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Canadian Journal of Gastroenterology logoLink to Canadian Journal of Gastroenterology
. 2009 Oct;23(10):699–704. doi: 10.1155/2009/760793

Adrenaline injection plus argon plasma coagulation versus adrenaline injection plus hemoclips for treating high-risk bleeding peptic ulcers: A prospective, randomized trial

Seyed Alireza Taghavi 1,2,, Seyed Mohammad Soleimani 2, Seyed Mohammad Kazem Hosseini-Asl 1,2, Ahad Eshraghian 1, Hajar Eghbali 2, Seyed Mohsen Dehghani 1, Bita Ahmadpour 2, Mehdi Saberifiroozi 1,2
PMCID: PMC2776614  PMID: 19826646

Abstract

BACKGROUND/OBJECTIVE:

Several combination endoscopic therapies are currently in use. The present study aimed to compare argon plasma coagulation (APC) + adrenaline injection (AI) with hemoclips + AI for the treatment of high-risk bleeding peptic ulcers.

METHODS:

In a prospective randomized trial, 172 patients with major stigmata of peptic ulcer bleeding were randomly assigned to receive APC + AI (n=89) or hemoclips + AI (n=83). In the event of rebleeding, the initial modality was used again. Patients in whom treatment or retreatment was unsuccessful underwent emergency surgery. The primary end point of rebleeding rate and secondary end points of initial and definitive hemostasis need for surgery and mortality were compared between the two groups.

RESULTS:

The two groups were similar in all background variables. Definitive hemostasis was achieved in 85 of 89 (95.5%) of the APC + AI and 82 of 83 (98.8%) of the hemoclips + AI group (P=0.206). The mean volume of adrenaline injected in the two groups was equal (20.7 mL; P=0.996). There was no significant difference in terms of initial hemostasis (96.6% versus 98.8%; P=0.337), rate of rebleeding (11.2% versus 4.8%; P=0.124), need for surgery (4.5% versus 1.2%; P=0.266) and mortality (2.2% versus 1.2%; P=0.526). When compared for the combined end point of mortality plus rebleeding and the need for surgery, there was an advantage for the hemoclip group (6% versus 15.7%, P=0.042).

CONCLUSION:

Hemoclips + AI has no superiority over APC + AI in treating patients with high-risk bleeding peptic ulcers. Hemoclips + AI may be superior when a combination of all negative outcomes is considered.

Keywords: Adrenaline, Argon plasma coagulation, Hemoclips


Acute, nonvariceal, upper gastrointestinal bleeding remains a common medical problem associated with significant morbidity, mortality and health care resource use. The annual incidence of acute upper gastrointestinal bleeding is approximately 50 to 170 per 100,000 population (13). The case fatality rate of upper gastrointestinal bleeding is approximately 5% to 10%, either directly caused by the bleeding episode or through deterioration of concurrent medical illnesses (4,5). Mortality is related to age, comorbidity, endoscopic stigmata and rebleeding as well as the degree of the initial bleeding, transfusion volume and rebleeding after endoscopic therapy (69).

Endoscopic therapy has generally been recommended as the first-line treatment for upper gastrointestinal bleeding because it has been shown to reduce recurrent bleeding, the need for surgery and mortality (10). The American Society of Gastrointestinal Endoscopy guidelines (11) and the United Kingdom guidelines (12) stated that no single modality has been shown to be superior for treating upper gastrointestinal bleeding caused by peptic ulcer disease and that hemoclips are particularly useful for actively bleeding large vessels, but they may be difficult to apply to awkwardly located ulcers. The Nonvariceal Upper GI Bleeding Consensus Conference Group, which consisted mostly of Canadian experts, proposed the most definitive recommendations: “no single method of endoscopic injection is superior to the others, no single method of endoscopic thermal coaptive therapy is superior to the others and the placement of clips is a promising endoscopic hemostasis therapy for high-risk stigmata” (13).

