- Research article
- Open Access
Intravenous non-high-dose pantoprazole is equally effective as high-dose pantoprazole in preventing rebleeding among low risk patients with a bleeding peptic ulcer after initial endoscopic hemostasis
BMC Gastroenterology volume 12, Article number: 28 (2012)
Many studies have shown that high-dose proton-pumps inhibitors (PPI) do not further reduce the rate of rebleeding compared to non-high-dose PPIs but we do not know whether intravenous non-high-dose PPIs reduce rebleeding rates among patients at low risk (Rockall score < 6) or among those at high risk, both compared to high-dose PPIs. This retrospective case-controlled study aimed to identify the subgroups of these patients that might benefit from treatment with non-high-dose PPIs.
Subjects who received high dose and non-high-dose pantoprazole for confirmed acute PU bleeding at a tertiary referral hospital were enrolled (n = 413). They were divided into sustained hemostasis (n = 324) and rebleeding groups (n = 89). The greedy method was applied to allow treatment-control random matching (1:1). Patients were randomly selected from the non-high-dose and high-dose PPI groups who had a high risk peptic ulcer bleeding (n = 104 in each group), and these were then subdivided to two subgroups (Rockall score ≥ 6 vs. < 6, n = 77 vs. 27).
An initial low hemoglobin level, serum creatinine level, and Rockall score were independent factors associated with rebleeding. After case-control matching, the significant variables between the non-high-dose and high-dose PPI groups for a Rockall score ≥ 6 were the rebleeding rate, and the amount of blood transfused. Case-controlled matching for the subgroup with a Rockall score < 6 showed that the rebleeding rate was similar for both groups (11.1% in each group).
Intravenous non-high-dose pantoprazole is equally effective as high-dose pantoprazole when treating low risk patients with a Rockall sore were < 6 who have bleeding ulcers and high-risk stigmata after endoscopic hemostasis.
Acute, non-variceal upper gastrointestinal bleeding is a common cause of hospitalization and mortality has remained at 6% to 8% despite recent advances in both pharmacological and endoscopic therapy [1, 2]. The risk of recurrent bleeding is increased in patients with high-risk stigmata found by endoscopy. Endoscopic hemostasis is able to control bleeding and reduce the rebleeding rate, morbidity and even mortality of this disease [3, 4]. The success of hemostasis, however, is highly dependent on the intragastric pH and studies have shown that, when the intra-gastric pH is low, platelet function is impaired and pepsin is activated, which disaggregates platelet plugs [5, 6]. The maintenance of an intragastric pH above 6.0 allows stabilization of the clot, which stops peptic ulcer (PU) bleeding and prevents rebleeding [7, 8]. Interestingly, in Hung's study , the time during which a intragastric pH above 6 was maintained was similar for both a non-high dose PPI group and a high dose group (49%, 59%, p = 0.182). This poses the question as to what is the optimal dose of PPI that is able to achieve the required therapeutic goal, This continues to be a controversial issue in clinical practice. Both the Vienna and Asia-Pacific consensus recommend intravenous high-dose PPI therapy after successful endoscopic hemostasis; however, the evidence related to the use of low-dose PPIs is limited [10, 11]. Many studies have shown that high-dose PPIs do not further reduce the rate of rebleeding compared to non-high-dose PPIs [12–14]. Nevertheless, we do not know whether the effect of intravenous non-high-dose PPIs is able to reduce the rebleeding rate among patients at low risk (Rockall score ≤ 6) or among those at high risk, both compared to high-dose PPIs. We can assume that intravenous high-dose PPI therapy is no doubt beneficial after successful endoscopic hemostasis but non-high dose treatment may be equally effective among certain subgroup of patients. If this is true, a change in strategy with respect to the use of PPIs may be both beneficial and cost-effective. The aim of this retrospective case-controlled study was to identify the subgroup of patients that might benefit from non-high-dose PPI treatment.
