Pregled bibliografske jedinice broj: 470865
Prophylactic administration of ranitidine after sclerotherapy of esophageal varices
Prophylactic administration of ranitidine after sclerotherapy of esophageal varices // International journal of clinical pharmacology, therapy and toxicology, 29 (1991), 347-351 (recenziran, članak, stručni)
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Naslov
Prophylactic administration of ranitidine after sclerotherapy of esophageal varices
Autori
Pulanić, Roland ; Vrhovac, Božidar ; Jokić, N. ; Rosandić, Marija ; Šalamon, Vladimir ; Opačić, Milorad ; Rustemović, Nadan ; Korać, Bojana ; Vucelić, Boris
Izvornik
International journal of clinical pharmacology, therapy and toxicology (0300-9718) 29
(1991);
347-351
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, stručni
Ključne riječi
ranitidine; sclerotherapy; esophageal varices
Sažetak
The present trial was carried out to determine the usefulness of H2-receptor antagonist drug therapy for the prevention of esophageal bleeding and esophageal varices in patients who underwent sclerotherapy. According to randomization, out of the 58 patients, 28 received, along with the usual standard therapy, ranitidine and 30 received placebo. Ranitidine, 50 mg, was administered intravenously over a period of 3 days every 8 hours, and then 150 mg of ranitidine was given per os in the evening for one month. For improvement of hemostasis and during the elective sclerotherapies, 1% polidocanol was used as the sclerosant. During each puncture, 2 ml was injected. Injections were paravasal and intravasal. After sclerotherapy, endoscopic examinations were carried out on the third day and one month later. Necrosis was noted in 42% of the patients and esophageal mucosal inflammation in 26%. Esophageal ulcers did not occur. There was no statistically significant difference between the two groups in terms of age, sex ratio, cause of liver cirrhosis, and the Child's classification. The size of the esophageal varices had no effect on the development of esophageal mucosal changes in correlation with the quantity of sclerosant. The comparison of the two groups of patients, sclerosed for hemorrhage and sclerosed electively, showed no statistically significant difference regarding esophageal mucosal changes. No differences between the ranitidine and placebo groups of patients were observed in this indication. It can be concluded that esophageal mucosal changes probably arise as a consequence of the sclerosant, its concentration, quantity and mode of application.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb
Profili:
Milorad Opačić
(autor)
Božidar Vrhovac
(autor)
Bojana Korać
(autor)
Nadan Rustemović
(autor)
Vladimir Šalamon
(autor)
Roland Pulanić
(autor)
Boris Vucelić
(autor)
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- SCI-EXP, SSCI i/ili A&HCI
Uključenost u ostale bibliografske baze podataka::
- MEDLINE