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Effect of COVID 19 pneumonia on hyperglycemia: Is it different from non COVID pneumonia?
Knox, Daniel B; Hirshberg, Eliotte L; Orme, James; Peltan, Ithan; Lanspa, Michael J.
  • Knox DB; Division of Pulmonary and Critical Care Medicine, Intermountain Medical Center, Murray, UT, USA; Division of Pulmonary and Critical Care Medicine, University of Utah, Salt Lake City, UT, USA. Electronic address: dan.knox@imail.org.
  • Hirshberg EL; Division of Pulmonary and Critical Care Medicine, Intermountain Medical Center, Murray, UT, USA; Division of Pulmonary and Critical Care Medicine, University of Utah, Salt Lake City, UT, USA.
  • Orme J; Division of Pulmonary and Critical Care Medicine, Intermountain Medical Center, Murray, UT, USA; Division of Pulmonary and Critical Care Medicine, University of Utah, Salt Lake City, UT, USA.
  • Peltan I; Division of Pulmonary and Critical Care Medicine, Intermountain Medical Center, Murray, UT, USA; Division of Pulmonary and Critical Care Medicine, University of Utah, Salt Lake City, UT, USA.
  • Lanspa MJ; Division of Pulmonary and Critical Care Medicine, Intermountain Medical Center, Murray, UT, USA; Division of Pulmonary and Critical Care Medicine, University of Utah, Salt Lake City, UT, USA.
Diabetes Metab Syndr ; 16(2): 102407, 2022 Feb.
Article in English | MEDLINE | ID: covidwho-1634135
ABSTRACT
BACKGROUND AND

AIMS:

Glycemic control in critical illness has been linked to outcomes. We sought to investigate if COVID pneumonia was causing disrupted glycemic control compared to historically similar diseases.

METHODS:

At Intermountain Healthcare, a 23-hospital healthcare system in the intermountain west, we performed a multicenter, retrospective cohort observational study. We compared 13,268 hospitalized patients with COVID pneumonia to 6673 patients with non -COVID-pneumonia.

RESULTS:

Patients with COVID-19 were younger had fewer comorbidities, had lower mortality and greater length of hospital stay. Our regression models demonstrated that daily insulin dose, indexed for weight, was associated with COVID-19, age, diabetic status, HgbA1c, admission SOFA, ICU length of stay and receipt of corticosteroids. There was significant interaction between a diagnosis of diabetes and having COVID-19. Time in range for our IV insulin protocol was not correlated with having COVID after adjustment. It was correlated with ICU length of stay, diabetic control (HgbA1C) and prior history of diabetes. Among patients with subcutaneous (SQ) insulin only percent of glucose checks in range was correlated with diabetic status, having Covid-19, HgbA1c, total steroids given and Elixhauser comorbidity score even when controlled for other factors.

CONCLUSIONS:

Hospitalized patients with COVID-19 pneumonia who receive insulin for glycemic control require both more SQ and IV insulin than the non-COVID-19 pneumonia counterparts. Patients with COVID-19 who received SQ insulin only had a lower percent of glucose checks in range.
Subject(s)
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia / Diabetes Mellitus / Glycemic Control / SARS-CoV-2 / COVID-19 / Hyperglycemia Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Limits: Aged / Female / Humans / Male / Middle aged Language: English Journal: Diabetes Metab Syndr Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pneumonia / Diabetes Mellitus / Glycemic Control / SARS-CoV-2 / COVID-19 / Hyperglycemia Type of study: Cohort study / Experimental Studies / Observational study / Prognostic study Limits: Aged / Female / Humans / Male / Middle aged Language: English Journal: Diabetes Metab Syndr Year: 2022 Document Type: Article