Skip to main content

Predicting the risk of early bleeding following endoscopic variceal ligation in cirrhotic patients with computed tomography

Abstract

Background

Life-threatening bleeding following endoscopic variceal ligation (EVL) in patients with cirrhosis rarely can occur. The present study aimed to evaluate the performance of computed tomography (CT) in predicting the risk of early bleeding following EVL in cirrhotic patients.

Methods

We retrospectively investigated 285 cirrhotic patients who had undergone EVL. EVL was performed for prophylaxis or acute variceal bleeding. The patients were classified into 2 groups: early bleeding (< 14 days after EVL) and non-early bleeding. We compared baseline characteristics including CT findings between the patient groups.

Results

Among the 285 patients who underwent EVL treatment, 19 patients (6.7%) experienced early bleeding. On average, these bleeding occurred 9.3 ± 3.5 days after the EVL, with a range of 3 to 13 days. Patients who experience early bleeding had a higher six-week bleeding-related mortality rate compared to those in the non-early bleeding group (31.6% vs. 10.2%; p = 0.014). There was a correlation between the grade of esophageal varix observed during endoscopy and the diameter of esophageal varix observed on CT (p < 0.001). The diameter of esophageal varix on CT was identified as the only significant predictive factor for early bleeding (p = 0.005).

Conclusion

A larger esophageal varix diameter observed on CT is associated with an increased risk of early bleeding after EVL treatment. Early identification of this high-risk group can provide a change of treatment strategies to improve patient outcomes.

Peer Review reports

Background

Gastroesophageal varices is one of the most common complications of advanced liver cirrhosis. Of Child-Pugh A patients, 45% have gastroesophageal varices and the prevalence increases up to 72% of Child-Pugh B/C patients [1]. Variceal bleeding, causative of 70% of all upper gastrointestinal bleeding, has an occurrence rate of 5–15% per year in patients with cirrhosis [2,3,4]. It remains one of the most severe and immediate life-threatening complications and mortality from esophageal variceal bleeding is as high as 20% [5]. The risk of variceal bleeding is related to variceal size and other reported predictors are decompensated cirrhosis (Child-Pugh B/C) and the endoscopic presence of red wale marks on the varices [6].

Current guidelines recommend non-selective beta-blockers or endoscopic variceal ligation (EVL) for primary prophylaxis of esophageal variceal bleeding. When acute variceal bleeding is confirmed by endoscopy, EVL should be performed. Despite treatment with vasoactive drugs plus EVL and prophylactic antibiotics, up to 10–15% of patients with acute variceal bleeding have persistent or early rebleeding [7,8,9].

Early bleeding after EVL is reported mainly due to early slippage of rubber bands and is fatal in some cases. Several previous studies have suggested the possible predictive factors for early bleeding after EVL: previous variceal bleeding, peptic esophagitis, low albumin, high D-dimer, presence of ascites, high aspartate aminotransferase to platelet ratio index (APRI) score, low prothrombin index, number of varices, extent of varices, and number of rubber bands [10,11,12,13]. Since these studies included heterogenous populations and the risk factors were not well validated, until now, there was no general consensus about the predictive factors and strategies to prevent early bleeding.

Patients with cirrhosis occasionally undergo multiphase computed tomography (CT) scans to screen for hepatocellular carcinoma (HCC). The evaluation of portosystemic collateral vessels, including gastroesophageal varices, using CT scans is possible. Several previous studies have evaluated the correlation between CT findings and endoscopy and have demonstrated that it was comparable to endoscopy in detecting varices [14,15,16]. In addition, other studies have shown that a CT scan is much better tolerated and more cost-effective than endoscopy [14, 17, 18]. Currently, however, studies have not examined the utility of CT scan in predicting the risk of early bleeding after EVL. The present study aimed to evaluate CT performance in predicting the risk of early bleeding following EVL, in patients with cirrhosis.

