Pharmacological treatment for aphasia following stroke

J Greener, P Enderby, R Whurr, J Greener, P Enderby, R Whurr

Abstract

Background: Aphasia describes language impairment associated with a brain lesion.

Objectives: The objective of this review was to assess the effects of drugs on language abilities when given to people with aphasia following stroke.

Search strategy: We searched the Cochrane Stroke Group Register (last searched: May 2001), and reference lists of relevant articles to December 1998. We also contacted academic institutions and other researchers to identify further published and unpublished trials. MEDLINE was searched from 1966-1998, and CINAHL from 1982-1998. We searched the International Journal of Disorders of Communication by hand (known by other names in the past), from 1969 to 1998.

Selection criteria: Randomised controlled trials comparing: ~bullet~Any drug given to improve language, versus no treatment, or versus placebo ~bullet~Any drug given to improve language versus speech and language therapy ~bullet~One drug given to improve language versus another drug given with the same aim

Data collection and analysis: The principal reviewer collected the data, and assessed the quality of the trials with independent data checking and methodological advice. If we could not perform a statistical combination of different studies, we sought missing data. Failing that we provided a description. We sought missing data from authors, or where appropriate, a drug company.

Main results: We considered fifty two studies in detail, from which we identified ten trials suitable for the review. In most cases the methodological quality was unassessable, and only one trial reported sufficient detail for us to complete a description and analysis. This study did lose a large number of patients during its course. Drugs used in the trials identified were piracetam, bifemalane, piribedil, bromocriptine, idebenone, and Dextran 40. We found weak evidence that patients were more likely to have improved on any language measure at the end of the trial if they had received treatment with piracetam (odds ratio 0.46, 95% confidence interval 0.3 to 0.7). The evidence is considered weak because of the large numbers of drop outs from the trials identified, who were lost to follow up. Patients who were treated with piracetam were no more likely (considering statistical significance) than those who took a placebo to experience unwanted effects, including death (odds ratio 1.29, 95% confidence interval for difference 0.9 to 1.7). However, the differences in death rates between the two groups, even though not not statistically significant, do give rise to some concerns that there may be an increased risk of death from taking piracetam. We could not determine if drug treatment is more effective than speech and language therapy. We could not determine whether one drug is more effective than another.

Reviewer's conclusions: The main conclusion of this review is that drug treatment with piracetam may be effective in the treatment of aphasia after stroke. Further research is needed to explore the effects of drugs for aphasia, in particular piracetam. If a trial is done, this must be large enough to have adequate statistical power. The safety of the drug should be of primary interest. Researchers should examine the long term effects of this treatment, and whether it is more effective than speech and language therapy.

Conflict of interest statement

The principal reviewer no longer practices speech and language therapy. The other two reviewers are both speech and language therapists with many years experience in the treatment of aphasia after stroke. Professor Enderby was an investigator in the Enderby 1994 trial.

Figures

1.1. Analysis
1.1. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 1 number of patients with aphasia not improved at end of study.
1.2. Analysis
1.2. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 2 number of patients with aphasia not resolved by 12 weeks on AAT.
1.3. Analysis
1.3. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 3 number of patients with aphasia not resolved by 24 weeks on AAT.
1.4. Analysis
1.4. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 4 number of all patients still aphasic on FAST scale at day 29 of study.
1.5. Analysis
1.5. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 5 number of all patients still aphasic on FAST scale at day 84 of study.
1.6. Analysis
1.6. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 6 number of patients with early treatment still aphasic on FAST scale at day 29 of study.
1.7. Analysis
1.7. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 7 number of patients with early treatment still aphasic on FAST scale at day 84 of study.
1.8. Analysis
1.8. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 8 difference in aphasia scale scores before and after treatment.
1.9. Analysis
1.9. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 9 spontaneous language rating (1) at week 12.
1.10. Analysis
1.10. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 10 spontaneous language rating (1) at week 24.
1.11. Analysis
1.11. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 11 spontaneous language rating (2) at week 12.
1.12. Analysis
1.12. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 12 spontaneous language rating (2) at week 24.
1.13. Analysis
1.13. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 13 spontaneous language rating (3) at week 12.
1.14. Analysis
1.14. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 14 spontaneous language rating (3) at week 24.
1.15. Analysis
1.15. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 15 spontaneous language rating (4) at week 12.
1.16. Analysis
1.16. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 16 spontaneous language rating (4) at week 24.
1.17. Analysis
1.17. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 17 spontaneous language rating (5) at week 12.
1.18. Analysis
1.18. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 18 spontaneous language rating (5) at week 24.
1.19. Analysis
1.19. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 19 spontaneous language rating (6) at week 12.
1.20. Analysis
1.20. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 20 spontaneous language rating (6) at week 24.
1.21. Analysis
1.21. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 21 score on token test at 12 weeks.
1.22. Analysis
1.22. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 22 score on token test at 24 weeks.
1.23. Analysis
1.23. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 23 score on repetition test at 12 weeks.
1.24. Analysis
1.24. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 24 score on repetition test at 24 weeks.
1.25. Analysis
1.25. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 25 score on written language test at 12 weeks.
1.26. Analysis
1.26. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 26 score on written language test at 24 weeks.
1.27. Analysis
1.27. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 27 score on confrontation naming test at 12 weeks.
1.28. Analysis
1.28. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 28 score on confrontation naming test at 24 weeks.
1.29. Analysis
1.29. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 29 score on comprehension test at 12 weeks.
1.30. Analysis
1.30. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 30 score on comprehension test at 24 weeks.
1.34. Analysis
1.34. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 34 Orgogozo Scale at end of 4 weeks.
1.35. Analysis
1.35. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 35 number of deaths, any type of patient, at end of trial.
1.36. Analysis
1.36. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 36 number of dropouts, any cause, by end of trial (ie people not included in test score analyses)..
1.37. Analysis
1.37. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 37 number of patients experiencing adverse events, including death, at end of trial.
1.38. Analysis
1.38. Analysis
Comparison 1 Piracetam compared with placebo, Outcome 38 number of deaths of aphasic patients at end of study.
6.1. Analysis
6.1. Analysis
Comparison 6 Dextran 40 compared with placebo, Outcome 1 number of patients worsened or not improved on four item language scale at end of trial.
6.2. Analysis
6.2. Analysis
Comparison 6 Dextran 40 compared with placebo, Outcome 2 number of patients died/experienced an adverse effect.

Source: PubMed

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