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Elizabeth S Draper a Department of Epidemiology and Public Health,
Leicester University Medical School, Leicester LE1 6TP, b Department of Child Health, Leicester Royal
Infirmary, Leicester LE2 7LX, c Department of Obstetrics and Gynaecology,
Queens Medical Centre, University of Nottingham, Nottingham NG7
2UH
Correspondence to: E S Draper msn{at}le.ac.uk
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Abstract |
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Objective:
To produce current data on survival of
preterm infants.
Design:
Retrospective population based study.
Setting:
Trent health region.
Subjects:
All European and Asian live births,
stillbirths, and late fetal losses from 22 to 32 weeks' gestation,
excluding those with major congenital malformations, in women resident
in the Trent health region between 1 January 1994 and 31 December 1997.
Main outcome measures:
Birth weight and gestational
age specific survival for both European and Asian infants (a)
known to be alive at the onset of labour, and (b)
admitted for neonatal care.
Results:
738 deaths occurred in 3760 infants born
between 22 and 32 weeks' gestation during the study period, giving an overall survival rate of 80.4%. The survival rate for the 3489 (92.8%) infants admitted for neonatal care was 86.6%. For European infants known to be alive at the onset of labour, significant variations in gestation specific survival by birth weight emerged from
24 weeks' gestation: survival ranged from 9% (95% confidence interval 7% to 13%) for infants of birth weight 250-499 g to 21% (16% to 28%) for those of 1000-1249 g. At 27 weeks' gestation, survival ranged from 55% (49% to 61%) for infants of birth weight 500-749 g (below the 10th centile) to 80% (76% to 85%) for those of
1250-1499 g. Infants who were large for dates (
27 weeks' gestation) had a slightly reduced, but not significant, predicted survival. Similar survival rates were observed for Asian infants. The odds ratio
for the survival of infants from a multiple birth compared with
singleton infants was 1.4 (1.1 to 1.8). Survival graphs for infants
admitted for neonatal care are presented by sex.
Conclusion:
Easy to use birth weight and gestational
age specific predicted survival graphs for preterm infants facilitate decision making for clinicians and parents. It is important that these
graphs are representative, are produced for a geographically defined
population, and are not biased towards the outcomes of particular
centres. Such graphs, produced in two stages, allow for the changing
pattern of survival of infants from the start of the intrapartum period
to immediately after admission for neonatal care.
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Key messages
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Introduction |
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Data on the probability of survival of infants in high risk pregnancies can be of great value in guiding management. This information can help both clinical staff and parents to decide if and when to intervene in a pregnancy. Unit based data on the survival of preterm infants by birth weight and gestation can be easily compiled, but such data are easily biased by variation in local casemix and local variations in attitude to the care of the most immature infants.1 To overcome these problems, data on birth weight and gestational age specific survival should be derived from geographically defined populations using data from all pregnancies within the relevant gestation band.
Geographically based graphs for liveborn infants were produced in the 1980s for a US population2 and for the Netherlands,3 but both are now out of date as they were produced before the introduction of many important advances in perinatal care such as antenatal steroids and exogenous surfactant therapy. Birth weight and gestational age specific survival graphs have yet to be produced for a UK population. Attempts to produce such graphs have been hampered by the absence of gestational age in the statutory dataset required by the Office of National Statistics.
We aimed to produce birth weight and gestational age specific survival
graphs for a population of infants born between 22 and 32 weeks'
gestation in the United Kingdom. To maximise clinical relevance, we
focused on two specific clinical situations. We aimed (a) to
develop one set of data to indicate the chance of an infant being
discharged alive from the neonatal service if it was known to be alive
at either the onset of labour or when the decision to deliver was made,
and (b) to develop a second set of data to describe the sex
specific survival to discharge home of infants admitted to a neonatal unit.
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Subjects and methods |
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Subjects
We studied Trent health region, a geographically defined
population, which comprises around 4.6 million people and about 60 000
births a year. We included all births and late fetal losses from 22 to
32 weeks' gestation inclusive to mothers resident in the Trent health
region between 1 January 1994 and 31 December 1997. We excluded infants
of less than 22 weeks' gestation as there were no survivors in this
group. The Trent confidential inquiry into stillbirths and deaths in
infancy (part of the national confidential inquiry into
stillbirths and deaths in infancy programme4) provided data on all late fetal losses of 22 and 23 weeks' gestation, all stillborn infants known to be alive at the onset of labour, and all
infant deaths before discharge from neonatal care, and the Trent
neonatal survey5 provided data for all infants of
32
weeks' gestation admitted to the 16 neonatal intensive care units in
the Trent health region.
sex, ethnic origin, and whether the infant was from a
multiple pregnancy. We defined gestation according to the hierarchy
specified by the national confidential inquiry into stillbirths
and deaths in infancy programme: mother certain of her dates (most
reliable); early dating scan (less than 20 weeks' gestation); late
dating scan (more than 20 weeks' gestation); and postnatal examination
(least reliable). If the difference between maternal date and early
dating scan was more than 7 days, we chose the early dating scan.
