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. 2023 Aug 11;12(16):5229. doi: 10.3390/jcm12165229

Table 5.

Associations with a change in D-dimer from before to after ESD in the subgroup analysis of midazolam users.

Change in D-Dimer from before to after ESD
<1.0 (n = 83) ≥1.0 (n = 20) Univariate OR 95%CI Multivariate
Sex (male/female) 57/26 17/3 0.177
Age (years) 68.7 ± 12.07 74.4 ± 7.23 0.034 a 1.1 0.87–1.00 0.098
Pathological examination (cancerous/non-cancerous) 64/19 18/2 0.233
ESD site (upper/lower) 47/36 17/3 0.011 a 1.2 0.25–6.71 0.818
Maximum diameter of resected sample (mm) 31 ± 14.8 36 ± 14.4 0.104
WBC the day after ESD (109/L) 7.9 ± 2.4 7.4 ± 2.5 0.364
CRP the day after ESD (mg/dL) 0.6 ± 0.9 1.2 ±1.5 0.068
Thrombosis (n) 18 3 0.391
Hypertension (n) 43 11 1.000
Hyperlipidemia (n) 23 4 0.423
Diabetes mellitus (n) 17 7 0.246
Dialysis (n) 1 1 0.335
Antiplatelet drug use (n) 9 3 1.000
Anticoagulant use (n) 8 0 0.206
Procedure duration (min) 113.3 ± 65.0 147.6 ± 65.9 0.028 a 1.0 0.99–1.00 0.202
Corrected midazolam doses 2.3 ± 1.3 3.9 ± 1.8 <0.001 a 1.5 0.43–0.95 0.030 a
Total pentazocine Hydrochloride dose (mg) 7.9 ± 8.2 1.1 ± 5.0 <0.001 a
Total pethidine Hydrochloride dose (mg) 20.5 ± 25.5 45.5 ± 25.0 <0.001 a 1.0 0.95–1.00 0.076
Total haloperidol dose (mg) 1.1 ± 2.2 2.6 ± 3.3 0.011 a 1.0 0.77–1.28 0.959

Continuous value variables are described as mean ± standard deviation. WBC, white blood cell count; ESD, Endoscopic submucosal dissection; CRP, C-reactive protein. a: p < 0.05.