Argon plasma coagulation (APC) is a new method that offers controlled, noncontact electrocoagulation. APC has proven to be safe and effective for coagulation of tissue to achieve hemostasis (14). It can be learned easily, is repeatable and induces limited tissue destruction (6). On the other hand, the depth of injury is unpredictable and may produce only shallow coagulation, which is insufficient for hemostasis (14).

There are variable success rates reported in the literature regarding hemostasis using endoscopic clips or APC, and studies comparing clips or APC with other endoscopic treatment modalities have yielded conflicting results. Most studies using clips or APC have been limited by relatively small sample sizes, variations in study design, and entry and outcome criteria. The endoscopic techniques used were also dissimilar in that some combined clips or APC with injection whereas others used clips or APC alone in actively bleeding ulcers (1517).

We conducted a randomized controlled trial to compare the efficacy and safety of endoscopic combination therapy using APC plus adrenaline injection (AI), with hemoclips plus AI.

METHODS

Patients

A prospective, randomized, comparative trial was conducted between March 2007 and June 2008, in medical centres affiliated with the Shiraz University of Medical Science, Shiraz, Iran. All patients with signs of upper gastrointestinal bleeding underwent endoscopy within 12 h of admission. Men and women older than 18 years of age were eligible for inclusion in the study if endoscopy showed a gastric or duodenal ulcer with an actively bleeding vessel (spurting or oozing), a nonbleeding visible vessel or an adherent clot. For those with a nonbleeding visible vessel, coffee-ground material or blood in the stomach and/or duodenum, hemodynamic instability or an initial hemoglobin level of less than 100 g/L, endoscopy was required to show recent bleeding. Exclusion criteria included having a platelet count of less than 50×109/L, an international normalized ratio of greater than 2, gastric malignancy, multiple bleeding sites or previous gastrectomy.

The clinical characteristics (age, sex, blood pressure, comorbid diseases, use of nonsteroidal anti-inflammatory drugs, smoking status, history of peptic ulcer disease or upper gastrointestinal bleeding) of each patient were recorded.

Randomization was performed at the time of endoscopy by means of numbered, sealed envelopes containing treatment assignments randomly generated by computer. All endoscopic hemostatic procedures were performed by two experienced endoscopists who did not participate in the postprocedure care of the patients.

Procedure

Adrenaline (1:10,000 dilution) in 0.5 mL or 1 mL doses was injected through multiple punctures into and around the bleeding site, with at least 10 mL being injected. After AI, patients in the APC group underwent treatment with an argon plasma coagulator unit (APC 2, VIO 300 D, Erbe, Germany). The spray mode was used with two power/gas settings for gastric and duodenal ulcers (70 W and 40 W and 2 L/min to 1 L/min, respectively). Suction was applied to remove smoke and prevent overinflation of the gastrointestinal tract. Endoscopic hemoclip therapy was performed with stainless steel hemoclips (HX-610-135, Olympus Medical Systems, Japan). Hemoclips were applied with a clip application device (HX-110LR, Olympus, Japan) passed through the 2.8 mm diameter accessory channel of a standard endoscope. Hemoclips were individually loaded and deployed. For ulcers with clots, the base of the clot was manually irrigated with a 50 mL syringe (200 mL of water total).

After hemostasis was achieved, the bleeding site was observed for at least 4 min. Initial hemostasis was defined as the absence of endoscopic evidence of bleeding during 4 min of observation after therapy. Following therapeutic endoscopy, patients were observed closely. While the patient was in the hospital, treatment included intravenous administration of pantoprazole (80 mg stat, 8 mg/h) for one day, started on arrival to hospital before endoscopic intervention. Subsequently, oral therapy with omeprazole 20 mg twice daily was started. Endoscopy was performed one day after initial hemostasis, with five biopsy specimens being obtained from the ulcer margin and base. The specimens were evaluated for the presence of malignancy and Helicobacter pylori infection. Individuals who were positive for H pylori infection, detected by histology, received appropriate eradication therapy. Evidence of recurrent bleeding included new hematemesis, aspiration of fresh blood from a nasogastric tube or continuous melena, with a pulse rate greater than 100 beats/min, a decrease in systolic blood pressure exceeding 30 mmHg or a decrease in hemoglobin of at least 20 g/L. A second endoscopy was performed in patients who displayed any evidence of recurrent bleeding, with the same endoscopic hemostatic treatment being performed.

