Treatment of Stable Angina with a New Fixed-Dose Combination of Ivabradine and Metoprolol: Effectiveness and Tolerability in Routine Clinical Practice.

INTRODUCTION: In this prospective, multicenter, observational cohort study, the effectiveness and tolerability of the first fixed-dose combination (FDC) formulation of the selective heart rate reducing agent ivabradine and the beta-blocker metoprolol was evaluated in stable angina pectoris (AP) patients in a clinical practice setting.
METHODS: Stable AP outpatients received a FDC of ivabradine and metoprolol (b.i.d.) for 4 months, in addition to cardiovascular standard therapy. Resting heart rate (HR), number of angina attacks, short-acting nitrate consumption, severity of symptoms (assessed by patient judgment and documented by CCS score) and tolerability were documented. Medication adherence was assessed by a modified four-item Morisky questionnaire. Descriptive statistics were performed on all data.
RESULTS: A total of 747 stable AP patients (mean age, 66.4 years, 62% male, 50% and 31% with previous PCI and myocardial infarction, respectively) were included. Apart from ivabradine and beta-blockers as free combination, most frequently used concomitant standard medications at baseline were aspirin (68%), statins (71%), ACEI/AT1-blockers (76%), diuretics (35%), and calcium antagonists (15%). Highly prevalent comorbidities were hypertension (86%), hyperlipidemia (65%), and diabetes (35%). After 4 months, switch to treatment with the FDC was associated with a significant reduction in mean HR by 10 bpm. Proportion of patients with ≥ 1 angina attacks/week decreased from 38 to 7%. Patients in CCS class 1 increased (25 to 63%), while they decreased in CCS class 3 (19 to 5%). Medication adherence was also significantly improved (p < 0.001 for all changes from baseline). Mostly mild adverse events were documented in 5.4% of patients.
CONCLUSIONS: In these stable AP patients in a real-life setting, treatment with a FDC of ivabradine and metoprolol was associated with reduced HR and angina symptoms, while exercise capacity (CCS score) was improved. These effects may be mainly mediated by the increased medication adherence of patients observed with use of the FDC formulation. FUNDING: Servier TRIAL REGISTRATION NUMBER: ISRCTN51906157.

Introduction

Elevated heart rate can disturb the myocardial oxygen balance by simultaneously increasing myocardial oxygen demand and limiting myocardial perfusion due to the shortening of diastolic perfusion time. Both mechanisms can either induce or worsen myocardial ischemia and thereby trigger angina symptoms and reduce exercise capacity [1]. As a consequence, there is a strong emphasis in guidelines on sufficient heart rate reduction as an important strategy to prevent oxygen imbalance and improve angina symptoms in stable AP patients [2, 3]. To control heart rate and reduce symptoms, beta-blockers are mostly recommended as a first-line strategy. However, in clinical practice, their use can be limited due to their broad mode of action and resulting side effects [4, 5]. Moreover, registry data have shown many patients to remain symptomatic under beta-blocker therapy [6, 7], indicating the need for combining heart rate reducing agents. In contrast to beta-blockers, ivabradine, an inhibitor of the funny channel pacemaker current (I f), selectively targets heart rate without reducing myocardial contractility or relaxation [8-10]. In recent studies the mechanisms of anti-ischemic and anti-anginal efficacy of ivabradine were further elucidated. In patients with chronic stable coronary artery disease (CAD), ivabradine was associated with an increase of myocardial diastolic perfusion time, an enhanced coronary flow reserve, improved endothelial function, and enhanced coronary collateral flow [11-15].

