throbber
J Neurol (2008) 255 [Suppl 6]:87–92
`DOI 10.1007/s00415-008-6016-8
`
`Thomas Klauer
`Uwe K. Zettl
`
`Compliance, adherence, and the treatment
`of multiple sclerosis
`
`■ Abstract With the availability of
`disease-modifying, immunomodu-
`
`Dr. T. Klauer (쾷)
`Medizinische Fakultät der Universität
` Rostock
`Klinik und Poliklinik für Psychosomatik
`und Psychotherapeutische Medizin
`Gehlsheimer Str. 20
`18147 Rostock, Germany
`E-Mail: thomas.klauer@med.uni-rostock.de
`Prof. Dr. U. K. Zettl
`Medizinische Fakultät der Universität
` Rostock
`Klinik und Poliklinik für Neurologie
`Gehlsheimer Str. 20
`18147 Rostock, Germany
`
`latory therapies (DMT) for multi-
`ple sclerosis (MS) and the first
`long-term studies, it became obvi-
`ous that problems of compliance to
`complex treatment regimens under
`chronic conditions would also ap-
`ply to these approaches. In a selec-
`tive overview, problems and find-
`ings of adherence research are
`depicted. Based on a discussion of
`basic concepts, issues of operation-
`ally defining and measuring adher-
`ence are outlined. Descriptive find-
`ings on adherence to DMTs and
`empirical predictors of nonadher-
`
`ence are then discussed. Referring
`to theoretical models of treatment
`motivation, selected problems (e. g.,
`indication) and strategies of pro-
`moting adherence are described.
`Finally, implications of modern
`concepts of the patient-therapist
`relationship for the issue of patient
`adherence are considered.
`
`■ Key words multiple sclerosis ·
`compliance · adherence ·
`immunomodulatory treatment ·
`counseling
`
`for further morbidity and mortality and as a waste of
`health care resources. Nevertheless, it is a frequent phe-
`nomenon with proportions from 12 % (HIV disease) up
`to 33 % (diabetes) of nonadherent patients in various di-
`agnostic groups with an average nonadherence rate of
`nearly 25 % [6]. This estimate from a meta-analysis is
`similar to findings on adherence to immunomodulatory
`treatment (disease-modifying therapy, DMT) of multi-
`ple sclerosis (MS). According to a recent review [12], em-
`pirically observed nonadherence rates in DMTs vary be-
`tween 6 % and 43 %. Differences in definitions and
`measures of adherence considerably contribute to these
`variations.
`
`Definition and assessment of (non-)adherence
`
`JON 6016
`
`Adherent behavior may constitute a difficult task for pa-
`tients especially in chronic and complex conditions. Ac-
`cording to Meichenbaum and Turk [14], this task com-
`prises six domains of behavior, i. e., (1) utilization and
`consequent maintenance of therapy, (2) to keep treat-
`
`Introduction
`
`Even highly potent medical treatments may be limited
`in their effectiveness by the degree to which patients
`continue to exactly follow the treatment procedure (e. g.,
`medication) over the entire treatment course (compli-
`ance). Recently, the term “adherence” has been preferred
`over the concept of compliance because of the authori-
`tative and paternalistic connotations of the latter. Ad-
`herence has been defined as “the extent to which a per-
`son’s behaviour – taking medication, following a diet,
`and/or executing lifestyle changes, corresponds with
`agreed recommendations from a health care provider”
`([30], p. 3). Frequently, more specific aspects of adher-
`ence like persistence (i. e., the time interval between the
`first application of a medicament and withdrawal from
`continuous application contrary to the health care pro-
`vider’s recommendation) and performance quality (i. e.,
`stability regarding dosation scheme and mode of appli-
`cation) are further distinguished [4].
`Nonadherence is usually seen as an unnecessary risk
`
`MYLAN INC. EXHIBIT NO. 1043 Page 1
`
`