Definitive hemostasis was defined as the absence of recurrent bleeding during the 30-day period following initial or secondary endoscopic hemostasis. The rate of recurrent bleeding, as a primary outcome, was compared between the two groups. The rate of initial hemostasis, definitive hemostasis, need for emergency surgery and bleeding-related deaths were compared as secondary outcomes.

Following discharge, patients were requested to return to the outpatient clinic two and four weeks after initial hemostasis. Individuals who did not revisit the outpatient clinic were followed by telephone.

Statistical analysis

With the assumption that the hemoclip + AI combination method would lower the expected risk of recurrent bleeding from 17% (18) after APC + AI to 3.8% (19), 81 patients would have been needed in each group for a power of 80% and a significance level of 0.05. Continuous data are summarized as mean (95% CI). The Student’s t test was used to compare the mean values of continuous variables, and the χ2 test was used for the comparison of categorical variables. The analyses were performed with SPSS version 11.5 (SPSS Inc, USA) for Windows (Microsoft Corporation, USA). A P<0.05 was considered to be statistically significant.

Ethics and consent

Possible complications of endoscopic treatment were discussed with the patients and their relatives, and written informed consent was obtained before trial entry. The present study was approved by the Research Council Ethics Committee of the Shiraz University of Medical Science. The present study was conducted in accordance with the Declaration of Helsinki (Edinburgh revision, 2000).

RESULTS

A total of 914 patients with upper gastrointestinal bleeding underwent emergency endoscopy. Of these, 574 had ulcer disease, 246 had esophageal or gastric variceal bleeding and 94 had nonulcer lesions. Peptic ulcers with an actively bleeding vessel (spurting or oozing), nonbleeding visible vessels or adherent clots were found in 196 patients. Twenty-four subjects were excluded because of previous gastrectomy, bleeding diathesis, gastric malignancy or multiple bleeding sources at endoscopy (Figure 1).

Figure 1).

Figure 1)

Flow diagram of the study, showing outcomes for all patients. AI Adrenaline injection; APC Argon plasma coagulation; GI Gastrointestinal

Clinical data for the patients at study entry are presented in (Table 1). There were no significant differences between the two groups with respect to age, sex, shock state, comorbid diseases, use of nonsteroidal anti-inflammatory drugs, H pylori status and history of previous upper gastrointestinal bleeding.

TABLE 1.

Baseline characteristics of the study groups

Characteristic Adrenaline injection
P
With argon plasma coagulation With hemoclips
Age, years (mean ± SD) 48.63±15.97 51.34±14.01 0.24
Sex (males/females), n/n 73/16 60/23 0.128
Smoking 39 (36) 46 (55.4) 0.01
Nonsteroidal anti-inflammatory drug use 46 (51.7) 33 (39.8) 0.117
Hypovolemic shock 2 (2.2) 3 (3.6) 0.467
Comorbidity 83 (93.3) 75 (90.4) 0.487
Ulcer history 29 (32.6) 12 (14.5) 0.05
Previous ulcer bleeding 7 (7.9) 5 (6) 0.636
Admitted for ulcer bleeding 85 (95.5) 82 (98.8) 0.206
In-hospital bleeding 4 (4.5) 1 (1.2) 0.206
Duration of admission, days (mean ± SD) 5.34±1.56 5.52±1.19 0.396
Helicobacter pylori-positive 65 (73) 63 (75.9) 0.288

Data presented as n (%) unless specified otherwise

In the evaluation of smoking, the difference between the groups was significant (P=0.01), with a greater proportion in the hemoclips + AI group. History of peptic ulcer disease was also significantly higher in the APC + AI group (P=0.05). Ulcer characteristics (Table 2) were comparable between the study groups.

TABLE 2.

