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  • 1
    In: Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy, Wiley, Vol. 38, No. 3 ( 2018-03), p. 349-356
    Abstract: Prior studies have identified risk factors for recurrent Clostridium difficile infection ( CDI ), but few studies have integrated these factors into a clinical prediction rule that can aid clinical decision‐making. The objectives of this study were to derive and validate a CDI recurrence prediction rule to identify patients at risk for first recurrence in a national cohort of veterans. Design Retrospective cohort study. Data Source Veterans Affairs Informatics and Computing Infrastructure. Patients A total of 22,615 adult Veterans Health Administration beneficiaries with first‐episode CDI between October 1, 2002, and September 30, 2014; of these patients, 7538 were assigned to the derivation cohort and 15,077 to the validation cohort. Measurements and Main Results A 60‐day CDI recurrence prediction rule was created in a derivation cohort using backward logistic regression. Those variables significant at p 〈 0.01 were assigned an integer score proportional to the regression coefficient. The model was then validated in the derivation cohort and a separate validation cohort. Patients were then split into three risk categories, and rates of recurrence were described for each category. The CDI recurrence prediction rule included the following predictor variables with their respective point values: prior third‐ and fourth‐generation cephalosporins (1 point), prior proton pump inhibitors (1 point), prior antidiarrheals (1 point), nonsevere CDI (2 points), and community‐onset CDI (3 points). In the derivation cohort, the 60‐day CDI recurrence risk for each score ranged from 7.5% (0 points) to 57.9% (8 points). The risk score was strongly correlated with recurrence (R 2  = 0.94). Patients were split into low‐risk (0–2 points), medium‐risk (3–5 points), and high‐risk (6–8 points) classes and had the following recurrence rates: 8.9%, 20.2%, and 35.0%, respectively. Findings were similar in the validation cohort. Conclusion Several CDI and patient‐specific factors were independently associated with 60‐day CDI recurrence risk. When integrated into a clinical prediction rule, higher risk scores and risk classes were strongly correlated with CDI recurrence. This clinical prediction rule can be used by providers to identify patients at high risk for CDI recurrence and help guide preventive strategy decisions, while accounting for clinical judgment.
    Type of Medium: Online Resource
    ISSN: 0277-0008 , 1875-9114
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2018
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  • 2
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 1999
    In:  PharmacoEconomics Vol. 16, No. 1 ( 1999), p. 43-57
    In: PharmacoEconomics, Springer Science and Business Media LLC, Vol. 16, No. 1 ( 1999), p. 43-57
    Type of Medium: Online Resource
    ISSN: 1170-7690
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 1999
    detail.hit.zdb_id: 2043876-X
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  • 3
    In: Clinical Therapeutics, Elsevier BV, Vol. 21, No. 8 ( 1999-8), p. 1358-1369
    Type of Medium: Online Resource
    ISSN: 0149-2918
    Language: English
    Publisher: Elsevier BV
    Publication Date: 1999
    detail.hit.zdb_id: 2025417-9
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  • 4
    In: Journal of Oncology Pharmacy Practice, SAGE Publications
    Abstract: Oncologists are increasingly prescribing oral antineoplastic agents which have benefits and challenges impacting patient outcomes. Practice guidelines recommend monitoring symptoms and adherence without outlining any specific tools or methods for monitoring. Pharmacists are successful in monitoring patients on therapy and improving outcomes. We aimed to assess the feasibility and utility of a pharmacist-delivered and medical record-integrated adherence and symptom monitoring program for patients on oral antineoplastic agents. Methods This single-center, prospective, interventional study designed and implemented an adherence and monitoring program. A pharmacist contacted patients twice between clinic visits for three months. During telephone encounters, patients were verbally screened for medication adherence and assessed for new or changing symptoms using the Edmonton Symptom Assessment System as a signal of possible adverse events. We measured feasibility via patient enrollment, completed proportion of scheduled contacts, and pharmacist time. Utility was assessed through patient adherence, satisfaction surveys, healthcare resource utilization, and pharmacist interventions (i.e., patient education, adherence assistance, and symptom management). Results Fifty-one patients participated. Ninety-one percent of scheduled patient contacts were completed. Edmonton Symptom Assessment System was administered by pharmacy personnel 102 times. Patient-reported adherence was 100%. Overall satisfaction was 85% and 100%, for patients and physicians, respectively. Fifty-one (98%) pharmacist recommendations were accepted. There were 14 total utilizations of healthcare resources—5.2 per 1000 patient days. Conclusions This study suggests a pharmacist monitoring program for patients taking oral antineoplastic agents is feasible and provides utility. Further research is needed to evaluate whether this program improves safety, adherence, and outcomes in patients using oral antineoplastic agents.
