Published online Dec 26, 2017. doi: 10.5662/wjm.v7.i4.129
Peer-review started: February 28, 2017
First decision: September 4, 2017
Revised: October 8, 2017
Accepted: November 1, 2017
Article in press: November 1, 2017
Published online: December 26, 2017
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Respiratory diseases, especially asthma, are common in children. While spirometry contributes to asthma diagnosis and management in older children, it has a limited role in younger children whom are often unable to perform forced expiratory manoeuvre. The development of novel diagnostic methods which require minimal effort, such as forced oscillation technique (FOT) is, therefore, a welcome and promising addition. FOT involves applying external, small amplitude oscillations to the respiratory system during tidal breathing. Therefore, it requires minimal effort and cooperation. The FOT has the potential to facilitate asthma diagnosis and management in pre-school children by faciliting the objective measurement of baseline lung function and airway reactivity in children unable to successfully perform spirometry. Traditionally the use of FOT was limited to specialised centres. However, the availability of commercial equipment resulted in its use both in research and in clinical practice. In this article, we review the available literature on the use of FOT in childhood asthma. The technical aspects of FOT are described followed by a discussion of its practical aspects in the clinical field including the measurement of baseline lung function and associated reference ranges, bronchodilator responsiveness and bronchial hyper-responsiveness. We also highlight the difficulties and limitations that might be encountered and future research directions.
Core tip: Respiratory diseases, such as asthma, are especially common in children. Although their diagnosis and management are facilitated by using spirometry in older children, the use of the latter remains limited in younger children because of their inability to perform forced expiratory manoeuvre. Therefore, the use of new methods which require minimal effort and cooperation from children, such as the forced oscillation technique (FOT) is a welcome and promising addition to identify children with underlying airway function abnormalities. In this article, we review the available literature on the use of FOT in childhood asthma.
- Citation: Alblooshi A, Alkalbani A, Albadi G, Narchi H, Hall G. Is forced oscillation technique the next respiratory function test of choice in childhood asthma. World J Methodol 2017; 7(4): 129-138
- URL: https://www.wjgnet.com/2222-0682/full/v7/i4/129.htm
- DOI: https://dx.doi.org/10.5662/wjm.v7.i4.129
Asthma is the most common chronic childhood disease worldwide[1]. It is often difficult to diagnose in infants and young children due to lack of objective measures, such as spirometry[2-4].
Spirometry is the gold standard method to assess lung function in older children and adults. However, obtaining acceptable and repeatable spirometry measures requires significant efforts and high level of cooperation[5-7]. Therefore, the diagnosis and management of childhood asthma remain suboptimal, in young children and older children who cannot perform an acceptable forced expiratory manoeuver.
One potential lung function method suitable for use in young children and older children unable to perform spirometry is the forced oscillation technique (FOT). The FOT was developed by DuBois et al[8] in 1956, to measure the mechanical behaviour of the respiratory system. Over the years, the FOT has been used in research and more recently in clinical practice[9-12]. The application of FOT has expanded to the point where commercial equipment are now widely available. Standardized approaches for the collection of FOT outcomes have been established by the European Respiratory Society (ERS) and the American Thoracic Society (ATS) in pre-school children[9].
One significant advantage of the FOT is its application during tidal breathing and the subsequent reduction in the level of active participation and cooperation required from the individual being tested. As a result, this technique can be feasibly used in children as young as two years of age[13]. Consequently, the FOT opens new frontiers in the application of objective measurements of respiratory function in young children and offers improvements in the diagnosis and management of asthma in young children.
In this review we have summarised the available literature on the use of FOT in childhood asthma. The technical aspects of FOT are briefly described followed by a discussion of its practical aspects in the clinical field, including the measurement of baseline lung function and associated reference ranges, bronchodilator responsiveness and bronchial hyper-responsiveness. We also highlight the difficulties and limitations that might be encountered and future research directions.