Ulcer characteristics

Adrenaline injection
P
With APC With hemoclips
Duodenal ulcers 53 (59.6) 38 (45.8) 0.71
  Anterior 33 (62.3) 21 (55.3)
  Posterior 15 (28.3) 12 (31.6)
  Superior 1 (1.9) 0
  Inferior 3 (5.7) 5 (13.2)
  D2 1 (1.9) 0
Gastric ulcers 36 (40.4) 45 (54.2) 0.71
  Antrum/Incisura 7 (19.5) 0
  Lesser curvature 14 (38.9) 33 (73)
  Fundus and body 5 (13.9) 5 (11.1)
  Cardia 10 (27.8) 7 (15.6)
Ulcer type 0.762
  Spurting artery 9 (10.1) 7 (8.4)
  Oozing 2 (2.2) 3 (3.6)
  Visible vessel 69 (77.5) 61 (73.5)
  Adherent clot 9 (10.1) 12 (14.5)
Ulcer size
  <10 mm 36 (41.6) 44 (53)
  10 mm to 20 mm 40 (44.9) 32 (38.6)
  >20 mm 12 (13.5) 7 (8.4)

Data presented as n (%) unless specified otherwise. APC Argon plasma coagulation

There was no statistically significant difference in terms of ulcer sites (stomach versus duodenum), ulcer size, bleeding stigmata or the specific location of ulcers within the stomach and duodenum. Clinical outcome data are summarized in (Table 3).

TABLE 3.

Clinical results

Adrenaline injection
P
With APC With hemoclips
Initial hemostasis, n (%) 86 (96.6) 82 (98.8) 0.337
Rebleeding, n (%) 10 (11.2) 4 (4.8) 0.124
Duodenal ulcer 1/53 2/38 0.569
  Anterior 0/33 1/21
  Posterior 1/15 1/12
  Superior 0 0
  Inferior 0 0
Gastric ulcer 9/36 2/45 0.01
  Antrum/incisura 0 0
  Lesser curvature 5/14 2/33
  Fundus and body 1/5 0/5
  Cardia 3/10 0/7
Ulcer type
  Spurting artery 2/9 0/7
  Oozing 0/2 0/3
  Visible vessel 7/69 4/61
  Adherent clot 1/9 0/12
Ulcer size
  <10 mm 4/36 1/44
  10 mm to 20 mm 5/40 3/32
  >20 mm 1/12 0/7
Definite hemostasis, n (%) 85 (95.5) 82 (98.8) 0.206
Need for surgery, n (%) 2 (2.2) 0 0.266
Mortality, n (%) 2 (2.2) 1 (1.2) 0.526

Data presented as n/n unless specified otherwise. APC Argon plasma coagulation

The mean volume of adrenaline used in the two groups was equal (20.7 mL; P=0.996). In the APC + AI group, the mean (± SD) number of APC pulses was 2.75±0.64, and the mean number of hemoclips in the hemoclips + AI group was 2.43±0.72.

Initial hemostasis was successfully achieved in 96.6% of the APC + AI group and 98.8% of the hemoclip + AI group (P=0.337). In the APC + AI group, two of three patients with uncontrolled bleeding died and one had successful emergency surgery. In the hemoclip + AI group, the only patient with uncontrolled bleeding died before undergoing surgery due to severe hemodynamic instability, similar to the two deaths in the APC + AI group.

Bleeding recurred in 10 patients in the APC + AI group (11.0%) and in four of the hemoclip + AI group (4.8%) (P=0.124). All 14 of these patients underwent the same repeated endoscopic intervention. Only one patient in the APC + AI group needed surgery due to failed endoscopic intervention. Need for surgery (2.2% in the APC + AI group versus 0% in the hemoclip + AI group; P=0.266) and mortality (2.2% in the APC + AI group versus 1.2% in the hemoclip + AI group; P=0.526) was not statistically different. Also, there was not a significant difference between the two groups in achieving definite hemostasis (95.5% in the APC + AI group versus 98.8% in the hemoclip + AI group; P=0.206) and mean length of hospital stay (5.34 days for the APC + AI group versus 5.52 days for the hemoclip + AI group; P=0.396).