Patients and methods

Patients

Consecutive patients who had undergone EVL in Pusan National University Yangsan Hospital from January 2009 to December 2018 were retrospectively analyzed. EVL was performed for prophylaxis or acute bleeding of esophageal varices (EV). All patients received vasoactive drugs (terlipressin/somatostatin) and intravenous broad-spectrum antibiotics according to the guidelines [6]. Food intake after EVL was allowed at the discretion of the physician. The exclusion criteria included patients with incomplete medical records, those with a long time interval between endoscopy and CT (> 60 days), and those with unmeasurable EV or portal veins on the CT scan (Fig. 1). Laboratory results for all patients were retrieved on the day of EVL procedure.

Fig. 1
figure 1

Flow diagram of patient enrollment

According to the occurrence of early bleeding after EVL (bleeding occurring between 24 h and 14 days after the procedure), the patients were classified into 2 groups. Bleeding after EVL was defined according to the Baveno criteria as follows: (1) recurrent hematemesis, and/or melena, and/or bloody fluid drained by the nasogastric tube or (2) a decrease in hemoglobin by at least 2 g/dL, or a transfusion of more than 2 units of packed RBCs needed within 24 h, or hypovolemic instability [19]. Proton pump inhibitors (PPIs) were not administered after EVL [20, 21]. Bleeding-related death was defined as death within 6 weeks of the index bleeding [22]. The present study was conducted in accordance to the ethical guidelines of the Declaration of Helsinki and was approved by the Institutional Review Boards (IRB) of Pusan National University Yangsan Hospital. Requirement for informed consent was waived after review of IRB of Pusan National University Yangsan Hospital because it was practically impossible and this study was of retrospective design.

Endoscopic procedure for EVL

Upper endoscopy was performed using Olympus GIFQ 260 or Pentax EG 2940 scope. The grade of EV was classified as small straight (F1); enlarged tortuous, occupying less than one third of the esophageal lumen (F2); or large sized, coil-shaped that occupy more than one-third of the esophageal lumen (F3) [23]. EVL was performed using a multiband ligator (6 shooter Saeed Multi-band ligator, Cook Medical Endoscopy, Limerick, Ireland).

CT measurements

All patients underwent abdominal CT imaging including portal venous phase image. Different CT systems (Somatom Definition Flash, Somatom Definition AS+, or Somatom Sensation 16, Siemens Medical Systems, Erlangen, Germany; and Discovery 750HD, Revolution, General Electric Medical Systems, Milwaukee, WI, USA) were used with slice thickness of 5 mm, and a 3 mm reconstruction interval. CT images were obtained with settings of 100 or 120 kVp, and mAs was set by automatic exposure control for each patient. Portal venous image was obtained 60 s after contrast media injection during suspended inspiration. The CT images were evaluated with consensus by two abdominal radiologists (T.U.K with 12 years of experience, and H.R with 6 years of experience) who were blinded to the patient’s medical history, and laboratory and endoscopic findings. Maximum short axis diameter of the largest esophageal varix and maximum main portal vein diameter of each patient were recorded. Maximum main portal vein diameters were measured at a point at least 1 cm distal to the confluence of the splenic and superior mesenteric veins and at least 1 cm proximal to the first branch of the main portal vein on axial portal venous phase images [24].

Statistical analysis

Continuous variables between the early and non-early bleeding groups were analyzed using a Student`s t-test. The Chi-square test or Fisher`s exact test was used to investigate the association between categorical factors and early bleeding. Differences between groups of continuous variables that were non-parametrically distributed were assessed using Kruskal–Wallis tests. All variables selected in univariate analysis (p < 0.20) were included in the multivariate model. In the multivariate analysis, logistic regression models were used to investigate the independent risk factors associated with early bleeding after EVL. Receiver operator characteristics (ROC) curves were used to evaluate the optimal cut-off value for EV diameter on CT. Statistical analysis was performed using SPSS for Windows (version 21; SPSS Inc., Chicago, IL, USA). All p-values < 0.05 were considered statistically significant.

Results

Baseline characteristics of the enrolled patients

A total of 285 patients who underwent EVL were included in our study. The baseline characteristics of the enrolled patients are shown in Table 1. Our study included 232 (81.4%) males and 53 (18.6%) females. The mean age was 60.5 ± 10.7 years. There were 89 (31.2%), 144 (50.5%), and 52 (18.3%) patients with Child-Pugh classification of A, B, and C, respectively. In 16 (5.6%), 92 (32.3%), and 177 (62.1%) patients, the EV grades were F1, F2, and F3, respectively. Eighty-three (29.1%) patients had a concomitant gastric varices (GV) and 33 (11.6%) patients had a previous history of variceal bleeding. Twenty six (9.1%) patients had portal vein thrombosis, and 122 (42.8%) patients had HCC. Model for end-stage liver disease (MELD) score was 13.7 ± 5.6 and prothrombin time (PT) was 16.3 ± 3.1 sec.

