Jump to: Page Content, Site Navigation, Site Search,
You are seeing this message because your web browser does not support basic web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.
time to change asthma guidelines?
Helen Reddel Insitute of Respiratory Medicine, Royal Prince
Alfred Hospital and University of Sydney, PO Box M77, Camperdown, NSW
2050, Australia
Correspondence to:
Dr Reddel hkr{at}mail.med.usyd.edu.au
Peak expiratory flow varies throughout the day in normal
subjects, and this diurnal variation is increased in people with asthma.1 Current asthma guidelines recommend that diurnal
variability of the peak expiratory flow rate should be calculated when
diagnosing asthma and assessing its severity, 2-7
including during exacerbations.
3 4
Diurnal variability of
peak flow has been used as a marker of airway
responsiveness,
8 9
particularly in epidemiological studies,
10 11
and as an outcome measure in clinical
asthma trials.12 However, there are problems associated
with its use.
Cumbersome calculations
Number of daily observations
Impact of timing
Effect of drug regimens
Summary points
Variation in peak flow over days or weeks provides helpful
information about asthma control
Asthma guidelines recommend that diurnal peak flow variability is
calculated to provide an index of airway lability
These calculations are too time consuming for normal clinical practice
Factors such as the time of recording or recent use of
2
agonist drugs result in minor changes in peak flow, but can
cause large errors in diurnal variability
Diurnal variability may fail to detect important changes in lung
function
An alternative, simpler index of peak flow variation such as the lowest
morning peak flow expressed as percentage of the patient's personal
best peak flow value should be evaluated for inclusion in asthma
guidelines
Although diurnal variability in peak flow has been included in
asthma guidelines for many years, doctors in primary and secondary care
settings rarely use it, because of the cumbersome calculations
involved. Several alternative equations may be used. The most
common are the amplitude percentage mean ((maximum
minimum)/mean)
or the amplitude percentage maximum ((maximum
minimum)/maximum), calculated for each day, and then averaged over a period of 1 to 2 weeks.13 Determining the amplitude percentage mean from as
few as 7 days of twice daily peak flow readings for one patient (see
fig 1) is complicated and tedious, even if calculator shortcuts (which
may increase the possibility of error) are used. Furthermore, the
calculations take too long for a standard medical consultation. Electronic recording and computerised processing of peak flow data are
still prohibitively expensive for general practice, and also have
pitfalls. For example, if a program is written to calculate daily
amplitude as (evening
morning) instead of (maximum
minimum), some
daily values may be negative, resulting in an underestimation of
average diurnal variability. It should be noted that the various equations currently used to estimate diurnal variability give results
that are not directly comparable.

View larger version (44K):
[in a new window]
Fig 1.
Peak expiratory flow (PEF) chart of a 36 year
old man. Diurnal variability been calculated for the last 7 days
only
Most asthma guidelines state that diurnal variability should
be calculated from two sets of peak flow readings each day
taken in
the morning and afternoon/evening.2-7 However, several
studies have now shown that diurnal variability is grossly underestimated unless peak flow is recorded four or more times a
day.
14 15
For example, one study showed that only
20%-45% of "true" diurnal variability (based on 13 daily peak
flow readings) was detected from two daily peak flow
readings.15 Two hourly peak flow readings are currently
used in diagnosing occupational asthma, but patients in normal clinical
practice often have difficulty recording peak flow even twice
daily,16 resulting in bias through non-compliance.17
A corollary of the above is that if patients record only two peak
flow sessions per day, the time at which peak flow is recorded may have
a major impact on the estimated diurnal variability. In most patients,
the acrophase (peak) of peak flow occurs at approximately 1400 to
1600,1 but asking patients to record peak flow at this
time on workdays is generally impractical. A delay in recording the
second daily set of peak flow readings which leads to a difference of
only 50 l/min in absolute peak flow may cause an underestimation of
diurnal variability for that day of as much as 50% (fig 2).
Clinical trials often try to standardise by specifying time
"windows" within which peak flow measurements should be performed.