When the two groups were compared for the combined end point of mortality plus rebleeding and the need for surgery, there was an advantage to hemoclips, with a slight margin of significance (6% versus 15.7% for hemoclips and APC groups, respectively, P=0.042)

No major procedure-related complication (eg, perforation or worsening of bleeding as a result of the hemostatic procedure) was observed in either group.

DISCUSSION

Endoscopic injection therapy is still commonly used for the treatment of bleeding peptic ulcers, with dilute adrenaline being among the most frequently used solutions. Although this technique can successfully stop the majority of ulcer bleeds, recurrent bleeding still occurs in 10% to 30% of cases (2).

Bleeding recurrence has been identified as the most important prognostic factor of mortality (20). Therefore, if recurrence of bleeding can be prevented, the rate of mortality from ulcer bleeding can potentially be reduced (21).

It is generally accepted that the combination of injection therapy with another method of hemostasis (eg, injection therapy + heater probe, injection therapy + hemoclips) is superior to injection therapy alone for definitive control of bleeding, especially in high-risk ulcers (19,22).

The main question for the practicing clinician is, therefore, the most suitable ‘type’ of combination therapy for the treatment of a high-risk, bleeding peptic ulcer.

Presently, both APC and clipping are commonly used worldwide for the treatment of high-risk bleeding peptic ulcers, both usually used in combination with injection therapy. There are, however, little data available to allow for the comparison of these two methods, and there are arguments in favour of each.

Animal studies have shown that only mechanical methods such as hemoclips may be effective in controlling bleeding for vessels larger than 2 mm in diameter (23). Tissue damage is minimized with this method (24).

In a meta-analysis performed by Sung et al (25), the pooled data from 15 studies indicated that endoscopic clipping, with or without injection, is more effective than endoscopic injection alone for the treatment of bleeding peptic ulcers, and at least as effective as thermal therapies for the induction of hemostasis and prevention of surgery and mortality.

APC, on the other hand, is easier to target to the bleeding sites than hemoclips (2628). Despite promising efficacy for the treatment of angiodysplasia, gastric antral vascular ectasia and radiation proctitis, there are few published trials regarding the efficacy of APC for bleeding peptic ulcers. The available data indicate a similar efficacy as heater probe in terms of initial hemostasis as well as recurrent bleeding, and a potential superiority in the speed of initial hemostasis (18,29,30).

The present head-to-head study compared APC and hemoclips in a randomized controlled trial. A high rate of initial hemostasis was achieved in both treatment groups. As expected, ulcers with visible vessels had the highest frequency of recurrent bleeding. A lower rate of recurrent bleeding was noted in gastric ulcers in the hemoclip + AI group than in the APC + AI group, although these differences were not statistically significant.

There was also no difference with respect to the predetermined end points of definitive hemostasis (95.5% versus 98.8%; P=0.206), need for surgery (2.2% versus 0%; P=0.266) and mortality (2.2% versus 1.2%; P= 0.526), which indicate a similar efficacy for both methods based on the present data. Therefore, clinicians may choose the method based on availability, experience and the clinical situation.

The statistically significant advantage of hemoclips over APC for the combined end point of rebleeding, need for surgery and mortality is interesting, and may suggest a potential trend for the superiority of hemoclips, at least in some subgroups of bleeding peptic ulcers. This, however, can only be confirmed in studies with a larger number of patients. It is also notable that hemoclips were able to stop bleeding in all patients who rebled after the intial application; this may translate to lower mortality in a larger number of patients, considering that the majority of deaths in peptic ulcer bleeding occur in those who rebleed. Hemoclips may also have a viable role as a rescue treatment for rebleeding following other methods of hemostasis.

Larger studies may also be able to elucidate possible differences between these two treatment methods for different subgroups of patients (eg, different vessel size, different locations), which could not be stratified in the current study due to the number of patients.

