Health care resource utilization before and after natalizumab initiation among patients with multiple sclerosis in Germany

Abstract

Background

Multiple sclerosis (MS), a progressive neurodegenerative disease, greatly impacts the quality of life and economic status of people affected by this disease. In Germany, the total annual cost of MS is estimated at €40,000 per person with MS. Natalizumab has shown to slow MS disease progression, reduce relapses, and improve the quality of life of people with MS.

Objective

To evaluate MS-related and all-cause health care resource utilization and costs among German MS patients during the 12 months before and after initiation of natalizumab in a real-world setting.

Methods

The current analysis was conducted using the Health Risk Institute research database. Identified patients were aged ≥18 years with ≥1 diagnosis of MS and had initiated natalizumab therapy (index), with 12-month pre– and post–index-period data. Patients were stratified by prior disease-modifying therapy (DMT) usage or no DMT usage in the pre-index period. Outcome measures included corticosteroid use and number of sick/disability days, inpatient stays, and outpatient visits. Health care costs were calculated separately for pre- and post-index periods on a per-patient basis and adjusted for inflation.

Results

In a final sample of 193 natalizumab-treated patients, per-patient MS-related corticosteroid use was reduced by 62.3%, MS-related sick days by 27.6%, and inpatient costs by 78.3% from the pre- to post-index period. Furthermore, the proportion of patients with MS-related hospitalizations decreased from 49.7% to 14.0% (P<0.001); this reduction was seen for patients with and without prior DMT use.

Conclusions

In a real-world setting in Germany, initiation of natalizumab treatment in people with MS significantly reduced MS-related hospitalizations, corticosteroid use, sick days, and associated costs.

Keywords:

• multiple sclerosis
• relapsing–remitting
• health care resource utilization
• costs
• outcomes
• natalizumab

Introduction

Multiple sclerosis (MS) is a progressive, degenerative disease of the central nervous system, characterized by multiple symptoms, including spasticity; problems with walking, balance, and coordination; fatigue, depression, and mood disorders; bladder, bowel, and sexual dysfunction; and cognitive impairment. As such, MS is the leading cause of disability among nonelderly individuals in industrialized countries.¹ In Germany, it is estimated that at least 120,000 people have MS,² with the total annual cost of MS in Germany estimated to be €40,000 per person with MS.^3,4 MS pathogenesis is characterized by inflammatory and neurodegenerative mechanisms,⁵ which manifest as relapses^6,7 and disability progression,⁸ respectively.

The most common form of MS is relapsing–remitting MS (RRMS), whereby an unpredictable course of relapses is followed by a period of remission and recovery.⁹ MS relapses have been shown to profoundly affect an individual’s quality of life, as occurrences interfere with the ability to perform daily activities, are linked to emotional distress and depression, and impact family, friends, and caregivers.¹⁰ Thus, the societal, economic, familial, and personal burden of MS relapses is enormous.

People with MS who experience relapses are often treated with corticosteroids and admitted to the hospital.¹¹ MS relapses contribute significantly to the costs associated with the disease,¹² which increase with disease severity.^12–14

Treatments that can slow or prevent the progression of MS have the potential to significantly improve the quality of life for people with MS and reduce the economic impact of the disease.^14,15 Natalizumab, a selective adhesion-molecule inhibitor, has been shown to reduce annualized relapse rates by 68% versus placebo among people with RRMS^16,17 and by 81% versus placebo among people with highly active RRMS.¹⁸ In the European Union, natalizumab is indicated in adults with highly active RRMS who failed to respond to an adequate course of interferon beta or glatiramer acetate, and in adults with rapidly evolving severe RRMS (with ≥2 relapses in 1 year and ≥1 gadolinium-enhancing lesion or a significant increase in T2 lesion load compared with a previous recent magnetic resonance imaging assessment).¹⁹

