Item | Yes | No | Unclear | |
1 | Was the spectrum of patients representative of the patients who will receive the test in practice? | |||
2 | Were selection criteria clearly described? | |||
3 | Is the reference standard likely to correctly classify the target condition? | |||
4 | Is the time period between reference standard and index test short enough to be reasonably sure that the target condition did not change between two tests? | |||
5 | Did the whole sample or a random selection of the sample, receive verification using a reference standard of diagnosis? | |||
6 | Did patients receive the same reference standard regardless of the index test result? | |||
7 | Was the reference standard independent of the index test (ie, the index test did not form part of the reference standard)? | |||
8 | Was the execution of the index test described in sufficient detail to permit replication of the test? | |||
9 | Was the execution of the reference standard described in sufficient detail to permit its replication? | |||
10 | Were the index test results interpreted without knowledge of the results of the reference standard? | |||
11 | Were the reference standard results interpreted without knowledge of the results of the index test? | |||
12 | Were the same clinical data available when test results were interpreted as would be available when the test is used in clinical practice? | |||
13 | Were uninterpretable/intermediate test results reported? | |||
14 | Were withdrawals from the study explained? |
Reproduced from Whiting et al.12 Copyright BioMed Central.