Elderly woman alone in hospice bed

(Photo by Lopolo on Shutterstock)

In A Nutshell

  • Starting benzodiazepines or antipsychotics in hospice was linked to higher 180-day mortality among nursing home residents with dementia.
  • Half the cohort began one of these drugs within a median of 3 days after hospice enrollment.
  • Each additional fill in the first 30 days raised risk further: 15% (benzodiazepines) and 6% (antipsychotics).
  • Prescribing varies widely by agency, and Medicare no longer tracks hospice medication use.

ANN ARBOR, Mich. — Nearly half of nursing home residents with dementia receive benzodiazepines during hospice care, and a new national study reveals these commonly prescribed sedatives are associated with a 41% increased risk of death within six months. Antipsychotics, given to about one in eight patients, showed a 16% increase in mortality risk.

The findings challenge current end-of-life prescribing practices for the 25% of hospice patients who have Alzheimer’s disease and related dementias. Unlike cancer patients, who typically have more predictable disease trajectories, people with dementia often live for months or even years after enrolling in hospice. One in five will outlive the six-month prognosis required for hospice eligibility.

“While these medications may provide symptom relief in appropriate clinical scenarios, their use is associated with substantial risks,” the researchers wrote in JAMA Network Open. The study examined 139,103 Medicare beneficiaries with dementia who enrolled in hospice between 2014 and 2018. Researchers then created carefully matched comparison groups totaling 53,859 participants to isolate the effects of these medications. The authors note the study was not designed to estimate national prevalence.

Hospice providers routinely prescribe benzodiazepines like lorazepam and antipsychotics such as haloperidol to manage agitation, anxiety, and terminal delirium. For dementia patients, these behaviors often distress not just the patient but also family members and nursing staff.

Both medication classes carry documented risks in older adults. Antipsychotics have an FDA boxed warning specifically for increased mortality in dementia patients. Benzodiazepines are linked to respiratory suppression, sedation, falls, and aspiration.

The research team, led by Dr. Lauren Gerlach, a geriatric psychiatrist from the University of Michigan Medical School, used Medicare claims data to track patients who started these medications after hospice enrollment. They compared outcomes to similar patients who didn’t receive the drugs. Most patients began taking benzodiazepines or antipsychotics within three days of entering hospice.

Among those who started benzodiazepines, 73.6% had died by 180 days. Only 58.3% of matched patients who didn’t receive the drugs died in the same timeframe. For antipsychotics, 70.7% of users died compared to 63.3% of nonusers.

The study controlled for age, cognitive function, overall health, functional status, disruptive behaviors, and baseline use of other medications affecting the central nervous system. The link between medication initiation and increased mortality held across multiple statistical approaches.

Woman with sick, dying husband
Researchers say the link to an increased death risk from these medications is a “blind spot” in end-of-life care. (© Photographee.eu – stock.adobe.com)

Prescribing Rates Vary Wildly Between Hospice Facilities

The lack of consistency in prescribing is striking. Previous research has shown benzodiazepine prescribing rates in hospice range from 12% to 80% across different agencies. Antipsychotic rates vary from 6% to 62%. Whether a dementia patient receives these medications appears to depend more on which hospice agency they use than on their actual symptoms or clinical needs.

Hospice clinicians themselves disagree about these medications. In one national survey, 40% of hospice physicians believed benzodiazepines were overused in their facilities. Only 8% of hospice nurses shared that view.

Gerlach and her colleagues argue for national guidelines for hospice prescribing in dementia. Standardized protocols could reduce unwarranted variation and promote safer practices.

Why Dementia Patients Face Unique Challenges in Hospice

Hospice was originally designed around a cancer care model. Cancer patients typically have weeks or a few months to live. Dementia follows a fundamentally different path. The condition involves gradual functional and cognitive decline over an extended, unpredictable timeline. Doctors struggle to determine when someone is truly at the end of life.

People with dementia have the longest hospice stays of all diagnosis groups. In this study, average hospice length of stay exceeded 130 days. For patients who aren’t actively dying, families may prioritize preserving alertness and communication during remaining months. Sedating medications could work against these priorities.

The researchers noted that patients earlier in the hospice trajectory, who may have months to live, face particular risks. Sedating effects may compromise quality of life, impair communication, and interfere with functional independence.