`
`88
`
`ment and aftercare appointments, (3) to take drugs cor-
`rectly, (4) to actively change health lifestyles, (5) to do
`treatment-related “homework” and (6) to reduce risk
`behaviors (e. g., smoking).
`The more complex the task of treatment adherence
`presents for patients, the more difficult it is to distin-
`guish nonadherence from incomplete adherence. For re-
`search purposes, operationally defined criteria have
`been introduced (e. g., taking correctly 80 % of the med-
`ication or more; 33 % missed applications over one
`month [19, 28]). When comparing different medication
`schedules and preparations (e. g., in the immunomodu-
`latory treatment of MS; [29]), operational standard mea-
`sures of adherence also have to be developed.
`In contrast to complete adherence, nonadherent be-
`havior is a manifold phenomenon. Major types of non-
`adherence are (1) complete refusal of therapy, (2) refusal
`of specific treatment options and (3) arbitrary or unin-
`tended modification of prescriptions. Moreover, several
`subtypes can be distinguished which include intentional
`clandestine (“covert”) noncompliance, but also supple-
`mentation of medication by commercially available
`drugs as well as drug intake without an indication (“hy-
`percompliance”; [19]).
`A number of instruments has been developed to as-
`sess adherence, which are usually divided into the cate-
`gories of direct and indirect measures. The most fre-
`quently applied and, at the same time, most unreliable
`assessment approach, i. e., the patient self-report, is sub-
`sumed among the indirect approaches in which adher-
`ence is inferred from indicator variables. Even when
`compared to other indirect measures like, e. g., pill
`counts, prescriptions and pharmacy files, patients (as
`well as their physicians) tend to overestimate adherence
`so much that this procedure is widely seen as inappro-
`priate. Among the indirect measures, electronic registra-
`tion of medication consumption by Medical Event Mon-
`
`Table 1 Adherence to immunomodulatory treatment of MS in selected studies
`
`itoring systems (e. g., electronic pill-boxes) are preferred
`especially in naturalistic studies and have been devel-
`oped for a wide range of medication modalities in inter-
`nal medicine, neurology, and ophthalmology.
`In clinical studies, direct measures of adherence are
`indispensable in which medication intake is assessed in
`an unmediated way. This is accomplished either by di-
`rect surveillance of intake, which can only rarely be re-
`alized in practical care, or by verification of the active
`agent or its metabolites, but also of marker substances in
`the blood or urine. These approaches require sensitive
`biochemical detection methods in order to avoid false
`negative findings.
`
`Adherence to immunomodulatory treatment of MS
`
`Immunomodulators like interferon beta (IFNβ-) 1a,
`IFNβ-1b, and glatiramer acetate are central components
`of MS platform therapy which should reduce the devel-
`opment of new lesions in the central nervous system, the
`frequency of exacerbations, and both physical and cog-
`nitive impairment. The most severe demand that immu-
`nomodulatory treatment imposes upon patients is that
`it involves medication that must be injected highly fre-
`quent (every day, every other day, or once a week) over
`an extended period of time (months or even years) sub-
`cutaneously or intramuscularly. Benefits of DMTs will
`not be positively experienced by the patients, but should
`appear as reduced frequency of exacerbations. Instead,
`flu-like side effects including flushing, chest pain, palpi-
`tations and dyspnea are frequent and challenge the pa-
`tient's adherence.
`In empirical studies of DMT adherence (Table 1),
`these side-effects and perceived lack of treatment effi-
`cacy were most frequently mentioned as reasons for dis-
`continuation by patients [12]. As in adherence studies in
`
`Sample
`size
`
`Course
`of MS
`
`Type of study
`
`Time frame
`
`Nonadherence %
`
`Remarks
`
`12.9
`15.3 – 41.1
`39.3
`27
`21.2
`30.2
`14 (RRMS)
`23 (SPMS)
`13.5 (RRMS)
`30 (SPMS)
`12.9
`45.8
`
`Trained patients
`
`Trained patients
`
`Switchers included
`
`Study
`
`Mohr et al. [17]
`Milanese et al. [15]
`Ruggieri et al. [23]
`Tremlett & Oger [28]
`Fraser et al. [[8]
`Haas & Firzlaff [9]
`O'Rourke & Hutchinson [18]
`
`Year
`
`2001
`2003
`2003
`2003
`2004
`2005
`2005
`
` 101
`1481
` 122
` 844
` 108
` 308
` 394
`
`RR
`RR
`RR
`RR
`RR, SP
`RR
`RR, SP
`
`Prospective, telephone report
`Prospective
`Prospective
`Retrospective, hospital charts
`Prospective
`Prospective
`Retrospective, hospital charts
`
`6 months
`3 years
`5 years
`6 months
`6 months
`2 years
`3 years
`
`Rio et al. [22]
`
`2005
`
` 622
`
`RR, SP
`
`Retrospective
`
`Md = 47 months
`
`Turner et al. [29]
`Portaccio et al. [20]
`
`2007
`2008
`
` 90
` 225
`
`n.a.
`RR
`
`Prospective
`Retrospective
`
`6 months
`M = 4.2 years
`
`M mean; Md median; RR relapse-remitting; SP secondary-progressive
`
`MYLAN INC. EXHIBIT NO. 1043 Page 2
`
`

