Item request has been placed! ×
Item request cannot be made. ×
loading  Processing Request

Diabetic ketoacidosis and hyperglycemic hyperosmolar state are associated with higher in-hospital mortality and morbidity in diabetes patients hospitalized with ST-elevation myocardial infarction, but not within 30 days of readmission.

Item request has been placed! ×
Item request cannot be made. ×
loading   Processing Request
  • Additional Information
    • Source:
      Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
    • Publication Information:
      Original Publication: San Francisco, CA : Public Library of Science
    • Subject Terms:
    • Abstract:
      Competing Interests: The authors have declared that no competing interests exist.
      Background: While the cardiovascular risk of hyperglycemia has been thoroughly elucidated in patients with type 2 diabetes (T2DM) hospitalized for myocardial infarction, the evidence surrounding acute severe hyperglycemia is less well-established. Our study aimed to explore the impact of diabetic ketoacidosis (DKA) and hyperglycemic hyperosmolar state (HHS), both severe hyperglycemic conditions, on cardiovascular outcomes in patients with T2D admitted for ST-elevation myocardial infarction (STEMI).
      Methods: We used the National Readmission Database (2016-2019) to extract patients with T2DM and STEMI at baseline. Subsequently, we selected cases of DKA and HHS. The primary endpoint was in-hospital mortality. Secondary endpoints included in-hospital acute renal failure, cardiogenic shock, and 30-day readmission and mortality.
      Results: The presence of DKA increased the adjusted odds of mortality and cardiogenic shock by almost 2-fold (adjusted Odds Ratios aOR = 2.30 [1.70-3.12], 2.055 [1.602-2.637], respectively) and renal failure by nearly 5-fold (aOR = 5.175 [4.090-6.546]). HHS was also associated with higher odds of mortality, acute renal failure, and cardiogenic shock. In 30 days, DKA and HHS increased the risk of readmission (aOR = 1.815 [1.449-2.75], 1.751 [1.376-2.228], respectively). There were no differences in the rates of cardiovascular disease, mortality, or other cardiovascular events between DKA and HHS patients. Within 30 days of readmission, DKA and HHS were associated with higher odds of readmission but not mortality. Cardiovascular disease was the most common etiology of readmission in all patients. The incidence of non-STEMI was the highest in DKA patients, and the incidence of STEMI was the highest in the HHS group.
      Conclusion: The presence of diabetic ketoacidosis or hyperglycemic hyperosmolar state is associated with higher odds of mortality, renal failure, cardiogenic shock, and 30-day readmission in STEMI patients with type 2 diabetes, highlighting the need for enhanced clinical management and monitoring of patients experiencing acute hyperglycemia.
      (Copyright: © 2025 Almutairi et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.)
    • References:
      Diabetes. 2004 Aug;53(8):2079-86. (PMID: 15277389)
      Crit Care Med. 2007 Oct;35(10):2262-7. (PMID: 17717490)
      Adv Exp Med Biol. 2021;1307:153-169. (PMID: 32020518)
      Cardiovasc Diabetol. 2021 Sep 24;20(1):192. (PMID: 34560876)
      Int J Mol Sci. 2023 May 27;24(11):. (PMID: 37298308)
      Diabetes Care. 2000 May;23(5):658-63. (PMID: 10834426)
      J Am Coll Cardiol. 1995 Jul;26(1):57-65. (PMID: 7797776)
      Crit Care Med. 2005 Jul;33(7):1624-33. (PMID: 16003073)
      Diabetes Care. 2009 Jul;32(7):1335-43. (PMID: 19564476)
      Nat Rev Cardiol. 2021 Apr;18(4):291-304. (PMID: 33188304)
      Lancet. 2014 Mar 22;383(9922):1068-83. (PMID: 24315620)
      Am J Med Sci. 2012 Apr;343(4):321-6. (PMID: 21946827)
      Front Cardiovasc Med. 2022 Oct 10;9:940035. (PMID: 36299875)
      Circulation. 2002 Oct 15;106(16):2067-72. (PMID: 12379575)
      Diabetes Care. 2006 Apr;29(4):765-70. (PMID: 16567812)
      Diabetes Care. 2009 Jul;32(7):1153-7. (PMID: 19564471)
      Am Heart J. 2003 Oct;146(4):674-8. (PMID: 14564322)
      BMC Cardiovasc Disord. 2020 Jan 30;20(1):36. (PMID: 32000678)
      Eur Heart J. 2005 Apr;26(7):650-61. (PMID: 15728645)
      Diabetes Care. 2003 May;26(5):1485-9. (PMID: 12716809)
      Med Clin North Am. 1995 Jan;79(1):9-37. (PMID: 7808097)
      Endocr Rev. 2004 Feb;25(1):153-75. (PMID: 14769830)
      BMJ. 2019 May 29;365:l1114. (PMID: 31142480)
      Cardiovasc Diabetol. 2018 Apr 18;17(1):57. (PMID: 29669543)
      N Engl J Med. 2009 Mar 26;360(13):1283-97. (PMID: 19318384)
      Diabetes Care. 2005 Dec;28(12):2901-7. (PMID: 16306552)
      Diabetes Care. 2024 Aug 1;47(8):1257-1275. (PMID: 39052901)
      JAMA. 2005 Jan 26;293(4):437-46. (PMID: 15671428)
      N Engl J Med. 2018 Aug 16;379(7):633-644. (PMID: 30110583)
      Cardiovasc Diabetol. 2023 Apr 12;22(1):85. (PMID: 37046267)
      Diabet Med. 1992 Jul;9(6):536-41. (PMID: 1643801)
    • Publication Date:
      Date Created: 20250206 Date Completed: 20250206 Latest Revision: 20250208
    • Publication Date:
      20250208
    • Accession Number:
      PMC11801527
    • Accession Number:
      10.1371/journal.pone.0318774
    • Accession Number:
      39913488