| Literature DB >> 27017344 |
Katie A Peterson1, George Savulich2, Dan Jackson3, Clare Killikelly2, John D Pickard4, Barbara J Sahakian2,5.
Abstract
We conducted a systematic review of the literature and used meta-analytic techniques to evaluate the impact of shunt surgery on neuropsychological performance in patients with normal pressure hydrocephalus (NPH). Twenty-three studies with 1059 patients were identified for review using PubMed, Web of Science, Google scholar and manual searching. Inclusion criteria were prospective, within-subject investigations of cognitive outcome using neuropsychological assessment before and after shunt surgery in patients with NPH. There were statistically significant effects of shunt surgery on cognition (Mini-Mental State Examination; MMSE), learning and memory (Rey Auditory Verbal Learning Test; RAVLT, total and delayed subtests), executive function (backwards digit span, phonemic verbal fluency, trail making test B) and psychomotor speed (trail making test A) all in the direction of improvement following shunt surgery, but with considerable heterogeneity across all measures. A more detailed examination of the data suggested robust evidence for improved MMSE, RAVLT total, RAVLT delayed, phonemic verbal fluency and trail making test A only. Meta-regressions revealed no statistically significant effect of age, sex or follow-up interval on improvement in the MMSE. Our results suggest that shunt surgery is most sensitive for improving global cognition, learning and memory and psychomotor speed in patients with NPH.Entities:
Keywords: Cognition; Neuropsychological tests; Neuropsychology; Normal pressure hydrocephalus; Shunt surgery
Mesh:
Year: 2016 PMID: 27017344 PMCID: PMC4971036 DOI: 10.1007/s00415-016-8097-0
Source DB: PubMed Journal: J Neurol ISSN: 0340-5354 Impact factor: 4.849
Characteristics of the studies included in meta-analyses
| Study | Patient | Patient selection | Age of patients mean (SD) years | Follow-up interval | % males |
|---|---|---|---|---|---|
| Andrén et al. [ | 69c | Patients with idiopathic NPH | 70 (48–84)a | 3 months | 54 |
| Duinkerke et al. [ | 10 | Patients with idiopathic NPH who showed improvement in at least one clinical symptom with temporary lumbar drainage | 70.9 (10.26) | 6–12 months | 40 |
| Foss et al. [ | 27 | Patients with idiopathic NPH | 72 (46–81)a | 6–9 months | 29.6 |
| Gleichgerrcht et al. [ | 10 | Patients with idiopathic NPH who showed clinical response to continuous CSF drainage | 69.4 (9.3) | 6–8 months | 70 |
| Hellström et al. [ | 47 | Patients with idiopathic NPH | 73 (24–84)a | 3 months | 47 |
| Hellström et al. [ | 142 | Patients with idiopathic NPH | 72.5 (30–87)a | 3 months | 51 |
| Hiraoka et al. [ | 11 | Patients with idiopathic NPH | 77.9 (4.1) | 3 months | 40 |
| Iddon et al. [ | 11 | Patients with idiopathic NPH | 69.64 (6.14) | 6 months | 72.7 |
| Katzen et al. [ | 12 | Patients with idiopathic NPH | 74.92 (7.72) | 6 months | 33.3 |
| Kazui et al. [ | 49c | Patients with idiopathic NPH | 76.4 (4.4) | 3 months | 41 |
| Lundin et al. [ | 35 | Patients with idiopathic NPH | 73 (49–81)b | 3 months | 45.7 |
| Mataró et al. [ | 8 | Patients with idiopathic NPH | 73.4 (6.8) | 6 months | 50 |
| Mataró et al. [ | 18 | Patients with idiopathic NPH | 74.56 (7.06) | 6 months | 50 |
| Moriya et al. [ | 32 | Patients with idiopathic NPH | 73.7 (6.8) | 12 months | 71.9 |
| Peterson et al. [ | 22 | Patients with NPH | 68.3 (10.8) | 3–9 months | 63.6 |
| Poca et al. [ | 43 | Patients with idiopathic NPH | 71.1 (6.9) | 6 months | 69.8 |
| Saito et al. [ | 32 | Patients with idiopathic NPH who showed ≥ 1 point reduction on the total iNPH Grading Scale following shunt surgery | 75.7 (4.5) | 12 months | 50 |
| Savolainen et al. [ | 51 | Patients with idiopathic NPH | 67.5 | 3–12 months | 52.9 |
| Solana et al. [ | 185 | Patients with idiopathic NPH | 73.96 (6.3) | 6 months | 60 |
| Stambrook et al. [ | 14 | Patients with NPH | 66.0 (14.16) | Mean = 23.73 weeks | 64.3 |
| Thomas et al. [ | 42 | Patients with idiopathic NPH | 73 (10) | 3–9 months | 45.2 |
| Virhammar et al. [ | 173 | Patients with idiopathic NPH | 74 (54–88)a | 12 months | 53 |
| Yamamoto et al. [ | 16 | Patients with idiopathic NPH | 75.8 (4.9) | 3 months | 50 |
CSF cerebrospinal fluid, NPH normal pressure hydrocephalus
aMedian (range)
bMean (range)
cTreatment-as-normal group
Fig. 1PRISMA flow chart for review
Meta-analyses results
| Cognitive domain | Test |
| Estimated average pre-shunt score | 95 % CI | Estimated average difference | 95 % CI |
| Cochran’s |
| Estimated between-study variance |
|---|---|---|---|---|---|---|---|---|---|---|
| Global function | MMSE | 19 | 23.10 points | 22.13, 24.08 | 2.20 points | 1.45, 2.95 | <0.001 | 99.62 (18; <0.001) | 81.9 | 1.99 |
| Learning and memory | RAVLT total | 7 | 22.73 words | 19.86, 25.61 | 5.64 words | 3.86, 7.43 | <0.001 | 14.02 (6; 0.03) | 57.2 | 2.68 |
| RAVLT delayed | 7 | 1.90 words | 1.22, 2.57 | 1.43 words | 0.55, 2.31 | 0.001 | 56.33(6; <0.001) | 89.3 | 1.11 | |
| Executive function | Backwards digit span | 6 | 2.92 digits | 2.38, 3.46 | 0.36 digits | 0.04, 0.67 | 0.03 | 38.61 (5; <0.001) | 87.0 | 0.12 |
| Phonemic verbal fluency | 8 | 19.67 words | 13.60, 25.74 | 2.73 words | 0.84, 4.63 | 0.005 | 10.55 (7; 0.16) | 33.6 | 2.32 | |
| TMT-B | 9 | 293.03 s | 221.09, 364.97 | −43.46 s | −83.23, −3.70 | 0.03 | 35.89 (8; <0.001) | 77.7 | 2494.80 | |
| Psychomotor speed | TMT-A | 13 | 132.48 s | 108.48, 156.49 | −25.90 s | −36.11, −15.69 | <0.001 | 18.78 (12; 0.09) | 36.1 | 104.03 |
MMSE Mini-Mental State Examination, RAVLT Rey Auditory Verbal Learning Test, TMT trail making test
Meta-regressions of average difference of MMSE on moderator variables
| Covariate | Estimate | Standard error |
| 95 % CI |
|---|---|---|---|---|
| Time-to-retest (months) | 0.01 | 0.13 | 0.96 | −0.24, 0.25 |
| Av. age (years) | −0.15 | 0.15 | 0.29 | −0.44, 0.13 |
| % male | 0.05 | 0.03 | 0.09 | −0.01, 0.11 |