`
`
`
`
`
`89
`
`other diagnostic groups, proportions of nonadherent
`patients vary within a broad range between nearly 13
`and nearly 46 % of patients, depending on type of study,
`follow-up interval, definition of nonadherence, course
`of MS, and immunomodulators. Results from pivotal
`clinical studies (which are not considered here) mostly
`yielded results below this range.
`While differences between the various immunomod-
`ulators are not consistent and confounded with type of
`study, adherence seems to be higher in patients with re-
`lapse-remitting (RR) than with secondary-progressive
`(SP) course [18, 22]. Most drop-outs seem to occur within
`the first two years of treatment [12]. Most studies con-
`verge in that the risk of nonadherence grows with higher
`extended disability scale scores (EDSS). Moreover, non-
`adherence rates are higher in studies from clinical prac-
`tice as compared to large-scale prospective studies.
`Besides selection biases, a reason for this observation
`might be that in clinical practice switches between im-
`munomodulatory drugs are common [18] and may have
`been erroneously categorized as cases of nonadherent
`behavior in some studies. Differences between studies
`may also result from differences in the amount of train-
`ing and information patients had received before enter-
`ing immunomodulatory treatment (e. g., [17]).
`
`Determinants of adherence
`
`Missing treatment effects or undesirable side effects em-
`pirically explain only medium amounts of variance in
`adherence. Besides characteristics of treatment, (1) dis-
`ease characteristics, (2) patient variables, (3) quality of
`the patient-therapist relationship, (4) treatment setting
`and (5) influences from the social environment can be
`distinguished as important determinants of adherent
`behavior [19].
`Among patient characteristics, informational defi-
`cits, motivational deficits, and psychological disorders
`have most frequently been discussed. Obviously, adher-
`ence is most strongly threatened by disorders that spe-
`cifically and directly interfere with medication applica-
`tion like, e. g. injection phobia in the immunomodulatory
`treatment of multiple sclerosis [17] or treatment of dia-
`betes. Depression represents a more general risk to ad-
`herent behavior.
`Informational deficits in the patients which can lead
`to problems like, e. g., instable intake contingencies, have
`long been regarded as a result of an inaccurate patient-
`physician communication. In many areas of medicine,
`attempts have been undertaken to optimize communi-
`cation and to place it on a more cooperative foundation
`(e. g., shared decision-making; [10]). In psychological
`approaches to subjective theories of illness [13], it is as-
`sumed that uncommunicated, dissenting lay concepts of
`patients lead to a selective encoding of illness-related in-
`
`formation and to biased information processing. Subse-
`quently, patients might avoid confronting therapists
`with their diverging ideas. In this process of developing
`nonadherence, risks of abandoning intake are frequently
`underestimated.
`Psychological models of adherence mostly refer to
`motivational factors like degree of suffering, lay etiology
`or treatment expectations [24]. Usually, it is assumed
`that higher levels of suffering and more positive expec-
`tations regarding treatment effectiveness should go
`along with greater adherence. However, the concept of
`treatment expectations is multidimensional: subjective
`probabilities of desired and undesired consequences of
`adherent and nonadherent behavior should similarly
`determine compliance to somatic as well as psychologi-
`cal treatment; these probabilities have been systemati-
`cally described within expectancy-values approaches
`(e. g., [19]).
`One of the first theoretical accounts for compliant be-
`havior was the Health Beliefs Model (HBM; [1]). Accord-
`ing to the HBM, the individual tendency to engage in
`preventive health behaviors as well as compliant behav-
`iors under treatment is influenced by four types of ex-
`pectations: (1) the perceived severity of an illness, (2)
`the perceived vulnerability to that illness, (3) the per-
`ceived benefits expected from a specific health behavior
`and (4) the perceived barriers to engage in a specific
`health behavior. Recently, the HBM has been applied to
`immunomodulatory treatment of MS [29] using one of
`the three beta interferon (IFNβ) preparations or glati-
`ramer acetate. Treatment adherence as well as satisfac-
`tion at the 2-, 4-, and 6-month follow-ups were consis-
`tently predicted only by perceived benefits but not by
`the other model variables. However, expectations re-
`garding treatment outcomes may also be unrealistically
`positive, and patients holding them are at risk to discon-
`tinue treatment because of frustration and disappoint-
`ment.
`Since treatment adherence over longer periods of
`time has turned out to be a dynamic and probably un-
`stable phenomenon, process or stage models of health
`behavior change have also been proposed to explain in-
`terindividual differences. In the Transtheoretical Model
`(TTM) of health behavior change [21] it is assumed that
`patients pass through a progressive sequence of stages
`of readiness for change. As defined in the model, these
`stages include (1) precontemplation (i. e., not thinking
`about changing behavior in the next six months), (2)
`contemplation (thinking about changing the behavior
`in the next six months but not in the next 30 days), (3)
`preparation (ready to change in the next 30 days), (4) ac-
`tion (changed fewer than six months ago) and (5) main-
`tenance (changed the behavior more than six months
`ago). Since empirical tests of the model challenged dis-
`tinctiveness of the stages as well as unidirectionality of
`the change process [7], criteria were reformulated less
`
`MYLAN INC. EXHIBIT NO. 1043 Page 3
`
`