We reviewed 477 consecutive medical records of subjects with confirmed gastric and duodenal ulcers bleeding by endoscopic study between Jan. 2009 and March. 2011. All subjects received endoscopic hemostatic therapy for high-risk stigmata (active bleeding or a visible vessel in an ulcer bed) and were prescribed intravenous pantoprazole. The non-high-dose PPI patients were those who received an 80 mg pantoprazole bolus, which was followed by intravenous pantoprazole 80 mg per day until alimentation was possible, and then they received 40 mg per day pantoprazole orally. On the other hand, high-dose PPI patients received an 80 mg pantoprazole intravenous bolus injection, then were treated with 8 mg per hour continuous infusion of pantoprazole for 3 days, which was followed by intravenous 80 mg per day. A video endoscope (Olympus GIF-XQ240 or GIF-XQ 260, Tokyo, Japan) was used to perform the endoscopic therapy on all patients at our hospital. Individuals were excluded if the ulcer was malignant; there was non ulcerative bleeding such as angiodysplasia or a Mallory-Weiss tear, if the subject was lost to follow up before 30 days except due to mortality, and if the patient did not successfully undergo the initial endoscopic hemostasis. A total of 413 patients were enrolled for further analysis. For comparison, the patients were classified into two groups: subjects who achieved sustained hemostasis (n = 324) and those who did rebleed (n = 89). The patients' demographic and clinical characteristics were recorded including age, gender, initial shock status, red blood cell count, the amount of blood transfusion as packed red blood cells (PRBC), time to endoscope, underlying morbidities, drug use, such as non-steroid anti-inflammatory drugs (NSAIDs), aspirin, clopidogrel or warfarin and the Rockall score calculated as described in a previous study . The characteristics of the ulcer, such as size, the presence of multiple ulcers in association, and the Forrest classification, which was determined as described in a previous study, were also investigated [16, 17].
Next nearest neighbor matching was implemented using the greedy matching algorithm (NCSS 2007, Kaysville, Utah 84037, USA) to reduce bias in this retrospective study. This matching algorithm was performed to find equivalent matched controls in high-dose pantoprazole group for each individual in the non-high-dose group. The matching variables were stage of chronic kidney disease (CKD), Forrest classification and Rockall score. Effectively, patients were randomly selected to form non-high-dose and high-dose PPI groups that had a high risk PU bleeding (n = 104 in each group); these groups were then subdivided to two subgroups, namely those with a Rockall score of ≥ 6, n = 77 and those with a Rockall score of ≤ 6, n = 27). Risk stratification was defined according to the Rockall scoring system. Patients with a score ≧ 6 were considered high risk patients. Otherwise, they were classified as low risk patients as validated by Church and colleagues . This study was approved in accordance with the principles of the Helsinki Declaration by both the Institutional Review Board and the Ethics Committee of Chang Gung Memorial Hospital, Taiwan (IRB 100-2003B).
The classification of chronic kidney disease was defined according to Kidney Disease: Improving Global Outcomes (KDIGO) . The primary end points were rebleeding, need for surgery, and mortality. Rebleeding was defined based on the clinical physician's evaluation as ongoing melena passage, hematemesis, fresh blood or coffee-ground material in nasogastric tube or a decline in the hemoglobin level with or without PRBC transfusion. Shock was defined as tachycardia, a heart rate > 100/min, or hypotension with a systemic blood pressure < 90 mmHg [14, 20].
High risk ulcers were defined according to the Forrest classification . With respect to high-risk stigmata, active bleeding was defined as a continuous blood spurting (Forrest IA) or oozing (Forrest IB) from the ulcer base. A non-bleeding visible vessel at endoscopy was defined as a discrete protuberance at the ulcer base (Forrest IIA). An adherent clot was one that was resistant to forceful irrigation or suction (Forrest IIB). With respect to low-risk stigmata, a flat base, a pigmented spot or a clean base were defined as Forrest grade IIC or III.
The Statistical Package for Social Sciences (SPSS15.0, Chicago, IL, USA) for Windows was used to analyze the data. The results are expressed as distributions, absolute frequencies, relative frequencies, medians and ranges, or means ± standard deviation (SD). The quantitative data were compared using the Student's t-test when the variables had a normal distribution. Differences between the proportions of categorical data were evaluated by Fisher's exact test when the number of expected subjects was less than five and otherwise by the χ2 test. A multivariate logistic regression model was used to assess the independent association between the rebreeding and non-rebleeding groups. A p value of < 0.05 was considered statistically significant. Further statistical analysis was performed after case-controlled matching the subgroups with Rockall scores ≥ 6 or < 6 by the greedy methods in order to compare rebleeding between the high-dose and non-high-dose PPI groups.
