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Journal articles on the topic 'Omeprazole'

Author: Grafiati

Published: 4 June 2021

Last updated: 9 March 2023

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1

Sartika, Eria, Eko Suhartono, and Agung Biworo. "PENGARUH LANSOPRAZOL DAN OMEPRAZOL TERHADAP AKTIVITAS ENZIM KATALASE HEPAR TIKUS." Berkala Kedokteran 12, no. 2 (October 7, 2016): 255. http://dx.doi.org/10.20527/jbk.v12i2.1875.

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Abstract: Lansoprazole and omeprazole is a Proton Pump Inhibitor class of drugs that are often used for the treatment of peptic ulcers. Lansoprazole and omeprazole have an influence on the various target organs exposed. Mechanism of lansoprazole and omeprazole in influencing the activity of the enzyme catalase is competing with absolute catalase enzyme substrate (H2O2) in the binding of the enzyme active site. This study aims to determine the effect of lansoprazole and omeprazole against liver catalase enzyme activity. This study was a laboratory experimental study conducted in three groups, namely the control group (P0), the treatment group (P1) is given lansoprazole 30 mg and a treatment group (P2) given omeprazole 20 mg. The result showed the value of Km of the control group (P0) of 13.482 mmol/dm3, the treatment group (P1) of 11,227 mmol/dm3 and the treatment group (P2) of 6,327 mmol/dm3. Analysis of statistical data shows the regression correlation value of p for P1 was 0,01 adn for P2 was 0,02 (p <0.05) and the R value approaching 1 with a linear graph Lineweaver Burk meaningful. Concluded that lansoprazole and omeprazole may affect the activity of the liver enzyme catalase. Keywords: lansoprazole, omeprazole, enzyme catalase, rat liver Abstrak: Lansoprazol dan omeprazol merupakan obat golongan proton pump inhibitor yang sering digunakan untuk pengobatan tukak lambung. Lansoprazol dan omeprazol memiliki berbagai pengaruh terhadap organ target yang terpajan. Mekanisme lansoprazol dan omeprazol dalam mempengaruhi aktivitas enzim katalase adalah berkompetisi dengan substrat absolut enzim katalase (H2O2) dalam mengikat sisi aktif enzim. Penelitian ini bertujuan untuk mengetahui pengaruh lansoprazol dan omeprazol terhadap aktivitas enzim katalase hepar. Penelitian ini merupakan penelitian quasi eksperimental yang dilakukan pada 3 kelompok, yakni kelompok kontrol (P0), kelompok perlakuan (P1) diberikan lansoprazol 30 mg dan kelompok perlakuan (P2) diberikan omeprazol 20 mg. Hasil penelitian didapatkan nilai Km pada kelompok kontrol (P0) sebesar 13,482 mmol/dm3, pada kelompok perlakuan (P1) sebesar 11,227mmol/dm3 dan pada kelompok perlakuan (P2) sebesar 6,327mmol/dm3. Analisis data statistik korelasi regresi menunjukkan nilai p pada P1 0,01 dan pada P2 0,02 (p<0,05) serta nilai R mendekati 1 dengan grafik linear Lineweaver Burk yang menanjak. Disimpulkan bahwa lansoprazol dan omeprazol dapat mempengaruhi aktivitas enzim katalase hepar mencit. Kata-kata kunci: lansoprazol, omeprazol, enzim katalase, hepar mencit

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2

Fienda, Adrully El, and Ainun Wulandari. "Analisis Efektivitas Biaya Penggunaan Omeprazol dan Pantoprazol dalam Terapi Peptic Ulcer pada Pasien Lansia Rawat Inap di Rumah Sakit Umum Adhyaksa." Jurnal Farmasi Higea 14, no. 2 (December 30, 2022): 169. http://dx.doi.org/10.52689/higea.v14i2.475.

