Gap finder

Search review questions

Each row is one question a systematic review asked: who, what, compared with what, and which outcome, with the effect it found and how certain that is. Words match anywhere in the field.

Limit to evidence status or GRADE (optional)

1,521 questions in 132 reviews · Hepato-Biliary

current versions
No studies 303 · 19.9%Ungraded 39 · 2.6%Very low 876 · 57.6%Low 216 · 14.2%Moderate 65 · 4.3%High 22 · 1.4%

Ungraded means an effect was reported without a GRADE rating; it is not a gap. No studies means the review found nothing to answer the question. The six categories are a display order, not a score.

QuestionEffectEvidenceStatus / GRADE
L‐ornithine L‐aspartate vs rifaximin
Mortality · people with cirrhosis who had minimal or overt hepatic encephalopathy or who were at risk for developing hepatic…
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
RR 0.33 [0.04, 3.03]2 studies · 105 participantsVery low
L‐ornithine L‐aspartate vs rifaximin
Hepatic encephalopathy assessed based on neurocognitive manifestations · people with cirrhosis who had minimal or overt hepatic encephalopathy or who were at risk for developing hepatic…
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
RR 1.06 [0.57, 1.96]2 studies · 105 participantsVery low
L‐ornithine L‐aspartate vs rifaximin
Serious adverse events assessed using ICH‐GCP · people with cirrhosis who had minimal or overt hepatic encephalopathy or who were at risk for developing hepatic…
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
RR 0.32 [0.01, 7.42]1 study · 43 participantsVery low
L‐ornithine L‐aspartate vs rifaximin
Quality of life assessed using questionnaires · people with cirrhosis who had minimal or overt hepatic encephalopathy or who were at risk for developing hepatic…
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
no estimate extractedNRNo studies
L‐ornithine L aspartate vs placebo or no intervention
Hepatic encephalopathy assessed based on neurocognitive manifestations
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
RR 0.7 [0.59, 0.83]22 studies · 1375 participantsVery low
L‐ornithine L‐aspartate vs rifaximin
Non‐serious adverse events assessed using ICH‐GCP · people with cirrhosis who had minimal or overt hepatic encephalopathy or who were at risk for developing hepatic…
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
RR 0.32 [0.01, 7.42]1 study · 43 participantsVery low
L‐ornithine L aspartate vs placebo or no intervention
Serious adverse events assessed using ICH‐GCP
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
RR 0.63 [0.45, 0.9]19 studies · 1489 participantsVery low
L‐ornithine L aspartate vs placebo or no intervention
Quality of life assessed using 3 different questionnaires
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
no estimate extractedNRVery low
L‐ornithine L aspartate vs placebo or no intervention
Non‐serious adverse events assessed using ICH‐GCP
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
RR 1.15 [0.75, 1.77]14 studies · 1076 participantsVery low
L‐ornithine L‐aspartate vs lactulose
Mortality · people with cirrhosis who had minimal or overt hepatic encephalopathy or who were at risk for developing hepatic…
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
RR 0.68 [0.11, 4.17]4 studies · 175 participantsVery low
L‐ornithine L‐aspartate vs lactulose
Hepatic encephalopathy assessed based on neurocognitive manifestations · people with cirrhosis who had minimal or overt hepatic encephalopathy or who were at risk for developing hepatic…
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
RR 1.13 [0.81, 1.57]4 studies · 175 participantsVery low
L‐ornithine L‐aspartate vs lactulose
Serious adverse events assessed using ICH‐GCP · people with cirrhosis who had minimal or overt hepatic encephalopathy or who were at risk for developing hepatic…
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
RR 0.69 [0.22, 2.11]3 studies · 144 participantsVery low
L‐ornithine L‐aspartate vs lactulose
Quality of life assessed using questionnaires · people with cirrhosis who had minimal or overt hepatic encephalopathy or who were at risk for developing hepatic…
L‐ornithine L‐aspartate for prevention and treatment of hepatic encephalopathy in people with cirrhosis (2018) · Cochrane
no estimate extractedNRNo studies
Exercise vs no exercise
All‐cause mortality · people with Child‐Pugh stage A or B cirrhosis
Physical exercise for people with cirrhosis (2018) · Cochrane