The basic principle of FOT involves the application of external signals into the respiratory system and measuring the resulting response of that system[10]. This response is termed the respiratory system impedance (Zrs). The Zrs can be determined when flow and pressure are measured across a known frequency range at the airway opening and is represented as the resistance (Rrs) and reactance (Xrs) of the respiratory system
Zrs = Pao / V’ao = Rrs + j Xrs
where Pao is the pressure V’ao is the flow measured at the airway opening and j = √ (-1)
Resistance (Rrs) represents the component of Zrs that is a function of both Pao and V‘ao, equating to the resistive properties of the respiratory system. Reactance (Xrs) is the out-of-phase component that is a function of both Pao and volume, reflecting elatic recoil of the respiratory system. Both Rrs and Xrs are determined when oscillatory (sound waves) signals are applied at the airway opening (and hence to the whole respiratory system).
It is important to be aware that the respiratory impedance is frequency-dependent: (1) At low frequencies, (2-4 Hz) as the oscillations are transmitted more distally into the lungs, Rrs and Xrs tend to reflect the properties of the peripheral respiratory system; (2) at higher frequencies, (> 20 Hz) the Zrs reflects the resistive and inertive properties of the proximal conducting airways.
It is critical to note that Rrs and Xrs reflect mechanical properties of the entire respiratory system, including the airway, lung and chest wall[10]. It is therefore not possible to assign specific anatomical changes (for example central airway obstruction) to changes in any one FOT outcome at a specific frequency (see below for further details).
As the airway and the lung tissue are both flow and volume-dependant, the characteristic of the oscillatory signals used is important. These signals can take any of the following common forms: (1) Single frequency; (2) impulse oscillation system[14]; (3) pseudorandom noise (the simultaneous application of several frequency components).
The oscillation signal that is most commonly applied encompasses the medium frequency range, generally including frequencies between 2 Hz and 20 Hz. The advantage of using mid-range frequencies is that the oscillatory signals can be superimposed on the tidal breathing and therefore result in a broader application[10]. For more details reviews on the technical aspects of FOT, readers are directed to review (oscillation mechanics of respiratory system) by Bates et al[15].
This section summaries the available equipment, feasibility, repeatability, and finally the collection and reporting of FOT data in young children.
The availability of FOT commercial equipment has resulted in the increased uptake of FOT in clinical practice and especially in young children. The FOT equipment includes (Figure 1): (1) A loudspeaker or similar to generate the oscillatory signals; (2) a pneumotachograph and pressure transducers to measure pressure and flow; (3) a mouth piece containing a bacterial filter to prevent cross infection between patients. A typical arrangement of the forced oscillatory impedance measurement, adapted from[9].
The feasibility and success rates of FOT are, understandably, age-dependent. The success rate in children 4 years of age and older exceeds 80%[13,16,17], while it ranges from 83% to 100% in healthy children aged 2-7 year[13,18] and between 57% to 100% in children with asthma aged between 3 to 5 years[13,16]. In young children with acute asthma the success rate of FOT reduced to 24% and 65% in three and eight-year-old children respectively, However, it was higher than that of spirometry in the same population[12]. Furthermore, the feasibility of FOT measurements increases noticeably with practice in children.
The feasibility of FOT with challenge testing has been assessed in several research studies and has been shown to be feasible in young children using either inhaled adenosine monophosphate (AMP)[19], free running[20], methacholine[21-23], hypertonic saline[21], cold air[24] or mannitol challenge[25].
For adequate collection of the data, the child should be seated with their back straight and their neck either in the neutral position or slightly extended. FOT is usually performed with the mouthpiece which incorporates a bacterial filter and a nose clip-on. A staff member or a parent needs to support the child’s cheeks as well as the floor of his mouth, as shown in Figure 2. An acquisition period should cover several breathing cycles, typically lasting 8-16 s. The results, computed as the mean value of the three to five acceptable measurements, also include the measurement of the coefficient of variation calculated from the standard deviation (SD) of the measurements. Acceptable measures are the one which have no artefacts such as leak, incomplete expiration, glottis closure, swallowing and the child obstructing the mouthpiece with their tongue are easily identified[9] (Figure 2).