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PPI (proton pump inhibitors) adalah salah satu obat yang umum diresepkan pada gangguan lambung. Penelitian ini bertujuan untuk mengetahui nilai efektivitas biaya pada penggunaan Omeprazol dan Pantoprazol pada pasien rawat inap di RSU Adhyaksa. Penelitian ini menggunakan metode deskriptif kuantitatif dengan pengambilan data secara retrospektif dengan membandingkan Direct Medical Cost (biaya medik langsung). Subjek dari penelitian ini adalah semua pasien rawat inap di RSU Adhyaksa yang mendapatkan terapi Omeprazol dan Pantoprazol dengan usia >50 tahun dalam periode Januari 2020 – Mei 2022. Hasil efektivitas terapi dapat dilihat dari data rekam medis pasien dan biaya pengobatan pasien yang dianalisis dengan perhitungan rasio rerata efektivitas biaya (ACER). Berdasarkan efektivitas terapi pantoprazol (95,2%) lebih efektif dibandingkan omeprazol (90,5%). Terdapat perbedaan nilai ACER pada pasien yang menggunakan pantoprazole sebesar Rp 1.802.501,- dan pada omeprazole sebesar Rp 2.022.952,-. ICER pada penelitian ini menunjukkan angka Rp. 601.510,-. Pada penelitian ini terdapat perbedaan efektivitas antara pantoprazol dan omeprazole sebagai terapi Peptik ulser. Biaya terapi peptic ulser pada pantoprazol lebih rendah dibandingkan omeprazole.

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3

Hutahaean, Amsaline, Gayatri Citraningtyas, and Defny S. Wewengkang. "ANALISIS EFEKTIVITAS BIAYA PADA PASIEN GASTRITIS RAWAT INAP DI RUMAH SAKIT BHAYANGKARA MANADO." PHARMACON 8, no. 4 (November 28, 2019): 767. http://dx.doi.org/10.35799/pha.8.2019.29351.

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ABSTRACTGastritis is an inflammatory process in the gastric mucosa and submucosa or health problems caused by irritation and infection factors. Treatment therapy used in gastritis is the proton pump inhibitor (PPI), H2 receptor antagonists, and antacids. Giving treatment therapy used by patients has an impact on the amount of medical expenses. The purpose of this study was to determine a more cost effective therapy between the use of omeprazole and lansoprazole in hospitalized gastrtitis patients at Bhayangkara Hospital, Manado. The method used in this study is Cost Effectiveness Analysis with a retrospective data collection on the period of January - December 2018. The sample in this study was 44 patients, consisting of 25 patients using with omeprazole therapy and 19 patients with lansoprazole therapy. The results showed that the most cost-effective PPI was omeprazole with an ACER value of IDR 643,210.37 and ICER value of IDR 631,023.17/ day for each increase in effectiveness if there is a transfer from lansoprazole to omeprazole Keywords: Cost Effectiveness Analysis, Gastritis, Omeprazole, Lansoprazol. ABSTRAKGastritis adalah proses inflamasi pada mukosa dan submukosa lambung atau gangguan kesehatan yang disebabkan oleh faktor iritasi dan infeksi. Terapi pengobatan yang digunakan pada penyakit gastritis yaitu proton pump inhibitor (PPI), antagonis reseptor H2, serta antasida. Pemberian terapi pengobatan yang digunakan oleh pasien berdampak pada besarnya biaya pengobatan. Tujuan penelitian ini untuk menentukan terapi yang lebih cost effective antara penggunaan omeprazol dan lansoprazol pada pasien gastrtitis rawat inap di RS Bhayangkaara Manado. Metode yang digunakan pada penelitian ini adalah Cost-Effectiveness Analysis dengan rancangan pengambilan data secara retrospektif pada periode Januari – Desember 2018. Sampel pada penelitian ini sebanyak 44 pasien, terdiri dari 25 pasien pengguna terapi omeprazol dan 19 pasien pengguna terapi lansoprazol. Hasil penelitian menunjukkan terapi PPI yang lebih cost-effective adalah omeprazol dengan nilai ACER sebesar Rp. 643.210,37 dan nilai ICER sebesar Rp. 631.023,17/hari untuk setiap peningkatan efektivitas jika akan dilakukan perpindahan dari lansoprazol ke omeprazol. Kata Kunci : Analisis Efektivitas Biaya, Gastritis, Omeprazol, Lansoprazol.

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4

Nasrullah, Mohammed Z., Khalid Eljaaly, Thikryat Neamatallah, Usama A. Fahmy, Abdulmohsin J. Alamoudi, Hussain T. Bakhsh, and Ashraf B. Abdel-Naim. "Omeprazole Prevents Colistin-Induced Nephrotoxicity in Rats: Emphasis on Oxidative Stress, Inflammation, Apoptosis and Colistin Accumulation in Kidneys." Pharmaceuticals 15, no. 7 (June 23, 2022): 782. http://dx.doi.org/10.3390/ph15070782.

