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©The Author(s) 2025.
World J Hepatol. Sep 27, 2025; 17(9): 109118
Published online Sep 27, 2025. doi: 10.4254/wjh.v17.i9.109118
Table 2 Patients excluded from granulocyte colony stimulating factor therapy in randomized trial
Ref.
Intervention/control arm and inclusion criteria
Exclusion criteria
Survival at day 90
Singh et al[19] (2014)GCSF+SOC, SMTUpper gastrointestinal bleeding during the previous 10 days, hepatocellular carcinoma or portal vein thrombosis, hepatorenal syndrome, grade 3 or 4 hepatic encephalopathy, uncontrolled bacterial infection, human immunodeficiency virus infection, and other liver disease etiologies18/23 (78.2%); 05/23 (21.7%)
Singh et al[18] (2018)GCSF+SMT, SMT+GCSF+NAC, SMTSame as above13/19 (68.42%); 16/18 (88.8%); 6/20 (30%)
Shasthry et al[16] (2018)GCSF, SMTLille score < 0.45 at day 7. Multiorgan failure9/14 (64.2%); 4/14 (28.4%)
Tayek et al[42] (2022)GCSF + SMT, SMTPregnancy, uncontrolled infection, known human immunodeficiency virus infection, recent upper gastrointestinal hemorrhage, white blood cell > 30000/mm3, creatinine > 2 mg/dL, and AH therapy for more than three days before randomization12/16 (75%); 15/18 (83.2%)
Mishra et al[17] (2024)GCSF, GCSF+Predni-solone, PrednisoloneSerum creatinine > 1.5 mg/dL, total leukocyte count > 25000/cmm, mDF > 90, hemoglobin of less than 10 g/dL, active infection, recent upper gastrointestinal bleeding, and the existence of any other liver disease33/42 (78.5%); 37/42 (88.1%); 27/42 (64.2%)


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