`
`90
`
`restrictively, and additional variables were integrated
`like, e. g., "pros" and "cons" of changing as well as per-
`ceived barriers. The TTM has been applied to the dis-
`continuation of immunomodulatory treatment of MS
`with IFNβ-1a and was found to correctly identify 82 %
`of the nonadherent and 81 % of the adherent patients to-
`gether with level of education and disability as predic-
`tors [2].
`Self-efficacy is another type of expectancy that has
`been frequently shown to predict a wide range health
`behaviors [25]. It is defined as the subjective probability
`to be able to perform a health-related behavior or, more
`specifically, concrete action in support of medical treat-
`ment. Self-efficacy expectations should be especially rel-
`evant in the "post-intentional" phase of treatment moti-
`vation when compliant behavior has to be maintained in
`the face of barriers and obstacles like, e. g., negative side
`effects [26]. Mohr et al. [17] found self-injection self-ef-
`ficacy before and during IFNβ-1a therapy to predict
`treatment adherence after six months. In a prospective
`study on glatiramer acetate [8], adherent and nonadher-
`ent patients significantly differed on the Multiple Scle-
`rosis Self-Efficacy Scale (MSSE; [27]).
`A comprehensive model of treatment adherence
`should not only integrate patient, therapist, illness and
`treatment factors but also exogenous influences espe-
`cially from the social environment. Social support from
`spouses and friends may contribute much to the adher-
`ent behavior of the patients: According to meta-analytic
`results [5], patients lacking instrumental social support
`(e. g., material aid, assistance in practical problem-solv-
`ing) bear a 3.6-fold higher risk of nonadherence. Thus,
`it might be useful to include patients' relatives in adher-
`ence-related interventions.
`
`Interventions to promote adherence
`
`Because determinants of nonadherence are manifold and
`heterogeneous, patients at risk should undergo detailed
`assessment along the above mentioned categories of vari-
`ables to ensure that adequate strategies of compliance
`promotion are assigned. For example, patient education
`focusing on illness-related information should not be ap-
`propriate to resolve motivational deficits which interfere
`with regular intake of medication. Following the identifi-
`cation of patients at risk by certain key features (e. g., neg-
`ative experiences with similar treatments; difficult social
`environment; [19]), a diagnostic sequence assessing defi-
`cits in illness-related knowledge (indication for informa-
`tion), deficits in practical skills (indication for education)
`and, finally, motivational deficits (indication for motiva-
`tional intervention) has been suggested [11]. More spe-
`cific diagnostic procedures may then be used to identify
`target variables for intervention in individual patients
`(e. g., unrealistic treatment expectations).
`
`While MS patients are often well equipped with in-
`formation and skills (e. g., by self-injection training),
`only few motivational interventions have been proposed
`for this group. To enhance treatment motivation and ad-
`herence, interventions have to be tailored to the specific
`deficits of the patients and to consider the more general
`aims and incentives patients are committed to in their
`lives as well as the stage of change patients are actually
`in. Group intervention approaches to promote adher-
`ence, thus, should be designed flexible as well as compre-
`hensive and involve informational, behavioral, and mo-
`tivational components.
`An initial aim of such interventions is to encourage
`patients to take responsibility for their treatment. For
`example, self-commitment to change is a central con-
`cept of motivational interviewing (MI), a counseling
`strategy which has been transferred from addiction
`therapy to many other areas of medicine and clinical
`psychology [16]. Basic principles of MI are cooperation,
`activation of intrinsic motivation, and autonomy. These
`principles are reflected in an empathetic style of coun-
`seling, active listening, abandonment of reasoning to
`avoid patient resistance and addressing the patients’
`ambivalence regarding treatment continuation. Specific
`strategies of MI are, e. g., enhancement of problem rec-
`ognition, the promotion of self-efficacy, and the config-
`uration of change plans with respect to time criteria.
`Some specific aspects of MI were integrated into a soft-
`ware-based telephone counseling intervention [3]; in a
`study with 366 patients, it could be shown that adher-
`ence to IFNβ treatment was remarkably higher in the in-
`tervention group (98.8 %) compared to standard care
`controls (91.3 %).
`
`Conclusions
`
`In many cases, treatment of chronic disease challenges
`the patients’ self-management skills and motivational
`resources by demanding medication intake, following a
`diet, and changing the individual lifestyle. This applies
`also to standard immunomodulatory therapies of mul-
`tiple sclerosis which require the careful maintenance of
`(self-)injection schedules and, sometimes, the tolerance
`of undesired side effects. As in other chronic conditions,
`a substantial proportion of patients does not adhere to
`treatment at least for some time.
`Nonadherence rates reported from studies with MS
`patients vary within a broad range between nearly 13
`and nearly 46 % of patients, depending on type of study,
`follow-up interval, definition of nonadherence, course
`of MS, and immunomodulators. Current evidence indi-
`cates that a progressive course of MS, higher disability,
`lower self-efficacy, lower motivation to change, and
`lower perceived benefits predict nonadherence to DMTs
`in multiple sclerosis. One of the few studies on adher-
`
`MYLAN INC. EXHIBIT NO. 1043 Page 4
`
`

