Fracture rates and economic outcomes in patients with osteoporosis prescribed risedronate gastro-resistant versus other oral bisphosphonates: a claims data analysis.

Patients with osteoporosis prescribed risedronate gastro-resistant had a lower incidence of fractures versus those prescribed other oral bisphosphonates. Administration of risedronate gastric-resistant does not require fasting, and this more convenient dosing administration may explain its improved efficacy.
PURPOSE: Up to half of patients do not follow complex dosing instructions of immediate-release bisphosphonates used for the prevention of osteoporotic fractures, which can result in suboptimal effectiveness. Risedronate gastro-resistant (GR) offers a more convenient dosing option by eliminating the need for fasting. This study compares fracture rates and outcomes between osteoporosis women treated with risedronate GR (GR cohort) versus other oral bisphosphonates (other cohort).
METHODS: Claims from women with osteoporosis in the USA were analyzed. Patients were classified into the two cohorts based on the first oral bisphosphonate observed (index date) and matched 1:1 based on patient characteristics. Patients were observed for ≥ 2 years following the index date. Fracture rates, health care resource utilization and costs, and treatment persistence were compared.
RESULTS: In total, 2,726 patients were selected in each cohort (median age: 60.0 years). The incidence of fractures was lower in the GR versus the other cohort for any fracture sites (incidence rate ratio, 95% CI: 0.83, 0.70-0.97) and spine fractures (0.71, 0.54-0.95), although the respective rate of medication discontinuation at 2 years was 80.5% and 74.4%. Time to first fracture was delayed for the GR cohort, reaching statistical significance after 36 months. The GR cohort incurred fewer hospitalizations (incidence rate per 1,000 patient-years: GR = 106.74; other = 124.20, p < 0.05) translating into lower hospitalization costs per patient per year (GR = $3,611; other = $4,603, p < 0.05).
CONCLUSIONS: Patients prescribed risedronate GR versus other bisphosphonates had a lower incidence of fractures, which may be explained by the fact that the GR formulation is absorbed even when taken with food.

Introduction

In Europe, in 2010, it was estimated that 22 million women and 5.5 million men aged between 50 and 84 years old were living with osteoporosis [1]. In the USA, approximately 12.3 million individuals older than 50 years were estimated to have osteoporosis in 2020 [2]. These numbers are expected to continue to increase over the next decades with the aging of the population [1]. Men and women with osteoporosis have an increased risk of fractures or bone breaks which can substantially impact their quality of life [3]. Osteoporosis fracture may lead to chronic pain and disability and higher risk of early mortality and pose a substantial financial burden on patients, their family, and the health care systems [4-7].

Oral bisphosphonates are the recommended first-line treatment for patients with osteoporosis in the USA and in Europe [8, 9]. Acting as antiresorptive agents, the use of oral bisphosphonate treatments has been associated with a significant reduction of the risk of fractures in patients with osteoporosis [7, 8, 10]. However, oral bisphosphonates are poorly absorbed, and lack of adherence to complex dosing instructions involving fasting and not lying down after taking the medication can further limit its absorption [11]. Real-world evidence indicates that more than 50% of patients do not follow all dosing instructions of the immediate-release formulation [12]. A poor absorption of bisphosphonates can result in suboptimal effectiveness and increased risk of fractures [13-15], leading to significant utilization of health care resources and costs [4, 16, 17].

Risedronate gastro-resistant (GR) was developed with the goal of providing more convenient dosing instructions and reducing the risk of gastrointestinal (GI) side effects by eliminating the need for fasting, without impacting the overall bioavailability and efficacy of the treatment [11, 18]. The GR formulation has the advantages of a better absorption independent of food intake, which is expected to translate into improved efficacy and a reduction in fracture rates compared to other immediate-release oral bisphosphonates, including alendronate sodium, ibandronate sodium, and risedronate sodium. However, there is limited real-world data comparing fracture rates between patients treated with risedronate GR versus other oral bisphosphonates.