Repeatability is an important issue when considering the role of a lung function measures. The short-term repeatability of FOT in heathy children has been assessed and it is summarized in Table 1 below. The long term (two weeks) and short term repeatability were both similar[19].
Commonly reported FOT outcomes include resistance (Rrs), reactance (Xrs) at different frequencies, resonance frequency (Fres), frequency dependence (Fdep), and the area under reactance curve (AX), as illustrated in Figure 3. The reported Rrs variable includes, in the same measurement, the Rrs of the airway, that of the chest wall, and that of the lung tissue. As airway Rrs dominates Rrs in the mid frequencies[26], it can be considered a surrogate of airway resistance[27,28]. As frequency decreases to below approximately 4 Hz Rrs will increasing include peripheral respiratory resistance and be reflective of the peripheral airways and the lung. As Xrs, on the other hand, is dominated by elastic properties of the respiratory tissue, reflecting the elastic and inertive properties of the respiratory system, it is negative at low frequencies. The point at which Xrs crosses the zero, representing the inertial properties of the larger airways[29], is called the Fres, which is the frequency at which elastive and inertive properties of the lung are balanced, and which becomes positive at higher frequencies[30]. The Fdep of that resistance is thought to reflect peripheral airway resistance[31], as, for example, in patients with obstructive airway diseases, it is generally higher than normal subjects due to the difference in airway resistance[30]. However, to date there are no studies directly confirming this.
The area under the reactance curve (AX) is the sum of the Xrs from a Xrs at 5 Hz until Fres (i.e., when Xrs is zero, as in Figure 3) [29]. Studies have shown that Xrs and AX are better representative of peripheral airway obstruction than Rrs[29] and that AX and Fres clearly distinguish healthy children from those with small airway disease and asthma[32].
The FOT outcomes alter with growth and therefore need to be reported as both absolute values and as a function of a predicted value. Expressing outcomes as z or SD scores is the most appropriate. Z scores allows the easy estimation of the lower limit of normal (being either -1.64 or -1.96) and avoids the diagnostic uncertainly that can arise when using percent predicted and a fixed cut off for the presence of abnormal lung function[33,34].
Numerous studies have reported reference data in healthy children using a variety of FOT outcomes[13,35-44]. The FOT outcomes are generally reported to change with age, height and gender. There is some variability due to the different ethnicity, gender, age, weight, height, equipment and the methodology used in those studies and it is important that users carefully review potential reference equations to match the populations, equipment and protocols used as closely as possible to their own circumstances[37,45]. Reporting and comparing the relevant z-scores for these measurements simplifies the interpretation as the possible confounders reported earlier have already been taken into consideration when calculating these scores. Table 2 below summarises those studies and shows those differences.
