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size assessment <strong>may</strong> be unfamiliar.<br />

The mechanisms of action and optimal<br />

patient selection need to be addressed<br />

in further rigorous clinical and scientific<br />

studies.<br />

Indications<br />

Candidates for bronchial thermoplasty<br />

include adults with severe persistent<br />

asthma who require regular<br />

maintenance medications of inhaled<br />

corticosteroids (>1000 µg/day of<br />

beclomethasone or the equivalent) and<br />

a long-acting beta agonist (≥100 µg/<br />

day of salmeterol or the equivalent).<br />

These patients would have received<br />

add-on therapies such as leukotriene<br />

modifiers, omalizumab, or oral<br />

corticosteroids (≤10 mg/day).<br />

These patients should be on stable<br />

maintenance asthma medications<br />

according to accepted guidelines,<br />

should have a pre-bronchodilator<br />

forced expiratory volume in 1 second<br />

(FEV1) of 60% or more of predicted,<br />

and should have a stable asthma<br />

status (FEV1 within 10% of the best<br />

value, no current respiratory tract<br />

infection, and no severe asthma<br />

exacerbation within the preceding 4<br />

weeks).<br />

Patients are usually selected<br />

on the basis of the AIR 2 trial. The<br />

patient should be stable in terms<br />

of asthma status, defined as a post<br />

bronchodilator FEV1 within 15% of<br />

baseline values with no respiratory<br />

tract infection or asthma exacerbations<br />

within the preceding 14 days.<br />

Contraindications<br />

Contraindications for BT include the<br />

following:<br />

• Presence of an implantable<br />

electronic device<br />

• Known hypersensitivity to drugs<br />

used during bronchoscopy<br />

• Severe comorbid conditions that<br />

would increase the risk of adverse<br />

events<br />

Patients are not considered<br />

candidates for BT if they had three or<br />

more hospitalisations for asthma, three<br />

or lower respiratory tract infections and<br />

four or more oral corticosteroids used<br />

for asthma in the previous year.<br />

Although the benefits of BT <strong>may</strong><br />

be large, the potential harm <strong>may</strong> be<br />

large as well, and the long-term side<br />

effects are unknown. Studies are still<br />

needed to assess exacerbation rates<br />

and long-term effects on lung function.<br />

It remains to be determined which<br />

phenotypes will respond best to BT,<br />

what the effects <strong>may</strong> be on obstructed<br />

patients with an FEV1 higher than<br />

60%, and what the applicability of the<br />

procedure <strong>may</strong> be in patients receiving<br />

systemic steroid therapy<br />

Procedure considerations<br />

BT is performed via fibreoptic<br />

bronchoscopy in three separate<br />

procedures, separated by<br />

approximately 3 weeks, as<br />

PATIENTS ARE NOT<br />

CONSIDERED CANDIDATES<br />

FOR BT IF THEY HAD THREE<br />

OR MORE HOSPITALISATIONS<br />

FOR ASTHMA<br />

demonstrated by previous studies.]<br />

Dividing the treatments into three<br />

bronchoscopy sessions minimizes<br />

the risk of inducing an asthma<br />

exacerbation or diffuse airway oedema.<br />

It also avoids excessive procedural<br />

length. BT takes longer (30-60<br />

minutes) than a standard fiber-optic<br />

bronchoscopy (5-20 minutes) does,<br />

and the longer duration implies the<br />

use of larger doses of medication for<br />

sedation.<br />

All accessible airways are treated,<br />

with the exception of the right middle<br />

lobe, because of the theoretical<br />

concern about the risk of inducing<br />

right-middle-lobe syndrome.]<br />

Oxygen delivery should be started<br />

via a nasal or oral cannula during<br />

the procedure, with appropriate<br />

monitoring of vital signs. Heart rate,<br />

pulse oximetry, and noninvasive blood<br />

pressure should be continuously<br />

monitored.<br />

Outcomes<br />

Patients <strong>may</strong> experience respiratoryrelated<br />

adverse events such as cough,<br />

wheezing, and chest tightness during<br />

the treatment period. Most of these<br />

symptoms occur within 1 day of the<br />

procedure and resolve in an average of<br />

7 days with standard therapy.<br />

It is unclear why an intervention<br />

aiming at a reduction of smoothmuscle<br />

mass would not affect<br />

FEV1. Given that the number of<br />

exacerbations is reduced with no<br />

change in FEV1, it <strong>may</strong> be that altered<br />

response to the inflammatory triggers<br />

plays a role in addition to the reduction<br />

in smooth-muscle mass.<br />

Complications<br />

Recurrent lung atelectasis secondary<br />

to fibrin plugs has been reported<br />

as an early complication of BT.<br />

In the susceptible patient, high<br />

thermal stimulation <strong>may</strong> lead to<br />

an inflammatory reaction with<br />

microvascular alteration, induced<br />

either by heat or by the release of<br />

inflammatory mediators. Lung abscess<br />

has also been described as a direct<br />

complication; thus, collecting and<br />

publishing safety data continue to<br />

be important. A prospective cohort<br />

study performed as part of the<br />

TASMA trial reported a high incidence<br />

of acute radiologic abnormalities<br />

after BT. Postprocedural CT of<br />

the chest identified four different<br />

radiologic patterns: (1) peribronchial<br />

consolidations with surrounding<br />

ground-glass opacities (94%), (2)<br />

atelectasis (38%), (3) partial bronchial<br />

occlusions (63%), and (4) bronchial<br />

dilatations (19%). These complications<br />

resolved without clinical impact in<br />

virtually all cases.<br />

The author is Head, Department of<br />

Respiratory Medicine, Medical Trust<br />

Hospitals, Cochin<br />

May 2019 / FUTURE MEDICINE / 31

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