DreamDiver wrote: will having an SV machine give me that much better results, or am I always going to have to live with a certain amount of headache and central apnea?
This is probably the best summary I have seen. It is from the powerpoint slides at the first link I posted this morning:
ADAPTIVE PRESSURE SUPPORT SERVO-VENTILATION
• Figure 2. Box plots of effect of treatment on central apnea
index. Horizontal bar: median; thick vertical line: interquartile
range; circles: outliers; thin bar: range excluding outliers.
Also shown are statistical significance of comparisons
between control and each of the four treatments, and
between ASV and the other four conditions.
I am not sure of the date on the data? It seems to indicate on the slide that they were from 2001, which is way too early! But I have seen the numbers in table form elsewhere - think maybe there were from Shahrokh Javaheri, in November, 2009?
Going through the hurdles to get approvaed for an ASV is another question! My centrals are from medication, so it is a different "sub-category" I believe. It won't just "go away." Approval is easier there I think.
The steps outlined in this BCBS Policy Manual are quite daunting! Section F, page 4:
http://www.bcbsnc.com/assets/services/p ... evices.pdf
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F. Complex Sleep Apnea:
“Complex Sleep Apnea” as used in this policy is defined as a clinical syndrome where central apneas develop during pressure titrations in the sleep lab in patients who have demonstrated obstructive sleep apnea either at initial p olysomnography or during an unattended (unsupervised) home sleep study.
Coverage of bilevel PAP device with a backup rate or an adaptive servo-ventilation (ASV) device may beconsidered medically necessary in patients with Complex Sleep Apnea syndrome when the central apneas
have failed to respond to:
1. Reduction in the administered CPAP or bilevel pressures in the sleep lab (’down titration’); and
2. Acclimation/desensitization to pressure therapy by a trial of auto bilevel PAP in the home setting with appropriate, gradual acclimation measures for a period of at least four weeks, followed by a bilevel PAP titration in the sleep lab for determination of definitive treatment pressures; and
3. Evaluation and treatment of underlying medical conditions or etiologies (e.g., thyroid disease, opiateuse, renal failure, etc.);
and when the back-up rate or ASV device has been shown to be effective in the sleep lab.
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