The anti-ischemic and anti-anginal efficacy of ivabradine had been proven in randomized clinical trials [16-20], supporting its guideline recommended use for symptomatic treatment in patients with stable AP either alone, if beta-blockers are contraindicated, or in combination with them if symptoms persist despite beta-blocker therapy. Combining a beta-blocker with ivabradine has been shown to further reduce the heart rate, resulting in less myocardial ischemia and angina symptoms along with a higher exercise capacity in a clinical trial [20]. Similar results were observed in three large observational studies with stable AP patients in daily routine practice [21-23]. In particular, a post hoc analysis of the ADDITIONS (prActical Daily efficacy anD safety of ivabradine In combinaTION with beta-blockerS) study as well as a pooled analysis of these three observational cohorts have proven beneficial effects for adding ivabradine to an existing therapy with the most commonly prescribed beta-blocker metoprolol in real-life populations of stable CAD patients [24, 25].

Although only scarce data are available on medication adherence for symptomatic therapies in stable CAD patients, studies on secondary prevention after a first cardiovascular event requiring a percutaneous coronary intervention (PCI) suggest a rapid decline in adherence to newly prescribed medications such as, for example, beta-blockers [26]. This phenomenon can be observed especially in patients with co-morbidities and complex therapy regimen [27]. To reduce the tablet burden and thereby increasing medication adherence in AP patients, a fixed-dose combination (FDC) of metoprolol and ivabradine was developed. However, data is still lacking on use of a FDC of these two drugs. The current study therefore aimed to evaluate the effectiveness and tolerability of the first FDC formulation of metoprolol and ivabradine in routine clinical practice, and to detect effects on medication adherence.

Methods

Stable AP patients fulfilling official criteria for treatment with the new ivabradine/metoprolol FDC (Implicor™ 5/25, 5/50, 7.5/25, 7.5/50) according to the approved EU indication were eligible for inclusion in this non-interventional observational cohort study by cardiologists, general practitioners and internists in an outpatient setting. Three visits were planned, consisting of baseline examination (visit 1), a control visit after 4 weeks (visit 2), and the final examination after 4 months (visit 3). All data was systematically documented using a standardized case report form (CRF).

All procedures followed were in accordance with the ethical standards of the responsible committee on human experimentation (institutional and national) and with the Helsinki Declaration of 1964, as revised in 2013. Informed consent was obtained from all patients for being included in the study. Ethical approval was granted by the independent ethics commission in Freiburg/Germany (FEKI). This trial is registered at controlled-trials.com with registration number ISRCTN51906157. Demographic data and general/disease-specific medical history, information about concomitant diseases, other relevant medical therapies and reasons for initiation of FDC treatment were recorded at baseline visit. According to the approved label, the starting dose of the FDC should be equivalent to the dosing of the individual components (ivabradine and metoprolol) before switch. If necessary to achieve symptom control, the dose could be adjusted during the study to a maximal dose of 7.5 mg ivabradine and 50 mg metoprolol twice daily. Dose reduction was possible in case of pronounced heart rate reduction < 50 beats per minute (bpm) or occurrence of bradycardic symptoms during treatment.

Patient status was clinically documented at each visit by recording HR, number of weekly angina symptoms, use of short-acting nitrates, and CCS class. Other parameters assessed at baseline and/or during the course of the study included history of myocardial infarction (MI), revascularization therapies like percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG), blood pressure profile, conduction disorders, use of pacemaker devices, NYHA class, left ventricular dysfunction (LVD). At visit 3, relevant changes in concomitant medications were analyzed. For assessment of the overall response rate to FDC treatment, response was defined as achieving a HR < 70 bpm and/or an absolute HR reduction of ≥ 10 bpm at study end (visit 3). Furthermore, an evaluation of the overall effectiveness and tolerability of therapy was made using a physician’s assessment scale with categories “very good”, “good”, “moderate”, and “poor”. Patient impression and satisfaction with the switch to a FDC treatment was documented by use of three open questions at visit 3.

An important objective of this study was to evaluate possible effects of a switch to FDC therapy on medication adherence of patients (by reduction of pill burden). For this purpose, a modified four-item Morisky questionnaire [28] was used to assess medication adherence at baseline compared to study end (visit 3) after 4 months of treatment. Proportion of patients with “complete adherence”, which was defined as the absence of any adherence-related problems reported in the questionnaire, was analyzed for both time points.