In Germany, ~90% of the population (~70 million individuals) is insured as part of the Statutory Health Insurance (SHI) program,^20,21 and the prevalence of MS among people insured by the SHI in 2010 was estimated to range from 120,000 to ≥200,000.²² The objective of this study was to evaluate MS-related and all-cause health care resource utilization (HRU) and costs among German people with MS during the 12 months before and 12 months after initiation of natalizumab in a real-world setting. In addition, HRU and costs were evaluated after stratifying people with MS by whether or not they had used a disease-modifying therapy (DMT) during the pre-index period. Although several studies have evaluated the economic burden of MS in Germany,^3,4,15 to our knowledge this is the first study to evaluate MS-related HRU and costs among natalizumab-treated people with MS based on their previous DMT exposure.

Methods

Database

The current analysis was conducted using the Health Risk Institute (HRI) research database, which contains anonymized, patient-level inpatient, outpatient, sick leave, and pharmacy claims data from about 80 health insurance companies, representing a high proportion of thê130 health insurance companies that comprise the SHI in Germany²⁰ and providing good external validity.²³ For 2008–2013, the HRI research database contained individual, de-identified claims data for about 4 million people, with a patient sample that is representative of the German population for age and gender.^24,25 The database is fully compliant with all data protection regulations in Germany and has been certified. As the HRI research database includes verified accounting data of the participating insurance companies, these claims data are regularly audited by the insurance companies for reimbursement purposes and are prepared in accordance with German Social Law (paragraphs 287 SGB V and 75 SGB X). This study utilized an existing data set in line with all data protection regulations, and patients were not identified for the purpose of this study.

This study is a retrospective database study based on fully anonymized claims data, and claims data are recorded for accounting purposes and not for clinical research. No electronic medical records or other clinical parameters were used. As a result, no ethical approval or consent from an ethics committee or review board was required for this study.

Case selection

The study sample included patients aged ≥18 years who initiated treatment with natalizumab (index date [Anatomical Therapeutic Chemical {ATC} code L04AA23] between January 1, 2009, and December 31, 2012). All patients had a primary or secondary diagnosis of MS (International Statistical Classification of Diseases and Related Health Problems, 10th revision, German Modification [ICD-10-GM] codes G35.xx) in the inpatient sector in the pre-index period or a verified diagnosis of MS in the outpatient sector during any of the four quarters before the index quarter. At least 24 months of continuous eligibility was required, including a 12-month pre-index period and a 12-month post-index period. Furthermore, patients had to have ≥1 natalizumab prescription in the fourth quarter of the post-index period to indicate continuous natalizumab use. Thus, the entire study covered the time interval from January 1, 2008, to December 31, 2013 (Figure 1).

Figure 1 Study design.

Patient groups

Outcomes were evaluated in the overall sample of patients who initiated treatment with natalizumab and in natalizumab initiators based on the prior use of other DMTs. Patients were categorized as having used (prior DMT use) or not used (no prior DMT use) another DMT during the 12-month pre-index period.

Outcome measures

Patient demographic and clinical characteristics included age, gender, and index year. The Deyo-Charlson Comorbidity Index (DCI),^26,27 a summary measure of comorbidity burden, is reported as both a continuous and categorical measure. Individual DCI comorbidities are reported as binary outcomes (i.e., present or not present). MS-related and all-cause hospitalizations were defined as having a primary MS-related ICD-10-GM code (G35.xx) or any ICD-10-GM code, respectively. For the total population, the total number of inpatient stays and total length of stay were each summed across all admissions for the pre- and post-index period.

The use of corticosteroids (intravenous [IV] and oral) was determined if a patient had ≥1 prescription claim for dexamethasone, methylprednisolone, prednisolone, prednisone, or adrenocorticotropic hormone. Similarly, immunosuppressant use was recorded affirmatively if a patient had ≥1 claim for an immunosuppressant. Per the German Association of Neurologists’ guidelines for diagnosis and treatment of MS,²⁸ drugs for MS symptom relief include antidementia agents, antidepressants, antiepileptics, muscle relaxants (i.e., baclofen, botulinum toxin, dantrolene, tizanidine, tolperisone, and tetrazepam), antispasmodics, and select medications to manage fatigue (i.e., amantadine and modafinil), tremor (i.e., propranolol), and sexual dysfunction (i.e., sildenafil, tadalafil, and tibolone). Use of MS symptom relief and all MS-related prescription medications was identified using the ATC classification system.