The two datasets were merged and validated. To ensure that infants
were only counted once, we deleted any duplicate records (infants
admitted to a neonatal unit who subsequently died were represented in
both datasets). Infants with lethal congenital anomalies were excluded
from the analysis.
Statistical analysis
We analysed data for two time periods: all infants known to
be alive at the onset of labour or when the decision to deliver was
made; and a subset of this group of all infants admitted to neonatal
units. As studies have shown that ethnic differences have a major
influence on outcome,6-8 we calculated the birth weight
and gestational age specific survival for both Asian (originating from
the Indian subcontinent) and European infants within each group. We
excluded infants from other ethnic groups owing to small numbers.
we then used
this to develop a simple equation for use in clinical
practice. The fit of the logistic model was assessed with the Hosmer
and Lemeshow goodness of fit test,9 with P<0.05 taken to
be evidence of a statistically significant difference between observed
and predicted survival. We then constructed a graph showing the
predicted proportional survival (with 95% confidence intervals) of
singleton infants by birth weight increments of 250 g and gestational
age intervals of 1 week both separately and together. Graphs for
infants admitted to neonatal care were constructed by sex for the
European but not Asian population as the sample size of the latter was
too small. Distribution free smoothed lines were added to the graphs to
show the observed 10th and 90th centiles for
birth weight.
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Results |
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Study population
Between 1 January 1994 and 31 December 1997 there were over
240 000 live births, stillbirths, and late fetal losses of
22
weeks' gestation within Trent health region. Of these, 3871 infants
were
32 weeks' gestation and known to be alive at the onset of
labour. We excluded six infants with missing data for birth weight, and
115 infants with lethal congenital anomalies, leaving 3760 infants of
which 944 (25.1%) were from multiple pregnancies. Overall, there were
738 deaths giving an overall survival rate of 80.4%, ranging from 6%
for infants of 23 weeks' gestation to 98% for those of 32 weeks'
gestation. In total, 271 infants were either intrapartum stillbirths or
died shortly after delivery leaving 3489 (92.8%) infants admitted to neonatal units: 3162 (86.6%) of these infants survived to discharge home from neonatal care.
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European infants
Figure 1 shows the proportional survival of singleton European
infants known to be alive at the onset of labour. The Hosmer and
Lemeshow goodness of fit statistic9 for this model was
2=7.06, df=8, P=0.53. At 22 weeks' gestation predicted
survival of European infants was 2%-3% irrespective of their size.
Significant variations in gestation specific survival by birth weight
emerged from 24 weeks' gestation: predicted survival ranged from 9%
(7% to 13%) for birth weights of 250-499 g to 21% (16% to 28%) for those of 1000-1249 g. At 28 weeks' gestation predicted survival was
63% (56% to 70%) for birth weights of 500-749 g (below the 10th
centile) and 90% (87% to 92%) for those of 1250-1499 g. At 32 weeks' gestation predicted survival was 80% (70% to 88%) for birth weights of 750-999 g and 98% (97% to 99%) for those of
1500-2499 g. A reduced predicted survival at gestations of
27 weeks
was seen in infants large for dates, although this finding was not significant.
Asian infants
Figure 2 shows the predicted survival of Asian infants known to be
alive at the onset of labour, derived from the same model as figure 1.
As with the European infants, only 2%-3% of Asian infants of 22 weeks' gestation were predicted to survive irrespective of their size.
Predicted survival at 28 weeks' gestation was 69% (63% to 74%) for
birth weights of 500-749 g (below the 10th centile) and 90% (87% to
92%) for those of 1250-1499 g. Predicted survival at 32 weeks'
gestation was 96% (93% to 97%) for birth weights of 750-999 g and
99% (98% to 100%) for those of 1500-2499 g.
