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High Rate of Potentially Inappropriate Prescribing of PPIs for Older People in Primary Care
abstract
This abstract is available on the publisher's site.
Access this abstract nowOBJECTIVES
To characterize prescribing of proton pump inhibitors (PPIs) and medicines that increase gastrointestinal bleeding risk (ulcerogenic) in older people from 1997 to 2012 and assess factors associated with maximal-dose prescribing in long-term PPI users.
DESIGN
Repeated cross-sectional study of pharmacy claims data.
SETTING
Eastern Health Board region of Ireland.
PARTICIPANTS
Individuals aged 65 and older from a means-tested health plan in 1997, 2002, 2007, and 2012 (range 78,489-133,884 individuals).
MEASUREMENTS
PPI prescribing prevalence was determined per study year, categorized according to duration (≤8 or >8 weeks), dosage (maximal or maintenance), and co-prescribed drugs. Logistic regression in long-term PPI users was used to determine whether age, sex, polypharmacy, and ulcerogenic medicine use were associated with being prescribed a maximal dose rather than a maintenance dose. Adjusted odds ratios (ORs) with 95% confidence intervals (CIs) are presented.
RESULTS
Half of this older population received a PPI in 2007 and 2012. Long-term use (>8 weeks) of maximal doses rose from 0.8% of individuals in 1997 to 23.6% in 2012. Although some ulcerogenic medicines and polypharmacy were significantly associated with maximal PPI doses, any nonsteroidal anti-inflammatory drug use was significantly associated with lower odds of maximal PPI dose (adjusted OR = 0.87, 95% CI = 0.85-0.89), as were aspirin use and older age. Adjusting for medication and demographic factors, odds of being prescribed a maximal PPI dose were significantly higher in 2012 than in 1997 (adjusted OR = 6.30, 95% CI = 5.76-6.88).
CONCLUSIONS
Long-term maximal-dose PPI prescribing is highly prevalent in older adults and is not consistently associated with gastrointestinal bleeding risk factors. Interventions involving prescribers and patients may promote appropriate PPI use, reducing costs and adverse effects of PPI overprescribing.
Additional Info
Characterizing Potentially Inappropriate Prescribing of Proton Pump Inhibitors in Older People in Primary Care in Ireland from 1997 to 2012
J Am Geriatr Soc 2016 Dec 01;64(12)e291-e296, F Moriarty, K Bennett, C Cahir, T FaheyFrom MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
This repeated cross-sectional study evaluated Irish pharmacy claims data of around 130,000 Irish older adults (≥65; 96.5% of Ireland’s older population) for proton pump inhibitor (PPI) prescriptions, every 5 years between 1997 and 2012.1
The use of PPI increased from 10.7% in 1997 to 50.3% in 2007 and 48.4% in 2012. The odds of being prescribed a maximal PPI dose were sixfold higher in 2012 than in 1997 (aOR, 6.30; 95% CI, 5.76–6.88). Long-term prescribing became more common, with the number of those taking a PPI for longer than 8 weeks increasing from 4.1% in 1997 to 35.5% in 2012. Analysis took into consideration ulcerogenic medications (eg, NSAIDS), comorbidities, and duration of high-dose PPI use.
The Beers criteria2 and the European corollary STOPP criteria, lists of medications to avoid or limit in the elderly, recommend no longer than 8 weeks of high-dose PPI for ulcers, gastritis, etc, and a reduction to low dose before stopping altogether. The same criteria also recommend against the use of NSAIDs or cox-2 inhibitors in elderly patients due to vasoconstriction contributing to cardiac and renal problems in addition to GI bleed.
I thought it was an academic medicine phenomenon that resident physicians forget to stop the PPI on discharge that was inappropriately started in the hospital for “GI prophylaxis.”3 But this study shows that, instead, the inappropriate prescribing has increased over time. Over the time of this study, polypharmacy of five or more medications also increased from 17.8% in 1997 to 60.4% in 2012, and those patients taking 10 or more regular medicines increased from 1.5% to 21.9%.4 Despite the increase in obesity and aging that may have contributed to higher arthritis rates and more use of NSAIDs, the incidence of PPI use without concurrent ulcerogenic medications has increased over time from 0.3% in 1997 to 4.7% in 2012. Especially noteworthy is that the number of patients at maximal PPI dose increased 30-fold from 0.8% in 1997 to 23.6% in 2012.
A somewhat surprising finding was that maximal dose use was inversely associated with the concomitant use of NSAIDs. The authors speculate that perhaps prescribing practices affected by history and comorbidities might account for some of this effect.
Hopefully, the slight decrease from 50.3% in 2007 to 48.4% in 2012 is a trend that will continue, given the risk of PPIs. PPIs place patients at higher risk of vitamin B12 and magnesium deficiencies, Clostridium difficile infection, dementia,5,6 cardiac mortality7 due to nitrous oxide depletion, and possibly pneumonia. (The increased rate of pneumonia has recently been put in question in a time sequence analysis.8)
After checking for gastritis, Barrett’s, or ulcers, I stop PPIs on hospital follow-up. In long-term users, I taper before stopping. I generally use antacids for several days to counteract the acid hypersecretion. Patients who have tried and failed antacids, I bridge with sucralfate for 1 week to 1 month, depending on the anxiety level of the patient or the doctor. University of Wisconsin Integrative Medicine Fellowship has helpful patient handouts for GERD and tapering.
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