From acute presentation to post-discharge outcomes: intentional Z-drug versus benzodiazepine overdose in a retrospective cohort

Background Z-drugs are alternatives to benzodiazepines (BZDs) for insomnia, but overdose safety remains uncertain. We compared acute and post-discharge outcomes after intentional Z-drug and BZD overdose. Methods This retrospective cohort included 239 adults (110 Z-drug; 129 BZD) treated at two emergency departments without flumazenil (2018–2024). Models adjusted for age, sex, dose category, intent, and center. Results Compared with BZD overdose, Z-drug overdose was associated with more recorded physical restraint use (adjusted odds ratio [aOR], 6.974; 95% confidence interval [CI], 3.358–14.483), more recorded patient-behavior-related medical interruption events (PB-MIEs; aOR, 5.955; 95% CI, 2.732–12.980), and a longer emergency-department stay (adjusted median difference, 2.516 h; 95% CI, 2.056–2.845), but fewer intensive care unit (ICU) admissions (aOR, 0.092; 95% CI, 0.031–0.272). Among admitted patients, total stay was longer after Z-drug overdose (228 vs 146 h, P < 0.001). The hazard of a first documented anxiety and/or depressive diagnosis was higher after Z-drug overdose (adjusted hazard ratio [aHR], 2.918; 95% CI, 1.928–4.416). Recurrence proportions were similar (25.5% vs 23.3%; log-rank P = 0.426), but timing differed. The recurrence Cox model violated the proportional-hazards assumption; the adjusted HR of 1.266 is descriptive, not a constant relative risk. Among 58 recurrent cases, standard single-dose (SSD) multiples declined and documented intent shifted toward sleep-related dose escalation; this pattern may partly reflect assessment or documentation differences. Conclusion Z-drug overdose was associated with more recorded behavioral-management events and a higher hazard of first documented psychiatric diagnosis, whereas BZD overdose was associated with more severe supportive-care outcomes. Initial care should integrate mental-status and respiratory monitoring with behavioral and self-harm assessment. Follow-up should address insomnia, medication safety, and mental health. Recurrence timing and intent shifts were documented associations, not causal effects.

Authors

Institutions

Publication Details

Journal
Frontiers in Psychiatry
Published
2026-11-09
DOI
https://doi.org/10.3389/fpsyt.2026.1991713
Primary Topic
Poisoning and overdose treatments
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
NOV
article

From acute presentation to post-discharge outcomes: intentional Z-drug versus benzodiazepine overdose in a retrospective cohort

黄蓓蓓, Chao Wu, Donglin Zhu, QinQin Liu et al.
Frontiers in Psychiatry
Poisoning and overdose treatments
article

From acute presentation to post-discharge outcomes: intentional Z-drug versus benzodiazepine overdose in a retrospective cohort

黄蓓蓓, Chao Wu, Donglin Zhu, QinQin Liu, 孙铭, Yao Tan, Liang Gu, Jie Lu
article en

Abstract

Background Z-drugs are alternatives to benzodiazepines (BZDs) for insomnia, but overdose safety remains uncertain. We compared acute and post-discharge outcomes after intentional Z-drug and BZD overdose. Methods This retrospective cohort included 239 adults (110 Z-drug; 129 BZD) treated at two emergency departments without flumazenil (2018–2024). Models adjusted for age, sex, dose category, intent, and center. Results Compared with BZD overdose, Z-drug overdose was associated with more recorded physical restraint use (adjusted odds ratio [aOR], 6.974; 95% confidence interval [CI], 3.358–14.483), more recorded patient-behavior-related medical interruption events (PB-MIEs; aOR, 5.955; 95% CI, 2.732–12.980), and a longer emergency-department stay (adjusted median difference, 2.516 h; 95% CI, 2.056–2.845), but fewer intensive care unit (ICU) admissions (aOR, 0.092; 95% CI, 0.031–0.272). Among admitted patients, total stay was longer after Z-drug overdose (228 vs 146 h, P < 0.001). The hazard of a first documented anxiety and/or depressive diagnosis was higher after Z-drug overdose (adjusted hazard ratio [aHR], 2.918; 95% CI, 1.928–4.416). Recurrence proportions were similar (25.5% vs 23.3%; log-rank P = 0.426), but timing differed. The recurrence Cox model violated the proportional-hazards assumption; the adjusted HR of 1.266 is descriptive, not a constant relative risk. Among 58 recurrent cases, standard single-dose (SSD) multiples declined and documented intent shifted toward sleep-related dose escalation; this pattern may partly reflect assessment or documentation differences. Conclusion Z-drug overdose was associated with more recorded behavioral-management events and a higher hazard of first documented psychiatric diagnosis, whereas BZD overdose was associated with more severe supportive-care outcomes. Initial care should integrate mental-status and respiratory monitoring with behavioral and self-harm assessment. Follow-up should address insomnia, medication safety, and mental health. Recurrence timing and intent shifts were documented associations, not causal effects.

Frontiers in PsychiatryVol. 17
Xuzhou Medical College (CN), Nanjing Brain Hospital (CN), Nanjing Drum Tower Hospital (CN), Yangzhou University (CN), Nanjing Medical University (CN), Nanjing University (CN)
Poisoning and overdose treatments
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Laika access coming soon