The main objective of the study was to quantify and compare fracture rates among women with osteoporosis treated with risedronate GR versus other oral bisphosphonates. Health care resource utilization (HCRU), health care costs (HCC), and medication persistence and adherence were also compared between the two treatment groups.

Methods

Data source

This study used data from the IBM® MarketScan® Commercial and Medicare Supplemental Databases (Q1 2009 to Q4 2019). The MarketScan Commercial and Medicare Supplemental Databases represent health services (both pharmacy and medical) of approximately 130 million employees, dependents, and retirees in the USA with primary or Medicare supplemental coverage through privately insured fee-for-service, point-of-service, or capitated health plans. The databases include de-identified patient-level claims and are compliant with the Health Insurance Portability and Accountability Act (HIPAA).

Study design

The study used a retrospective observational design. Outcomes were compared between women with osteoporosis treated with risedronate GR (GR cohort) versus other oral bisphosphonates (other bisphosphonates cohort). For each patient, the date of the first observed prescription fill for an oral bisphosphonate was defined as the index date and the treatment initiated on that date as the index treatment. The 6-month period prior to the index date was defined as the baseline period. The observation period of patients spanned the period from the index date to the earliest of the data cut-off date or end of continuous eligibility.

Sample selection and construction of study cohorts

Adult women with at least one medical claim associated with a diagnosis for osteoporosis (ICD-9 codes, 733.0x; ICD-10 codes, M80.xx, M81.xx) were identified. Patients were included in the study if they had at least one prescription fill for an oral bisphosphonate (alendronate sodium, ibandronate sodium, and risedronate sodium).

Selected women were also required to have continuous eligibility (both pharmacy and medical benefits) for at least 6 months prior to the index date and for at least 2 years following the index date to allow sufficient time to observe fracture events. Furthermore, no treatment switch (i.e., from risedronate GR to other oral bisphosphonates or from other oral bisphosphonates to risedronate GR) were allowed during the minimum 2-year period.

As bisphosphonates can also be used to treat Paget’s disease and bone damages from some types of cancer, patients with a diagnosis for Paget’s disease or malignant neoplasm recorded during the 6-month baseline period were excluded.

Patients were classified into two mutually exclusive study cohorts based on the treatment initiated on the index date, i.e., risedronate GR cohort and other oral bisphosphonates cohort (including immediate-release risedronate).

Matching

To balance the patients’ profile between cohorts, each woman in the risedronate GR cohort was matched to one woman in the other bisphosphonates cohort with similar demographic and clinical characteristics. Matching factors, evaluated on the index date or at baseline as appropriate, included age, year of the index date, insurance plan type (e.g., comprehensive, preferred provider organization, exclusive provider organization/point-of-service, health maintenance organization), region, Charlson Comorbidity Index [19] categories (≤ 2 and > 2), selected comorbid conditions [20] with statistically significant differences between cohorts, presence of a fracture, and the use of selected drugs affecting bone density (abaloparatide, aromatase inhibitors, estrogens, denosumab, gonadotropin-releasing hormone agonists, injectable bisphosphonates, romosozumab, systemic corticosteroids, and teriparatide).

Definition of outcomes and statistical analyses

Outcomes were compared between the risedronate GR cohort and the other oral bisphosphonates cohort. For fracture rates, a subgroup analysis was performed among patients initiated on alendronate on the index date—the majority of patients in the other oral bisphosphonates cohort.

Fracture rates

Fracture events were identified based on the presence of medical claims associated with a diagnosis code of fracture during the observation period (see Online Resource 1 for list of diagnosis codes). The incidence of fractures was assessed overall as well as stratified by the main skeletal sites (i.e., hip, pelvis, spine, wrist/arm).