Among the 477 subjects who had their health records reviewed, four subjects were lost to follow up before 30 days other than by death, two subjects failed their initial endoscopic hemostasis, thirteen suffered from angiodysplasia, twenty five had gastric cancers, seventeen had gastric antral vascular ectasia and three had a Mallory-Weiss tear; these individuals were all excluded and eventually 413 subjects were enrolled for further analysis. Among these 413 enrolled patients, 219 were treated by endoscopic epinephrine injection, clips or thermocoagulation alone and 194 were treated by clips, or thermocoagulation in combination with epinephrine injection. There were no significant differences between the two study groups with respect to sustained hemostasis vs. rebleeding groups in terms of age, drug use (such as NSAIDs, aspirin or warfarin), shock at presentation, time to endoscopy, ulcer size and stage of Forrest classification(Table 1). Significant differences were observed for variables such as gender (female: 26.8% vs. 39.3%, p = 0.022), creatinine (2.0 ± 2.3 g/L vs. 3.6 ± 3.3 g/L, p = 0.010), initial hemoglobin level (96.7 ± 28.2 g/L vs. 82.5 ± 24.1 g/L, p ≤ 0.001), platelet count (197.4 ± 87.3 × 109/L vs. 188.0 ± 129.0 × 109/L, p = 0.031), CKD stage III to V (38.9% vs. 70.8%, p ≤ 0.001), DM (26.9% vs. 41.6%, p = 0.007), Rockall score (6.0 ± 1.6 vs. 6.8, ± 17, p < 0.001), amount of blood transfused as PRBC (1203.2 ± 1640.4 mL vs. 2192.6 ± 2077.3 mL, p < 0.001), surgery (0.3 vs.7.9, p < 0.001), hospital stay (11.5 ± 13.5 vs. 29.9 ± 46.0, p < 0.001)and mortality (6.8% vs. 29.2%, p < 0.001). On multivariate analysis, an initial low hemoglobin level, serum creatinine level, and Rockall score were independent factors associated with rebleeding (Table 2).
The greedy method (NCSS 2007) was used to create treatment-control random matching of individuals based on stage of CKD and Rockall score, and 104 patients were randomly selected to form the non-high-dose and high-dose patient groups (Table 3). Among high risk patients (n = 77), the significant variables were the rebleeding rate (14.3% vs. 40.2%, p = 0.001), and amount of blood transfused as PRBC (1373.4 ± 1309.5 mL vs. 2539.0 ± 2271.1 mL, p ≤ 0.001). On the other hand, among the low risk patients (Rockall score ≤ 6), the baseline demographic and clinical characteristics such as rebleeding rate (3/27, 11.1% in each group), surgical interventions, and mortality were similar for both the high-dose and non-high-dose groups (Table 4).
There have been a number of studies in the literature that have reported there to be no difference in the magnitude of risk reduction between intensive high-dose and non-high-dose intravenous PPI therapy and these include those conducted by the Hung and Yuksel groups [9, 21]. In addition, meta-analysis by Wang and Wu came to a similar conclusion, namely that low-dose intravenous PPI can achieve the same efficacy as high-dose PPI following endoscopic hemostasis [22, 23]. A more recent prospective study conducted by Songür and colleagues also showed that high-dose esomeprazole infusion therapy following endoscopic hemostasis treatment is not superior to low-dose PPI therapy in the terms of re-bleeding, need for surgery and mortality . Moreover, Chen and colleagues from Taiwan concluded in a randomized clinical trial that PPI dosage is not associated with rebleeding following combined endoscopic haemostasis of bleeding ulcers . Obviously, the findings remain somewhat unconvincing with respect to the optimal dosage of PPI for ulcer bleeding despite the publication of updated Vienna and Asian-pacific consensus statements [10, 11]. In parallel with the above findings, we still do not know whether the effect of intravenous non-high-dose PPIs is as good as high-dose PPIs in terms of reducing rebleeding rates among patients at low risk (Rockall score ≤ 6) or among those at high risk (Rockall score ≥ 6).