Doing this may, however, introduce more error, because the timing of
the peak flow acrophase seems to be determined by the time at which the
patient wakes on that day, and, unlike other circadian rhythms, changes
almost immediately with a change in waking time.18 In one
study, peak flow determinations performed "immediately upon waking"
were recorded, on average, 81 minutes later on weekends than on
weekdays.19 Gannon et al found that the peak flow
acrophase occurred more than 2 hours later on rest days than on
workdays,14 presumably because of differences in waking
time. Thus, normal lifestyle variations can have a substantial impact
on estimated diurnal variability.

View larger version (21K):
[in a new window]
Fig 2.
A sample stylised cosinor distribution of peak
flow with a bathyphase (trough) of 300 l/min at 0400 and an acrophase
(peak) of 400 l/min at 1600. "True" diurnal variability (amplitude
percentage mean) is (400-300)×100/350=29%. Diurnal variability for
peak flow recorded at 0600 and 2000 is (375-305)×100/340=21%, while
that for peak flow recorded at 0600 and 2200 is
(350-305)×100/328=14%
The validity of diurnal variability as a measure of asthma
severity was originally established when the recommended treatment
regimen for
2 agonist drugs was routine
inhalation two to four times daily, but its continuing validity cannot
be assumed now that
2 agonists are usually
taken only on demand. If a
2 agonist drug is
inhaled to relieve symptoms rather than at a routine time, the elapsed
time before the next scheduled peak flow recording is likely to vary
from day to day, and errors caused by the augmentation of peak flow by
a residual bronchodilator effect may occur. Once again (as in fig 2), a
small change in the absolute peak flow can cause a large change in the
calculated diurnal variability.
2 agonist drugs. This is also standard
practice in most clinical trials. However, in clinical practice,
patients with asthma that is poorly controlled cannot be asked to delay taking a needed
2 agonist for several hours so
that a "pretreatment" peak flow can be recorded. In a recent study
we found that people who used a bronchodilator more than 2.2 times a
day were unable to delay its use for 4 hours before 31% of scheduled
peak flow measurements.20 Including these potentially
augmented peak flow values resulted in positive bias in the average
morning peak flow and average evening peak flow, but diurnal
variability was affected in an unpredictable way. It was increased or
decreased on any day depending on whether the morning peak flow or
evening peak flow, or both, were augmented by bronchodilator use before
the recording.21
2 agonist treatment (provided peak flow is
recorded consistently before this medication is taken), as the
frequency of use of short acting
2 agonist
drugs usually falls. Long acting
2 agonists
themselves increase evening and, to a greater extent, morning peak
flow,22 with a resulting reduction in peak flow amplitude,
and hence a reduction in diurnal variability.
Diurnal variability and exacerbations
Calculating diurnal variability in peak flow during
exacerbations of asthma is included in two current guidelines. The
guidelines of the British Thoracic Society recommend that diurnal
variability should be used to assess whether a patient admitted to
hospital for an exacerbation of asthma can be discharged home safely.
However, not all asthma exacerbations are associated with increased
variability in peak flow. During presumed viral asthma exacerbations in
patients with previously well controlled asthma, diurnal variability
did not increase despite an average fall in morning peak flow of
27%.23 In these exacerbations, both daily peak flow
amplitude and mean peak flow fell, so that the amplitude percentage
mean was unchanged. Diurnal variability may thus fail to detect
important and sustained changes in lung function, and cannot be
recommended for assessing the severity of asthma exacerbations.
Other indices of variation in peak flow
Despite the problems with diurnal variability discussed
above, visual inspection of peak flow charts suggests that peak flow
variation over a period of days or weeks can provide helpful
information about the severity of asthma and the response to
treatment.25-27 This process of visual inspection has
been validated for occupational asthma,28 but requires
considerable experience, and is thus not appropriate for inclusion in
asthma guidelines for general clinical practice. Other measures of peak
flow variation such as the standard deviation or coefficient of
variation have been examined,24 but these indices require
computerised processing and are therefore not currently suitable for
normal clinical practice.
