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Accès ouvert déclaré 2025 article

Identifying In-Hospital Risk Factors for Post-liver Transplant Seizures

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2Pays d’affiliation déclarés

Rattachement africain : ar, gb. Niveau de preuve : code pays fourni par la source.

Le résumé fourni par la source

Background Liver transplantation (LT) is a life-saving intervention for end-stage liver disease; however, postoperative complications, particularly neurological issues such as seizures, pose significant challenges. This study aims to identify perioperative factors associated with seizures following LT and develop a predictive risk model. By recognizing these in-hospital risk factors, clinicians may tailor perioperative management to mitigate seizure risk and improve neurological outcomes. Methodology We conducted a retrospective observational study of adult patients who underwent LT at a tertiary referral center between January 2009 and January 2019. Data were collected for the perioperative period, spanning seven days pre-LT to 30 days post-LT. Variables included demographic, clinical, neurological, and liver-related data. Statistical analyses compared patients with and without seizures using appropriate tests for categorical and continuous variables. A predictive model for seizures was developed using in-hospital factors. It was then internally validated and evaluated for accuracy, sensitivity, specificity, and receiver operating characteristic curve. From this model, a practical clinical risk score was created. Results Of 376 patients, 40 (10.6%) experienced seizures within 30 days post-LT. The median age was 54.8 years, and 41% were males. Chronic liver failure was the primary indication for LT, with alcohol abuse, hepatitis C, and hepatitis B being the most common etiologies. Patients' preoperative conditions included hepatocellular carcinoma (23%), chronic hyponatremia (22.6%), and prior kidney failure (22.1%). Portosystemic encephalopathy (PSE) was present in 46.5% of patients. Patients' preoperative blood tests revealed low hemoglobin (mean: 10.8 g/dL, SD: 2.2), hyponatremia (mean: 134 mEq/L, SD: 5), elevated international normalized ratio (mean: 2.21, SD: 1.56), high bilirubin (mean: 8.74 mg/dL, SD: 10.23), and creatinine (mean: 1.41 mg/dL, SD: 1.95). Combined liver and kidney transplantation was performed in 9.2% of cases, while 15.4% were emergency procedures. Graft complications occurred in 25% of patients, with functional delay being the most frequent (14.5%). Immunosuppressive regimens included prednisone with tacrolimus or mycophenolate. Seizures typically occurred on post-LT day seven (interquartile range: 5-13) and included uncertain onset (40%), non-convulsive status epilepticus (30%), generalized seizures (22.5%), convulsive status epilepticus (5%), and focal seizures (2.5%). Treatment was administered to 85% of seizure patients, primarily with levetiracetam (75%). Using seven acute perioperative variables, i.e., age at transplantation, history of PSE, pre-LT epilepsy diagnosis, pre-LT hemoglobin, procedure duration, graft cold ischemia time, and intraoperative blood transfusion, we developed a risk score for post-LT seizures. This score achieved an accuracy of 0.72 (95% CI: 0.63-0.80) and an area under the curve (AUC) of 0.90. Conclusions This study identifies key in-hospital factors associated with seizures following LT and presents a predictive risk model based on clinical preoperative and surgical variables. With an AUC of 0.90, the model demonstrates strong discriminative ability, suggesting it is a robust tool for predicting seizures in the immediate post-LT period. Further prospective multicenter studies are needed to externally validate the model and risk score, thereby enhancing its clinical applicability.

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Le contrôle bibliographique ouvert

DOI retrouvé dans Crossref DOI retrouvé ; titre concordant.

Titre Crossref
Identifying In-Hospital Risk Factors for Post-liver Transplant Seizures
Date Crossref
30/01/2025
Éditeur
Springer Science and Business Media LLC
Type
journal-article

Ce recoupement confirme des métadonnées liées au DOI. Il ne confirme ni la méthode ni les conclusions de l’étude, et il ne compte pas comme une seconde source scientifique indépendante.

Où se fait cette recherche

  • Favaloro Foundation Institute of Neurosciences pays non établi dans la notice
    Structure de recherche
  • Chartered Institute of Management Accountants pays non établi dans la notice
    Institution
  • Muscular Dystrophy UK pays non établi dans la notice
    Organisation à but non lucratif
  • Hospital CIMA Sanitas Department of Neurology pays non établi dans la notice
    Établissement de santé
  • John Walton Muscular Dystrophy Research Centre Department of Neurology pays non établi dans la notice
    Structure de recherche

Institute of Neurosciences — Favaloro Foundation, Chartered Institute of Management Accountants et Muscular Dystrophy UK, avec 2 autres affiliations.

Une affiliation ne permet pas de déduire la nationalité d’un auteur.

Les sujets associés

Epilepsy research and treatmentNeurological Complications and SyndromesPharmacological Effects and Toxicity Studies

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