`
`
`
`
`
`91
`
`ence interventions in MS patients showed that tele-
`phone-based counseling using a motivational interview-
`ing strategy contributed to a reduction of discontinuation
`rates. Nevertheless, nonadherence remains a serious
`problem in the treatment of MS.
`Usually, nonadherence is regarded as a risk for pa-
`tient morbidity and mortality and as an unnecessary
`economical burden for the health care system. Nonad-
`herent behavior has mostly been attributed to deficits in
`cognitive or motivational characteristics of the patient,
`in the patient-therapist communication, in the treat-
`ment setting or in the social support networks of the pa-
`tients. However, in modern reformulations of the pa-
`tient-therapist relationship preferring strategies like
`empowerment and shared decision-making, the concept
`of nonadherence has also undergone a change of mean-
`ing [10]: From the perspective of the expert patient, who
`
`is well informed about the limitations of treatment ef-
`fectiveness, nonadherent behavior may well be the result
`of critical reflection of treatment options against the
`background of more general aspirations and aims in life.
`The heterogeneity of variations of (post-)intentional
`nonadherence suggests that the simple dichotomy of ad-
`herent and nonadherent patients might be too simple
`and not helpful in modern health care. Open communi-
`cation between patients and health-care providers as
`well as shared decision-making should help to “uncover”
`intentional nonadherence of the clandestine type and,
`thus, to make the treatment process more efficient with
`regard to medical and economical outcomes.
`
`■ Conflict of interest The authors have no conflict of interest to de-
`clare.
`
`References
`
` 1. Becker MH (1974) The health-belief
`model and personal health behavior.
`Charles B. Slack, Thorofare
` 2. Berger BA, Hudmon KS, Liang H
`(2004) Predicting treatment discontin-
`uation among patients with multiple
`sclerosis: Application of the transtheo-
`retical model of change. J Am Pharm
`Assoc 44:445–454
` 3. Berger BA, Liang H, Hudmon KS
`(2005) Evaluation of software-based
`telephone counseling to enhance
` medication persistency among pa-
`tients with multiple sclerosis. J Am
`Pharm Assoc 45:466–472
` 4. Cramer JA, Roy A, Burrell A, Fairchild
`CJ, Fuldeore MJ, Ollendorf DA, Wong
`PK (2008) Medication compliance and
`adherence. Value in Health 11:44–47
` 5. DiMatteo MR (2004) Social support
`and patient adherence to medical
`treatment: A meta-analysis. Health
`Psychol 23:207–217
` 6. DiMatteo MR (2004) Variations in
` patients’ adherence to medical re-
`commendations: A quantitative review
`of 50 years of research. Med Care 42:
`200–209
` 7. Drieschner KH, Lammers SMM, van
`der Staak CPF (2004) Treatment moti-
`vation: An attempt for clarification of
`an ambiguous concept. Clin Psychol
`Rev 23:1115–1137
` 8. Fraser C, Morgante L, Hadjimichael O,
`Vollmer T (2004) A prospective study
`of adherence to glatiramer acetate in
`indivuals with multiple sclerosis.
`J Neurosc Nurs 36:120–129
`
` 9. Haas J, Firzlaff M (2005) Twenty-four
`month comparison of immunomodu-
`latory treatments – a retrospective
`open label study in 308 RRMS patients
`treated with beta interferons or glati-
`ramer actetate. Eur J Neurol 12:
`425–431
`10. Heesen C, Berger B, Hamann J, Kasper
`J (2006) Empowerment, Adhärenz,
` evidenzbasierte Patienteninformation
`und partizipative Entscheidungs-
`findung bei MS – Schlagworte oder
`Wegweiser? Neurol Rehabil 12:232–238
`11. Kanfer FH, Reinecker H, Schmelzer D
`(1996) Selbstmanagementtherapie (2nd
`ed.) Springer, Berlin
`12. Kern S, Reichmann H, Ziemssen T
`(2008) Therapieadhärenz in der neu-
`rologischen Praxis. Nervenarzt 79:
`877–890
`13. Leventhal H, Meyer D, Nerenz D (1980)
`The common sense representation of
`illness danger. In: Rachman S (ed)
`Contributions to medical psychology
`(vol. 2). Pergamon, New York, pp 7–30
`14. Meichenbaum D, Turk DC (1987)
` Facilitating treatment adherence: A
`practitioner’s guidebook. Plenum, New
`York
`15. Milanese C, LaMantia L, Palombo R,
`et al (2003) A post-marketing study on
`interferon β 1b and 1a treatment in
` relapse-remittting multiple sclerosis:
`Different response in drop-outs and
`treated patients. J Neurol Neurosurg
`Psychiatry 74:1689–1692
`16. Miller WR, Rollnick S (1991) Motiva-
`tional interviewing: Preparing people
`to change addictive behavior. Guilford,
`New York
`
`17. Mohr DC, Boudewyn AC, Likosky W,
`Levine E, Goodkin DE (2001) Inject-
`able medication for the treatment of
`multiple sclerosis: The influence of
`self-efficacy expectations and injection
`anxiety on adherence and ability to
`self-inject. Ann Behav Med 23:125–132
`18. O’Rourke KET, Hutchinson M (2005)
`Stopping beta-interferon therapy in
`multiple sclerosis: An analysis of stop-
`ping patterns. Mult Scler 11:46–50
`19. Petermann F, Mühlig S (1998) Grund-
`lagen und Möglichkeiten der Compli-
`ance-Verbesserung. In: Petermann F
`(ed) Compliance und Selbstmanage-
`ment. Hogrefe, Göttingen, pp 73–102
`20. Portaccio E, Zipoli V, Siracusa G, Sorbi
`S, Amato MP (2008) Long-term adher-
`ence to interferon β therapy in relapse-
`remitting multiple sclerosis. Eur Neu-
`rol 59:131–135
`21. Prohaska JO, DiClemente CC (1982)
`Transtheoretical psychotherapy:
` Toward a more integrative model of
`change. Psychother Theory Res Pract
`19:276–288
`22. Rio J, Porcel J, Téllez N, Sánchez-
`Betancourt A, Tintoré M, Arévalo MJ,
`Nos C, Montalban X (2005) Factors
` related with treatment adherence to
`interferon β and glatiramer acetate
`therapy in multiple sclerosis. Mult
`Scler 11:306–309
`23. Ruggieri RM, Settipani N, Viviano L,
`Attanasio M, Giglia L, Almasio P, La
`Bella V, Piccoli F (2003) Long-term
` interferon-beta treatment for multiple
`sclerosis. Neurol Sci 24:361–364
`
`MYLAN INC. EXHIBIT NO. 1043 Page 5
`
`

