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Table 1 Efficacy (% resolution of incontinence) and discontinuation data included into the economic model

From: Cost-effectiveness analysis of antimuscarinics in the treatment of patients with overactive bladder in Spain: A decision-tree model

% Resolution of incontinence (<1 episode/24 hrs)

W2

W8

W12

W12|W8

W12|~W8

Placebo

20,99%

34,66%

27,84%

80,33%

14,16%

Fesoterodine 4 mg

30,41%

50,00%

43,67%

87,34%

21,05%

Fesoterodine 8 mg

40,59%a

55,38%a

50,21%

90,65%

24,20%

Tolterodine

29,23%

49,47%

38,18%

77,17%

13,04%

Solifenacin 5 mgc

31,49%

51,99%

41,76%

80,33%d

21,24%

Solifenacin 10 mge

32,11%a

53,01%a

42,58%

80,33%d

21,66%b

Other data

% Nocturia (> = 2 episodes/night) % of patients with nocturia at baseline without nocturia at W12

Constipation

Placebo

54,34%

1,99%

Fesoterodine 4 mg

55,56%

4,15%

Fesoterodine 8 mg

55,90%

6,01%

Tolterodine

57,69%

2,76%

Solifenacin 5 mg

54,34%i

3,53%j

Solifenacin 10 mg

88,72%j

7,72%j

Discontinuation

W2

W8

W12

W24 f

W52 f

Placebo

100%

92,84%

90,64%

79,32%

59,27%

Fesoterodine 4 mg

100%

92,67%g

equal to placebo data h

Fesoterodine 8 mg

--

--

equal to placebo data h

Tolterodine

100%

95,76%

equal to placebo data h

Solifenacin 5 mg

100%

94,06%

equal to placebo data h

Solifenacin 10 mg

--

--

equal to placebo data h

  1. The symbol "|" denotes conditional response rates; the response at week 12 given response at week 8. The symbol "~" denotes non-response; no-response at week 12 given no-response at week 8
  2. Source: Fesoterodine phase III trials, except when a different source is described [17, 18].
  3. a - values not used in the decision tree; only used to calculate conditional response rates
  4. b - conditional response rates estimated by applying the W8 low dose: high dose response ratio to the W12|~W2(~W8) non-titrating response rate
  5. c - equal to 1,5 times the placebo rates [29]
  6. d - conditional response equal to placebo rate
  7. e - equal to 1,5294 times the placebo rates [29]
  8. f - W24 and W52 values were extrapolated from clinical trial data using an exponential decay curve fitted to W2, W8, and W12 discontinuation values
  9. g - discontinuation rate of fesoterodine 4 mg at W8 in the trial data was greater than that of placebo at W12, therefore this value was set equal to the W12 rate.
  10. h - discontinuation rates at week 12 were found to be not statistically significant for any treatment [30], therefore the values are equal to placebo discontinuation
  11. i - relative rates from published literature [42]; solifenacin 5 mg not found to be significantly different than placebo; solifenacin 10 mg 63.28% higher than placebo
  12. j - relative rates from published literature [29]; solifenacin 5 mg 1,778 times placebo; solifenacin 10 mg 3,889 times higher than placebo