Jump to: Page Content, Site Navigation, Site Search,
You are seeing this message because your web browser does not support basic web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.
Melbourne F Hovell a Center for Behavioral Epidemiology and
Community Health (C-BEACH), Graduate School of Public Health, San Diego
State University, San Diego, CA 92182, USA, b Centers for Disease Control
and Prevention, National Center for Environmental Health, Division of
Laboratory Sciences, Atlanta, GA 30341-3724, USA
Correspondence to: M F
Hovell behepi{at}rohan.sdsu.edu
| |
Abstract |
|---|
|
|
|---|
Objective:
To test the efficacy of behavioural
counselling for smoking mothers in reducing young children's exposure
to environmental tobacco smoke.
The World Health Organization has estimated that the health of
almost half of the world's children is threatened by exposure to
environmental tobacco smoke.1 In the United States the
prevalence of US children living in homes with a smoker has been
estimated to be 43%, with state specific estimates of exposure in the
home ranging from 12% to 34%2; nationally, about 15 million US children and adolescents are exposed.3
Similarly, about 43% of Australian children,4 33% of
Canadian children,5 and 41% of British children are
exposed to environmental tobacco smoke.6 Exposure increases children's risk of respiratory tract infections, otitis media, asthma, and the sudden infant death syndrome.7-9
The costs to children's medical care from exposure were $703m-$897m
(£439m-£561m) in the United States, $239.5m (£150m) in Canada, and
$267m (£167m) in Great Britain (in 1997 prices).10
Two trials reported significant decreases in children's exposure to
environmental tobacco smoke after counselling of parents. Greenberg et
al decreased children's reported exposure, but infants' urine
cotinine concentrations increased.11 Hovell and colleagues found similar reductions in reported exposure, which were sustained over two years, but did not measure cotinine
concentrations.
12 13
We extended our earlier research by
measurement of cotinine concentrations and by testing counselling (in
person and by telephone) with high risk, ethnically diverse, and low
income families recruited from the US supplemental nutrition programme
for women, infants, and children. We hypothesised that counselling
would decrease children's exposure, decrease mothers' smoking, and
increase rates of stopping smoking.
Protocol
Inclusion criteria
Recruitment
Counselled group
Design:
Randomised double blind controlled trial.
Setting:
Low income homes in San Diego county, California.
Participants:
108 ethnically diverse mothers who
exposed their children (aged <4 years) to tobacco smoke in the home.
Intervention:
Mothers were given seven counselling
sessions over three months.
Main outcome measures:
Children's reported exposure
to environmental tobacco smoke from mothers in the home and from all
sources; children's cotinine concentrations in urine.
Results:
Mothers' reports of children's exposure to their smoke in the home declined in the counselled group from 27.30 cigarettes/week at baseline, to 4.47 at three months, to 3.66 at 12 months and in the controls from 24.56, to 12.08, to 8.38. The
differences between the groups by time were significant (P=0.002).
Reported exposure to smoke from all sources showed similar declines,
with significant differences between groups by time (P=0.008). At 12 months, the reported exposure in the counselled group was 41.2% that
of controls for mothers' smoke (95% confidence interval 34.2% to
48.3%) and was 45.7% (38.4% to 53.0%) that of controls for all
sources of smoke. Children's mean urine cotinine concentrations
decreased slightly in the counselled group from 10.93 ng/ml at baseline
to 10.47 ng/ml at 12 months but increased in the controls from 9.43 ng/ml to 17.47 ng/ml (differences between groups by time P=0.008). At
12 months the cotinine concentration in the counselled group was 55.6%
(48.2% to 63.0%) that of controls.
Conclusions:
Counselling was effective in reducing
children's exposure to environmental tobacco smoke. Similar
counselling in medical and social services might protect millions of
children from environmental tobacco smoke in their homes.
![]()
Introduction
Top
Abstract
Introduction
Participants and methods
Results
Discussion
References
![]()
Participants and methods
Top
Abstract
Introduction
Participants and methods
Results
Discussion
References
We included English and Spanish speaking mothers who smoked at
least two cigarettes a day and exposed their child (aged <4 years) to
the smoke from at least one cigarette a day. We excluded women who were
currently breast feeding, to avoid confounded cotinine
analyses,
14 15
and women who did not have a telephone, to
ensure exposure to the intervention.