Table 1 Baseline clinical characteristics of the enrolled patients

Comparison of baseline characteristics between early bleeding and non-early bleeding groups

Among the 285 patients treated with EVL, 19 patients (6.7%) developed early bleeding. Early bleeding occurred with a mean day of 9.3 ± 3.5 days (range: 3–13 days). Six weeks bleeding-related death rate was 11.6% (33/285).

The characteristics of both the early and non-early bleeding groups are presented in Table 2. There was no difference between groups regarding various factors except six-week bleeding-related mortality rate. The severity of the liver disease was similar in both groups [Child Pugh class score (p = 0.313) and MELD (p = 0.223)]. Previous history of variceal bleeding (p = 0.553)], indication of EVL (p = 0.835), presence of ascites (p = 0.197), the presence of portal vein thrombosis (p = 0.943), PT (p = 0.157) and total bilirubin (p = 0.050) were not significantly different between groups. Six-week bleeding-related mortality rate was significantly higher in early bleeding group than in the non-early bleeding group (31.6% vs. 10.2%; p = 0.014).

Table 2 Comparison of baseline characteristics between the patient groups

Comparison of imaging parameters

Correlation between the grade of EV observed during endoscopy and the diameter of EV on CT was significant (p < 0.001) (Fig. 2). The imaging data of both the early and non-early bleeding groups are presented in Table 3. There was no difference of the endoscopic findings. The grade of EV (p = 0.238), number of varices (p = 0.244), presence of concomitant gastric varices (p = 0.807), and number of EVL (p = 0.676) were not significantly different between groups. On CT findings, EV diameter was significantly different between groups. The EV diameter was larger in the early than non-early bleeding group (8.42 ± 2.74 vs. 6.84 ± 2.33; p = 0.005).

Fig. 2
figure 2

A Relationship between CT variceal diameter and endoscopic grading. B, C 44-year-old man with liver cirrhosis and large esophageal varices. Portal phase CT image of esophagus shows multiple nodular, enhancing, intraluminally protruding lesions (arrows) within esophagus wall. In this patient, largest varix was measured as 10.7 mm. Endoscopic image shows multiple large varices

Table 3 Comparison of imaging date between the patient groups

Multivariate analysis of risk factors for early bleeding after EVL

Four variables (p < 0.20) were identified in univariate analysis; total bilirubin, PT, presence of ascites, and EV size. In multivariate analysis, EV diameter on CT was the only independent predictive factor for early bleeding after EVL (OR 1.336, 95% CI 1.099–1.624, p = 0.004) (Table 4). We calculated the cut off value, which was 7.5 mm and had a sensitivity and specificity of 63.2% and 61.7% (area under the curve of 0.7), respectively; to determine the optimal EV diameter on CT (Fig. 3).

Table 4 Multivariate analysis of risk factors for early bleeding after EVL
Fig. 3
figure 3

ROC curve shows the predictive ability of esophageal diameter on CT for predicting the early bleeding after EVL.

Discussion

EVL is an effective method to treat or prevent esophageal variceal bleeding. Bleeding after EVL, which was mainly associated with EVL-induced ulcer bleeding, occurs in 2.8 to 7.8% of patients [10,11,12, 25, 26], and the mortality is reported to be as high as 52% [10]. Previous studies suggested several factors associated with early bleeding after EVL. Poor liver function has been well known as a predictive factor of early bleeding in patients with liver cirrhosis. Yang et al. demonstrated that end-stage liver cirrhosis (Child-Pugh C) was an independent risk factor for early bleeding within 14 days of EVL [27]. Berreta et al. reported that Child-Pugh C classification was an independent predictive factor for rebleeding-related death [28]. Other studies found that each variable for Child-Pugh classification was an independent risk factor for early bleeding or rebleeding within 4 weeks of EVL. PT or index, albumin, presence or severity for ascites, and MELD were reported as independent predictive factors for early bleeding or rebleeding after EVL [10,11,12,13, 26].

