Author, date and country | Patient group | Study type (level of evidence) | Outcomes | Key results | Study Weaknesses |
---|---|---|---|---|---|
Ioannou GN, Doust J, Rockey DC 20 jan 2003 USA | patients with oesophageal variceal bleeding and receiving treatment with terlipressin;including one high quality RCT comparing in 219 patients terlipressin versus Emergency Sclerotherapy | Cochrane review comparing terlipressin treatment to various other treatments including Emergency Sclerotherapy | Mortality | Terlipressin (26/105); Sclerotherapy(19/114) OR 1.64 [ 0.85, 3.15 ] CI 95%; p-0.14 | only one study out of review relates to the topic, though that particular trial was of a high quality; comparing only to one out of possible endoscopic intervention- laser, banding etc. |
Failure of initial haemostasis | 20/105( Terlipressin); 20/114( Sclerotherapy) OR 1.11 [ 0.56, 2.19 ] CI 95%, p- 0.77 | ||||
Rebleedings | 26/105(Terlipressin); 29/114(Sclerotherapy); OR 0.96 [ 0.52, 1.78 ], CI95%, p-0.91 | ||||
number of other procedures required to control Bleeding ( TIPS, Thamponade, Sclerotherapy, Surgery) | 17/105(Terlipressin); 21/114( Sclerotherapy) OR 0.86 [ 0.43, 1.72 ] CI95%, p-0.66 | ||||
Number of blood transfusions | mean(SD)4.7(4.8)(Terlipressin);mean(SD) 4.5(4.3)(Sclerotherapy)- Mean Difference 0.20 [ -1.01, 1.41 ], CI95%, p-0.75 | ||||
Length of Hospitalization | Mean(SD)17 (10) (Terlipressin); Mean(SD)18 (10)(Sclerotherapy), Mean Difference- -1.00 [ -3.65, 1.65 ] CI95%, p-0.46 | ||||
D’Amico G, Pagliaro L, Pietrosi G, Tarantino I 2001 Italy | 1146 cirrhotic patients with acute variceal bleeding | Cochrane review of 12 RCT comparing sclerotherapy versus various vasoactive treatments (vasopressin (± nitroglycerin), terlipressin, somatostatin, or octreotide) | failure to control bleeding (11 RCTs, 977 pts) | Risk Differrence( Combined)CI95% -0.03 (-0.07 to 0.01)p=0.14 | only sclerotherapy is chosen as endoscopic treatment selection includes patients only with variceal UGIB |
Five-day failure rate(7 RCTs, 759 pts) | Risk Differrence( Combined)CI95% -0.05 (-0.12 to 0.01)p=0.087 | ||||
rebleeding (11 RCTs, 1082 pts) | Risk Differrence( Combined)CI95% -0.01(-0.06 to 0.04)p=0.68 | ||||
rebleeding before other elective treatments (9 RCTs, 975 pts) | Risk Differrence( Combined)CI95% -0.02 (-0.06 to 0.03) p=0.46 | ||||
mortality(12 RCTs, 1146 pts) | Risk Differrence( Combined)CI95% -0.04 (-0.08 to 0.00) p= 0.079 | ||||
mortality before other elective treatments (5 RCTs, 474 pts) | Risk Differrence( Combined)CI95% -0.02 (-0.07 to 0.04) p= 0.54 | ||||
transfused blood units (7 RCTs, 793 pts) | (weighted mean difference CI95%) -0.17 (-0.52 to 0.19) p= 0.36 | ||||
Adverse events (11 RCTs, 1082pts) | Risk Differrence( Combined)CI95% 0.08 (0.02 to 0.14) p= 0.0066 | ||||
serious adverse events (5 RCTs, 602 pts) | Risk Differrence( Combined)CI95% 0.05 (0.02 to 0.08) p= 0.0032 | ||||
Brennan M. R. Spiegel, MD; Nimish B. Vakil, MD; Joshua J. Ofman, MD, MSHS june 11, 2001 USA | Patients presenting with nonvariceal bleeding | Systematic Review of 23 articles, though only 4 randomised | early discharge in stable NVUGIB | 46% immediate discharge afterimmediate endoscopy(110 pts, Lee); no significant differences in the rest of the studies | |
mortality | no difference in all studies | ||||
rebleeding | |||||
need for surgery | |||||
desaturations | early | ||||
Alan Barkun, MD, MSc; Marc Bardou, MD, PhD; and John K. Marshall, MD, MSc 2003 | Patients with Nonvariceal Upper Gastrointestinal Bleeding | Clinical Guideline | < 24 h endoscopy in low risk patients | allows for safe and prompt discharge of patients classified as low risk (Recommendation: A [vote: a, 92%; b, 8%]; Evidence: I) | applies only to non variceal bleedings |
< 24 h endoscopy in high risk patients | improves patient outcomes for patients classified as high risk (Recommendation: C [vote: a, 64%; b, 36%]; Evidence: II-2) | ||||
< 24 h endoscopy | reduces resource utilization for patients classified as either low or high risk (Recommendation: A [vote: a, 88%; b, 12%]; Evidence: I) | ||||
David J. Bjorkman, MD, MSPH, SM, Atif Zaman, MD, M. Brian Fennerty, MD, David Lieberman, MD, James A 2000 USA | 93 patients with acute nonvariceal upper gastrointestinal bleeding | randomised controlled trial comparing < than 6 h endoscopy versus 6-48h | total length of stay | OR 3.98 days: 95% CI[2.84, 5.11], median, 3 days; and OR 3.26 days: 95% CI[2.32-4.21], median, 3 days, for <6h Endoscopy and 6-48h Endoscopy, respectively; p = 0.45. | Unstable patients were excluded from the study, thus possibly removing the group that would have benefit the most from emergent endoscopy |
transfusions requirement | 19 patients in early vs 15patients in 6-24h endoscopy(p=0.43); The mean number of transfusions was 1.54 for the Emergent Endoscopy group and 2.14 for the 6-48h Endoscopy group (p = 0.34) | ||||
mortality | 0 in both groups | ||||
surgery requirements | 1 in each group |