Health care–related costs (in Euros [€]) were calculated separately for the pre- and post-index periods on a per-patient basis and converted to 2013 € using the general rate of inflation for Germany.²⁹ MS-related inpatient costs were defined as the total costs for patient hospitalizations with a primary ICD-10-GM code for MS, and all-cause costs were defined as the total costs for admissions for any reason. Total costs for corticosteroids (IV, oral, and self-injectable) and immunosuppressants were summed across all relevant prescription claims. Total costs for MS-related outcomes were calculated as the sum of all costs for MS-related hospitalizations, corticosteroids, and immunosuppressants. Costs were collected in the HRI database and the reported costs were those for which the SHIs pay. In the inpatient sector, a German diagnosis-related group system was used.

Additional end points included the percentage of patients having any sick or disability days (sick leave >6 weeks), the number of MS-related and all-cause sick days, and all-cause disability days.

Statistical analyses

Results for baseline demographic and clinical characteristics, HRU and costs, and sick days and disability days are summarized descriptively. Continuous variables are presented as means (with standard deviations [SDs]) or medians (with ranges), depending on the distributions of the data. Categorical variables are presented as frequency distributions and percentages. Statistical comparisons of baseline demographic and clinical characteristics between those with and without prior DMT use were performed using nonpaired t-tests for means and Mann–Whitney U tests for medians; chi-square and Fisher’s exact tests were used for comparisons of proportions.

Statistical comparisons of the changes from the pre- to post-index period for HRU, costs, sick days, and disability days were performed using one-sample t-tests for means and Wilcoxon signed-rank tests for medians; McNemar chi-square tests were used for comparisons of categorical data. Statistical comparisons of the changes from the pre- to post-index period between patients with and without prior DMT use were performed using Two-sample t-tests for means and Wilcoxon rank-sum tests for medians; Mantel–Haenszel chi-square tests were used for categorical data.

Results

Patient disposition and characteristics

The final sample included 193 patients who initiated treatment with natalizumab between 2009 and 2012 and met all selection criteria (Figure 2). The majority of patients (75%; n=145) had used another DMT during the pre-index period. The mean (SD) age was 37.1 (10.2) years, and 65% of the sample was female. Overall, hemiplegia or paraplegia (20.7%) and chronic pulmonary disease (19.7%) were the most prevalent conditions contributing to the DCI. With the exception of mean DCI, which was significantly higher among patients with prior DMT use, baseline demographic and clinical characteristics were comparable regardless of prior DMT use (Table 1).

Figure 2 Patient selection process.

Abbreviation: MS, multiple sclerosis.

Table 1 Baseline demographic and clinical characteristics of patients initiating treatment with natalizumab

