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.
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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
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.
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
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.
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.
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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).
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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
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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Associated Data
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Supplementary Materials
bmjopen-2019-035562supp001.pdf (48.1KB, pdf)
bmjopen-2019-035562supp002.pdf (85.7KB, pdf)
bmjopen-2019-035562supp003.pdf (40.5KB, pdf)
bmjopen-2019-035562supp004.pdf (40.2KB, pdf)
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bmjopen-2019-035562supp007.pdf (14.3KB, pdf)
bmjopen-2019-035562supp008.pdf (16.8KB, pdf)