To ensure capturing new fracture as opposed to follow-up care, a definitional algorithm was applied for patients who had more than one medical claim associated with a diagnosis of fracture over the observation period [21, 22]. For two claims indicative of fractures occurring at the same skeletal site, to be considered a new fracture, the date of the second medical claim was required to occur ≥ 90 days after the first claim. Subsequent medical claims occurring < 90 days apart were considered follow-up care/fracture aftercare. For two claims indicative of fractures occurring at distinct skeletal sites, to be considered a new fracture, the date of the second medical claim was required to occur ≥ 30 days after the date of the initial medical claim. Subsequent medical claims occurring < 30 days apart were considered a single event involving multiple skeletal sites.

For each cohort, the incidence rate (IR) of fractures was calculated as the number of fracture events divided by the total patient-years of observation to account for the different lengths of observation. The IR was compared between cohorts using generalized linear models (GLMs) with a log link and negative binomial distribution, adjusting for matched pairs. Results were reported as incidence rate ratios (IRRs) along with their respective confidence intervals (CIs) and p-values.

Time from initiation of the index treatment to the date of the first fracture event was also described using Kaplan–Meier (KM) curves and compared between the two cohorts using the log-rank test.

HCRU and HCC

All-cause HCRU and HCC during the observation period were assessed and compared between the two cohorts. Health resources components and associated costs evaluated included inpatient stays, emergency department (ED) visits, outpatient visits, and other ambulatory encounters. Total medical costs (i.e., inpatient, ED, outpatient, and other ambulatory encounters costs) as well as all-cause and bisphosphonate-related pharmacy costs were also assessed.

To account for the varying observational time across patients, HCRU were reported as IRs per 1,000 patient-years of observation, and HCC were calculated as weighted average costs and reported per patient per year (PPPY).

HCRU were compared between cohorts using GLMs with a log link and negative binomial distribution, adjusting for matched pairs. Results were reported as IRRs along with their respective CIs and p-values.

For HCC, to account for the non-normality of the cost distribution as well as matched pairs, p-values and 95% CIs were estimated using non-parametric bootstrap re-sampling techniques. Results were reported as incremental HCC with their corresponding p-values and CIs. All costs were standardized and reported in 2019 US dollars using the medical care component of the Consumer Price Index [23].

Persistence and adherence to the index medication

Treatment persistence with the index medication was defined as the time from the date of initiation of the index treatment to the date of discontinuation of the index treatment. Treatment discontinuation was defined as a treatment gap of ≥ 90 consecutive days—measured between the end of the days of supply of a filled prescription and the date of the subsequent filled prescription for the index treatment, if any. Patients who did not discontinue the index treatment were censored on the date of the first switch to another oral bisphosphonate, the data cut-off date, or the end of insurance eligibility, whichever occurred first. Results were presented graphically using KM curves and compared between the two cohorts using the log-rank test.

Adherence to the index treatment was measured with the medication possession ratio (MPR), calculated as the number of days covered by the treatment over the period of interest divided by the numbers of days during the period. Adherence while on treatment (i.e., from the first to the last dispensing of the index treatment plus the days of supply of the last dispensing) and over fixed periods of 6 months, 1 year, and 2 years was considered.

Results

Patient characteristics

Out of the 1,364,890 women with ≥ 1 dispensing for an oral bisphosphonate in the database (risedronate GR, 16,737; other oral bisphosphonates, 1,348,153), 2,726 women prescribed risedronate GR and 2,726 matched women prescribed other oral bisphosphonates were selected after applying the inclusion and exclusion criteria. Among patients in the other bisphosphonates cohort, the majority were initiated on alendronate (66.3%) followed by ibandronate (20.2%) and risedronate immediate release (13.5%). Median age was 60.0 years old in both cohorts, and most patients were from the South region (45.2%) or Northeast region (29.5%) of the USA (Table 1). Overall, 1.7% of patients in both cohorts had a diagnosis of fracture recorded during the baseline period. The proportion of patients with a wrist/arm fracture at baseline was slightly higher among GR patients (0.9% vs. 0.5%, p = 0.031).

