Reportinbg Quality Item |
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   1. Are the inclusion and exclusion criteria clearly reported? |
   2. Is information regarding the number of patients who did not gave informed consent and who were not willing to participate adequately reported? |
   3. Are the baseline characteristics of included patients reported? |
   4. Is the surgical technique adequately reported? |
   5. Are the prosthesis brand and fixation reported with enough detail? |
   6. Are the reasons or definitions for revision adequately reported? |
   7. Are the number of revisions (N) and revision rates regarding aseptic loosening (either Kaplan-Meier or life table or revisions per 100 observed component years) adequately reported? |
   8. Is the number of deaths, lost-to-follow up (e.g. no show at clinic or emigration), amputations, and revisions other than the primary endpoint adequately reported? |
Methodological Quality Item |
   1. Is there a clear primary research question/hypothesis?* |
   2. How were the cohorts constructed? |
a. Consecutivelya |
b. Non-consecutively |
c. Unknown |
   3. How adequate was the follow-up (FU)? |
a. Fully completed FU |
b. 5% or less lost-to-FU or FU quotientb is 1 or less |
c. More than 5% lost-to-FU or FU quotient is more than 1 |
d. Unknown |
   4. How was the FU performed? |
a. Predefined e.g. yearly |
b. When patients had complaints or chart review (of non-predefined FU) |
c. Unknown |
   5. How many arthroplasties are at risk at the FU of interest? |
a. 20 or more |
b. Less than 20 |
b. Unknown |
   6. Has a worst case analysis or competing risk analysis for competing endpoints [14] been performed? |