RR 0.19 [0.01, 3.73]6 studies · 173 participantsModerate
Exercise vs no exercise
Serious adverse events · people with Child‐Pugh stage A or B cirrhosis
Physical exercise for people with cirrhosis (2018) · Cochrane
RR 0.61 [0.19, 1.94]6 studies · 173 participantsLow
Exercise vs no exercise
Health‐related quality of life ‐ CLDQ (total score 1–7, high score corresponds to a better HRQoL) · people with Child‐Pugh stage A or B cirrhosis
Physical exercise for people with cirrhosis (2018) · Cochrane
no estimate extracted3 studies · 81 participantsLow
Exercise vs no exercise
Anthropometric measurements: mid‐arm circumference (cm) · people with Child‐Pugh stage A or B cirrhosis
Physical exercise for people with cirrhosis (2018) · Cochrane
no estimate extracted3 studies · 72 participantsLow
Exercise vs no exercise
Anthropometric measurements: mid‐thigh circumference (cm) · people with Child‐Pugh stage A or B cirrhosis
Physical exercise for people with cirrhosis (2018) · Cochrane
no estimate extracted5 studies · 128 participantsLow
Exercise vs no exercise
Physical fitness: peak exercise oxygen uptake (mL/kg/minute) · people with Child‐Pugh stage A or B cirrhosis
Physical exercise for people with cirrhosis (2018) · Cochrane
no estimate extracted4 studies · 100 participantsLow
Exercise vs no exercise
Physical fitness: 6‐Minute Walk Test (min in total) · people with Child‐Pugh stage A or B cirrhosis
Physical exercise for people with cirrhosis (2018) · Cochrane
no estimate extracted4 studies · 105 participantsVery low
Branched‐chain amino acids (BCAA) vs control
Mortality Clinically · people with hepatic encephalopathy.
Branched‐chain amino acids for people with hepatic encephalopathy (2017) · Cochrane
RR 0.88 [0.69, 1.11]15 studies · 760 participantsModerate
Branched‐chain amino acids (BCAA) vs control
Hepatic encephalopathy Psychometric and clinical assessments · people with hepatic encephalopathy.
Branched‐chain amino acids for people with hepatic encephalopathy (2017) · Cochrane
RR 0.73 [0.61, 0.88]16 studies · 827 participantsHigh
Branched‐chain amino acids (BCAA) vs control
Nausea and diarrhoea Clinically · people with hepatic encephalopathy.
Branched‐chain amino acids for people with hepatic encephalopathy (2017) · Cochrane
RR 3.39 [0.7, 16.46]5 studies · 945 participantsLow
Branched‐chain amino acids (BCAA) vs control
Albumin Laboratory assessment · people with hepatic encephalopathy.
Branched‐chain amino acids for people with hepatic encephalopathy (2017) · Cochrane
no estimate extracted3 studies · 176 participantsLow
Branched‐chain amino acids (BCAA) vs control
Nitrogen balance Laboratory assessment · people with hepatic encephalopathy.
Branched‐chain amino acids for people with hepatic encephalopathy (2017) · Cochrane
no estimate extracted3 studies · 108 participantsLow
Flumazenil vs placebo
All‐cause mortality · people with hepatic encephalopathy
Flumazenil versus placebo or no intervention for people with cirrhosis and hepatic encephalopathy (2017) · Cochrane
RR 0.75 [0.48, 1.16]11 studies · 842 participantsLow
Flumazenil vs placebo
Hepatic encephalopathy · people with hepatic encephalopathy
Flumazenil versus placebo or no intervention for people with cirrhosis and hepatic encephalopathy (2017) · Cochrane
RR 0.75 [0.71, 0.8]9 studies · 824 participantsLow
Flumazenil vs placebo
Serious adverse events · people with hepatic encephalopathy
Flumazenil versus placebo or no intervention for people with cirrhosis and hepatic encephalopathy (2017) · Cochrane
no estimate extracted11 studies · 842 participantsLow
Terlipressin vs placebo or no intervention
Mortality · people with hepatorenal syndrome
Terlipressin versus placebo or no intervention for people with cirrhosis and hepatorenal syndrome (2017) · Cochrane
RR 0.85 [0.73, 0.98]9 studies · 534 participantsLow
Terlipressin vs placebo or no intervention
Hepatorenal syndrome · people with hepatorenal syndrome
Terlipressin versus placebo or no intervention for people with cirrhosis and hepatorenal syndrome (2017) · Cochrane
RR 0.63 [0.48, 0.82]7 studies · 510 participantsLow
Terlipressin vs placebo or no intervention
Serious adverse events · people with hepatorenal syndrome
Terlipressin versus placebo or no intervention for people with cirrhosis and hepatorenal syndrome (2017) · Cochrane
RR 0.91 [0.68, 1.21]9 studies · 534 participantsLow
Terlipressin vs placebo or no intervention
Serious cardiovascular adverse events · people with hepatorenal syndrome