Nine months' screening at sites of the supplemental nutrition
programme for women, infants, and children identified 1147 possibly
eligible families. Of these, we contacted 832: 162 (19.5%) qualified
and were offered financial incentives ($60-$90) to participate. We
enrolled the first 108 women who signed informed consent forms, an
adequate sample size based on previous research.12 After
we had taken baseline measures, we randomly assigned the families to
counselling or control conditions.
Counselled mothers were told that quitting smoking was not
required. They were given seven individualised counselling sessions
(three in person and four by telephone) during three months.
Counselling was based on shaping procedures.16 The mean
duration of sessions ranged from 12.6 to 28.0 minutes. Graduate
students with 20 hours of training and weekly supervision by case
review provided the counselling.
Control group
Mothers received the usual nutritional counselling of the
supplemental nutrition programme and brief advice to quit smoking and
not expose their children to environmental tobacco smoke.
Measures of exposure to environmental tobacco smoke
Mothers' reports
Interviews were conducted at baseline, at three months (after
counselling), and at six and 12 months. The baseline interview was
conducted in person in the mothers' homes, and follow up interviews
were by telephone. The mean length of interviews was 57.2 (SD 15.8)
minutes. Content included information on mothers' demographics and
tobacco use and their child's exposure to environmental tobacco smoke.
Children's urine cotinine concentrations
Urine samples (collected at baseline and three and 12 months) were
analysed for cotinine (a metabolite of nicotine and recommended
biomarker)20 at the Centers for Disease Control and
Prevention by means of isotope dilution liquid chromatography and
tandem mass spectrometry with a limit of detection of <50 parts per
trillion. We obtained samples from children who were not toilet trained
by placing two sterile 15 cm cotton rolls in diapers and removing these
when they were wet. The cotton rolls were packed into a sterile 20 ml
syringe (without needle), and the urine was expressed into a 5 ml vial.
Previous research showed that cotton rolls do not alter the cotinine
concentration.21 Samples from toilet trained children were
collected with a standard urine collection cup. Samples were frozen at
-29°C and packed in dry ice for shipping. The laboratory was blind
to subjects' identity and group assignment.
Mothers' saliva cotinine concentrations
Mothers' saliva was obtained at each interview with Episcreen
collection devices (Epitope, Beaverton, OR) and stored frozen at
-29°C until laboratory analysis by enzyme linked immunoassay (STC,
Bethlehem, PA). The laboratory was blind to subjects' identity and
group assignment. Mothers who reported stopping smoking were tested and
cessation confirmed by cotinine concentrations <30 ng/ml.
Nicotine monitors
We conducted nicotine monitoring to provide objective validation
of mothers' reported levels of smoking and to enhance reporting
accuracy.22 Inactive monitors were placed in three rooms
per household where children's greatest exposure to environmental
tobacco smoke was reported. These were used to sensitise the mothers to
possible confirmation of their reports of exposure. One week before the
three month interview, we placed an active monitor in the room of
greatest exposure for a randomly selected half of the families. The
monitor was a 37 mm diameter cassette containing a Teflon coated glass
fibre filter (Emfab TX 40h120WW, Pallflex, Putnam, CT) saturated with
4% sodium bisulphate and 5% ethanol and dried. Gas chromatography was
used to assess nicotine levels.
23 24
Assays confirmed the
validity of mothers' reports.19
Assignment and masking
Random numbers were used to stratify assignment by three ethnic
groups. After the baseline measures, assistants opened an envelope to
reveal assignments. Measurement assistants were blind to group
assignment. Control families were unaware of counselling procedures,
and investigators were blind to results until all data were collected.
Statistical analyses
Analyses were based on intention to treat. We adjusted dependent
variables by logarithmic or square root transformation to reduce
skewness and present geometric and untransformed means. Differential
rate of change in reported exposure and cotinine estimates of exposure
relied on analyses of repeated measures over time. Estimated power to
detect differential change between groups exceeded 0.80 for all
dependent variables. We analysed the effects of counselling using the
generalised estimating equations approach, with linear components of
time as "within subjects" factors and the interaction as a
"between subjects" factor (SAS version 6.12).25
Modelling procedures based on generalised estimating equations are
superior to models based on analysis of variance in that they do not
require repeated measures to be equally spaced from one another and
they retain cases with missing data at one or more times. We first
calculated differential change from baseline to end of follow up and
then repeated this for baseline to three months (counselling effect)
and from three months to end of follow up (maintenance effect).
|
| |
Results |
|---|
|
|
|---|
Participant flow and follow up
Figure 1 shows the number of mothers enrolled through completion
of measures. Forty nine (92%) of the mothers assigned to the
counselling group completed all seven counselling sessions.
