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Objective: The goal of this study was to characterize the pre-, peri-, and postoperative risk factors associated with early hyponatremia (defined as a serum sodium level < 135 mEq/L on or before postoperative day [POD] 3) following transsphenoidal pituitary surgery.
Methods: This retrospective study was performed using a single-institution database for patients undergoing surgery for pituitary adenoma (PA). Serum values were collected routinely throughout the postoperative period. Uni- and multivariable statistical analyses were performed to identify independent predictors of early hyponatremia. Patients with diabetes insipidus receiving desmopressin were excluded from the analysis.
Results: Of 254 patients with nonfunctional PAs (NFPAs), 65 (25.6%) developed early-onset hyponatremia. Univariable analysis showed that older age, higher preoperative serum sodium, higher preoperative serum glucose, BMI > 30 kg/m2, and pituitary apoplexy were significantly associated with early hyponatremia (p < 0.05). Multivariable logistic regression modeling revealed that the factors most strongly associated with early hyponatremia were thiazide diuretic use (OR 7.84, 95% CI 1.01-72.11; p = 0.049), pituitary apoplexy (OR 21.33, 95% CI 2.86-271.37; p = 0.006), preoperative glucose level (OR 1.16 per 10 mg/dl, 95% CI 1.02-1.36; p = 0.032), and BMI > 27 kg/m2 (OR 0.05, 95% CI 0.00-0.36; p = 0.010).
Conclusions: Early-onset hyponatremia is a common electrolyte derangement following transsphenoidal pituitary surgery for NFPAs. Clinical factors including low BMI, thiazide diuretic use, and elevated preoperative serum glucose were associated with an increased risk of early-onset hyponatremia. Higher BMI, in contrast, was protective against early-onset hyponatremia. Understanding the factors related to postoperative hyponatremia can aid in earlier detection, monitoring, and treatment for high-risk patients following PA surgery.
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http://dx.doi.org/10.3171/2024.12.JNS241384 | DOI Listing |
J Neurosurg
August 2025
Departments of2Neurosurgery and.
Objective: The goal of this study was to characterize the pre-, peri-, and postoperative risk factors associated with early hyponatremia (defined as a serum sodium level < 135 mEq/L on or before postoperative day [POD] 3) following transsphenoidal pituitary surgery.
Methods: This retrospective study was performed using a single-institution database for patients undergoing surgery for pituitary adenoma (PA). Serum values were collected routinely throughout the postoperative period.
AACE Clin Case Rep
March 2024
Division of Endocrinology, Department of Medicine, Montefiore Medical Center, Bronx, New York.
Background/objective: Immune checkpoint inhibitors (ICI), including Programmed Cell Death 1, Programmed Cell Death Ligand 1, and Cytotoxic T-lymphocyte Associated Antigen 4 inhibitors, upregulate T-cell responses against tumor cells and are becoming a cornerstone in the treatment of various advanced solid and hematological cancers. Mulvihill-Smith Syndrome (MSS) is a rare genetic syndrome that has been associated with metabolic abnormalities and early-onset tumors, including malignancies. We report the first known case of ICI-induced hyponatremia attributable to syndrome of inappropriate antidiuretic hormone ADH release (SIADH) in a patient with MSS.
View Article and Find Full Text PDFActa Paediatr
August 2024
Department of Paediatrics, Groote Schuur Hospital, University of Cape Town, Cape Town, South Africa.
Aim: There is limited literature available about necrotising enterocolitis (NEC) in low- and middle-income countries. This study sought to determine the proportion, pattern and risk factors for mortality among very low birth weight (VLBW) neonates with NEC in a middle-income setting.
Methods: A retrospective observational cohort study was conducted on all infants with birth weights less than 1501 g admitted from 2018 to 2020 at Groote Schuur Hospital, Cape Town, South Africa.
Am J Case Rep
December 2023
Department of Nephrology, Children's Hospital Affiliated to Capital Institute of Pediatrics, Beijing, China (mainland).
BACKGROUND Gitelman syndrome (GS) is a rare inherited autosomal recessive salt-losing renal tubulopathy. Early-onset GS is difficult to differentiate from Bartter syndrome (BS). It has been reported in some cases that cyclooxygenase (COX) inhibitors, which pharmacologically reduce prostaglandin E2(PGE2) synthesis, are helpful for GS patients, especially in children, but the long-term therapeutic effect has not yet been revealed.
View Article and Find Full Text PDFJ Obstet Gynaecol Res
February 2024
Department of Obstetrics and Gynecology, Chiba University Hospital, Chiba, Japan.
Aim: To identify the symptoms and relevant factors associated with acute adrenal insufficiency of early-onset Sheehan syndrome.
Methods: We retrospectively reviewed the charts of 125 women admitted to our intensive care unit because of postpartum hemorrhage between January 2011 and December 2021. Three women developed acute adrenal insufficiency.