Terlipressin versus placebo or no intervention for people with cirrhosis and hepatorenal syndrome (2017) · Cochrane
RR 7.26 [1.7, 31.05]4 studies · 234 participantsLow
Terlipressin vs placebo or no intervention
Abdominal pain · people with hepatorenal syndrome
Terlipressin versus placebo or no intervention for people with cirrhosis and hepatorenal syndrome (2017) · Cochrane
RR 1.54 [0.97, 2.43]4 studies · 294 participantsLow
Terlipressin vs placebo or no intervention
Diarrhoea · people with hepatorenal syndrome
Terlipressin versus placebo or no intervention for people with cirrhosis and hepatorenal syndrome (2017) · Cochrane
RR 5.76 [2.19, 15.15]2 studies · 240 participantsLow
Hepatitis B immunoglobulin (HBIG) vs no intervention
All‐cause mortality or other serous adverse events of the newborn
Hepatitis B immunoglobulin during pregnancy for prevention of mother‐to‐child transmission of hepatitis B… (2017) · Cochrane
no estimate extracted0 studies · 1 participantsUngraded
Hepatitis B immunoglobulin (HBIG) vs no intervention
All‐cause mortality or other serous adverse events of the mothers
Hepatitis B immunoglobulin during pregnancy for prevention of mother‐to‐child transmission of hepatitis B… (2017) · Cochrane
no estimate extracted0 studies · 1 participantsUngraded
Hepatitis B immunoglobulin (HBIG) vs no intervention
Newborn with HBsAg‐positive result
Hepatitis B immunoglobulin during pregnancy for prevention of mother‐to‐child transmission of hepatitis B… (2017) · Cochrane
RR 0.3 [0.24, 0.38]29 studies · 5310 participantsVery low
Hepatitis B immunoglobulin (HBIG) vs no intervention
Newborn with HBeAg‐positive result
Hepatitis B immunoglobulin during pregnancy for prevention of mother‐to‐child transmission of hepatitis B… (2017) · Cochrane
RR 0.68 [0.43, 1.05]7 studies · 1764 participantsVery low
Hepatitis B immunoglobulin (HBIG) vs no intervention
Newborn with HBV‐DNA‐positive result
Hepatitis B immunoglobulin during pregnancy for prevention of mother‐to‐child transmission of hepatitis B… (2017) · Cochrane
RR 0.25 [0.15, 0.42]16 studies · 2130 participantsLow
Intervention NR
All‐cause mortality ( · people with hepatic encephalopathy
Probiotics for people with hepatic encephalopathy (2017) · Cochrane
RR 0.58 [0.23, 1.44]7 studies · 404 participantsLow
Intervention NR
Adverse events ‐ Change of/or withdrawal from treatment ( · people with hepatic encephalopathy
Probiotics for people with hepatic encephalopathy (2017) · Cochrane
RR 1.27 [0.88, 1.82]7 studies · 490 participantsVery low
Intervention NR
Quality of life ( · people with hepatic encephalopathy
Probiotics for people with hepatic encephalopathy (2017) · Cochrane
no estimate extracted1 study · 69 participantsVery low
Intervention NR
Plasma ammonia concentration (final and change scores) (μmol/L) ( · people with hepatic encephalopathy
Probiotics for people with hepatic encephalopathy (2017) · Cochrane
no estimate extracted6 studies · 325 participantsVery low
Intervention NR
No‐recovery (incomplete resolution of clinical symptoms) ( · people with hepatic encephalopathy
Probiotics for people with hepatic encephalopathy (2017) · Cochrane
RR 0.67 [0.56, 0.79]10 studies · 574 participantsModerate
Intervention NR
Adverse events ‐ Overt hepatic encephalopathy ( · people with hepatic encephalopathy
Probiotics for people with hepatic encephalopathy (2017) · Cochrane
RR 0.29 [0.16, 0.51]10 studies · 585 participantsLow
Intervention NR
Adverse events ‐ Change of/or withdrawal from treatment ( · people with hepatic encephalopathy
Probiotics for people with hepatic encephalopathy (2017) · Cochrane
RR 0.7 [0.46, 1.07]9 studies · 551 participantsVery low
Intervention NR
Quality of life ( · people with hepatic encephalopathy
Probiotics for people with hepatic encephalopathy (2017) · Cochrane
no estimate extracted3 studies · 115 participantsLow
Intervention NR
Plasma ammonia concentration (final and change scores) (μmol/L) ( · people with hepatic encephalopathy
Probiotics for people with hepatic encephalopathy (2017) · Cochrane
no estimate extracted10 studies · 705 participantsLow
Intervention NR
All‐cause mortality ( · people with hepatic encephalopathy
Probiotics for people with hepatic encephalopathy (2017) · Cochrane
RR 5 [0.25, 102]2 studies · 200 participantsVery low
Intervention NR
No‐recovery (incomplete resolution of clinical symptoms) ( · people with hepatic encephalopathy
Probiotics for people with hepatic encephalopathy (2017) · Cochrane
RR 1.01 [0.85, 1.21]7 studies · 430 participantsVery low