 (1.73–3.58) <0.001
 2 3.32 (2.26–4.86) <0.001
 3 5.53 (3.74–8.20) <0.001
 4 9.28 (6.48–13.28) <0.001
 5 7.31 (4.53–11.80) <0.001
Medication
 Analgesics 0.87 (0.66–1.16) 0.345
 Antidementia agents 0.31 (0.08–1.29) 0.108
 Antidepressants 1.48 (0.93–2.35) 0.097
 Antiemetics 0.84 (0.25–2.81) 0.771
 Antiepileptics 1.86 (0.93–3.68) 0.077
 Antihistamines 2.47 (1.30–4.71) 0.006
 Antiparkinsonian agents 1.68 (0.52–5.47) 0.387
 Antipsychotics, a-/typical 1.17 (0.65–2.09) 0.6
 Cardiovascular drugs 1.84 (1.40–2.41) <0.001
 Laxatives 1.03 (0.34–3.14) 0.962
 Migraine agents 1.40 (1.75–3.63) 0.362
 Muscle relaxants 1.19 (0.28–5.05) 0.81
 Platelet aggregation inhibitors 0.78 (0.49–1.23) 0.285
 Sedatives, hypnotics 1.66 (0.94–2.92) 0.078
 Systemic antibiotics 1.16 (0.82–1.64) 0.405
 Urological spasmolytics 0.83 (0.26–2.67) 0.753
Preceding medication
 Insulin 0.58 (0.37–0.91) 0.017
 Phenprocoumon 2.95 (1.71–5.09) <0.001
Preceding event
 Hospitalization 1.69 (1.32–2.16) <0.001
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a-/typical typical and atypical, CI confidence interval, OR odds ratio, PIM potentially inappropriate medication

Results

Final Study Population

Our final study cohort comprised 35,696 patients. PSM led to comparable study groups, each with a size of 17,848 patients. Table 1 shows the characteristics of the final study population. These patients received a drug from one of the 18 therapeutic groups for the first time in the observation year, 2010. About half of the study population had no comorbidity as defined by the CCI. Nearly 20 % were hospitalized within 90 days preceding the intake of any new medication, and 10 % had a diagnosis potentially caused by an adverse drug reaction, which resulted in hospitalization. Most incident prescriptions in 2010 belonged to the following therapeutic classes: analgesics (41.66 %), cardiovascular medications (36.14 %), antibiotics (17.44 %), antidepressants (5.73 %), platelet aggregation inhibitors (4.43 %) and sedatives (2.85 %).

Table 1.

Characteristics of the final matched study population with incident PIM use and no PIM use

Characteristic Non-PIM PIM Total
Patients [N (%)] 17,848 (50.00) 17,848 (50.00) 35,696
Sex [N (%)]
 Female 11,030 (50.56) 10,785 (49.44) 21,815
 Male 6818 (49.12) 7063 (50.88) 13,881
Age [N (%)]
 65–69 years 3937 (49.80) 3969 (50.20) 7906
 70–74 years 5050 (49.75) 5100 (50.25) 10,150
 75–79 years 3857 (51.65) 3611 (48.35) 7468
 80–84 years 2752 (48.13 2966 (51.87) 5718
 85–89 years 1503 (51.86) 1395 (48.14) 2898
 90–94 years 531 (48.67) 560 (51.33) 1091
 95+ years 218 (46.88) 247 (53.12) 465
Charlson comorbidity index score [N (%)]
 0 9675 (50.65) 9428 (49.35) 19,103
 1 3580 (50.33) 3533 (49.67) 7113
 2 2051 (49.53) 2090 (50.47) 4141
 3 1113 (48.97) 1160 (51.03) 2273
 4 990 (47.55) 1092 (52.45) 2082
 5+ 439 (44.61) 545 (55.39) 984
Adverse drug event: hospitalization [N (%)] 127 (39.44) 195 (60.56) 322
 OR for hospitalization (95 % CI) Reference 1.54 (1.23–1.93)
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CI confidence interval, OR odds ratio, PIM potentially inappropriate medication

Risk of Hospitalization

The incidence of hospitalization differed significantly between groups, with 127 cases (39.44 %) in the control group and 195 cases (60.56 %) in the intervention group. The odds ratio (OR) for hospitalization was 1.54 [95 % confidence interval (CI) 1.23–1.93] for those receiving PIMs in comparison with those receiving equivalent non-PIMs.

