Table 1.
Overview of the included studies
Definition based on time (n=51) | ||||||
Studies of side effects related to long-term PPI use (n=29) | ||||||
Author, year | Country | Setting | Study design | Aim | Definition of long-term use | Rationale |
Haastrup et al, 20185 | Denmark | N/A | Review | Overview of side effects of long-term PPI use | >2 weeks | Earlier studies showing no important side effects if used ≤2 weeks |
Revaiah et al, 201820 | India | Secondary sector | Single-centre, cross-sectional | Risk of small bacterial overgrowth in PPI users | >3 months | No |
Torvinen-Kiiskinen et al, 201821 | Finland | Primary sector | Case–control | Risk of hip fractures among community-dwelling residents with Alzheimer’s | ≥1 year | No |
Biyik et al, 201722 | Turkey | Outpatient gastroenterology clinic | Cohort study | Risk of hypomagnesaemia in PPI users | ≥6 months | No |
Takahari et al, 201723 | Japan | Secondary sector | Cross-sectional | Frequency of gastric cobblestone-like lesions in PPI users undergoing endoscopy | ≥6 months | No |
Lochhead et al, 201724 | USA | Nurses’ health study | Cross-sectional | Association between PPI use and cognitive function | ≥2 years | No |
Kearns et al, 201725 | UK | Primary sector | Case–control | Association between PPI use and pancreatic cancer | >2 years | Avoiding reverse causation |
Targownik et al, 201726 | Canada | General population | Cross-sectional | Association between PPI use and bone structure | ≥5 years | No |
Bahtiri et al, 201727 | Turkey | General population | Cohort | Risk of hypomagnesaemia | 12 months | No |
Huang et al, 201628 | Taiwan | General population | Cohort | Association between PPI use and risk of spontaneous bacterial peritonitis in patients with decompensated liver cirrhosis | >180 days | No |
Takeda et al, 201529 | Japan | Outpatients | Cross-sectional | Prevalence of hypomagnesaemia | >1 year | No |
Lundell et al, 201514 | N/A | Systematic review | Systematic review | Effects of PPI on serum gastrin levels and gastric histology | >48 months | FDA requesting 3-year safety data from manufacturers |
Song et al, 201430 | Cochrane review | N/A | Systematic review | Risk of gastric pre-malignant lesions in PPI users | ≥6 months | No |
Lewis et al, 201431 | Australia | General population | Cohort | PPIs and risk of falls and fractures in elderly women | ≥1 year | No |
Helgadóttir, 201432 | Iceland | Secondary sector | Cross-sectional | Serum gastrin levels in PPI users | ≥2 years | No |
Bektas et al, 201233 | Turkey | Secondary sector | Cross-sectional | ECL hyperplasia in PPI users | ≥6 months | No |
Pregun et al, 201134 | Hungary | Secondary sector | Cohort | Effect of PPI on serum chromogranin-A and gastrin levels | >6 months | No |
Sarzynski et al, 201135 | USA | Primary sector | Retrospective cohort | Association between PPI use and iron-deficiency anaemia | >1 year | No |
Fujimoto and Hongo, 201136 | Japan | Multicentre | Cohort | Efficacy and safety of 104 weeks treatment with rabeprazole | 104 weeks | No |
Lombardo et al, 201037 | Italy | Secondary sector | Cohort | Incidence of small intestinal bacterial overgrowth among PPI users | >2 months | No |
Yoshikawa et al, 200938 | Japan | Secondary sector | Case–control | Body mass index changes during PPI therapy in patients with GORD | >10 months | No |
Ally et al, 200939 | USA | Outpatient clinic | Retrospective | Risk of fundic gastric polyps in PPI users | >48 months | No |
Van Soest et al, 200840 | The Netherlands | General practice | Case–control | Risk of colorectal cancer among PPI users | >365 days within 5 years | No |
Hashimoto et al, 200741 | Japan | Secondary sector | Clinical trial | PPI-induced tolerance to histamine-2-receptor antagonists | >4 weeks | No |
Yang et al, 200742 | UK | General practice | Case–control | Risk of colorectal cancer among PPI users | ≥5 years cumulative use | The definition is argued to be able to demonstrate an accelerative effect on the transformation from adenomas to carcinomas |
Robertson et al, 200743 | Denmark | Population based | Case–control | Risk of colorectal cancer among PPI users | >7 years | The definition is argued to be able to demonstrate an accelerative effect on the transformation from adenomas to carcinomas |
Jalving et al, 200644 | The Netherlands | Secondary sector | Cross-sectional | Risk of fundic gastric polyps in PPI users | ≥1 years | No |
Hritz et al, 200545 | Hungary | Secondary sector | Clinical trial | Effect of PPI on gastric cell proliferation | 6 months | No |
ClinicalTrials.gov | Austria | Secondary sector | Clinical trial | Intestinal microbiota in PPI users | ≥6 months | No |
Studies of treatment effects of long-term PPI use (n=13) | ||||||
Kiso et al, 201746 | Japan | Outpatient clinic | Cross-sectional | Endoscopic findings in patients undergoing gastric screening | >8 weeks | No |
Funaki et al, 201747 | Japan | Outpatient clinic | Cross-sectional | Efficacy of PPI in patients with NERD with and without irritable bowel syndrome | >6 months | ROME III criteria for functional disorders (duration >6 months) |
