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  • 1
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2001
    In:  Disease Management and Health Outcomes Vol. 9, No. 4 ( 2001), p. 203-213
    In: Disease Management and Health Outcomes, Springer Science and Business Media LLC, Vol. 9, No. 4 ( 2001), p. 203-213
    Type of Medium: Online Resource
    ISSN: 1173-8790
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2001
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  • 2
    Online Resource
    Online Resource
    American Society of Clinical Oncology (ASCO) ; 2014
    In:  Journal of Clinical Oncology Vol. 32, No. 4_suppl ( 2014-02-01), p. 267-267
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO), Vol. 32, No. 4_suppl ( 2014-02-01), p. 267-267
    Abstract: 267 Background: Oral medications have become more widely available for treatment of various cancers, and adherence to dosing/ refill patterns, or medication possession, are important considerations for treatment. Abiraterone acetate (AA), prodrug of aberaterone, is a novel oral androgen biosynthesis inhibitor approved for metastatic castration resistant prostate cancer. This study reports adherence to AA dosing and administration recommendations by prostate cancer (PC) patients as observed in two separate data sources. Methods: PC patients with ≥1 AA prescription fill were identified in two retrospective pharmacy claim data sources: (1) Truven Commercial Claims and Encounters; and (2) Symphony ProMetis. Patients with no evidence of recent chemotherapy (NRC) or with evidence of recent chemotherapy (RC) were identified in the 6 months prior to AA initiation. The average AA daily dose per prescription per patient was reported. To evaluate adherence, the Medication Possession Ratio (MPR), a measure of consistency calculated as the sum of the AA days of supply divided by the total number of days between first and end of last AA fill, was assessed for patients with ≥2 AA fills. Data were summarized by descriptive statistics. Results: In both datasets the mean medication consistency/MPR was greater than 90% and the mean daily dose was within 1% of the recommended daily dose (1,000 mg). Medication consistency and AA daily dose per patient appeared similar between patients with recent chemotherapy and patients without recent chemotherapy (Table). Conclusions: Results from two observational studies representing 〉 3,700 PC patients reported high levels of AA adherence to AA dosing and administration consistent with prescribing information. Such data support providers’ understanding of the consistency to which AA treated PC patients adhere to AA medication use. [Table: see text]
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
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    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2014
    detail.hit.zdb_id: 2005181-5
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  • 3
    Online Resource
    Online Resource
    SAGE Publications ; 2012
    In:  Journal of Diabetes Science and Technology Vol. 6, No. 3 ( 2012-05), p. 555-562
    In: Journal of Diabetes Science and Technology, SAGE Publications, Vol. 6, No. 3 ( 2012-05), p. 555-562
    Type of Medium: Online Resource
    ISSN: 1932-2968 , 1932-2968
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2012
    detail.hit.zdb_id: 2467312-2
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  • 4
    In: Annals of General Psychiatry, Springer Science and Business Media LLC, Vol. 10, No. 1 ( 2011-12)
    Abstract: Because wide variations in mental health care utilization exist throughout the world, determining long-term effectiveness of psychotropic medications in a real-world setting would be beneficial to physicians and patients. The purpose of this analysis was to describe the effectiveness of injectable risperidone long-acting therapy (RLAT) for schizophrenia across countries. Methods This was a pragmatic analysis of data from two prospective observational studies conducted in the US (Schizophrenia Outcomes Utilization Relapse and Clinical Evaluation [SOURCE]; ClinicalTrials.gov registration number for the SOURCE study: NCT00246194) and Spain, Australia, and Belgium (electronic Schizophrenia Treatment Adherence Registry [eSTAR] ). Two separate analyses were performed to assess clinical improvement during the study and estimate psychiatric hospitalization rates before and after RLAT initiation. Clinical improvement was evaluated using the Clinical Global Impressions-Severity (CGI-S) and Global Assessment of Functioning (GAF) scales, and change from baseline was evaluated using paired t tests. Psychiatric hospitalization rates were analyzed using incidence densities, and the bootstrap resampling method was used to examine differences between the pre-baseline and post-baseline periods. Results The initial sample comprised 3,069 patients (US, n = 532; Spain, n = 1,345; Australia, n = 784; and Belgium, n = 408). In all, 24 months of study participation, completed by 39.3% (n = 209), 62.7% (n = 843), 45.8% (n = 359), and 64.2% (n = 262) of patients from the US, Spain, Australia, and Belgium, respectively, were included in the clinical analysis. Improvements compared with baseline were observed on both clinical assessments across countries ( P 〈 0.001 at all post-baseline visits). The mean improvement was approximately 1 point on the CGI-S and 15 points on the GAF. A total of 435 (81.8%), 1,339 (99.6%), 734 (93.6%), and 393 (96.3%) patients from the US, Spain, Australia, and Belgium, respectively, had ≥1 post-baseline visit and were included in the analysis of psychiatric hospitalization rates. Hospitalization rates decreased significantly in all countries regardless of hospitalization status at RLAT initiation ( P 〈 0.0001) and decreased significantly in the US and Spain ( P 〈 0.0001) when the analysis was limited to outpatients only. Conclusions RLAT in patients with schizophrenia was associated with improvements in clinical and functional outcomes and decreased hospitalization rates in the US, Spain, Australia, and Belgium, despite differences in health care delivery systems.