Multivariate regression analyses assessed the influence of different covariates on hospitalization rates. Table 2 shows that the odds were significantly increased with PIM prescription [OR 1.46 (95 % CI 1.16–1.84)]. Other risks for hospitalization were greater age, higher CCI scores (with the exception of a CCI score of 5), preceding events of hospitalization [OR 1.69 (95 % CI 1.32–2.16)] and two drug classes: antihistamines [OR 2.47 (95 % CI 1.30–4.71)] and cardiovascular drugs [OR 1.84 (95 % CI 1.40–2.41)].

The main diagnoses responsible for hospitalization were either directly or indirectly related to the cardiovascular system, such as ‘atrial fibrillation and flutter’, ‘atrioventricular block’, ‘volume depletion’ or ‘hypo-osmolality and hyponatraemia’, which might have resulted in negative effects on the heart (Table 3).

Table 3.

Diagnoses registered at the time of hospitalization

Non-PIM PIM
ICD code Patients (N) ICD code description ICD code Patients (N) ICD code description
A047 3 Enterocolitis due to Clostridium difficile A047 8 Enterocolitis due to Clostridium difficile
D690 1 Allergic purpura E86 19 Volume depletion
E86 9 Volume depletion E870 1 Hyperosmolality and hypernatraemia
E876 1 Hypokalaemia E871 4 Hypo-osmolality and hyponatremia
F115 1 Mental and behavioural disorders due to use of opioids E875 1 Hyperkalaemia
I260 6 Pulmonary embolism with mention of acute cor pulmonale H539 1 Visual disturbance, unspecified
I269 4 Pulmonary embolism without mention of acute cor pulmonale I260 3 Pulmonary embolism with mention of acute cor pulmonale
I441 1 Atrioventricular block, second degree I269 2 Pulmonary embolism without mention of acute cor pulmonale
I442 2 Atrioventricular block, complete 1 Pulmonary embolism without mention of acute cor pulmonale
I470 1 Re-entry ventricular arrhythmia I441 3 Atrioventricular block, second degree
I471 1 Supraventricular tachycardia I442 2 Atrioventricular block, complete
I4810 26 Atrial fibrillation and flutter I447 1 Left bundle-branch block, unspecified
I490 1 Ventricular fibrillation and flutter I471 1 Supraventricular tachycardia
I495 3 Sick sinus syndrome I472 1 Ventricular tachycardia
I499 1 Cardiac arrhythmia, unspecified I4810 61 Atrial fibrillation and flutter
I610 1 Intracerebral haemorrhage in hemisphere, subcortical I495 3 Sick sinus syndrome
I612 1 Intracerebral haemorrhage in hemisphere, unspecified I616 1 Intracerebral haemorrhage, multiple localized
I613 1 Intracerebral haemorrhage in brain stem I800 1 Phlebitis and thrombophlebitis of superficial vessels of lower extremities
I619 1 Intracerebral haemorrhage, unspecified I802 3 Other venous embolism and thrombosis
I801 2 Phlebitis and thrombophlebitis of femoral vein I808 1 Phlebitis and thrombophlebitis of other sites
I802 2 Other venous embolism and thrombosis I951 5 Orthostatic hypotension
I803 1 Phlebitis and thrombophlebitis of lower extremities, unspecified K290 4 Acute haemorrhagic gastritis
I808 1 Phlebitis and thrombophlebitis of other sites K521 1 Toxic gastroenteritis and colitis
I951 2 Orthostatic hypotension K922 4 Gastrointestinal haemorrhage, unspecified
K290 6 Acute haemorrhagic gastritis N178 4 Other acute renal failure
K717 1 Toxic liver disease with fibrosis and cirrhosis of liver N179 7 Acute renal failure, unspecified
K922 5 Gastrointestinal haemorrhage, unspecified N184 3 Chronic kidney disease, stage 4
N178 2 Other acute renal failure N185 3 Chronic kidney disease, stage 5
N179 7 Acute renal failure, unspecified N189 1 Chronic kidney disease, unspecified
N183 1 Chronic kidney disease, stage 1–5 R060 2 Dyspnoea
N185 1 Chronic kidney disease, stage 5 R11 5 Nausea and vomiting
R060 2 Dyspnoea R33 1 Retention of urine
R11 1 Nausea and vomiting R400 1 Somnolence
R21 1 Rash and other nonspecific skin eruption R42 3 Dizziness and giddiness
R33 1 Retention of urine R51 2 Headache
R42 1 Dizziness and giddiness R55 21 Syncope and collapse
R451 1 Restlessness and agitation T460 1 Cardiac-stimulant glycosides and drugs of similar action
R51 1 Headache T783 1 Angioneurotic oedema
R55 9 Syncope and collapse
1 Syncope and collapse
T400 1 Opioid
T424 1 Benzodiazepines
T464 1 Angiotensin-converting-enzyme inhibitors
T783 2 Angioneurotic oedema
Total 119 Total 187
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PIM potentially inappropriate medication

Discussion

In this cohort study, we found a significant positive association between incident PIM prescription and subsequent risk of hospitalization. After mimicking randomization via PSM, patients with a PIM prescription had a 1.54-fold higher risk (95 % CI 1.23–1.93) of being hospitalized within 30 days after the first dispensing of the PIM, in comparison with the control group.

