Medication review versus usual care to improve drug therapies in older inpatients not admitted to geriatric wards: a quasi-experimental study (RASP-IGCT)

Inappropriate drug use remains common in older persons and has been associated with a lower quality of life, increased health-care utilization and an increased readmission risk [1]. Causes are many and frequently complex, yet have been shown to be at least partially amenable to change [1‐8].

Multiple comprehensive interventions have already been demonstrated to improve the quality of prescribing and to reduce the number of potentially inappropriate medications (PIMs). Most interventions have been limited to the inpatient setting, which might partially be explained by the provision of increased monitoring during hospital stay and also by higher baseline risk of the hospitalized patient population for adverse (drug) events, resulting in a relatively lower needed sample size for interventional studies [9]. In several trials, such interventions relied on the addition of ward-based hospital pharmacists to the multidisciplinary care team [4]. Hospital pharmacists provided several services, such as medication reconciliation on admission, supporting the implementation and adjustment of clinical decision support systems (CDSS), patient education and medication review [2, 5, 8, 10]. Pharmacist-led interventions affect clinical outcome; a decrease in the number of unplanned drug-related readmissions and emergency department visits has been observed, as concluded in recent meta-analyses [1, 4]. More data are still needed however to corroborate previous findings on the perceived benefit of medication review in older adults and also to further confirm the perceived benefits in specific subgroups [1, 4, 11, 12].

To ascertain the appropriateness of drug therapies in older adults, several screening tools have been made available [13]. We have developed the RASP (Rationalization of Home Medication by an Adjusted STOPP in Older Patients) list, which was subsequently investigated as part of a pharmacist-led medication review in a controlled trial which took place on several acute geriatric wards in a large teaching hospital [2, 13]. This approach was shown to improve the quality of prescribing without increasing harm in a very old, predominantly octogenarian, inpatient population [2]. The intervention was however restricted to patients admitted to dedicated acute geriatric care units, limiting the benefits to a select subgroup of older adults. In many hospitals the majority of octogenarians are admitted to non-geriatric wards rather than to acute geriatric care units.

Previous reports have shown that a comprehensive geriatric assessment (CGA) by the interdisciplinary geriatric consultation team (IGCT) improved care in selected inpatient populations [14‐16]. Considering the manner in which the CGA is offered, it is still not completely elucidated whether to opt for a fully decentralized assessment of geriatric patients, to develop a co-management model or to transfer and admit high risk older patients to dedicated acute geriatric wards [17‐19]. It has furthermore not been established whether IGCT involvement might lead to an improvement in drug use in older patients. Dalleur et al. performed a randomized controlled trial to investigate this subject. The authors concluded that the use of the STOPP criteria by trained geriatricians, as members of the IGCT, led to a doubling of the reduction of PIMs in older inpatients admitted to non-geriatric medical units in a Belgian hospital [20]. The decentral IGCT team composition and provided care have however been shown to be highly heterogeneous and results by Dalleur et al. can hence not be readily extrapolated [20, 21].

As of 2014, Belgian law has provided a fixed budget for a minimum of two full time equivalents (mostly nursing staff), excluding fees for geriatricians, who are to be financed through other means. While improving care in older inpatients is central to the IGCT care model, the specific tasks and composition of IGCTs differ substantially across hospitals [21]. In our hospital, a medication review is not performed systematically by the IGCT. Frequently, the IGCT has rather recommended to perform additional blood tests, to screen for and treat low haematocrit or haemoglobin, to organize transfer to a rehabilitation centre or to organize professional home care [14].

The aim of this pilot study (RASP-IGCT) was to evaluate whether a medication review carried out by non-geriatricians using the RASP list and provided within the context of a CGA might result in an increase of drug-related recommendations in frail older patients, who had been evaluated by the IGCT and who were admitted to non-geriatric wards. Furthermore, this study aimed to evaluate the acceptance of the recommendations, to reduce the number of PIMs and to identify significant determinants for the number of IGCT provided drug-related recommendations.

Both investigators (JH and LD) showed a favourable reproducible approach in the training set of patient cases, respectively scoring a Cohen’s kappa of 0.72 and 0.73.

In total, 60 patients were enrolled consecutively of whom 59 were included in the analysis of the primary outcome measure. One patient was excluded from analysis due to the institution of end-of-life care during hospital stay which precluded any IGCT counselling. Detailed information on patient flow through the study is depicted in Fig. 1.

Patient characteristics did not differ significantly between both cohorts. Average age-adjusted CCI was 7.12 (95% confidence interval (CI): 6.39, 7.84). Patients were drawn from 20 nursing wards, covering a total of 14 medical and surgical disciplines. More information has been provided in Table 1. Most common disciplines were the trauma ward (19/59) and cardiology units (15/59). In total, 24 and 35 patients were admitted to a surgical or medical unit, respectively. Twenty-three patients (23/59) were admitted to the hospital due to a fall as the main reason or as one of multiple reasons for admission. There was no difference seen in the number or type of RASP PIMs at baseline in the usual care vs. intervention patients, except a higher frequency of potentially inadequate inhalation in COPD in the intervention cohort (usual care vs. intervention: 0/29 vs 6/30, p = 0.024). Other prevalent pre-admission RASP PIMs have been summarized in Table 2.

