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BMJ Open logoLink to BMJ Open
. 2020 Oct 5;10(10):e035562. doi: 10.1136/bmjopen-2019-035562

Maternal trauma due to motor vehicle crashes and pregnancy outcomes: a systematic review and meta-analysis

Carmen Amezcua-Prieto 1,2,3, Jennifer Ross 4, Ewelina Rogozińska 5,6, Patritia Mighiu 5, Virginia Martínez-Ruiz 1,2,3, Karim Brohi 4, Aurora Bueno-Cavanillas 1,2,3,, Khalid Saeed Khan 1,2,5, Shakila Thangaratinam 5
PMCID: PMC7537450  PMID: 33020077

Abstract

Objectives

To systematically review and quantify the effect of motor vehicle crashes (MVCs) in pregnancy on maternal and offspring outcomes.

Design

Systematic review and meta-analysis of observational data searched from inception until 1 July 2018. Searching was from June to August 2018 in Medline, Embase, Web of Science, Scopus, Latin-American and Caribbean System on Health Sciences Information, Scientific Electronic Library Online, TRANSPORT, International Road Research Documentation, European Conference of Ministers of Transportation Databases, Cochrane Database of Systematic Reviews and Cochrane Central Register.

Participants

Studies were selected if they focused on the effects of exposure MVC during pregnancy versus non-exposure, with follow-up to verify outcomes in various settings, including secondary care, collision and emergency, and inpatient care.

Data synthesis

For incidence data, we calculated a pooled estimate per 1000 women. For comparison of outcomes between women involved and those not involved in MVC, we calculated ORs with 95% CIs. Where possible, we statistically pooled the data using the random-effects model. The quality of studies used in the comparative analysis was assessed with Newcastle–Ottawa Scale.

Results

We included 19 studies (3 222 066 women) of which the majority was carried out in high-income countries (18/19). In population-level studies of women involved in MVC, maternal death occurred in 3.6 per 1000 (95% CI 0.25–10.42; 3 studies, 12 000 women; Tau=1.77), and fetal death or stillbirth in 6.6 per 1000 (95% CI 3.81–10.12; 8 studies, 47 992 women; I2=92.6%). Pooled incidence of complications per 1000 women involved in MVC was labour induction (276.43), preterm delivery (191.90) and caesarean section (166.65). Compared with women not involved in MVC, those involved had increased odds of placental abruption (OR 1.43, 95% CI 1.27–1.63; 3 studies, 1 500 825 women) and maternal death (OR 202.27; 95% CI 110.60–369.95; 1 study, 1 094 559 women).

Conclusion

Pregnant women involved in MVC were at higher risk of maternal death and complications than those not involved.

PROSPERO registration number

CRD42018100788.

Keywords: pregnancy, motor vehicle crashes, pregnancy complications


Strengths and limitations of this study.

  • This is the first systematic review examining the link between involvement in motor vehicle crashes (MVCs), mortality and adverse outcomes that includes evaluation of study quality assessment.

  • This is the second systematic review looking at outcomes following MVC in pregnancy.

  • We conducted our review using a prospectively registered protocol and reported it in accordance with the international standards.

  • Outcomes variables correspond to any trimester, not to specific trimesters.

  • Outcomes according to seat belt use are scarce, since only two studies use population-level data.

Introduction

Up to half of all women in developed countries drive motor vehicles1 and the consequences of road traffic-related injuries involving pregnant women can be severe.2 Indeed, motor vehicle crashes (MVCs) are the most common cause of non-obstetric trauma associated with fetal deaths (2.3 per 100 000 live births).3 The risk of adverse outcomes resulting from an MVC increases in the second trimester of pregnancy if the pregnant women were the driver4; however, this does not appear to be the case for pregnant passengers or pedestrians.5 A maternal mortality rate of 3.5 women per 100 000 is reported following MVCs in pregnant women.6 Mechanisms of injury recorded within the pregnant population of the UK national trauma registry, the Trauma Audit and Research Network, saw an increased rate of vehicular collision in pregnant women when compared with the non-pregnant cohort.7 In 2001–2008, 2.9% of pregnant women in North Carolina were drivers in one or more crashes.8 In the USA, data from the National Automotive Sampling System/Crashworthiness Data System reflect that when vehicles with pregnant women are involved in collision, 50% of those women will sustain an injury.9 There are few safety guidelines on travelling by car during pregnancy.10–12 The focus of these tends to be on questions around the use of seat belts and the activation of airbags in the car.12