Regarding the endoscopic findings of varices, previous studies suggested several risk factors. Xu et al. reported that varices throughout the whole extent of the esophagus are more dangerous than those that are limited to the middle and lower esophagus for early rebleeding [11]. Cho et al. reported that concomitant F3 GV was a risk factor for EVL-induced ulcer bleeding [12]. The risk factors not only related to severity of liver function, but also related to EVL procedure. Lee et al. found that the higher number of EV ligations was significantly associated with rebleeding within 6 weeks of EVL due to extensive surface area of the mucosal injury [29]. Xu et al. also proved that the more rubber bands that were used for ligation, the greater the possibility of rebleeding within 2 weeks [11]. Sinclair et al. found that a higher band-induced ulcer bleeding rate within 4 weeks were observed following EVL for acute variceal hemorrhage, which EVL is unavoidable than prophylactic EVL [26]. In our study, we collected data previously reported as risk factors and evaluated whether they were useful as predictors for early bleeding, however, we could not draw convincing conclusions. This can be explained by sampling differences, heterogenous populations, different definitions such as early bleeding and bleeding period, and selection bias due to retrospective study design.

Considering the morbidity and mortality associated with variceal hemorrhage in patients with cirrhosis, it is recommended that these patients should undergo endoscopic screening for the evaluation of gastroesophageal varices [4]. However, it has been observed that there are costs and risks associated with endoscopy and endoscopy, which can be poorly tolerated, particularly in patients with cirrhosis [30,31,32]. Patients with cirrhosis sometimes undergo CT scans to screen for HCC when ultrasound surveillance is suboptimal [33, 34]. With the recent advancement in multiphase CT, the evaluation of portosystemic collateral vessels using CT scan is possible. Previous studies have evaluated the correlation for varices between CT and endoscopy findings and have reported that CT results were comparable to those of endoscopy in detecting varices. Furthermore, agreement between radiologists, regarding the size of varices, was better than between endoscopists [14,15,16]. In a prospective study, CT was found to have approximately 90% sensitivity and 50% specificity in detecting esophageal varices [14]. A recent retrospective study reported a CT sensitivity of 98.96%, specificity of 100%, and diagnostic accuracy of 98.97% for EV in patients with chronic liver disease [35]. Therefore, CT can be considered as a potential noninvasive, less expensive and more compliant EV detection method compared to the invasive endoscopic screening modality.

To date, previous studies investigated the diagnostic accuracy and correlation between CT and endoscopic findings, these studies have not evaluated CT findings associated with variceal bleeding. There was only one study which evaluated the CT findings to predict variceal hemorrhage, but no studies have explored the prognostic value of CT in predicting the risk of early bleeding after EVL. To our knowledge, our study is the first to investigate the associations between CT findings and early bleeding after EVL in patients with cirrhosis. Results from our study show that a larger EV diameter on CT is the only independent predictive factor for early EV bleeding. Differences in distension of the esophagus, which cause some of the discrepancy in accessing variceal size during endoscopy and CT, may account for our results. While the esophagus is insufflated or deflated during endoscopy, the transluminal pressure and, consequently, EV size are variable. When the esophagus is nondistended during CT, the hemodynamics of the varices are maintained. Therefore, the assessment of varices in a nondistended state during CT may allow for a more accurate measurement of varix diameter.

There are several limitations of our study. First, this was a retrospective study with selection bias and the number of patients who experienced early bleeding were relatively few. Second, early bleeding events were not all confirmed by endoscopy and therefore, we could not classify bleeding events as EVL-induced ulcer bleeding or new variceal bleeding. Third, although we confined time interval between endoscopy and CT (≤ 60 days), interval progression or regression of EV cannot be entirely ruled out. Fourth, imaging measurements had variability in findings. There may be the variability in CT findings between radiologists, as well as in endoscopic findings between endoscopists. Furthermore, in endoscopic findings, there may be inaccuracy for assessing the grade of EV during the acute variceal bleeding. Lastly, although we suggest the specific cut-off value of diameter of EV diameter on CT, we could not perform further validation.