The overall rebleeding rate in current study was high at 21.5% (89/413) with Hung and Yuksel reported rebleeding rates of 3.9% (4/103) and 7.2% (7/97), respectively [9, 21]. The differences can be explained by the enrollment in the present study of more patients with concurrent illness resulting in a mean Rockall score of 6.1. The prevalence of CKD in Yuksel's study was only 2.06% (2/97), and the mean score of American Society of Anesthesiologist (ASA) criteria was only 1.5 to 1.6 in Hung's study. As is well known, severe concurrent illness may dilute the results attained when assessing the effect of high-dose PPI treatment. All these studies, including ours, observed that intravenous high-dose pantoprazole treatment did not appear to be more effective at reducing rebleeding compared to a non-high-dose regimen among patients with high-risk stigmata. The greatest limitation with a retrospective case-controlled study like the current study is that, despite the attempt to minimize the possible selection bias between the two treatment groups by conducting greedy matching, prejudice is still inevitable among the high-dose group. For instance, there were still more rebleeding patients in the high risk patients with Rockall score ≥ 6 (14.3% vs. 40.2%, p = 0.001).
Most interestingly, after case-controlled matching, the low risk patient subgroup (Rockall score ≤ 6) analysis actually showed that the rebleeding rate was similar for both the high-dose and non-high-dose groups (3/27, 11.1% in each group) (Table 4). This implies that non-high-dose intravenous PPI is enough to preventing rebleeding among low risk patient. Theoretically, there is no doubt about the effectiveness of the anti-secretory effect of high-dose PPI. Evidence points clearly towards the fact that continuous intravenous infusion of PPI is able to maintain an intragastric pH > 6 for 59% to 98% of the time during monitoring [26–28]. In contrast, other studies have shown that low-dose intravenous PPI can be as effective as a high-dose regimen at maintaining a consistent pH of around 4-6 [29, 30]. Choi and colleagues reported that low-dose continuous infusion of pantoprazole (40 mg bolus followed by 4 mg/h) was able to maintain an intragastric pH > 6 in a manner similar to that of a high-dose group (80 mg bolus followed by 8 mg/h) among Korean patients with PU bleeding requiring endoscopic hemostasis . At least two other meta-analysis studies have revealed that high-dose PPIs are not superior to non-high-dose PPIs in terms of reducing the rate of rebleeding, neither with respect to the need for surgical intervention, nor in terms of mortality after endoscopic treatment among patients with bleeding PUs. This suggests that the non-high dose PPI treatment strategy may provide an equal clinical benefit among ulcer bleeding patients [24, 25, 32]. Therefore, it makes sense that non-high-dose intravenous PPI might be sufficient to reduce the rebleeding of PUs after initial endoscopic hemostasis among Taiwanese, at least among the subgroup of low risk patients that have a Rockall score < 6.
Co-morbidities influence the rate of recurrent bleeding . Recurrent PU bleeding may be prolonged in individuals with co-morbidities and therefore Cheng and colleagues suggested a extended low dose infusion of intravenous PPIs for up to 7-days may result in better control of recurrent bleeding of PUs . For instance, the fact that patients have a more severe stage of kidney disease (CKD V) might be relevant to increased rebleeding . This is consistent with the present study in that CKD stage III to V was found to be an influencing risk factor for recurrent bleeding on univariate analysis in spite of the fact that all subjects with end stage renal disease (ESRD) received heparin-free dialysis at our hospital. Uremic platelet function impairment may be responsible for this higher risk of ulcer rebleeding . The reason behind uremic platelet dysfunction involving the interaction of von Willebrand factor (vWf) with various platelet membrane glycoproteins, namely Ib and IIb to IIIa, which do not normalize after dialysis .
From the cost-effectiveness point of view, Leontiadis and colleagues reported that high-dose PPI therapy is more expensive, and that non-high dose is relatively inexpensive ; however, Barkun and colleagues proved that high-dose intravenous esomeprazole strategy is more effective and less costly than a non-intravenous esomeprazole strategy .
Several limitations of this study must be recognized. Firstly, this retrospective analysis is dependent on the completeness of the medical charts. If the chart report of ulcer pattern was not complete, we reviewed the image obtained by endoscopy or watching the recorded video in order to record the ulcer characteristics. Therefore, the investigation reliability might vary in this area. Secondly, selection bias definitely existed among high-dose group due to the clinicians' decision with respect to the dosage used for the more severely ill patients, even though we attempted to minimize this selection bias using the greedy matching method after controlling the baseline conditions of the subjects. Thirdly, some patients were treated by endoscopic epinephrine injection alone, which was suboptimal. Therefore, the intention to compare the overall efficacies between the non-high-dose and high-dose PPIs is hampered by these limitations. However, the interesting part of this study remains our observed in terms of the low risk subgroup and treatment strategy.
