Τόμος 5 (1991) – Τεύχος 3 – Άρθρο 4 – Επιθεώρηση Κλινικής Φαρμακολογίας και Φαρμακοκινητικής-Διεθνής Έκδοση – Volume 5 (1991) – Issue 3 – Article 4 – Epitheorese Klinikes Farmakologias και Farmakokinetikes-International Edition

Title Management of patients with peptic ulcer receiving streptokinase for acute myocardial infarction
Authors John Kanonidis, Constantine Papadopoulos, John Papayannis, Stavros Konstantinidis, Stylianos Savatis, Panayotis Kotridis, Constantine Gitsios and George Sakadamis

2nd Department of Cardiology, University of Thessaloniki, Greece

Citation Kanonidis, J., Papadopoulos, C., Papayannis, J., Konstantinidis, S., Savatis, S. et al.: Management of patients with peptic ulcer receiving streptokinase for acute myocardial infarction, Epitheorese Klin. Farmakol. Farmakokinet. 5(3): 143-147 (1991)
Publication Date Received for publication: 25 October 1991

Accepted for publication: 5 November 1991

Full Text Language English
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Keywords Acute myocardial infarction, streptokinase, peptic ulcer.
Other Terms review article
Summary The aim of this study is to evaluate the role of H2 inhibitors in preventing gastrointestinal bleeding (GIB) in patients (pts) with peptic ulcer (PU) undergoing thrombolysis for acute myocardial infarction (AMI). Thirty nine pts (mean age 57±6 years) with known PU, receiving streptokinase (SK) for AMI, were studied. These pts were divided in two groups (G). G1 included 22 pts who had been free from symptoms of PU for at least six months prior to AML G2 included 17 pts, 8 with relapsing symptoms of PU for the six month period prior to AMI and 9 with a history of PU complications. As a supplement to thrombolytic treatment, pts in G1 received Ranitidine 150 mgr per os t.i.d. for one week and in G2 Ranitidine 50 mgr i.v. t.i.d. for 3 days, followed by 150 mgr per os t.i.d. up to the end of the first week. No pts developed clinically recognizable GIB. In 5 pts (2 in G1 and 3 in G2) a noticeable decrease of Hb occurred without clinical evidence of blood loss. In 7 pts (4 in G1 and 3 in G2) adverse reactions from the gastrointestinal system (vomiting, nausea) were attributed to hypersensitivity to SK infusion. In conclusion, a protective role of H2 inhibitors, although. cannot be claimed due to the non randomised nature of the study, is nevertheless strongly indicative and can be recommended for those pts with PU which are considered at high risk for GIB.
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