When should oxygen be given to children at high
altitude?
Primary Reviewers: Rami Subhi 1,
Secondary Reviewer: Dr
Robert Tasker 2
1University of Melbourne,
Australia
2Department of Paediatrics,
University of Cambridge, UK
The World Health
Organization has produced guidelines for the
management of common illnesses in hospitals with limited resources.
This series reviews the scientific evidence behind WHO's
recommendations. The WHO guidelines, and more reviews are available at
http://www.who.int/child-adolescent-health/publications/CHILD_HEALTH/PB.htm
This
review addresses the question: This review
addresses the question: When should oxygen be given to children at high
altitude?
Introduction:
Each year pneumonia
causes more than 3 million deaths in children under 5 years of age
(including neonates), and results in 11-20 million hospitalizations.[1;2]
98% of deaths from pneumonia in children occur in developing countries.[3]
Hypoxaemia is a significant risk factor for mortality,[4-6]
and a strong predictor of radiographic pneumonia.[5;7;8]
The recognition of hypoxaemia among children with pneumonia is crucial
in management, may assist in diagnosis and helps determine
prognosis.
Currently the World
Health Organization (WHO) recommends clinical signs to guide the
starting and stopping of oxygen therapy. Where pulse oximetry
is available, WHO recommends an arterial oxygen saturation measured by
pulse oximetry (SpO2) of 90% as the threshold for oxygen administration.[9] The latter approach
may only be implementable in settings where oxygen supplies are not
limited. At high altitudes, where normal oxygen saturation
levels are lower than at sea level, a threshold of 90% may be less
relevant. A clearer definition of the lower limit of normal
SpO2 among children at different altitudes would enable protocols for
oxygen therapy to be adapted to local conditions, and enable resources
to be appropriately applied.
To assist in the
identification and management of hypoxaemia, this study aimed to use
the published literature to define normal values of SpO2 in children
and to propose a model for defining hypoxaemia at varying altitudes.
Methodology
Search strategy and inclusion criteria
A review was
conducted using OVID Medline (1950-August week 2 2007) and Embase
(1980-2007 week 33). The abstracts of potentially relevant
publications were reviewed, and the complete texts of studies
addressing the inclusion criteria (outlined below) were
obtained. References cited by these articles, as well as the
link option ‘Find similar’ in OVID and Embase were
then used to widen the search.
Studies were included if they reported SpO2 of healthy, awake children
aged 1 week to 12 years, permanently residing in the study
location. In order to ensure that study data used in the
analysis provides a reasonable estimate of the normal SpO2 of the
populations it represents, we set the cut-off for sample size as
greater than 30 children. Studies including SpO2 measurements of
preterm, hospitalised, anaesthetised or chronically ill children were
excluded. Only papers in English were reviewed, and no
attempts were made to obtain unpublished data.
The inclusion
criteria were designed to include the largest sample of children for
whom such data are available, but it was considered important to
exclude studies that described normal episodes of desaturation during
the foetal-neonatal transition throughout the first hours of
life. Although recovery to adult SpO2 levels has been
previously demonstrated within 15 minutes after birth [10], a
minimum age of one week was set to ensure that such normal fluctuations
were not represented.
Data extracted from
studies were age, sample size, mean (standard deviation) SpO2, oximeter
type, and altitude above sea level. Where the standard
deviation (SD) was not reported, either the 95% confidence interval
(CI) or the standard error (SE) was extracted, depending on the
information reported. Missing standard errors and standard
deviations were then derived from available statistics using standard
methods.[11]
All altitudes less than 100 metres above sea level were considered to
be equivalent to sea level (0 metres). If a study reported
SpO2 for different age categories without providing overall summary
data, one subgroup was chosen to be included in the analysis, on the
basis of the greatest number of subjects and avoiding a sub-group which
included the neonatal period.
We defined hypoxaemia as any SpO2 value at or below the 2.5th centile
for a population of healthy children at a given altitude. If the values
of SpO2 are normally distributed, this definition corresponds to a SpO2
reading of more than 2 standard deviations below the mean.
Statistical
analysis
Data were entered
into Microsoft Excel, and analysed using Stata version 10.12
The 2.5th centile of the distribution of SpO2 values could not be
estimated directly, as only one study in the literature reported this
statistic.[6]
For this reason, the hypoxaemia threshold was estimated by predicting
mean SpO2 based on altitude, and subtracting two standard deviations
from the prediction. The prediction equation was obtained using a
linear random effects meta-regression, which was implemented using the
user-contributed Stata command “metareg”.[13] The between-studies variance
was estimated using restricted maximum likelihood.
