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. 2019 May 20;14(5):e0216994. doi: 10.1371/journal.pone.0216994

Table 1. Demographics for control subjects and patients with SCD with and without chronic pain.

Sickle Cell Disease Control Group Sickle Cell Disease- Pain phenotype
Demographics Overall (n = 22) No chronic pain (n = 10) P-value Chronic pain (n = 15) No chronic pain (n = 7) P-value
Age, years, median (IQR) 28 (25–37) 31 (24–41) 0.7 31.4 (26–43) 24.1 (21–27) 0.002
Gender, n (% female) 13 (59) 5 (50) 0.7 10 (67) 3 (43) 0.4
SCD genotype (n, %)
 HbSS 17 (77) NA NA 10 (67) 7 (100) 0.4
 HbSC 4 (18) 4 (27) 0 (0)
 HbSbthal0 1 (5) 1 (7) 0 (0)
Hydroxyurea use, n (% yes) 8 (36) NA NA 7 (47) 1 (14) 0.2
Baseline Labs, median (IQR)
 WBC (#/ul) 9.1 (5.6–10.9) 6.3 (4.7–8.3) 0.08 9.1 (5.3–10.5) 8.2 (5.7–12.1) 0.9
 Hgb (g/dl) 9.3 (8.5–10.5) 13.8 (11.8–15.8) <0.0001 9.5 (9.1–10.6) 8.5 (8.2–9.1) 0.01
 reticulocyte percent (%) 7.0 (5.5–14.0) 1.5 (1.2–1.8) <0.0001 7.0 (4.8–12.6) 6.9 (5.9–17.6) 0.5
Hospital Utilization (median number over last 3 years)
 Unscheduled Clinic Visit 1.5 (0–8.3) NA NA 1 (0–13) 2 (1–6) 0.8
 ED Visit 3 (1–6.3) NA NA 3 (1–8) 4 (1–5) 0.8
 Inpatient Hospitalization 3 (1.8–6) NA NA 3 (1–6) 3 (2–6) 0.8
Morphine milligram equivalent (mg), median (IQR) 72.3 (50.3–240) NA NA 190.7 (72.3–317.1) 33.7 (6.7–62.1) 0.002