Summary of findings 3. Summary of findings: Substitutive interventions versus control.
Substitutive interventions compared with control for visual field defects in patients with stroke | ||||
Patient or population: stroke survivors with visual field defects Settings: any rehabilitation setting Intervention: compensative interventions Comparison: control, placebo, or no intervention | ||||
Outcomes | Relative effect (95% CI) | No of Participants (studies) | Quality of the evidence (GRADE) | Comments |
Functional ability in activities of daily living (Barthel Index) After 4 weeks of treatment |
Wearing prisms MD ‐4.00 (‐17.86 to 9.86) (no significant effect) |
39 (1 study, Rossi 1990) |
⊕⊝⊝⊝ very low | Reasons for downgrades:
|
Visual field (change in visual field area & change in error scores, from baseline) After intervention |
Not wearing prisms SMD 0.12 (‐0.46 to 0.70) Wearing prisms SMD 1.12 (0.44 to 1.80) |
85 (2 studies, Rossi 1990; Rowe 2010) |
⊕⊝⊝⊝ very low | Reasons for downgrades:
|
Extended activities of daily living (Change in EADL from baseline; mobility improvement scores, in Logits) After intervention |
Not wearing prisms SMD 0.20 (‐0.44 to 0.85) Wearing prisms SMD 0.24 (‐0.26 to 0.75) |
99 (2 studies, Bowers 2014; Rowe 2010) |
⊕⊝⊝⊝ very low | Reasons for downgrades:
|
Reading ability | Not wearing prisms MD 2.80 (‐7.13 to 12.73) (no significant effect) |
45 (1 study, Rowe 2010) |
⊕⊕⊝⊝ Low | Reasons for downgrades:
|
Falls (number of falls) After intervention |
Wearing prisms OR 1.21, (0.26 to 5.76) (no significant difference) |
39 (1 study, Rossi 1990) |
⊕⊝⊝⊝ very low | Reasons for downgrades:
|
Quality of life (Visual Function Questionnaire (VFQ‐25)) After intervention |
Not wearing prisms MD 8.40 (‐4.18 to 20.98) (no significant effect) |
43 (1 study, Rowe 2010) |
⊕⊕⊝⊝ Low | Reasons for downgrades:
|
Scanning ‐ cancellation (line cancellation errors) After intervention |
Wearing prisms MD 9.80 (1.91 to 17.69) (favours substitutive) |
39 (1 study, Rossi 1990) |
⊕⊝⊝⊝ very low | Reasons for downgrades:
|
Adverse events (number of participants with reported events during intervention period) |
OR 87.32 (4.87 to 1564.66) (favours control) |
59 (1 study, Rowe 2010) |
⊕⊕⊝⊝ Low | Reason for downgrades:
|
GRADE Working Group grades of evidence High quality: Further research is very unlikely to change our confidence in the estimate of effect. Moderate quality: Further research is likely to have an important impact on our confidence in the estimate of effect and may change the estimate. Low quality: Further research is very likely to have an important impact on our confidence in the estimate of effect and is likely to change the estimate. Very low quality: We are very uncertain about the estimate. |
EADL: extended activities of daily living MD: mean difference OR: odds ratio SMD: standardised mean difference VFQ‐25: Visual function questionnaire