Table 1

Demographic and clinical characteristics

	GR patients	Other patients	p-valuea
	n = 2,726	n = 2,726
Demographics
Age, mean ± SD [median]	62.0 ± 10.2 [60.0]	62.1 ± 10.3 [60.0]	0.815
Age category, n (%)
18–49 yrs	139 (5.1%)	139 (5.1%)	-
50–54 yrs	440 (16.1%)	440 (16.1%)	-
55–59 yrs	755 (27.7%)	755 (27.7%)	-
60–64 yrs	562 (20.6%)	562 (20.6%)	-
65–69 yrs	241 (8.8%)	241 (8.8%)	-
70–74 yrs	197 (7.2%)	197 (7.2%)	-
75–79 yrs	172 (6.3%)	172 (6.3%)	-
80 + yrs	220 (8.1%)	220 (8.1%)	-
Census region, n (%)
Northeast	804 (29.5%)	804 (29.5%)	-
North Central	379 (13.9%)	379 (13.9%)	-
South	1,231 (45.2%)	1,231 (45.2%)	-
West	300 (11.0%)	300 (11.0%)	-
Unknown	12 (0.4%)	12 (0.4%)	-
Commercial insurance plan type, n (%)
Basic	0 (0.0%)	0 (0.0%)
Comprehensive	312 (11.4%)	312 (11.4%)
EPO/POS	246 (9.0%)	246 (9.0%)
HMO/POS with capitation	244 (8.9%)	244 (8.9%)
PPO	1,702 (62.3%)	1,702 (62.3%)
CDHP/HDHP	183 (6.7%)	183 (6.7%)
Unknown	43 (1.6%)	43 (1.6%)
Comorbidities during the 6-month baseline period
Patients with ≥ 1 comorbidity, n (%)	1,783 (65.4%)	1,776 (65.2%)	0.820
Cardiovascular disease	424 (15.6%)	424 (15.6%)	-
Celiac disease	12 (0.4%)	10 (0.4%)	0.831
Chronic pulmonary disease	266 (9.8%)	261 (9.6%)	0.853
Depression	248 (9.1%)	248 (9.1%)	-
Diabetes	291 (10.7%)	258 (9.5%)	0.145
Fatigue	283 (10.4%)	252 (9.2%)	0.166
Gastrointestinal mucositis or urination problem	330 (12.1%)	330 (12.1%)	-
Hyperparathyroidism	37 (1.4%)	34 (1.2%)	0.807
Hypertension	857 (31.4%)	833 (30.6%)	0.463
Hypertensive chronic kidney disease	11 (0.4%)	11 (0.4%)	-
Inflammatory bowel disease	34 (1.2%)	20 (0.7%)	0.077
Joint inflammatory disease	126 (4.6%)	126 (4.6%)	-
Vitamin D deficiency	262 (9.6%)	262 (9.6%)	-
Charlson Comorbidity Index
CCI, mean ± SD [median]	0.1 ± 0.8 [0.0]	0.0 ± 0.8 [0.0]	0.028*
CCI category, n (%)
≤ 2	2,708 (99.3%)	2,708 (99.3%)	-
Fractures during the 6-month baseline period
Any site	47 (1.7%)	47 (1.7%)	-
Hip	6 (0.2%)	10 (0.4%)	0.453
Pelvis	4 (0.1%)	2 (0.1%)	0.683
Spine	13 (0.5%)	23 (0.8%)	0.089
Wrist/arm	25 (0.9%)	13 (0.5%)	0.031*
Dispensing of ≥ 1 drug affecting bone density during the 6-month baseline periodb, n (%)	1,001 (36.7%)	1,001 (36.7%)	-
Duration of observation period (months), mean ± SD [median]	52.0 ± 21.7 [46.8]	56.4 ± 22.6 [52.4]	< .001*

Notes:

SD standard deviation

ap-values were calculated using paired t-tests for continuous variables, and McNemar tests for categorical variables

bDrugs included abaloparatide, aromatase inhibitors, estrogens, denosumab, gonadotropin-releasing hormone agonists, injectable bisphosphonates, romosozumab, systemic corticosteroids, and teriparatide