There is a reported association between MVC and maternal mortality.13 Moreover, further associations such as the trigger for immediate delivery or being more likely to die are reported with severe blunt injury (Injury Severity Score (ISS) of 9 or above, or systolic blood pressure <90 mm Hg on arrival).14 Involvement in MVC is also associated with perinatal mortality,15 injuries to the abdominal region,16 placental abruption secondary to increased intra-abdominal pressure,17 preterm birth and caesarean section.6 However, more data are required in relation to areas such as fetal outcomes and higher risk pregnancies, particularly regarding sociodemographic characteristics of the mother, specific trimester of pregnancy when exposed to trauma, socioeconomic country conditions, severity and type of trauma, and collision characteristics such as speed. A systematic review on trauma in pregnancy (including five studies reporting complications of involvement in MVC, and fourteen other studies on other forms of trauma) showed that MVC and domestic violence were the most common causes of traumatic injury during pregnancy.4 No quality assessment of the included studies was reported in this review. Previous non-systematic reviews have published strategies used to monitor women and fetuses after a crash.18–21 However, to our knowledge there is no systematic review or meta-analysis focused on the maternal and fetal outcomes after MVC in pregnancy.

Review objectives

As the clinical impact on the mother and fetus after MVC has not been well documented, we conducted a systematic review of the effect on maternal and fetal outcomes of MVC in pregnant women, compared with those not involved in a collision.

Methods

We conducted a systematic review and reported it according to recommended standards.22

Literature search

Searching was from June to August 2018. The following databases were used to identify relevant literature: Medline, Embase, Web of Science, Scopus, Latin-American and Caribbean System on Health Sciences Information, Science Citation Index, Scientific Electronic Library Online, TRANSPORT, International Road Research Documentation, European Conference of Ministers of Transportation Databases, Cochrane Database of Systematic Reviews and Cochrane Central Register of Controlled Trials. We also sought to identify unpublished research or research reported in the grey literature by searching a range of relevant databases, including the Inside Conferences, Systems for Information on Grey Literature and Dissertation Abstracts. Furthermore, the searches of the medical database were supplemented with the internet search using a general search engine (eg, Google, www.google.co.uk/) and safetylit.org. Language and date restrictions were not applied to electronic searches. Relevant studies were identified using a combination of, but not limited to, the medical subject headings and keywords for “motor vehicle collision” (OR road traffic collision OR crash OR collision) and “pregnancy” (OR pregnant women OR gravid women OR childbearing women OR maternal).

Review inclusion criteria

Papers were selected if they studied the effects of exposure to trauma due to involvement in an MVC during pregnancy versus non-exposure, with follow-up to verify outcomes in various settings including secondary care, collision and emergency, and inpatient care. Observational studies (cohort studies, case–control design, non-intervention arms of randomised controlled trials) were included. Case series and case reports were excluded. Online supplemental appendix 1 shows the search strategy for Medline (via Ovid) and online supplemental appendix 2 the excluded studies with reasons.

