BMJ No. 7051 Volume 313 Saturday 27 July 1996
Sleeping position in babies who died from the sudden infant death syndrome and matched controls | |||
| Detail | No (%) of babies who died | No (%) of controls | Odds ratio (95% confidence interval) |
| Position put down: | |||
| Back | 82 (43.6) | 509 (65.8) | 1.00 |
| Side | 76 (40.4) | 241 (31.1) | 2.01 (1.38 to 2.93) |
| Front | 30 (16.0) | 24 (3.1) | 9.58 (4.86 to 18.87) |
| No with data available | 188 | 774 | |
| Position found: | |||
| Back | 67 (35.8) | 618 (81.9) | 1.00 |
| Side | 43 (23.0) | 92 (12.2) | 4.51 (2.65 to 7.66) |
| Front | 77 (41.2) | 45 (6.0) | 21.36 (11.67 to 39.08) |
| No with data available | 187 | 755 | |
Thermal environment - Significantly more of the mothers
of control infants than of babies who died worried about their babies becoming
too hot (0.47; 0.28 to 0.76). Twice as many babies who died (21.8%) as controls
(11.9%) slept in rooms in which the heating was on for the whole duration of the
last or reference sleep (2.14; 1.33 to 3.15). Table 2 shows the thermal
resistance (tog value) of bedding and clothing for sleep, usually and during the
last or reference sleep for babies who died and controls. The babies who died
were more heavily wrapped than the controls, both usually and during the last or
reference sleep, the risk increasing as the tog value increased. A small but
significant proportion of babies who died wore a hat to sleep, both usually at
night (3.1%
Bed sharing and room sharing - Routine bed sharing with
parent(s) (two or more nights a week) was commoner among babies who died (26%)
than controls (14.2%) (2.04; 1.36 to 3.07). During the last or reference sleep
this difference was significant only for those who had been in bed with the
parent(s) for more than one hour (25.7% versus 15.3% controls; 1.86; 1.23 to
2.81) or for the whole night (14.9%
Use of dummies - There was no difference in the
proportion of the babies who died and controls who routinely used a dummy, but
for the last or reference sleep there was a significant excess of control infants
(52.8%) who used a dummy compared with babies who died (39.8%) (0.59; 0.42 to
0.84).
Breast feeding or bottle feeding - More of the control
infants (60.3%) than the babies who died (45.1%) had ever been breast fed (0.50;
0.35 to 0.71), but the protective effect did not increase with increasing
duration of breast feeding. Breast feeding was significant independently of dummy
use, the cumulative protective effect of both being additive (0.26; 0.15 to
0.44). Bottle feeding was strongly associated with lower socioeconomic status and
with smoking. When breast feeding was adjusted for socioeconomic status its
apparent protective effect became non-significant (0.69; 0.47 to 1.02).
MULTIVARIATE MODEL
From the univariate analysis various factors seem to be associated with an
increased or decreased risk of the sudden infant death syndrome. To examine their
significance, however, we need to look at their relation to each other and to
control for other significant risk factors. Table 4 shows how the significance of
the variables associated with the sleeping environment changes when they are put
in the multivariate model with each other and how it changes further when we
control for other significant risk factors.
** Controlled for all sleeping environment factors listed in table.
*** Controlled for maternal age, parity, gestation, birth weight, whether
family received family income supplement, exposure to tobacco smoke, and factors
in sleeping environment that remain significant.
**** Fisher's exact test,
hence odds ratio not given. The results of this, the first large scale case-control study of the sudden
infant death syndrome after the national risk reduction campaign, demonstrate the
effects of the changes introduced and shed new light on the aetiology and
epidemiology of the syndrome.
SLEEPING POSITION AND BED SHARING
The
significance of the prone sleeping position as a risk factor for the syndrome has
been confirmed. A new finding is that the side sleeping position, previously
recommended as a safer alternative to prone sleeping, is itself associated with a
significantly increased risk of death when compared with supine. This added risk
seems to result mainly from the tendency of babies placed on their sides to roll
prone and was not influenced by the position of the infant's arm. The higher
prevalence of side sleeping than prone sleeping in the present population means
that the population attributable risk from side sleeping (18.4%) is higher than
that of prone sleeping (14.2%) despite a much lower odds ratio.(15)
Interpretation of the effects of bed sharing on the risk of death is
complicated by the interactions with several other factors. Mothers who
habitually take their babies into bed with them are not homogeneous but come from
disparate ethnic, social, and cultural groups with very different approaches to
child care, breast feeding, smoking, and alcohol misuse. The data confirm the
conclusion of the New Zealand study(17) that there is a significant
risk from bed sharing if the parents smoke and support a previous suggestion (not
borne out in the New Zealand study) that bed sharing is a risk if the mother has
recently consumed alcohol.(18) There is no suggestion that taking the
baby into bed for a short time for feeding or for comfort poses any risk - except
that the mother may then fall asleep and keep the baby in her bed all night long.
THERMAL ENVIRONMENT
Thermal stress emerges in the present study as a smaller independent risk
factor for the syndrome than previously reported.(2) This might be
expected from the known interaction between heavy wrapping and prone sleeping,
the prevalence of which has sharply declined. It is postulated that the
interaction may arise from a reduction in heat loss from the face of a baby lying
prone.(19)
In the present study most babies slept supine or on their sides so that
adverse effects of heavy wrapping would be less likely, unless the head became
totally covered and heat loss from both face and scalp was prevented. Total
covering by the bedding emerged from the multivariate analysis as the most potent
of all risk factors. The fact that babies who died had been previously found
totally covered more often than the controls suggests that the way the bedding is
usually arranged might be partly responsible. This lends support to the recent
"Feet to Foot" initiative from the Foundation for the Study of Infant Deaths,
which advocates that a baby's bedding should be made up so that the baby's feet
are at the foot of the cot and risk of slipping beneath the covers is reduced.
