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T h o m a s J . K a l l s t r o m , r r t, f a a r c AARC Representative, National Asthma Education and Prevention Program Focus on Asthma A Sneak Peek at Soon-to-Be-Released Asthma Drugs F our years ago, the National Heart, Lung, and Blood Institute published the National Asthma Education and Prevention Program’s Expert Panel Report 2: Asthma Guidelines for the Diagnosis and Management of Asthma.1 A significant amount of research has been published since. In fact, a recent MEDLINE search revealed more than 13,000 asthma-related citations since 1997, a large proportion of which was related to changes in pharmacotherapy. We will continue to see many improvements in the drugs we use to treat asthma. Below are highlights of what 2001 promises. A d va i r D i s ku s Combination drugs are no strangers to asthmatic patients and are a logical approach that simplifies the administration of medications. Patient compliance is enhanced when drugs can be combined. Such drugs have been used successfully and efficiently to treat hypertension, tuberculosis, and AIDS. GlaxoSmithKline plans to release a new combination drug this spring: fluticasone and salmeterol will be combined in a dry diskus powder inhaler named Advair Diskus. 10 A AR C Tı m e s April 2001 In a study by Kavuru et al,2 a 12week randomized, double-blind, multicenter study consisting of 356 patients (over age 12), found that a combination of fluticasone and salmeterol reduced the symptom scores and overall need for rescue drug (albuterol). Additionally, nocturnal awakenings decreased, while days with no symptoms increased (compared to those receiving placebo and salmeterol). Many new The combination of these two drugs causes a synergistic response as the inhaled corticosteroid provides a protective effect on the betaagonist receptor. At the same time, the long-acting agonists prime the glucocorticoid receptor, which in turn intensifies the antiinflammatory action of the glucocorticoid. Once released, Advair will be available in 100 asthma medications will soon be available, and RTs should become knowledgeable about what these drugs have to offer. Shapiro et al3 reached a similar conclusion when they noted significantly decreased asthma symptom scores and need for rescue drug. Patients in this study who received fluticasone and salmeterol had a significantly greater probability of remaining in the study without being withdrawn because of deterioration of symptoms than did patients receiving the placebo, salmeterol, or fluticasone. mcg, 250 mcg, and 500 mcg strengths. F o rm o t e r o l a n d omalizumab Novartis Pharmaceuticals plans to release two products in 2001: formoterol (sold as Foradil Aersolizer) and omalizumab (sold as Xolair). Formoterol has been used since 1991 outside of the United States in more than 60 countries. This long-acting Focu s on Asthma beta-2 adrenergic provides control for up to 12 hours when given twice daily. The onset of action is 10 to 20 minutes. A recently published study by Bensch et al4 noted that formoterol had a rapid onset and was effective for 12 hours. Morning and evening peak expiratory flow rates improved, and patients were less likely to use a rescue medication than those who received albuterol or placebo. Use of formoterol also provided significantly greater improvements in asthma symptom scores compared to both albuterol and placebo. This breath-actuated powder drug is administered by an aersolizer device, which delivers the medication from a capsule. Another interesting development on the horizon is the Novartis and Genentech drug omalizumab. Omalizumab is a genetically engineered recombinant humanized monoclonal antibody. Omalizumab is given to the patient via a subcutaneous route. Once administered, it binds to the IgE antibody, thereby preventing it from binding to receptors on mast cells and basophils. As a result, the cross-linking of the IgE and the degranulation of mast cells and basophils are inhibited. It is this sequence that stops the allergic response. Once patients start taking this medication, they should observe dramatic and prompt reductions in IgE levels within the first few days of initial administration. Omalizumab has been studied in more than 1,700 patients with allergic asthma, and in more than 750 with allergic rhinitis. Patients who received the drug in a study done by Milgrom et al5 noted a significant improvement in asthma symptom scores (compared to those who received placebo) and a reduction in use of inhaled corticosteroids. There was also an association with those treated with omalizumab and an improvement in asthma-specific quality of life. The therapy was well tolerated; and after 20 weeks, none of the patients who received the drug developed antibodies against it. Once on the market there will need to be significant patient education about omalizumab. Patients will need to understand that unlike a rescue medication, this drug will not provide shortacting relief. Education should be focused on the route of administration, dosing, and expected clinical