128 research outputs found

    Proposing a Method for Determining the Appropriate Purchasing Strategy Based on the Purchasing Portfolio Approach

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    The aim of purchasing portfolio is commodity classification to determine the suitable purchasing strategy. In this research, we propose a new method for the classification of commodities with the extension of purchasing portfolio approaches. Indeed, the purpose of this research is to determine the appropriate purchasing strategy for commodities with the consideration of purchasing portfolio. Furthermore, first, by reviewing the literature and surveying the specialists and databases, the dimensions of profit impact, market complexity, and the balance of supplier and buyer power were considered and appropriate criteria for classifying commodities and services were determined. After determining the number of dimensions, the weight of the criteria in each dimension was calculated using the best-worst method. Then, using the TOPSIS method, the score of commodities was obtained in each dimension and the position of the commodities and services was determined on a matrix. To determine the most suitable strategy by considering commodity position based on three defined dimensions, at first, the appropriate strategies were collected by reviewing the research literature, and then, the most appropriate strategy for each category of commodities was determined. Finally, the proposed method was implemented for the commodities of a company, and the results were presented

    Patientâ reported outcomes in a large North American cohort living with chronic hepatitis B virus: a crossâ sectional analysis

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    Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/153747/1/apt15618_am.pdfhttps://deepblue.lib.umich.edu/bitstream/2027.42/153747/2/apt15618.pd

    Diabetes and prediabetes in patients with hepatitis B residing in North America

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    Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/115977/1/hep28110-sup-0001-suppinfo01.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/115977/2/hep28110.pdfhttp://deepblue.lib.umich.edu/bitstream/2027.42/115977/3/hep28110_am.pd

    Withdrawal of Long-Term Nucleotide Analog Therapy in Chronic Hepatitis B:Outcomes From the Withdrawal Phase of the HBRN Immune Active Treatment Trial

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    INTRODUCTION:Withdrawal of nucleos(t)ide analog therapy is increasingly being evaluated in chronic hepatitis B infection as a strategy to induce hepatitis B surface antigen (HBsAg) loss. The Hepatitis B Research Network Immune-Active Trial evaluated treatment with tenofovir (TDF) for 4 years ± an initial 6 months of peginterferon-α (PegIFN) (NCT01369212) after which treatment was withdrawn.METHODS:Eligible participants (hepatitis B e antigen [HBeAg]-/anti-HBe+, hepatitis B virus [HBV] DNA &lt;103IU/mL, no cirrhosis) who discontinued TDF were followed for at least 1 year with optional follow-up thereafter. Retreatment was based on predefined criteria.RESULTS:Among 201 participants who received 4 years of treatment, 97 participants (45 TDF and 52 TDF + PegIFN arm, 79 Asian) discontinued TDF. HBsAg loss occurred in 5 participants, 2 within 25 weeks and 3 within 89-119 weeks postwithdrawal (cumulative rate 4.3% by 2 years). Alanine aminotransferase (ALT) flares (&gt;5× upper limit of normal) after TDF withdrawal occurred in 36 (37.1%) participants and occurred more frequently and earlier in those HBeAg- compared with HBeAg+ at treatment initiation. ALT flares were associated with older age and higher HBV DNA pretreatment and at the visit before the flare. ALT flares were not significantly associated with HBsAg decline or loss but were associated with immune active disease at 1 year (70.6% vs 11.9%, P &lt; 0.0001) and 2 years (66.7% vs 25.9%, P = 0.03) postwithdrawal. Treatment reinitiation was required in 13 (13.4%) participants, and 13 others remained in a sustained inactive carrier state by the end of the study follow-up. No criteria reliably predicted safe treatment withdrawal.DISCUSSION:Results from this trial do not support TDF withdrawal as a therapeutic strategy. HBsAg loss was infrequent within 2 years of stopping long-term TDF. If withdrawal is considered, HBV DNA should be carefully monitored with reinitiation of therapy if levels rise above 4 log10IU/mL to reduce the risk of ALT flares, as they were not associated with subsequent HBsAg decline or loss.</p
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