Characteristic	All patients (N=193)	With prior DMT use (n=145)	Without prior DMT use (n=48)	P-valuea
Age, years
Mean (SD)	37.1 (10.2)	37.1 (9.8)	37.1 (11.4)	0.818
Median (range)	37 (19, 61)	38 (19, 60)	36 (21, 61)
Female gender, n (%)	125 (64.8)	91 (62.8)	34 (70.8)	0.384
Index year, n (%)
2009	37 (19.2)	26 (17.9)	11 (22.9)	0.747
2010	39 (20.2)	30 (20.7)	9 (18.8)
2011	55 (28.5)	40 (27.6)	15 (31.3)
2012	62 (32.1)	49 (33.8)	13 (27.1)
DCI score
Mean (SD)	0.88 (1.2)	0.99 (1.3)	0.54 (0.9)	0.031
Median (range)	0 (0.0, 5.0)	0 (0.0, 5.0)	0 (0.0, 3.0)
DCI conditions ≥5%, n (%)
Hemiplegia or paraplegia	40 (20.7)	34 (23.4)	6 (12.5)	0.149
Chronic pulmonary disease	38 (19.7)	31 (21.4)	7 (14.6)	0.403
Diabetes without complications	12 (6.2)	10 (6.9)	2 (4.2)	0.733
Mild liver disease	11 (5.7)	9 (6.2)	2 (4.2)	0.734
Prior DMT, n (%)
Glatiramer acetate (Copaxone^®)	42 (21.8)	42 (29.0)	0 (0.0)	Not applicable
Intramuscular interferon beta-1a (Avonex^®)	34 (17.6)	34 (23.4)	0 (0.0)
SC interferon beta-1b (Betaferon^®)	28 (14.5)	28 (19.3)	0 (0.0)
SC interferon beta-1a (Rebif^®)	28 (14.5)	28 (19.3)	0 (0.0)
SC interferon beta-1b (Extavia^®)	7 (3.6)	7 (4.8)	0 (0.0)
Fingolimod (Gilenya^®)	6 (3.1)	6 (4.1)	0 (0.0)
No prior DMT	48 (24.9)	0 (0.0)	48 (100)
Multiple sclerosis–related medications, n (%)
Corticosteroidsb	146 (75.6)	116 (80.0)	30 (62.5)	0.020
Immunosuppressants	10 (5.2)	7 (4.8)	3 (6.3)	0.712

Notes:

a P values for the comparison of the subgroups of patients with and without prior DMT use;

b dexamethasone, methylprednisolone, prednisolone, prednisone, or adrenocorticotropic hormone.

Abbreviations: DCI, Deyo-Charlson comorbidity index; DMT, disease-modifying therapy; SC, subcutaneous; SD, standard deviation.

Inpatient hospitalizations and expenditures

MS-related and all-cause inpatient HRU and expenditures were reduced after initiating natalizumab compared with the pre-index period. In the overall sample, the proportion of patients with MS-related hospitalizations decreased significantly on natalizumab therapy, from 49.7% to 14.0% (P<0.001; Figure 3A), with a corresponding decrease in the per-patient mean number of MS-related hospitalizations from 1.1 to 0.2 (P<0.001; Table 2). The mean number of MS-related inpatient days among those with hospital stays decreased by 61.3%, from 7.0 days (n=96) in the pre-index period to 2.7 (n=27) on natalizumab therapy (P<0.001; Table 2).

Figure 3 Multiple sclerosis–related (A) hospitalizations and (B) inpatient costs.

Abbreviation: DMT, disease-modifying therapy.

Table 2 Health care resource utilization among overall patient sample before and after initiating treatment with natalizumab

Health care resource utilization	All patients (N=193)
	Pre-index	Post-index	Change	P-value
Number of hospitalizations
MS-related
Mean (SD)	1.1 (1.5)	0.2 (0.7)	−0.9 (1.4)	<0.001
Median (range)	0 (0, 8)	0 (0, 5)	0 (−6, 3)
All-cause
Mean (SD)	1.3 (1.8)	0.4 (1.1)	−0.9 (1.8)	<0.001
Median (range)	1 (0, 9)	0 (0, 11)	0 (−8, 9)
Number of inpatient days
MS-related
Mean (SD)	7.0 (10.7)	2.7 (20.5)	−4.3 (20.5)	<0.001
Median (range)	0 (0, 62)	0 (0, 277)	0 (−62, 238)
All-cause
Mean (SD)	9.6 (16.6)	5.0 (23.5)	−4.6 (25.0)	<0.001
Median (range)	4 (0, 113)	0 (0, 277)	0 (−113, 238)
Corticosteroid use
Mean (SD)	2.4 (2.5)	0.6 (1.3)	−1.8 (2.4)	<0.001
Median (range)	2 (0, 19)	0 (0, 8)	−1 (−19, 3)
Number of sick days
MS-related
Mean (SD)	29.8 (53.1)	21.8 (55.8)	−8.0 (59.7)	<0.001
Median (range)	1 (0, 326)	0 (0, 366)	0 (−308, 311)
All-cause
Mean (SD)	36.2 (58.5)	27.9 (61.4)	−8.3 (63.8)	<0.001
Median (range)	5 (0, 330)	0 (0, 366)	0 (−312, 256)
Number of all-cause disability days
Mean (SD)	33.2 (84.9)	39.7 (97.9)	6.6 (61.5)	0.436
Median (range)	0 (0, 365)	0 (0, 366)	0 (−158, 365)

