Table 2

Associations of elevated frailty risk groups with adverse clinical outcomes the low frailty risk group

OutcomeOverall, n (%)Low risk, n (%)Intermediate risk, n (%)High risk, n (%)P valueIntermediate risk, OR (95% CI), P valueHigh risk, OR (95% CI), P value
UnadjustedFully adjustedUnadjustedFully adjusted
 All-cause 30-day mortality524 (10.7%)221 (7.1%)267 (16.2%)36 (25.2%)<0.0012.53 (2.09 to 3.06), p<0.0012.65 (2.17 to 3.25), p<0.0014.4 (2.94 to 6.57), p<0.0014.83 (3.17 to 7.37), p<0.001
 Length of stay, median (IQR)*5 (2, 9)4 (2, 7)7 (4, 12)11.5 (7, 18)<0.0013.74 (3.34 to 4.14), p<0.0013.77 (3.39 to 4.15), p<0.00110.04 (8.92 to 11.16), p<0.00110.07 (9.02 to 11.13), p<0.001
 Long hospital stay >10 days1010 (20.4%)386 (12.3%)543 (32.7%)81 (56.2%)<0.0013.47 (2.99 to 4.02), p<0.0013.66 (3.14 to 4.28), p<0.0019.21 (6.51 to 13.01), p<0.0019.75 (6.83 to 13.92), p<0.001
 30-day readmission586 (11.8%)372 (11.8%)195 (11.7%)19 (13.2%)0.871.04 (0.88 to 1.24), p=0.6431.04 (0.87 to 1.24), p=0.691.47 (0.95 to 2.26), p=0.0811.67 (1.08 to 2.59), p=0.022
Functional impairment, n (%)
 Barthel Index, median (IQR)*95 (70, 100)100 (85, 100)80 (55, 100)50 (20, 75)<0.001−15.76 (-17.87 to −13.64), p<0.001−14.59 (-16.69 to −12.48), p<0.001−40.55 (-47.01 to −34.09), p<0.001−39.7 (-46.06 to −33.33), p<0.001
 Barthel Index <95 points1052 (46.5%)529 (36.3%)472 (62.9%)51 (92.7%)<0.0012.98 (2.48 to 3.58), p<0.0012.87 (2.37 to 3.47), p<0.00122.37 (8.04 to 62.23), p<0.00125.03 (8.91 to 70.32), p<0.001
Quality of life, n(%)
 Impairment of mobility408 (18.0%)162 (11.1%)217 (28.9%)29 (51.8%)<0.0013.25 (2.59 to 4.08), Pp<0.0013.1 (2.46 to 3.92), p<0.0018.61 (4.97 to 14.91), p<0.0018.45 (4.82 to 14.81), p<0.001
 Impairment of self-care1010 (44.5%)480 (32.9%)484 (64.4%)46 (82.1%)<0.0013.69 (3.07 to 4.44), p<0.0013.63 (2.99 to 4.4), p<0.0019.40 (4.7 to 18.79), p<0.0019.59 (4.74 to 19.41), p<0.001
 Impairment of usual activities1366 (60.2%)767 (52.5%)553 (73.5%)46 (82.1%)<0.0012.51 (2.08 to 3.05), p<0.0012.35 (1.92 to 2.87), p<0.0014.16 (2.08 to 8.31), p<0.0013.98 (1.97 to 8.06), p<0.001
 Pain/discomfort910 (42.7%)574 (40.8%)314 (46.3%)22 (48.9%)0.0391.25 (1.04 to 1.51), p=0.0171.21 (1 to 1.47), p=0.0471.39 (0.77 to 2.52), p=0.2781.28 (0.7 to 2.33), p=0.43
 Anxiety/depression629 (30.3%)394 (28.2%)213 (33.2%)22 (56.4%)<0.0011.26 (1.03 to 1.55), p=0.0231.26 (1.02 to 1.55), p=0.0293.29 (1.73 to 6.26), p<0.0013.11 (1.62 to 5.99), p=0.001
 EQ-VAS, mean (SD)*70.8 (18.3)72.1 (17.9)68.2 (19.0)61.8 (17.6)<0.001−3.9 (-5.83 to −1.97), p<0.001−3.75 (-5.69 to −1.81), p<0.001−10.3 (-17.53 to −3.08), p=0.005−11.12 (-18.29 to −3.94), p=0.002
Discharge other than home1092 (22.0%)504 (16.0%)530 (31.9%)58 (40.3%)<0.0012.46 (2.13 to 2.83), p<0.0012.53 (2.18 to 2.92), p<0.0013.54 (2.5 to 5.01), p<0.0013.81 (2.68 to 5.42), p<0.001
  • Quality of life measures were adapted from EQ-5D. We dichotomised levels into ‘no impairment’ (level 1) and ‘impairment’ (levels 2 and 3). Frequencies of reported impairment (levels 2 and 3) were analysed.

  • The fully adjusted model was adjusted for age, gender and comorbidities not included in the score.

  • *Linear regression analyses were calculated reporting regression coefficient, 95% CI, p value.

  • EQ-VAS, EuroQol visual analogue health scale.