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      Statin use, survival and incidence of thrombosis among older patients with polycythemia vera and essential thrombocythemia

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          Abstract

          Background

          Polycythemia vera (PV) and essential thrombocythemia (ET) are linked to increased risk of cardiovascular morbidity and mortality. In addition to the reduction in of arterial thrombotic events, statins may prevent venous thrombosis including among patients with cancer. As previous registry‐ and claims‐based studies revealed that the use of statins may improve the survival of patients with various malignancies we evaluated their impact on outcomes of older adults with PV and ET.

          Methods

          We identified 4010 older adults (aged 66–99 years at diagnosis) with PV ( n = 1809) and ET ( n = 2201) in a population‐based cohort study using the Surveillance, Epidemiology, and End Results‐Medicare database with median follow‐up of 3.92 (interquartile range: 2.58–5.75) years. Propensity score matching (PSM) and inverse probability of treatment weighting (IPTW) approaches were utilized to assess potential association between statins and overall survival. Multivariable competing risk models with death as a competing risk were used to evaluate possible relationship between statins and the incidence of thrombosis.

          Results

          55.8% of the patients used statins within the first year after PV/ ET diagnosis, and statin use was associated with a 22% reduction in all‐cause mortality ( PSM: hazard ratio [ HR] = 0.78, 95% confidence interval [ CI]: 0.63–0.98, p = 0.03; IPTW: HR = 0.79, 95% CI: 0.64–0.97, p = 0.03). Statins also reduced the risk of thrombosis in this patient population ( PSM: HR = 0.63, 95% CI: 0.51–0.78, p < 0.01; IPTW: HR = 0.57, 95% CI: 0.49–0.66, p < 0.01) as well as in PV and ET subgroups.

          Conclusions

          These findings suggest that it may be important to incorporate statins into the therapeutic strategy for older adults with PV and ET.

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          Most cited references49

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          A Proportional Hazards Model for the Subdistribution of a Competing Risk

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            Comorbidity measures for use with administrative data.

            This study attempts to develop a comprehensive set of comorbidity measures for use with large administrative inpatient datasets. The study involved clinical and empirical review of comorbidity measures, development of a framework that attempts to segregate comorbidities from other aspects of the patient's condition, development of a comorbidity algorithm, and testing on heterogeneous and homogeneous patient groups. Data were drawn from all adult, nonmaternal inpatients from 438 acute care hospitals in California in 1992 (n = 1,779,167). Outcome measures were those commonly available in administrative data: length of stay, hospital charges, and in-hospital death. A comprehensive set of 30 comorbidity measures was developed. The comorbidities were associated with substantial increases in length of stay, hospital charges, and mortality both for heterogeneous and homogeneous disease groups. Several comorbidities are described that are important predictors of outcomes, yet commonly are not measured. These include mental disorders, drug and alcohol abuse, obesity, coagulopathy, weight loss, and fluid and electrolyte disorders. The comorbidities had independent effects on outcomes and probably should not be simplified as an index because they affect outcomes differently among different patient groups. The present method addresses some of the limitations of previous measures. It is based on a comprehensive approach to identifying comorbidities and separates them from the primary reason for hospitalization, resulting in an expanded set of comorbidities that easily is applied without further refinement to administrative data for a wide range of diseases.
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              2018 AHA/ACC/AACVPR/AAPA/ABC/ACPM/ADA/AGS/APhA/ASPC/NLA/PCNA Guideline on the Management of Blood Cholesterol

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                Author and article information

                Contributors
                nikolai.podoltsev@yale.edu
                Journal
                Cancer Med
                Cancer Med
                10.1002/(ISSN)2045-7634
                CAM4
                Cancer Medicine
                John Wiley and Sons Inc. (Hoboken )
                2045-7634
                13 September 2023
                September 2023
                : 12
                : 18 ( doiID: 10.1002/cam4.v12.18 )
                : 18889-18900
                Affiliations
                [ 1 ] Section of Hematology, Department of Internal Medicine Yale School of Medicine New Haven Connecticut USA
                [ 2 ] Cancer Outcomes, Public Policy, and Effectiveness Research (COPPER) Center Yale University New Haven Connecticut USA
                [ 3 ] Department of Chronic Disease Epidemiology Yale School of Public Health New Haven Connecticut USA
                [ 4 ] Section of Cardiology, Department of Internal Medicine Yale School of Medicine New Haven Connecticut USA
                [ 5 ]Present address: Division of Hematology and Oncology University of Alabama School of Medicine Birmingham Alabama USA
                [ 6 ]Present address: Investigational Drug Branch, Cancer Therapy Evaluation Program National Cancer Institute Bethesda Maryland USA
                Author notes
                [*] [* ] Correspondence

                Nikolai A. Podoltsev, Section of Hematology, Department of Internal Medicine, Yale School of Medicine, New Haven, Connecticut, USA.

                Email: nikolai.podoltsev@ 123456yale.edu

                Author information
                https://orcid.org/0000-0002-3657-778X
                https://orcid.org/0000-0002-8542-2944
                https://orcid.org/0000-0001-7071-6475
                https://orcid.org/0000-0002-1827-5032
                Article
                CAM46528 CAM4-2023-06-2939.R1
                10.1002/cam4.6528
                10557879
                37702132
                772569e8-6e9d-4584-b66c-c5448c74f550
                © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 22 August 2023
                : 17 June 2023
                : 31 August 2023
                Page count
                Figures: 3, Tables: 3, Pages: 12, Words: 5717
                Funding
                Funded by: Frederick A. DeLuca Foundation , doi 10.13039/100017683;
                Categories
                Research Article
                RESEARCH ARTICLES
                Clinical Cancer Research
                Custom metadata
                2.0
                September 2023
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.3.4 mode:remove_FC converted:06.10.2023

                Oncology & Radiotherapy
                mpn,statins,survival,thrombosis
                Oncology & Radiotherapy
                mpn, statins, survival, thrombosis

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