Inspection of the
summary statistics reported in Table 1
indicates that the distribution of SpO2 values for many studies is
negatively skewed rather than normally distributed; adding two standard
deviations to the mean produces a value exceeding the theoretical
maximum of 100% for the six studies at 1600m of altitude or less. We
required the outcome to be normally distributed, both to satisfy the
assumptions of the analysis method, and because we wished for the mean
minus 2 SD to correspond to the 2.5th centile. For these
reasons, meta-regression was performed on the log-transformed scale. A
prediction equation for hypoxaemia threshold was derived by subtracting
two standard deviations from the predicted mean SpO2 on the transformed
scale, and back-transforming the resulting equation to the natural
scale.
Results
24 studies
fulfilled the selection criteria.[5-7;14-34]
Eleven studies were subsequently excluded. These
included a study in Peru of a 6 to 18 year old population which did not
meet the age criteria [22],
and one in Nepal of children presenting with cough and coryza.[15] An
additional 6 studies did not report a mean SpO2 value and appropriate
measure of variation, [6;16;20;26;27;35] and 3 studies were excluded
due to having a sample size less than [28;30;31;32]
Mean SpO2,
altitude, sample size and an appropriate measure of variation were
reported in the remaining 13 studies (Table1).
Of these 13 studies, 9 reported a standard deviation, 2 a standard
error and the remaining 2 a 95% confidence interval. One study examined
two populations living at different altitudes [7], reporting summary statistics
separately. Each population was treated as a separate population for
the purpose of the meta-regression. In total therefore, the analyses of
SpO2 values included 14 data points from 13
studies.
Very strong
evidence was found for an association between study altitude and the
study’s mean SpO2 value (p<0.001). The equation
obtained for predicting mean SpO2 at a given altitude was:
The equation obtained for predicting the hypoxaemia threshold at a
given altitude was:
Both prediction equations are graphically depicted in Figure 1. At an
altitude of approximately 2500 metres above sea level, the 2.5th
centile of the distribution of SpO2 in normal, healthy children is 90%.
This decreases to 85% at approximately 3200 metres above sea level.
Discussion
Oxygen therapy has
been shown to improve outcomes in pneumonia.[4;36] Ensuring a reliable
and efficient system for detecting hypoxaemia and supplying oxygen and
having clear and simple guidelines for its use is therefore vital to
good quality paediatric care. This is particularly so in
developing countries given the magnitude of the burden of
pneumonia. And yet, such systems are often of poor quality or
non-existent where they are most needed, where oxygen administration is
often dictated more by availability than by need.
There have been
many hurdles to implementing effective systems for oxygen therapy in
developing countries: the cost and scarcity of cylinder oxygen and the
unreliability of clinical signs in predicting hypoxaemia. In
recent times, the introduction of pulse oximetry in developing country
health facilities has been advocated for its accuracy in detecting
hypoxaemia and cost-effectiveness in limiting oxygen wastage.[37;38]
If pulse oximetry is to be widely used and understood by health
workers, consensus as to the SpO2 level below which oxygen
supplementation should be given is needed.
There are
physiological and ‘safe practice’ arguments for
maintaining SpO2 above 90% at sea level, to ensure that the
relationship between SaO¬2 and Po2 is on the flat segment of
the oxygen dissociation curve. While SpO2 levels below 90% at
sea level indicate severe respiratory pathology, in high altitude
locations such levels are found in normal local children owing to the
low barometric pressure. Despite this, the oxygen balance in
these children remains adequate in health due to several physiological
adaptations, including hyperventilation, polycythemia, enhanced
alveolar growth and increased capillary proliferation. [39;40]
For ill children living at such high altitudes, the aim of oxygen
supplementation should not therefore be based on normal levels at sea
level, but should aim to achieve an adjusted expected normal SpO2 for
that setting. Our study quantifies the expected reduction in
SpO2 levels with increasing altitudes. The strong association found
between study altitude and a study’s average SpO2 value
suggests that a lower threshold for giving oxygen may be appropriate at
very high altitude if supplies are limited.