Participants
Table 1 shows the demographic characteristics of the mothers and
children. Families were white, black, or Hispanic and had low income
with limited education.
|
Sampling and success of random assignment
The two groups were well matched in their demographic and
dependent variables, suggesting successful random assignment.
Analyses
Reported exposure
Figure 2 shows that in both groups the children's reported
exposure to their mothers' tobacco smoke in the home declined steeply
from baseline to three months (end of counselling) and then only
slightly during follow up. Our analyses of repeated measures showed
significant differences between groups by time (P=0.002), indicating
that exposure declined more for the counselled group than for the
control group. Analyses of changes from baseline to three months also
showed significant differences between groups by time (P=0.011). From
three months to 12 months, the difference between the two groups
remained significant (P=0.017), but neither showed any significant
change over time, suggesting that the counselling effect was maintained
but that no later improvement occurred. Student's t tests
showed a significant cross sectional difference between the groups at
three months only (t(99)=
2.74 (95% confidence interval
1.503 to
0.240); P=0.007). Thus, the effects of counselling were
obtained by three months and sustained through follow up. Table 2 shows
the geometric means for children's exposure to environmental tobacco
smoke at baseline, three months, and 12 months.
|
|
2.30 (
1.244 to
0.092); P=0.024) and 12 months (t(91)=
2.10 (
1.430 to
0.039); P=0.039),
suggesting that counselling had an effect and that this was maintained.
Children's urine cotinine concentration
Figure 3 shows that children's cotinine concentrations increased
from baseline to three months in both groups but that the concentration
then declined slightly in the counselled group whereas it continued to
increase in the control group. Our analyses of repeated measures showed
significant differences between groups by time (P=0.008). Student's
t tests showed significant differences between the two
groups only at 12 months (t(90)=
2.05 (
0.948 to
0.015); P=0.043). These results suggested a prevention effect that
lasted through follow up.
|
Mothers' saliva cotinine concentration
From baseline to three months, the mothers' cotinine
concentrations increased significantly in both groups
from 75.8 ng/ml
to 91.2 ng/ml for counselled women and from 76.9 ng/ml to 89.7 ng/ml
for controls (P<0.001). During follow up, counselled mothers'
cotinine concentrations decreased to 80.6 ng/ml at 12 months, while
those of the controls increased to 112.9 ng/ml. This difference between
groups by time neared significance (P=0.06), suggesting a possible
decrease in the relative level of smoking for counselled mothers
compared with controls. There were no significant differences in the
numbers of mothers who stopped smoking (six in the counselling group
and four in the control group).
| |
Discussion |
|---|
|
|
|---|
This is the first study to show therapeutic benefits of counselling mothers on their children's exposure to environmental tobacco smoke based on cotinine concentrations. In the counselled group the children's cotinine concentrations decreased slightly (4%) by 12 months, whereas those in the control group increased substantially (85%), suggesting that counselling prevented an increase in exposure to environmental tobacco smoke. Reported exposure to environmental tobacco smoke decreased more after counselling and was sustained for nine months, suggesting maintenance of effects consistent with our previous findings.13
Our present results extend earlier work by showing the efficacy of counselling delivered in part by telephone to women receiving services from the supplemental nutrition programme for women, infants, and children. The successful decrease (or prevention of increase) in children's exposure to environmental tobacco smoke in this low income, racially and ethnically diverse, high risk population suggests that counselling is generalisable, as does the similarity of our results to those from earlier studies.11-13 Such counselling in medical and social services might protect millions of children from exposure to environmental tobacco smoke.
Smoking decreased slightly among counselled mothers but increased by half among controls. Counselling may have prevented an increase in mothers' smoking over time, although it did not result in more mothers quitting. Increased smoking among the controls probably contributed to their children's increased cotinine concentrations.
Parental reports of reducing their children's exposure could reflect the parents smoking in a different room but still close enough for the child to inhale smoke. Similarly, as children begin walking, they may be exposed to nicotine from dust on carpets and furniture. This would not be easily monitored or reported by parents and might account for the control mothers reporting decreased exposure to environmental tobacco smoke whereas their children had increased cotinine concentrations. Additional research is needed to determine the source of increasing cotinine concentrations in control children.
