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. 2017 Jul 7;2017(7):CD006396. doi: 10.1002/14651858.CD006396.pub4

Muhr 2016.

Methods CBA study
Participants Army conscripts (n= 1234)
Control group: before military service in 2002‐2004 (n = 839),
Intervention group: in military service 2004‐2005 (n = 395),
40 servicemen from the armoured regiment included in the control‐group are also included in the intervention group.
Mean age: intervention, 19 years, control, 18 years at enrolment
Gender: male
Hearing ability: most participants had maximum hearing thresholds of 25 dB for frequencies 0.5 to 8 kHz in both ears at enrolment to study (I 88.4%, C 85.5%)
Exposure: intervention group exposed to impulse noise from shooting
Sweden
 Military
Interventions Intervention: HLPP including HPDs and administrative controls (n = 395)
Control: non‐exposed to military noise, waiting for training period (n = 839)
Outcomes STS ≥ 15 dB at 1 or both ears at any of 0.25, 0.5, 1, 2, 3, 4, 6 or 8 kHz between baseline and follow‐up, hearing test with average follow‐up of 8 months (intervention group) and 13 months (control group)
Notes  
Risk of bias
Bias Authors' judgement Support for judgement
14. Blinding (subjects) High risk no blinding
15. Blinding (outcome assessors) High risk no blinding
16. Retrospective unplanned subgroup analyses Low risk no subgroup analysis, data dredging unlikely
17. Follow‐up Unclear risk approximate difference of 5 months in follow‐up between intervention and control, 1.5 times longer for control
18. Statistical tests Low risk RR (95%CI)
19. Compliance Unclear risk not reported
20. Outcome measures Low risk audiometry quality reported
21. Selection bias (population) Low risk all subjects recruits to the army
22. Selection bias (time) High risk different time periods, 2004/2005 vs 2002‐2004
23. Randomization High risk no randomisation
24. Allocation concealment High risk no randomisation
25. Adjustment for confounding Low risk Control and intervention groups of similar age and hearing, baseline for other confounders not reported
26. Incomplete outcome data Unclear risk loss of follow‐up not reported