Supplementary data

bmjopen-2019-035562supp001.pdf (48.1KB, pdf)

Supplementary data

bmjopen-2019-035562supp002.pdf (85.7KB, pdf)

Data extraction and study quality assessment

A double screening of papers was carried out. Two reviewers (CA-P and JR) independently extracted the relevant data from each full-text article and data were recorded using a standardised data extraction form. A data extraction form was piloted for each study design and amended as required. Discrepancies were resolved by consensus or by a discussion with a third senior author (ER). We extracted data on (a) severe adverse maternal outcomes such as maternal death, miscarriage and preterm birth (<37/40 and <34/40); (b) severe adverse fetal outcomes such as intrauterine death/stillbirth and neonatal death. Secondary outcomes were: (a) individual components of maternal outcomes such as preterm labour, mode of delivery (vaginal delivery vs caesarean section), premature rupture of membranes (PROM), preterm PROM, placental abruption, chorioamnionitis/sepsis and maternal admission to an intensive care unit (ICU) or high dependency unit; (b) individual components of fetal outcomes: respiratory distress syndrome, neonatal ICU admission, low birth weight and small for gestational age.

We also extracted data on (1) adverse outcomes in pregnant women involved in MVC and their offspring in subgroups according to maternal characteristics (low, high and any risk), trimester of exposure, country (low and middle income, high income), type of trauma (penetrating, blunt, burns), severity of trauma (mild, moderate, severe), seat belt use (yes, no), study quality (low, high); (2) risk factors for pregnancy complications following MVC such as maternal characteristics (age, parity, high risk pregnancy, gestational age), type of trauma, type of motor vehicle, type of collision, collision characteristic (stationary, high or moderate speed) and seat belt use.

The quality assessment of studies was independently evaluated by two reviewers (JR and CA-P) using the Newcastle–Ottawa Scale.23 This scale includes 8 items, 4 items about selection criteria of cases or cohorts in case–control or cohort designs, respectively; 2 items about comparability between groups (in both designs); and 3 items about exposure criteria in case–control designs and about outcomes in cohort designs. Any of those studies could be awarded a maximum of one star for each numbered item within the selection and exposure categories. A maximum of two stars could be given for comparability. For the incidence analysis, we considered six aspects24 : (1) representativeness of cohort; (2) design; (3) method of sampling; (4) adequacy of follow-up; (5) if the outcomes were adequately ascertained and (6) if measurement or misclassification bias was minimised. Studies without these features or with unclear reporting were classified to have a high risk of bias.

Patient and public involvement

No patient involved.

Data synthesis

We undertook random-effects meta-analysis to determine the ORs with 95% CIs for maternal and offspring complications from MVC. We estimated heterogeneity between the included studies with Χ2 test of Q (I2) excepting when not enough studies were in the meta-analysis,2 3 and we pooled the rates of maternal/fetal complications and reported with 95% CI. For each primary outcome, a meta-analysis was conducted for studies sufficiently homogeneous in terms of the characteristics of participants and exposure. The subgroup analysis was applied in: (a) trimester of pregnancy during which the trauma occurred; (b) maternal risk status (low, high, any risk); (c) type of trauma; (d) severity of trauma (using the ISS to categorise the severity of trauma sustained following MVC)25; (e) setting (low/middle-income, high-income country); (f) year of study publication: (before or after the introduction of mandatory seat belt legislature in the country of study); and (g) study quality according to the Newcastle and Ottawa Scale.23

Results

Study selection

Out of 1739 retrieved references, 19 studies met the eligibility criteria (figure 1). Five of these reported data allow us to compare pregnancy complications between pregnant women involved in MVC and those not involved in MVC.6 8 26–28 The totality of the studies (n=19) contributed to the analysis of the incidence of pregnancy complications among women involved in MVC.6 17 26–40

Figure 1.

Figure 1

The study selection process in the systematic review of outcomes on pregnant women involved in motor vehicle crashes.*references of relevant non-systematic reviews and Google Scholar.

Characteristics of included studies

The characteristics of included studies are in table 1. Included studies were published between 1993 and 2016. Most of them were carried out in developed, high-income countries such as the USA (14/18),8 26 28–30 32–39 Sweden (1/19),27 Kuwait (1/19)17 and Israel (1/19).40 The number of included pregnant women varies, ranging from 39 to 1 094 559. The data were sourced from hospital records/trauma registries (7/19)17 30 31 34 37 38 40 or from population-level databases (12/19).2 6 8 26–29 32 33 35 36 39 The majority of studies collected information on outcomes of pregnant women involved in MVC during any trimester of pregnancy. Eight out of 19 studies reported information about the use of safety devices such as seat belts and/or airbags.26 29 32 34 36–38 Also in eight studies, the authors assessed the severity of MVC injuries with five of these using a validated tool28 30 34 37 40 —most of them reporting ISS28 30 34 40 and one the Revised Trauma Scale.37

Table 1.