`
`92
`
`24. Schneider W (1990) Die Psychothera-
`piemotivation – Behandlungs-
`voraussetzung oder ein zu vernachläs-
`sigendes Konstrukt? In: Schneider W
`(ed), Indikationen zur Psychotherapie.
`Beltz, Weinheim, pp 183–201
`25. Schwarzer R (1992) Self-efficacy in the
`adoption and maintenance of health
`behaviors: Theoretical approaches and
`a new model. In: Schwarzer R (ed) Self-
`efficacy: Thought control of action.
`Hemisphere, Washington, pp 217–242
`
`26. Schwarzer R, Luszczynska A (2005)
`Compliance als universelles Problem
`des Gesundheitsverhaltens. In:
`Schwarzer R (ed) Gesundheitspsycho-
`logie (Enzyklopädie der Psychologie,
`Vol. C/X/1). Hogrefe, Göttingen,
`pp 585–601
`27. Schwartz CE, Coulthard-Marris L,
`Zeng Q, Retzlaff P (1996) Measuring
`self-efficacy in people with multiple
`sclerosis: A validation study. Arch Phys
`Med Rehab 77:394–398
`
`28. Tremlett HL, Oger J (2003) Interrupted
`therapy: Stopping and switching of the
`ß-interferons prescribed for MS. Neu-
`rol 61:551–554
`29. Turner AP, Kivlahan DR, Sloan AP,
`Haselkorn JK (2007) Predicting ongo-
`ing adherence to disease modifying
`therapies in multiple sclerosis: Utility
`of the Health Beliefs Model. Mult Scler
`13:1146–1152
`30. World Health Organization (2003)
` Adherence to long-term therapies:
` Evidence of action. WHO, Geneva
`
`MYLAN INC. EXHIBIT NO. 1043 Page 6