*Significant at the 5% level

Fracture rates

During the observation period, regardless of the site, patients in the GR cohort had a lower incidence of fractures compared to patients in the other bisphosphonates cohort (Table 2). Statistically significant differences were observed for any site of fractures and spine fractures—patients in the GR cohort were associated with a 17% reduction in overall risk of fracture (IR per 1,000 patient-years: GR, 34.65 vs. other, 42.13; p < 0.05) and 29% reduction in the risk of spine fractures (IR per 1,000 patient-years: GR, 10.84 vs. other, 15.13; p < 0.05). A stratification by age group showed that the incidence of fractures, including hip fractures, more than doubled when comparing patients < 65 to those ≥ 65 years old as of the index date (Table 3). At each time point considered over the observation period, the rate of incident fractures was lower in the GR cohort compared to the other bisphosphonates cohort, reaching statistical significance at 36 months (GR, 7.08%; other, 8.67%; p = 0.037) (Fig. 1).

Table 2

Fracture rates

GR vs. other patients
	GR patients			Other patients
	n = 2,726			n = 2,726			IRR(95% CI)a,bUnadjusted
	Total number of fractures	Total patient-years of observation	IR of fractures, per 1,000 patient-years	Total number of fractures	Total patient-years of observation	IR of fractures, per 1,000 patient-years
Any site	409	11,804	34.65	540	12,818	42.13	0.83 (0.70–0.97)*
Hip	100	11,804	8.47	114	12,818	8.89	0.98 (0.69–1.40)
Pelvis	28	11,804	2.37	43	12,818	3.35	0.71 (0.41–1.23)
Spine	128	11,804	10.84	194	12,818	15.13	0.71 (0.54–0.95)*
Wrist/arm	180	11,804	15.25	215	12,818	16.77	0.91 (0.73–1.13)
GR vs. alendronate patients
	GR patients			Alendronate patients
	n = 1,807			n = 1,807			IRR (95% CI)a,b Unadjusted
	Total number of fractures	Total patient-years of observation	IR of fractures, per 1,000 patient-years	Total number of fractures	Total patient-years of observation	IR of fractures, per 1,000 patient-years
Any site	262	7,712	33.97	354	8,323	42.53	0.81 (0.66–0.98)*
Hip	71	7,712	9.21	80	8,323	9.61	0.99 (0.65–1.51)
Pelvis	16	7,712	2.07	26	8,323	3.12	0.68 (0.35–1.33)
Spine	83	7,712	10.76	132	8,323	15.86	0.69 (0.49–0.97)*
Wrist/arm	112	7,712	14.52	132	8,323	15.86	0.91 (0.70–1.20)

Notes:

CI confidence interval, IR incidence rate, IRR incidence rate ratio

aIncidence rate ratios were estimated with generalized linear models with log link and negative binomial distribution with robust error variances to account for the matched pairs. Incidence rate ratios may differ from the ratio of the incidence rates because of adjustments for overdispersion

bAn IRR < 1 indicates a lower incidence of fracture per patient-year among women treated with risedronate GR

*Significant at the 5% level

Table 3

Fracture rates by age group

Patients < 65 years
	GR patients			Other patients
	n = 1,896			n = 1,896			IRR(95% CI)a,bUnadjusted
	Total number of fractures	Total patient-years of observation	IR of fractures, per 1,000 patient-years	Total number of fractures	Total patient-years of observation	IR of fractures, per 1,000 patient-years
Any site	192	8,104	23.69	214	8,783	24.37	0.96 (0.75–1.24)
Hip	36	8,104	4.44	22	8,783	2.50	1.80 (0.85–3.83)
Pelvis	4	8,104	0.49	9	8,783	1.02	0.48 (0.14–1.69)
Spine	45	8,104	5.55	69	8,783	7.86	0.67 (0.42–1.08)
Wrist/arm	114	8,104	14.07	120	8,783	13.66	1.03 (0.77–1.37)
Patients ≥ 65 years
	GR patients			Other patients
	n = 830			n = 830			IRR (95% CI)a,b Unadjusted
	Total number of fractures	Total patient-years of observation	IR of fractures, per 1,000 patient-years	Total number of fractures	Total patient-years of observation	IR of fractures, per 1,000 patient-years
Any site	217	3,700	58.65	326	4,035	80.79	0.74 (0.60–0.91)*
Hip	64	3,700	17.30	92	4,035	22.80	0.78 (0.52–1.17)
Pelvis	24	3,700	6.49	34	4,035	8.43	0.78 (0.42–1.42)
Spine	83	3,700	22.43	125	4,035	30.98	0.74 (0.52–1.05)
Wrist/arm	66	3,700	17.84	95	4,035	23.54	0.76 (0.55–1.05)