Characteristics of included studies

Study ID
author, year, country
Design Sample size Time period Inclusion criteria Data source Trimester Seat belt use
(with data)
Assessment of trauma severity
(with data)
Method of assessing trauma severity Maternal outcomes Offspring outcomes
Population-level data
Azar et al,2
2015,
USA
Population-based matched retrospective cohort
(incidence only)
5936 2003–2011 Admitted to hospital following MVC while pregnant Population-based cohort Any No No N/A Maternal death
Hyde et al,26
2003,
USA
Retrospective cohort
(incidence and comparison)
322 704 1992–1999 Pregnant drivers involved in MVC Linked databases (police registry and birth/death certificates) Any Yes Yes Study-specific definition‡  Fetal death
Kvarnstrand et al,27
2008,
Sweden
Retrospective cohort (incidence and comparison) 1 094 559 1991–2001 Maternal inclusion on the accident register >28 GW Linked databases (police registry and birth/death certificates) 2nd No Yes Study-specific definition§ Maternal death Fetal/neonatal death
Kuo et al,33
2007,
USA
Retrospective chart/database review (incidence only) 16982 injuries
4479 (in MVC)
2002 Pregnant women hospitalised with injury (only MVC used) Sample from population level cohort (National Inpatient Sample) Any No No N/A Delivery, hospitalisation
Schiff and Holt,28
2005,
USA
Retrospective cohort
(incidence and comparison)
17 899 1989–2001 Hospitalised for
MVC and with
a singleton live birth or fetal death
Linked databases (hospital discharge data and birth/death certificates) Any No Yes ISS Preterm birth, PROM,
C-section, placental abruption
Stillbirth,
LBW, SGA,
fetal distress,
RDS, meconium
Schiff et al,36
2010,
USA
Retrospective cohort (incidence only) 3348 2002–2005 Non-rollover
MVC among pregnant front seat occupants
Linked databases (hospital discharge data and birth/death certificates) Any Yes (airbag); no (seat belt) No N/A Preterm birth, placental abruption, labour induction, C-section Stillbirth, LBW,
SGA, RDS,
fetal distress,
meconium
Vivian-Taylor et al,6
2012,
Australia
Retrospective cohort
(incidence and comparison)
604 380 2000–2007 Women who gave birth exposed and not exposed to MVC Linked databases (hospital discharge data and birth/death certificates) 2nd No Yes Study-specific definition¶ Admission, placental abruption, APH, PPH, preterm birth, C-section Perinatal death (>20th GW), neonatal transfer
Vladutiu
et al,8
2013,
USA
Retrospective cohort
(incidence and comparison)
878 546 2001–2008 Pregnant women 16–46
years, >20 GW, delivering a live/stillbirth singleton infant
Linked databases (police registry and birth/death certificates) 2nd Yes (seat belt); yes (airbag) No N/A Placental abruption, PROM, preterm birth Stillbirth
Weiss and Strotmeyer,32
2002,
USA
Crash database pregnant versus non-pregnant (NASS/CDS)
(incidence only)
32 810 1995–1999 Pregnant and non-pregnant women 15–39 years Sample from population-level database of traffic accidents Any Yes No N/A Maternal death
Weiss et al,35
2008,
USA
Retrospective cohort
(incidence only)

