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Molecular, pathological and clinical assessments were collected in a mutually blinded manner in a retrospective cohort approach.
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Both percent positivity of cells and staining intensity were decided in a double blinded manner.
Histological sections were analyzed by a pathologist in a double blinded manner.
All examiners were mutually blinded to the results of other examiners.
The two specialists were mutually blinded, and used structured and pre-determined questionnaire to improve objectiveness of decision making.
Observer bias was unlikely, since different and mutually blind research assistants conducted EE and SBAS interviews.
The study was designed in a double blind manner.
This test was conducted in a double-blind manner to eliminate examiner bias.
Another limitation is that the PLR test was not performed in a blind manner.
All counting was performed in a blind manner.
This blood assay was also performed in a blind manner.
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