Conclusions
Both mothers' reports and cotinine analyses confirmed the
benefits of counselling on children's exposure to environmental
tobacco smoke. The most conservative interpretation of the results
suggests that counselling prevented an increase in exposure to
environmental tobacco smoke. Future studies should be directed to
interventions that combine formal counselling for quitting smoking with
counselling for reducing children's exposure to environmental tobacco
smoke. Future studies should also extend follow up to assess how long
the effects of counselling are maintained and the developmental trends
in exposure to environmental tobacco smoke. These results set the stage
for research to determine the effects of reducing exposure to
environmental tobacco smoke on morbidity and
mortality.
|
What is already known on this topic
The World Health Organization has estimated that the health of almost half of the world's children is threatened by exposure to environmental tobacco smoke Two trials reported significant decreases in children's exposure to environmental tobacco smoke after counselling of mothers, but neither provided an objective outcome measure of efficacy What this study addsA randomised trial of counselling to reduce children's exposure to environmental tobacco smoke used measures of cotinine concentrations in addition to mothers' reports Counselled mothers reported significantly greater decreases in exposure to environmental tobacco smoke compared with controls, and children's urine cotinine concentrations decreased slightly for counselled families while increasing substantially for controls The findings confirm the efficacy of counselling to reduce children's exposure to environmental tobacco smoke |
| |
Acknowledgments |
|---|
We thank the following investigators for their assistance during the conduct of this trial: Chris Ake, Department of Family and Preventive Medicine, University of California at San Diego; S Katharine Hammond, Environmental Health Sciences Division, School of Public Health, University of California, Berkeley; Doug Hoffman, Neurochemistry Laboratory, Dartmouth Medical School; Sarah Nordahl Larson, San Diego State University Foundation WIC programme; Brian P Leaderer, Division of Environmental Health Sciences, Yale University School of Medicine.
Contributors: MFH, as principal investigator, had primary responsibility for the study design, administration, quality assurance, planning of statistical analyses, and writing of the manuscript. JMZ, as project coordinator, was responsible for overseeing data collection, intervention delivery, and data preparation and also conducted statistical analyses and contributed to writing the manuscript. GEM collaborated on design of measures, statistical analyses, and editing the manuscript. CRH conducted statistical analyses and assisted with study design and editing the manuscript. JTB conducted urine cotinine analyses and assisted with interpretation of results and editing the manuscript. JP assisted with the study design and editing the manuscript. MFH and JMZ are the guarantors of the paper.
| |
Footnotes |
|---|
Funding: This research was supported by Grant No 027946 SFP awarded to MFH from the Robert Wood Johnson Foundation Smoke-Free Families Program, and by discretionary funds from the Center for Behavioral Epidemiology and Community Health.
Competing interests: None declared.
| |
References |
|---|
|
|
|---|
| 1. | World Health Organization, Division of Noncommunicable Diseases, Tobacco Free Initiative. International consultation on environmental tobacco smoke (ETS) and child health. Consultation report. Geneva: WHO, 1999. www.who.int/toh/TFI/consult.htm (accessed 26 July 2000). |
| 2. | Pirkle JL, Flegal KM, Bernert JT, Brody DJ, Etzel RA, Maurer KR. Exposure of the US population to environmental tobacco smoke. The third national health and nutrition examination survey, 1988 to 1991. JAMA 1996; 275: 1233-1240[Abstract]. |
| 3. |
Centers for Disease Control.
State-specific prevalence of cigarette smoking among adults, and children's and adolescents' exposure to environmental tobacco smoke United States, 1996.
MMWR Morb Mortal Wkly Rev
1997;
46:
1038-1043[Medline].
|
| 4. | National Health and Medical Research Council. The health effects of passive smoking. Australia: NHMRC, 1997. |
| 5. | Physicians for a Smoke-Free Canada. Highlight sheet No 1. Smoking in Canadian homes: Are children at risk? , 1999. Available from: www.smoke-free.ca/eng_home/news_press_Jun99.htm (accessed 26 July 2000). |
| 6. | Jarvis MJ. Children's exposure to passive smoking: survey methodology and monitoring trends. Background paper. , 1999. Available from: Tobacco Free Initiative www.who.int/toh/TFI/consult.htm (accessed 7 May 2000). |
| 7. | US Department of Health and Human Services (PHS), NIH, US Environmental Protection Agency. Respiratory health effects of passive smoking: lung cancer and other disorders. Washington DC: Office of Research and Development, Office of Air and Radiation, 1993. (NIH publication No 93-3605.) |
| 8. | Charlton A. Children and passive smoking: a review. J Fam Pract 1994; 38: 267-277[Medline]. |
| 9. | Klonoff-Cohen HS, Edelstein SL, Lefkowitz ES, Srinivasan IP, Kaegi D, Chang JC, et al. The effect of passive smoking and tobacco exposure through breast milk on sudden infant death syndrome. JAMA 1995; 273: 795-798[Abstract]. |
| 10. | Adams EK, Melvin C, Merritt R, Worrall B. The costs of environmental tobacco smoke (ETS): an international review. , 1999. Available from: Tobacco Free Initiative www.who.int/toh/TFI/consult.htm (accessed 7 May 2000). |
| 11. | Greenberg RA, Strecher VJ, Bauman KE, Boat BW, Fowler MG, Keyes LL, et al. Evaluation of a home-based intervention program to reduce infant passive smoking and lower respiratory illness. J Behav Med 1994; 17: 273-290[CrossRef][Medline]. |
| 12. |
Hovell MF, Meltzer SB, Zakarian JM, Wahlgren DR, Emerson JA, Hofstetter CR, et al.