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Infants from multiple births
Infants from multiple births had, for the same birth weight,
gestation, and ethnic origin as singleton infants, a greater chance of
survival (odds ratio 1.4, 1.1 to 1.8). From this odds ratio we
developed a simple equation for use in clinical practice to adjust for
the predicted survival of multiple births (to the nearest percentage
point):
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for example, at 24 weeks'
gestation the predicted survival of male infants was 22% (17% to
27%) for birth weights of 500-749 g and 29% (24% to 35%) for those
of 750-999 g whereas the predicted survival of female infants was 29%
(23% to 35%) and 37% (30% to 44%) respectively. Owing to the small
number of Asian infants (n=232), figure 5 shows the predicted survival
for all Asian infants (not subdivided by sex) admitted for neonatal
care.
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Discussion |
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Data on gestational age is not collected routinely in the United
Kingdom. Consequently it has been difficult to provide national data on
survival after preterm delivery, despite the need for such information
when counselling women with an anticipated preterm delivery. The
improving prognosis for infants of very short gestations makes it
important to give parents an accurate prediction of outcome for their
child.10 Our data provide gestational age specific survival rates for singleton Asian and European infants, by birth weight groupings, for a geographically defined population, at two
separate time periods
all infants known to be alive at the onset of
labour, when the sex of the infant is generally unknown; and a subset
of this group of all infants admitted to neonatal units. Trent health
region is considered representative of England and Wales, with a
mixture of urban and rural populations and similar mortality and
morbidity measures
for example, in 1996 the perinatal mortality rate
was 8.6 per 1000 births for England and Wales and 8.7 per 1000 births
for Trent, and the proportion of babies weighing less than 2500 g was
7.3% for both England and Wales and Trent.
Additional factors affecting infant survival
Factors known to affect the survival of infants (ethnic origin,
sex, and multiple pregnancy) were included in the modelling process.
For ease of use, separate graphs were produced for European and Asian
infants. Previous reports indicating improved survival of female
infants requiring intensive care are confirmed in our study among
European infants.
11 12
International perspectives
Several other studies have looked at birth weight and gestational
age specific survival, all of which have limitations. In two US
studies
2 14
geographically based survival graphs were
produced for liveborn infants. The first study,2 however,
was carried out before the introduction of many important new
management strategies
for example, exogenous surfactant therapy and
the widespread use of antenatal steroids. In the second
study,14 the survival of infants was described by birth
weight and gestation separately but not together. That study produced
data for the actuarial survival of infants by weeks of gestation or 100 g birth weight groupings and showed that the survival in the smallest infants improved dramatically during the first few days of life although the risk of a late death was high in the smallest of these
infants. As a result we are planning to supplement our current data
with a third set of graphs including late deaths among those infants
surviving the perinatal period, as well as investigating the prediction
of morbidity in preterm infants. A further geographically based study
reported for the national livebirth cohort of the Netherlands in
19833 is also now of limited relevance. Geographically defined studies
15 16
of the survival of preterm infants
in the United Kingdom have either concentrated on gestation specific or
birth weight specific survival alone or have considered the total
population of deliveries including deaths before the onset of labour.
None of these studies present data for all infants known to be alive at
the onset of labour and therefore are of limited use to obstetricians.
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Conclusion |
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Birth weight and gestational age specific predicted survival
graphs for preterm infants facilitate decision making for
obstetricians, neonatologists, and parents and give a range of
predicted survival for any given gestational age by estimated or actual
birth weight. It is important that such graphs are produced for a
geographically defined population so that they are representative and
not biased towards the outcomes of particular centres. The production
of such graphs in two stages allows for the changing pattern of
survival from the start of the intrapartum period to the immediate
period after admission for neonatal care. A continual process of
updating needs to be in place to allow for improvements in survival of infants.
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Acknowledgments |
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We thank Sue Wood (regional coordinator), Jayne Bennett (administrator), and all the district coordinators for the Trent confidential inquiry into stillbirths and deaths in infancy, the staff (medical, nursing, and clerical) of the 16 perinatal units in Trent, those units adjacent to Trent that allowed us access to data on cross boundary flows of patients, and Keith Abrams and Nicky Spiers for their statistical advice.
Contributors: DJ, ESD, and DJF conceived the original idea for the study; they will act as guarantors for the paper. All authors contributed to the writing of the paper. BM carried out the statistical analysis.
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Footnotes |
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Funding: The Trent neonatal survey and Trent confidential inquiry into stillbirths and deaths in infancy are funded through the Trent regional office
Competing interests: None declared.
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References |
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(Accepted 13 July 1999)
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