Notes:

CI confidence interval, IR incidence rate, IRR incidence rate ratio

aIncidence rate ratios were estimated with generalized linear models with log link and negative binomial distribution with robust error variances to account for the matched pairs. Incidence rate ratios may differ from the ratio of the incidence rates because of adjustments for overdispersion

bAn IRR < 1 indicates a lower incidence of fracture per patient-year among women treated with risedronate GR

*Significant at the 5% level

Fig. 1

Development of first fracture (any site)

(95% CI)

(95% CI)

Results remained consistent and numerically similar when comparing fracture rates between patients treated with risedronate GR versus alendronate (Table 2). When compared to patients initiated on alendronate, patients initiated on risedronate GR were associated with a 19% reduction in the overall risk of fracture (IR per 1,000 patient-years: GR, 33.97 vs. other, 42.53; p < 0.05) and 31% reduction in the risk of spine fracture (IR per 1,000 patient-years: GR, 10.76 vs. other, 15.86; p < 0.05).

HCRU and HCC

Compared to patients who were prescribed other bisphosphonates, those who were prescribed risedronate GR had fewer inpatient stays during the observation period (106.74 inpatient stays per 1,000 patient-years for GR vs. 124.20 inpatient stays per 1,000 patient-years for other, IRR = 0.86 [0.76–097]). The incidence of ED, outpatient, and other ambulatory encounter visits was not statistically significantly different between the two cohorts (Table 4).

Table 4

Health care resource utilization and costs

HCRU, per 1,000 patient-years	GR patients	Other patients	IRR (95% CI)a
	n = 2,726	n = 2,726
Inpatient visits	106.74	124.20	0.86 (0.76–0.97)*
ED visits	533.29	549.38	0.97 (0.88–1.07)
Outpatient visits	16,384.69	15,681.44	1.04 (0.99–1.08)
Other ambulatory encounterb	2,775.82	2,726.07	1.04 (0.95–1.13)
HCC PPPYc, mean ± SD	GR patients	Other patients	Cost difference[95% CI]
	n = 2,726	n = 2,726
Inpatient	3,611 ± 11,367	4,603 ± 16,230	− 993	(− 1,805; − 285)*
Emergency department	890 ± 2,762	900 ± 2,360	− 10	(− 156; 128)
Outpatient	7,305 ± 13,691	6,768 ± 12,471	538	(− 195; 1,311)
Other ambulatory encounterb	694 ± 3,396	792 ± 3,720	− 97	(− 293; 102)
Total medical costs	12,500 ± 23,005	13,063 ± 25,778	− 562	(− 1,995; 819)
Pharmacy	4,335 ± 12,980	3,655 ± 9,192	680	(64; 1,485)*
Oral bisphosphonates	387 ± 523	149 ± 297	238	(214; 262)*

Notes:

Costs are reported in 2019 US dollars

CI confidence interval, ED emergency department, HCC health care costs, HCRU health care resource utilization, IRR incidence rate ratio, PPPY per patient per year

aIncidence rate ratios were estimated with generalized linear models with log link and negative binomial distribution with robust error variances to account for the matched pairs

bOther ambulatory encounters include mainly patient home, independent laboratory, skilled nursing facilities, and other unlisted facilities

cCosts PPPY are weighed by the number of days in the patients’ observation period

*Significant at the 5% level

Consistent with their lower utilization of inpatient services, inpatient costs were $993 per patient per year lower in the GR cohort compared to the other bisphosphonates cohort (GR = $3,611 vs. other = $4,603, p < 0.05). No statistically significant differences were observed for costs associated with ED, outpatient, and other ambulatory encounter visits. When compared to patients in the other bisphosphonates cohort, patients in the GR cohort incurred incremental total pharmacy costs of $680 per patient per year—partly driven by higher dispensing costs for oral bisphosphonates (Table 4).

