Some characteristics of hyperglycaemic crisis differ between patients with and without COVID-19 at a safety-net hospital in a cross-sectional study
dc.creator | Shah, Arnav | |
dc.creator | Deak, Andrew | |
dc.creator | Allen, Shaneisha | |
dc.creator | Silfani, Elayna | |
dc.creator | Koppin, Christina | |
dc.creator | Zisman-Ilani, Yaara | |
dc.creator | Sirisena, Imali | |
dc.creator | Rose, Christina | |
dc.creator | Rubin, Daniel | |
dc.date.accessioned | 2021-10-18T15:52:12Z | |
dc.date.available | 2021-10-18T15:52:12Z | |
dc.date.issued | 2021-09-11 | |
dc.identifier.citation | Arnav Shah, Andrew Deak, Shaneisha Allen, Elayna Silfani, Christina Koppin, Yaara Zisman-Ilani, Imali Sirisena, Christina Rose & Daniel Rubin (2021) Some characteristics of hyperglycaemic crisis differ between patients with and without COVID-19 at a safety-net hospital in a cross-sectional study, Annals of Medicine, 53:1, 1642-1645, DOI: 10.1080/07853890.2021.1975042 | |
dc.identifier.issn | 1365-2060 | |
dc.identifier.doi | http://dx.doi.org/10.34944/dspace/6952 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12613/6971 | |
dc.description.abstract | Objective: To compare patients with DKA, hyperglycaemic hyperosmolar syndrome (HHS), or mixed DKA-HHS and COVID-19 [COVID (+)] to COVID-19-negative (−) [COVID (−)] patients with DKA/HHS from a low-income, racially/ethnically diverse catchment area. Methods: A cross-sectional study was conducted with patients admitted to an urban academic medical center between 1 March and 30 July 2020. Eligible patients met lab criteria for either DKA or HHS. Mixed DKA-HHS was defined as meeting all criteria for either DKA or HHS with at least 1 criterion for the other diagnosis. Results: A total of 82 participants were stratified by COVID-19 status and type of hyperglycaemic crisis [26 COVID (+) and 56 COVID (−)]. A majority were either Black or Hispanic. Compared with COVID (−) patients, COVID (+) patients were older, more Hispanic and more likely to have type 2 diabetes (T2D, 73% vs 48%, p < .01). COVID(+) patients had a higher mean pH (7.25 ± 0.10 vs 7.16 ± 0.16, p < .01) and lower anion gap (18.7 ± 5.7 vs 22.7 ± 6.9, p = .01) than COVID (−) patients. COVID (+) patients were given less intravenous fluids in the first 24 h (2.8 ± 1.9 vs 4.2 ± 2.4 L, p = .01) and were more likely to receive glucocorticoids (95% vs. 11%, p < .01). COVID (+) patients may have taken longer to resolve their hyperglycaemic crisis (53.3 ± 64.8 vs 28.8 ± 27.5 h, p = .09) and may have experienced more hypoglycaemia <3.9 mmol/L (35% vs 19%, p = .09). COVID (+) patients had a higher length of hospital stay (LOS, 14.8 ± 14.9 vs 6.5 ± 6.0 days, p = .01) and in-hospital mortality (27% vs 7%, p = .02). Discussion: Compared with COVID (−) patients, COVID (+) patients with DKA/HHS are more likely to have T2D. Despite less severe metabolic acidosis, COVID (+) patients may require more time to resolve the hyperglycaemic crisis and experience more hypoglycaemia while suffering greater LOS and risk of mortality. Larger studies are needed to examine whether differences in management between COVID (+) and (−) patients affect outcomes with DKA/HHS. | |
dc.format.extent | 5 pages | |
dc.language | English | |
dc.language.iso | eng | |
dc.relation.ispartof | Open Access Publishing Fund | |
dc.relation.haspart | Annals of Medicine, Vol. 53, Iss. 1 | |
dc.relation.isreferencedby | Taylor & Francis Open Access | |
dc.rights | Attribution CC BY | |
dc.rights.uri | https://creativecommons.org/licenses/by/4.0/ | |
dc.subject | COVID-19 | |
dc.subject | Hyperglycaemic emergencies | |
dc.subject | Diabetic ketoacidosis | |
dc.subject | Hyperglycaemic hyperos | |
dc.subject | Molar syndrome | |
dc.title | Some characteristics of hyperglycaemic crisis differ between patients with and without COVID-19 at a safety-net hospital in a cross-sectional study | |
dc.type | Text | |
dc.type.genre | Journal article | |
dc.description.department | Endocrinology, Diabetes, and Metabolism | |
dc.description.department | Social and Behavioral Sciences | |
dc.relation.doi | https://doi.org/10.1080/07853890.2021.1975042 | |
dc.ada.note | For Americans with Disabilities Act (ADA) accommodation, including help with reading this content, please contact scholarshare@temple.edu | |
dc.description.schoolcollege | Lewis Katz School of Medicine | |
dc.description.schoolcollege | Temple University. School of Pharmacy | |
dc.description.schoolcollege | Temple University. College of Public Health | |
dc.description.sponsor | Temple University Libraries Open Access Publishing Fund, 2021-2022 (Philadelphia, Pa.) | |
dc.creator.orcid | Zisman-Ilani|0000-0001-6852-2583 | |
dc.temple.creator | Shah, Arnav | |
dc.temple.creator | Deak, Andrew | |
dc.temple.creator | Allen, Shaneisha | |
dc.temple.creator | Silfani, Elayna | |
dc.temple.creator | Koppin, Christina | |
dc.temple.creator | Zisman-Ilani, Yaara | |
dc.temple.creator | Sirisena, Imali | |
dc.temple.creator | Rose, Christina | |
dc.temple.creator | Rubin, Daniel | |
refterms.dateFOA | 2021-10-18T15:52:12Z |