Abbreviations: MS, multiple sclerosis; SD, standard deviation.

In the overall sample, the proportion of patients with MS-related hospitalizations decreased by 71.8% while on natalizumab therapy (P<0.001; Figure 3A). Similarly significant reductions were observed for patients with (70.2%, P<0.001) and without (77.3%, P<0.001) prior DMT use. The mean number of MS-related hospitalizations also decreased significantly in both groups, from 1.1 to 0.2 in patients with prior DMT use (P<0.001) and from 0.9 to 0.1 in patients without prior DMT use (P<0.001; Table S1). Among all MS patients, the mean duration of hospital stays decreased by 52.8% in patients with prior DMT use (from 7.2 to 3.4 days; P<0.001) and by 90.5% in patients without prior DMT use (from 6.3 to 0.6 days; P<0.001).

Mean annual per-patient MS-related inpatient costs decreased by 78.3%, from €3,759 (median, €706; range, €0–€60,583) in the pre-index period to €815 (median, €0; range, €0–€25,934) in the post-index period in the overall sample, and by 76.6% and 83.9% in patients with and without prior DMT use, respectively (all P<0.001; Figure 3B).

In the overall sample, the proportion of patients hospitalized for any cause decreased by 52.4% while on natalizumab therapy (P<0.001; Figure 4A). The mean number of all-cause hospitalizations was 1.3 in the pre-index period and 0.4 in the post-index period (P<0.001), and the mean duration of these stays decreased by 48.2%, from 9.6 to 5.0 days (P<0.001; Table 2). Similar reductions after natalizumab initiation were observed in the subgroups of patients with and without prior DMT use (Figure 4A; Table S1).

Figure 4 All-cause (A) hospitalizations and (B) inpatient costs.

Abbreviation: DMT, disease-modifying therapy.

Mean annual per-patient all-cause inpatient costs decreased by 64.0%, from €4,610 (median, €2,365; range, €0–€60,583) in the pre-index period to €1,660 (median, €0; range, €0–€33,719) in the post-index period in the overall sample and by 58.9% and 78.7% in patients with and without prior DMT use, respectively (all P<0.001; Figure 4B).

Corticosteroid use

In the first year of treatment with natalizumab, statistically significant reductions from the pre-index period in the proportions of patients using corticosteroids were observed among all patients (62.3% reduction) and among those with (63.8% reduction) and without (56.6% reduction) prior DMT use (all P<0.001; Figure 5A). Similarly, a significant decrease was observed in the mean number of corticosteroid prescriptions for all patients (from 2.4 to 0.6; P<0.001). Patients who had received prior DMTs showed a larger change in corticosteroid use (from 2.6 to 0.6) than those who did not receive prior DMTs (from 2.1 to 0.9; all P<0.001; Table 2; Table S1). Mean expenditures associated with corticosteroid use also significantly declined in each patient group (decreased by 78.9%, 79.0%, and 78.2% for patients overall, with prior DMT use, and without prior DMT use, respectively; all P<0.001; Figure 5B).

Figure 5 Corticosteroid (A) use and (B) costs.

Abbreviation: DMT, disease-modifying therapy.