Intravenous non-high-dose pantoprazole is equally effective as high-dose pantoprazole when treating low risk patients with bleeding ulcers and high-risk stigmata after endoscopic hemostasis and who have a Rockall sore that is < 6.
Chronic kidney disease
Packed red blood cell
Non-steroid anti-inflammatory drugs
End stage renal disease
von Willebrand factor
Platelet membrane glycoproteins.
Blatchford O, Davidson LA, Murray WR, Blatchford M, Pell J: Acute upper gastrointestinal haemorrhage in west of Scotland: case ascertainment study. BMJ. 1997, 315: 510-514. 10.1136/bmj.315.7107.510.
Jiranek GC, Kozarek RA: A cost-effective approach to the patient with peptic ulcer bleeding. Surg Clin North Am. 1996, 76: 83-103. 10.1016/S0039-6109(05)70424-2.
Lin HJ, Wang K, Perng CL, Chua RT, Lee FY, Lee CH, Lee SD: Octreotide and heater probe thermocoagulation for arrest of peptic ulcer hemorrhage. A prospective, randomized, controlled trial. J Clin Gastroenterol. 1995, 21: 95-98. 10.1097/00004836-199509000-00006.
Laine L: Multipolar electrocoagulation versus injection therapy in the treatment of bleeding peptic ulcers. A prospective, randomized trial. Gastroenterology. 1990, 99: 1303-1306.
Green FW, Kaplan MM, Curtis LE, Levine PH: Effect of acid and pepsin on blood coagulation and platelet aggregation. A possible contributor prolonged gastroduodenal mucosal hemorrhage. Gastroenterology. 1978, 74: 38-43.
Patchett SE, O'Donoghue DP: Pharmacological manipulation of gastric juice: thrombelastographic assessment and implications for treatment of gastrointestinal haemorrhage. Gut. 1995, 36: 358-362. 10.1136/gut.36.3.358.
Chaimoff C, Creter D, Djaldetti M: The effect of pH on platelet and coagulation factor activities. Am J Surg. 1978, 136: 257-259. 10.1016/0002-9610(78)90241-6.
Netzer P, Gaia C, Sandoz M, Huluk T, Gut A, Halter F, Hüsler J, Inauen W: Effect of repeated injection and continuous infusion of omeprazole and ranitidine on intragastric pH over 72 hours. Am J Gastroenterol. 1999, 94: 351-357.
Hung WK, Li VK, Chung CK, Ying MW, Loo CK, Liu CK, Lam BY, Chan MC: Randomized trial comparing pantoprazole infusion, bolus and no treatment on gastric pH and recurrent bleeding in peptic ulcers. ANZ J Surg. 2007, 77: 677-681. 10.1111/j.1445-2197.2007.04185.x.
Barkun AN, Bardou M, Kuipers EJ, Sung J, Hunt RH, Martel M, Sinclair P, International Consensus Upper Gastrointestinal Bleeding Conference Group: International consensus recommendations on the management of patients with nonvariceal upper gastrointestinal bleeding. Ann Intern Med. 2010, 152: 101-113.
Sung JJ, Chan FK, Chen M, Ching JY, Ho KY, Kachintorn U, Kim N, Lau JY, Menon J, Rani AA, Reddy N, Sollano J, Sugano K, Tsoi KK, Wu CY, Yeomans N, Vakil N, Goh KL: Asia-Pacific Working Group. Asia-Pacific Working Group consensus on non-variceal upper gastrointestinal bleeding. Gut. 2011, 60: 1170-1177. 10.1136/gut.2010.230292.
Andriulli A, Loperfido S, Focareta R, Leo P, Fornari F, Garripoli A, Tonti P, Peyre S, Spadaccini A, Marmo R, Merla A, Caroli A, Forte GB, Belmonte A, Aragona G, Imperiali G, Forte F, Monica F, Caruso N, Perri F: High- versus low-dose proton pump inhibitors after endoscopic hemostasis in patients with peptic ulcer bleeding: a multicentre, randomized study. Am J Gastroenterol. 2008, 103: 3011-3118. 10.1111/j.1572-0241.2008.02149.x.
Cheng HC, Kao AW, Chuang CH, Sheu BS: The efficacy of high- and low-dose intravenous omeprazole in preventing rebleeding for patients with bleeding peptic ulcers and comorbid illnesses. Dig Dis Sci. 2005, 50: 1194-1201. 10.1007/s10620-005-2759-6.
