BMJ 2001;323:476-479 [Abridged] ( 1 September )

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Teenage pregnancy and risk of adverse perinatal outcomes associated with first and second births: population based retrospective cohort study

Gordon C S Smith, specialist registrar in maternal-fetal medicine aJill P Pell, consultant b

a Department of Obstetrics and Gynaecology, University of Glasgow, Queen Mother's Hospital, Glasgow G3 8SH, b Department of Public Health, Greater Glasgow Health Board, Glasgow G3 8YU

Correspondence to: G C S Smith, Department of Obstetrics and Gynaecology, University of Cambridge, Rosie Hospital, Cambridge CB2 2SW gcss2{at}cam.ac.uk


    Abstract
Top
Abstract
Introduction
Methods
Results
Discussion
References

Objective: To determine whether first and second births among teenagers are associated with increased risk of adverse perinatal outcomes after confounding variables have been taken into account.
Design: Population based retrospective cohort study using routine discharge data for 1992-8.
Setting: Scotland.
Main outcome measures: Stillbirth, preterm delivery, emergency caesarean section, and small for gestational age baby among non-smoking mothers aged 15-19 and 20-29.
Results: The 110 233 eligible deliveries were stratified into first and second births. Among first births, the only significant difference in adverse outcomes by age group was for emergency caesarean section, which was less likely among younger mothers (odds ratio 0.5, 95% confidence interval 0.5 to 0.6). Second births in women aged 15-19 were associated with an increased risk of moderate (1.6, 1.2 to 2.1) and extreme prematurity (2.5, 1.5 to 4.3) and stillbirth (2.6, 1.3 to 5.3) but a reduced risk of emergency caesarean section (0.7, 0.5 to 1.0).
Conclusions: First teenage births are not independently associated with an increased risk of adverse pregnancy outcome and are at decreased risk of delivery by emergency caesarean section. However, second teenage births are associated with an almost threefold risk of preterm delivery and stillbirth.


What is already known on this topic
Teenage mothers are more likely to deliver prematurely and to have a perinatal death than older women

Teenage mothers are also more likely to smoke, be having a first baby, and live in adverse social circumstances

What this study adds
Non-smoking women aged 15-19 having a first birth were not at increased risk of adverse obstetric outcomes compared with women aged 20-29 after potential confounding variables were adjusted for

Non-smoking women aged 15-19 having a second birth were at significantly increased risk of both premature delivery and stillbirth compared with women aged 20-29 



    Introduction
Top
Abstract
Introduction
Methods
Results
Discussion
References

Teenage pregnancy is an important public health problem as it often occurs in the context of poor social support and maternal wellbeing. Some studies have suggested that first teenage pregnancies have a higher frequency of adverse perinatal outcomes. 1 2 However, there is argument about whether this is an independent association 1 2 or explained by confounding factors.3-5 In general, the risk of adverse outcomes is lower in second pregnancies. However, longitudinal studies comparing outcomes in first and second pregnancies in teenagers have produced inconsistent results.6-9 Cross sectional studies comparing the outcome of second births in teenagers and older women have observed increased rates of preterm birth, low birth weight, and perinatal death 10 11 but have failed to adjust for potential confounding factors such as smoking and socioeconomic deprivation.

Scotland is well placed to study the outcomes of teenage pregnancy. Teenage pregnancy rates in the United Kingdom are the highest in western Europe. Routine obstetric data have been collected on more than 99% of births in Scotland for over 20 years.12 Scotland has a population that is relatively homogeneous in terms of race, and health care is free at the point of access, including all medical, surgical, drug, and dental treatment during pregnancy. The aims of this study were to determine whether teenage pregnancy was associated with increased rates of adverse perinatal outcome, whether the association differed by parity, and whether any associations were independent of confounding factors.


    Methods
Top
Abstract
Introduction
Methods
Results
Discussion
References

We used the Scottish morbidity record 2 (SMR2) database to identify all singleton births resulting in a live or stillborn baby during 1992-8. Inclusion in the main study group was restricted to first or second births, gestation at birth of between 24 and 43 weeks, birth weight >500 g, maternal age between 15 and 29 years, and non-smoking mothers. We also selected a second cohort who fulfilled all the above criteria except that they were classified as smokers at the time of first attendance for antenatal care.

Definitions and denominators
First births were defined as births to women who had had no previous pregnancies or whose previous pregnancies had all ended in either therapeutic abortion or miscarriage. Second births were defined as having been preceded by only one pregnancy that did not result in abortion. Gestational age at birth was defined as the number of completed weeks of gestation based on the estimated delivery date in the clinical record. A small for gestational age baby was defined as a live baby who was less than the 5th percentile of birth weight for the given week of gestation, using percentiles derived from all Scottish singleton live births recorded in the SMR2 database with values for both birth weight and gestational age in 1992-8 (n=409 541). The denominator was all live births.

