Proton pump inhibitors receiving and prognosis of patients after scheduled percutaneous coronary interventions
The urgency of the study is determined by the lack of data necessary in order to assess the safety of prolonged use of proton pump inhibitors (PPI) in patients with IHD combined with anti-aggregant therapy. The aim of the study was to study the relationship between the use of PPI and the risk of thr...
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doaj-4085fca02c9144c58f56d7f8119e62672020-11-25T03:11:58Zrus"Consilium Medicum" Publishing houseТерапевтический архив0040-36602309-53422018-09-019099210010.26442/terarkh201890992-10029746Proton pump inhibitors receiving and prognosis of patients after scheduled percutaneous coronary interventionsA L Komarov0O O Shakhmatova1V Muraseeva2E S Novikova3E V Guskova4E P Panchenko5Department of Clinical Problems of Atherothrombosis of the National Medical Research Center for CardiologyDepartment of Clinical Problems of Atherothrombosis of the National Medical Research Center for CardiologyDepartment of Clinical Problems of Atherothrombosis of the National Medical Research Center for CardiologyDepartment of Clinical Problems of Atherothrombosis of the National Medical Research Center for CardiologyPirogov National Medical and Surgical CenterDepartment of Clinical Problems of Atherothrombosis of the National Medical Research Center for CardiologyThe urgency of the study is determined by the lack of data necessary in order to assess the safety of prolonged use of proton pump inhibitors (PPI) in patients with IHD combined with anti-aggregant therapy. The aim of the study was to study the relationship between the use of PPI and the risk of thrombotic complications in patients undergoing planned procedures of percutaneous coronary interventions (PCI) and receiving dual antiplatelet therapy. Materials and methods. The study is a prospective register of patients who successfully underwent planned percutaneous coronary intervention (PCI). The effect of PPI (omeprazole and pantoprazole) on the frequency of the combined end point cardiovascular death, ACS, AI, TIA, peripheral arterial thrombosis and PE was assessed using the Log-Rank criterion, as well as in a multivariate analysis (Cox proportional risk regression model). Results. A total of 391 patients were included in the study (23.1% women, mean age 61.2 [Symbol] 10.4 years). The median duration of follow-up was 18 months. During this period of time, 34 adverse events were recorded. Log-Rank analysis showed that the proportion of patients without adverse events in the omeprazole group was significantly lower in comparison with patients who did not receive PPI (0.56 vs. 0.84, Log-Rank p=0.003), and for pantoprazole no such pattern was found (0.89 against 0.84, Log-Rank p=0.21). The average level of residual platelet reactivity (ORT), as well as the number of patients with high ORT (> 208 PRU), did not differ significantly between the groups of omeprazole, pantoprazole and the group of patients not receiving PPI. According to multivariate analysis, omeprazole was an independent predictor of thrombotic complications after a planned PCI (OR 3.75, 95% confidence interval 1.72-8.17, p=-0.0009). Conclusion. Long-term use of omeprazole (at least 30 days) is an independent predictor of thrombotic complications in patients who underwent planned PCI.https://ter-arkhiv.ru/0040-3660/article/viewFile/32996/pdfproton pump inhibitorsomeprazolepantoprazoleihdpercutaneous coronary interventionsrisk of cardiovascular complications |
collection |
DOAJ |
language |
Russian |
format |
Article |
sources |
DOAJ |
author |
A L Komarov O O Shakhmatova V Muraseeva E S Novikova E V Guskova E P Panchenko |
spellingShingle |
A L Komarov O O Shakhmatova V Muraseeva E S Novikova E V Guskova E P Panchenko Proton pump inhibitors receiving and prognosis of patients after scheduled percutaneous coronary interventions Терапевтический архив proton pump inhibitors omeprazole pantoprazole ihd percutaneous coronary interventions risk of cardiovascular complications |
author_facet |
A L Komarov O O Shakhmatova V Muraseeva E S Novikova E V Guskova E P Panchenko |
author_sort |
A L Komarov |
title |
Proton pump inhibitors receiving and prognosis of patients after scheduled percutaneous coronary interventions |
title_short |
Proton pump inhibitors receiving and prognosis of patients after scheduled percutaneous coronary interventions |
title_full |
Proton pump inhibitors receiving and prognosis of patients after scheduled percutaneous coronary interventions |
title_fullStr |
Proton pump inhibitors receiving and prognosis of patients after scheduled percutaneous coronary interventions |
title_full_unstemmed |
Proton pump inhibitors receiving and prognosis of patients after scheduled percutaneous coronary interventions |
title_sort |
proton pump inhibitors receiving and prognosis of patients after scheduled percutaneous coronary interventions |
publisher |
"Consilium Medicum" Publishing house |
series |
Терапевтический архив |
issn |
0040-3660 2309-5342 |
publishDate |
2018-09-01 |
description |
The urgency of the study is determined by the lack of data necessary in order to assess the safety of prolonged use of proton pump inhibitors (PPI) in patients with IHD combined with anti-aggregant therapy. The aim of the study was to study the relationship between the use of PPI and the risk of thrombotic complications in patients undergoing planned procedures of percutaneous coronary interventions (PCI) and receiving dual antiplatelet therapy. Materials and methods. The study is a prospective register of patients who successfully underwent planned percutaneous coronary intervention (PCI). The effect of PPI (omeprazole and pantoprazole) on the frequency of the combined end point cardiovascular death, ACS, AI, TIA, peripheral arterial thrombosis and PE was assessed using the Log-Rank criterion, as well as in a multivariate analysis (Cox proportional risk regression model). Results. A total of 391 patients were included in the study (23.1% women, mean age 61.2 [Symbol] 10.4 years). The median duration of follow-up was 18 months. During this period of time, 34 adverse events were recorded. Log-Rank analysis showed that the proportion of patients without adverse events in the omeprazole group was significantly lower in comparison with patients who did not receive PPI (0.56 vs. 0.84, Log-Rank p=0.003), and for pantoprazole no such pattern was found (0.89 against 0.84, Log-Rank p=0.21). The average level of residual platelet reactivity (ORT), as well as the number of patients with high ORT (> 208 PRU), did not differ significantly between the groups of omeprazole, pantoprazole and the group of patients not receiving PPI. According to multivariate analysis, omeprazole was an independent predictor of thrombotic complications after a planned PCI (OR 3.75, 95% confidence interval 1.72-8.17, p=-0.0009). Conclusion. Long-term use of omeprazole (at least 30 days) is an independent predictor of thrombotic complications in patients who underwent planned PCI. |
topic |
proton pump inhibitors omeprazole pantoprazole ihd percutaneous coronary interventions risk of cardiovascular complications |
url |
https://ter-arkhiv.ru/0040-3660/article/viewFile/32996/pdf |
work_keys_str_mv |
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