This Lille score for alcoholic hepatitis calculator determines mortality risk in patients suffering from alcoholic hepatitis and not reacting to steroid therapy. Below the form you can find more information on the Lille model factors, the formula and its guidelines.
How does this Lille score for alcoholic hepatitis calculator work?
This is a health calculator that predicts mortality in patients with alcoholic hepatitis and stratifies risk in said cases that don’t respond to steroid therapy. It evaluates the patient condition for the past 7 days since the diagnosis has been put and corticosteroid medication has been initialized, considering these criteria:
■ Age is used as a risk factor in the prognosis score and is given an important weigh in the final result.
■ Albumin, measured in g/dL or g/L is used as one of the main proteins, the serum determination allows a quick check of the liver function. Normal values are between 3.5 – 5 g/dL.
■ Bilirubin level at admission and bilirubin determination from day 7 measured in either mg/dL or µmol/L in order to monitor evolution and see whether the patient has responded to the steroid treatment in the past week.
■ Creatinine measured in either mg/dL or µmol/L, providing information on the clearance job of the kidneys and in general presenting elevated levels in patients with history of significant alcohol consumption.
■ Prothrombin time in seconds that shows liver function in terms of blood clotting and evidences any metabolic issues still present.
The formula used by the Lille score for alcoholic hepatitis calculator accounts for the factors above and involves different weighs, according to each individual importance:
Lille Model Score = Exp(-R)/(1 + Exp(-R))
R = [3.19 - (0.101 x age in years)] + (1.47 x albumin in g/dL) + [0.28215 x (bilirubin initial - bilirubin day7 in mg/dL)] - (0.206 x creatinine in mg/dL) - (0.11115 x bilirubin initial in mg/dL) - (0.0096 x prothrombin time in seconds)
Lille score guidelines
The Lille model is a risk stratification tool aiming to give a prognostic in cases unresponsive to corticosteroids at around 7 days since the therapy has begun. The score originated in the CHRU Lille center is applied usually in cases in which the Maddrey score was above 32 and determined the urgent administration of the treatment.
If the patient status doesn’t improve and if bilirubin determinations don’t show any signs of amelioration, there might be the case of a poor prognosis.
The model guidelines describe scores below 0.45 to be consistent with a 6 month survival rate of 85% while what is above the 0.45 cut off, to predict a 6 month survival rate of 25%. In the second scenario, the clinical management should focus on finding alternative therapies and refer the patient for a transplant waiting list.
Response to steroid medication is often crucial in determining the outcome of a patient suffering from AH and such prognosis models are implemented after the other liver disease assessments such as the Child-Pugh severity score.
The original model supervised the evolution of 320 patients in the development cohort and of 118 in the validation program. Baseline data from admission was taken as well as another determination of bilirubin in the 7th day of the study. One of the conclusions was that in severe cases, nonresponders presented an increased mortality risk in the following 3 months from treatment.
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