Conclusions
In the absence of a "gold standard," clinical practice
guidelines for assessing asthma severity and monitoring asthma control
usually include several measures such as symptoms, lung function, and
airway lability. Airway lability is estimated by diurnal variability
when bronchial provocation testing is unavailable. These clinical
practice guidelines must be scientifically valid, but the extent of
their implementation, and hence their effectiveness, also depends
greatly on how simple and straightforward they are in
practice.33 Diurnal variability seems to be deficient on both counts
its calculation is subject to errors and is impractical clinically in that it takes too long to calculate. We propose that
asthma guidelines on peak expiratory flow monitoring be reviewed, and
that a simpler measure such as the lowest % personal best should be
evaluated as an index of peak flow lability in assessing asthma
severity and monitoring of asthma control.
| |
Acknowledgments |
|---|
HR is a research scholar with the National Health and Medical Research Council of Australia. CJ is chairman of the National Asthma Campaign of Australia. AW is a member of the executive of the Global Initiative for Asthma and was a participant and author for the conference report, "The assessment and treatment of asthma."
| |
References |
|---|
| 1. | Hetzel MR, Clark TJH. Comparison of normal and asthmatic circadian rhythms in peak expiratory flow rate. Thorax 1980; 35: 732-738[Abstract]. |
| 2. | National Asthma Education and Prevention Program. Guidelines for the diagnosis and management of asthma expert panel. Report 2. Bethesda, MD: National Institutes of Health , 1997(NIH publication No 97-4051, NHLBI.) |
| 3. | British Thoracic Society, National Asthma Campaign and Royal College of Physicians of London in association with the General Practitioner in Asthma Group, British Association of Accident and Emergency Medicine, British Paediatric Respiratory Society, Royal College of Paediatric and Child Health. The British guidelines on asthma management. 1995 review and position statement. Thorax 1996; 52(suppl 1): S1-21. |
| 4. | Global Initiative for Asthma. In: Global strategy for asthma management and prevention. Bethesda, MD: National Institutes of Health , 1995(NIH publication No 96-3659A, NHLBI.) |
| 5. | National Heart Lung and Blood Institute. International consensus report on the diagnosis and management of asthma. Clin Exp Allergy 1992; 22(suppl 1): 1-72. |
| 6. | Newhouse MT, ed. The assessment and treatment of asthma: a conference report. J Allergy Clin Immunol 1990; 85: 1098-1111[Medline]. |
| 7. | National Asthma Campaign [Australia]. Asthma management handbook. Melbourne: National Asthma Campaign , 1998. |
| 8. | Ryan G, Latimer KM, Dolovich J, Hargreave FE. Bronchial responsiveness to histamine: relationship to diurnal variation of peak flow rate, improvement after bronchodilator, and airway calibre. Thorax 1982; 37: 423-429[Medline]. |
| 9. | Neukirch F, Liard R, Segala C, Korobaeff M, Henry C, Cooreman J. Peak expiratory flow variability and bronchial responsiveness to methacholine. Am Rev Respir Dis 1992; 146: 71-75[Medline]. |
| 10. | Lebowitz MD, Krzyzanowski M, Quackenboss JJ, O'Rourke MK. Diurnal variation of PEF and its use in epidemiological studies. Eur Respir J 1997; 10 (suppl 24): 49-56s. |
| 11. | Higgins BG, Britton JR, Chinn S, Cooper S, Burney PGJ, Tattersfield AE. Comparison of bronchial reactivity and peak expiratory flow variability measurements for epidemiologic studies. Am Rev Respir Dis 1992; 145: 588-593[Medline]. |
| 12. | Toogood JH, Andreaou P, Baskerville J. A methodological assessment of diurnal variability of peak flow as a basis for comparing different inhaled steroid formulations. J Allergy Clin Immunol 1996; 98: 555-562[Medline]. |
| 13. | Connolly CK. The effect of bronchodilators on diurnal rhythms in airway obstruction. Br J Dis Chest 1981; 75: 197-203[Medline]. |
| 14. |
Gannon PFG, Newton DT, Pantin CFA, Burge PS.
Effect of the number of peak expiratory flow readings per day on the estimation of diurnal variation.
Thorax
1998;
53:
790-792 |
| 15. | D'Alonzo GE, Volker WS, Keller A. Measurements of morning and evening airflow grossly underestimate the circadian variability of FEV1 and peak expiratory flow rate in asthma. Am J Resp Crit Care Med 1995; 152: 1097-1099[Abstract]. |
| 16. |
Côté J, Cartier A, Malo J-L, Rouleau M, Boulet L-P.
