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Introduction |
A wide range of risk factors are associated with fetuses being
small for gestational age,1 and the prognosis for such
fetuses varies according to the presence of chromosomal or other
congenital malformations.2-4 In pregnancies of small for
gestational age fetuses without congenital malformations it has been
assumed that constitutionally small fetuses
for example, twins, or
infants born to short mothers
are at lower risk of adverse outcomes
than fetuses affected by other situations such as pre-eclampsia or cigarette consumption.
5 6
In fact, such an assumption
underlies recent pleas for customised or individualised definitions of
a fetus being small for gestational age.
7 8
Unfortunately, this assumption has rarely been critically
tested.
9 10
In Sweden the population based birth register includes information on
risk factors for fetuses being small for gestational age including
maternal age, height, parity, smoking habits, blood pressure status,
and type of pregnancy (single or multiple). We used this information to
study the differences in late fetal death rates in association with
fetal size and underlying determinants of a fetus being small for
gestational age.
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Subjects and methods |
Swedish birth register
In Sweden data from all hospital births, including demographics,
reproductive history, and complications during pregnancy and delivery,
are collected prospectively and recorded in a birth register.11 From 1983 to 1992 1 083 367 births were
recorded. Our study was restricted to singleton or twin pregnancies
without congenital malformations, according to ICD-8 (international
classification of diseases, 8th revision) and ICD-9 (9th revision)
codes 740-759, in women aged 15 to 44 years (n=1 026 249).
Maternal height and smoking habits are recorded at the time of
registration for antenatal care. Parity is defined as the number of
previous births, including stillbirths. Maternal age is defined as
completed years at delivery. Any maternal disorders are noted by an
obstetrician at the time of the woman's discharge. Hypertension is
defined as12: essential (ICD-8 code 401 and ICD-9 codes
642A-C); gestational (non-proteinuric) (ICD-8 code 637.01 and ICD-9
codes 640D and 642X); mild (proteinuric) pre-eclampsia (ICD-8 code
637.03 and ICD-9 code 642E); severe (proteinuric) pre-eclampsia (ICD-8 code 637.04 and ICD-9 code 642F); and eclampsia (ICD-8 code 637.1 and
ICD-9 code 642G). The 250 women with eclampsia were grouped with 5145 women with severe pre-eclampsia.
Birthweight ratio was defined as the ratio of observed to expected
birth weight on the basis of the fetuses' gestational age and sex.
Explanatory variables were the fetuses' sex, a third degree polynomial
of gestational age in days, and interaction between the fetuses' sex
and gestational age. A normal birthweight ratio was defined as
0.90
and that of mildly and extremely small for gestational age fetuses as
>0.75 but <0.90 or
0.75 respectively. Late fetal death was defined
as a stillbirth delivered at 28 completed weeks of gestation or later.
When available, ultrasonography was used to estimate gestational age
during the second trimester otherwise gestational age was estimated
from the last menstrual period. At the start of the study 50% of the
obstetric departments performed routine ultrasonography. From 1990 onwards all pregnant women in Sweden were offered ultrasonography
before 18 weeks' gestation.
13 14
We used multiple logistic regression analyses to estimate the effect of
independent variables on late fetal death.
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Results |
Risk factors
Late fetal death rates were increased in women who were 35 years
or older, were nulliparous, smoked, or were <155 cm in height (table
1). Essential hypertension, severe pre-eclampsia, and twin pregnancies
were associated with greatly increased late fetal death rates. In
pregnancies of normal birthweight ratio the late fetal death rate was
2.1 per 1000 compared with 4.7 and 32.8 per 1000 in pregnancies of
mildly and extremely small for gestational age fetuses
respectively.
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Table 1
Number of births and late fetal deaths
associated with maternal characteristics, type of birth, and
birthweight ratio in Sweden from 1983 to1992
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Table 1 shows the relation between maternal and fetal characteristics
and birthweight ratio. Maternal smoking habits and height influenced
the mean birthweight ratio in a dose dependent manner but the largest
effects were observed in women with severe pre-eclampsia or twin
pregnancies.