Our finding that very few mothers, index or control, practised this technique
during the study, which preceded the initiative, suggests that there is a large
potential for change. Duvets or quilts were associated with added risk both in
themselves and through their propensity to total covering; this reinforces the
advice that the use of duvets or quilts should be strongly discouraged for
infants under 1 year.
BREAST FEEDING AND DUMMY USE
As in the Avon study,(5) no independent protective effect was
identified from breast feeding when we controlled for other significant factors.
In the univariate analysis the lack of any "dose-response" effect from breast
feeding suggests that it is acting as a marker of the lifestyle of mothers who
breast feed rather than showing a biological effect in itself. The loss of
significance when account is taken either of smoking or of socioeconomic status
supports this interpretation, as does the very small protective effect among the
infants of non-smoking mothers. There are of course other good reasons to
continue recommending breast feeding. The apparent protective effect of a
dummy is in agreement with the observation in New Zealand,(3) but in
that study a high proportion of infants were sleeping prone. Dummy use is more
common in the more socioeconomically deprived groups in the United Kingdom and is
the only factor over-represented in these groups that is associated with a
significantly reduced risk of the syndrome. It is not clear whether use of a
dummy is a marker of a particular pattern of infant care in this group. These
findings should not be used to claim that dummies prevent cot death, but it may
not be appropriate for health care professionals routinely to discourage the use
of dummies in young infants. Further research is needed to identify any adverse
effects of dummy use, in particular the reported adverse effects on breast
feeding.(20)
Funding: National Advisory Body for the confidential inquiry into
stillbirths and deaths in infancy.
Conflict of interest: None.
Friarage Hospital,
Northallerton,
Operational Research Division,
Nuffield Institute for
Health,
Sheffield Children's Hospital,
University
of Bristol,
Institute of Child Health,
Department of Child Health,
Correspondence
to:Professor Fleming.
1 Wigfield R, Fleming P J. The prevalence of risk factors for SIDS:
impact of an intervention campaign. In: Rognum TO, ed.
2 Fleming P J, Gilbert R E, Azaz Y, Berry P J, Rudd P T,
Stewart A, et al . The interaction between bedding and sleeping
position in sudden infant death syndrome: a population based case-control study.
3 Mitchell E A, Taylor B J,
Ford R P K, Stewart A W, Becroft D M O, Thompson J M D, et al . Dummies and
the sudden infant death syndrome. Arch Dis Child 1993;68
:501-4.
4 Klonoff-Cohen H, Edelstein S L. Bed sharing and the sudden infant
death syndrome. BMJ 1995;311 :1269-72.
5 Gilbert
RE, Wigfield R E, Fleming P J, Berry P J, Rudd P T. Bottle feeding and the sudden
infant death syndrome. BMJ 1995;310 :88-90.
6 Ford RP K, Taylor B J, Mitchell E A, Enright S A, Stewart A W, Becroft
D M O, et al . Breastfeeding and the risk of sudden infant death
syndrome. Int J Epidemiol 1993;22 :885-90.
7 National Advisory Body for CESDI. Annual report for
1994. London: Department of Health, 1996.
8 Blair P, Fleming P,
Bensley D, Smith I, Bacon C, Taylor E. Plastic mattresses and sudden infant death
syndrome. Lancet 1995;345 :720.
9 Wigfield R E, Fleming P J, Berry P J, Rudd P T, Golding J. Can the
fall in Avon's sudden infant death rate be explained by the observed sleeping
position changes? BMJ 1992;304 :282-3.
10 Taylor
EM, Emery J L. Categories of preventable infant deaths. Arch Dis Child
1990;63 :535-9.
11 Gilbert R E, Rudd P T, Berry P J, Fleming
P J, Hall E, White D G, et al . Combined effect of infection and heavy
wrapping on the risk of sudden infant death. Arch Dis Child
1992;67 :272-7.
12 Cordner S M, Willinger M. The definition of the sudden infant
death syndrome. In: Rognum TO, ed. Sudden infant death syndrome, new
trends in the nineties . Oslo: Scandinavian University Press, 1995.
13 SAS Institute. SAS user's guide. Version 6. 4th ed.
Cary, NC: SAS Institute, 1989.
14 Microsoft Corporation. Fox-Pro . Redmond, Washington:
Microsoft Corporation, 1995.
15 Bruzzi P, Green S B, Byar D P, Brunton L A, Schaiver C. Estimating
the population attributable risk for multiple risk factors using case control
data. Am J Epidemiol 1985;122 :904-14.
16 Blair
P S, Fleming P J, Bensley D, Smith I, Bacon C, Taylor E, et al . Smoking
and the sudden infant death syndrome: results from 1993-5 case-control study for
confidential inquiry into stillbirths and deaths in infancy. BMJ
1996;313 :195-8.
17 Scragg R, Mitchell E A, Tayloret B, Stewart AW, Ford RPK, Thompson
JMD, et al . Bed sharing, smoking and alcohol in the sudden infant
death syndrome. BMJ 1993;307 :1313-8.