Additional multivariate regression analyses showed that other factors associated with hospitalization were age and CCI score. This finding correlates with PIM prescribing patterns, correlating positively with age, the number of comorbidities and female sex [39–41]. Incident prescriptions of two drug classes—antihistamines and cardiovascular drugs—were associated with hospitalization, whereas those for other drug classes were not statistical significant. This was probably due to the study design and the small number of remaining cases.

Other drugs that made up large proportions of the incident prescriptions, e.g. analgesics, with typical side effects on the gastrological, nephrological and cardiovascular systems, did not show statistically significant associations. However, these medications have been positively correlated with hospital admissions [42]. The reason why we could not display this correlation in our study was probably due to the study design, since classical analgesic-induced ADEs, such as severe gastric ulcers, would tend to occur after our study’s cut-off time of 30 days [43]. This is generally the case, with some ADEs evolving at a later stage being missed. Further research analysing specific drug classes, with larger numbers of cases and designed particularly for particular drug classes and indications, is necessary for clarification [44].

Results in Relation to Other Studies

It is difficult to compare prior studies with our study, as in many of those studies the sample sizes were small and not representative, there was no adjustment for important covariates included in the analyses, or a temporal relationship between drug use and ADEs was not taken into account [11, 19]. Even differences in coding and identification of ADEs need to be considered. Most mainly US studies have measured hospitalizations, either in general in the case of PIM studies, or after coding as ICD Y diagnoses in other studies. These Y codes include ‘drugs, medicaments and biological substances causing adverse effects in therapeutic use’ and suggest a causal relationship to ADE-related hospitalizations.

For example, Lau et al. (OR 1.27) and Dedhiya et al. (OR 1.27) also identified hospitalizations in general and reported findings similar to those in our study, though those studies had some of the previously mentioned methodological issues [32, 45].

Budnitz et al. analysed emergency hospitalizations caused by ADEs [28] identified via ICD Y codes.

The main drugs causing ADEs in these studies were warfarin (17.3 %), insulin (13 %) and digoxin (3.2 %). Conversely, PIMs (as defined by the Beers Criteria of 2003) played only a small role (3.6 %).

It is not surprising that this kind of identification primarily captures cases that are obvious and easy to detect, such as insulin overdosing in cases of hypoglycaemia or a pathological international normalized ratio (INR) in cases of bleeding associated with warfarin. But this kind of measurement tends to underestimate many ADEs that are more ambiguous—for example, anticholinergic side effects (such as those influencing the heart rhythm or causing dizziness), for which it is harder to prove causality, especially in multimorbid patients [46]. But anticholinergic and sedative medications are a major part of PIM lists and are well known to be associated with poorer performance on physical mobility and cognitive tasks [47]. In a systematic review of ambulatory-based studies, for example, ADEs resulted most frequently in central nervous system (CNS) symptoms (25.1 %), followed by gastrointestinal symptoms (22.7 %) and electrolyte/renal symptoms (12.4 %) [2]. Transferred to our study results, diagnoses such as ‘atrial fibrillation and flutter’ may be associated with side effects of a new anticholinergic PIM such as an antidepressant or neuroleptic, and alpha blockers such as doxazosin may be responsible for ‘orthostatic hypotension’.

We wanted to learn from previous studies, and we refined their approaches by building comparable groups via PSM and implementing a temporal relationship to the new PIM drug intake. We detected hospitalizations in general but adapted detection to country-specific conditions by limiting our analysis to particular diagnoses that are potentially related to ADEs, as defined by Stausberg, for a retrospective study design. Our intent was to reduce bias as much as possible [48].

Our results matched those of newer studies using outcome detection in general, which achieved similar results regarding PIM and hospitalization. Using the so-called Screening Tool of Older Persons’ Potentially Inappropriate Prescriptions (STOPP) criteria, developed by Gallagher et al. in Ireland, Hamilton et al. found significantly higher rates of hospitalization in patients receiving PIMs (OR 1.85) and positive effects of PIM lists [14, 49, 50].

A study design similar to ours was used by Price et al. who analysed the health profiles of 383,150 hospitalized subjects, showing that overall PIM exposure was associated with an elevated risk of hospitalization (adjusted OR 1.18) [51]. This trend was confirmed in a recently published prospective study in Italian hospitals [52]. A recent study in Switzerland analysed determinants of PRISCUS-PIMs and revealed that PIM use was significantly associated with hospitalization [39].

