Table 2. Newcastle-Ottawa quality assessment scale.
| Selection |
|---|
| (1) Representativeness of the exposed cohort |
| (a) Truly representative of the average patients with colorectal cancers in the community* |
| (b) Somewhat representative of the average patients with colorectal cancers in the community* |
| (c) Selected group of users (e.g., nurses, volunteers) |
| (d) No description of the derivation of the cohort |
| (2) Selection of the non exposed cohort |
| (a) Drawn from the same community as the exposed cohort* |
| (b) Drawn from a different source |
| (c) No description of the derivation of the non exposed cohort |
| (3) Ascertainment of exposure (Proof of colorectal cancers and osteopontin measurement) |
| (a) Secure record (e.g., surgical records)* |
| (b) Structured interview* |
| (c) Written self report |
| (d) No description |
| (4) Demonstration that outcome of interest was not present at start of study |
| (a) Yes* |
| (b) No |
| Comparability |
| (1) Comparability of cohorts on the basis of the design or analysis |
| (a) Study controls for recurrence or metastasis* |
| (b) Study controls for any additional factor (Age, gender, grade, KPS score, etc.)* |
| Outcome |
| (1) Assessment of outcome |
| (a) Independent blind assessment* |
| (b) Record linkage* |
| (c) Self report |
| (d) No description |
| (2) Was follow-up long enough for outcomes to occur? (Death or recurrence) |
| (a) Yes (60 months)* |
| (b) No |
| (3) Adequacy of follow up of cohorts |
| (a) Complete follow up- all subjects accounted for* |
| (b) Subjects lost to follow up unlikely to introduce bias-small number lost- (25%) follow up, or description provided of those lost)* |
| (c) Follow up rate (<75%) and no description of those lost |
| (d) No statement |
A maximum of one star (*)*: can be given for each numbereditem within the ‘Selection’ and ‘Outcome’ categories. While a maximum of twostars**: can be given for ‘Comparability’.