18 Norvenious S G. Sudden infant death syndrome in Sweden in
1973-1977 and 1979. Acta Paediatr Scand Suppl 1987;333 :1-138.
19 Fleming P J, Levine M R, Azaz Y, Wigfield R. The development of
thermoregulation and interactions with the control of respiration in infants:
possible relationship to sudden infant death. Acta Paediatr Scand
1993;389 (suppl):57-9.
20 Barros F C, Victora C G, Semer T C,
Filho S T, Tamosi E, Weiderpass E. Use of pacifiers is associated with decreased
breastfeeding duration. Pediatrics 1995;95 :497-9.
(Accepted 19 June 1996)
Design - Two year population based case-control study. Parental
interviews were conducted for each infant who died and four controls matched for
age and date of interview.
Setting - Three regions in England
with a total population of 17 million people.
Subjects - 195 babies who died and 780 matched controls.
Results - More index than control mothers (62.6% versus
25.1%) smoked during pregnancy (multivariate odds ratio = 2.10; 95%
confidence interval 1.24 to 3.54). Paternal smoking had an additional independent
effect when other factors were controlled for (2.50; 1.48 to 4.22). The risk of
death rose with increasing postnatal exposure to tobacco smoke, which had an
additive effect among those also exposed to maternal smoking during pregnancy
(2.93; 1.56 to 5.48). The population attributable risk was over 61%, which
implies that the numbers of deaths from the syndrome could be reduced by almost
two third if parents did not smoke. Alcohol use was higher among index than
control mothers but was strongly correlated with smoking and on multivariate
analysis was not found to have any additional independent effect. Illegal drug
use was more common among the index parents, and paternal use of illegal drugs
remained significant in the multivariate model (4.68; 1.56 to 14.05).
Conclusions - This study confirms the increased risk of the
sudden infant death syndrome associated with maternal smoking during pregnancy
and shows evidence that household exposure to tobacco smoke has an independent
additive effect. Parental drug misuse has an additional small but significant
effect.
Although the incidence of sudden unexpected deaths in infancy in the United
Kingdom has fallen, especially since the "Back to Sleep" campaign in 1991, such
deaths remain the largest single group of deaths of infants between 1 week and 1
year old.(1) The study of sudden unexpected deaths in infancy (part of
the national confidential inquiry into stillbirths and deaths in infancy (CESDI),
funded by the Department of Health) conducted a detailed case-control study and
confidential inquiry of all sudden unexpected deaths in infancy in the
participating regions of the United Kingdom in the two year period one year after
the national intervention campaign. A summary of the preliminary results of this
study has been published.(2)
Several case-control studies have shown an association between the risk of
maternal smoking during pregnancy and the sudden infant death
syndrome.(3-13) A recent meta-analysis of these studies, including
cohort and smaller case-control studies, estimate a pooled relative risk
(adjusted for prone sleeping position) of 2.99 (95% confidence interval 2.79 to
3.19) for maternal smoking during pregnancy.(12) Many of these studies,
however, were conducted before the recent decreases in the incidence of such
deaths which followed risk reduction campaigns in several countries.
Several studies have shown evidence of increasing risk of the syndrome with
increasing exposure to tobacco smoke within the
household.(6) (13-15) We investigated the risk of the
sudden infant death syndrome associated with exposure to tobacco smoke after the
national campaign to reduce the risk of such deaths. Exposure was measured in
terms of both the in utero effect and the effect once the infant is born. The
effects of alcohol consumption and parental use of illegal drugs in relation to
smoking were also studied.
The study
aimed to include all cases of the sudden infant death syndrome in infants aged 7
to 364 days inclusive in two NHS regions in the United Kingdom (Southwest and
Yorkshire) from February 1993 and a third region (Trent) from September 1993
until January 1995 inclusive, the total population of the study area being about
17 million.
As in previous studies in Avon, Sheffield, and Yorkshire cases
were ascertained by means of a communication network of professionals and lay
organisations who reported all deaths within 24 hours. All sudden unexpected
deaths in infancy were initially reported and investigated.
Data were collected on a standard questionnaire by four research
interviewers for each region, consistency of approach being maintained by cross
regional initial training and regular meetings thereafter. Four controls for each
case were selected by the method previously used in Avon.(16-18) The
same interviewer visited each control family, usually within a week of the death,
to collect the same data as for the index case.
Full details of the methods and the statistical analysis are given in the
accompanying paper.(19)
Ascertainment of cases and controls - Details of the
ascertainment are given in the accompanying paper.(19) During the study
period, 266 sudden unexpected deaths in infancy were identified, of which 216
were classified as the sudden infant death syndrome. This analysis deals with the
195 babies who died (90.3% of the total) for whom full data are available and
their 780 matched controls.
Time to first
interview - The median time from the discovery of the death until the
first interview of the index parents was 4.5 days; 82% of families were
interviewed within 14 days and 95% within 28 days of the death.
Matching for age - Over two thirds of the controls were
matched within 2 weeks and over 90% within 1 month of the age of the index baby.
SMOKING
Table 1 shows the univariate statistics (controlled for matching) for
maternal smoking before, during, and after pregnancy; paternal smoking; and
others, excluding parents, who smoked in the
household.