The application of hemoclips to the posterior part of the duodenum and lesser curvature of the stomach is theoretically difficult. In the present study, difficulties were encountered in the application of hemoclips to the posterior wall of the duodenum in three of 12 (25%) patients and to the lesser curvature of the stomach in seven of 33 (21%) patients; however, all of these patients achieved initial hemostasis. Although APC has a theoretical advantage in the above mentioned areas (because of the potential for tangential application), the present study demonstrated a lower rebleeding rate in the hemoclips + AI group in the lesser curvature compared with the APC + AI group; however, these differences were not statistically significant. These intriguing results may need further studies to be confirmed.

It may be surprising that despite a limited depth of penetration, APC was shown to be effective for the treatment of bleeding from large vessels in the present trial. Although the actual mechanism of efficacy cannot be determined without a microscopic study of the application site, a combination of compression from inflammation in the burned surrounding tissues as well as possible thrombosis of the involved vessel due to vessel wall damage may be able to explain the efficacy of APC in this subgroup.

The risk of perforation after APC is a matter of debate (10,3135) and is estimated to be approximately 0.31% (30). Although this potential risk may be regarded as a disadvantage for APC compared with hemoclips (which induce less demonstrable tissue damage), no perforation was encountered in either of the groups to substantiate this disadvantage in the present study.

No report of bloating or abdominal discomfort (which may be caused by the high gas flow with APC) was reported in either of the groups.

CONCLUSION

There is no statistically significant superiority for either APC or hemoclips regarding the end points of mortality, need for surgery and rebleeding based on data from the present study.

Acknowledgments

This study was supported by the Gastroenterohepatology Research Centre of the Shiraz University of Medical Sciences, Shiraz, Iran. The authors appreciate the cooperation of the endoscopy staff of the Nemazee hospital, Shiraz, Iran.

Footnotes

FUNDING: This study was supported by a grant from the Research Council of the Shiraz University of Medical Sciences, Shiraz, Iran.