In conclusion, a larger EV diameter on CT is a risk factor for early bleeding after EVL treatment. The optimal cut-off value for EV size remains to be determined. Therefore, further large cohort, prospective design are required to determine the optimal cut-off value and role of CT as a noninvasive screening tool for the early identification of high-risk groups and change of treatment strategies to improve patient outcomes.

Data availability

The datasets generated and/or analysed during the current study are not publicly available due to protect the privacy of the patient, but are available from the corresponding author on reasonable request.

References

  1. Kovalak M, Lake J, Mattek N, Eisen G, Lieberman D, Zaman A. Endoscopic screening for varices in cirrhotic patients: data from a national endoscopic database. Gastrointest Endosc. 2007;65(1):82–8.

    Article  PubMed  Google Scholar 

  2. Groszmann RJ, Garcia-Tsao G, Bosch J, Grace ND, Burroughs AK, Planas R, Escorsell A, Garcia-Pagan JC, Patch D, Matloff DS, et al. Beta-blockers to prevent gastroesophageal varices in patients with Cirrhosis. N Engl J Med. 2005;353(21):2254–61.

    Article  CAS  PubMed  Google Scholar 

  3. Abraldes JG, Bureau C, Stefanescu H, Augustin S, Ney M, Blasco H, Procopet B, Bosch J, Genesca J, Berzigotti A, et al. Noninvasive tools and risk of clinically significant portal Hypertension and varices in compensated Cirrhosis: the anticipate study. Hepatology. 2016;64(6):2173–84.

    Article  CAS  PubMed  Google Scholar 

  4. de Franchis R, Baveno VIF. Expanding consensus in portal Hypertension: report of the Baveno VI Consensus Workshop: stratifying risk and individualizing care for portal Hypertension. J Hepatol. 2015;63(3):743–52.

    Article  PubMed  Google Scholar 

  5. D’Amico G, Garcia-Tsao G, Pagliaro L. Natural history and prognostic indicators of survival in Cirrhosis: a systematic review of 118 studies. J Hepatol. 2006;44(1):217–31.

    Article  PubMed  Google Scholar 

  6. Garcia-Tsao G, Sanyal AJ, Grace ND, Carey W. Practice Guidelines Committee of the American Association for the Study of Liver D, Practice Parameters Committee of the American College of G: Prevention and management of gastroesophageal varices and variceal Hemorrhage in Cirrhosis. Hepatology. 2007;46(3):922–38.

    Article  CAS  PubMed  Google Scholar 

  7. Garcia-Tsao G, Bosch J. Management of varices and variceal Hemorrhage in Cirrhosis. N Engl J Med. 2010;362(9):823–32.

    Article  CAS  PubMed  Google Scholar 

  8. Avgerinos A, Nevens F, Raptis S, Fevery J. Early administration of somatostatin and efficacy of sclerotherapy in acute oesophageal variceal bleeds: the European Acute bleeding Oesophageal Variceal episodes (ABOVE) randomised trial. Lancet. 1997;350(9090):1495–9.

    Article  CAS  PubMed  Google Scholar 

  9. Levacher S, Letoumelin P, Pateron D, Blaise M, Lapandry C, Pourriat JL. Early administration of terlipressin plus glyceryl trinitrate to control active upper gastrointestinal bleeding in cirrhotic patients. Lancet. 1995;346(8979):865–8.

    Article  CAS  PubMed  Google Scholar 

  10. Vanbiervliet G, Giudicelli-Bornard S, Piche T, Berthier F, Gelsi E, Filippi J, Anty R, Arab K, Huet PM, Hebuterne X, et al. Predictive factors of bleeding related to post-banding Ulcer following endoscopic variceal ligation in cirrhotic patients: a case-control study. Aliment Pharmacol Ther. 2010;32(2):225–32.

    Article  CAS  PubMed  Google Scholar 

  11. Xu L, Ji F, Xu QW, Zhang MQ. Risk factors for predicting early variceal rebleeding after endoscopic variceal ligation. World J Gastroenterol. 2011;17(28):3347–52.