    Type of Medium: Online Resource
    ISSN: 1744-859X
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2011
    detail.hit.zdb_id: 2090401-0
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  • 5
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2010
    In:  Annals of General Psychiatry Vol. 9, No. 1 ( 2010-12)
    In: Annals of General Psychiatry, Springer Science and Business Media LLC, Vol. 9, No. 1 ( 2010-12)
    Type of Medium: Online Resource
    ISSN: 1744-859X
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2010
    detail.hit.zdb_id: 2090401-0
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  • 6
    Online Resource
    Online Resource
    American Society of Hematology ; 2016
    In:  Blood Vol. 128, No. 22 ( 2016-12-02), p. 5934-5934
    In: Blood, American Society of Hematology, Vol. 128, No. 22 ( 2016-12-02), p. 5934-5934
    Abstract: Introduction: The goal of multiple myeloma (MM) treatment is to control disease, prolong survival and improve quality of life (Colson 2015). One piece of evidence that a therapy is working well is the ability to maintain therapy without change. The purpose of this analysis was to describe treatment patterns and costs among MM patients who maintain first line of therapy (LOT) for at least six months. Results of this analysis will provide clinicians and payers with information about factors associated with faster progression through treatment. Methods:A US claims database (Truven Health MarketScan®) was used to identify adult patients with ≥2 MM diagnoses (ICD-9 203.0x) between Jan 1, 2005-Dec 31, 2014 (end of study) with; 1) MM treatment between Jan 1, 2007-Jun 30, 2014 and within 90 days of an MM diagnosis code (date of first MM treatment set as index date); 2) continuous medical insurance 24 months pre and ≥6 months postindex). Patients were excluded if they had 1) MM treatment preindex; 2) non-MM chemo; 3) stem cell transplant, pregnancy or HIV diagnoses. An algorithm was used to identify LOTs based on treatment gaps, changes in therapy and refractory status. Patient characteristics, treatment patterns and costs were assessed for patients without a new LOT within 6 months of starting their first LOT and for patients with a new LOT within 6 months of starting their first LOT. Treated days was defined as the time between the first day of treatment in the LOT until the last day a treatment was available based on the dispensing dates and days supplies. Categorical and continuous measures were tested with Chi-Square tests or independent t-tests, respectively. Differences in costs were tested in a general linear model with a gamma distribution and a log link. Results: Of the 2,936 patients included, 74.7% maintained LOT 1 for at least 6 months (i.e., did not have a LOT 2 within 6 months of starting their LOT 1). The average age of patients who maintained LOT 1 was 71.3 (SD 10.8) years and 56.3% were male. The average age of patients with an LOT 2 (i.e. started LOT 2 within 6 months of starting their LOT 1) was 69.7 (SD 11.0) years and 57.3% were male. Fewer patients without an LOT 2 had Commercial insurance compared to the group with an LOT 2 (25.8% vs. 29.5%). Patients without a LOT 2 were more likely to have had a lenalidomide-based (no PI) regimen for LOT 1 than patients who had an LOT 2 (35.8% vs. 22.3%; p 〈 0.0001) Mean total costs were lower among patients without a LOT 2 compared to patients with a LOT 2 ($211,115 vs. $242,177; p 〈 0.0001). Most of the cost difference was driven by outpatient costs, which were $90,906 for patients without an LOT 2 and $119,221 for the group with an LOT 2 (p 〈 0.0001). The average number of treated days among patients without an LOT 2 was 143.1 days out of the possible 180 days of observation compared to 133.9 days among patients with a LOT 2 (p 〈 0.0001). Among patients with a second LOT, based on the treatment algorithm, the observed reasons for initiating the second LOT included, 51.1% had a change in therapy with 〈 60 day gap in therapy, 24.8% were refractory to an initial proteasome inhibitor (PI) or immunomodulatory (IMiD) therapy, 12.0% had ≥60-day gap in all therapy with a restart of the same drug and 12.1% had some other combination of reasons (i.e., change, restart of the same drug after a 60-day gap and/or 60-day gap in all therapy). Cost per day using the number of days between the start of the LOT and the end of treatment during the LOT were lowest among patients who did not progress to a second LOT during the first 180 days ($1,475/treated day). This was followed by patients who had a change in therapy alone ($1,704), those who were refractory to the initial therapy ($1,912), those who restarted after a 90-day gap with no therapy and ($1,999), and those with a combination of reasons for initiating the second LOT ($2,082). Conclusions:During the first 6-months after initiation of first LOT, approximately 75% of patients maintained LOT 1. Patients who maintained LOT 1 tended to be older, have lower costs, more treated days, and more frequently treated with lenalidomide-based (no PI) regimens at LOT 1. This analysis suggests that maintaining lines of therapy longer is associated with reduced healthcare costs and using a lenalidomide-based regimen in LOT 1 may be associated with longer time to next therapy, which may be helpful when considering treatment sequencing. Disclosures Maiese: Janssen Scientific Affairs, LLC: Employment. Slaton:CK Consulting Associates, LLC: Employment. Kozma:CK Consulting Associates, LLC: Employment.