1816 1999–2002 Injury-related emergency department visits by pregnant women (only MVC used) Linked databases (hospital discharge data and birth/death certificates) Any No No N/A Hospital admission
Whitehead,39
2013,*
USA
PRAMS survey database
(incidence only)
235 329 2000–2005 Survey of women who recently delivered a live-born infant Population-based cohort (PRAMS) Any No No N/A Preterm birth, UTI, PROM
Wolf et al,29
1993,
USA
Population-based retrospective cohort
(incidence only)
2582 1980–1988 Pregnant women drivers involved in MVC >20GW Linked databases (police registry and birth/death certificates) 2nd and 3rd Yes No N/A Preterm birth, placental abruption,
C-section
Stillbirth,
LBW,
RDS
Single hospital records/trauma registry
Aboutanos,34
2007,
USA
Retrospective chart/database review
(incidence only)
148 2001–2005 Single hospital records from trauma centre Any Yes
(only in miscarriage)
Yes ISS Maternal death, miscarriage Fetal death hydrops fetalis
Baerga-Varela et al,30
2000,
USA
Retrospective chart/database review
(incidence only)
39 1986–1996 Single hospital records Any No Yes ISS Maternal death, miscarriage Stillbirth
Brookfield et al,37
2013,
USA
Retrospective chart/database review
(incidence only)
256 1990–2007 Single hospital records from trauma centre Any Yes Yes ISS and RTS Maternal death, admission to hospital
Chibber
et al,17
2015,
Kuwait
Retrospective chart/database review
(incidence only)
728 2009–2012 Single hospital records 2nd No No N/A Maternal death, placental abruption, preterm birth, uterine rupture,
C-Section, admission
Fetal death, fetal distress
Luley et al,38
2013,
USA
Retrospective chart/database review
(incidence only)
126 1994–2010 Single hospital trauma database 2nd and 3rd Yes No N/A Maternal death, placental abruption,
C-section
Stillbirth
Miller et al,40
2016,
Israel
Retrospective cohort
(incidence only)
3794 2006–2013 National trauma registry Any No No ISS Maternal death, miscarriage, placental abruption,
C-section
Stillbirth
Orji et al,31
2002,
Nigeria
Retrospective chart/database review
(incidence only)
84 1980–2000 Single hospital records† Any No No N/A Maternal death, placental abruption, uterine rupture, C-section Perinatal death (fetal death), fetal tachycardia

*National survey.

†Two hospitals in same region included.

‡Possible/probable/incapacitated/fatal.

§Fatal/major/minor/uninjured.

Severe’= admission to ICU and/or blood transfusion and/or injury to abdomen/pelvis/lower back.

APH, antepartum haemorrhage; GW, gestational week; ICU, intensive care unit; ISS, Injury Severity Score; LBW, low birth weight; MVCs, motor vehicle crashes; N/A, not applicable; NASS/CDS, National Automotive Sampling System/Crashworthiness Data System; PPH, postpartum haemorrhage; PRAMS, Pregnancy Risk Assessment Monitoring System; PROM, premature rupture of membranes; RDS, respiratory distress syndrome; RTS, Revised Trauma Score; SGA, small for gestational age; UTI, urinary tract infection.

Quality assessment

Sixty per cent of studies had a low risk of bias with regards to the adequacy of representativeness and random sample selection (12/19). None of the studies was prospective. The categories of follow-up of more than 80% of participants, outcome ascertainment and misclassification bias showed low risk (figure 2). The five papers included for comparison of complication rates between pregnant women exposed to MVC and those who were not exposed (assessed using the Newcastle–Ottawa Scale) showed generally high quality, with four papers scoring 9/9 (6, 26, 28, 29). The remaining paper scored 8/9, losing 1 point for the comparability as it did not control for any secondary factors.27

Figure 2.

Figure 2

The quality assessment of the included studies.