A number of additional subgroups were specified according to gender, age (CCS class (I–IV), patients with or without PCI, LVD, and pre-treatment with ivabradine and/or metoprolol at baseline. All adverse events (AE) and adverse drug reactions (ADR) occurring during the study period had to be documented and assessed by the treating physicians on a standardized AE/ADR reporting form at each patient visit after baseline examination. Coding of all AE/ADR data was performed in accordance with the Medical Dictionary for Regulatory Activities (MedDRA) version 19.1.

Due to the observational design of the study, statistical analysis of the results was performed by a descriptive approach. Data are presented as mean values ± standard deviations (SD) for continuous variables and numbers of patients and/or percentages for categorical variables. Analysis of effectiveness data was performed with data imputation according to the last value carried forward method (LVCF). Wilcoxon’s signed-rank test, Fisher’s exact test and Chi-square test were applied as appropriate for assessment of changes between baseline and follow-up visits. Corresponding p values should be interpreted in a descriptive-exploratory way. The p values reported are two-tailed and an alpha level of 0.05 was used to assess statistical significance. No correction of alpha level for multiple testing was performed. All study data were evaluated by an independent statistical institute (ANFOMED GmbH, Möhrendorf, Germany). All statistical analyses have been performed by means of the SAS software system (version 9.4 for Microsoft Windows 10; SAS Institute Inc., Cary, NC, USA).

Results

Baseline Characteristics

A total of 747 patients with chronic stable AP (intention to treat population) were enrolled in this non-interventional study in 260 centers in Germany. Data of 741 patients (99.2%) were available for all three visits. The mean study duration was 3.9 months (range, 0.10–7.9 months). The mean age of the cohort was 66.4 ± 10.8 years (24.7% ≥ 75 years), 62.4% of the patients were male. On average, patients suffered from CAD for 70.0 months and from AP for 59.4 months. 31.3% of the study cohort had a history of myocardial infarction (MI), 50.3 and 10.2% underwent PCI or CABG, respectively. 32.8% of the study cohort had left ventricular dysfunction (LVD), mean LV ejection fraction (LVEF) was 44.6 ± 11.5%. Valvular heart defects were present in 20.1%, and conduction disturbances in 22.7% of patients. Nearly all participants presented with cardiovascular risk factors or concomitant diseases (Table 1), most commonly with hypertension (86.4%), hyperlipidemia (65.2%), obesity (42.0%), type 2 diabetes (34.9%), nicotine abuse (30.9%), COPD (15.1%), depression (13.8%), and renal impairment (8.8%).

Table 1

Baseline characteristics of study population

Characteristics	(N = 747)
Demographic characteristics
Age (years)	66 ± 10.8
≥ 75 years	184 (25%)
Sex (male)	455 (62%)
Body mass index (kg/m2)	28.6 ± 4.8
Medical history
Previous myocardial infarction	233 (31%)
Previous PCI	376 (50%)
Previous CABG	76 (10%)
Hypertension	645 (86%)
Hyperlipidemia	487 (65%)
Obesity	314 (42%)
Diabetes mellitus	261 (35%)
Chronic obstructive pulmonary disease/asthma	144 (19%)
Renal impairment	66 (9%)
Clinical findings
Heart rate (bpm)	76.8 ± 11.8
Number of angina attacks per week	1.0 ± 2.5
Use of short-acting nitrates per week	1.3 ± 3.0
Systolic blood pressure (mmHg)	137.6 ± 15.1
Diastolic blood pressure (mmHg)	81.8 ± 10.1
Canadian Cardiovascular Society
Class I	170 (25%)
Class II	371 (55%)
Class III	128 (19%)
Class IV	3 (< 1%)
Medication
Beta-blockers	706 (95%)
Metoprolol	664 (94%)
Ivabradine	665 (89%)
Calcium channel blockers	115 (15%)
Long acting nitrates	47 (6%)
Molsidomine	46 (6%)
Ranolazine	31 (4%)
Angiotensin-converting enzyme inhibitors	386 (52%)
Angiotensin II receptor antagonists	184 (25%)
Statins	529 (71%)
Aspirin	504 (68%)
Diuretics	258 (35%)