Strengths and Limitations of This Study

The strengths of this study were the large and representative sample and the comprehensiveness of the data. Our complex method differed from those used in other studies analysing PIMs and clinical outcomes in various respects. First, to fulfil important aspects of the Naranjo algorithm in the identification of an ADE, we focused on analysing hospitalizations and their temporal relationship to receiving a new medication [53]. Second, we chose an observation time period of 30 days after intake of the new medication, since most ADEs occur soon after the initial prescribing, when the patient is not yet accustomed to the medication [29, 30], as in the case of falls [33, 34, 54]. Also, by implementing a wash-out period and using PSM, we reduced selection bias and potential unintended influences of confounders.

Since previous studies found differing results, depending on whether matching was done or not, our intent was to reduce bias as much as possible [48], although this resulted in a decreased study sample. Our goal was to give precision priority over quantity.

Besides its strengths, our study suffered from some of the common limitations of a retrospective design. Although control for a number of potential confounders was possible by matching, uncontrolled confounding due to missing clinical information and other unknown covariates is likely to have occurred, i.e. our analyses were not suited to studying dose dependency of subsequent ADEs, nor did we have information about the influence of over-the-counter (OTC) drugs on outcomes. Patients taking PIMs have been shown to have a slightly worse health status, which was partly accounted for by PSM and was therefore also reflected in our study population. The aforementioned advantage of analysing new use of PIMs could conversely have been a disadvantage, since some ADEs might develop only after more than 30 days, as discussed previously. Therefore, some ADEs might not have been detected. In addition, choosing to consider only individuals with a PIM-free period prior to the study may have resulted in a somehow healthier population in comparison with the average patient population. However, the CCI scores of our study population were not particularly low and could be judged to be in the average range, in comparison with the populations of other studies. Finally, given the retrospective nature of the study, one cannot conclude certainly if it was the PIM drugs per se that were dangerous for patients or if the PIM prescribing was an indicator of dangerous prescribing. We conclude that the results suggest the presence of a relationship between PIM use and specific ADEs but cannot demonstrate causality.

Value of PIM Lists

PIM lists should not be seen as standalone criteria, nor do they replace individually tailored consideration of risks and benefits for the individual patient. Yet they have to be viewed in contrast to individual medication reviews, which involve a thoroughly active, time-consuming assessment of each medication, after consideration of its indication, effectiveness, dosage and other clinical information to determine its appropriateness [55, 56].

PIM lists are universally available, inexpensive and a time-efficient screening tool, which are an important instrument for medical reviews and can be implemented in computer software to support physicians.

This is of special interest, as the mean physician contact times with patients are only 9.0 min in Germany, 11.8 min in the UK and 20.3 min in the USA [57]. Hence, hints in computer software may be valuable at the time of prescribing to prevent suboptimal drug choices—for example, through prior physician education [40]. Mattison et al. reported a decrease in PIM prescribing after implementation of an effectively computerized provider order entry warning system [58].

Conclusion

Use of PIMs in the elderly is a major public health concern. These explicit (criterion-based) PIM lists should not be seen as standalone criteria, nor do they replace individually tailored consideration of risks and benefits for the individual patient.

Implicit (judgment-based) criteria might perform better concerning clinical outcomes. However, implicit criteria also require considerable time for assessment of each medication, after consideration of its indication, effectiveness, dosage and other clinical information to determine its appropriateness [55, 56]. Instead, PIM lists are universally available, inexpensive and a time-efficient screening tool, which are an important instrument for medical reviews and can be implemented in computer software to support physicians.

Our study suggests that elderly patients taking PRISCUS-PIMs are more likely to suffer from ADEs, leading to an increased risk of hospitalization. This study supports the increasing consensus to avoid new prescribing of PIMs [11, 56, 59].

Acknowledgments

The authors are grateful to the statutory health insurance organization Allgemeine Ortskrankenkasse (AOK) Rheinland-Hamburg for providing this comprehensive data set.

Compliance with Ethical Standards

Funding

This research project was funded by the non-profit foundation Dr Werner Jackstädt-Stiftung, (Wuppertal, Germany) (http://www.jackstaedt-stiftung.de).

Conflict of interest

Prof. Stock and Drs. Siegel, Redaelli and Henschel have no conflict of interest.

Ethical issues

The authors state that for this retrospective and pseudonymized study, no ethical approval was needed.

Contributor Information

Frank Henschel, Email: frank.hen@gmx.de.

Stephanie Stock, Email: stephanie.stock@uk-koeln.de.

References

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