Incidence of complications among pregnant women involved in MVCs

The assessment of adverse outcome incidence among women involved in MVC (using population-level data) demonstrated incidence estimations of 276.43 per 1000 for induction of labour (95% CI 262.54–290.54), 191.90 per 1000 for preterm delivery (95% CI 45.98–405.74) and 166.65 per 1000 for caesarean section (95% CI 47.34–339.00). The estimated incidence rates for other complications included 42.33 per 1000 for PROM, 17.08 per 1000 requiring admission to hospital, 16.14 per 1000 for placental abruption and 15.19 per 1000 for neonatal respiratory distress. A pooled incidence of maternal death was 3.60 per 1000 women (95% CI 0.25–10.42, 3 studies, 12 000 women, Tau=1.77). The pooled incidence of perinatal death (fetal death or stillbirth) per 1000 women was 6.60, (95% CI 3.81–10.12; 8 studies, 47 992 women; I2=92.6%) (table 2). The representation of the maternal and offspring outcomes according to trauma severity are in appendices (online supplemental appendices 3 and 4). Using data from single hospital centres, the random pooled estimation for the incidence of admission to hospital was 117.92 per 1000 women (95% CI 109.82–126.40)17 37; for maternal death was 135.05 per 1000 women (95% CI 131.37–138.80) and for fetal death was 5.73 per 1000 women (95% CI 3.05–9.77) (online supplemental appendices 5 and 6).

Table 2.

Incidence of adverse outcomes per 1000 women involved in motor vehicle crashes

Outcome and study Number of studies Number of women Incidence estimate per 1000 women 95% CI
Maternal
Maternal death 3 12 000 3.60 0.25–10.42
Azar et al,2 2005 6.57 4.68–8.97
Kvarnstrand et al,27 2008 6.61 3.70–10.88
Miller et al,40 2016 0.26 0.01–1.47
Admission to hospital 2 3838 17.08 13.20–21.46
Vivian-Taylor et al,6 2012 8.90 5.28–14.03
Weiss et al,35 2008 29.19 21.94–38.0
Placenta abruption 6 36 737 16.14 7.04–28.78
Wolf et al,29 1993 8.10 5.02–12.36
Miller et al,40 2016 1.05 0.29–2.70
Schiff and Holt,28 2005 113.40 88.80–142.01
Schiff et al,36 2010 12.25 8.80–16.58
Vivian-Taylor et al,6 2012 16.32 11.26–22.84
Vladutiu et al,8 2013 7.17 6.15–8.31
Preterm delivery 5 265 680 191.90 45.98–405.74
Schiff and Holt,28 2005 316.15 278.53–355.65
Schiff et al,36 2010 97.37 87.53–107.92
Vivian-Taylor et al,6 2012 83.09 71.42–95.98
Vladutiu et al,8 2013 110.33 106.43–114.33
Whitehead,39 2013 437.00 435.00–439.01
PROM 3 260 310 42.33 5.87–109.24
Schiff and Holt,28 2005 22.34 11.95–37.89
Vladutiu et al,8 2013 23.53 21.66–25.51
Whitehead,39 2013 96.00 94.81–97.20
Labour induction 2 3930 276.43 262.54290.54
Schiff and Holt,28 2005 223.37 190.15–259.42
Schiff et al,36 2010 286.14 270.87–301.78
Caesarean section 5 12 338 166.65 47.34–339.00
Miller et al,40 2016 6.06 3.85–9.08
Schiff and Holt,28 2005 254.30 219.38–291.73
Schiff et al,36 2010 259.26 244.48–274.46
Vivian-Taylor et al,6 2012 260.14 241.13–279.85
Wolf et al,29 1993 171.68 157.35–186.76
Offspring
Perinatal death 8 47 992 6.60 3.81–10.12
Kvarnstrand et al,27 2008 Fetal/neonatal 17.62 12.62–23.92
Hyde et al,26 2003 Fetal 5.01 3.66–6.70
Miller et al,40 2016 Stillbirth 0.79 0.16–2.31
Schiff and Holt,28 2005 Fetal 12.03 4.85–24.62
Vivian-Taylor et al,6 2012 Stillbirth 16.82 11.67–23.42
Vladutiu et al,8 2013 Stillbirth 5.25 4.38–6.23
Schiff et al,36 2010 Fetal 4.18 2.29–7.01
Wolf et al,29 1993 Fetal 3.47 1.59–6.58
Fetal distress 2 3930 60.09 52.85–67.77
Schiff and Holt,28 2005 132.30 105.84–162.56
Schiff et al,36 2010 50.48 43.31–58.44
Meconium at delivery 2 3930 52.61 45.82–59.85
Schiff and Holt,28 2005 63.57 45.15–86.57
Schiff et al,36 2010 51.08 43.86–59.08
RDS 3 6522 15.19 5.83–28.68
Schiff and Holt,28 2005 32.65 19.77–50.51
Schiff et al,36 2010 14.64 10.85–19.30
Wolf et al,29 1993 6.17 3.53–10.00

