Hyperbaric oxygen for idiopathic suddensensorineural hearing loss and tinnitus (Cochrane Review).
Citation: Bennett M, Kertesz T, Yeung P. Hyperbaric oxygen for idiopathic suddensensorineural hearing loss and tinnitus (Cochrane Review). In: The Cochrane Library (Issue 1 2005). Chichester, UK: John Wiley & Sons, Ltd.
Background
Idiopathic sudden sensorineural hearing loss (ISSHL)
with or without tinnitus is common and presents a health problem with
significant effect on quality of life. Hyperbaric oxygen therapy (HBOT) may
improve oxygen supply to the inner ear and it is postulated that application of
HBOT to these patients may result in an improvement in hearing and/or a
reduction in the intensity of tinnitus.
To assess the benefits and harms of HBOT for treating
ISSHL and/or tinnitus.
We searched the Cochrane ENT Specialist Register (June
2004), CENTRAL (The Cochrane Library Issue 3, 2004), MEDLINE (1966 - 2004),
EMBASE (1974 - 2004), CINAHL (1982 - 2004), DORCTHIM (1996 - 2004), and
reference lists of articles. Relevant journals were hand searched and
researchers in the field were contacted.
Randomised studies comparing the effect on ISSHL and/or
tinnitus of therapeutic regimens which include HBOT with those that exclude HBOT.
Three reviewers independently evaluated the quality of
the relevant trials using the validated Oxford-Scale (Jadad
1996) and extracted the data from the included trials.
Five trials contributed to this review (254 subjects).
Pooled data from two trials involving 114 patients did not show any significant
improvement in the chance of a 50% increase in hearing threshold on Pure Tone
Average (PTA) when HBOT was used (relative risk [RR] with HBOT 1.53, 95% CI 0.85
to 2.78, P=0.16), but did show a significantly increased chance of a 25%
increase in PTA (RR 1.39, 95% CI 1.05 to 1.84, P=0.02). There was a 22% greater
chance of improvement with HBOT, and the number need to treat (NNT) to achieve
one extra good outcome was 5 (95% CI 3 to 20). A single trial involving 50
subjects also suggested significant more improvement in the mean PTA threshold
with HBOT, expressed as a percentage of baseline (WMD 37%, 95% CI 22% to 53%,
P<0.001). The significance of
any improvement following HBOT in a subjective rating of tinnitus could not be
assessed due to poor reporting.
There were no significant improvements in hearing or
tinnitus reported in the single study to examine chronic presentation (six
months) of ISSHL and/or tinnitus.
For people with early presentation of ISSHL, the
application of HBOT significantly improved hearing loss, but the clinical
significance of the level of improvement is not clear. We could not assess the
effect of HBOT on tinnitus by pooled data analysis. The routine application of
HBOT to these patients cannot be justified from this review. In view of the
modest number of patients, methodological shortcomings and poor reporting, this
result should be interpreted cautiously, and an appropriately powered trial of
high methodological rigour is justified to define those patients (if any) who
can be expected to derive most benefit from HBOT.