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  • 1
    In: Nuclear Medicine Communications, Ovid Technologies (Wolters Kluwer Health), Vol. 42, No. 9 ( 2021-09), p. 990-997
    Abstract: Cardiac resynchronization therapy (CRT) reduces morbidity and mortality in heart failure patients. The purpose of this study was to assess the value of gated myocardial perfusion single-photon emission computed tomography (GMPS) phase analysis for predicting survival in heart failure patients undergoing CRT. Methods This retrospective cohort study evaluated heart failure patients who underwent GMPS prior to CRT. Phase histogram bandwidth (PHB) and phase SD (PSD) were calculated using GMPS data. Cox proportional hazards model was used to identify independent predictors of overall survival (OS). Results A total of 35 patients (age 65.1 ± 13.3, 27 men and 8 women), who were followed for mean of 4.1 ± 2.9 years, were enrolled in the study. PSD of greater than 45° was found to be an independent predictor of poor OS (hazard ratio = 12.63, P  = 0.011) when compared with age (hazard ratio = 1.00, P  = 0.922), gender (hazard ratio = 0.31, P  = 0.155), NYHA class (hazard ratio = 0.45, P  = 0.087), QRS duration greater than 150 ms (hazard ratio = 2.38, P  = 0.401), pre-CRT left ventricular ejection fraction (LVEF) (hazard ratio = 0.95, P  = 0.175) and etiology of heart failure (hazard ratio = 1.42, P  = 0.641). Furthermore, PHB greater than 140° was also found to be an independent predictor of poor OS (hazard ratio = 5.63, P  = 0.040) when compared with age, gender, NYHA class, QRS duration greater than 150 ms, pre-CRT LVEF and etiology of heart failure. Conclusions PSD and PHB, measured by GMPS, may serve as biomarkers for the prediction of survival in patients undergoing CRT.
    Type of Medium: Online Resource
    ISSN: 0143-3636
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2021
    detail.hit.zdb_id: 2028880-3
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  • 2
    Online Resource
    Online Resource
    Society of Student Run Free Clinics ; 2022
    In:  Journal of Student-Run Clinics Vol. 8, No. 1 ( 2022-12-20)
    In: Journal of Student-Run Clinics, Society of Student Run Free Clinics, Vol. 8, No. 1 ( 2022-12-20)
    Abstract: Background: Student-run free clinics (SRFC) provide comprehensive primary care for uninsured populations throughout the country. However, imaging remains a barrier to care for underserved communities that experience inequitable access to healthcare. In this study, we describe the establishment of a radiology specialty clinic (RSC) that served as an in-house ultrasound imaging service at our institution's SRFC. Methods: Between September 2019 and March 2020, patients were scheduled for imaging at the free clinic site, and studies were performed and read by institutional radiologists. Patient data were reviewed to assess patient demographics, study indication, ultrasound type, and time between referral and appointment. Lastly, imaging utilization was examined seven months prior to and seven months after implementing the free ultrasound clinic to assess any changes in usage, wait time, or referral patterns using Fischer’s exact test and unpaired student t-tests. Results: A total of 10 patients were seen during the clinic’s operation, with 11 studies being performed.  Overall, usage patterns stayed consistent pre and post-implementation. There was no significant difference in wait times between referral and appointment (pre-RSC 15 days vs. post-RSC 18.5 days, p=0.91) and the RSC demonstrated a total cost savings of $770 to the clinic. Conclusions: We describe the implementation of an in-house ultrasound imaging service at our SRFC. The RSC provided increased access to imaging, demonstrated cost-savings to the SRFC, and had no negative effects on ultrasound usage or wait times between referrals and appointments.
    Type of Medium: Online Resource
    ISSN: 2474-9354
    URL: Issue
    Language: Unknown
    Publisher: Society of Student Run Free Clinics
    Publication Date: 2022
    detail.hit.zdb_id: 3103477-9
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  • 3
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 113, No. 15 ( 2016-04-12), p. 4027-4032
    Abstract: Deoxycytidine kinase (dCK), a rate-limiting enzyme in the cytosolic deoxyribonucleoside (dN) salvage pathway, is an important therapeutic and positron emission tomography (PET) imaging target in cancer. PET probes for dCK have been developed and are effective in mice but have suboptimal specificity and sensitivity in humans. To identify a more suitable probe for clinical dCK PET imaging, we compared the selectivity of two candidate compounds—[ 18 F]Clofarabine; 2-chloro-2′-deoxy-2′-[ 18 F]fluoro-9-β- d -arabinofuranosyl-adenine ([ 18 F]CFA) and 2′-deoxy-2′-[ 18 F]fluoro-9-β- d -arabinofuranosyl-guanine ([ 18 F]F-AraG)—for dCK and deoxyguanosine kinase (dGK), a dCK-related mitochondrial enzyme. We demonstrate that, in the tracer concentration range used for PET imaging, [ 18 F]CFA is primarily a substrate for dCK, with minimal cross-reactivity. In contrast, [ 18 F]F-AraG is a better substrate for dGK than for dCK. [ 18 F]CFA accumulation in leukemia cells correlated with dCK expression and was abrogated by treatment with a dCK inhibitor. Although [ 18 F]CFA uptake was reduced by deoxycytidine (dC) competition, this inhibition required high dC concentrations present in murine, but not human, plasma. Expression of cytidine deaminase, a dC-catabolizing enzyme, in leukemia cells both in cell culture and in mice reduced the competition between dC and [ 18 F]CFA, leading to increased dCK-dependent probe accumulation. First-in-human, to our knowledge, [ 18 F]CFA PET/CT studies showed probe accumulation in tissues with high dCK expression: e.g., hematopoietic bone marrow and secondary lymphoid organs. The selectivity of [ 18 F]CFA for dCK and its favorable biodistribution in humans justify further studies to validate [ 18 F]CFA PET as a new cancer biomarker for treatment stratification and monitoring.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2016
    detail.hit.zdb_id: 209104-5
    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
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