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Assessing the Impact of Smoke-free Legislation on Perinatal Health in the Netherlands

Assessing the Impact of Smoke-free Legislation on Perinatal Health in the Netherlands

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02189265
Enrollment
2069695
Registered
2014-07-14
Start date
2000-01-31
Completion date
2014-07-31
Last updated
2014-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infant, Low Birth Weight, Infant Mortality, Infant, Small for Gestational Age, Infant, Very Low Birth Weight, Perinatal Mortality, Premature Birth, Stillbirth, Sudden Infant Death

Keywords

Live birth [MeSH], Infant [MeSH], Infant, newborn [MeSH], Second-hand smoke, Tobacco smoke pollution [MeSH], Smoke-free, Smoke-free policy [MeSH]

Brief summary

The purpose of this study is to investigate whether there has been a change in perinatal outcomes following the phased smoking ban introduction (January 2004 for workplaces; July 2008 for bars and restaurants) workplaces in the Netherlands.

Detailed description

Primary research questions 1. Is the phased introduction of smoke-free legislation in The Netherlands associated with reductions in adverse perinatal outcomes (e.g. perinatal mortality, preterm birth, small for gestational age)? 2. How do these associations compare with those described for other European countries in comparable studies (i.e. Belgium (Cox 2013), England (Been et al under review), Scotland (Mackay 2012))? Study design Retrospective cohort study (using prospective routinely collected health care data) Study population All singleton births in the Netherlands between January 1st 2000 and December 31st 2011. Intervention The intervention under study is the ban on smoking in workplaces, and in bars and restaurants implemented in the Netherlands on January 1st, 2004 and July 1st, 2008, respectively. Inclusion and exclusion criteria We will include all registered singleton births in the Netherlands occurring between January 1st, 2000 and December 31st, 2011. This is the maximum time period surrounding the ban's introduction for which the required birth data are available through the data source. Multiple pregnancies, neonates with chromosomal anomalies, pregnancies with unknown gestational age, pregnancies that ended before 24 weeks and pregnancies resulting in the birth of a child weighing less than 500 grams will be excluded. Outcome The primary outcomes are: * Perinatal mortality (stillbirth + early neonatal mortality, i.e. within the first 7 days of life) * Preterm birth (live birth with gestational age \<37+0 weeks) * Small for gestational age (SGA; live birth with birth weight below 10th centile; The Dutch PRN reference curves for birth weight by gestational age according to parity, sex and ethnic background will be used) To assess whether smoke-free legislation had a selective impact on certain subgroups of outcomes we furthermore identified a number of secondary outcomes: * Stillbirth (born dead from 24+0 weeks of gestation) * Early neonatal mortality (live birth and death within first 7 days) * Very preterm birth (live birth with gestational age \<32+0 weeks) * Low birth weight (live birth with birth weight \<2500 grams) * Very low birth weight (live birth with birth weight \<1500 grams) * Very small for gestational age (live birth with birth weight below percentile 2.3rd centile) * Major congenital anomalies (based on reported associations with antenatal smoke exposure (Hackshaw 2011)). Data sources Individual level health care data will be extracted from The Netherlands Perinatal Registry (PRN). Linked midwifery, obstetric, and neonatal data are available from 2000 to 2011 (including 2011). Data extraction and handling All relevant variables regarding our outcomes, as well as relevant potential confounders will be extracted from the database. Sample size Power calculation for interrupted time series modelling is complicated given the complexity of the analysis. Similar previous studies have demonstrated statistically significant and clinically relevant effects of smoke-free legislation on preterm birth (Cox 2013; Mackay 2012; Page 2012), low birth weight (Mackay 2012), SGA (Mackay 2012; Kabir 2013), and perinatal mortality (Mackay et al. and Been et al. both under review). Given the larger population size of the Netherlands as opposed to the regions in which these studies were carried out (except for Been et al. under review), we expect our study to have sufficient power to detect similar effect sizes, should these be present. Statistical analysis Incidences for each outcome will be presented graphically for each time period to facilitate visualisation of temporal fluctuations and trends in changes of incidence levels. To facilitate timing of the events, date of delivery and expected term date are required for each pregnancy. Data will be presented as outlined in different Tables. Interrupted time series analyses with adjustment for potential confounders will be performed to assess the associations between implementation of smoke-free legislation and primary and secondary outcome measures. Individual-level analysis will be performed using logistic regression analysis. The models will account for the underlying temporal trend in incidence, and will allow for a sudden change in incidence ('step change') following the introduction of the smoking bans. We will test and adjust for any non-linearity in the underlying time trends, and seasonality will be accounted as appropriate. Sensitivity analyses (primary outcomes only) In recent years, gestational age is usually estimated based on early ultrasonography findings, which is more reliable than estimation based on the last menstrual period. Although the method of ascertainment is not recorded in PRN, there is an item indicating 'certainty' of the gestational age, which is positive in about 93% of records. For the primary outcomes preterm birth and SGA we will perform a sensitivity analysis including only cases in whom gestational age estimation is considered reliable according to this item. Recent perinatal management changes have been implemented in The Netherlands resulting in increased active management of babies born at the edge of viability (i.e. 23-24 weeks gestation) (NVOG 2010). This has resulted in increased survival at this gestational age as well as altered management of 25-26 week infants, which likely affects the number of babies born preterm (although this effect is expected to be small given the small percentage of all preterm babies being born at this stage), as well as mortality indicators. For the primary outcomes preterm birth and perinatal mortality we will therefore perform a sensitivity analysis excluding babies born before 26 completed weeks of gestation. Smoking during pregnancy is known to be underreported in the PRN database. Definitions between different caregivers differ; (any) smoking and heavy smoking (\>20 cigarettes daily). We will consider performing subgroup analyses of the impact of smoke-free legislation on the primary outcomes according to maternal smoking status during pregnancy. In a sensitivity analysis we will investigate whether smoke-free legislation has any differential impact on spontaneous preterm birth versus medically indicated preterm birth. All analyses will be performed using Stata 13.0.