    Type of Medium: Online Resource
    ISSN: 0006-4971 , 1528-0020
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    Language: English
    Publisher: American Society of Hematology
    Publication Date: 2016
    detail.hit.zdb_id: 1468538-3
    detail.hit.zdb_id: 80069-7
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  • 7
    Online Resource
    Online Resource
    American Society of Clinical Oncology (ASCO) ; 2016
    In:  Journal of Clinical Oncology Vol. 34, No. 15_suppl ( 2016-05-20), p. 8052-8052
    In: Journal of Clinical Oncology, American Society of Clinical Oncology (ASCO), Vol. 34, No. 15_suppl ( 2016-05-20), p. 8052-8052
    Type of Medium: Online Resource
    ISSN: 0732-183X , 1527-7755
    RVK:
    RVK:
    Language: English
    Publisher: American Society of Clinical Oncology (ASCO)
    Publication Date: 2016
    detail.hit.zdb_id: 2005181-5
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  • 8
    Online Resource
    Online Resource
    SAGE Publications ; 2018
    In:  Multiple Sclerosis Journal - Experimental, Translational and Clinical Vol. 4, No. 4 ( 2018-10), p. 205521731881903-
    In: Multiple Sclerosis Journal - Experimental, Translational and Clinical, SAGE Publications, Vol. 4, No. 4 ( 2018-10), p. 205521731881903-
    Abstract: Administrative-claims data enable comparative effectiveness assessment using large numbers of patients treated in real-world settings. Objective To evaluate real-world relapses, healthcare costs and resource use in patients with MS newly initiating subcutaneous interferon beta-1a (sc IFNβ-1a) v. oral disease-modifying drugs (DMDs: dimethyl fumarate, fingolimod, teriflunomide). Methods Patients from an administrative claims database (1 Jan 2012–31 Dec 2015) were selected if they: were 18–63 years old; had an MS diagnosis; had newly initiated sc IFNβ-1a, dimethyl fumarate, fingolimod, or teriflunomide (first claim = index); had no evidence of DMD 12-months pre-index; and had 12-month eligibility pre- and post-index. Relapse was defined as an MS-related inpatient stay, emergency room visit, or outpatient visit with a corticosteroid prescription ± 7 days. Outcomes were evaluated using logistic regression and generalized linear models. Results A total of 4475 patients met inclusion criteria: 21.9% sc IFNβ-1a, 51.0% dimethyl fumarate, 19.7% fingolimod, 7.4% teriflunomide. Teriflunomide patients had 1.357 (95% CI 1.000, 1.831; p = 0.0477) greater odds of 1-year relapse than sc IFNβ-1a patients. Estimated mean all-cause 1-year costs were higher after fingolimod (US$72,376) v. sc IFNβ-1a initiation (US$65,408; p  〈  0.0001). Non-DMD costs were not significantly different. Conclusion Patients initiating sc IFNβ-1a had better relapse outcomes v. teriflunomide, and lower all-cause costs v. fingolimod.
    Type of Medium: Online Resource
    ISSN: 2055-2173 , 2055-2173
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2018
    detail.hit.zdb_id: 2841884-0
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  • 9
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 1996
    In:  PharmacoEconomics Vol. 10, No. 1 ( 1996-07), p. 4-13
    In: PharmacoEconomics, Springer Science and Business Media LLC, Vol. 10, No. 1 ( 1996-07), p. 4-13
    Type of Medium: Online Resource
    ISSN: 1170-7690
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1996
    detail.hit.zdb_id: 2043876-X
    SSG: 15,3
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  • 10
    Online Resource
    Online Resource
    Academy of Managed Care Pharmacy ; 2014
    In:  Journal of Managed Care Pharmacy Vol. 20, No. 8 ( 2014-08), p. 800-807
    In: Journal of Managed Care Pharmacy, Academy of Managed Care Pharmacy, Vol. 20, No. 8 ( 2014-08), p. 800-807
    Type of Medium: Online Resource
    ISSN: 1083-4087 , 1944-706X
    Language: English
    Publisher: Academy of Managed Care Pharmacy
    Publication Date: 2014
    detail.hit.zdb_id: 2059704-6
    detail.hit.zdb_id: 2772684-8
    SSG: 15,3
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