Score | Quality Evaluation Criteria |
---|---|
Essential internal validity | |
 ✓ | The sampling method and exclusion criteria did not introduce sampling bias. |
 ✓ | The design or analysis allowed for comparability between parameter and minimized co-intervention bias. |
 ✓ | The outcomes were reliable (e.g., all infants screened were accounted for; there was no error in the result tallies). |
 ✓ | The outcomes were valid (e.g., based on objective measures; did not contain bias). |
Sample | |
 * | The community was described from which all infants were drawn. |
 - | The community was not described from which infants were drawn. |
 * | The sample size was 1000 or more for each group described. |
 - | The sample size was less than 1000 for each group described. |
 * | The coverage rate was described and was 95% or more, as recommended by the Joint Committee of Infant Hearing. |
 - | The coverage rate was not described, or if described, coverage was less than 95%. |
 * | The infants included were described with respect to risk factors, NICU admission, well babies, all babies born, etc. |
 - | The infants included were not described. |
Screening | |
 * | The screening protocol was described and included at least four of the five following factors: infant age at screening, test method, number of screens performed in screening step 1, the test device, and referral criteria (If not automatic) including one or both ears. |
 - | Less than four of the five above-mentioned factors pertaining to the screening protocol were described. |
Outcome | |
 * | The method for collecting data was described (e.g., paper records, centralized database, etc). |
 - | The method for collecting data was not described. |
 * | The criteria for determining loss to follow-up (or nonattendance) was describeda. |
 - | The criteria for determining loss to follow-up (or nonattendance) was not describeda. |