The majority of both index and control mothers (85.7% and 87.5%,
respectively) remained smokers or non-smokers in the periods before, during, and
after pregnancy. Table 2 shows the dose-response effects of exposure to tobacco
smoke. The more the mother smoked during pregnancy the greater the associated
risk. For other household members this trend was less clear.
Table 3 shows that smoking by partners and others in the household was both
significant and independent of maternal smoking during pregnancy. The data
suggest that the risks associated with tobacco smoke are not restricted to an in
utero effect from maternal smoking.
Table 4 shows the effect of
postnatal exposure to tobacco smoke. The first two measures show the number of smokers and the number of cigarettes smoked daily in those households where smoking was allowed in a room with the baby present. The third measure gives a parental
estimation of the infants' daily exposure to smoke, both within and outside the
household. The risk increased with increasing numbers of smokers in the
household, increasing total number of cigarettes smoked a day, and increasing
daily exposure to tobacco smoke.
** Of the nine sets of index and control parents who did not answer this
question, at least one parent smoked.
SMOKING AND ALCOHOL CONSUMPTION
There was no significant difference between the index and control partners
regarding usual alcohol consumption (P = 0.901) or consumption of 3 or
more units (17.3%
Usual alcohol consumption became non-significant when we adjusted for
socioeconomic status (no alcohol: 1.22; 0.81 to 1.85; \g10 units a week: 1.75;
0.91 to 3.36). Alcohol consumption in the last 24 hours became non-significant
when we further adjusted for maternal smoking (1.62; 0.53 to 4.91).
{headb}smoking and illegal substance use
The parents were given a list of
illegal drugs and asked if they had taken any of these more than once. The list
included heroin, crack, cocaine, ecstasy, speed, LSD, amphetamines, barbiturates,
cannabis, and glue. We expected that parents might be reluctant to answer this
question, but in the event they did so readily. Table 6 shows the results.
By far the commonest drug used was cannabis, which was used by 6.8% of
index mothers during pregnancy and 1% of control mothers. The use of illegal
drugs among parents remained a significant risk factor even after adjustment for
tobacco smoking.
MULTIVARIATE ANALYSIS Several factors remained significant in the multivariate analysis but are
not amenable to change. These included younger mothers, mothers without a
partner, high parity, multiple births, short gestation, and low socioeconomic
status. After we controlled for all of these factors along with sleeping position
and possible confounders such as maternal alcohol consumption, parental use of
illegal drugs, parental bed sharing, and the protective effect of breast feeding
maternal smoking during pregnancy remained significant (2.10; 1.24 to 3.54). When
we added birth weight (adjusted for gestation and sex) to the model as a known
outcome, maternal smoking during pregnancy remained significant (1.78; 1.04 to
3.05). Paternal smoking had an additional independent effect (2.50; 1.48 to
4.22), but smoking by other members of the household became non-significant. The
risk associated with smoking if one or both parents smoked was 3.79 (2.09 to
6.88) when we controlled for other factors. In only 16.9% of index households did
neither parent smoke; the population attributable risk for smoking by at least
one parent was 61.2%.(20) When we considered parental estimation of the
infant's daily exposure to tobacco smoke as a postnatal marker for smoking, this
marker was significant when we controlled for other factors
(P = 0.008). If maternal smoking during pregnancy was added to the
model, however, the postnatal marker lost its independent effect
(P = 0.1601). This may be explained by the strong correlation between
maternal smoking during and after pregnancy. The additive effect of smoking in
pregnancy and postnatal exposure was significant (2.93; 1.56 to 5.48).
Maternal use of illegal drugs became non-significant in the multivariate
model, whether we looked at use before, during, or after pregnancy. Paternal use
of illegal drugs after the baby's birth remained significant in the multivariate model (4.68; 1.56 to
14.05).
The results of this study, the first after the national intervention
campaign, give the strongest evidence to date of the risk of the sudden infant
death syndrome associated with smoking. Even after we had controlled for a wide
range of confounders, including socioeconomic status, maternal smoking during
pregnancy remained significant. Furthermore, we were able to show a biological
gradient: the more the mother smoked the greater the risk to the infant. Paternal
smoking had an additional independent effect when we controlled for other factors
including maternal smoking during pregnancy. In 83.1% of index households at
least one parent smoked. The population attributable risk of 61.2% implies that
the number of deaths from the syndrome could be reduced by almost two thirds if
parents did not smoke. The risk to the infant is therefore twofold: from maternal
smoking during pregnancy and from those that smoke either in the presence of the
pregnant mother or in the presence of the infant. Trying to quantify the risk of
the separate effects is difficult because many of the mothers who smoke during
pregnancy are a main source of exposure after pregnancy. Evidence that postnatal
exposure has a dose related effect is very strong, however, whether measured by
the number of smokers in the household, the number of cigarettes the infant is
exposed to, or the number of hours of exposure. Those infants exposed both to
maternal smoking during pregnancy and postnatal tobacco smoke are at increased
risk.
The index mothers drank slightly more alcohol, but these differences were
not significant when we adjusted for maternal smoking. A worrying finding from
this study is the use of illegal drugs by the parents. Although the numbers are
small and partly reflect the social deprivation of the index group, drug use
among the index partners after pregnancy remained a significant risk after many
other factors were controlled for.
CONCLUSION
Despite clear health warnings, many people continue to smoke. The
responsibility of minimising the risk of the sudden infant death syndrome lies
not just with the mother who smokes but all smokers. An appropriate public health
message might be that smoking in the same environment as a pregnant mother or
child is as unacceptable as drinking and driving. Parents who have been unable to
give up or reduce their smoking habit should be strongly advised to keep their
baby in a "smoke-free zone." This, however, should not be regarded as an
alternative to the much better precaution of not smoking at all.