Values are means ± standard deviations or numbers and corresponding percentages

bpm beats per minute, PCI percutaneous coronary intervention, CABG coronary artery bypass graft

Apart from ivabradine (mean daily dose 9.9 mg) and beta-blockers (metoprolol in 94.1% with a mean daily dose of 93.6 mg) as free combination, concomitant cardiovascular standard medication included statins (70.8%), aspirin (67.5%), ACE-inhibitors/AT1-blockers (76.3%), diuretics (34.5%), oral anticoagulants (10.7%), calcium antagonists (15.4%), aldosterone antagonists (8.7%), and long-acting nitrates (6.3%).

The main reasons of physicians for prescribing the FDC of metoprolol and ivabradine were to improve adherence by reducing tablet burden (89.2%), and save therapy costs (42.0%). Most frequently used metoprolol/ivabradine FDC dosage forms at the start of therapy were 50/5 mg b.i.d. (47.5%), and 25/5 mg b.i.d. (35.5%), followed by 50/7.5 mg b.i.d. (9.5%), and 25/7.5 mg b.i.d. (6.5%). At study entry and last visit, mean daily dose of metoprolol in the FDC was 78.4 and 81.6 mg, respectively, for ivabradine it was 10.8 mg at baseline and 11.1 mg at the end of the study.

Effectiveness

At study entry, mean HR was 76.8 ± 11.8 bpm in all patients, with HR ≥ 70 bpm in 69.3% (n = 518). After 4 months of treatment, transition to FDC significantly reduced mean HR by 9.6 bpm to 67.2 ± 8.2 bpm (Fig. 1) in the total study cohort (p < 0.0001 from baseline); 78.8% (n = 577) of all patients with available HR measurements at study end (n = 732) were classified as responders at the end of follow-up, defined as HR reduction to < 70 bpm and/or absolute reduction by ≥ 10 bpm from baseline to last visit. Total response rate (74.9%) was very similar in magnitude for the main patient group with initial HR ≥ 70 bpm.

Fig. 1

Mean resting heart rate during FDC treatment over 4 months. x, mean; –, median; [], interquartile range; -, minimum and maximum. FDC fixed-dose combination; *p < 0.0001

At admission, the average number of angina attacks per week (reported 7 days prior to each visit) was 1.0 ± 2.5. After 4 months of therapy, the FDC of metoprolol/ivabradine led to a significant decrease of the average number of angina attacks per week to 0.2 ± 0.9 (p < 0.0001 from baseline). Proportion of patients with ≥ 1 angina attacks per week in the last 7 days prior to visit decreased from initially 37.8 to 6.5% after 4 months of FDC therapy (Table 2). In those 278 patients, the mean number of angina attacks was reduced from 2.7 at baseline to 0.4 after 4 months (p < 0.0001 from baseline), and 86.0% of them were free from limiting angina symptoms at last visit.

Table 2

Angina symptoms and short-acting nitrate use

	Baseline		4 months
	n	%	n	%
≥ 1 angina attack(s) per week (n = 736)	278	37.8	48	6.5*
≥ 1 short-acting nitrate use(s) per week (n = 717)	202	28.2	43	6.0*

Values represent patient numbers (n) and corresponding percentages (%) at baseline and study end

* p < 0.0001 versus baseline

The average baseline consumption of short-acting nitrates per week (reported 7 days prior to each visit) was 1.3 ± 3.0 units. After 4 months of therapy with the FDC, average consumption of short-acting nitrates per week dropped significantly to 0.2 ± 1.3 units (p < 0.0001 from baseline). Percentage of patients in need of ≥ 1 short-acting nitrate units per week fell from 28.2% at study entry to 6.0% after 4 months (Table 2). In those 202 patients, the mean number of nitrate uptake was reduced from 4.4 units at baseline to 0.7 units after 4 months (p < 0.0001 from baseline), and in 81.7% of them there was no further need for the use of short-acting nitrates at last visit.