    Type of Medium: Online Resource
    ISSN: 1078-1552 , 1477-092X
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2023
    detail.hit.zdb_id: 2026590-6
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  • 5
    Online Resource
    Online Resource
    SAGE Publications ; 2003
    In:  Annals of Pharmacotherapy Vol. 37, No. 9 ( 2003-09), p. 1276-1286
    In: Annals of Pharmacotherapy, SAGE Publications, Vol. 37, No. 9 ( 2003-09), p. 1276-1286
    Abstract: To review the electrocardiographic (ECG) and cardiovascular effects of 5-hydroxytryptamine 3 (5-HT 3 ) receptor antagonists preclinically, in healthy volunteers, and in patients undergoing chemotherapy or surgery. DATA SOURCES: A MEDLINE search was performed of clinical trials and preclinical data published between 1963 and December 2002 assessing the ECG and cardiovascular effects of 5-HT 3 receptor antagonists, supplemented with reviews and secondary sources. STUDY SELECTION AND DATA EXTRACTION: All of the articles identified were evaluated and all information deemed relevant was included in this review. DATA SYNTHESIS: There are no clinically relevant differences in efficacy and safety among the available 5-HT 3 receptor antagonists for prevention and treatment of chemotherapy-induced and postoperative nausea and vomiting. As a class, they have well-defined electrophysiologic activity. Changes in ECG parameters (PR, QRS, QT, QTc, JT intervals) are small, reversible, clinically insignificant, and independent of the patient population studied, and patients are asymptomatic during these changes. ECG changes are most prominent 1–2 hours after a dose of dolasetron, ondansetron, and granisetron and return to baseline within 24 hours. Clinically important adverse cardiovascular events associated with these changes are rare. No serious cardiac events (including torsade de pointes) arising from ECG interval changes have been attributed to 5-HT 3 receptor antagonist use. CONCLUSIONS: Clinical data demonstrate that ECG interval changes are a class effect of the 5-HT 3 receptor antagonists. Theoretical concern regarding cardiovascular adverse events with these agents is not supported by clinical experience. The significant benefits of these agents outweigh the theoretical small risk of meaningful cardiovascular events.
    Type of Medium: Online Resource
    ISSN: 1060-0280 , 1542-6270
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2003
    detail.hit.zdb_id: 2053518-1
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  • 6
    Online Resource
    Online Resource
    SAGE Publications ; 2003
    In:  Annals of Pharmacotherapy Vol. 37, No. 12 ( 2003-12), p. 1918-1919
    In: Annals of Pharmacotherapy, SAGE Publications, Vol. 37, No. 12 ( 2003-12), p. 1918-1919
    Type of Medium: Online Resource
    ISSN: 1060-0280 , 1542-6270
    Language: English
    Publisher: SAGE Publications
    Publication Date: 2003
    detail.hit.zdb_id: 2053518-1
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  • 7
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 1999
    In:  American Journal of Health-System Pharmacy Vol. 56, No. 24 ( 1999-12-15), p. 2540-2542
    In: American Journal of Health-System Pharmacy, Oxford University Press (OUP), Vol. 56, No. 24 ( 1999-12-15), p. 2540-2542
    Type of Medium: Online Resource
    ISSN: 1079-2082 , 1535-2900
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 1999
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  • 8
    In: Antibiotics, MDPI AG, Vol. 12, No. 1 ( 2022-12-28), p. 51-
    Abstract: While efforts have been made in the United States (US) to optimize antimicrobial use, few studies have explored antibiotic prescribing disparities that may drive future interventions. The objective of this study was to evaluate disparities in antibiotic prescribing among US ambulatory care visits by patient subgroups. This was a retrospective, cross-sectional study utilizing the National Ambulatory Medical Care Survey from 2009 to 2016. Antibiotic use was described as antibiotic visits per 1000 total patient visits. The appropriateness of antibiotic prescribing was determined by ICD-9 or ICD-10 codes assigned during the visit. Subgroup analyses were conducted by patient race, ethnicity, age group, and sex. Over 7.0 billion patient visits were included; 11.3% included an antibiotic prescription. Overall and inappropriate antibiotic prescription rates were highest in Black (122.2 and 78.0 per 1000) and Hispanic patients (138.6 and 79.8 per 1000). Additionally, overall antibiotic prescription rates were highest in patients less than 18 years (169.6 per 1000) and female patients (114.1 per 1000), while inappropriate antibiotic prescription rates were highest in patients 18 to 64 years (66.0 per 1000) and in males (64.8 per 1000). In this nationally representative study, antibiotic prescribing disparities were found by patient race, ethnicity, age group, and sex.