Figure 1 suggests
that at altitudes above 2500 metres, using an SpO2 threshold of 90% to
administer oxygen is conservative, and may result in oxygen
supplementation to some children with SpO2 in the normal
range. In facilities with limited oxygen supplies located at
these altitudes, therefore, a lower level of SpO2 can be used, and an
approximation could be an SpO2 <85%. Above 3200
metres, even this lower definition is conservative, and may become too
sensitive as a screening test for oxygen need. Such
guidelines are based on statistical definitions, and their clinical
relevance needs to be further studied. The use of thresholds
of hypoxaemia below 90% to indicate oxygen therapy at altitude has been
reported in the literature [7;19;20], but clearly, in addition
to locally-relevant thresholds of SpO2, oxygen therapy should be based
on the overall clinical picture of each child, as well as a careful
consideration of resource availability.
In many health
facilities, the scarcity of oxygen means that health workers are faced
not with the question of which children need oxygen, but which children
need it most. It is optimal practice to cohort children
requiring oxygen together in a high dependency area of the ward,
allowing for regular observation and monitoring. This
necessitates the accurate identification of the proportion of sick
children requiring such attention. Oxygen saturation by pulse
oximetry can be used to facilitate this process and to indicate the
severity of respiratory disease.[4;5;41] In high altitude settings,
consideration of the normally lower levels of SpO2 and being able to
approximate these quantitatively, will be useful in informing clinical
decisions.
It should be
emphasized that ultimately what is important in maintaining adequate
tissue oxygenation is the oxygen content in the blood, not the oxygen
saturation. This is given by the equation (1.30 x [Hb] x
SaO2) + 0.003 PaO2. Children with severe anaemia or infants
in their physiological nadir of haemoglobin concentration may be
hypoxic despite having an SpO2 level within the normal range.
Ideally, oxygen therapy needs to be guided by pulse oximetry as well as
measurement of the haemoglobin concentration. However, in the
absence of an immediate measure of Hb, emphasis may be placed on
identifying the clinical signs of anaemia or identifying children in
their nadir of Hb, in whom more liberal thresholds for giving oxygen
would be appropriate.
Previous studies
have used the mean SpO2 minus 2 SD to define hypoxaemia in children,
and assumed normally distributed saturation levels.[5;7;18;19]
Our study has taken into account the skewed distribution of normal
SpO2, and has weighted each study estimate by its precision. We have
also attempted to include the largest number of relevant studies that
reported results in a format which would allow a pooled analysis of the
data. Our findings suggest that the definition of hypoxaemia as mean
SpO2 minus 2 SD may not accurately capture the lowest 2.5% of values at
low and moderate altitudes. We recommend that future studies check
distributional assumptions and explicitly report centile values such as
the 2.5th centile and/or median.
There are a number
of limitations to the study design we used. Where children
were selected on grounds of ethnic background, the normal SpO2 reported
may not be representative of unstudied populations of children living
at comparable altitudes. In addition, variations between
study findings could be due to differences in sampling, ethnicity and
age ranges studied, as well as the use of different oximeters and/or
protocols for measuring SpO2. Also, there was no way of
controlling for either the precision or the accuracy of the oximeters
used in each study. The statistical model employed assumes reliable
estimates of study means and standard deviations, as well as assuming
that the transformation applied would have resulted in an approximately
normal distribution for study populations at all altitudes. Ideally,
had raw data been available, summary statistics would have been
calculated on an appropriate scale rather than estimated.
Summary
Above altitudes of
2500 metres, giving oxygen for SpO2 less than 90% may be too liberal
for facilities with limited oxygen supplies. There is
evidence that for altitudes greater than 2500 metres a threshold of
SpO2 of 85% can be used to identify children most in need of
oxygen. A balance needs to be achieved between using accurate
altitude-specific definitions of hypoxaemia, and ensuring simple and
safe indications for oxygen that can be taught to and used by health
workers. We hope the model proposed for predicting normal
SpO2 and the definition of hypoxaemia at different altitudes will be
useful for clinicians in determining when to give oxygen.
Table 1: Studies of normal SpO2 in children resident at different altitudes
>
Please click image for full size
Figure
1 Estimated threshold of hypoxaemia at different altitudes

References
1. Rudan I, Tomaskovic L, Boschi-Pinto C,
Campbell H, WHO Child Health Epidemiology Reference Group. Global
estimate of the incidence of clinical pneumonia among children under
five years of age. Bulletin of the World Health Organization
82(12):895-903, 2004.[Medline]
2. UNICEF/WHO. Pneumonia: the forgotten
killer of children. 2006. Geneva.
