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February 10, 2012

Diabetes Treatment (cont.)

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Inhaled Insulin

Inhaled insulin, marketed by Pfizer in 2006, was approved by the FDA. This inhaled form of insulin is called Exubera. The insulin is packaged in dry blister packs that are inserted into an inhalation device. This device lances the powder packs allowing the insulin to enter a chamber that has a mouth piece through which the user can inhale the insulin. Exubera has a peak of action similar to Humalog (rapid acting), and a duration of action similar to regular insulin (short acting). It can be combined with oral medication in patients with type 2 diabetes or used alone. In patients with type 1 diabetes the insulin should be combined with a longer acting basal insulin such as glargine.

The side effect profile of inhaled insulin is similar to other insulins, and the user must be aware of hypoglycemia. In addition, since the insulin is absorbed through the lungs, there was initial concern regarding lung function. While there is a slight decrease in lung function with the initial use of Exubera, this stabilizes quickly and returns to baseline of aged matched controls when the Exubera is discontinued. Since this is still a new product, it is recommended that any patient starting on inhaled insulin have lung function tests done prior to starting treatment. If baseline values of FEV1 (a measure of lung function) are < 70%, Exubera is not given. After six months of use lung function tests are performed again; if deterioration is noted, Exubera is discontinued.

Exubera is not to be used in regular or intermittent smokers and patients requiring very small doses of insulin. Nevertheless, in the right population, this is a great option.

Note: Unfortunately, acceptance of Exubera was poor over the year or so it was available since it's launch in 2006. Recently in October 2007, the company Pfizer decided not to sell the product anymore. Part of this issue was the time required to teach the device and the uniqueness of the format of delivery. While no major medical concerns were noted with it's use, it simply has not been accepted by patients and doctors. Perhaps we will see this modality come back in a new easier to use incarnation.


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