Reduction of environmental tobacco smoke exposure among asthmatic children: a controlled trial [published erratum appears in Chest 1995;107:1480].
Chest
1994;
106:
440-446 |
| 13. |
Wahlgren DR, Hovell MF, Meltzer SB, Hofstetter CR, Zakarian JM.
Reduction of environmental tobacco smoke exposure in asthmatic children: a 2-year follow-up.
Chest
1997;
111:
81-88 |
| 14. | Schulte-Hobein B, Schwartz-Bickenbach D, Abt S, Plum C, Nau H. Cigarette smoke exposure and development of infants throughout the first year of life: influence of passive smoking and nursing on cotinine levels in breast milk and infant's urine. Acta Paediatr 1992; 81: 550-557[Medline]. |
| 15. |
Mascola MA, Vunakis HV, Tager IB, Speizer FE, Hanrahan JP.
Exposure of young infants to environmental tobacco smoke: breast-feeding among smoking mothers.
Am J Public Health
1998;
88:
893-896 |
| 16. | Mattanini MA, Thyer B, eds. Finding solutions to social problems: behavioral strategies for change. Washington DC: American Psychological Association, 1996. |
| 17. | Hovell MF, Zakarian JM, Matt GE, Hofstetter CR, Bernert JT, Pirkle J. Decreasing environmental tobacco smoke exposure among low income children: preliminary findings. Tobacco Control 2000; 9(suppl 3): iii0-1. |
| 18. | Emerson JA, Hovell MF, Meltzer SB, Zakarian JM, Hofstetter CR, Wahlgren DR, et al. The accuracy of environmental tobacco smoke exposure measures among asthmatic children. J Clin Epidemiol 1995; 48: 1251-1259[CrossRef][Medline]. |
| 19. | Matt GE, Hovell MF, Zakarian JM, Bernert JT, Pirkle JL, Hammond SK. Measuring second-hand tobacco smoke exposure in babies: the reliability and validity of mother-reports in a sample of low-income families. Health Psychol 2000; 19: 232-241[CrossRef][Medline]. |
| 20. | Hovell MF, Zakarian JM, Wahlgren DR, Matt GE, Emmons KM. Measurement of environmental tobacco smoke exposure: trials and tribulations. Tobacco Control 2000; 9: 0-6. |
| 21. |
Matt GE, Wahlgren DR, Hovell MF, Zakarian JM, Bernert JT, Meltzer SB, et al.
Measuring ETS exposure in infants and young children through urine cotinine and memory-based parental reports: empirical findings and discussion.
Tobacco Control
1999;
8:
282-289 |
| 22. | Murray DM, O'Connell CM, Schmid LA, Perry CL. Validation of smoking by self-report by adolescents: a re-examination of the bogus pipeline procedures. Addict Behav 1987; 12: 7-15[CrossRef][Medline]. |
| 23. | Hammond SK, Leaderer BP. A diffusion monitor to measure exposure to passive smoking. Environ Sci Technol 1987; 21: 494-497[CrossRef]. |
| 24. | Leaderer BP, Hammond SK. Evaluation of vapor-phase nicotine and respirable suspended particle mass as markers for environmental tobacco smoke. Environ Sci Technol 1991; 25: 770-777[CrossRef]. |
| 25. | Diggle PJ, Liang KY, Zeger SL. Analysis of longitudinal data. Oxford: Clarendon Press, 1995. |
(Accepted 3 July 2000)
Read all Rapid Responses
What can you learn from this BMJ paper? Read Leanne Tite's Paper+