Compliance with peak expiratory flow monitoring in home management of asthma.
Chest
1998;
113:
968-972 |
| 17. | Higgins BG, Britton JR, Chinn S, Jones TD, Jenkinson D, Burney PGJ, et al. The distribution of peak flow variability in a population sample. Am Rev Respir Dis 1989; 140: 1368-1372[Medline]. |
| 18. | Clark THJ, Hetzel MR. Diurnal variation of asthma. Br J Dis Chest 1977; 71: 87-92[Medline]. |
| 19. | Reddel HK, Ware SI, Salome CM, Jenkins CR, Woolcock AJ. Pitfalls in processing electronic spirometric data in asthma. Eur Respir J 1998; 12: 853-858[Abstract]. |
| 20. | Reddel HK, Ware SI, Salome CM, Marks GB, Jenkins CR, Woolcock AJ. Standardization of ambulatory peak flow monitoring: the importance of recent beta 2-agonist inhalation. Eur Respir J 1998; 12: 309-314[Abstract]. |
| 21. | Salome C, Reddel H, Ware S, Jenkins C, Woolcock A. Diurnal variability from twice daily PEF is unreliable for assessment of asthma severity. Am J Resp Crit Care Med 1998; 157: A631. |
| 22. | Dahl R, Earnshaw JS, Palmer JB. Salmeterol: a four week study of a long-acting beta-adrenoceptor agonist for the treatment of reversible airways disease. Eur Respir J 1991; 4: 1178-1184[Abstract]. |
| 23. | Reddel HK, Ware SI, Marks GB, Salome CM, Jenkins CR, Woolcock AJ. Differences between asthma exacerbations and poor asthma control. Lancet 1999; 353: 364-369[Medline]. (Erratum. Lancet 1999;353:758.) |
| 24. | Siersted HC, Hansen HS, Hansen N-CG, Hyldebrandt N, Mostgaard G, Oxhoj H. Evaluation of peak expiratory flow variability in an adolescent population sample. The Odense schoolchild study. Am J Resp Crit Care Med 1994; 149: 598-603[Abstract]. |
| 25. | Turner-Warwick M. On observing patterns of airflow obstruction in chronic asthma. Br J Dis Chest 1977; 71: 73-86[Medline]. |
| 26. | Cross D, Nelson HS. The role of the peak flow meter in the diagnosis and management of asthma. J Allergy Clin Immunol 1991; 87: 120-128[Medline]. |
| 27. | Brand PL, Duiverman EJ, Postma DS, Waalkens HJ, Kerrebijn KF, Van Essen-Zandvliet EE. Peak flow variation in childhood asthma: relationship to symptoms, atopy, airways obstruction and hyperresponsiveness. Eur Respir J 1997; 10: 1242-1247[Abstract]. |
| 28. | Côté J, Kennedy S, Chan-Yeung M. Quantitative versus qualitative analysis of peak expiratory flow in occupational asthma. Thorax 1993; 48: 48-51[Abstract]. |
| 29. | Reddel HK, Salome CM, Peat JK, Woolcock AJ. Which index of peak expiratory flow is most useful in the management of stable asthma? Am J Resp Crit Care Med 1995; 151: 1320-1325[Abstract]. |
| 30. | Connolly C, Prescott R, Alcock S, Gatnash A. Actual over best function as an outcome measure in asthma. Respir Med 1994; 88: 453-459[Medline]. |
| 31. | Meijer RJ, Kerstjens HAM, Postma DS. Comparison of guidelines and self-management plans in asthma. Eur Respir J 1997; 10: 1163-1172[Abstract]. |
| 32. | Fishwick D, Beasley R. Use of peak-flow based self-management plans by adult asthmatic patients. Eur Respir J 1996; 9: 861-865[Medline]. |
| 33. |
Grol R, Dalhuijsen J, Thomas S, Veld C, Rutten G, Mokkink H.
Attributes of clinical guidelines that influence use of guidelines in general practice: observational study.
BMJ
1998;
317:
858-861 |
(Accepted 26 March 1999)
Read all Rapid Responses