Conflict of interest: None.
Operational Research Division,
Nuffield Institute for Health,
Friarage Hospital,
Sheffield Children's Hospital,
University of Bristol,
Institute of Child Health,
Department of Child Health,
Correspondence to: Professor Fleming.
1 Wigfield R, Fleming P J. The prevalence of risk factors for SIDS:
the impact of an intervention campaign. In: Rognum TO, ed. Sudden infant
death syndrome: new trends in the nineties . Oslo: Scandinavian University
Press, 1995:124-8.
2 The National Advisory Body for CESDI.
Annual report for 1994 . London: Department of Health, 1996.
3 Naeye R L, Ladis B, Drage J S. Sudden infant death syndrome: a
prospective study. Am J Dis Child 1976;130 :1207-12.
4 Hoffman H J, Hunter J C, Ellish N J, Janerick D T, Goldberg J. Adverse
reproductive factors and the sudden infant death syndrome. In: RM Harper, HJ
Hoffman eds. Sudden infant death syndrome: risk factors and basic
mechanisms. New York: PMA Publishing, 1988:153-75.
5 Gilbert R E, Fleming P J, Azaz Y, Rudd P. Signs of illness preceding
sudden unexpected death in infants. BMJ 1990;300 :1237-9.
6 McGlashan N D. Sudden infant death in Tasmania 1980-1986: a seven
year prospective study. Soc Sci Med 1989;29 :1015-26.
7 Engelberts A. Cot death in the Netherlands: an epidemiological
study. Amsterdam: VU University Press, 1991. (MD Thesis.)
8 Li D-K,
Dalang J R. Maternal smoking, low birth weight and ethnicity in relation to sudden
infant death syndrome. Am J Epidemiol 1991;134 :958-64.
9 Mitchell E A, Taylor B J, Ford R P K, Stewart A W, Becroft D M, Thompson
J M, et al . Four modifiable and other major risk factors for cot
death: the New Zealand study. J Paediatr Child Health
1992;28 (suppl):S3-8.
10 Nicholl J P, O'Cathain A. Antenatal
smoking, postnatal passive smoking, and sudden infant death syndrome. In:
Poswillo D, Alberman E, eds. Effects of smoking on the fetus, neonate and
child . Oxford: Oxford Medical Publications, 1992.
11 Schoendorf
KC, Kiely J L. Relationship of sudden infant death syndrome to maternal smoking
during and after pregnancy. Paediatrics 1992;90 :905-8.
12 Mitchell E A. Smoking: the next major and modifiable risk factor.
In: Rognum TO, ed. Sudden infant death syndrome: new trends in the
nineties . Oslo: Scandinavian University Press, 1995:114-8.
13 Mitchell E A, Ford R P K, Stewart A W, Taylor B J, Becroft D M,
Thompson J M, et al . Smoking and the sudden infant death syndrome.
Paediatrics 1993;91 :893-6.
14 Haglund B,
Cnattingius S. Cigarette smoking as a risk factor for sudden infant death
syndrome. Am J Public Health 1990;80 :29-32.
15 Klonoff-Cohen H S, Edelstein S L, Lefkowitz E S, Srinivasan I P,
Kaegi D, Chun Chang J, et al . The effect of passive smoking and
tobacco exposure through breast milk on sudden infant death syndrome. JAMA
1995;273 :795-8.
16 Fleming P J, Gilbert R E, Azaz Y, Berry
P J, Rudd P T, Stewart A, Hall E. The interaction between bedding and sleeping
position in sudden infant death syndrome: a population-based case-control study.
BMJ 1990;301 :85-9.
17 Wigfield R E, Fleming P J, Berry P J, Rudd P T, Golding J. Can the
fall in Avon's sudden infant death rate be explained by the observed sleeping
position changes? BMJ 1992;304 :282-3.
18 Gilbert
RE, Rudd P T, Berry P J, Fleming P J, Hall E, White D G, et al .
Combined effect of infection and heavy wrapping on the risk of sudden infant death.
Arch Dis Child 1992;67 :272-7.
19 Fleming P J, Blair P S, Bacon C, Bensley D, Smith I, Taylor,
et al . Environment of infants during sleep and risk of the sudden
infant death syndrome: results of 1993-5 study for confidential inquiry into
stillbirths and deaths in infancy. BMJ 1996;313 :191-5.
20 Bruzzi P, Green S B, Byar D P, Brunton L A, Schaiver C. Estimating
the population attributable risk for multiple risk factors using case control
data. Am J Epidemiol 1985;122 :904-14.