This document is available on Docket Alarm but you must sign up to view it.


Or .

Accessing this document will incur an additional charge of $.

After purchase, you can access this document again without charge.

Accept $ Charge
throbber

Still Working On It

This document is taking longer than usual to download. This can happen if we need to contact the court directly to obtain the document and their servers are running slowly.

Give it another minute or two to complete, and then try the refresh button.

throbber

A few More Minutes ... Still Working

It can take up to 5 minutes for us to download a document if the court servers are running slowly.

Thank you for your continued patience.

This document could not be displayed.

We could not find this document within its docket. Please go back to the docket page and check the link. If that does not work, go back to the docket and refresh it to pull the newest information.

Your account does not support viewing this document.

You need a Paid Account to view this document. Click here to change your account type.

Your account does not support viewing this document.

Set your membership status to view this document.

With a Docket Alarm membership, you'll get a whole lot more, including:

  • Up-to-date information for this case.
  • Email alerts whenever there is an update.
  • Full text search for other cases.
  • Get email alerts whenever a new case matches your search.

Become a Member

One Moment Please

The filing “” is large (MB) and is being downloaded.

Please refresh this page in a few minutes to see if the filing has been downloaded. The filing will also be emailed to you when the download completes.

Your document is on its way!

If you do not receive the document in five minutes, contact support at support@docketalarm.com.

Sealed Document

We are unable to display this document, it may be under a court ordered seal.

If you have proper credentials to access the file, you may proceed directly to the court's system using your government issued username and password.


Access Government Site

We are redirecting you
to a mobile optimized page.





Document Unreadable or Corrupt

Refresh this Document
Go to the Docket

We are unable to display this document.

Refresh this Document
Go to the Docket