Ref. | Year of publication | Ethnic group - Country of study | Subject number | Age in years | Height (cm) | Reported prediction equation variables |
Frei et al[35] | 2005 | Caucasian - Canadian | 222 | 3-10 | 90-155 | Rrs at 5-35 Hz Xrs at 5-35 Hz Fres, AX |
Dencker et al[36] | 2006 | Caucasian - Scandinavian | 360 | 2-11 | 90-162 | Rrs at 5-20 Hz Xrs at 5-20 Hz Fres |
Amra et al[37] | 2008 | Asian - Iranian | 509 | 5-18 | 127-197 | Rrs at 5-25 Hz Xrs at 5-25 Hz |
Nowowiejska et al[38] | 2008 | Caucasian - Polish | 626 | 3-18 | 95-193 | Rrs at 5-35 Hz Xrs at 5-35 Fres |
Vu et al[39] | 2008 | Asian - Vietnamese | 175 | 6-11 | 111-154 | Rrs at 8 Hz Xrs at 8 Hz |
Vu et al[40] | 2010 | Asian - Vietnamese | 95 | 6-11 | 111-134 | Rrs at 8 Hz Xrs at 8 Hz |
Calogero et al[41] | 2010 | Italian | 163 | 2-6 | 101-114 | Rrs at 6-10 Hz Xrs at 6-10 Hz |
Park et al[42] | 2011 | Korean | 133 | 3-6 | 95-121 | Rrs at 5, 10 Xrs at 5, 10 RF, AX |
Calogero et al[43] | 2013 | Caucasian Italian and Australian | 760 | 2-13 | 90-160 | Rrs at 6, 8, 10 Hz Xrs at 6, 8, 10 Hz Fres, AX |
Shackleton et al[44] | 2013 | Mexican | 584 | 3-5 | 87-119 | Rrs at 6 and 8 Hz Xrs at 6 and 8 Hz |
Hagiwara et al[46] | 2014 | Japanese | 537 | 6-15 | 111-174 | Rrs at 5 and 20 Hz Rrs5-20 |
By incorporating measurements of bronchodilator Responsiveness (BDR) and bronchial hyper-responsiveness (BHR), the utility of FOT to assist in the diagnosis of asthma in young children may be increased[47]. The official ATS/ERS statement on pulmonary function testing in preschool children stated that FOT is a promising tool in diagnosing and following up children with asthma[9]. Other studies also suggest that the FOT may be useful in assessing asthma control, compliance to medication, and in the follow up of these young children[48].
In children aged 5 years and above, spirometry adequately assesses baseline lung function and the results correlate well with asthma severity[49]. When comparing spirometry and FOT in children older than 6 years of age, those with asthma have lower baseline FOT than with spirometry when compared to healthy children[50]. Whilst few studies have examined baseline airway obstruction in young children with asthma using FOT. Klug et al[51] reported that young children with stable asthma demonstrated impaired baseline lung function when assessed using FOT. Oostveen et al[17] showed that, when compared to healthy 4-year-old children, those children with persistent wheeze had worse baseline lung function than those with transient wheeze as assessed by FOT. Children with a history of recurrent wheeze and/or asthma recruited from clinics tend to have worse lung function expressed in FOT even when asymptomatic[18,52]. However, other studies conducted in children with history of wheeze and recruited from the community have similar FOT outcomes to healthy children[53,54]. The ability of FOT to determine asthma severity remains therefore questionable, especially in children on asthma medication[49]. Further studies are therefore needed to explore the relationship between baseline lung function using FOT and asthma severity in young children with asthma.
The assessment of bronchodilator responsivess using FOT in young children with asthma has been encouraged in clinical practice[10]. Critical the the assessment of increased responsiveness associated with asthma is an understanding of the response of healthy children with bronchodilators. The assessment of change in FOT outcomes during the assessment of BDR has been expressed as absolute change or relative change from the baseline in the Rrs, Xrs and AX, the use of AX has been explored in a few studies and is shown to be a good outcome in assessing the BDR in children with asthma[17,29,32].
In the most recent study which assessed BDR in children (Calogero et al[43]), cut-offs for a positive BDR in healthy Caucasian children were defined as 34% and 50% for Rrs and Xrs, respectively expressed as a relative change from the baseline lung function. In a study looking at the uses of pseudorandom FOT signal (4–48 Hz) in quantifying BDR in healthy young children, children with cystic fibrosis, neonatal chronic lung disease and children with asthma and/or current wheeze, Thamrin et al[53] recommended a positive BD response of 40% and 65% for Rrs and Xrs, respectively expressed as a relative change from the baseline lung function[53]. Another study, conducted by Oostveen et al[17] in Belgium on 4 years old healthy and wheezy children (n = 325) using FOT, recommended a positive BDR at Rrs 4 of 43% expressed as absolute changes. Cut-off values for BDR in previous studies are summarized and listed in Table 3. In general, > 30% decrease in Rrs after bronchodilator is suggestive of asthma.