Sick days and disability days

After initiation of natalizumab, the percentage of patients with MS-related and all-cause sick days decreased from the pre-index period by 27.6% (P<0.001) and 14.0% (P=0.011), respectively (Figure 6A, B). The percentages of patients with sick days also decreased in patients with and without prior DMT use; however, only the changes in the former group were statistically significant (Figure 6A, B). In contrast, changes in the mean number of MS-related and all-cause sick days were statistically significant for all patients regardless of previous DMT use (Table 2; Table S1). The mean number of MS-related sick days per patient was reduced by 8.0 days (P<0.001) for patients overall, by 7.7 days (P=0.003) for those with prior DMT use, and by 8.9 days (P=0.012) for those without prior DMT use. Similarly, the mean number of all-cause sick days was reduced by 8.3 days (P<0.001), 9.0 days (P=0.001), and 6.2 days (P=0.026), respectively. Both for patients with and without prior DMT use, changes in the proportion of patients with all-cause disability days and in the mean number of all-cause disability days (Table 2; Table S1) were not statistically significant.

Figure 6 Percentage of patients with (A) multiple sclerosis–related and (B) all-cause sick days.

Abbreviation: DMT, disease-modifying therapy.

Discussion

Natalizumab has been available in Germany since 2006.³⁰ Among German people with MS initiating natalizumab treatment between January 2009 and December 2012 in real-world settings, this study demonstrated significant reductions at 12 months in MS-related and all-cause hospitalizations and corticosteroid use. Administrative medical and pharmacy claims data from the German HRI research database showed that, from the pre- to the post-index period, the proportion of people with MS hospitalized for MS-related and all-cause events decreased by 72% and 52%, respectively, and the percentage of people with MS using corticosteroids was reduced by 62%. For MS-related and all-cause hospitalizations, per-person costs were reduced by nearly €3,000; for corticosteroid use, per-person costs were reduced by a mean of approximately €300. In this study, 75% of people with MS had used another DMT in the 12 months before starting treatment with natalizumab. The reductions in MS-related and all-cause hospitalizations and costs and MS-related and all-cause sick days were larger among people with MS without prior DMT use. In contrast, reductions in corticosteroid use and disability days were comparable between people with MS with and without prior DMT use. These findings are supported by studies in other countries of people with MS starting or switching to natalizumab.^31–33 In a similarly designed US-based analysis, significant reductions were observed in MS-related and all-cause hospitalizations, corticosteroid use, and associated costs after starting treatment with natalizumab.³¹ Seventy percent of people with MS had used pre-index DMT; for MS-related hospitalizations and costs, reductions were larger in the cohort of people with MS who had not used pre-index DMT.³¹ In an Italian observational study of people with RRMS who had continued disease activity after interferon beta or glatiramer acetate therapy, a significantly larger percentage of those who switched their therapy to natalizumab showed no evidence of disease activity compared with those who switched to another DMT after 24 months.³² In other studies, people with MS with breakthrough disease after the first-line therapy showed larger reductions in disease activity after switching from another DMT to natalizumab.^17,33,34

In a 2006 German cost-of-illness analysis, the mean total annual cost of MS per person was estimated at €40,000, two-fifths of which was related to decreased productivity owing to sick leave and early retirement.³ Decreased numbers of MS-related sick days (8.0 days) and all-cause sick days (8.3 days) in the first year following natalizumab treatment initiation in this study could correlate with a significant decline in the indirect costs of MS. In combination with the declines in direct medical costs also observed here, the addition of natalizumab to a treatment regimen for a person with MS could have a positive impact on the economic burden of MS in Germany. While decreases in the number of disability-related days were observed, these changes did not reach statistical significance. This may be due to the short 12-month followup period and/or the small number of disabled people with MS. In addition, DMT treatment may mitigate the number of people with MS who become disabled as 70% of the population is pretreated. Natalizumab significantly reduced MS and all-cause HRU and the associated costs. These reductions and cost offsets suggest that natalizumab may be a cost-effective treatment option for MS in Germany.