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The clinical value of colistin, a polymyxin antibiotic, is limited by its nephrotoxicity. Omeprazole is a commonly prescribed proton pump inhibitor. The current study aimed to evaluate the effects of the concomitant administration of omeprazole on colistin-induced nephrotoxicity in rats. Omeprazole significantly ameliorated colistin nephrotoxicity as evidenced by prevention in the rise in the serum level of creatinine, urea and cystactin C as well as urinary N-acetylglucosamine activity. This was confirmed by histological studies that indicated a decreased incidence of interstitial nephritis, degenerative cortical changes and collagen deposition. This was accompanied by the prevention of oxidative stress as omeprazole significantly inhibited the lipid peroxidation, glutathione depletion and enzymatic exhaustion of superoxide dismutase as well as catalase. Additionally, omeprazole inhibited the expression of interleukin-6 and tumor necrosis factor-α. Further, omeprazole inhibited the colistin-induced rise in Bax and the down-regulation of Bcl2 mRNA expression. An assessment of the serum levels of colistin revealed that omeprazole had no significant impact. However, it was observed that omeprazole significantly inhibited the accumulation of colistin in kidney tissues. In conclusion, omeprazole protects against colistin-induced nephrotoxicity. This can be attributed to, at least partly, omeprazole’s anti-oxidant, anti-inflammatory and anti-apoptotic activities in addition to its ability to prevent the toxic accumulation of colistin in kidneys.

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5

&NA;. "Omeprazole see Furosemide/omeprazole." Reactions Weekly &NA;, no. 354 (June 1991): 11. http://dx.doi.org/10.2165/00128415-199103540-00049.

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6

Javed, Mamoona, Muhammad Hayder Ali, Muhammad Saad Tanveer, and Muhammad Hassan Tanveer. "Omeprazole vs Lansoprazole in the Management of Gastroesophageal Reflux Disease: A Systematic Literature Review." Journal of Medical Research and Innovation 4, no. 2 (March 29, 2020): e000204. http://dx.doi.org/10.32892/jmri.204.

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Objective: To evaluate the effectiveness and safety of omeprazole compared to lansoprazole in Gastroesophageal reflux disease patients (GERD). Methods: A systematic search of MEDLINE, EMBASE (inception to December 2019) and CENTRAL (January 2011 to December 2019) was conducted to identify the relevant articles. A detailed inclusion-exclusion criterion was developed and implemented to screen the abstracts. Full texts of the selected abstracts were then assessed to establish their inclusion or exclusion in our review. Cochrane risk of bias criterion was used to assess the methodological quality of the included studies. All relevant data were extracted and the results were summarised narratively. Results: 9 studies met our inclusion-exclusion criteria and were included in this review. In all three trials reporting on heartburn and regurgitation, both omeprazole and lansoprazole were found to be effective in relieving the symptoms of heartburn and regurgitation; however, there was no evidence that one is better than the other. Five out of six studies reporting on intragastric pH provided the evidence of omeprazole’s superiority over lansoprazole in controlling gastric pH. Omeprazole lowered intragastric pH faster and the results lasted longer compared to lansoprazole. The results were statistically significant. Conclusion: There is no significant difference in the clinical effectiveness of omeprazole and lansoprazole in relieving symptoms of heartburn and regurgitation. However, omeprazole is more effective in reducing gastric acidity than lansoprazole.

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7

Skvortsova, T. A., G. Yu Knorring, and E. N. Kareva. "Use of Omeprazole in Paediatric Patients in Russia." Doctor.Ru 20, no. 10 (2021): 39–43. http://dx.doi.org/10.31550/1727-2378-2021-20-10-39-43.

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Objective of the Review: To analyse clinical and pharmacological characteristics and normative documents in the use of modern proton pump inhibitors (PPI) in paediatric patients in the Russian Federation. Key Points. PPIs remain a widely used and efficient therapy of acid-related disorders in children; however, prescription should be based not only on clinical characteristics of a patient, but also on normative documents, e.g., instructions for the use of PPIs in paediatric population for certain indications approved by the Ministry of Health of Russia, since healthcare providers are responsible for off-label prescriptions. Conclusion. Omeprazole is one of the most well-studied PPIs; it has good evidence base for the use in children; however, in Russia, most omeprazoles have contraindications in paediatric population. Omez is indicated for the management of gastroesophageal reflux and duodenal ulcer caused by Helicobacter pylori in children. Keywords: acid-related disorders, children, paediatrics, proton pump inhibitors, Omeprazole.

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8

&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1382 (December 2011): 28. http://dx.doi.org/10.2165/00128415-201113820-00100.