Simon-Rudler M, Massard J, Bernard-Chabert B, DIM V, Ratziu V, Poynard T, Thabut D: Continuous infusion of high-dose omeprazole is more effective than standard-dose omeprazole in patients with high-risk peptic ulcer bleeding: a retrospective study. Aliment Pharmacol Ther. 2007, 25: 49-54.
Rockall TA, Logan RF, Devlin HB, Northfield TC: Risk assessment after acute upper gastrointestinal haemorrhage. Gut. 1996, 38: 316-321. 10.1136/gut.38.3.316.
Forrest JA, Finlayson ND, Shearman DJ: Endoscopy in gastrointestinal bleeding. Lancet. 1974, 2: 394-397.
Consensus conference: Therapeutic endoscopy and bleeding ulcers. JAMA. 1989, 262: 1369-1372.
Church NI, Dallal HJ, Masson J, Mowat NA, Johnston DA, Radin E, Turner M, Fullarton G, Prescott RJ, Palmer KR: Validity of the Rockall scoring system after endoscopic therapy for bleeding peptic ulcer: a prospective cohort study. Gastrointest Endosc. 2006, 63: 606-612. 10.1016/j.gie.2005.06.042.
Levey AS, Eckardt KU, Tsukamoto Y, Levin A, Coresh J, Rossert J, De Zeeuw D, Hostetter TH, Lameire N, Eknoyan G: Definition and classification of chronic kidney disease: a position statement from Kidney Disease: Improving Global Outcomes (KDIGO). Kidney Int. 2005, 67: 2089-2100. 10.1111/j.1523-1755.2005.00365.x.
Xu HW, Wang JH, Tsai MS, Wu KL, Chiou SS, Changchien CS, Hu TH, Lu SN, Chuah SK: The effects of cefazolin on cirrhotic patients with acute variceal hemorrhage after endoscopic interventions. Surg Endosc. 2011, 25: 2911-2918. 10.1007/s00464-011-1642-0.
Yuksel I, Ataseven H, Koklu S, Ertugrul I, Basar O, Odemiş B, Ibiş M, Saşmaz N, Sahin B: Intermittent versus continuous pantoprazole infusion in peptic ulcer bleeding: a prospective randomized study. Digestion. 2008, 78: 39-43. 10.1159/000158227.
Wang CH, Ma MH, Chou HC, Yen ZS, Yang CW, Fang CC, Chen SC: High-dose vs non-high-dose proton pump inhibitors after endoscopic treatment in patients with bleeding peptic ulcer: a systematic review and meta-analysis of randomized controlled trials. Arch Intern Med. 2010, 170: 751-758. 10.1001/archinternmed.2010.100.
Wu LC, Cao YF, Huang JH, Liao C, Gao F: High-dose vs low-dose proton pump inhibitors for upper gastrointestinal bleeding: a meta-analysis. World J Gastroenterol. 2010, 16: 2558-2565. 10.3748/wjg.v16.i20.2558.
Songür Y, Balkarli A, Acartürk G, Senol A: Comparison of infusion or low-dose proton pump inhibitor treatments in upper gastrointestinal system bleeding. Eur J Int Med. 2011, 22: 200-204. 10.1016/j.ejim.2010.11.007.
Chen CC, Lee JY, Fang YJ, Hsu SJ, Han ML, Tseng PH, Liou JM, Hu FC, Lin TL, Wu MS, Wang HP, Lin JT: Randomised clinical trial: high-dose vs. standard-dose proton pump inhibitors for the prevention of recurrent haemorrhage after combined endoscopic haemostasis of bleeding peptic ulcers. Aliment Pharmacol Ther. 2012, 35: 894-903. doi:10.1111/j.1365-2036.2012.05047.x
Netzer P, Gaia C, Sandoz M, Huluk T, Gut A, Halter F, Hüsler J, Inauen W: Effect of repeated injection and continuous infusion of omeprazole and ranitidine on intragastric pH over 72 hours. Am J Gastroenterol. 1999, 94: 351-357.
Javid G, Zargar SA, U-Saif R, Khan BA, Yatoo GN, Shah AH, Gulzar GM, Sodhi JS, Khan MA: Comparison of p.o. or i.v. proton pump inhibitors on 72-h intragastric pH in bleeding peptic ulcer. J Gastroenterol Hepatol. 2009, 24: 1236-1243. 10.1111/j.1440-1746.2009.05900.x.