An analysis of SHI claims data showed that the prevalence of MS in Bavaria had increased by 42% from 2005 to 2009, corresponding to an overall projected prevalence of 142,856 people with MS in Germany in 2009.³⁰ In addition, the percentage of people with MS receiving ≥1 DMT increased from 46% in 2005 to 51% in 2009. Thus, given the increasing prevalence of MS and the increasing proportion of people with MS receiving multiple DMTs in Germany, the findings from the current study suggest that natalizumab may positively impact the high economic burden associated with HRU among German people with MS.⁴

As this is a descriptive study, these results should be interpreted in the context of certain limitations. First, although the HRI research database is generally representative of the German population, the relatively small sample size of this study restricts the extent to which the findings are generalizable to the German population of people with MS, at large. Furthermore, the study results may not be generalizable to pregnant women, as they were excluded from this analysis. It was not possible to evaluate clinical measures of effectiveness, including disability progression, as typically assessed by changes in Expanded Disability Status Scale scores, clinically identified relapses, and severity of the relapses, as this information is not available from the HRI research database. In addition, the time period of the analysis does not allow for a complete record of a person’s history with MS, including disease duration, prior treatment, or relapse, all of which may differ over time. Also, to have a comparable patient sample, only patients staying on natalizumab therapy were included.

These analyses were limited by the 1-year pre- and post-index periods, and future analyses can examine 2-year pre- and post-index periods, provided that sample sizes are large enough. These analyses were also limited to HRU (i.e., hospitalizations, corticosteroid use, and sick days) related to MS outcomes and did not include any DMT costs, such as the cost of natalizumab or DMT costs in the pre-index period. In addition, corticosteroid use may be underestimated in this study because its use in the inpatient setting could not be included in this analysis. Corticosteroid use was evaluated as a dichotomous outcome, and corticosteroid dosing changes around natalizumab were not evaluated. Future research should expand on this issue and describe corticosteroid dosing over time. Finally, in German claims data, outpatient visits are not coded with a diagnosis code, and emergency room (ER) visits cannot be assessed; therefore, MS-specific outpatient visits and ER visits were not included in this analysis.

Further research is warranted, including a more detailed analysis to evaluate study outcomes among people with MS by disease severity and to evaluate hospitalizations that may be preventable, thereby reducing HRU-related costs.

Conclusions

In a real-world setting in Germany, people with MS who initiated treatment with natalizumab demonstrated significant reductions in MS-related and all-cause inpatient stays and corticosteroid use with associated costs. Natalizumab was also associated with significant decreases from the pre-index period in the percentage of people with MS-related and all-cause sick days and in the mean number of MS-related and all-cause sick days. These findings suggest that the benefits of natalizumab, as demonstrated in clinical trials, translate into real-world reductions in MS-related and all-cause hospitalizations and corticosteroid use. In addition, people with MS without DMT use had a greater magnitude of reduction in both MS-related and all-cause inpatient utilization and costs following natalizumab initiation than people with MS with prior DMT use, further highlighting the need to start treatment early.

Acknowledgments

The study was sponsored by Biogen, and Biogen provided funding for editorial support in the development of this manuscript; Linda A. Goldstein (Infusion Communications, Haddam, CT, USA) wrote the first draft of the manuscript based on input from authors, and Joshua Safran and Melissa Austin (Infusion Communications) copyedited and styled the manuscript per journal requirements. Biogen reviewed and provided feedback on the manuscript to the authors. The authors had full editorial control of the manuscript and provided their final approval of all content.

The data analysis was performed with cooperation from Xcenda and Elsevier Health Analytics.

The abstract of this paper was presented at the ISPOR 20th Annual International Meeting in Philadelphia on May 16–20, 2015, as a poster presentation; the poster’s abstract was published in Value Health 2015;18(3):A284; available at http://www.valueinhealthjournal.com/article/S1098-3015(15)01716-7/abstract?_returnURL=http%3A%2F%2Flinkinghub.elsevier.com%2Fretrieve%2Fpii%2FS1098301515017167%3Fshowall%3Dtrue.