    Article  PubMed  PubMed Central  Google Scholar 

  12. Cho E, Jun CH, Cho SB, Park CH, Kim HS, Choi SK, Rew JS. Endoscopic variceal ligation-induced Ulcer bleeding: what are the risk factors and treatment strategies? Med (Baltim). 2017;96(24):e7157.

    Article  Google Scholar 

  13. Rui Sun XQ, Zou D, Shao X, Li H, Guo X. Risk factors for 5-day bleeding after endoscopic treatments for gastroesophageal varices in liver Cirrhosis. AME Med J 2017, 2(3).

  14. Perri RE, Chiorean MV, Fidler JL, Fletcher JG, Talwalkar JA, Stadheim L, Shah ND, Kamath PS. A prospective evaluation of computerized tomographic (CT) scanning as a screening modality for esophageal varices. Hepatology. 2008;47(5):1587–94.

    Article  PubMed  Google Scholar 

  15. Yu NC, Margolis D, Hsu M, Raman SS, Lu DS. Detection and grading of esophageal varices on liver CT: comparison of standard and thin-section multiplanar reconstructions in diagnostic accuracy. AJR Am J Roentgenol. 2011;197(3):643–9.

    Article  PubMed  Google Scholar 

  16. Shen M, Zhu KS, Meng XC, Zhang JS, Liu LY, Shan H. [Evaluation of esophageal varices and predicting the risk of esophageal varices bleeding with multi-detector CT in patients with portal Hypertension]. Zhonghua Yi Xue Za Zhi. 2010;90(41):2911–5.

    PubMed  Google Scholar 

  17. Kim SH, Kim YJ, Lee JM, Choi KD, Chung YJ, Han JK, Lee JY, Lee MW, Han CJ, Choi JI, et al. Esophageal varices in patients with Cirrhosis: multidetector CT esophagography–comparison with endoscopy. Radiology. 2007;242(3):759–68.

    Article  PubMed  Google Scholar 

  18. Kim YJ, Raman SS, Yu NC, To’o KJ, Jutabha R, Lu DS. Esophageal varices in cirrhotic patients: evaluation with liver CT. AJR Am J Roentgenol. 2007;188(1):139–44.

    Article  PubMed  Google Scholar 

  19. de Franchis R, Baveno VF. Revising consensus in portal Hypertension: report of the Baveno V consensus workshop on methodology of diagnosis and therapy in portal Hypertension. J Hepatol. 2010;53(4):762–8.

    Article  PubMed  Google Scholar 

  20. de Franchis R, Bosch J, Garcia-Tsao G, Reiberger T, Ripoll C, Baveno VIIF. Baveno VII - renewing consensus in portal Hypertension. J Hepatol. 2022;76(4):959–74.

    Article  PubMed  Google Scholar 

  21. Zhang YY, Wang L, Shao XD, Zhang YG, Ma SZ, Peng MY, Xu SX, Yin Y, Guo XZ, Qi XS. Effects of postoperative use of proton pump inhibitors on gastrointestinal bleeding after endoscopic variceal treatment during hospitalization. World J Gastrointest Surg. 2023;15(1):82–93.

    Article  PubMed  PubMed Central  Google Scholar 

  22. de Franchis R, Primignani M. Natural history of portal Hypertension in patients with Cirrhosis. Clin Liver Dis. 2001;5(3):645–63.

    Article  PubMed  Google Scholar 

  23. Beppu K, Inokuchi K, Koyanagi N, Nakayama S, Sakata H, Kitano S, Kobayashi M. Prediction of variceal Hemorrhage by esophageal endoscopy. Gastrointest Endosc. 1981;27(4):213–8.

    Article  CAS  PubMed  Google Scholar 

  24. Stamm ER, Meier JM, Pokharel SS, Clark T, Glueck DH, Lind KE, Roberts KM. Normal main portal vein diameter measured on CT is larger than the widely referenced upper limit of 13 mm. Abdom Radiol (NY). 2016;41(10):1931–6.

    Article  PubMed  Google Scholar 

  25. Jamwal KD, Maiwall R, Sharma MK, Kumar G, Sarin SK. Case Control Study of post-endoscopic Variceal Ligation Bleeding Ulcers in severe Liver Disease: outcomes and management. J Clin Transl Hepatol. 2019;7(1):32–9.

