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  • 1
    Online Resource
    Online Resource
    Baishideng Publishing Group Inc. ; 2019
    In:  World Journal of Gastroenterology Vol. 25, No. 18 ( 2019-5-14), p. 2229-2239
    In: World Journal of Gastroenterology, Baishideng Publishing Group Inc., Vol. 25, No. 18 ( 2019-5-14), p. 2229-2239
    Type of Medium: Online Resource
    ISSN: 1007-9327
    Language: Unknown
    Publisher: Baishideng Publishing Group Inc.
    Publication Date: 2019
    detail.hit.zdb_id: 2084831-6
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  • 2
    In: American Journal of Gastroenterology, Ovid Technologies (Wolters Kluwer Health), Vol. 114, No. 1 ( 2019-10), p. S588-S588
    Abstract: Approved HCV DAA regimens can cure nearly all patients; however, barriers to care in community practices include patients with a large number of medical co-morbidities, advanced liver damage and insurance approval of DAA regimens. This study assesses medical conditions, liver staging methods, and the drug prior auth process in HCV-infected patients managed in community practices partnered with a dedicated pharmacy team with expertise in liver disorders. METHODS: This IRB-approved, ongoing study captures outcomes on a cohort of 705 patients from community practices across Texas. Patients had chronic hepatitis C and were treated with DAA regimens selected by the physician. Insurance carrier and prior auth process data were also captured. RESULTS: 96% of prior auth requests to Medicare and Medicaid were accepted upon first request; however, only 84% of requests to private insurance were accepted upon first request and did not require an appeal. This cohort included many patients with complicated medical histories including HCC (4.4%), ESRD (2.7%), liver transplant (2.1%) and seizure disorders (4.5%). Liver staging was done via Fibrotest (71%), Fibroscan (22%), Fibrosure (13%) and liver biopsy (0.6%). Medicaid patients had proportionately more advanced disease (79% F3/F4) and were less likely to be previously treated with DAA therapy (1.6%). The most common co-morbid conditions were hypertension (66%), diabetes (28%), GERD (23%), depression (20%), anxiety (16%) dyslipidemia (16%), renal disease (9%) and COPD (9%). Medicaid patients had the highest rates of dyslipidemia, obesity, renal disease and COPD. Overall, 90% of patients had undetectable virus at week 4, 96.7% completed follow-up and 97% achieved SVR, regardless of health insurance type. All patients with ESRD or with seizure disorders treated with oxcarbazepine achieved SVR as did 87% of patients with prior liver transplant. SVR was also achieved in 86% of patients with a history of HCC. CONCLUSION: HCV treatment in the community setting resulted in 97% cure. This cohort includes a wide variety of patients including those on dialysis or post-liver transplant. Partnership with a dedicated and liver focused pharmacy team resulted in 90% approval of first-time prior auth requests. Knowledge of and management of co-morbid conditions is critical for maximizing overall patient adherence, compliance and outcomes. Close monitoring through a chronic care management model can lead to better overall patient management.
    Type of Medium: Online Resource
    ISSN: 0002-9270 , 1572-0241
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2019
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  • 3
    In: American Journal of Gastroenterology, Ovid Technologies (Wolters Kluwer Health), Vol. 114, No. 1 ( 2019-10), p. S588-S589
    Abstract: The prevalence of cirrhosis is on the rise in the US and predisposes patients to multiple costly complications, including hepatic encephalopathy (HE). Hospital readmissions among patients with decompensated cirrhosis are common and ∼1/3 are due to recurrent HE. Recommended treatment of HE is lactulose +/- rifaximin; however, access to rifaximin is sometimes difficult to access due to formulary restrictions or cost. This study assesses health outcomes, the rifaximin approval process and compliance in patients with HE in community GI/hep practices that use a dedicated pharmacy team with expertise in liver disorders. METHODS: This IRB-approved, observational protocol captures long-term health outcomes and pharmacy support data every 6 months for up to 10 years. Patients have cirrhosis, at least stage 1 HE and are already receiving or newly starting rifaximin. The concomitant use of lactulose was allowed at the discretion of the physician. Patients from community practices across Texas were included in this patient cohort followed over the first 6 months. RESULTS: The first cohort of 744 patients received rifaximin with (45%) or without (55%) lactulose and were insured through Medicare (39%), private (36%) or Medicaid (24%). In this cohort, 99% of rifaximin prescriptions were accepted with the first prior auth request and the majority of patients started treatment 〈 14 days of prescription submission. DDI assessment and dosing compliance were reviewed resulting in 94% medication compliance during Month 1. During the first 6 months, 17.4% had 〉 1 ER/urgent care visit and 4.4% were hospitalized due to an HE-related event. Thirteen patients had a new HCC diagnosis and 9 patients underwent liver transplant. After 6 months, 73% remained on rifaximin, 14% no longer wanted to participate, 8% were lost to follow up and 5% died. Overall medical condition was stable/improved for 90% compared to 6 months prior. CONCLUSION: Patients with HE who are treated at community sites with a specialized pharmacy team can receive rifaximin in an expedited manner. Continued patient education and communication with the health care team can lead to high adherence rates which can minimize ER/urgent care visits and hospitalizations. HCV remains the most common underlying disease in this cohort. In spite of rigorous monitoring, a large % of patients with advanced liver disease die or are lost to follow up. Close monitoring through a chronic care management model can lead to early diagnosis and better patient management.
    Type of Medium: Online Resource
    ISSN: 0002-9270 , 1572-0241
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2019
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  • 4
    In: Medicine, Ovid Technologies (Wolters Kluwer Health), Vol. 98, No. 26 ( 2019-06), p. e16254-
    Abstract: The aim of this study was to obtain real-world, US, observational data on the effect of baseline resistance-associated substitutions (RASs) on achieving sustained virologic response (SVR) in hepatitis C (HCV) patients treated with direct-acting antiviral (DAA) regimens; the need for long-term follow-up in post-SVR patients. It is uncertain if the presence of RASs limits efficacy to DAAs. Once SVR is achieved, society guidelines recommend long-term surveillance for hepatocellular carcinoma in certain patients. Real-world data are limited on these topics. Adult patients treated with DAAs at community hepatitis clinics between January 2015 and April 2017 were included in this study. Baseline resistance testing was performed before treatment. Per guidelines, post-SVR long-term monitoring was required in patients with F3 to F4 fibrosis before treatment or with elevated ALT levels ( 〉 19 U/L females; 〉 30 U/L males). A total of 875 chronic, mostly GT1a (60%) HCV patients were treated with an approved DAA regimen. Average baseline AST and ALT were 75 and 67 U/L, respectively, and 47% had F3 to F4 fibrosis at baseline. SVR was achieved in 863 (98.6%) patients despite a high presence of baseline RASs (61%). Long-term monitoring was required post-SVR in 539 patients (62%). In a real-life, US cohort of HCV-infected patients, nearly all patients achieved SVR with available DAA regimens regardless of baseline RASs. Approximately two-thirds of these patients required long-term follow-up, despite viral eradication.
    Type of Medium: Online Resource
    ISSN: 0025-7974 , 1536-5964
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2019
    detail.hit.zdb_id: 2049818-4
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