
For an adult 65 or older taking a benzodiazepine or Z-drug for insomnia, the 2018 deprescribing.org guideline strongly recommends a slow, collaborative taper, for example about 25 percent every 2 weeks with 12.5 percent steps or drug-free days near the end, combined with CBT-I and follow-up every 1 to 2 weeks. For an adult whose GERD or esophagitis symptoms have resolved after at least 4 weeks of a PPI, the 2017 guideline recommends lowering the dose or stopping and using the PPI on demand, with review at 4 and 12 weeks; Barrett esophagus, severe esophagitis, a bleeding ulcer history and high-risk NSAID use are reasons to continue.
Benzodiazepine receptor agonists (benzodiazepines and the Z-drugs) and proton pump inhibitors are the two drug classes most often deprescribed in older adults, and the deprescribing.org guidelines give each a clear pathway. For a benzodiazepine or Z-drug taken for insomnia by an adult 65 or older, recommend a slow taper regardless of how long it has been used: about 25 percent of the dose every 2 weeks, 12.5 percent steps or planned drug-free days near the end, CBT-I alongside, and contact every 1 to 2 weeks. For a PPI whose indication has run its course, lower the dose or stop it and use it on demand, then check for returning symptoms at 4 and 12 weeks.
The 2023 Beers Criteria list all benzodiazepines and the nonbenzodiazepine hypnotics (zolpidem, eszopiclone, zaleplon) to avoid in older adults because of cognitive impairment, delirium, falls, fractures and motor vehicle crashes, with little lasting gain in sleep. The deprescribing.org guideline adds physical dependence, memory disorder, functional impairment and daytime sedation, and notes that sleep benefits wane after about 4 weeks while the harms continue and grow with age.
PPIs are on the Beers list to avoid beyond 8 weeks unless the patient is high risk (oral corticosteroids or chronic NSAID use), has erosive esophagitis, Barrett esophagus or a hypersecretory condition, or has shown a need for maintenance. The PPI algorithm lists the associated harms as fractures, C. difficile infection and diarrhea, community-acquired pneumonia, vitamin B12 deficiency and hypomagnesemia. Many older adults remain on a PPI started for a short-term indication, such as hospital stress-ulcer prophylaxis, that no one revisited.
The 2018 guideline applies to adults taking a BZRA for insomnia on its own, or for insomnia whose underlying comorbidities are managed.
| Population | Recommendation | Strength |
|---|---|---|
| 65 and older, taking a BZRA for insomnia for any duration | Taper slowly, then stop | Strong (GRADE) |
| 18 to 64, taking a BZRA for insomnia for more than 4 weeks | Taper slowly, then stop | Weak (GRADE) |
| Other sleep disorder (for example restless legs), unmanaged anxiety or depression, a benzodiazepine effective specifically for anxiety, alcohol withdrawal | Outside the algorithm; treat the condition and individualize | Not covered |
If the indication is unclear, find out whether there is a history of anxiety, a past psychiatric consultation, or whether the drug was started in hospital for sleep or during a grief reaction.
Explain the reason (the risks of continued use and the loss of effect over time), what withdrawal feels like and that it is usually mild and short, and that the patient controls the pace. The algorithm lists the expected benefits of stopping: better alertness and cognition, less daytime sedation and fewer falls.
The algorithm suggests reducing by about 25 percent every 2 weeks and, if possible, using 12.5 percent reductions near the end or planned drug-free days. Reductions are calculated from the starting dose, so the steps stay equal.
| Weeks | Nightly dose as a share of the starting dose |
|---|---|
| 0 to 2 | 75 percent |
| 2 to 4 | 50 percent |
| 4 to 6 | 25 percent |
| 6 to 8 | 12.5 percent, or 25 percent on alternate nights (planned drug-free days) |
| After week 8 | Stop |
Practical rules from the algorithm:
The 2025 Joint Clinical Practice Guideline on Benzodiazepine Tapering, led by the American Society of Addiction Medicine, addresses long-term users and those with physical dependence more broadly. It calls for an individualized taper, commonly starting with reductions of 5 to 10 percent every 2 to 4 weeks and generally not exceeding 25 percent every 2 weeks, slowed further when withdrawal is significant, and it warns that some tapers take months or longer. For an older adult on a long-standing, higher dose, the slower schedule is the safer default.
For patients 65 and older, monitor every 1 to 2 weeks for the duration of the taper. Withdrawal symptoms are insomnia, anxiety, irritability, sweating and gastrointestinal upset, usually mild and lasting days to a few weeks. Ask about sleep with a sleep diary, daytime function, falls, mood and any substitution with alcohol or over-the-counter sedating antihistamines such as diphenhydramine, which the Beers Criteria also list to avoid.
CBT-I is the treatment that replaces the hypnotic. It usually involves 5 to 6 sessions covering sleep education, stimulus control, sleep restriction, sleep hygiene and relaxation, and it produces sustained benefits; combined with tapering, it improves the chance of stopping. Psychologists usually deliver it, but trained clinicians and self-help programs can provide parts of it. Behavioral advice for primary care:
In long-term care, the algorithm adds daytime light exposure, more daytime activity, short naps only before 2 pm, toileting before bed, minimal alarm noise and avoiding waking residents for care at night.
