PMID- 34738287 OWN - NLM STAT- MEDLINE DCOM- 20220325 LR - 20220325 IS - 1099-1557 (Electronic) IS - 1053-8569 (Linking) VI - 31 IP - 3 DP - 2022 Mar TI - Utilization trend of gastric acid-suppressing agents in relation to analgesics. PG - 314-321 LID - 10.1002/pds.5381 [doi] AB - BACKGROUND: Controversies exist about excessive use of gastric acid-suppressing agents or lack of adequate indications, especially when co-prescribed with analgesics for gastroprotection. We aimed to analyze the nationwide trend of gastric acid-suppressing agents and analgesics. METHODS: We obtained nationwide consumption data of analgesics (nonsteroidal anti-inflammatory drugs [NSAIDs], opioids, others) and gastric acid-suppressing agents (proton pump inhibitors [PPI] and histamine-2 receptor antagonists [H2RAs]) between years of 2014-2018 from IQVIA Turkey. Drug utilization was measured by defined daily dose (DDD)/1000 inhabitants/day (DID) unit. Drug sales data were further used to test the correlation of PPIs and H2RAs to analgesics. RESULTS: During the study period, analgesic utilization increased from 65.7 to 67.4 DID. NSAIDs constituted 82.7%-84.9% of all analgesic utilization. The consumption of NSAIDs increased by 3.1%, and the most commonly consumed analgesic was diclofenac (18.5 +/- 1.5 DID), constituting 25.4%-29.0% of all analgesics. PPI utilization was found to regularly raise from 52.1 DID in 2014 to 72.0 DID in 2018 with an overall increment of 38.2%. Use of H2RAs was found to increase from 11.4 DID in 2014 to 14.0 DID in 2018. The physician visit-adjusted utilization of both antirheumatic NSAIDs and non-antirheumatic analgesics showed significantly moderate-strong positive correlations with PPIs (r: 0.63, 0.48-0.76 and r: 0.63, 0.47-0.75, respectively) and H2RAs (r: 0.61, 0.44-0.73 and r: 0.57, 0.41-0.71, respectively). CONCLUSION: The utilization trend exhibited a dramatic increase of the gastric acid-suppressing agents -more pronounced for PPIs, with a modest increase in analgesics. Excessive utilization of PPIs does not seem to imply a tendency toward only NSAID-related gastroprotection. CI - (c) 2021 John Wiley & Sons Ltd. FAU - Kirmizi, Neriman Ipek AU - Kirmizi NI AD - Department of Medical Pharmacology, School of Medicine, Istanbul Medipol University, Istanbul, Turkey. FAU - Aydin, Volkan AU - Aydin V AD - Department of Medical Pharmacology, International School of Medicine, Istanbul Medipol University, Istanbul, Turkey. FAU - Akici, Ahmet AU - Akici A AUID- ORCID: 0000-0002-8593-0818 AD - Department of Medical Pharmacology, School of Medicine, Marmara University, Istanbul, Turkey. LA - eng PT - Journal Article DEP - 20211117 PL - England TA - Pharmacoepidemiol Drug Saf JT - Pharmacoepidemiology and drug safety JID - 9208369 RN - 0 (Anti-Inflammatory Agents, Non-Steroidal) RN - 0 (Gastrointestinal Agents) RN - 0 (Histamine H2 Antagonists) RN - 0 (Proton Pump Inhibitors) SB - IM MH - Anti-Inflammatory Agents, Non-Steroidal/therapeutic use MH - *Gastric Acid MH - *Gastrointestinal Agents MH - Histamine H2 Antagonists/therapeutic use MH - Humans MH - Proton Pump Inhibitors/therapeutic use OTO - NOTNLM OT - analgesics OT - diclofenac OT - gastric acid-suppressing agents OT - pantoprazole OT - ranitidine OT - utilization trend EDAT- 2021/11/06 06:00 MHDA- 2022/03/26 06:00 CRDT- 2021/11/05 07:03 PHST- 2021/10/18 00:00 [revised] PHST- 2021/02/24 00:00 [received] PHST- 2021/10/31 00:00 [accepted] PHST- 2021/11/06 06:00 [pubmed] PHST- 2022/03/26 06:00 [medline] PHST- 2021/11/05 07:03 [entrez] AID - 10.1002/pds.5381 [doi] PST - ppublish SO - Pharmacoepidemiol Drug Saf. 2022 Mar;31(3):314-321. doi: 10.1002/pds.5381. Epub 2021 Nov 17.