Hatlebakk et al, 201648 | Europe (several countries) | Secondary sector | RCT | Comparing anti-reflux surgery with PPI treatment in patients with chronic GERD | 5 years | No |
Yoon et al, 201449 | South Korea | HP-positive patients | RCT | Eradication rates with different durations of pretreatment with PPI | ≥56 days | No |
Poh et al, 201117 | USA | Outpatient clinic | RCT | Comparing stimulus response functions to acid in users and non-users of PPI undergoing acute stress | 8 weeks | No |
Labenz et al, 200950 | Sweden | Secondary sector | RCT | Predictors of symptom resolution in patients with GERD during maintenance PPI therapy | >6 months | Maintenance phase after healed oesophagitis |
Sugano et al, 201351 | Japan | Outpatient clinic | Clinical trial | Gastroprotective effect of omeprazole | 1 year | No |
Fujimoto and Hongo, 201052 | Japan | Secondary sector | Cohort | Relapse of GERD during long-term PPI therapy | 104 weeks | No |
Kandil et al, 201015 | Egypt | Outpatient clinic | Cohort | Effect of exogenous melatonin in patients with GERD | 4 and 8 weeks | No |
Mason et al, 200853 | UK | General practice | RCT | Effect of HP eradication in long-term users of PPI | A repeat prescription for PPI begun at least 12 months ago | Previous article by Hungin et al54 |
Raghunath et al, 200955 | UK | Primary care | Cross-sectional | Symptoms in patients on long-term PPI therapy | A repeat prescription for PPI begun at least 12 months ago | Previous article by Hungin et al54 |
Usai et al, 200816 | Italy | Secondary sector | Cohort | Recurrence of reflux symptoms in patients with coeliac disease with NERD | >8 weeks | No |
Frazzoni et al, 200756 | Italy | Secondary sector | Cohort | Efficacy of long-term PPI on intraoesophageal acid suppression | 2 years of continuous use | No |
Studies of deprescribing long-term PPI (n=6) | ||||||
Pezeshkian and Conway, 201857 | USA | N/A | Review | Guidance on deprescribing PPI in older adults | >12 weeks | Approved duration of treatment |
Boghossian et al, 201758 | Cochrane review | N/A | Systematic review | Effects of deprescribing PPI in adults | ≥28 days | No |
Walsh et al, 201659 | Canada | General practice | Cross-sectional | Deprescribing | ≥8 weeks | Guideline recommending reassessment of PPIs after 8 weeks |
Van der Velden et al, 201360 | The Netherlands | Primary care | RCT | Deprescribing | ≥1 year | No |
Bjornsson et al, 200661 | Sweden | Secondary sector | Clinical trial | Discontinuation | >8 weeks | No |
Krol et al, 200462 | The Netherlands | General practice | RCT | Discontinuation | ≥12 weeks | No |
Pharmacoepidemiological studies of long-term PPI use (n=3) | ||||||
Othman et al, 201663 | UK | General population | Cohort | Prevalence and pattern of PPI prescribing | ≥1 year continuous use | No |
Lødrup et al, 201464 | Denmark | General population | Survey | Use of PPIs | ≥120 days the past year | No |
Haroon et al, 201365 | Ireland | Secondary sector | Survey | Reasons for treatment | 2 years | No |
Definition based on quantity of PPI (n=10) | ||||||
Studies of side effects related to long-term PPI use (n=6) | ||||||
Imfeld et al, 201866 | UK | General population | Case–control | Risk of dementia | ≥100 prescriptions | No |
Shao et al, 201867 | Taiwan | General population | Case–control | Risk of hepatocellular carcinoma | >28 DDDs | No |
Sieczkowska et al, 201868 | Poland | Outpatient clinic and general practice | Cohort | Risk of small intestinal bacterial overgrowth | PPI for at least 75% of the time during the previous 3 months at a minimum dose of 20 mg per day | No |
Chien et al, 201669 | Taiwan | General population | Case–control | Risk of periampullar cancer | >180 DDDs | No |
Clooney et al, 201670 | Canada | General population | Cross-sectional | Gut microbiome in long-term PPI users | >180 tablets each year in a 5-year period | No |
Den Elzen et al, 200871 | The Netherlands | General population | Cross-sectional | Risk of vitamin B12 deficiency | >810 DDDs in 3 years | No |
Studies of deprescribing long-term PPI (n=2) | ||||||
Reimer and Bytzer, 201072 | Denmark | Primary care | Cross-sectional | Discontinuation in symptomatically treated patients | 120 tablets of any PPI in the previous 12 months | No |
Clinicaltrials.gov | USA | Primary care | Clinical trial | Evaluation of a deprescribing programme | 90-day prescription within 120 days | No |
Pharmacoepidemiological studies of long-term PPI use (n=2) | ||||||
Wallerstedt et al, 20174 | Sweden | General population | Cross-sectional | Prevalence of PPI use among residents ≥65 years | Filled prescriptions for PPI covering ≥75% of the year | No |
Haastrup et al, 20162 | Denmark | General population | Cohort | Predictors of incident long-term use among first-time users | >60 DDDs within 6 months | Definition used in other studies |
DDDs, defined daily doses; ECL, enterochromaffin-like; FDA, Food and Drug Administration; GERD, gastro-oesophageal reflux disease; HP, Helicobacter pylori; N/A, not available; NERD, non-erosive reflux disease; PPI, proton pump inhibitor; RCT, randomised controlled trial.