I refer to the paper by Nixon et al(1) on the use of McGill Oximetry
Score (MOS) in planning adenotonsillectomy (T&A) in children with
obstructive sleep apnea. His approach resulted in 22% of positive oximetry
(MOS category 2 or above). In other words, 78% eventually required a
formal sleep study. I think the proportion of positive oximetry is too low
to be helpful in reducing polysomngography (PSG) workload. For patients
having MOS 1 requiring subsequent sleep study, the waiting time for T&A
was actually prolonged by 2.5 times. Besides, the majority of patients
needed two procedures instead of one. This is obviously not desirable.
In Phase 2 of the study, patients with MOS 1 (normal + inconclusive
oximetry) have an average apnea-hypopnea index (AHI) of 4.1 (95% CI 3.0-
5.1). I think patients with normal oximetry should have much lower AHI.
Unfortunately both inconclusive and normal oximetries were grouped under
category 1, and we do not know how many within these two subcategories
eventually received T&A. In Phase 3, OSAS was later diagnosed in 58 (49%)
among 119 with either MOS 1 or failed oximetry. A second oximetry done
simultaneously was ¡§inconclusive¡¨ in all 58. That means that patients
with normal oximetry are unlikely to have OSAS. Even if they have mild
OSAS, most parents will prefer medical treatment rather than T&A. I have
actually tried the MOS on 40 snoring children, the average AHI for normal
VS inconclusive oximetry was 0.86 VS 2.37 (unpublished data).
MOS is a semi-quantitative measure of the ¡§depth¡¨ of desaturation,
while desaturation index (DI) is a quantitative measure of the
¡§frequency¡¨ of desaturation. Hence, MOS and DI are looking at different
aspects of the same hypoxic process. MOS is unable to detect frequent,
mild desaturations >90%, a situation probably classified as MOS 1-
inconclusive. In fact, the ability to detect this ¡§fluctuating pattern¡¨
can enhance the sensitivity of oximetry(2). This may be achieved by
introducing DI to supplement MOS.
The average DI in asymptomatic normal children is below 1(3). MOS 1
with DI >1 may indicate the presence of significant OSAS. On the other
hand, MOS 1-normal with a DI <1 can be quite reassuring, especially if
the symptoms and signs are mild. These patients can be safely followed up
with conservative treatment. PSG can be spared, unless symptoms persist or
get worse. A larger scale study that combines MOS and DI in diagnosing
OSAS is indicated to test this modified approach.
Reference:
1. Nixon GM, Kermack AS, Davis GM, Manoukian JJ, Brown KA,
Brouillette RT. Planning Adenotonsillectomy in Children With Obstructive
Sleep Apnea: The Role of Overnight Oximetry. Pediatrics. 2004;113;e19-e25.
2. Epstein LJ, Dorlac GR. Cost-effectiveness analysis of nocturnal
oximetry as a method of screening for sleep apnea-hypopnea syndrome.
Chest. 1998;113(1):97-103.
3. Urschitz MS, Wolff J et al. Reference values for nocturnal home
pulse oximetry during sleep in primary school children. Chest.
2003;123(1):96-101.
Conflict of Interest:
None declared