Linda Rogers and Joan Reibman Curr Opin Pulm Med. (2012) January Vol. 18 Stepping down asthma treatment: how and when Journal club 2013.06.10 R4. Yoo,

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Linda Rogers and Joan Reibman Curr Opin Pulm Med. (2012) January Vol. 18 Stepping down asthma treatment: how and when Journal club R4. Yoo, Jung-sun

Asthma guidelines focus on achieving and maintaining asthma control and balancing the risk of medications with control of disease Once symptoms are controlled for at least 3 months, therapy can be reduced to the lowest dose that maintains control.  Despite these recommendations, questions remain about when and how to reduce asthma therapy Benefits of inhaled corticosteroids (ICS) are well established, and adverse effects are uncommon at low and moderate doses  particularly with sustained high doses, and include osteoporosis, adrenal axis suppression, cataracts, hoarseness, dysphonia, oral candidiasis, and dermal thinning and bruising. Introduction Eur Resp J 2008; 31:143–178

Recent links of ICS to diabetes and pneumonia are cause for concern and require further investigation Safety concerns about long-acting beta agonists (LABAs) create questions about the optimal way to reduce combination ICS/LABA therapy This review will discuss the current state of knowledge of how one should reduce therapy when asthma control is sustained. Introduction Am J Respir Crit Care Med 2011; 183:589–595 N Engl J Med 2007; 356:775–789

Once on low-dose therapy, the risk of adverse effects of ICS is low However, patients and some providers still have doubts about ICS safety, leading to the desire to reduce or stop When mild asthma is controlled, ICS can often be reduced by 50%, but reducing therapy is less successful with rapid medication tapering and in moderate-to-severe disease Inhaled corticosteroid in mild to moderate asthma Am J Respir Crit Care Med 2011; 183:589–595 N Engl J Med 2000; 343:1054–1063 Chest 2006; 130:65S–72S. N Engl J Med 1994; 331:700–705 JAMA 2001; 285:2594–2603

Roughly 50% of children and adults will redevelop symptoms within 1–12 months if ICS are stopped. Seasonal effects are noted, with greater success weaning in spring and summer, and more failure in the fall. In adults with persistent asthma, the ability to achieve sustained discontinuation of ICS with good control: rare Inhaled corticosteroid in mild to moderate asthma Am J Respir Crit Care Med 2011; 183:589–595 N Engl J Med 2000; 343:1054–1063 Ann Allergy Asthma Immunol 2008; 101:144–152. J Asthma 2008; 45:445–451.

Although data are mixed, biomarkers including FeNO, sputume eosinophilia, are not clearly helpful at determining which patients can have therapy reduced and are often not available in many practice settings. Approaches using low-dose ICS plus additional as needed ICS or as-needed ICS/SABA combination require further study. Inhaled corticosteroid in mild to moderate asthma Am J Respir Crit Care Med 2011; 183:589–595 N Engl J Med 2007; 356:2040–2052

When escalating therapy in uncontrolled asthma, addition of nonsteroid agents is favored over increasing to high-dose ICS for most patients Less data are available to suggest that this approach ‘works in reverse’ – that lowering ICS prior to removing nonsteroid drugs is effective at sustaining asthma control. Recent systematic reviews reinforce that LABAs are effective at controlling asthma with lower ICS doses Stepping down Inhaled corticosteroid Cochrane Database Syst Rev 2010:CD Eur Resp J 2008; 31:143–178

There are ample data documenting that omalizumab (anti-IgE) allows reduced ICS dosing.  A 2011 systematic review including eight trials and 3429 patients found that omalizumab-treated patients were able to reduce their ICS by 50% or discontinue it entirely Although perhaps justified in moderate-to-severe disease, enthusiasm for this approach must by tempered by the fact that omalizumab has an average whole sale price of $4000– $ per year Significant long-term side-effects of low-to-moderate dose ICS: low  A large body of data now support omalizumab as a treatment that can allow for reduction of ICS dosing, but its use is limited by expense and logistics of administration Stepping down Inhaled corticosteroid N Engl J Med 2006; 354:2689–2695 Chest 2011; 139:28–35.

One of the most common dilemmas: how to reduce ICS/LABA once asthma is controlled.  Guidelines recommend a two-step approach: reducing the ICS by 50% and maintaining the LABA, and stopping the LABA if control is sustained with low-dose ICS Risk of adverse effects of LABA: important, significant controversy  upcoming US FDA mandated LABA safety mega-trial Stepping down fixed dose combination therapy Eur Resp J 2008; 31:143–178

Once asthma control is achieved and sustained, how low should the ICS dose be reduced?  Low and moderate dose ICS do not differ in terms of symptom control, but moderate- dose ICS may have a slight advantage in terms of lung function (FEV1 in adults but not children) and at reducing exacerbations Good data suggest that the long-term safety profile of low-to-moderate dose ICS: favorable Is stepping down beyond moderate Inhaled corticosteroid in adult ? Thorax 2004; 59:1041–1045 J Allergy Clin Immunol 2010; 126:389–392 Thorax 2004; 59:1041–1045

In adults with persistent asthma, continuation of moderate dose (FSC 250) ICS/LABA resulted in marginally better symptom control and lung function compared to adjustable and maintenance Bud/Form, but a striking 50% lower exacerbation rate. At the end of 1 year, both groups ended up on just under 500 mg daily of either fluticasone or budesonde, respectively.  suggests patient-dictated adjustment of medication according to symptoms slightly lowers ICS exposure, but possibly at the cost of a higher exacerbation rate.  also suggests that there is a minimum daily ICS dose needed to prevent exacerbations, at least in adults. Is stepping down beyond moderate Inhaled corticosteroid in adult ? Thorax 2004; 59:1041–1045 J Allergy Clin Immunol 2011; 128:278–281

Use low-dose ICS and then increase ICS at the first signs of an exacerbation. Data evaluating this approach show that doubling ICS does not prevent exacerbations  It seems that once control is lost, it may not be easily regained.  These findings highlight the critical need for long-term, step-down studies in both children and adults. Both children and adults and comparing reducing ICS vs. maintaining stable dosing and evaluating long term outcomes and adverse effects Is stepping down beyond moderate Inhaled corticosteroid in adult ? J Allergy Clin Immunol 2011; 128:278–281

Although step-down of asthma therapy is recommended once asthma control is sustained for at least 3 months, questions remain about when and how to reduce treatment. In milder patients, ICS can often be reduced by 50%,and intermittent ICS treatment, often in fixed combination with short-acting beta agonist, is an emerging strategy for control of mild asthma. A large body of data now support omalizumab as a treatment that can allow for reduction of ICS dosing, but its use is limited by expense and logistics of administration. Key points

Although data are mixed, biomarkers including FeNO are not clearly helpful at determining which patients can have therapy reduced and are often not available in many practice settings. In patients on fixed-dose combination ICS/LABA, data currently suggests that reducing ICS dose before discontinuing LABA may be the more effective approach for patients on combination therapy, but more data are needed Key points

Conclusion Although step-down of controller medication to the lowest dose which controls asthma is an appropriate goal, many unanswered questions remain regarding how to best accomplish this, and what the ultimate ‘lowest’ dose should be. Current data is overrepresented with short-term studies that may underestimate the risk of exacerbations on lower medication dosing and may overstate the benefits of lower dosing compared to risks. More data are needed regarding the ideal duration of control prior to tapering, and the best approach to stepping down patients with severe asthma, particularly those on moderate-to-high dose ICS/LABA.