Data source: population database

PROM, premature rupture of membranes; RDS, respiratory distress syndrome.

Supplementary data

bmjopen-2019-035562supp003.pdf (40.5KB, pdf)

Supplementary data

bmjopen-2019-035562supp004.pdf (40.2KB, pdf)

Supplementary data

bmjopen-2019-035562supp005.pdf (57.3KB, pdf)

Supplementary data

bmjopen-2019-035562supp006.pdf (63.8KB, pdf)

Pregnancy complications in women involved versus not involved in MVCs

We observed a statistically significant link between involvement in MVC and maternal death (OR 202.3, 95% CI 110.60–370.00; single study)27 (data not shown in table or graphic). Figure 3 shows pooled results from population-level data, demonstrating a positive association between MVC and placental abruption (OR 1.43 95% CI 1.27–1.63). Two studies contributed data used in sensitivity analyses stratifying by seat belt use, where the pooled estimation26 of fetal death decreased with seat belt devices, but the association was not statistically significant (OR 0.66 95% CI 0.36–1.19) (online supplemental figure 1). The review manager forest plot displays a positive but not statistically significant association between fetal death and MVC without seat belt use (OR 5.78 95% CI 0.17–201.12, Tau2=6.51) (online supplemental figure 2).

Figure 3.

Figure 3

Comparison of outcomes between women involved and not involved in motor vehicle crashes (MVCs).

Supplementary data

bmjopen-2019-035562supp007.pdf (14.3KB, pdf)

Supplementary data

bmjopen-2019-035562supp008.pdf (16.8KB, pdf)

Discussion

Statement of principal findings

This review estimated that for women involved in MVC, maternal death occurrence was 3.6 per 1000 and perinatal death 6.6 per 1000 women. Compared with women not involved in MVC, those involved had an increased odds of placental abruption, antepartum haemorrhage and maternal death. The pooled incidence of complications per 1000 women involved in MVC was, from the higher incidence to the lower, induction of labour, preterm delivery, caesarean section, PROM and placental abruption (population level-data).

Strengths and weaknesses of this study

This is the second systematic review, after the one of Mendez-Figueroa et al,4 looking at outcomes following MVC in pregnancy. We conducted our review using a prospectively registered protocol and reported it in accordance with the international standards.41 This review, to our best knowledge, is the first one examining the link between involvement in MVC, mortality and adverse outcomes that involves evaluation of study quality assessment; 14 studies looking at outcome incidence related to MVC2 17 29–40 and 5 studies comparing outcomes in pregnant women involved in MVC and those who were not.6 8 26–28 We used established tools to assess outcome reporting quality for the incidence rates42 and comparability.23 We included data from population-level and single-centre studies, but the analysis and reporting of the results were independent in order to get precision and validity in the estimations. However, a couple of graphics of the maternal and offspring’s outcomes incidences have been included as online supplemental appendices 3 and 4. Between August 2018 and March 2020, there have been no new studies eligible to include in the systematic review.

