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  1. AU="Abdallah G. Kfoury"
  2. AU="Zaeske, C"
  3. AU="Hammerich, Kristoff"
  4. AU="Paul J. Burgess"
  5. AU="Valek, Lucie"
  6. AU="Mandal, Surajit"
  7. AU="Krumm, Laura"
  8. AU="Shimura, Hidetoshi"
  9. AU="Munguia-Lopez, Jose Gil"
  10. AU="Eysert, Fanny"
  11. AU="Qazi Arisa, Fakhar Ali"
  12. AU="Guan, Yunshan"
  13. AU="Ayachi, Jihene"
  14. AU="Boulvard Chollet, Xavier L E"
  15. AU="Kwon, Sohee"
  16. AU=Fra-Bido Sigrid
  17. AU="Delgado, Teresa Cardoso"
  18. AU="Judy Ly"
  19. AU="E Richtig"
  20. AU="Jones, D. C."
  21. AU="Revillet, Hélène" AU="Revillet, Hélène"
  22. AU="Lee, Ji Ye"
  23. AU="Yoshinaga, Kazuaki"
  24. AU="Moturi, Krishna"
  25. AU="Loizeau, J"
  26. AU="Gentry, Matthew S"
  27. AU="Drury, Lucy S"
  28. AU="Caraman, Irina"

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  1. Artikel ; Online: Donor Age, Sex, and Cause of Death and Their Relationship to Heart Transplant Recipient Cardiac Death

    Margo E. Hammond / Charles Zollinger / Andrija Vidic / Gregory L. Snow / Joseph Stehlik / Rami A. Alharethi / Abdallah G. Kfoury / Stavros Drakos / M Elizabeth H. Hammond

    Journal of Clinical Medicine, Vol 12, Iss 24, p

    2023  Band 7629

    Abstract: Background: Recent studies indicate that donor innate immune responses participate in initiating and accelerating innate responses and allorecognition in the recipient. These immune responses negatively affect recipient outcomes and predispose recipients ...

    Abstract Background: Recent studies indicate that donor innate immune responses participate in initiating and accelerating innate responses and allorecognition in the recipient. These immune responses negatively affect recipient outcomes and predispose recipients to cardiovascular death (CV death). We hypothesized that a donor cause of death (COD) associated with higher levels of innate immune response would predispose recipients to more adverse outcomes post-transplant, including CV death. Methods: We performed a single-institution retrospective analysis comparing donor characteristics and COD to recipient adverse cardiovascular outcomes. We analyzed the medical records of local adult donors (age 18–64) in a database of donors where adequate data was available. Donor age was available on 706 donors; donor sex was available on 730 donors. We linked donor characteristics (age and sex) and COD to recipient CV death. The data were analyzed using logistic regression, the log-rank test of differences, and Tukey contrast. Results: Donor age, female sex, and COD of intracranial hemorrhage were significantly associated with a higher incidence of recipient CV death. Conclusions: In this single institution study, we found that recipients with hearts from donors over 40 years, donors who were female, or donors who died with a COD of intracranial hemorrhage had a higher frequency of CV death. Donor monitoring and potential treatment of innate immune activation may decrease subsequent recipient innate responses and allorecognition stimulated by donor-derived inflammatory signaling, which leads to adverse outcomes.
    Schlagwörter innate immunity ; intracranial hemorrhage ; heart transplantation ; donor factors ; antibody mediated rejection ; cardiovascular death ; Medicine ; R
    Thema/Rubrik (Code) 610
    Sprache Englisch
    Erscheinungsdatum 2023-12-01T00:00:00Z
    Verlag MDPI AG
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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  2. Artikel ; Online: Repeated measurement of the intermountain risk score enhances prognostication for mortality.

    Benjamin D Horne / Donald L Lappé / Joseph B Muhlestein / Heidi T May / Brianna S Ronnow / Kimberly D Brunisholz / Abdallah G Kfoury / T Jared Bunch / Rami Alharethi / Deborah Budge / Brian K Whisenant / Tami L Bair / Kurt R Jensen / Jeffrey L Anderson

    PLoS ONE, Vol 8, Iss 7, p e

    2013  Band 69160

    Abstract: BACKGROUND: The Intermountain Risk Score (IMRS), composed of the complete blood count (CBC) and basic metabolic profile (BMP), predicts mortality and morbidity in medical and general populations. Whether longitudinal repeated measurement of IMRS is ... ...

    Abstract BACKGROUND: The Intermountain Risk Score (IMRS), composed of the complete blood count (CBC) and basic metabolic profile (BMP), predicts mortality and morbidity in medical and general populations. Whether longitudinal repeated measurement of IMRS is useful for prognostication is an important question for its clinical applicability. METHODS: Females (N = 5,698) and males (N = 5,437) with CBC and BMP panels measured 6 months to 2.0 years apart (mean 1.0 year) had baseline and follow-up IMRS computed. Survival analysis during 4.0±2.5 years (maximum 10 years) evaluated mortality (females: n = 1,255 deaths; males: n = 1,164 deaths) and incident major events (myocardial infarction, heart failure [HF], and stroke). RESULTS: Both baseline and follow-up IMRS (categorized as high-risk vs. low-risk) were independently associated with mortality (all p<0.001) in bivariable models. For females, follow-up IMRS had hazard ratio (HR) = 5.23 (95% confidence interval [CI] = 4.11, 6.64) and baseline IMRS had HR = 3.66 (CI = 2.94, 4.55). Among males, follow-up IMRS had HR = 4.28 (CI = 3.51, 5.22) and baseline IMRS had HR = 2.32 (CI = 1.91, 2.82). IMRS components such as RDW, measured at both time points, also predicted mortality. Baseline and follow-up IMRS strongly predicted incident HF in both genders. CONCLUSIONS: Repeated measurement of IMRS at baseline and at about one year of follow-up were independently prognostic for mortality and incident HF among initially hospitalized patients. RDW and other CBC and BMP values were also predictive of outcomes. Further research should evaluate the utility of IMRS as a tool for clinical risk adjustment.
    Schlagwörter Medicine ; R ; Science ; Q
    Thema/Rubrik (Code) 310
    Sprache Englisch
    Erscheinungsdatum 2013-01-01T00:00:00Z
    Verlag Public Library of Science (PLoS)
    Dokumenttyp Artikel ; Online
    Datenquelle BASE - Bielefeld Academic Search Engine (Lebenswissenschaftliche Auswahl)

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