At study entry, 25.3% of patients were classified as CCS grade I, 55.2% as CCS grade II, 19.1% as CCS grade III, and 0.5% as CCS grade IV. A pronounced improvement in CCS grade distribution towards lower classes was observed. At the end of follow-up, percentage of patients classified as CCS grade I increased to 63.0%, while the proportion of patients in CCS class III declined to 5.4% (p < 0.0001 for all class changes from baseline; Fig. 2). Moreover, in the subgroup of patients with CHF or LVD at study entry, an improvement of NYHA class distribution and LVEF classification was demonstrated (data not shown).

Fig. 2

Distribution of patients according to CCS class at baseline and study end. CCS Canadian Cardiovascular Society; *p < 0.0001

All described effects concerning reduction of HR, number of weekly angina attacks, use of short-acting nitrates and improvement of CCS grade distribution were comparable and consistent for a number of predefined subgroups (e.g., according to gender, age CCS grading, switch of treatment or previous PCI). The effectiveness of therapy with the metoprolol/ivabradine FDC was mostly judged as “very good” (70.6%) or “good” (26.9%) by the treating physicians.

Adherence

After 4 months of therapy with the new metoprolol/ivabradine FDC, a “complete adherence” (defined as the absence of any adherence-related problems reported in the modified four-item Morisky questionnaire), was achieved in 58.2% of study population (Fig. 3), marking a pronounced increase compared to 33.8% of patients with this classification at study entry (p < 0.0001 from baseline). In particular, at the end of follow-up, 70.6% of the participants noted, that they “never” forget to take their current medication, 88.8% declared, that they never consciously decide not to take their current medication, 84.2% stated, that they never refrain from taking their current medication because of feeling good, and, finally, 71.5% declared to never have difficulties remembering when to take their current medication. With regards to all four items of the questionnaire, the remaining patients in their majority stated to be “sometimes” non-adherent, while only ≤ 1% stated to be non-adherent either “often” or “very often”, respectively.

Fig. 3

Patients with “complete adherence” at baseline and study end. *p < 0.0001

Additionally, 94.4% of patients stated that the FDC preparation is a simplification or relief in treatment of their heart disease in daily life, 88.9% noted that they are more satisfied with their treatment than before the switch to the FDC, and 82.4% declared that the FDC treatment improved their everyday quality of life (e.g., improved physical capacity). In line with those results, 75.2% of patients judged the tolerability of FDC therapy as “very good”, and a further 23.6% as “good”. Again, no marked differences in terms of medication adherence could be identified between the investigated subgroups.

Safety

Mostly mild AE occurred in 5.4% of all patients. ADR (considered related to treatment) have been reported for 2.5% of patients. No unexpected safety signals have been detected. As the most common AE dizziness, increased blood pressure, headache, and dyspnea (all < 1%) were reported, while, e.g., bradycardia and hypotension (each 0.3%) were just rarely seen. Serious AE were observed in four cases, but none of them was judged to be related to therapy. All safety aspects in the study were comparable and consistent for the above-mentioned subgroups.

Discussion

In this cohort of stable AP patients already receiving an intense anti-anginal pre-treatment at study entry, switching from free combination of a beta-blocker and ivabradine to the metoprolol/ivabradine FDC formulation was associated with a relevant further reduction of heart rate, frequency of angina attacks and nitrate use, accompanied by an improvement of exercise capacity as indicated by a pronounced shift of the participants to lower CCS classes. The above-mentioned effects were consistently seen in all pre-defined subgroups, irrespective of e.g., gender, age (CCS grading, status of (pre-)treatment with ivabradine and metoprolol or history of previous PCI. Moreover, the metoprolol/ivabradine FDC was generally well tolerated by patients. Within 4 months of follow-up, a considerable improvement in self-reported medication adherence was demonstrated. Positive effects on HR, angina symptoms and exercise tolerance (assessed by patient judgment/CCS score) are likely to be associated with the simplification of anti-anginal therapy leading to a better medication adherence in heavily pre-treated stable CAD patients with several cardiovascular and non-cardiovascular co-morbidities. The symptomatic benefits have been achieved on the basis of an already-effective concomitant anti-anginal baseline medication, indicated by the relatively low level of angina symptoms and nitrate use at study start.