For the incidence analysis, we evaluated the quality of the 19 studies of this systematic review. The highest risk was in the design. None of the studies had a prospective design. The representativeness of cohort and the random method of sampling were other limitations of the quality of studies, with 7 out of 19 studies having a high risk of bias in these areas.17 30 31 34 37 38 40 However, the quality assessment of the five papers included for comparison of complication rates between pregnant women involved and not involved in MVC using the Newcastle–Ottawa Scale showed generally high quality, with four papers scoring 9/9.6 8 26 28

The weaknesses of this systematic review are as follows. First, outcomes were not reported by trimester, with 13 out of 19 papers focused on MVC at any trimester. Second, outcomes, according to seat belt use, are scarce as only two studies using population-level data looked at safety features as a stratification factor.8 26 Two studies with data sourced from hospital records/single-site trauma registries37 38 and three studies using population-level databases8 26 29 reported some outcomes regarding seat belt use. Third, we found a limited number of relevant studies comparing outcomes between women involved and not involved in MVC. The majority of the studies were carried out in the USA8 26 28 with most recent one published in 2013.8 Fourth, the included studies differed in study design with seven of them using hospital records/single-site trauma registry17 30 31 34 37 38 40 and twelve population databases.2 6 8 26–29 32 33 35 36 39 Despite analysing the data within the respective study designs and incorporation of anticipated variation into the statistical model (random-effects),43 we encountered substantial statistical heterogeneity in the pooled estimates that could not be formally explored due to a limited number of studies and poor reporting of important factors such as trauma severity. As a fifth point, these data apply to developed countries—only one of the papers included data from an underdeveloped country, perhaps influencing the outcomes that might otherwise be seen in the developed world. Finally, in only eight studies did authors assess severity of MVC injuries, with only five of these using a validated tool.28 30 34 37 40 This was a challenge when aiming to analyse results according to the severity of the crash.

Meaning of the study

The strongest association was found between placental abruption6 8 28 and MVC. Maternal death was associated with involvement in MVC but this finding needs to be treated with caution as the data come from a single study.27 The outcomes in descending order of incidence estimate per 1000 (population-level data) were the induction of labour, preterm delivery, caesarean section, PROM and admission to hospital, placental abruption and maternal death. In the analyses stratified by use of seat belts, we observed an association of fetal death with lack of seat belt use by pregnant women involved in an MVC. However, this finding was not statistically significant and informed by a limited number of studies. Previous studies have shown that pregnant women wearing seat belts during the MVC did not experience a significantly higher risk of adverse fetal outcomes than women who were not involved in MVC.26 Furthermore, airbags seem to be contributing to the protection of both pregnant drivers and their fetuses.44

The results of this systematic review provide evidence informing primary prevention measures, recommendations and educational interventions for pregnant women in the context of MVC that should be incorporated into the primary care guidelines.

Unanswered questions and future research

The effects of MVC in pregnant women is a specific field that requires further research and an improved methodological approach to determine the risks of adverse maternal and fetal outcomes.

Additional variables such as trauma severity, the position of the women in the car, use of seat belts, deployment or non-deployment of an airbag, severity of the crash and gestational week of pregnancy should be recorded in relation to MVC exposure in order to allow more precision when analysing outcomes. A greater number of well-designed studies in a variety of global settings would strengthen current evidence-base.

Conclusions

Pregnant women involved in MVC seem to be at increased risk of maternal death and complications, especially placental abruption, than those not involved in MVC. The risk of complications such as preterm delivery, PROM and caesarean section were also increased. However, these findings need to be treated with caution due to the small number of studies included in the review and considerable differences between studies. Road traffic authorities should be conscious and strict in targeting preventive measures aimed at pregnant users of motor vehicles due to risk associated with potential involvement in MVC.

Supplementary Material

Reviewer comments
Author's manuscript

Footnotes

Contributors: PM conducted literature searches and screened publications jointly with JR. CA-P and JR extracted the data. CA-P and ER drafted the manuscript and conducted the statistical analyses. KSK and ST designed the study review. CA-P is the guarantor. VM-R, KB, ABC, ST and KSK gave critical revision of the manuscript. All authors had full access to the data and take responsibility for the data analyses.

Funding: The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

Competing interests: None declared.

Patient consent for publication: Not required.

Provenance and peer review: Not commissioned; externally peer reviewed.

Data availability statement: All data relevant to the study are included in the article or uploaded as supplemental information.

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