Very preterm delivery was defined as birth of a live baby at 24 to 32 weeks' gestation, and the denominator was all live births at or after 24 weeks' gestation. Moderately preterm delivery was defined as live births at 33 to 36 weeks' gestation, and the denominator was all live births at or after 33 weeks' gestation. Stillbirth was defined as delivery of a dead baby at or after 24 weeks' gestation, and the denominator was all births at or after 24 weeks' gestation. Neonatal death was defined as death of a liveborn baby in the first 28 days of life, and the denominator was all live births. Emergency caesarean section was defined as any unplanned caesarean delivery, and the denominator was all live births.

Maternal age was defined as the age of the mother in completed years at the time of birth because many of the outcomes were delivery related. Maternal height was measured in centimetres. Postcode of residence was used to derive Carstairs socioeconomic deprivation scores.13 These are based on 1991 census data on car ownership, unemployment, overcrowding, and social class within postcode sectors. The deprivation scores were then used to categorise women into quintiles based on the study population. Non-smoking was defined as never having smoked at the time of first attendance for antenatal care, and smokers were defined as women who were current smokers at the time of first attendance for antenatal care. Details of the statistical analyses are available on the BMJ's website.


    Results
Top
Abstract
Introduction
Methods
Results
Discussion
References

Data were complete in 371 531 (90.3%) cases, and the main study group comprised the 110 233 non-smoking women aged between 15 and 29 years having a first or second birth between 24 and 43 weeks gestation of a baby weighing over 500 g.

Table 1 shows the demographic characteristics and the frequency of adverse outcomes in the study group.


                              
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Table 1. Study group characteristics and crude outcomes. Values are numbers (percentages) of women unless stated otherwise

We then compared the risk of adverse outcomes associated with maternal age 15-19 between first and second births. This indicated that the risk of delivering a small for gestational age baby and of having an emergency caesarean section did not differ significantly by parity. However, when the risk of adverse obstetric outcomes associated with maternal age 15-19 was compared for first and second births, there were significant differences in the odds ratios of moderately premature birth (P=0.01), extremely premature birth (P=0.004), and stillbirth (P=0.03) (table 2). Therefore, the multivariate analyses were stratified by parity.


                              
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Table 2. Univariate and multivariate logistic regression analysis of the risk of adverse perinatal outcomes among women aged 15 to 19 years of age compared with women aged 20-29 years (non-smokers)

On multivariate analysis, women aged 15-19 years having first births were not at increased risk of any of the six adverse outcomes studied compared with women aged 20-29 (table 2). However, among second births, mothers aged 15-19 were at significantly increased risk of moderately and extremely premature birth and stillbirth (table 2). Emergency caesarean section was less likely among younger mothers at both first and second births. There were no significant interactions between maternal age at the time of delivery and socioeconomic deprivation quintile, height, year of delivery, or previous abortions for any of the outcomes for either first or second births.

When the risk of adverse outcome was compared within the age range 15-19, there was no significant variation in the risk of moderately or extremely premature birth, stillbirth, neonatal death, or delivery by emergency caesarean section. However, compared with 19 year old women, the risk of delivering a baby weighing less than the fifth percentile for gestational age was significantly lower among women aged 16 to 18 (figure).



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Adjusted odds ratios and 95% confidence intervals for delivering a small for gestational age baby (less than the 5th percentile for gestational age) associated with maternal age among first teenage births to non-smokers. Odds ratios were adjusted for maternal height category, socioeconomic deprivation quintile, previous spontaneous and therapeutic abortions, and year. The reference category was women giving birth aged 19

The proportion of women who were current smokers but fulfilled the other inclusion criteria at the time of first attendance for antenatal care varied by age and parity. Among women aged 15-19, 12 862 (47.5%) of first births and 2148 (54.8%) of second births were to smokers, whereas among women aged 20-29, 28 875 (27.4%) of first births and 26 120 (34.1%) of second births were to smokers (P<0.001).

When outcomes among 70 005 smokers were analysed, the risks associated with maternal age 15-19 again varied by parity. Among first births to smokers, there was a weak positive association between being aged 15-19 and moderately premature birth (table 3). Among second births to smokers, women aged 15-19 were at increased risk of moderately and extremely premature delivery and neonatal death. For both first and second births among smokers, being aged 15-19 was associated with a decreased risk of delivering a small for gestational age baby and being delivered by emergency caesarean section (table 3).


                              
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Table 3. Adjusted odds ratiosdagger (95% confidence intervals) for adverse outcomes in first and second births to women aged 15 to 19 compared with women aged 20-29 (smokers)




    Discussion
Top
Abstract
Introduction
Methods
Results
Discussion
References

Compared with older women, women who had a first birth during their teenage years were not at increased risk of any of the adverse outcomes studied and, indeed, were at significantly decreased risk of requiring emergency caesarean section. A previous study from the United States found that first teenage birth was independently associated with an increased risk of intrauterine growth restriction and of premature delivery,1 and a Swedish study observed that first teenage births were at increased risk of perinatal death.2 The main weakness of both studies was the failure to adjust for maternal smoking. Smoking is one of the strongest risk factors for adverse perinatal outcomes,14 and previous studies have shown that pregnant teenagers are more likely to smoke than pregnant older women. 15 16 Our findings in non-smoking mothers suggest that the positive associations previously reported among first births might simply reflect inadequate adjustment for confounding variables. Indeed, when outcomes were compared within the age range 15-19, women aged 16-18 had a decreased risk of intrauterine growth retardation, which is consistent with a previous population based study from the United States.17

By contrast, we found that second births among women aged between 15 and 19 years were associated with an almost threefold risk of extremely premature birth and stillbirth compared with women aged between 20 and 29 years (table 2). A similar pattern was observed among women who smoked. However, the Scottish mortality record database does not include information on the number of cigarettes smoked a day or the duration of smoking. Both of these might be expected to vary systematically with age. Since there is a dose-effect relation between smoking and adverse outcomes,18 the findings among smokers should be interpreted with caution.