    PubMed  PubMed Central  Google Scholar 

  26. Sinclair M, Vaughan R, Angus PW, Gow PJ, Parker F, Hey P, Efthymiou M. Risk factors for band-induced Ulcer bleeding after prophylactic and therapeutic endoscopic variceal band ligation. Eur J Gastroenterol Hepatol. 2015;27(8):928–32.

    Article  PubMed  Google Scholar 

  27. Yang MT, Chen HS, Lee HC, Lin CL. Risk factors and survival of early bleeding after esophageal variceal ligation. Hepatogastroenterology. 2007;54(78):1705–9.

    PubMed  Google Scholar 

  28. Berreta J, Kociak D, Corti R, Morales G, Ortiz M, Laplacette M, Bellido F, Romero G, Salgado P, Tumilasci O. [Predictors of intrahospitalary mortality in the upper gastrointestinal variceal bleeding due to chronic Liver Disease treated endoscopically]. Acta Gastroenterol Latinoam. 2008;38(1):43–50.

    PubMed  Google Scholar 

  29. Lee SW, Lee TY, Chang CS. Independent factors associated with recurrent bleeding in cirrhotic patients with esophageal variceal Hemorrhage. Dig Dis Sci. 2009;54(5):1128–34.

    Article  PubMed  Google Scholar 

  30. Assy N, Rosser BG, Grahame GR, Minuk GY. Risk of sedation for upper GI endoscopy exacerbating subclinical hepatic encephalopathy in patients with Cirrhosis. Gastrointest Endosc. 1999;49(6):690–4.

    Article  CAS  PubMed  Google Scholar 

  31. Vasudevan AE, Goh KL, Bulgiba AM. Impairment of psychomotor responses after conscious sedation in cirrhotic patients undergoing therapeutic upper GI endoscopy. Am J Gastroenterol. 2002;97(7):1717–21.

    Article  CAS  PubMed  Google Scholar 

  32. Eisen GM, Baron TH, Dominitz JA, Faigel DO, Goldstein JL, Johanson JF, Mallery JS, Raddawi HM, Vargo JJ 2nd, Waring JP, et al. Complications of upper GI endoscopy. Gastrointest Endosc. 2002;55(7):784–93.

  33. Singal AG, Llovet JM, Yarchoan M, Mehta N, Heimbach JK, Dawson LA, Jou JH, Kulik LM, Agopian VG, Marrero JA et al. AASLD practice guidance on prevention, diagnosis, and treatment of hepatocellular carcinoma. Hepatology 2023.

  34. Korean Liver Cancer A, National Cancer Center K. 2022 KLCA-NCC Korea practice guidelines for the management of hepatocellular carcinoma. Clin Mol Hepatol. 2022;28(4):583–705.

    Article  Google Scholar 

  35. Hassan M, Husen Y, Abbasi SU, Hussain Z. Diagnostic accuracy of Multidetector Computed Tomography in detection of esophageal varices. Cureus. 2019;11(1):e3933.

    PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

This research received no external funding.

Author information

Authors and Affiliations

Authors

Contributions

Conceptualization: Hwaseong Ryu, Young Mi Hong; Data curation: Young Mi Hong, Hwaseong Ryu, Tae Un Kim; Formal analysis: Ki Tae Yoon, Young Mi Hong; Methodology: Young Mi Hong; Writing – original draft: Hwaseong Ryu, Young Mi Hong; Writing – review & editing: Young Mi Hong.

Corresponding author

Correspondence to Young Mi Hong.

Ethics declarations

Competing interests

The authors declare no competing interests.

Ethics approval and consent to participate

The present study was conducted in accordance to the ethical guidelines of the Declaration of Helsinki and was approved by the Institutional Review Boards (IRB) of Pusan National University Yangsan Hospital. Requirement for informed consent was waived after review of IRB of Pusan National University Yangsan Hospital because it was practically impossible and this study was of retrospective design.

Consent for publication

Not applicable for our study.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Ryu, H., Kim, T.U., Yoon, K. et al. Predicting the risk of early bleeding following endoscopic variceal ligation in cirrhotic patients with computed tomography. BMC Gastroenterol 23, 410 (2023). https://doi.org/10.1186/s12876-023-03038-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12876-023-03038-1

Keywords