Journal of Clinical Medicine Research, ISSN 1918-3003 print, 1918-3011 online, Open Access
Article copyright, the authors; Journal compilation copyright, J Clin Med Res and Elmer Press Inc
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Original Article

Volume 17, Number 11, November 2025, pages 601-607


Assessment of the Treatment for Alcohol Withdrawal Syndrome With and Without Dexmedetomidine: A Retrospective Cohort Study

Tables

Table 1. Patients Characteristics
 
No dexmedetomidine (n = 371)With dexmedetomidine (n = 623)Total (n = 994)P value
aChi-square P value. bKruskal-Wallis P value. SD: standard deviation; IQR: interquartile range; COPD: chronic obstructive pulmonary disease; CAD: coronary artery disease.
Sex, n (%)
  Female77 (20.8%)125 (20.1%)202 (20.3%)0.7936a
  Male294 (79.2%)498 (79.9%)792 (79.7%)
Race, n (%)
  American Indian or Alaska Native0 (0.0%)1 (0.2%)1 (0.1%)
  Asian4 (1.1%)2 (0.3%)6 (0.6%)
  Black or African American7 (1.9%)18 (2.9%)25 (2.5%)
  Unknown1 (0.3%)4 (0.6%)5 (0.5%)0.3559a
  White359 (96.8%)598 (96.0%)957 (96.3%)
Ethnicity, n (%)
  Hispanic or Latino2 (0.5%)15 (2.4%)17 (1.7%)
  Non-Hispanic or Latino361 (97.3%)597 (95.8%)958 (96.4%)
  Unknown8 (2.2%)11 (1.8%)19 (1.9%)0.0827a
Age at encounter, years
  Mean (SD)52.8 (12.98)54.0 (12.24)53.6 (12.53)
  Median (IQR)54.0 (45.0, 61.0)55.0 (47.0, 62.0)55.0 (46.0, 62.0)0.0833b
  Range18.0, 85.018.0, 88.018.0, 88.0
Phenobarbital (yes = 1, no = 0), n (%)
  No313 (84.4%)476 (76.4%)789 (79.4%)0.0027a
  Yes58 (15.6%)147 (23.6%)205 (20.6%)
Benzodiazepines (yes = 1, no = 0), n (%)
  Yes371 (100.0%)623 (100.0%)994 (100.0%)Not applicable
  No0 (0%)0 (0%)0 (0%)
COPD (yes = 1, no = 0), n (%)
  No285 (76.8%)484 (77.7%)769 (77.4%)
  Yes86 (23.2%)139 (22.3%)225 (22.6%)0.7514a
CAD (yes = 1, no = 0), n (%)
  No314 (84.6%)527 (84.6%)841 (84.6%)0.9847a
  Yes57 (15.4%)96 (15.4%)153 (15.4%)
Asthma (yes = 1, no = 0), n (%)
  No344 (92.7%)572 (91.8%)916 (92.2%)0.6064a
  Yes27 (7.3%)51 (8.2%)78 (7.8%)

 

Table 2. Primary and Secondary Outcomes
 
No dexmedetomidine (n = 371)With dexmedetomidine (n = 623)Total (n = 994)P value
aIndependent sample t-test. bChi-square P value. cUnadjusted for ICU LOS. SD: standard deviation; IQR: interquartile range; ICU: intensive care unit; LOS: length of stay.
Primary outcomes - hospital LOS (days)
  Mean (SD)7.7 (8.32)12.3 (11.29)10.6 (10.51)
  Median (IQR)5.0 (3.0, 9.0)10.0 (6.0, 16.0)8.0 (5.0, 14.0)
  Range0.0, 73.01.0, 203.00.0, 203.0< 0.0001a
Primary outcomes - ICU LOS (days)
  Mean (SD)3.1 (3.77)6.9 (7.44)5.5 (6.59)
  Median (IQR)1.9 (1.0, 3.4)4.9 (2.9, 9.0)3.6 (1.8, 7.1)
  Range0.0, 31.10.1, 122.30.0, 122.3< 0.0001a
Secondary outcomes - lorazepam equivalent (mg)
  Mean (SD)41.19 (82.45)40.8 (59.17)40.95 (68.60)
  Median (IQR)24.8 (42.2)24.8 (42.2)24 (42.87)
  Range0.5, 14100.5692
Secondary outcomes - re-admission in 30 days (n)
  Yes262 (70.6%)475 (76.2%)737 (74.1%)0.0990b, c
  No109 (29.4%)148 (23.8%)257 (25.9%)
Secondary outcomes - re-admission in 60 days (n)
  Yes308 (83.0%)541 (86.8%)849 (85.4%)0.0334b, c
  No63 (17.0%)82 (13.2%)145 (14.6%)
Secondary outcomes - re-admission in 90 days (n)
  Yes314 (84.6%)556 (89.2%)870 (87.5%)0.0426b, c
  No57 (15.4%)67 (10.8%)124 (12.5%)

 

Table 3. Primary Outcomes Adjusted for Age and Dexmedetomidine Use
 
OutcomePredictorB95% CI (B)P valueExp(B)% Change in LOS
ICU: intensive care unit; LOS: length of stay; CI: confidence interval.
Hospital LOSAge (per year)0.0150.012 to 0.018< 0.0011.015+1.5%
Precedex use0.4610.380 to 0.542< 0.0011.586+58.6%
ICU LOSAge (per year)0.0110.008 to 0.014< 0.0011.011+1.1%
Precedex use0.6480.564 to 0.733< 0.0011.912+91.2%