Table 1:

Summary of evidence of harms associated with screening for type 2 diabetes*

No. of studiesutcome measureMean score ± SDAbsolute effect (95% CI)GRADE quality of evidence
No invitation to screeningInvitation to screening
Anxiety
1 RCT18
n = 355
Spielberger State
Anxiety Inventory
6 wk after last contactMean score 3.5
higher (0.22 to 6.78)
Moderate§**
34.1 ± 12.1
n = 168
37.6 ± 12.2
n = 77
AnxietyAt baseline††Mean score 0.53
lower (−2.60 to 1.54)
Low**‡‡§§
1 RCT19
n = 7380
Spielberger State
Anxiety Inventory
32.7 ± 11.5
n = 199
32.7 ± 11.6
n = 2 468
At 3–6 moMean score 1.51
higher (−0.17 to 3.20)
31.8 ± 11.4
n = 358
33.5 ± 12.0
n = 2 504
At 12–15 moMean score 0.57
higher (−1.11 to 2.24)
32.8 ± 11.8
n = 304
35.5 ± 12.2
n = 2 377
Hospital Anxiety and Depression Scale: Anxiety SubscaleAt baseline††Mean score 0.46
lower (−0.99 to 0.07)
Low§**‡‡§§
6.42 ± 4.39
n = 255
6.04 ± 3.79
n = 3 140
At 3–6 moMean score 0.12
lower (−0.55 to 0.32)
5.97 ± 3.86
n = 442
5.91 ± 3.89
n = 3 159
At 12–15 moMean score 0.01
lower (−0.47 to 0.45)
5.81 ± 3.87
n = 377
5.85 ± 3.87
n = 3 034
Depression
Hospital Anxiety and Depression Scale: Depression SubscaleAt baseline††Mean score 0.37
lower (−0.93 to 0.18)
Low**‡‡§§
4.52 ± 3.48
n = 256
4.24 ± 3.31
n = 3 161
At 3–6 moMean score 0.01
higher (−0.51 to 0.54)
4.18 ± 3.38
n = 444
4.24 ± 3.40
n = 3 177
At 12–15 moMean score 0.22
higher (−0.31 to 0.74)
4.03 ± 3.35
n = 378
4.28 ± 3.40
n = 3 049
  • Note: CI = confidence interval, RCT = randomized controlled trial, SD = standard deviation.

  • * ur systematic review of harms associated with screening for type 2 diabetes in adults of any age identified 2 RCTs.

  • Eborall et al.19 used adjusted mean differences for age and comorbidity (use of antihypertensives) to compute absolute effect.

  • Questionnaire was sent 6 weeks after last contact (either test or invitation).

  • § Unclear allocation concealment.

  • No information regarding blinding.

  • ** Quality rating is for a single study; thus, imprecision and publication bias criteria were rated as “no” and “unlikely.”

  • †† Questionnaire was given immediately after the initial blood test for those who attended screening, or after first contact for controls; data for those who attended screening were included in the analysis only if the questionnaire was completed and returned before the results of the test were received.

  • ‡‡ A nonrandomized sample of screening practices was used.

  • §§ Large loss to follow-up (for the follow-up periods 3–6 and 12–15 mo).