    Type of Medium: Online Resource
    ISSN: 2079-6382
    Language: English
    Publisher: MDPI AG
    Publication Date: 2022
    detail.hit.zdb_id: 2681345-2
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  • 9
    Online Resource
    Online Resource
    Wiley ; 2017
    In:  Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy Vol. 37, No. 3 ( 2017-03), p. 278-286
    In: Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy, Wiley, Vol. 37, No. 3 ( 2017-03), p. 278-286
    Abstract: To evaluate nationwide chronic myeloid leukemia (CML) treatment practices over an extended period and across multiple lines of tyrosine kinase inhibitor ( TKI ) therapy with imatinib, dasatinib, and nilotinib. Design Retrospective cohort study. Data Source Veterans Health Administration ( VHA ) national database. Patients A total of 2873 VHA beneficiaries aged 18–89 years who had at least one encounter at any of the ~150 VHA hospitals and 800 VHA clinics, had a diagnosis code for CML, and filled at least one prescription for imatinib, nilotinib, or dasatinib between October 1, 2001, and September 30, 2010. Measurement and Main Results The VHA database was used for the time period of October 1, 2000, to September 30, 2012, allowing for a 1‐year observation period to identify CML treatments prior to study enrollment and a minimum of a 2‐year follow‐up period to assess study end points. Primary study end points included change in TKI treatment, gaps in TKI treatment, TKI treatment persistence, and patient survival. Persistence for each distinct line of treatment was defined as the time of continuous therapy, quantified by the number of days covered by the drug from treatment initiation until a 60‐day gap in treatment was identified or a switch in treatment occurred. A Kaplan‐Meier model was used to evaluate persistence and survival. Of the 2873 patients receiving first‐line TKI treatment, 586 (20.4%) switched to a different TKI , constituting second‐line treatment. Overall, 245 patients (8.5%) were switched again to third‐line treatment. Only 4.4% of patients receiving first‐line treatment experienced a gap in therapy of 60 or more days. First‐line treatment persistence rates were 75%, 65%, and 55% for the first, second, and third years of treatment, respectively. Five‐year survival with first‐line treatment was 62%. Conclusion In this national cohort of VHA patients, 1‐year persistence of first‐line TKI treatment was similar to that in prior studies. Five‐year survival was comparable with that in other observational studies but was lower than that in prospective clinical trials. Persistence rates declined after the introduction of the new TKI s.
    Type of Medium: Online Resource
    ISSN: 0277-0008 , 1875-9114
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2017
    detail.hit.zdb_id: 2061167-5
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  • 10
    Online Resource
    Online Resource
    SAGE Publications ; 1991
    In:  DICP Vol. 25, No. 5 ( 1991-05), p. 505-517
    In: DICP, SAGE Publications, Vol. 25, No. 5 ( 1991-05), p. 505-517
    Abstract: Because of its in vitro activity in leukemic cell lines and Phase I studies of acute leukemia, Phase II and III clinical trials with idarubicin hydrochloride were conducted in patients with acute lymphocytic leukemia or acute nonlymphocytic leukemia. In the Phase III comparative trials between the combinations of idarubicin and cytarabine and daunorubicin hydrochloride and cytarabine, the idarubicin/cytarabine combination resulted in significantly greater complete remission rates and longer overall survival in two of three studies conducted in the US. As a result, the Food and Drug Administration approved intravenous idarubicin with a Class 1A rating in September 1990 for use in combination with other antileukemic drugs (e.g., cytarabine) for the treatment of acute myelogenous leukemia in adults. The recommended dose of idarubicin is 12 mg/m 2 daily for three days by slow intravenous injection in combination with cytarabine. Although idarubicin causes myelosuppression similar to that described with daunorubicin, the incidence of cardiotoxicity in animal models is lower. Idarubicin also has the advantage of oral administration, but the oral formulation of the drug remains investigational. The use of idarubicin in pediatric patients also remains to be established.
    Type of Medium: Online Resource
    ISSN: 1042-9611
    Language: English
    Publisher: SAGE Publications
    Publication Date: 1991
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