The median number of accepted recommendations differed significantly in favor of the intervention cohort group (usual care vs. intervention: 0.0 (0.0–0.5) vs. 3.0 (0.0–5.3), p < 0.001). The median acceptance rate did not differ between both cohorts (usual care vs. intervention: 45% vs 50%, p = 0.140).

At least one IGCT recommendation was adopted into the discharge letter in more patients in the intervention (24/29) than in the usual care cohort (4/29) (p < 0.001). In the intervention cohort, 47.2% (IQR: 33.2–50.0%) of the drug-related recommendations was based on the RASP list, which was significantly more than in usual care patients (0.0%, IQR: 0.0–0.0%) (p < 0.001). Additionally, other drug-related recommendations, that were not based on RASP list, were observed more frequently in intervention patients (median (IQR): usual care vs. intervention: 0.0 (0.0–0.0) vs. 3.0 (2.0–5.0), P < 0.001).

In the intervention cohort, patients were discharged with fewer drugs compared to admission than in the usual care cohort (proportion of drugs on admission, relative to discharge (%): usual care vs. intervention: 108.5%, IQR: 100.0–135.8% vs. 92%, IQR: 80.5–103.5%; p = 0.002). More RASP PIMs were discontinued in intervention patients during hospital stay, i.e. a mean difference was observed of 1.49 RASP PIMs (95% CI: 0.70, 2.23; p < 0.001). Patients in the intervention cohort received furthermore fewer RASP PIMs at discharge (usual care vs. intervention: 2.50, IQR: 2.0–3.8 vs. 1.0, IQR: 0.0–3.0; p = 0.008).

None of the individual RASP PIMs had been significantly discontinued more frequently in the intervention than in the usual care cohort. Trends towards higher discontinuation rates in favour of the intervention were observed for the following RASP items: prolonged use of benzodiazepines, zolpidem, zopiclone or zaleplon; prolonged use of antidepressants; use of inhalation corticosteroids in the treatment of COPD GOLD I-II; duplicate therapy (e.g. two different beta blockers). The content of the non-RASP based recommendations was very diverse (i.e. low prevalence per type of recommendation); they could largely be reduced to clinically relevant medication discrepancies and drug therapies lacking or with unclear indications. More information on drug use has been provided in Table 3.

The Poisson regression analysis identified two significant determinants for the dependent outcome measure of number of IGCT provided drug-related recommendations: application of the systematic medication review in the intervention cohort coincided with an incidence rate ratio (IRR) of 14.1 (95% CI: 8.3, 23.8, p < 0.001) and the number of preadmission drugs with an IRR of 1.06 (95% CI: 1.03, 1.09). No other significant determinants were observed. Model A is the unadjusted model with intervention vs. usual care as the sole determinant. Model B is the adjusted model which shows a small effect of the number of preadmission drugs. Both models have been depicted in Table 4.

A before-after study was undertaken in a large teaching hospital to increase the number of drug-related recommendations provided by the IGCT. Enrolled patients were older adults who had been admitted to other than acute geriatric wards and in whom a IGCT consultation had been requested. The intervention on top of usual care provided by the IGCT was able to significantly increase the number of drug-related recommendations. In this study, we found a very low number of drug-related recommendations in the before cohort (usual care). This might largely be explained by nurse IGCT members having been the first and predominant contact with the patients. These nurses were not yet accustomed with performing medication reconciliation and review.

The following secondary outcome measures should be considered exploratory. The criteria of the RASP list accounted for 47.2% (IQR: 33.3–55.0%) of the provided recommendations in the intervention cohort, which is in accordance with our previous experiences with the RASP list [2]. A median of 45% of the recommendations was accepted by the ward-based physicians in the intervention cohort, with a significant uptake of the IGCT recommendations into the final discharge letter. The latter was unexpected, given that drug-related recommendations were added to the patient’s file without further oral communication. Ward-based physicians were however found ready to apply the recommendations, which suggests promising results on the applicability of such interventions. We hypothesize that a different approach, with active publicity within the hospital for this type of additional IGCT service, would probably increase the downstream uptake of the drug-related recommendations.

Our results are in line with those found in a previous investigation, in which the intervention had also been based on the use of the RASP list [2]. Both this and the previous study were performed in a geriatric inpatient population and investigated comparable interventions. Several differences should be noted however. First, patients were enrolled from acute geriatric care wards as opposed to non-geriatric care wards. As a consequence, usual care consisted of geriatricians in the previous study, who were already trained in improving drug therapies. Second, patients were on average 2 years older and suffered from worse renal function. Third, the medication review service at the time was done solely by hospital pharmacists and pharmaceutical services were furthermore provided during the complete hospital stay, i.e. from admission to discharge. Nonetheless, both investigations comprised comparable comorbid patients who took nearly identical numbers of preadmission drugs. More importantly, the interventions in both studies led to similar reductions of RASP PIMs at discharge, which further corroborates the applicability of a RASP-based intervention in older inpatients.

