Table 5

Change in VKA control measures reported in studies published between 2000–2003 and 2004–2013

VariableStudies published in 2000–2003 (N=23)
n (%)
Studies published in 2004–2013 (N=125)
n (%)
p Value*
Number of measures reported (mean±SD)1.48±0.792.23±1.430.02
 115 (65.2)51 (40.8)
 26 (26.1)35 (28.0)
 31 (4.3)15 (12.0)
 41 (4.3)12 (9.6)
 508 (6.4)
 603 (2.4)
 701 (0.8)
≥28 (34.8)74 (59.2)0.05
Percentage of time in range (INR=2–3)15 (65.2)102 (81.6)0.14
Proportion of INR tests in range (INR=2–3)4 (17.4)20 (16.0)0.89
Mean/median INR7 (30.4)31 (24.8)0.76
Mean/median VKA dose1 (4.3)16 (12.8)0.42
Frequency of INR monitoring2 (8.7)36 (28.8)0.08
INR variability08 (6.4)0.46
INR testing interval4 (17.4)26 (20.8)0.98
Proportion of patients in/out of range†1 (4.3)28 (22.4)0.09
Other‡012 (9.6)0.26
  • *p Value for the comparison of studies published in 2000–2003 vs 2004–2013.

  • † For example, point prevalence, proportion of patients in range >50% of time or proportion of patients with ≥50% of INR measures <3.0.

  • ‡Other measures include: number of dosage changes; INR measure after a previously subtherapeutic or supratherapeutic INR; proportion of patients with ≥1INR measure below range after reaching an adequate INR; number of days until the next INR measure after an extreme measure; proportion of days with treatment stability (two consecutive INR measures in range); days to reach a therapeutic INR; mean time until stable (6 months within target INR range); minimum and maximum INR values per patient.

  • INR, international normalised ratio; VKA, vitamin K antagonist.