Late fetal death rates and mean birthweight ratios were similar for
women aged 20-24, 25-29, and 30-34 years. Compared with severe
pre-eclampsia other hypertensive disorders were either uncommon or had
a comparatively small influence on late fetal death or birthweight
ratio. In the logistic regression analyses maternal age was grouped as
15-19, 20-34, and 35-44 years, and hypertension as none, severe
pre-eclampsia, and other hypertensive disorders. Multiple logistic
regression analyses showed that there was an increased risk of late
fetal death in women who were 35 years or older, were nulliparous,
smoked, had twin pregnancies, or had severe pre-eclampsia (table
2).
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Table 2
Adjusted odds ratios (95% confidence
intervals) of late fetal death compared with maternal characteristics
of women recorded in the Swedish birth register from 1983 to 1992
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In a second logistic model we estimated the crude effect of being small
for gestational age on the risk of late fetal death. Compared with
fetuses of a normal birthweight ratio the risk was doubled in fetuses
mildly small for gestational age (odds ratio 2.3, 95% confidence
interval 2.1 to 2.5) and greatly increased in fetuses extremely small
for gestational age (16.5, 15.2 to 17.9).
Risk factors and birthweight ratio
To determine whether the increased risk of late fetal death
related to a fetus being small for gestational age was modified by
underlying determinants, we introduced interaction terms in the
logistic regression models. Important interaction terms were found
between birthweight ratio and all determinants studied except maternal
age, and predicted rates of late fetal death were calculated as a
function of birthweight ratio and its determinants (table 3). In
extremely small for gestational age fetuses late fetal death rates
ranged from 16 to 45 per 1000, which varied according to underlying
determinants. In mildly small for gestational age fetuses late fetal
death rates ranged from 2.3 to 8.7 per 1000, and from 1.3 to 4.6 per
1000 in fetuses of a normal birthweight ratio.
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Table 3
Adjusted rates and 95% confidence intervals
of late fetal death compared with characteristics of pregnancy and
birthweight ratio based on multiple logistic regression. Model includes
significant interactions between risk factors and birthweight ratio
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In extremely small for gestational age fetuses the predicted late fetal
death rate was 33.1 per 1000 in women aged less than 35 years
v 44.9 per 1000 in older women. Late fetal death rates also increased with maternal height, and were higher in singletons compared with twins and in non-hypertensive pregnancies compared with
pregnancies complicated by hypertensive disorders. Slightly higher late
fetal death rates were also observed in nulliparous women and in
non-smokers. In mildly small for gestational age fetuses late fetal
death rates were increased in women who were 35 years or older, were
155 cm in height, had twin pregnancies, or had severe
pre-eclampsia. In fetuses of a normal birthweight ratio late fetal
death rates were increased among women who were 35 years or older, were
<155 cm in height, were nulliparous, smoked, had twin pregnancies, or
had severe pre-eclampsia. Of the late fetal deaths, 51% were in the
preterm period and 49% were at or after term. When the analyses in
table 3 were restricted to full term pregnancies late fetal death rates
were reduced: 0.9 per 1000 in non-small for gestational age fetuses and
2.3 and 9.8 in mildly and extremely small for gestational age fetuses
respectively. The comparative increase in late fetal death rates by
risk factors and birthweight ratio, however, remained unchanged (data
not shown).
The impact of maternal height on late fetal death rate is shown when
using birthweight ratio as a continuous variable (figure). Late fetal
death rates consistently increased with decreasing birthweight ratio
regardless of maternal height, but the increase was most pronounced
among women
175 cm in height.
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Discussion |
This study shows that late fetal death rates associated with a
fetus being extremely small for gestational age are low in women who
are less than 35 years,
155 cm in height, have twin pregnancies, or
have severe pre-eclampsia or other hypertensive disorders. Hypertensive
disorders are well documented determinants of a fetus being small for
gestational age, and close antenatal supervision may contribute to the
favourable prognosis in these pregnancies. The reduced risks associated
with short stature and multiple births, however, support the assumption
that a small for gestational age fetus may be the result of
constitutional rather than pathological factors.5-8 Even
in short mothers, however, late fetal death rates were more than
10-fold higher in extremely small for gestational age fetuses compared
with fetuses of a normal birthweight ratio clearly indicating that even
in short mothers the consequences of a fetus being small for
gestational age may be serious.