3. Murray CJ, Lopez AD. Mortality by
cause for eight regions of the world: Global Burden of Disease
Study.[see comment]. Lancet 349(9061):1269-76, 1997.[Medline]
4. Duke T, Mgone J, Frank D. Hypoxaemia
in children with severe pneumonia in Papua New Guinea. Int J Tuberc
Lung Dis 2001; 5(6):511-519.[Medline]
5. Onyango FE, Steinhoff MC, Wafula EM,
Wariua S, Musia J, Kitonyi J. Hypoxaemia in young Kenyan children with
acute lower respiratory infection. BMJ 1993; 306(6878):612-615.[Medline]
6. Smyth A, Carty H, Hart CA. Clinical
predictors of hypoxaemia in children with pneumonia. Ann Trop Paediatr
1998; 18(1):31-40.[Medline]
7. Reuland DS, Steinhoff MC, Gilman RH,
Bara M, Olivares EG, Jabra A et al. Prevalence and prediction of
hypoxemia in children with respiratory infections in the Peruvian
Andes. J Pediatr 1991; 119(6):900-906.[Medline]
8. Lozano JM, Steinhoff M, Ruiz JG, Mesa
ML, Martinez N, Dussan B. Clinical predictors of acute radiological
pneumonia and hypoxaemia at high altitude. Arch Dis Child 1994;
71(4):323-327.[Medline]
9. World Health Organization. Pocket book
of hospital care for children: guidelines for the management of common
illnesses with limited resources. Geneva: World Health Organization;
2005.
10. Toth B, Becker A, Seelbach-Gobel B.
Oxygen saturation in healthy newborn infants immediately after birth
measured by pulse oximetry. Arch Gynecol Obstet 2002; 266(2):105-107.[Medline]
11. Kirkwood BR, Sterne JAC. Essential
Medical Statisitics. 2nd ed. Malden, MA: Blackwell Publishing; 2003.
12. Stata Satistical Software: Release 10
[ College Station TX: Stata Corp LP; 2007.
13. Sharp S. Meta-analysis Regression.
Stata Technical Bulletin Reprints. 7, 148-155. 1998.
14. Balasubramanian S, Suresh N,
Ravichandran C, nesh Chand GH. Reference values for oxygen saturation
by pulse oximetry in healthy children at sea level in Chennai. Ann Trop
Paediatr 2006; 26(2):95-99.[Medline]
15. Basnet S, Adhikari RK, Gurung CK.
Hypoxemia in children with pneumonia and its clinical predictors.
Indian J Pediatr 2006; 73(9):777-781.[Medline]
16. Beall CM. Oxygen saturation increases
during childhood and decreases during adulthood among high altitude
native Tibetians residing at 3,800-4,200m. High Alt Med Biol 2000;
1(1):25-32.[Medline]
17. Beebe SA, Heery LB, Magarian S,
Culberson J. Pulse oximetry at moderate altitude. Healthy children and
children with upper respiratory infection. Clin Pediatr (Phila) 1994;
33(6):329-332.[Medline]
18. Bruce N, Weber M, Arana B, Diaz A,
Jenny A, Thompson L et al. Pneumonia case-finding in the RESPIRE
Guatemala indoor air pollution trial: standardizing methods for
resource-poor settings. Bull World Health Organ 2007; 85(7):535-544.[Medline]
19. Duke T, Blaschke AJ, Sialis S,
Bonkowsky JL. Hypoxaemia in acute respiratory and non-respiratory
illnesses in neonates and children in a developing country. Arch Dis
Child 2002; 86(2):108-112.[Medline]
20. Dyke T, Lewis D, Heegaard W, Manary
M, Flew S, Rudeen K. Predicting hypoxia in children with acute lower
respiratory infection: a study in the highlands of Papua New Guinea. J
Trop Pediatr 1995; 41(4):196-201.[Medline]
21. Gamponia MJ, Babaali H, Yugar F,
Gilman RH. Reference values for pulse oximetry at high altitude. Arch
Dis Child 1998; 78(5):461-465.[Medline]
22. Huicho L, Pawson IG, Leon-Velarde F,
Rivera-Chira M, Pacheco A, Muro M et al. Oxygen saturation and heart
rate in healthy school children and adolescents living at high
altitude. Am J Human Biol 2001; 13(6):761-770.[Medline]
23. Lodha R, Bhadauria PS, Kuttikat AV,
Puranik M, Gupta S, Pandey RM et al. Can clinical symptoms or signs
accurately predict hypoxemia in children with acute lower respiratory
tract infections? Indian Pediatr 2004; 41(2):129-135.[Medline]
24. Lozano JM, Duque OR, Buitrago T,
Behaine S. Pulse oximetry reference values at high altitude. Arch Dis
Child 1992; 67(3):299-301.[Medline]
25. Madico G, Gilman RH, Jabra A, Rojas
L, Hernandez H, Fukuda J et al. The role of pulse oximetry. Its use as
an indicator of severe respiratory disease in Peruvian children living
at sea level. Respiratory Group in Peru. Arch Pediatr Adolesc Med 1995;
149(11):1259-1263.[Medline]
