Results 31 to 40 of about 39,924 (117)
Hyperkalemia: A persisting risk. A case report and update on current management
We report a case of hemodynamic instability due to bradycardia on the basis of severe hyperkalemia. Diabetic ketoacidosis and acute kidney injury together with polypharmacy triggered the acute onset.
Sebastian Schnaubelt +7 more
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Normoglycemic diabetic ketoacidosis in a type 2 diabetes patient on dapagliflozin: A case report
A 48‐year‐old male patient with Type 2 diabetes mellitus(T2D), on insulin replacement therapy, glipizide, and dapagliflozin presented with generalized weakness with weight loss of 40 pounds in 6 months ever since he was started on dapagliflozin.
Venkata Vinod Kumar Matli +3 more
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John A D’Elia,1 Alissa R Segal,1,2 George P Bayliss,3 Larry A Weinrauch1 1Kidney and Hypertension Section, Joslin Diabetes Center, Harvard Medical School, 2Department of Pharmacy Practice, MCPHS University, Boston, MA, 3Division of Kidney Diseases ...
D'Elia JA +3 more
doaj
Background/objectives Pregnant and postpartum women have a higher risk for developing severe Covid-19 and other clinical and obstetric complications. This study aims to evaluate the frequency of metabolic acidosis with elevated anion gap and describe a ...
Isabel Cristina Melo Mendes +8 more
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Clinical profile of diabetic ketoacidosis in tertiary care hospital of Eastern Nepal
Introduction: Diabetes ketoacidoisis (DKA) is characterized by hyperketonaemia, metabolic acidosis, and hyperglycemia. Aims: The aim of this study was to describe the demographic profile, clinical characterstics of patients admitted with diabetic ...
Robin Maskey +7 more
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Rhino-Orbital-Cerebral Mucormycosis: Successful Medical Management in a Resource Poor Setting [PDF]
Mucormycosis is commonly associated in diabetes. Rhino orbital cerebral mucormycosis (RCOM) is the most common type of presentation. Here we present a case of rhino orbital cerebral type of mucormycosis in a naïve Type 1 diabetic whose symptoms ...
Pravat Kumar Thato +4 more
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Background. Heterozygous intragenic mutations of the hepatocyte nuclear factor 1 homeobox b gene (HNF1B) located on chromosome 17 and microdeletion of 17q12 region (17q12MD) leads to the complete loss of this gene, which causes renal cystic ...
Can Aydın +7 more
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Beyond RPE: The Perception of Exercise Under Normal and Ketotic Conditions
AimSubjective perceptions of exercising exertion are integral to maintaining homeostasis. Traditional methods have utilized scores of ‘rating of perceived exertion’ (RPE) to quantify these subjective perceptions, and here we aimed to test whether RPE may
Olivia K. Faull +4 more
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Mitochondrial carbonic anhydrase VA (CA‐VA) deficiency is a rare inherited metabolic disorder caused by biallelic variants of the CA5A gene. It presents with hyperammonemia, lactic acidosis, and ketonuria, with or without hypoglycemia. We report the long‐
Shaymaa Shurrab +5 more
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Aim: Cerebral edema associated with diabetes ketoacidosis (CEDKA) is the most important clinical challenge in children with type-1 diabetes mellitus (T1DM). CEDKA is associated with a high rate of morbidity and mortality.
Masoumeh Sarvari +4 more
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