Ref. | Ethnic group age, yr | n | Variable | Dose | Waiting time (n) | Absolute BDR | Relative BDR, (%) |
Thamrin et al[53], 2007 | Healthy Caucasian (3-7) | 78 | Rrs 6,8,10 Xrs 6,8,10 | Salbutamol 600 mg | 15 | Rrs 6 -35.0, -3.1 Rrs 8 -35.0, -4.4 Rrs 10 -32.3, -3.7 Xrs 6 -0.27, 1.66 Xrs 8 - 0.04, 1.82 Xrs 10 -0.00, 2.03 | Rrs 6: 42% Rrs 8: 37% Rrs 10: 39% Xrs 6: 61% Xrs 8: 67% Xrs 10: 63% |
Thamrin et al[53], 2007 | Asthmatics Caucasian (3-7) | 57 | Rrs 6, 8, 10 Xrs 6, 8, 10 | Salbutamol 600 µg | 15 | Rrs 6 -37.0, 8.8 Rrs8 -33.1, 9.7 Rrs 10 -33.4, 4.5 Xrs 6 -0.21, 2.30 Xrs 8 -0.13, 2.47 Xrs 10 -0.12, 2.22 | Rrs 6: 42% Rrs 8: 37% Rrs 10: 39% Xrs 6: 61% Xrs 8: 67% Xrs 10: 63% |
Lan Vu et al[39], 2008 | Healthy Vietnamese (6–11) | 175 | Rrs 8 Hz Xrs 8 Hz | Salbutamol 200 µg | 5 | Rrs 8 -11.8,13.4 Xrs 8 4.09, - 5.78 | Rrs 8: 38% Xrs 8: 16% |
Lan Vu et al[40], 2010 | Asthmatic Vietnamese (6-10) | 103 | Rrs 8 Hz Xrs 8 Hz | Salbutamol 200 µg | 5 | -- | Rrs 8: 13% Xrs: 32% |
Oostveen et al[55], 2010 | Asthmatic Belgian -4 | 313 | Rrs 4 | Salbutamol 200 µg | 15 | -- | Rrs 4: 22% AX: 15.77% |
Calogero et al[41], 2010 | Healthy Italian (3-6) | 163 | Rrs 8 Xrs8 | Salbutamol 200 µg | 15 | -- | Rrs 8: 35% Xrs 8: 34%-61% |
LEE et al[57], 2012 | Healthy Korean | 161 | Rrs 5, 10, 15, 20, 25, 35 Xrs 5, 10, 15, 20, 25, 35 | Salbutamol 200 µg | 15 | Rrs 5 -0.127 Rrs 10 -0.098 Rrs 15 -0.073 Rrs 20 -0.056 Rrs 25 -0.056 Rrs 35 -0.057 Xrs 5 0.062 Xrs 10 0.057 Xrs 15 0.059 Xrs 20 0.044 Xrs 25 0.033 Xrs 35 0.054 Fres -2.167 | Rrs 5: 11.8 Rrs 10: 10.8 Rrs 15: 8.7 Rrs 20: 6.972 Rrs 25: 7.029 Rrs 35: 6.095 Xrs 5: 13.474 Xrs 10: 25.946 Fres: 10.457 |
Calogero et al[43], 2013 | Healthy Australian and Italian (2-16) | 502 | Rrs 6, 8, 10 Xrs 6, 8, 10 Fres, AX | Salbutamol 200 µg | 15 | Rrs 6 -2.9 Rrs 8 -2.74 Rrs 10 -2.39 Xrs 6 -1.80 Xrs 8 - 1.93 Xrs 10 -1.90 AX -33 Fres -12 | Rrs 6: 34 Rrs 8: 32 Rrs 10: 31 Xrs 6: 50 Xrs 8: 65 Xrs 10: 74 AX: 81 Fres: 47 |
The previous studies in healthy and wheezy young children have not conducted a ROC analysis to formally establish the sensitivity and specificity of a certain BDR cut off to be assessed. Limitations to the wider use of FOT in assessing BDR include the variability of medications, their timing and dosage between the different studies (Table 3).