26. Mau MK, Yamasato KS, Yamamoto LG.
Normal oxygen saturation values in pediatric patients. Hawaii Med J
2005; 64(2):42.[Medline]
27. Meyts I, Reempts PV, Boeck KD.
Monitoring of haemoglobin oxygen saturation in healthy infants using a
new generation pulse oximeter which takes motion artifacts into
account. Eur J Pediatr 2002; 161(12):653-655.[Medline]
28. Mok JY, McLaughlin FJ, Pintar M, Hak
H, Maro-Galvez R, Levison H. Transcutaneous monitoring of oxygenation:
what is normal? J Pediatr 1986; 108(3):365-371.[Medline]
29. Muhe L, Weber M. Oxygen delivery to
children with hypoxaemia in small hospitals in developing countries.
Int J Tuberc Lung Dis 2001; 5(6):527-532.[Medline]
30. Nicholas R, Yaron M, Reeves J. Oxygen
saturation in children living at moderate altitude. J Am Board Fam
Pract 1993; 6(5):452-456.[Medline]
31. Niermeyer S, Shaffer EM, Thilo E,
Corbin C, Moore LG. Arterial oxygenation and pulmonary arterial
pressure in healthy neonates and infants at high altitude. J Pediatr
1993; 123(5):767-772.[Medline]
32. Niermeyer S, Yang P, Shanmina,
Drolkar, Zhuang J, Moore LG. Arterial oxygen saturation in Tibetan and
Han infants born in Lhasa, Tibet. N Engl J Med 1995; 333(19):1248-1252.[Medline]
33. Saleu G, Lupiwa S, Javati A, Namuigi
P, Lehmann D. Arterial oxygen saturation in healthy young infants in
the highlands of Papua New Guinea. P N G Med J 1999; 42(3-4):90-93.[Medline]
34. Thilo EH, Park-Moore B, Berman ER,
Carson BS. Oxygen saturation by pulse oximetry in healthy infants at an
altitude of 1610 m (5280 ft). What is normal? Am J Dis Child 1991;
145(10):1137-1140.[Medline]
35. Poets CF, Stebbens VA, Lang JA,
O'Brien LM, Boon AW, Southall DP. Arterial oxygen saturation in healthy
term neonates. Eur J Pediatr 1996; 155(3):219-223.[Medline]
36. World Health Organization. Oxygen
therapy for acute respiratory infections for young children in
developing countries. Programme for the Control of Acute Respiratory
Infections of the World Health Organization. Geneva: World Health
Organization; 1993.
37. Weber MW, Mulholland EK. Pulse
oximetry in developing countries. Lancet 1998; 351(9115):1589.[Medline]
38. Steinhoff M, Black R. Childhood
pneumonia: we must move forward.[comment]. Lancet 369(9571):1409-10,
2007.[Medline]
39. West John B. Respiratory Physiology:
The Essentials. 7th ed. Baltimore, Maryland, USA: Lippincott Williams
& Wilkins; 2000.
40. de MK, Heymans HS, Zijlstra WG.
Physical adaptation of children to life at high altitude. [Review] [79
refs]. European Journal of Pediatrics 154(4):263-72, 1995.[Medline]
41. Djelantik IG, Gessner BD, Sutanto A,
Steinhoff M, Linehan M, Moulton LH et al. Case fatality proportions and
predictive factors for mortality among children hospitalized with
severe pneumonia in a rural developing country setting. Journal of
Tropical Pediatrics 49(6):327-32, 2003.[Medline]
42. Nicholas R, Yaron M, Reeves J. Oxygen
saturation in children living at moderate altitude. J Am Board Fam
Pract 1993; 6(5):452-456.[Medline]
43. Mood AM, Graybill FA, Boes DC.
Introduction to the Theory of Statistics. Tokyo: McGraw-Hill Kogakusha;
1974.
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