The study found that more frequent prescriptions compounded the mortality risk. The analysis of medication patterns during the first 30 days of hospice showed that each additional benzodiazepine prescription was associated with a 15% higher risk of death by 180 days. Each additional antipsychotic prescription was associated with a 6% higher risk. Patients typically received their last prescription about two weeks before death for benzodiazepines and three weeks before death for antipsychotics.

Medicare No Longer Tracks Hospice Medications

From 2014 to 2018, Medicare briefly required hospice agencies to report medications billed to the hospice benefit. That program has expired. Hospice medication use now goes entirely unmonitored.

The researchers called this a blind spot in oversight of end-of-life care. They urged renewed efforts to track and evaluate medication use in hospice to guide evidence-based practice and protect patient safety.

The study focused on nursing home residents with Medicare fee-for-service coverage. Findings may not apply to all hospice patients. The researchers couldn’t measure actual medication consumption, only prescriptions filled. They also lacked information about symptom severity that might have prompted prescribing decisions.

Roughly 30% of all hospice patients have a dementia diagnosis, even when enrolled for other primary conditions like heart disease or stroke. The researchers included all dementia patients regardless of their primary hospice-qualifying diagnosis. This approach reflects the reality that dementia often coexists with other terminal conditions.


Paper Summary

Methodology

This retrospective case-control study analyzed national Medicare claims and nursing home assessment data from July 2014 through September 2018. Researchers identified long-term nursing home residents with Alzheimer’s disease and related dementias who newly enrolled in hospice and had no benzodiazepine or antipsychotic use in the prior six months. From the initial cohort of 139,103 participants, they created two separate matched cohorts for analysis, one examining benzodiazepine initiation and another for antipsychotic initiation. Patients who started these medications during hospice were matched one-to-one with similar patients who didn’t receive the drugs, based on enrollment timing, age, sex, comorbidity burden, cognitive function, and baseline use of other central nervous system medications. The study followed patients for 180 days from hospice enrollment, tracking all-cause mortality.

Results

The study examined 139,103 participants with a mean age of 87.6 years, of whom 75.8% were female. Among 100,058 residents at risk for benzodiazepine exposure, 47.8% initiated use during hospice. Among 114,933 at risk for antipsychotic exposure, 13.4% initiated use. After matching procedures, the benzodiazepine cohort included 26,872 matched pairs, and the antipsychotic cohort included 10,240 pairs, for a total of 53,859 participants in the matched analysis cohorts. Patients who initiated benzodiazepines had a 41% higher hazard of death at 180 days compared to matched nonusers (hazard ratio 1.41). Those who initiated antipsychotics had a 16% higher hazard of death (hazard ratio 1.16). These associations remained consistent across multiple sensitivity analyses, including propensity score weighting and examination of cumulative exposure through multiple prescription fills. For each additional benzodiazepine prescription fill in the first 30 days, the hazard of 180-day mortality increased by 15% (hazard ratio 1.15), and for antipsychotics, it increased by 6% (hazard ratio 1.06).

Limitations

The study has several limitations. Residual confounding from unmeasured factors like symptom severity is possible despite matching on observable characteristics. Analyses relied on prescription claims, which may not fully capture actual medication use, and hospice claims don’t record days supplied. Findings are limited to Medicare fee-for-service beneficiaries in nursing homes and may not generalize to other populations such as home hospice patients or those in Medicare Advantage plans. The data reflect prescribing practices from 2014 to 2018 and may not capture more recent trends. The study examined all-cause mortality but didn’t measure symptom burden or quality of life, which are meaningful outcomes in end-of-life care.

Funding and Disclosures

This study was supported by grants K23AG066864 and R01AG087073 from the National Institute on Aging. Dr. Donovan Maust reported holding stock in Predictably Human and receiving personal fees from American Society for Addiction Medicine outside the submitted work. No other authors reported conflicts of interest. The funder had no role in study design, conduct, data analysis, manuscript preparation, or publication decisions.

Publication Details

Gerlach LB, Zhang L, Kim HM, Teno J, Maust DT. “Benzodiazepine or Antipsychotic Use and Mortality Risk Among Patients With Dementia in Hospice Care,” was published online October 14, 2025 in JAMA Network Open. doi:10.1001/jamanetworkopen.2025.37551

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