The effect of perendoscopic sclerosing agent injection in Forrest's II ulcers- A pilot study from Turkey
dc.contributor.author | Saruc M. | |
dc.contributor.author | Ozden N. | |
dc.contributor.author | Kucukmetin N. | |
dc.contributor.author | Tuzcuoglu I. | |
dc.contributor.author | Yuceyar H. | |
dc.date.accessioned | 2024-07-22T08:25:12Z | |
dc.date.available | 2024-07-22T08:25:12Z | |
dc.date.issued | 2002 | |
dc.description.abstract | Background: We aimed to clarify the outcome of perendoscopic prophylactic injection of sclerosing agent in Forrest's II ulcers. Material/Methods: Patients with upper gastrointestinal bleeding in last 6 hours were performed emergency endoscopy and were enrolled. The patients in group-1 were performed prophylactic injection therapy with 1% aethoxysclerol and then given medical treatment with intravenous 40 mg omeprazole twice a day and somatostatin infusion at the dose of 6 mg/day during 3 days. Group-2 patients were only given medical treatment with same agents and at same doses without having any perendoscopic therapy. Results: There were 32 patients in group-1 and 20 in group-2. In emergency endoscopy, 20 (62.5%) patients had IIa ulcers and 12 (37.5%) patients had IIb ulcers in group-1. These patients underwent prophylactic perendoscopic hemostasis by 1% aethoxysclerol in addition to medical treatment. Early rebleeding occurred in 9 (28.1%) patients of group-1 and 3 (15%) in group-2 (p<0.001). At the endoscopic control after 48 hours 13 (40.6%) patients in the group-1 and 15 (75%) patients in group-2 showed improved local ulcer stigmata (p<0.001). The numbers of blood units transfused were lower in the group-2 (p=0.002). The hospital stay was longer in group-1 (p=0.01). In the group-1, more endoscopic intervention was needed. Any death and the need for surgical intervention did not occurred in any groups. Conclusion: According to our results; the indication of perendoscopic prophylactic injection of sclerosing agent in non-bleeding ulcers with high risk of rebleeding must be reviewed by large population based, prospective, radomized trials. | |
dc.identifier.issn | 12341010 | |
dc.identifier.uri | http://akademikarsiv.cbu.edu.tr:4000/handle/123456789/20309 | |
dc.language.iso | English | |
dc.subject | Adult | |
dc.subject | Anti-Ulcer Agents | |
dc.subject | Endoscopy | |
dc.subject | Female | |
dc.subject | Humans | |
dc.subject | Male | |
dc.subject | Middle Aged | |
dc.subject | Peptic Ulcer | |
dc.subject | Pilot Projects | |
dc.subject | Sclerosing Solutions | |
dc.subject | Turkey | |
dc.subject | omeprazole | |
dc.subject | polidocanol | |
dc.subject | sclerosing agent | |
dc.subject | somatostatin | |
dc.subject | antiulcer agent | |
dc.subject | adult | |
dc.subject | article | |
dc.subject | controlled study | |
dc.subject | endoscopic sclerotherapy | |
dc.subject | endoscopy | |
dc.subject | female | |
dc.subject | gastrointestinal hemorrhage | |
dc.subject | hemostasis | |
dc.subject | hospitalization | |
dc.subject | human | |
dc.subject | major clinical study | |
dc.subject | male | |
dc.subject | peptic ulcer | |
dc.subject | pilot study | |
dc.subject | prophylaxis | |
dc.subject | treatment indication | |
dc.subject | treatment outcome | |
dc.subject | Turkey (republic) | |
dc.subject | clinical trial | |
dc.subject | controlled clinical trial | |
dc.subject | middle aged | |
dc.subject | peptic ulcer | |
dc.title | The effect of perendoscopic sclerosing agent injection in Forrest's II ulcers- A pilot study from Turkey | |
dc.type | Article |