Bronchial hyper-responsiveness, usually assessed using spirometry, is the gold standard for confirming a diagnosis of asthma in older children and adults[58,59]. However, false negative or false positive results can occur in young children who cannot perform an acceptable manoeuvre. BHR has been assessed in young children using other methods including FOT, interrupter technique, whole-body plethysmography and transcutaneous oxygen measurement SPO2[5,47,60-63].
Bronchial hyper-responsiveness studies comparing FOT with different lung function measures have reported FOT to be as effective as spirometry[63-69] and as sensitive as body plethysmography[70] and transcutaneous PO2[50] in older children with asthma. BHR has been assessed using FOT in children younger than 7 years of age with a range of challenge tests including adenosine monophosphate (AMP)[19], cold air[24], normal saline[21] methacholine[22,62,63,66,68,71], mannitol[25] and exercise[20,72] demonstrating that FOT can be reliably used in young children for challenge testing.
FOT characterization of BHR has been shown to be correlated to asthma severity[73] and to be sensitive to the response to immune therapy[74]. Another study has shown that cough variant asthma showed less BHR in comparison to classical asthma children[75].
Despite the above studies have clearly demonstrated the use of FOT to assess BHR in children, there are few studies demonstrating the best cut off value of BHR between healthy and children with asthma using FOT. Further work is needed before establishing FOT use as clinical tool to assess BHR in children.
Although forced oscillation technique can contribute to the diagnosis and management of childhood asthma, it has some limitations. Although, unlike spirometry, it does not require forced expiratory manoeuvres, it still require some cooperation by children to achieve successful repeatable measures. It is therefore both age and cooperation dependant. The practical advantage of the availability and affordability of different FOT commercial equipment, the Rrs and Xrs output are not always measured at the same frequencies by all these devices. This makes the comparison between different studies challenging. The standardization of the available commercial equipment is therefore still needed and FOT guidelines are currently being reviewed by the ATS and ERS.
As the available FOT reference equations have been constructed in specific populations, these findings cannot be generalised to other ethnic groups. Further studies are therefore still required to establish FOT reference values in other populations or ethnic groups. The assessment of BDR using FOT is not widely implemented because of differences amongst the relevant studies, including differences in the medications used, as well as their timing and dosage. Further studies are therefore required to establish an international standard protocol for this assessment as currently BDR still has not been studied in relation to recent symptoms in young children with wheeze, developing such studies would help not only in the follow up of children with wheeze, but also to ascertain the level of control of asthma symptoms and the compliance to medication in children with asthma.
Further research is also required to assess BHR, particularly in young children, in addition to standardise the use of FOT in young children for BHR assessment.
Recently there are new studies that have reported Rrs or Xrs from either expiration or inspiration (or both), including flow limitation within a breath. Those studies suggest that this approach is more sensitive than standard reporting of FOT. However, significant work is required prior to the intrdocution of these outcomes into clinical practice and this remains an area for the future studies[76,77].
In conclusion, with the relatively high prevalence of childhood asthma, FOT has been proven to be a useful tool to aid in its diagnosis and management especially in children unable to perform spirometry. As the recent availability of commercial equipment has increased its use both in research and in clinical practice, clinicians have to understand the emerging role of FOT in clinical practice and how to interpret its results in order to optimise clinical management of children with asthma.
Manuscript source: Invited manuscript
Specialty type: Medical laboratory technology
Country of origin: United Arab Emirates
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