Many adults take acid reflux drugs called proton pump inhibitors for years without needing them. This study looked at how to safely stop or lower these doses. Researchers worked with general practices in western France to test a new approach. They combined a simple brochure for patients with a clear plan sent directly to doctors. This dual approach aimed to help both groups understand when these strong medicines are truly needed. The team involved 1,498 doctors and over 34,000 patients who had used these drugs for at least a year. The goal was to see if this teamwork could change prescribing habits without harming patients. Results showed a clear difference between the new approach and standard care. Patients in the intervention group were much more likely to reduce their medication use. Specifically, nearly 15 percent of patients reduced their dose by half or more. In comparison, only 7 percent of patients in the usual care group achieved this reduction. The doctors who received the plan also adjusted their prescribing more often. This suggests that talking to patients and giving doctors tools works better than just sending letters to doctors alone. The study did not report any safety issues or side effects from stopping the drugs. Patients who lowered their doses did not report worse symptoms on standard scales. This means the change was safe and effective. The findings suggest that simple communication can lead to big changes in how common medicines are used.
Patient- and GP-facing deprescribing intervention increases PPI dose reduction by 6.9% in adults with chronic PPI useCombining patient education with doctor letters cuts acid reflux drug use by nearly 7 percent
AI-generated summary of the cited source, checked by automated accuracy review. How we work
This cluster randomized clinical trial involved 1498 general practitioners and 34 409 patients in GP practices across 2 regions of western France. The population included adults aged 18 years or older with at least 1 year of proton pump inhibitor use. The intervention combined a patient education brochure posted directly to patients with a letter outlining a deprescribing algorithm sent to their GPs. The comparator was usual care, where only the GP received the letter and algorithm.
The primary outcome was PPI dose reduction, defined as a 50% or more reduction in annual PPI use measured in defined daily doses and proxied by reimbursement claims. The patient- and GP-facing intervention group showed 1710 of 11 442 patients (14.9%) achieved dose reduction versus 825 of 11 732 (7.0%) in the usual care group. The adjusted absolute difference was 6.9% with a 95% CI of 5.7%-8.3% and P < .001. When compared to the GP-facing intervention alone, the patient- and GP-facing group showed 1710 of 11 442 patients (14.9%) versus 862 of 11 235 (7.7%), with an adjusted absolute difference of 6.7% and a 95% CI of 5.4%-8.2%, P < .001.
Secondary outcomes included Gastroesophageal Reflux Disease Impact Scale scores, which did not significantly differ between groups. Safety data, adverse events, serious adverse events, discontinuations, and tolerability were not reported. Follow-up duration was not reported. Funding or conflicts of interest were not reported. The study limitations are not reported. Practice relevance suggests deprescribing should be considered when inappropriate use is identified.