Supplementary material

Table S1 Health care resource utilization among the subgroups of patients with and without prior DMT use before and after initiating treatment with natalizumab

Health care resource utilization	Patients with prior DMT use (n =145)				Patients without prior DMT use (n =48)
	Pre-index	Post-index	Change	P-value	Pre-index	Post-index	Change	P-value
Number of hospitalizations
MS-related
Mean (SD)	1.1 (1.5)	0.2 (0.7)	−0.9 (1.4)	<0.001	0.9 (1.3)	0.1 (0.4)	−0.8 (1.2)	<0.001
Median (range)	1 (0, 8)	0 (0, 5)	0 (−6, 3)		0 (0, 5)	0 (0, 2)	0 (−4, 1)
All-cause
Mean (SD)	1.4 (1.8)	0.50 (1.3)	−0.9 (1.8)	<0.001	1.2 (1.7)	0.3 (0.6)	−1.0 (1.7)	<0.001
Median (range)	1 (0, 9)	0 (0, 11)	0 (−7, 9)		1 (0, 8)	0 (0, 3)	−0.5 (−8, 2)
Number of inpatient days
MS-related
Mean (SD)	7.2 (11.2)	3.4 (23.5)	−3.8 (23.2)	<0.001	6.3 (9.3)	0.6 (2.1)	−5.7 (8.6)	<0.001
Median (range)	4 (0, 62)	0 (0, 277)	0 (−62, 238)		0 (0, 36)	0 (0, 13)	0 (−35, 2)
All-cause
Mean (SD)	9.8 (16.0)	5.6 (25.6)	−4.1 (25.2)	<0.001	9.2 (18.4)	3.0 (15.3)	−6.2 (24.5)	<0.001
Median (range)	4 (0, 104)	0 (0, 277)	0 (−66, 238)		1.5 (0, 113)	0 (0, 105)	−1.5 (−113, 105)
Corticosteroid use
Mean (SD)	2.6 (2.5)	0.5 (1.0)	−2.0 (2.4)	<0.001	2.1 (2.4)	0.9 (1.9)	−1.2 (2.1)	<0.001
Median (range)	2 (0, 19)	0 (0, 4)	−2 (−19, 3)		1 (0, 10)	0 (0, 8)	−0.5 (−7, 3)
Number of sick days
MS-related
Mean (SD)	32.6 (55.5)	24.9 (61.2)	−7.7 (65.2)	0.003	21.4 (44.5)	12.5 (33.8)	−8.9 (39.0)	0.012
Median (range)	4 (0, 326)	0 (0, 366)	0 (−308, 311)		0 (0, 209)	0 (0, 165)	0 (−162, 146)
All-cause
Mean (SD)	39.4 (61.1)	30.4 (64.5)	−9.0 (66.3)	0.001	26.7 (49.5)	20.5 (50.8)	−6.2 (56.1)	0.026
Median (range)	10 (0, 330)	1 (0, 366)	0 (−312, 256)		0 (0, 213)	0 (0, 270)	0 (−166, 249)
Number of all-cause disability days
Mean (SD)	37.8 (90.9)	45.7 (105.5)	7.9 (65.1)	0.386	19.1 (61.9)	21.7 (68.0)	2.6 (49.1)	1.000
Median (range)	0 (0, 365)	0 (0, 366)	0 (−158, 365)		0 (0, 365)	0 (0, 366)	0 (−123, 249)

Abbreviations: DMT, disease-modifying therapy; MS, multiple sclerosis; SD, standard deviation.

Disclosure

Crystal Watson, Erika Gleissner, and Sarah Naoshy are employees of and hold stock/stock options in Biogen. Chris-tine Prosser, Sebastian Braun, and Pamela B Landsman-Blumberg are employees of Xcenda, which has a research consultancy agreement with Biogen. The authors report no other conflicts of interest in this work.