Conclusions
Our findings suggest a causal relation between second teenage birth and adverse pregnancy outcome. It is unlikely that the association can be explained by differences in the interval between pregnancies among teenage and older mothers since the associations observed were much greater than those previously reported for short intervals between pregnancies.19 Furthermore, teenage mothers were not at increased risk of a small for gestational age baby, which is known to be more common after a short interval between pregnancies.19 A biological cause could be confirmed or refuted only by access to more detailed socioeconomic information at the individual level. This would require prospective collection of data.

    Acknowledgments

We thank Jim Chalmers, consultant in public health medicine, at the Information and Statistics Division for providing the crude Scottish morbidity record (SMR2) data.

    Footnotes

Funding: None.

Competing interests: None declared.

The full version of this paper is available on the BMJ's website


    References
Top
Abstract
Introduction
Methods
Results
Discussion
References

1. Fraser AM, Brockert JE, Ward RH. Association of young maternal age with adverse reproductive outcomes. N Engl J Med 1995; 332: 1113-1117[Abstract/Full Text].
2. Olausson PO, Cnattingius S, Haglund B. Teenage pregnancies and risk of late fetal death and infant mortality. Br J Obstet Gynaecol 1999; 106: 116-121[Medline].
3. Strobino DM, Ensminger ME, Kim YJ, Nanda J. Mechanisms for maternal age differences in birth weight. Am J Epidemiol 1995; 142: 504-514[Abstract].
4. Berenson AB, Wiemann CM, McCombs SL. Adverse perinatal outcomes in young adolescents. J Reprod Med 1997; 42: 559-564[Medline].
5. Lao TT, Ho LF. The obstetric implications of teenage pregnancy. Hum Reprod 1997; 12: 2303-2305[Abstract].
6. Elster AB. The effect of maternal age, parity, and prenatal care on perinatal outcome in adolescent mothers. Am J Obstet Gynecol 1984; 149: 845-847[Medline].
7. Hellerstedt WL, Pirie PL, Alexander GR. Adolescent parity and infant mortality, Minnesota, 1980 through 1988. Am J Public Health 1995; 85: 1139-1142[Abstract].
8. Sweeney PJ. A comparison of low birth weight, perinatal mortality, and infant mortality between first and second births to women 17 years old and younger. Am J Obstet Gynecol 1989; 160: 1361-1367[Medline].
9. Blankson ML, Cliver SP, Goldenberg RL, Hickey CA, Jin J, Dubard MB. Health behavior and outcomes in sequential pregnancies of black and white adolescents. JAMA 1993; 269: 1401-1403[Medline].
10. Lumley J. The epidemiology of preterm birth. Baillieres Clin Obstet Gynaecol 1993; 7: 477-498[Medline].
11. McCormick MC, Shapiro S, Starfield B. High-risk young mothers: infant mortality and morbidity in four areas in the United States, 1973-1978. Am J Public Health 1984; 74: 18-23[Abstract].
12. Cole SK. Scottish maternity and neonatal records. In: Chalmers I, McIlwaine GM, eds. Perinatal audit and surveillance. London: Royal College of Obstetricians and Gynaecologists, 1980:39-51.
13. McLoone P, Boddy FA. Deprivation and mortality in Scotland, 1981 and 1991. BMJ 1994; 309: 1465-1470[Abstract/Full Text].
14. DiFranza JR, Lew RA. Effect of maternal cigarette smoking on pregnancy complications and sudden infant death syndrome. J Fam Pract 1995; 40: 385-394[Medline].
15. Olausson PM, Cnattingius S, Goldenberg RL. Determinants of poor pregnancy outcomes among teenagers in Sweden. Obstet Gynecol 1997; 89: 451-457[Medline].
16. Lao TT, Ho LF. Obstetric outcome of teenage pregnancies. Hum Reprod 1998; 13: 3228-3232[Abstract].
17. Lee KS, Ferguson RM, Corpuz M, Gartner LM. Maternal age and incidence of low birth weight at term: a population study. Am J Obstet Gynecol 1988; 158: 84-89[Medline].
18. Kyrklund-Blomberg NB, Cnattingius S. Preterm birth and maternal smoking: risks related to gestational age and onset of delivery. Am J Obstet Gynecol 1998; 179: 1051-1055[Medline].
19. Zhu BP, Rolfs RT, Nangle BE, Horan JM. Effect of the interval between pregnancies on perinatal outcomes. N Engl J Med 1999; 340: 589-594[Abstract/Full Text].

(Accepted 4 June 2001)


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