Case Control Study
Copyright ©The Author(s) 2025.
World J Gastroenterol. Mar 28, 2025; 31(12): 99846
Published online Mar 28, 2025. doi: 10.3748/wjg.v31.i12.99846
Table 4 Clinical characteristics and outcomes matched by propensity score, n (%)

Normal LES-IRP group (n = 69)
Increased LES-IRP group (n = 69)
P value
Sex, male/female (n)35/3441/280.305
Age, median (Q1-Q3) (years)45.0 (34.0-55.0)44.0 (35.5-56.0)0.797
BMI, median (Q1-Q3) (kg/m2)21.5 (19.1-23.7)20.9 (19.0-24.1)0.764
Duration of symptoms, median (Q1-Q3) (months)60.0 (24.0-174.0)60.0 (24.0-120.0)0.582
Previous treatment19 (27.5)18 (26.1)0.848
ASA classification0.573
    I68
    II6259
    III12
Ling classification0.145
    Type Ling I6 (8.7)16 (23.2)
    Type Ling IIa21 (30.4)18 (26.1)
    Type Ling IIb17 (24.7)16 (23.2)
    Type Ling IIc21 (30.4)18 (26.1)
    Type Ling III4 (5.8)1 (1.4)
Pre-treatment HRM
    LES basal pressure, median (Q1-Q3) (mmHg)14.8 (12.0-20.3)31.9 (22.5-40.4)0.000
    LES-IRP, median (Q1-Q3) (mmHg)11.4 (9.3-12.5)22.3 (19.0-28.4)0.000
Follow-up period, median (Q1-Q3) (month)25.0 (18.5-54.5)42.0 (28.5-63.5)0.002
Clinical success (Eckardt score ≤ 3)61 (88.4)62 (89.9)0.784
Intraoperative adverse events5 (7.1)8 (11.5)1.000
    Bleeding1 (1.4)1 (1.4)
    Mucosal injury3 (4.3)4 (5.8)
    Gas-related adverse events1 (1.4)3 (4.3)
        Pneumothorax0 (0.0)1 (1.4)
        Pneumoperitoneum1 (1.4)2 (2.9)
Eckardt score, median (Q1-Q3)
    Pre-treatment7.0 (5.0-8.0)7.0 (6.0-9.0)0.021
    Post-treatment1.0 (0.0-2.0)1.0 (1.0-2.0)0.201
    Pre-post change5.0 (4.0-7.0)6.0 (4.0-8.0)0.086
GerdQ score, median (Q1-Q3)6.0 (6.0-7.0)6.0 (6.0-7.0)0.917
GerdQ score ≥ 96 (8.7)7 (10.1)0.771