Table A1.
(1) Representativeness of the exposed cohort |
(★)-moderate-to-severe tinnitus |
(★)-tinnitus patients |
(☆)-selection of individuals |
(☆)-no description |
(2) Selection of the non-exposed cohort |
(★)-same as exposed cohort |
(☆)-other source |
(☆)-no description |
(3) Ascertainment of exposure |
(★)-objective measure |
(☆)-questionnaire |
(☆)-no description |
(4) Demonstration that outcome of interest was not present at start of study |
(★)-pre-stimulation tinnitus outcome available |
(☆)-pre-stimulation tinnitus outcome not available |
(1) Comparability of cohorts on the basis of the design or analysis |
(★)-inclusion based on tinnitus severity |
(☆)-no inclusion based on tinnitus severity |
(★)-inclusion based on HL |
(☆)-no inclusion based on HL |
(1) Assessment of outcome |
(★)-questionnaire |
(☆)-self report |
(☆)-no description |
(☆)-other |
(2) Was follow-up long enough for outcomes to occur |
(★)-at least during stimulation |
(☆)-no data |
(3) Adequacy of follow up of cohorts |
(★)-no missing data |
(★)-<10% missing data |
(☆)->10% missing data |
(☆)-no description |
★ 1 point; ☆ 0 point.