Persistence on the index treatment

Overall, in both cohorts, most patients discontinued their index treatment within the first 2 years from its initiation. At 2 years after the index date, the rate of discontinuation of the index medication was 80.5% in the GR cohort and 74.4% in the other bisphosphonates cohort. The persistence on the index treatment was overall statistically significantly lower for patients in the GR cohort, mainly driven by a higher discontinuation rate within the first few months of treatment initiation (Fig. 2). Average MPR while on treatment at 6 months, 1 year, and 2 years was not statistically significantly different between the two cohorts (Fig. 2).

Fig. 2

Persistence and adherence to the index medication

Discussion

Results from the current study indicate that over an average observation period of more than 50 months, patients prescribed risedronate GR had lower rates of fracture and in particular a lower rate of spine fractures compared to patients prescribed other bisphosphonates. Of note, although the proportion of patients who had experienced a fracture at any site during the 6-month baseline period was the same in the two treatment cohorts, a slightly higher proportion of patients prescribed risedronate GR experienced a wrist/arm fracture, perhaps indicative of a higher risk of subsequent fractures.

As expected, the incidence of hip fracture, the most expensive fracture type [17], was the lowest among patients under 65 years old and increased sharply in older patients. Overall, the incidence of fractures more than doubled in patients ≥ 65 versus < 65 years old. In general, the lower rates of fractures observed in the present study compared to previously published results from observational studies are consistent with the relatively young age of the studied population [24-26].

Indeed, in a study using claims data from commercially insured patients (all patients < 65 years old; mean age: 56.0 years old), the authors estimated incidence rates of fractures at any site between 15.4 and 16.1 per 1,000 patient-years for bisphosphonates [25]. In a similar study using claims from Medicare insured patients (all patients ≥ 65 years old; mean age, 78.2 years old), the authors estimated at 56.3 per 1,000 patient-years the incidence rate of fractures at any site [24].

Compared to patients prescribed other bisphosphonates, those who were prescribed risedronate GR were associated with a higher rate of treatment discontinuation, especially during the first few months after the index date. A potential explanation for this observation could be the 4 to 6 times higher out-of-pocket costs observed for risedronate GR than that for other bisphosphonates (mean [median] out-of-pocket costs per dispensing, 28–30-day supply, GR, $42.39 [$37.95] vs. other, $10.72 [$6.10]; 84–90-day supply, GR, $83.69 [$69.71] vs. other, $21.13 [$11.88]). This observation is further supported by a well-documented body of literature on the detrimental impact of increased out-of-pocket costs on medication compliance and persistence, in particular for chronic conditions [27-32].

This study offers a unique perspective on the fracture rates of patients prescribed risedronate GR versus other oral bisphosphonates in real-world settings. Several randomized clinical trials have assessed the efficacy of bisphosphonates, and the body of evidence from these studies suggests no differential effect on fracture rates between bisphosphonates [33]. However, in real-world settings, patients’ behavior towards their medication may impact the ability of bisphosphonates to prevent fractures.

Lack of persistence and poor compliance are known challenges with bisphosphonates, all of which may impact the overall efficacy of bisphosphonates [14, 33–35]. A systematic literature review of 89 prospective and retrospective observational studies examining patient adherence and persistence to oral bisphosphonates in adults with osteoporosis found that mean persistence rates ranged from 17.7 to 74.8% at 1 year and from 12.9 to 60.6% at 2 years. Similarly, compliance rates ranged from 31.7 to 72.0% at 1 year and from 34.5 to 47.9% at 2 years across studies [33]. Although reasons for the lack of persistence and compliance are likely multifactorial, complex dosing instructions as well as GI side effects have been reported as potential reasons [15, 33–35].