Interventions

The intervention under study is the ban on smoking in workplaces, and in bars and restaurants implemented in the Netherlands on January 1st, 2004 and July 1st, 2008, respectively.

Sponsors

Maastricht University Medical Center
CollaboratorOTHER
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
CollaboratorOTHER
The Netherlands Perinatal Registry (PRN)
CollaboratorUNKNOWN
University of Edinburgh
Lead SponsorOTHER

Study design

Observational model
ECOLOGIC_OR_COMMUNITY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 1 Weeks
Healthy volunteers
Yes

Inclusion criteria

Data are obtained via The Netherlands Perinatal Registry (PRN) (6). All registered stillbirths and livebirths occurring in the Netherlands between 1 January 2000 and 31 December 2011 are included. Inclusion Criteria: * Singleton birth occurring in the Netherlands between January 1st, 2000 and December 31st, 2011 * Liveborn (for all outcomes other than stillbirth and congenital anomalies)

Exclusion criteria

* No chromosomal anomalies

Design outcomes

Primary

MeasureTime frameDescription
Perinatal mortalityfrom 24+0 weeks gestation (for stillbirth); up to 7 days postnatally (for early neonatal mortality)stillbirth (i.e. intrauterine death from 24+0 weeks gestation) or early neonatal mortality (i.e. death within the first 7 days postnatally)
Preterm birthgestational age >= 24+0 weeks and <37+0 weekslive birth with gestational age \>= 24+0 weeks and \<37+0 weeks
Small for gestational agegestational age >= 24+0 weekslive birth at gestational age \>= 24+0 weeks with birth weight below 10th centile

Secondary

MeasureTime frameDescription
Low birth weightgestational age >= 24+0 weekslive birth at gestational age \>= 24+0 weeks with birth weight \<2500 grams
Very low birth weightgestational age >= 24+0 weekslive birth at gestational age \>= 24+0 weeks with birth weight \<1500 grams
Stillbirthgestational age >= 24+0 weeksborn dead from 24+0 weeks of gestation
Major congenital anomaliesgestational age >= 24+0 weeksbirth at \>= 24+0 weeks of gestation with a major birth defect (birth defects known to be influenced by antenatal smoke exposure based on recent systematic review (Hackshaw 2011))
Very small for gestational agegestational age >= 24+0 weekslive birth at gestational age \>= 24+0 weeks with birth weight below 2.3rd centile
Early neonatal mortalityup to 7 days postnatally after live birth at gestational age >= 24+0 weeksdeath within first 7 days after live birth at gestational age \>= 24+0 weeks
Very preterm birthgestational age >= 24+0 weeks and <32+0 weekslive birth with gestational age \>= 24+0 weeks and \<32+0 weeks

Countries

Netherlands, United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 13, 2026