(Accepted 19
June 1996)
Tog
value of bedding used for babies who died from sudden infant death syndrome and
matched controls Odds ratio (95%
confidence interval) Tog value No
(%) of
babies who died No (%) of controls Not adjusted
Adjusted* Usually by night: <6 togs 81 (42.0) 391 (50.2)
1.00 1.00 6-9 togs 80 (41.5) 318 (40.8)
1.27 (0.86 to 1.87) 1.27 (0.83 to 1.95) 10 togs and over 32 (16.6) 70 (9.0)
2.27 (1.32 to 3.90) 1.65 (0.90 to 3.04) No with data available 193
779 Usually by day: <6 togs 135 (70.0) 643 (82.6)
1.00 1.00 6-9 togs 43 (22.3) 117
(15.0)
2.00 (1.26 to 3.15) 2.07 (1.24 to 3.46)
10 togs and over 15 (7.8) 18
(2.3) 4.32 (1.97 to 9.46) 3.94 (1.64
to 9.49) No with data available 193 778
When put down: <6 togs 90 (47.1) 456 (58.5)
1.00 1.00 6-9 togs 68 (35.6)
263 (33.8) 1.50 (0.99 to 2.26) 1.52 (0.96
to 2.42) 10 togs an over 33 (17.3) 60
(7.7) 3.38 (1.94 to 5.87) 2.78 (1.49
to 4.16) No with data available 191
779 When found:
<6 togs 112 (58.9) 556
(71.4) 1.00 1.00 6-9 togs 51 (26.8) 183 (23.5)
1.61 (1.05 to 2.47) 1.57 (0.97 to 2.54)
10 togs and over 27 (14.2) 40
(5.2) 4.41 (2.20 to 7.62) 3.52 (1.74 to
7.11) No with data available 190
779 * Controlled for socioeconomic status (with family income
supplement).
Arrangement of bedding - Table 3 shows
the type of bedding, how the bedding was arranged, where the infant was put in
the bed, and whether the infant was usually found or found after the last or
reference sleep with covers over the head. Very few babies who died or control
infants were put down for the last or reference sleep at the bottom of the bed;
this reflected usual practice. Significantly more babies who died (9.0%
versus 3.2%) were found at the bottom of the bed after the last or
reference sleep (3.02; 1.42 to 6.25). More babies who died than controls were found with
covers over their heads, and of these, more were sleeping under duvets (64%
versus 33% controls).
Table 3 -
Arrangement of bedding in
babies who died from the sudden infant death syndrome and matched
controlsDetail of bedding No (%) of
babies who died No (%) of
controls Odds ratio
(95%
confidence interval) Duvet used for last or reference
sleep: No 112 (57.7) 602
(77.3) 1 Yes 82 (42.3) 177
(22.7) 2.82 (1.95 to 4.08) No with data available 194
779 Bedding for last or reference sleep: Tucked in or no bedding 82 (44.3)
467 (60.3) 1 Lying loosely over
103 (55.7) 307 (39.7) 1.92 (1.35 to
2.73) No with data available 185 774
Where in bed: Top or middle 169 (98.3)
689 (98.1) Bottom 3 (1.7) 13 (1.9)
P = 1.0* No with data available 172
702 Usually found with covers over head: Sometimes or never 181 (94.3)
763 (97.9) Often or always 11 (5.7)
16 (2.1) 2.72 (1.11 to 6.77) No with data available 192
779 Found with covers over head after
last or reference sleep: No 148 (81.3)
747 (97.6) Yes 34 (18.7) 18 (2.4) 18.93
(8.05 to 44.8) No with data
available 182 765 * Fisher's exact test.
Table 4 -
Multivariate analysis of significant factors in sleeping environment for risk
of the sudden infant death syndrome.
Figures are
odds ratios (95% confidence intervals)
Multivariate Variable* Univariate
Sleeping**
All factors*** Prone sleeping 9.58 (4.86 to
18.87) 10.03 (4.33 to 23.24)
9 (2.84 to 28.47) Side sleeping 2.01 (1.38 to
2.93)
2.16 (1.36 to 3.43) 1.84 (1.02 to
3.31) Infant found with
covers over head 18.93 (8.05 to
44.48)
31.38 (10.4 to 95.0) 21.58 (6.21 to
74.99) Tog value (6-9 togs) 1.5 (0.99 to
2.26) 0.95 (0.55 to 1.63) 0.89 (0.45
to 1.76) Tog value (10 togs and
over) 3.38 (1.94 to 5.87) 1.04 (0.44 to
2.46) 0.94 (0.31 to 2.83) Wearing hat P = 0.015****
6.21 (0.74 to 51.93) 4.13 (0.22 to 77.89) Heating on all night 2.14 (1.30 to 3.50)
3.14 (1.60 to 6.17) 2.37 (0.96 to 5.84) Whether mother ever breast fed 0.5
(0.35 to 0.71) 0.42 (0.26 to 0.67) 1.06
(0.57 to 1.98) Bed sharing with parents all night 4.12
(2.30 to 7.40) 4.06 (1.78 to 9.23) 4.36
(1.59 to 11.95) Using dummy 0.59
(0.42 to 0.84) 0.44 (0.27 to 0.70) 0.38
(0.21 to 0.70) Using duvet 2.82 (1.95 to 4.08)
1.88 (1.14 to 3.12) 1.72 (0.90 to 3.30) Loose bed
covering 1.92 (1.35 to 2.73) 1.25
(0.79 to 1.99) 1.07 (0.61 to 1.89) * All variables are for last or reference sleep except for
breast feeding.
The risk associated with prone sleeping, side sleeping, and covering of the
head by bedding and the protective effect of using a dummy remained significant
when we controlled for other factors. Bed sharing also remained significant, but
a subgroup analysis showed that the associated risk was significant only among
smokers (multivariate odds ratio 9.25; 2.51 to 34.02) rather than non-smokers
(2.27; 0.41 to 12.54). The risks associated with heating and using a duvet were
significant among the factors associated with the sleeping environment but just
failed to reach significance when we controlled for other risk factors. No
protective effect of breast feeding was identifiable when we controlled for all
other factors.