response to the drug. ( c on t in ue d on p a ge 94) A AR C Tı m e s A pri l 20 0 1 11 A A RC Ti m e s F oc us o n Asthma Ve n t i l a t i o n fo r L i f e (c on ti nu e d f ro m p a g e 11) ( con tin u ed fr om p ag e 2 6) Indeed, many new drugs will soon be available. All respiratory therapists involved in the management of asthma should become knowledgeable about what these drugs have to offer. While not all of these drugs will be given by the bedside respiratory therapist, it is essential that we are knowledgeable and able to teach our patients about them. • the delivery of non-acute care ventilation. The acute care setting has generated a group of patients requiring an extended time to wean. Also, there is earlier recognition of the decidedly ventilator-dependent patient. The diagnosis-related group (DRG) reimbursement system and the managed care movements have driven the VAI from the expensive, acute care setting. The options then are a specialized unit for further attempts at weaning, a skilled nursing facility (SNF), a group home setting, or “home.” The important reimbursement issue then becomes, primarily, a caregiver issue. If the weaning unit, SNF, group home, or home health agency can employ caregivers, placement can be made to that setting. If the family can arrange payment for caregivers or provide care themselves, the situation is greatly simplified and placement at home is the preferred choice. Reimbursement for ventilators and caregivers is available through government programs, but the caregivers must be skilled and the care must be continual and dependable. While the ventilator is usually rented and reimbursed, the caregiver situation is complex. For example, if an SNF accepts a VAI, reimbursement does not often cover continual care by an RT. Afacility can contract for the therapist’s services; but without continual involvement of an RT, active weaning attempts are often halted. Inadequate airway care, ventilation monitoring, or ventilator management often result in readmission to the acute care setting. If nursing personnel provide ventilator care, they must be skilled and comfortable with airway care, ventilator settings, and pressure/volume alarms. Thomas J. Kallstrom is director of cardiopulmonary services at Fairview Hospital in Cleveland, OH. REFERENCES 1. U.S. Department of Health and Human Services. (1997, July). National Asthma Education and Prevention Program, Expert panel report 2: Guidelines for the diagnosis and management of asthma (NIH Publication No. 97-4051). Bethesda, MD: National Institutes of Health, National Heart, Lung, and Blood Institute. 2. Kavuru, M., Melamed, J., Gross, G., et al. (2000). Salmeterol and fluticasone propionate combined in a new powder inhalation device for the treatment of asthma: A randomized, double-blind, placebo-controlled trial. Journal of Allergy and Clinical Immunology, 105(6), 11081116. 3. Shapiro, G., Lumry, W., Wolfe, J., et al. (2000). Combined salmeterol 50 microg and flutucasone propionate 250 microg in the diskus device for the treatment of asthma. American Journal of Respiratory and Critical Care Medicine, 161(2), 527534. 4. Bensch, G., Lapidus, R.J., Levine, B.E., et al. (2001). A randomized, 12-week, double-blind, placebo-controlled study comparing formoterol dry powder inhaler with albuterol metered-dose inhaler. Annals of Allergy, Asthma & Immunology, 86(1), 19-27. 5. Milgrom, H., Fick, R.B., Su, J.Q., et al. (1999). Treatment of allergic asthma with monoclonal anti-IgE antibody. New England Journal of Medicine, 341(26), 1966-1973. 94 A AR C Tı m e s April 2001 With the current shortage of nursing personnel — particularly those with experience in ventilator care — and limited reimbursement for respiratory therapy, the VAI can become a refugee in the health care system dependent on finding caregivers with experience in nonacute care ventilation. • Alexander B. Adams is senior research associate at Regions Hospital in St. Paul, MN, and can be reached at Alex.b. [email protected]. Peter Bliss is an engineer at Valley Inspired Products in Eden Prairie, MN, and can be reached at [email protected]. Tak in g a B re a t h e r ( con tin u ed fr om p a ge 9 6) garbled, as if he were using his forefinger to flap his lips. “Have a little respect,” I said. “What if you lost your teeth?” “I’ll never lose my teeth.” “Spoken like a true teenager,” I said. “But suppose you did.” He was quiet for a moment. “I’d sneak in here and steal them back — you know — like — take a bite out of crime.” I laughed. “That’s it. Wrap them in the napkins and leave them where you found them, next to the Certs.” Later that evening Shannon called to say that a gentleman wearing a porkpie hat had come in. His collar was turned up, and he took a long time browsing the magazines. When Shannon moved into the second aisle to dust pickle jars, the man headed for the check stand, snatched the messy little wad of napkins, and escaped into the night. • Jean Blackmon Waszak is a columnist for the Corrales Comment in Corrales, NM. Her essays have been widely reprinted. Jean Blackmon Waszak, ©2001