No. of studies | utcome measure | Mean score ± SD | Absolute effect (95% CI)† | GRADE quality of evidence | |
---|---|---|---|---|---|
No invitation to screening | Invitation to screening | ||||
Anxiety | |||||
1 RCT18 n = 355 | Spielberger State Anxiety Inventory | 6 wk after last contact‡ | Mean score 3.5 higher (0.22 to 6.78) | Moderate§¶** | |
34.1 ± 12.1 n = 168 | 37.6 ± 12.2 n = 77 | ||||
Anxiety | At 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 mo | Mean 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 mo | Mean 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 Subscale | At 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 mo | Mean 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 mo | Mean 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 Subscale | At 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 mo | Mean 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 mo | Mean 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).