Discussion
The regional coordinators of the
confidential inquiry into stillbirths and deaths in infancy were Ms Lesley Anson
(Yorkshire); Mrs Rosanne Sodzi (South Western, 1993-5); Mrs Rosie Thompson (South
Western, from 1995); Ms Sue Wood (Trent). The research health visitors of the
inquiry were Mrs Christine Ahronson, Mrs Lindsay Cansfield, Mrs Carmel Davis, Mrs
Margaret Griffin, Mrs Pat Johnson, Mrs Lynette Lovelock, Mrs Lynne Middleton, Mrs
Pam Mueller, Mrs Shirley Stephenson, Mrs Dawn Taylor, Mrs Lorraine Wright, and
the research midwives were Mrs Chris Laws and Mrs Rosie McCabe.
Foundation
for the Study of Infant Deaths Research Unit,
Institute of Child Health,
Royal
Hospital for Sick Children,
Bristol BS2 8BJ
Peter J Fleming,
professor of infant health and developmental physiology
Peter S
Blair,
North Yorkshire DL6 1JG
Chris Bacon,
consultant paediatrician
NHS Executive,
Quarry House,
Leeds LS2
9UA
David Bensley,
statistician
Leeds LS2 9PL
Iain Smith,
Sheffield S10 2TH
Elizabeth
Taylor,
consultant senior lecturer in paediatrics
St Michael's Hospital,
Bristol BS2 8EG
Jem Berry,
Royal Hospital for Sick Children,
Bristol BS2 8BJ
Jean Golding,
professor of paediatric and perinatal epidemiology
Postgraduate Medical School,
Royal Devon and Exeter Hospital,
Exeter EX2 5DW
John Tripp,
consultant paediatrician
REFERENCES
Smoking and the sudden infant death syndrome: results from 1993-5
case-control study for confidential inquiry into stillbirths and deaths in
infancy
Peter S Blair, Peter J Fleming, David Bensley, Iain Smith, Chris Bacon,
Elizabeth Taylor, Jem Berry, Jean Golding, John Tripp, Confidential Enquiry into
Stillbirths and Deaths Regional Coordinators and Researchers
Abstract
Objective - To investigate the effects of exposure to tobacco
smoke and of parental consumption of alcohol and illegal drugs as risk factors
for the sudden infant death syndrome after a national risk reduction campaign
which included advice on prenatal and postnatal avoidance of tobacco smoke.
Introduction
Methods
STUDY DESIGN, CASE NOTIFICATION, AND SELCTION OF CONTROLS
Results
Table 1 -
Univariate statistics for smoking and sudden infant death syndromeDetail No (%) of
babies who died No (%) of controls Odds ratio
(95%
confidence interval) Maternal smoking:
Before
pregnancy 138 (70.8) 255
(32.7) 5.07 (3.45 to 7.45) During
pregnancy 122 (62.6) 196 (25.1) 4.84 (3.33
to 7.04) After pregnancy 129 (66.2) 209
(26.8) 5.19 (3.57 to 7.55) Paternal smoking 118 (60.5) 282
(36.2) 3.04 (2.13 to 4.36) Others smoking in home 28 (14.3)
46 (5.9) 2.99 (1.71 to 5.25)
Table 2 -
Dose-response
effects of smoking on risk of sudden infant death syndromeNo of cigarettes smoked No
(%) of
babies who died No (%) of controls Odds ratio
(95% confidence interval) Mother during
pregnancy: None 73 (37.4) 584
(74.9) 1.00 1-9 53 (27.2) 108 (13.8)
4.59 (2.71 to 7.77) 10-19 42 (21.5) 58
(7.4) 5.38 (2.96 to 9.75) 20 and over 27 (13.8) 30
(3.8) 7.88 (3.87 to 12.26)
Father: None 77 (39.5) 498 (63.8)
1.00 1-9 33 (16.9) 100 (12.8)
2.18 (1.28 to 3.69) 10-19 52
(26.7) 112 (14.4) 3.81 (2.31 to 6.29) 20 and over
33 (16.9) 70 (9.0) 3.50 (1.86
to 6.56) Others (excluding parents): None 167 (85.6) 734
(94.1) 1.00 1-9 6 (3.1) 15 (1.9) P
= 0.257* 10-19 7 (3.6) 15 (1.9)
P = 0.161* 20 and over 15
(7.7) 16 (2.1) 4.12 (1.85
to 9.08) * Fisher's exact test; if these groups are combined: odds
ratio = 1.96 (0.93 to 4.13).
Table 3 - Effects of smoking by fathers and others (excluding
parents) in households, controlled for maternal smoking during pregnancy on risk
of sudden death syndrome
Smoking
status No (%) of
babies who died No (%) of
controls Odds ratio
(95%
confidence interval) Father non-smoker/mother non-smoker
33 (16.9) 421
(54.0) 1.00 Father smoker/mother non-smoker 40 (20.5) 163
(20.9) 3.41 (1.98 to 5.88) Father non-smoker/mother
smoker 44 (22.6) 77 (9.9) 7.01 (3.91 to
12.56) Father
smoker/mother smoker 78 (40.0) 119 (15.3)
8.41 (5.08 to 13.92) Other non-smoker/mother
non-smoker 65 (33.3) 561 (71.9)
1.00 Other smoker/mother non-smoker 8 (4.1)
23 (2.9) P = 0.007*
Other
non-smoker/mother smoker 102 (52.3) 173
(22.2)
6.01 (4.12 to 8.78) Other smoker/mother smoker
20 (10.3) 23 (2.9) 7.27 (3.46 to
14.94) *Fisher's exact
test.