In general, the beneficial effects of the metoprolol/ivabradine FDC complement those seen in the clinical ASSOCIATE (evaluation of the Antianginal efficacy and Safety of the aSsociation Of the funny Current Inhibitor ivAbradine with a beTa-blockEr) trial evaluating the free addition of ivabradine to an existing beta-blocker therapy in still symptomatic stable AP patients. After 4 months of co-therapy with ivabradine, a significant decline of HR, reduction of myocardial ischemia, and improvement of exercise capacity was demonstrated [20], supporting recent guideline recommendations for the use of such a combination in patients with uncontrolled HR (≥ 70 bpm) and angina symptoms despite beta-blocker therapy in maximally tolerated dosage [2, 3]. Moreover, a pilot study had shown that adding ivabradine to medium-dose beta-blockers more effectively increased exercise capacity than up-titration of beta-blockers in patients with stable AP [29, 30]. Given the known difficulties to up-titrate beta-blockers to higher doses in a real-life setting [4-7], setting a lower bar for combining them with ivabradine appears to be a viable alternative allowing lower doses of beta-blockers with less limiting side-effects.

In our study, the baseline characteristics of the population were comparable to those of three other prospective, observational cohort studies successfully testing the concept of (free) combination of beta-blockers with ivabradine in real-life populations, e.g., the ADDITIONS [21], REDUCTION (Reduction of ischemic Events by reDUCtion of heart rate In treatment Of stable aNgina with ivabradine) [22], and RESPONSIfVE (Evaluation of effectiveness and therapeutic response to ivabradine in daily practical use for chronic stable angina patients) study [23], with the exception of a slightly lower HR and angina frequency at study entry, which can be mainly explained by the high percentage of patients not only being pre-treated with beta-blocker but as well with ivabradine in the current study. A subgroup analysis of the ADDITIONS trial and post hoc analysis of the above-mentioned three non-interventional studies had consistently revealed a pronounced further reduction of HR, weekly angina attacks and nitrate consumption, respectively, as well as an improvement of exercise capacity and health-related quality of life (QoL) after 4 months of therapy with the free combination of metoprolol and ivabradine [24, 25]. At last follow-up, the results obtained with the new metoprolol/ivabradine FDC in terms of heart rate (67 bpm), frequency of angina attacks per week (0.3), weekly short-acting nitrate use (0.2 unit) and CCS class distribution were nearly identical to those with the free combination of both drugs in, e.g., the aforementioned ADDITIONS subgroup analysis [24]. Interestingly, in our study population the mean ivabradine dosage at study entry (10.8 mg) and after 4 months (11.1 mg) was roughly comparable with that used in the ADDITIONS metoprolol subgroup (9.6 and 12.6 mg, respectively), while the mean metoprolol dosage of 78.4 and 81.6 mg, respectively, was considerably lower than in the ADDITIONS cohort (102.5 and 108 mg, respectively). This finding suggests that the lower mean dosage of metoprolol used in the context of a FDC strategy in our study population may have been sufficient to achieve a similar effectiveness.