Consult psychiatry, addiction medicine or a sleep specialist when the patient has a substance use disorder, concurrent opioid use, a history of withdrawal seizures or delirium, a benzodiazepine prescribed for a psychiatric disorder, suspected sleep apnea or restless legs, or repeated failed tapers.
The algorithm sorts patients by why they take the PPI.
| Indication | Action |
|---|---|
| Mild to moderate esophagitis or GERD treated 4 to 8 weeks, esophagitis healed and symptoms controlled | Deprescribe (strong recommendation) |
| Peptic ulcer disease treated 2 to 12 weeks (NSAID-related or H. pylori) | Deprescribe |
| Upper GI symptoms without endoscopy, asymptomatic for 3 consecutive days | Deprescribe |
| ICU stress ulcer prophylaxis continued beyond the ICU admission | Stop |
| Uncomplicated H. pylori treated for 2 weeks and asymptomatic | Stop |
| Barrett esophagus, severe esophagitis, documented history of bleeding GI ulcer, chronic NSAID use with bleeding risk | Continue the PPI, or consult gastroenterology if considering deprescribing |
| Indication unknown | Ask about past endoscopy, hospitalization for a bleeding ulcer, past chronic NSAID use, prior heartburn or dyspepsia |
Lower the dose, for example from twice daily to once daily, halving the dose, or taking it every second day; the evidence suggests no increased risk of symptom return compared with continuing the higher dose. Or stop and use the PPI on demand: take it daily until symptoms resolve, then stop until they recur; about 1 in 10 patients may have symptoms return. The algorithm treats these as equally recommended, strong options and states that no tapering approach has been shown better than another, so choose what is most convenient and acceptable to the patient.
Standard and low daily doses from the algorithm:
| PPI | Standard (healing) dose, once daily | Low (maintenance) dose, once daily |
|---|---|---|
| Omeprazole | 20 mg | 10 mg |
| Esomeprazole | 20 or 40 mg | 20 mg |
| Lansoprazole | 30 mg | 15 mg |
| Dexlansoprazole | 30 or 60 mg | 30 mg |
| Pantoprazole | 40 mg | 20 mg |
| Rabeprazole | 20 mg | 10 mg |
Review at 4 and 12 weeks. In patients who can describe symptoms, ask about heartburn, regurgitation, dyspepsia and epigastric pain; in patients who cannot (advanced dementia), watch for loss of appetite, agitation and weight loss.
If symptoms return:
Alarm features such as GI bleeding, anemia, dysphagia, persistent vomiting or unintended weight loss are not rebound; they need prompt evaluation and gastroenterology referral.
A 78-year-old man presents for a medication review with his wife. He has taken temazepam 30 mg nightly for 9 years, started during a hospital stay, and omeprazole 20 mg daily for 4 years, started for heartburn that resolved within the first months; he has never had endoscopy, GI bleeding or regular NSAID use. He has no anxiety disorder, depression screen is negative, and his wife reports no snoring or witnessed apneas. He had one fall last winter and describes morning grogginess. He is interested in reducing his medications. Which of the following is the most appropriate plan?
Answer: C. He is over 65 and takes a BZRA for insomnia, so the guideline strongly recommends a slow, collaborative taper with behavioral therapy and close follow-up, and his fall and morning grogginess are the harms the taper addresses. His PPI was started for symptoms that resolved, with no Barrett esophagus, severe esophagitis, bleeding history or NSAID risk, so lowering the dose or using it on demand is appropriate, with review at 4 and 12 weeks. Option A stops a 9-year benzodiazepine abruptly, risking significant withdrawal, and substitutes a sedating drug without addressing the insomnia behaviorally. Option B uses a conversion that is not shown to reduce withdrawal and a 2-week taper that is far too fast, and it keeps a PPI without an indication. Option D ignores a fall and daytime sedation in a patient on two drugs listed in the Beers Criteria.
Common follow-up questions on Geriatrics & Prescribing (AGNP).
Not after regular use. Abrupt discontinuation in a physically dependent patient can cause severe withdrawal, including seizures, so the guidelines call for a gradual taper that the patient helps control. A short course of a few days is the exception.
Not routinely. The deprescribing.org algorithm notes that no published evidence shows switching to a long-acting agent reduces withdrawal or works better than tapering the short-acting drug. If tablet strengths do not allow 25 percent steps, it suggests drug-free days late in the taper or switching to lorazepam or oxazepam for the final steps.
The 2017 guideline found no evidence that one tapering approach is better than another. Lowering the dose (for example from twice daily to once daily, halving the dose, or every second day) and stopping with on-demand use are equally reasonable options; choose the one the patient finds most acceptable.
Use non-drug measures and manage occasional symptoms with an antacid, alginate, H2 receptor antagonist or an as-needed PPI. If symptoms persist for 3 to 7 days and interfere with normal activity, test and treat for H. pylori and consider returning to the previous dose; alarm features need endoscopic evaluation.
FNP and AGNP board questions written as primary-care cases, with guideline-based explanations, for the AANP and ANCC exams. Create a free account and pick your track.
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