In pregnancies of a normal birthweight ratio the risks of late fetal
death were influenced by maternal age, smoking habits, multiple births,
and severe pre-eclampsia. These factors increase the risks of severe
placental complications,15-18 which may cause fetal death
without affecting the birthweight ratio.
Late fetal death rates were higher among women older than 35 years
regardless of the birthweight ratio. The risk of late fetal death has
been reported to increase progressively with gestational age and this
increase is pronounced among women older than 35 years.
19 20
Risks of placental complications increase
with maternal age, and vascular degenerative changes have been observed in the uterine and myometrial arteries of women of older childbearing age
21 22
; this suggests that late fetal death may be due
to an age related effect as a consequence of uteroplacental
underperfusion.
Methodological considerations
Chance is an unlikely explanation for our findings because of the
large size of the study and the correspondingly narrow confidence intervals of our observed rates and odds ratios. The prospective nature
of data collection precludes recall bias. As some risk factors of a
fetus being small for gestational age are associated with increased
risks of congenital anomalies the study was restricted to pregnancies
without congenital malformations.
The conclusions from this investigation are, however, limited by the
risk factors included in the birth register. We lacked information on
the womens' socioeconomic position, prepregnancy body mass index, and
weight gain during pregnancy, which are important determinants of
birthweight ratio.1 Socioeconomic position and
prepregnancy body mass index are also associated with the risk of late
fetal death.
23 24
The association between weight gain
during pregnancy and late fetal death, however, is less
certain.
24 25
The risks of a fetus being small for
gestational age and late fetal death related to maternal age and
smoking habits, however, seem to be largely independent of
socioeconomic position and prepregnancy body mass
index.
1 23 24 26
Maternal height was not an important factor in the overall risk of late fetal death, which agrees with a
previous investigation.24 The effect of maternal height on birthweight ratio is reported to be the same both before and after adjusting for confounders. The effect of maternal height on the risk of
late fetal death associated with birthweight ratio is therefore
unlikely to be due to residual confounding.
27 28
An accurate estimation of the birthweight ratio in cases of late fetal
death is limited as estimates of gestational age and fetal weight are
based on time of delivery rather than time of death. This not only
leads to an overestimation of gestational age but the dead fetus may
also have lost weight before delivery,29 and the
birthweight ratio may therefore be underestimated in these pregnancies.
The extent of this bias is, however, probably limited. Firstly, almost
all pregnant women in Sweden follow the routine schedule of visiting
their antenatal clinic every second week from 24 weeks' gestation and
weekly from 36 weeks, and fetal heart activity is registered at each
visit. Secondly, the women are routinely told to contact their
antenatal clinic or obstetric department immediately if there is a
decrease in fetal movements. Thirdly, the time from diagnosis of a late
fetal death to delivery is generally reported as less than 24 hours.30 These factors should ensure a comparatively short
delay between the time of fetal death and the time of delivery. In a
study of fetal histology and stillbirth in the United States, it was
estimated that 80% of all stillbirths were delivered within one week
of death.31
Conclusions
Highlighting the risk factors of late fetal death in small for
gestational age fetuses is especially important in countries with low
infant mortality rates. In the present study, in which all infants with
congenital malformations were excluded, late fetal deaths accounted for
more than 50% of all late fetal and infant deaths in Sweden from 1983 to 1992. This study shows that the risk of late fetal death in a small
for gestational age fetus may be modified by the underlying
determinants of birthweight ratio. The very strong relation between
late fetal death and a small for gestational age fetus should, however,
be re-emphasised; a fetus that is extremely small for gestational age
is associated with a high risk of late fetal death, regardless of
cause, and must therefore be monitored.
Dr Kramer is a distinguished scientist of the Medical Research
Council of Canada.
Contributors: SC participated in the discussion of the study
hypothesis and study design, contributed to the analyses, and was
mainly responsible for writing the paper; he will act as guarantor of
the paper. BH participated in the discussion of the study hypothesis
and study design, performed the analyses, and contributed to writing
the paper. MSK initiated the study, participated in the discussions of
the study hypothesis and study design, contributed to the analyses, and
helped write the paper.