Laine L, Shah A, Bemanian S: Intragastric pH with oral vs intravenous bolus plus infusion proton-pump inhibitor therapy in patients with bleeding ulcers. Gastroenterology. 2008, 134: 1836-1841. 10.1053/j.gastro.2008.03.006.
Laterre PF, Horsmans Y: Intravenous omeprazole in critically ill patients: a randomized, crossover study comparing 40 with 80 mg plus 8 mg/hour on intragastric pH. Crit Care Med. 2001, 29: 1931-1935. 10.1097/00003246-200110000-00014.
Kiilerich S, Rannem T, Elsborg L: Effect of intravenous infusion of omeprazole and ranitidine on twenty-four-hour intragastric pH in patients with a history of duodenal ulcer. Digestion. 1995, l56: 25-30.
Choi KD, Kim N, Jang IJ, Park YS, Cho JY, Kim JR, Shin JM, Jung HC, Song IS: Optimal dose of intravenous pantoprazole in patients with peptic ulcer bleeding requiring endoscopic hemostasis in Korea. J Gastroenterol Hepatol. 2009, 24: 1617-1624. 10.1111/j.1440-1746.2009.05939.x.
Dokas SM, Lazaraki GI, Kontoninas Zl: Bolus intravenous omeprazole b.i.d. vs. continuous intravenous omeprazole infusion combined with endoscopic hemostasis in the treatment of peptic ulcer bleeding. Preliminary results [abstract]. Gut. 2004, 53 (supplement 6): A290-
Cheng HC, Sheu BS: Intravenous proton pump inhibitors for peptic ulcer bleeding: Clinical benefits and limits. World J Gastrointest Endosc. 2011, 3: 49-56.
Cheung J, Yu A, LaBossiere J: Peptic ulcer bleeding outcomes adversely affected by end-stage renal disease. Gastrointest Endosc. 2010, 71: 44-49. 10.1016/j.gie.2009.04.014.
Sabovic M, Lavre J, Vujkovac B: Tranexamic acid is beneficial as adjunctive therapy in treating major upper gastrointestinal bleeding in dialysis patients. Nephrol Dial Transplant. 2003, 18: 1388-1391. 10.1093/ndt/gfg117.
Sreedhara R, Itagaki I, Lynn B, Hakim RM: Defective platelet aggregation in uremia is transiently worsened by hemodialysis. Am J Kidney Dis. 1995, 25: 555-563. 10.1016/0272-6386(95)90123-X.
Leontiadis GI, Sreedharan A, Dorward S, Barton P, Delaney B, Howden CW, Orhewere M, Gisbert J, Sharma VK, Rostom A, Moayyedi P, Forman D: Systematic reviews of the clinical effectiveness and cost-effectiveness of proton pump inhibitors in acute upper gastrointestinal bleeding. Health Technol Assess. 2007, 11: 1-164.
Barkun AN, Adam V, Sung JJ, Kuipers EJ, Mössner J, Jensen D, Stuart R, Lau JY, Nauclér E, Kilhamn J, Granstedt H, Liljas B, Lind T: Cost Effectiveness of High-Dose Intravenous Esomeprazole for Peptic Ulcer Bleeding. Pharmacoeconomics. 2008, 28: 217-230.
The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-230X/12/28/prepub
The authors would like to acknowledge Miss Chih-Yun Lin for statistical analysis.
The authors declare that they have no competing interests.
CML and JHL participated in the design of the study, coordinated the study, performed the statistical analysis and wrote the manuscript. YHK, KLW, YCC, YPC, MLH, WCT, KWC, and THH participated in the design of the study and consulted on the statistical analysis. SKC consulted on design of the study and on the interpretation of results. All authors read and approved the final manuscript.
Chih-Ming Liang, Jyong-Hong Lee contributed equally to this work.
Authors’ original submitted files for images
Below are the links to the authors’ original submitted files for images.
About this article
Cite this article
Liang, C., Lee, J., Kuo, Y. et al. Intravenous non-high-dose pantoprazole is equally effective as high-dose pantoprazole in preventing rebleeding among low risk patients with a bleeding peptic ulcer after initial endoscopic hemostasis. BMC Gastroenterol 12, 28 (2012). https://0-doi-org.brum.beds.ac.uk/10.1186/1471-230X-12-28
- Intravenous proton-pump inhibitors
- Peptic ulcer bleeding
- Endoscopic hemostasis
- Rockall scores