The beneficial effects of the metoprolol/ivabradine FDC that were demonstrated after 4 months of therapy in stable AP patients mostly pre-treated with the free combination of beta-blocker and ivabradine may be mainly attributed to the observed increase in “complete adherence” to their medication from initially 34 to 58% at the end of follow-up as reported in a modified four-item Morisky questionnaire. Simplification of complex therapy regimens is a well-established concept, e.g., in cardiovascular secondary prevention or hypertension. A large meta-analysis revealed the use of FDC to significantly reduce the risk of non-adherence when compared with free combination regimens, with a decrease in relative risk of approximately 25% [31]. Patients taking only one drug were also more likely to adhere to treatment than those on multidrug regimens, and treatment was as well more likely to be effective [32]. Another study similarly demonstrated that, after a year of taking a fixed combination of treatments, adherence was significantly higher when compared with patients taking medication separately [33]. For the metoprolol/ivabradine FDC, given twice daily, and in co-morbid CAD patients with already high tablet burden, positive effects on medication adherence can be expected to be even more pronounced. In extension to the above mentioned data our study reinforces the view that even relatively small reductions in pill burden of already heavily treated patients may generate considerable effects on adherence to therapy. In the long term, an improved adherence accompanied by an increased effectiveness could result in decreased medical costs [34].

For every single item of the modified Morisky questionnaire, absence of any self-reported adherence issues was noted for at least 70% of patients at study end. Almost 90% of patients claimed to never consciously decide not to take their medication, indicating a high satisfaction with their current therapy. Additionally, this finding is not only in line with the effectiveness of the FDC, but as well with its tolerability rated as very good/good for 98% of patients. It further confirms the physician’s reporting of safety information of the FDC with only few patients experiencing AE/ADR such as phosphenes or symptomatic bradycardia. A favorable safety profile of the free combination of ivabradine and metoprolol was already observed in the aforementioned observational studies’ subgroups [24, 25]. Additionally, the medium-dose of metoprolol (maximally 2 × 50 mg/day) used in the FDC may as well have contributed to the low rate of side-effects. Although not directly addressed in our study, patient answers on satisfaction with FDC therapy and its influence on their therapy management, reduction of symptoms and everyday quality of life indicate further positive effects on health-related QoL.

Limitations

One limitation of this study was its relatively short duration of 4 months. Although the follow-up period seems to be fully sufficient for assessment of effectiveness and tolerability of the FDC [21-23], data on evaluation of medication adherence in such a setting are not available. As well, assessment of medication adherence was performed indirectly by analyzing a modified, four-item Morisky patient questionnaire. Possible effects on health-related QoL were not evaluated with validated measurement scales. To a minor degree, in patients taking only one of the two drugs at study entry, additional effects of switching to the FDC cannot be ruled out, although subgroup analyses did not reveal any relevant influence of baseline medication on the overall results. Additionally, this was an open-label study without a placebo or free metoprolol/ivabradine combination for comparison of treatment effects of the metoprolol/ivabradine FDC.

The main strength of this study was that it was carried out in a large outpatient population of stable AP patients in 260 centers in Germany. Furthermore, due to the non-interventional design of the study, it was possible to assess treatment in routine clinical practice in terms of effectiveness, safety and medication adherence. Patient groups usually underrepresented in controlled clinical trials (e.g., elderly, women, patients with multiple co-morbidities) can only be covered and evaluated by such open-label, observational cohort studies [35].

Conclusions

In this cohort of stable AP patients in a real-life setting, presenting with already intense anti-anginal pre-treatment at baseline, therapy with a metoprolol/ivabradine FDC preparation was associated with a further reduction in HR by 10 bpm. At study end, a clinically relevant reduction of angina symptoms and nitrate consumption by more than 80% was observed. Moreover, exercise capacity was markedly improved as reflected by a significant shift of patients towards lower CCS classes. The tolerability of the FDC was favorable with no unexpected safety signals during follow-up.

Results were consistently confirmed in different subgroups, including patients ≥ 75 years of age, with high CCS grading or previous PCI. These positive effects may be mainly mediated by the pronounced improvement in medication adherence associated with use of the FDC. Taken together, in stable AP patients pre-treated with beta-blocker (e.g., metoprolol) and ivabradine the metoprolol/ivabradine FDC improves medication adherence and increases symptom control in clinical practice.