REFERENCES

  • 1.Blatchford O, Davidson LA, Murray WR, Blatchford M, Pell J. Acute upper gastrointestinal hemorrhage in west of Scotland: Case ascertainment study. BMJ. 1997;315:510–4. doi: 10.1136/bmj.315.7107.510. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Longstreth GF. Epidemiology of hospitalization for acute upper gastrointestinal hemorrhage: A population-based study. Am J Gastroenterol. 1995;90:206–10. [PubMed] [Google Scholar]
  • 3.Vreeburg EM, Snel P, de Bruijne JW, Bartelsman JF, Rauws EA, Tytgat GN. Acute upper gastrointestinal bleeding in the Amsterdam area: Incidence, diagnosis and clinical outcome. Am J Gastroenterol. 1997;92:236–43. [PubMed] [Google Scholar]
  • 4.Rockall TA, Logan RF, Devlin HB, Northfield TC. Incidence of and mortality from acute upper gastrointestinal hemorrhage in the United Kingdom. Steering Committee and members of the National Audit of Acute Upper Gastrointestinal Hemorrhage. BMJ. 1995;311:222–6. doi: 10.1136/bmj.311.6999.222. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Targownik LW, Nabalamba A. Trends in management and outcomes of acute non-variceal upper gastrointestinal bleeding: 1993–2003. Clin Gastroenterol Hepatol. 2006;4:1459–66. doi: 10.1016/j.cgh.2006.08.018. [DOI] [PubMed] [Google Scholar]
  • 6.Khan K, Schwarzenberg SJ, Sharp H, Weisdorf-Schindele S. Argon plasma coagulation: Clinical experience in pediatric patients. Gastrointest Endosc. 2003;57:110–2. doi: 10.1067/mge.2003.13. [DOI] [PubMed] [Google Scholar]
  • 7.Kim HG, Park JK, Jung YD. Risk factors for early rebleeding after initial endoscopic hemostasis in patients with bleeding peptic ulcers. Gastrointest Endosc. 2000;51:208. [Google Scholar]
  • 8.Lau JY, Sung JJ, Lam YH, et al. Endoscopic retreatment compared with surgery in patients with recurrent bleeding after initial endoscopic control of bleeding ulcers. N Eng J Med. 1999;340:751–6. doi: 10.1056/NEJM199903113401002. [DOI] [PubMed] [Google Scholar]
  • 9.Fallah MA, Prakash C, Edmundowicz S. Acute gastrointestinal bleeding. Med Clin North Am. 2000;84:1183–208. doi: 10.1016/s0025-7125(05)70282-0. [DOI] [PubMed] [Google Scholar]
  • 10.Cook DJ, Guyatt GH, Salena BJ, Laine LA. Endoscopic therapy for acute non-variceal hemorrhage: A meta-analysis. Gastroenterology. 1992;102:139–48. doi: 10.1016/0016-5085(92)91793-4. [DOI] [PubMed] [Google Scholar]
  • 11.American Society of Gastrointestinal Endoscopy Guideline: The role of endoscopy in acute non-variceal upper GI hemorrhage. Gastrointest Endosc. 2004;60:497–504. doi: 10.1016/s0016-5107(04)01568-8. [DOI] [PubMed] [Google Scholar]
  • 12.Palmer KR.Non-variceal upper gastrointestinal hemorrhage: Guideline Gut 2002511–6.12077078 [Google Scholar]
  • 13.Barkun A, Bardou M, Marshall JK, for the Nonvariceal Upper GI Bleeding Consensus Conference Group Consensus recommendation for managing patients with nonvariceal upper gastrointestinal bleeding. Ann Intern Med. 2003;139:843–57. doi: 10.7326/0003-4819-139-10-200311180-00012. [DOI] [PubMed] [Google Scholar]
  • 14.Grund KE, Farin G. Annual of Gastrointestinal Endoscopy. 10th edn. London: Rapid Science; 1997. [Google Scholar]
  • 15.Chou YC, Hsu PI, Lai KH, et al. A prospective, randomized trial of endoscopic hemoclip placement and distilled water injection for treatment of high-risk bleeding ulcers. Gastrointest Endosc. 2003;57:324–8. doi: 10.1067/mge.2003.103. [DOI] [PubMed] [Google Scholar]
  • 16.Lin HJ, Perng CL, Sun IC, Tseng GY. Endoscopic haemoclip versus heater probe thermocoagulation plus hypertonic saline-epinephrine injection for peptic ulcer bleeding. Digest Liver Dis. 2002;35:898–902. doi: 10.1016/j.dld.2003.07.006. [DOI] [PubMed] [Google Scholar]
  • 17.Saltzman JR, Strate LL, Di Sena V, et al. Prospective trial of endoscopic clips versus combination therapy in upper GI bleeding. Am J Gastroenterol. 2005;100:1503–8. doi: 10.1111/j.1572-0241.2005.41561.x. [DOI] [PubMed] [Google Scholar]
  • 18.Cipolletta L, Bianco MA, Rotondano G, Piscopo R, Prisco A, Garofano ML. Prospective comparison of argon plasma coagulator and heater probe in the endoscopic treatment of major peptic ulcer bleeding. Gastrointest Endosc. 1998;48:191–5. doi: 10.1016/s0016-5107(98)70163-4. [DOI] [PubMed] [Google Scholar]