Table 4 - Postnatal exposure to tobacco smoke
and risk of sudden death syndrome Level of exposure No (%) of
babies who died No (%) of
controls Odds ratio
(95%
confidence interval) No of smokers in household*: None 101 (52.3) 615 (80.4)
1 1 22 (11.4) 66 (8.6)
2.44 (1.36 to 4.37) 2 59
(30.6) 77 (10.1) 5.15 (3.24 to 8.21) 3 and over 11 (5.7) 7
(0.9)
10.43 (3.34 to 32.54) No with data
available 193 765 No of
cigarettes smoked daily*: None 101 (52.3) 615
(80.4)
1
1-19 18 (9.3) 56 (7.3)
2.47 (1.29 to 4.73) 20-39 40 (20.7) 67
(8.8) 3.96 (2.40 to 6.55) 40 and over 34 (17.6)
27 (3.5) 7.57 (4.00 to 14.32) No with data available 193
765 Infant's daily exposure to tobacco smoke
(hours): 0 85 (45.7) 593
(76.9) 1 1-2 26 (14) 90 (11.7)
1.99 (1.14 to 3.46) 3-5 22 (11.8) 45 (5.8)
3.84 (1.97 to 7.48) 6-8 19 (10.2) 18 (2.3)
6.78 (3.17 to 14.49) >8 34 (18.3) 25 (3.2)
8.29 (4.28 to 16.05) No with data
available 186** 771** * In households where smoking was allowed in the
same room as the infant. Table
5-- Odds ratio (95%
confidence interval) Consumption of alcohol (units)
No (%)
of babies
who died No (%)
of
controls Not adjusted
Adjusted* Weekly before
pregnancy: 1-10 75 (39.7)
396 (50.9) 1.00** 1.00** None
91 (48.1) 333 (42.9) 1.44 (1.01
to 2.06) 1.34 (0.90 to 1.99)
>10 23 (12.2) 48 (6.2)
2.68 (1.46 to 4.82) 1.82 (0.96 to 3.46)
In
past 24 hours: 0-2 168 (88.5)
743 (95.5) 1.00** 1.00** 3 and over 22 (11.5) 35 (4.5)
2.62 (1.40 to 4.90) 1.91 (0.97 to 3.76) * Adjusted for maternal smoking.
** Reference group.Table 6 - Parental
use of illegal drugs and risk of sudden infant death syndrome Odds ratio (95%
confidence interval) Drug use No (%)
of
babies who died No (%)
of controls Not adjusted Adjusted* Mother: Before pregnancy 31/191 (16.2)
41/778 (5.3) 3.93 (2.18 to 7.09) 2.37
(1.25 to 4.47) During pregnancy 16/190 (8.4)
11/775 (1.4) 7.05 (2.58 to 19.29) 4.34 (1.51 to
12.43) After pregnancy 16/191 (8.4)
19/777 (2.4) 4.54 (1.92 to 10.71) 2.80 (1.10 to
7.18) Partner: Year before birth 37/172 (21.5)
50/755 (6.6) 3.76 (2.21 to 6.37) 3.28 (1.88 to
5.71) After birth 29/169 (17.2) 31/753
(4.1) 5.35 (2.71 to 10.53) 4.18 (2.06 to
8.48) *Adjusted for maternal (before, during, or after
pregnancy) and paternal smoking as appropriate. Discussion
The regional coordinators of the confidential inquiry into stillbirths
and deaths in infancy were Ms Lesley Anson (Yorkshire); Mrs Rosanne Sodzi (South
Western, 1993-5); Mrs Rosie Thompson (South Western, from 1995); Ms Sue Wood
(Trent). The research health visitors of the inquiry were Mrs Christine Ahronson,
Mrs Lindsay Cansfield, Mrs Carmel Davis, Mrs Margaret Griffin, Mrs Pat Johnson,
Mrs Lynette Lovelock, Mrs Lynne Middleton, Mrs Pam Mueller, Mrs Shirley
Stephenson, Mrs Dawn Taylor, Mrs Lorraine Wright, and the research midwives were
Mrs Chris Laws and Mrs Rosie McCabe. {funding}Funding: National Advisory Body for
the confidential inquiry into stillbirths and deaths in infancy.
Foundation
for the Study of Infant Deaths Research Unit,
Institute of Child Health,
Royal
Hospital for Sick Children,
Bristol BS2 8BJ
Peter S Blair,
medical
statistician
Peter J Fleming,
professor of infant health and
developmental physiology
NHS
Executive,
Quarry House,
Leeds LS2 9UA
David Bensley,
Leeds LS2 9PL
Iain Smith,
Northallerton,
North Yorkshire DL6 1JG
Chris Bacon,
consultant
paediatrician
Sheffield S10 2TH
Elizabeth Taylor,
consultant senior lecturer in
paediatrics
St Michael's Hospital,
Bristol BS2 8EG
Jem Berry,
Royal Hospital for Sick Children,
Bristol BS2 8BJ
Jean Golding,
professor of paediatric and perinatal epidemiology
Postgraduate Medical School,
Royal Devon and Exeter Hospital,
Exeter EX2 5DW
John Tripp,
consultant paediatrician
REFERENCES