Adding to the detrimental impact on bisphosphonates effectiveness of poor medication persistence and compliance is the poor compliance with dosing instructions. Absorption of oral bisphosphonate by the system is poor—usually less than 1% on average—and may be further limited by concurrent intake of food and beverage [11]. As such, to derive the full benefits of immediate-release formulations of oral bisphosphonates, patients are required to follow a strict dosing schedule—the drug is typically required to be taken on an empty stomach ≥ 30 to 60 min before the first food, drink, or other medications of the day. Furthermore, patients must not lie down for 30 min after taking the medication [36-38].

Real-world evidence indicates that a significant fraction of patients do not follow the complex dosing instructions of the immediate-release formulation of bisphosphonates [12]. In a survey of 363 women with osteoporosis aged ≥ 55 years old, 40.5% reported not being compliant with dosing instructions ensuring adequate absorption, 34.7% were not compliant with dosing instructions preventing adverse events, and as many as 56.5% were not compliant with all dosing instructions [12]. Other external factors, such as the calcium content in tap water, may also interfere with the absorption of bisphosphonates [39].

The lower rates of fractures observed among patients in the risedronate GR cohort, despite their lower persistence on the medication, could be explained by its more convenient dosing administration. Indeed, among patients remaining on bisphosphonates, those on risedronate GR are more likely to receive an improved medication benefit because of its absorption irrespective of fasting compared to the complex and, hence often not followed, dosing administration of immediate-release bisphosphonates.

Likely reflecting their lower incidence of fractures, patients prescribed risedronate GR were associated with a lower utilization of inpatient services, which translated into lower inpatient costs. The amount of health care resources and the associated costs diverted by osteoporotic fractures are substantial [4, 16, 17, 40]. For instance, using claims data from the USA, Tran et al. found that the all-cause incremental yearly health care costs of commercially insured women with versus without incident osteoporotic fracture over a period of 5 years following the fracture were $77,370, $28,737, $23,155, $21,478, and $18,835, respectively [40]. Even a small decrease in the risk of fracture has thus the potential for significant health care resources and health care costs saving on the long term.

Results from this study should be interpreted in light of some limitations. First, given the retrospective nature of the data used, this study did not attempt to establish causal inference. Instead, findings should be interpreted as association-level results. Second, because the databases used include patients with a commercial health plan or a Medicare Supplemental health plan, the study sample may not be representative of the general osteoporosis population. This is underscored by the relatively young age of studied patients. Third, the higher out-of-pocket cost associated with risedronate GR compared to that of other bisphosphonates may be the source of a selection bias. Another potential source of confounding comes from the fact that the database used does not include the necessary clinical information to identify patients at a higher risk of fracture. Fourth, osteoporosis and other conditions considered in this study were identified based on diagnostic codes recorded on administrative claims used for billing purposes, which in some instance could reflect suspected rather than confirmed clinical diagnoses. It is also possible that not all diagnoses are systematically recorded on claims; thus, underreporting of certain conditions is also a possibility. Similarly, the incidence of spine fracture may be underestimated as most cases do not come to medical attention. Fifth, claims data only provide information on filled prescriptions, not on how medications are actually consumed. Finally, the HCC reported are likely to be an underestimation of the total costs resulting from fractures as they do not capture administrative costs of third-party payers for claims processing, out-of-pocket costs, indirect costs (e.g., productivity loss), or other intangible costs.

Despite their lower persistence, patients prescribed risedronate GR were associated with a lower incidence of fractures compared to those prescribed other oral bisphosphonates, leading to lower utilization of inpatient services which translated into lower inpatient costs. These results are consistent with the hypothesis that the more convenient dosing administration of risedronate GR could improve the absorption of bisphosphonate and help patients with osteoporosis get an improved benefit of treatment.

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