  • 19.Lo CC, Ping I, Lo GH. Comparison of hemostatic efficacy for epinephrine injection alone and injection combined hemoclip therapy in treating high risk bleeding peptic ulcers. Gastrointest Endosc. 2006;63:767–73. doi: 10.1016/j.gie.2005.11.048. [DOI] [PubMed] [Google Scholar]
  • 20.Turner IB, Jones M, Piper DW. Factors influencing mortality from bleeding peptic ulcers. Scand J Gastroenterol. 1991;26:661–6. doi: 10.3109/00365529109043641. [DOI] [PubMed] [Google Scholar]
  • 21.Brullet E, Campo R, Calvet X, Coroleu D, Rivero E, Simo Deu J. Factors related to the failure of endoscopic injection therapy for bleeding gastric ulcer. Gut. 1996;43:111–6. doi: 10.1136/gut.39.2.155. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.Chung SS, Lau JY, Sung JJ, et al. Randomized comparison between adrenaline injection alone and adrenaline injection plus heater probe treatment for actively bleeding ulcers. BMJ. 1997;314:1307–11. doi: 10.1136/bmj.314.7090.1307. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Hepworth CC, Kadirkamanathan SS, Gong G, Swain CP. A randomized controlled comparison of injection, thermal and mechanical endoscopic methods of hemostasis on mesenteric vessels. Gut. 1998;42:462–9. doi: 10.1136/gut.42.4.462. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Yuan Y, Wang C, Hunt RH. Endoscopic clipping for acute nonvariceal upper-GI bleeding: A meta-analysis and critical appraisal of randomized controlled trials. Gastrointest Endosc. 2008;68:339–51. doi: 10.1016/j.gie.2008.03.1122. [DOI] [PubMed] [Google Scholar]
  • 25.Sung JJ, Tsoi KK, Lai LH, Wu JC, Lau JY. Endoscopic clipping versus injection and thermo-coagulation in the treatment of nonvariceal upper gastrointestinal bleeding: A meta-analysis. Gut. 2007;56:1364–73. doi: 10.1136/gut.2007.123976. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Grund KE, Storek D, Farin G. Endoscopic argon plasma coagulation (APC) first clinical experiences in flexible endoscopy. Endosc Surg Allied Technol. 1994;2:42–6. [PubMed] [Google Scholar]
  • 27.Canard JM, Vedrenne B. Clinical application of argon plasma coagulation in gastrointestinal endoscopy: Has the time come to replace the laser? Endoscopy. 2001;33:353–7. doi: 10.1055/s-2001-13686. [DOI] [PubMed] [Google Scholar]
  • 28.Farin G, Grund KE. Technology of argon plasma coagulation with particular regard to endoscopic applications. Endosc Surg Allied Technol. 1994;2:71–7. [PubMed] [Google Scholar]
  • 29.Chau CH, Siu WT, Law BKB, et al. Randomized controlled trial comparing epinephrine injection plus heat probe coagulation versus epinephrine injection plus argon plasma coagulation for bleeding peptic ulcers. Gastrointest Endosc. 2003;57:455–61. doi: 10.1016/s0016-5107(03)80008-1. [DOI] [PubMed] [Google Scholar]
  • 30.Havanond C, Havanond P. Argon plasma coagulation therapy for acute non-variceal upper gastrointestinal bleeding (review) Cochrane Database Syst Rev. 2005;18:CD003791. doi: 10.1002/14651858.CD003791.pub2. [DOI] [PubMed] [Google Scholar]
  • 31.Grund KE, Zindel C, Farin G. Agron plasma coagulation through a flexible endoscope. Evaluation of a new therapeutic method after 1606 uses. Deutche Medizinische Wochenschrift. 1997;122:432–8. doi: 10.1055/s-2008-1047634. [DOI] [PubMed] [Google Scholar]
  • 32.Sugawa C, Takekuma Y, Lucas CE, et al. Experimental studies of thermal therapy for severe non-variceal bleeding in dogs. Surg Endosc. 1999;13:1203–7. doi: 10.1007/pl00009621. [DOI] [PubMed] [Google Scholar]
  • 33.Hoyer N, Thouet R, Zellweger U. Massive pneumoperioneum after endoscopic argon plasma coagulation. Endoscopy. 1998;30:934. doi: 10.1055/s-2007-1001275. [DOI] [PubMed] [Google Scholar]
  • 34.Norton ID, Wang L, Levine SA, et al. In vivo characterization of colonic thermal injury caused by argon beam coagulation. Gastrointest Endosc. 2002;55:631–6. doi: 10.1067/mge.2002.123418. [DOI] [PubMed] [Google Scholar]
  • 35.Norton ID, Wang L, Levine SA, et al. Efficacy of colonic submucosal saline solution injection for the reduction of iatrogenic thermal injury. Gastrointest Endosc. 2002;56:95–9. doi: 10.1067/mge.2002.125362. [DOI] [PubMed] [Google Scholar]

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