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9

&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1386 (January 2012): 29–30. http://dx.doi.org/10.2165/00128415-201213860-00102.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1390 (February 2012): 28. http://dx.doi.org/10.2165/00128415-201213900-00108.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1391 (March 2012): 32. http://dx.doi.org/10.2165/00128415-201213910-00116.

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12

&NA;. "Omeprazole." Reactions Weekly &NA;, no. 703 (May 1998): 10. http://dx.doi.org/10.2165/00128415-199807030-00035.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 713 (August 1998): 9. http://dx.doi.org/10.2165/00128415-199807130-00025.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 716 (August 1998): 12. http://dx.doi.org/10.2165/00128415-199807160-00041.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 716 (August 1998): 13. http://dx.doi.org/10.2165/00128415-199807160-00046.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 723 (October 1998): 10. http://dx.doi.org/10.2165/00128415-199807230-00032.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 743 (March 1999): 10–11. http://dx.doi.org/10.2165/00128415-199907430-00030.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 743 (March 1999): 11. http://dx.doi.org/10.2165/00128415-199907430-00033.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 746 (April 1999): 9. http://dx.doi.org/10.2165/00128415-199907460-00028.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 751 (May 1999): 10. http://dx.doi.org/10.2165/00128415-199907510-00034.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 758 (July 1999): 10. http://dx.doi.org/10.2165/00128415-199907580-00032.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1194-1195 (March 2008): 28. http://dx.doi.org/10.2165/00128415-200811940-00103.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1135 (January 2007): 24. http://dx.doi.org/10.2165/00128415-200711350-00095.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1136 (January 2007): 21. http://dx.doi.org/10.2165/00128415-200711360-00064.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1138 (February 2007): 21. http://dx.doi.org/10.2165/00128415-200711380-00061.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1143 (March 2007): 20. http://dx.doi.org/10.2165/00128415-200711430-00066.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1149 (April 2007): 19. http://dx.doi.org/10.2165/00128415-200711490-00060.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1153 (May 2007): 21. http://dx.doi.org/10.2165/00128415-200711530-00070.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1158 (June 2007): 22. http://dx.doi.org/10.2165/00128415-200711580-00061.

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&NA;. "Omeprazole." Inpharma Weekly &NA;, no. 1203 (September 1999): 16. http://dx.doi.org/10.2165/00128413-199912030-00026.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1359 (July 2011): 29. http://dx.doi.org/10.2165/00128415-201113590-00112.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1361 (July 2011): 31. http://dx.doi.org/10.2165/00128415-201113610-00112.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1361 (July 2011): 31. http://dx.doi.org/10.2165/00128415-201113610-00114.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 1366 (August 2011): 23–24. http://dx.doi.org/10.2165/00128415-201113660-00089.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 532 (December 1994): 13. http://dx.doi.org/10.2165/00128415-199405320-00047.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 533 (January 1995): 9. http://dx.doi.org/10.2165/00128415-199505330-00033.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 538 (February 1995): 12. http://dx.doi.org/10.2165/00128415-199505380-00049.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 540 (March 1995): 10. http://dx.doi.org/10.2165/00128415-199505400-00033.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 547 (April 1995): 10. http://dx.doi.org/10.2165/00128415-199505470-00027.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 551 (May 1995): 9. http://dx.doi.org/10.2165/00128415-199505510-00035.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 558 (July 1995): 10. http://dx.doi.org/10.2165/00128415-199505580-00029.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 560 (July 1995): 9. http://dx.doi.org/10.2165/00128415-199505600-00027.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 564 (August 1995): 10. http://dx.doi.org/10.2165/00128415-199505640-00027.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 566 (September 1995): 10. http://dx.doi.org/10.2165/00128415-199505660-00038.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 567 (September 1995): 9. http://dx.doi.org/10.2165/00128415-199505670-00031.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 567 (September 1995): 10. http://dx.doi.org/10.2165/00128415-199505670-00033.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 585 (January 1996): 10. http://dx.doi.org/10.2165/00128415-199605850-00038.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 594 (March 1996): 10. http://dx.doi.org/10.2165/00128415-199605940-00036.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 424 (October 1992): 10. http://dx.doi.org/10.2165/00128415-199204240-00053.

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&NA;. "Omeprazole." Reactions Weekly &NA;, no. 428 (November 1992): 10. http://dx.doi.org/10.2165/00128415-199204280-00048.

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