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Table 2 Numerical scoring system used to allocate a score-based grade for the overall risk of bias in each of the twenty-six reviewed studies

From: Treatment in canine epilepsy – a systematic review

Studies

Randomisation sequence generation

Allocation concealment

Blinding of participants and personnel

Blinding of outcome assessment

Incomplete outcome data

Selective reporting

Other bias

Overall `risk of bias' category

Boothe et al. [11]

1

1

1

2

2

2

2

Low/moderate (11)

       

Primary investigator could potentially influence the treatment.

 

Chung et al. [24]

3

3

3

3

1

2

2

Moderate/high (17)

       

Research support but unclear if it was financial.

 

Cunningham et al. [29]

3

3

3

3

2

2

2

Moderate/high (18)

       

Conference abstract

 

Dewey et al. [18]

3

3

3

3

2

2

2

Moderate/high (18)

       

Less than 6 months study duration.

 

Dewey et al. [19]

3

3

3

3

2

2

1

Moderate/high (17)

EMEA pseudo-trial [13]

1

2

1

3

1

2

2

Low/moderate (12)

       

The follow up assessment of efficacy was not blinded. Different drug formulations were used compared to the final formulation.

 

Govendir et al. [21]

3

3

3

3

2

2

3

High (19)

       

A few cases were treated by the referring vets. The study had financial support. Less than 6 months study duration.

 

Heynold et al. [36]

3

3

3

3

2

2

3

High (19)

       

The study had financial support but unclear if it influenced the results. Less than 6 months study duration.

 

Kiviranta [17]

3

3

3

3

2

2

1

Moderate/high (17)

Löscher et al. [26]

3

3

3

3

2

2

3

High (19)

       

Part of the study was retrospective

 

Morton et al. [31]

3

3

3

3

2

2

3

High (19)

       

A few cases were treated by the referring vets. The study had financial support but unclear if it influenced the results.

 

Muñana et al. [12]

1

1

1

1

2

2

2

Low/moderate (10)

       

The study had financial support but unclear if it influenced the results.

 

Nafe [25]

3

3

3

3

2

2

3

High (19)

       

Less than 6 months study duration.

 

Pearce [32]

3

3

3

3

2

2

2

Moderate/high (18)

Platt et al. [22]

3

3

3

3

1

2

3

Moderate/high (18)

       

Less than 6 months study duration.

 

Podell et al. [33]

3

3

3

3

2

2

3

High (19)

       

Retrospective nature of study.

 

Rieck et al. [27]

3

3

3

3

2

2

3

High (19)

       

Part of the study was retrospective

 

Ruehlmann et al. [35]

3

3

3

3

1

2

3

Moderate/high (18)

       

Part of the study was retrospective. No clarification of statistical analysis

 

Schwartz-Porsche [28]

3

3

3

3

2

2

2

Moderate/high (18)

Schwartz-Porsche et al. [15]

2

2

3

3

2

2

2

Moderate/high (16)

       

The study had research support but unclear if it influenced the results. No clarification of statistical analysis

 

Schwartz-Porsche et al. [30]

3

3

3

3

2

2

1

Moderate/high (17)

Steinberg [23]

3

3

3

3

2

2

2

Moderate/high (18)

       

Conference abstract

 

Tipold et al. [14]

1

2

1

1

1

2

3

Low/moderate (11)

       

Statistical analysis was conducted before unblindingonly on the per-protocol population and not on the intent-to-treat population. A high and unbalanced population of animals was excluded. The reasons for exclusion were in many cases treatmet-related (post-randomization bias). Conflict of interest about imepitoin reported.

 

Trepanier et al. [34]

3

3

3

3

2

2

2

Moderate/high (18)

       

Some samples were submitted by the referring vets.

 

Volk et al. [16]

3

3

3

3

1

2

3

Moderate/high (18)

       

The study had financial support but unclear if it influenced the results. Part of the study was retrospective

 

Von Klopmann et al. [20]

3

3

3

3

2

2

3

High (19)

       

Less than 6 months study duration.

 
  1. Each aspect the risk of bias was categorised as `high’, `moderate’, `low’ or `unclear’. These categories were assigned a numerical score as follows: High risk of bias =3, moderate or unclear risk of bias =2, low risk of bias =1. Within each study these seven scores were summed to form a total score. This score translates to an overall estimated risk of bias associated with the findings of the study in question, as follows: Score 19–21 = overall high risk of bias, score 16 – 18 = overall moderate/high risk of bias, score 13 – 15 = overall moderate risk of bias, score 10 – 12 = overall low/moderate risk of bias, score 7 – 9 = overall low risk of bias.