Providing a structured medication review, such as the one investigated in this study, can improve the quality of prescribing and might also impact several clinical outcome measures, such as drug-related readmissions [2, 8, 26, 27]. The evidence remains limited however to a small number of positive studies, many of which involved ward-based pharmacists, who were frequently incorporated into multidisciplinary teams [4, 5, 28]. Pharmacist interventions frequently entail providing a medication reconciliation, a medication review, patient education and follow-up after discharge [28]. As team members, pharmacists offer an additional perspective on how to improve drug therapies in older patients and have been identified as suitable candidates to apply medication reviews [5, 28]. A structured medication review, whether or not involving pharmacists, has however not been rigorously been investigated within the context of a CGA [5]. This specific context might offer distinct advantages as opposed to providing an ad hoc medication review. Not only the medical and social, but also functional capabilities are ascertained within the CGA context, supporting individualized drug-related recommendations; frailty, life expectancy, cognitive reserve among others all play a significant role in determining whether certain drug therapies should be initiated, changed or discontinued [29].

To the best of our knowledge, only Dalleur et al. have investigated a comparable IGCT based approach, in which a systematic medication review was also provided as part of the CGA [20]. Enrolled participants had similar profiles, having a comparable age and overall drug use. Their intervention was performed however by geriatricians of the IGCT, who applied a medication review that was based on the STOPP criteria. Hence, both study designs differ regarding the specific screening tool and involvement of the specific health-care professional (trained geriatricians versus clinical pharmacy/medicine students). They concluded that using an explicit screening tool was operational in different settings, including the decentral IGCT setting, and that the intervention resulted in a doubling of PIM reduction, which is comparable to our results.

Following strengths of our study can be noted. Due to the design no teaching contamination could have occurred. With an additional effort, in this case performed by two healthcare professionals-in-training having been provided with limited training themselves, the IGCT care delivery model was able to significantly impact drug prescribing for older inpatients. Time investment of the investigators was limited as well: medication reconciliation and review if applied systematically was not considered to be overly time consuming (i.e. less than 30 min per patient). The external validity is furthermore reassuring as the main intervention was carried by two junior investigators under the supervision of a senior investigator. Also, our trial results are in line with results gathered in previous investigations [2, 20].

Several limitations should however be taken into account. This was an exploratory before-after study (n = 59), which means that our results might have been overestimated or be explained by unmeasured confounders. Hence, results should be interpreted with caution. Yet, temporal trends would likely be of no influence, as the study was completed in a two-month period within one hospital. Also, other determinants for the primary outcome measure were found to be of no or at best minimal impact in a predefined regression analysis. Lastly, no heterogeneity was observed across multiple outcome measures (e.g. more recommendations, less drugs, less RASP PIMs). Another major limitation is that no clinically relevant patient outcomes were evaluated. A larger and in particular controlled study with less stringent enrolment criteria should hence be undertaken to confirm our findings in a broader inpatient sample and to investigate the impact of the intervention on clinical outcome measures such as adverse drug reactions or unplanned drug-related hospital readmissions. We also did not follow-up patients after discharge, which limits our conclusions regarding the long-term impact of our intervention. Furthermore, not every hospital has access to trained pharmacists or geriatricians to oversee the training of involved health-care professionals, which might limit the external validity of our findings. The latter could however be mitigated by providing education through e-learning [30, 31].

Finally, the following issues should be targeted in future investigations. First, trained pharmacists can play an important role in an IGCT approach and have only been involved infrequently in this specific setting as can be inferred from the scarcity in the literature. Second, further studies should investigate whether ward-based nurses could undertake a relevant role in the medication review process by screening for potentially inappropriate therapies or aiding and implementing therapy changes for potentially inappropriate therapies or aiding in implementing therapy changes [32]. Previous investigations in different settings have already shown that trained nurses can have a beneficial impact on drug use, e.g. in the outpatient follow-up of heart failure patients or the management of atrial fibrillation patients, both settings with a high degree of polypharmacy [33, 34]. Third, CDSS might play an important role in expanding medication review services in the hospital setting and decreasing therapeutic inertia (e.g. alerting to the inappropriate use of sotalol in heart failure patients, or the use of flecainide in patients with previous coronary ischemia). We eagerly await the results of two ongoing European trials, OPERAM and SENATOR, both incorporating software packages to manage inappropriate drug use in older hospitalized adults [35]. Fourth, more studies should be performed to further confirm the benefits of complementing CGA with structured medication reviews.

Adding a systematic medication review to a CGA performed by the IGCT may have benefits. A large association was seen in this before-after study between providing a systematic medication review and an increase of drug-related recommendations provided by the IGCT. Regression analysis identified the number of preadmission drugs to be another potential determinant for the number of drug-related recommendations. More RASP PIMs were discontinued during hospital stay in the intervention cohort, which coincided with a relative decrease in the number of drugs. Due to the quasi-experimental design, results should be interpreted with caution.