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1.
Arch Dis Child ; 106(9): 855-861, 2021 09.
Article in English | MEDLINE | ID: mdl-33419730

ABSTRACT

PURPOSE: To estimate the minimum incidence of congenital Zika syndrome (CZS) and severe microcephaly in Canada and describe key clinical, epidemiological, aetiological and outcome features of these conditions. METHODS: Two separate national surveillance studies were conducted on CZS and severe microcephaly using the well-established Canadian Paediatric Surveillance Program from 2016 to 2019. Over 2700 paediatricians across Canada were surveyed monthly and asked to report demographic details, pregnancy and travel history, infant anthropometry, clinical features and laboratory findings of newly identified cases. Reports were reviewed to assign an underlying aetiology of severe microcephaly. Incidence rates were estimated using monthly live birth denominators. RESULTS: Thirty-four infants met the case definition for severe microcephaly and <5 met the case definition for CZS. The associated minimum incidence rates were 4.5 per 100 000 live births for severe microcephaly and 0.1-0.5 per 100 000 live births for CZS. Of severe microcephaly cases, 53% were attributed to genetic causes, 15% to infectious or ischaemic causes and 32% to unknown causes. The median head circumference-for-age Z-score at birth was -3.2 (IQR -3.8 to -2.6), and catch-up growth was often not achieved. Common clinical features included intracranial abnormalities (n=23), dysmorphology (n=19) and developmental delays (n=14). Mothers of infants with non-genetic aetiologies travelled during pregnancy more often (10/16) than mothers of infants with genetic aetiologies (<5/18; p<0.01). CONCLUSION: Severe microcephaly and CZS are both rare in Canada. Minimum incidence rates can be used as a baseline against which novel or re-emergent causes of severe microcephaly or CZS can be compared.


Subject(s)
Microcephaly/epidemiology , Population Surveillance/methods , Pregnancy Complications, Infectious/virology , Zika Virus Infection/congenital , Adult , Anthropometry/methods , Birth Weight/physiology , Canada/epidemiology , Female , Gestational Age , Humans , Incidence , Infant , Infant, Newborn , Live Birth/epidemiology , Male , Microcephaly/etiology , Microcephaly/genetics , Pregnancy , Pregnancy Complications, Infectious/epidemiology , Premature Birth/epidemiology , Severity of Illness Index , Surveys and Questionnaires , Zika Virus/isolation & purification , Zika Virus Infection/epidemiology
3.
J Obstet Gynaecol Can ; 37(1): 32-39, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25764034

ABSTRACT

OBJECTIVE: This analysis was undertaken to determine the rates and determinants of smoking cessation during pregnancy and smoking relapse after childbirth in Canada. METHODS: We used data from the Maternity Experiences Survey, a cross-sectional study of mothers who gave birth to a singleton baby in Canada in 2006. A total of 1586 mothers who smoked occasionally or daily before pregnancy were included in the analysis. RESULTS: The rate of smoking cessation during pregnancy was 53.0% (95% CI 50.3% to 55.7%). Higher pre-pregnancy smoking frequency, Inuit origin, being aged ≥ 35 years, lower education, not attending prenatal classes, lack of social support, stress before or during pregnancy, and living with a smoker were independently associated with higher risk of continued smoking, while First Nations (off-reserve) origin was associated with a lower risk. Among those who had quit smoking, 47.1% (95% CI 43.5% to 50.6%) relapsed postpartum. Living with a smoker, not having breastfed, and having stopped breastfeeding were independently associated with a higher risk of relapse. CONCLUSION: This study highlights the need to tailor smoking cessation and prevention interventions for some high-risk groups of women.


Objectif : Cette analyse a été menée pour déterminer les taux et les déterminants de l'arrêt tabagique pendant la grossesse et de la rechute post-partum au Canada. Méthodes : Nous avons utilisé les données de l'Enquête sur l'expérience de la maternité, soit une étude transversale sur des mères ayant accouché à la suite d'une grossesse simple au Canada en 2006. En tout, 1 586 mères ayant fumé occasionnellement ou quotidiennement avant la grossesse ont été incluses dans l'analyse. Résultats : Le taux d'arrêt tabagique pendant la grossesse était de 53,0 % (IC à 95 %, 50,3 % - 55,7 %). Une consommation de cigarettes plus élevée avant la grossesse, être d'origine inuite, être âgée de 35 ans ou plus, être moins scolarisée, la non-participation à des cours prénataux, le manque de soutien social, le stress avant ou pendant la grossesse et la cohabitation avec un fumeur étaient associés de façon indépendante à un risque accru de poursuite du tabagisme, tandis que le fait d'être issue des Premières Nations (hors-réserve) était associé à un risque moindre. Parmi les mères qui avaient cessé de fumer, 47,1 % (IC à 95 %, 43,5 % - 50,6 %) ont recommencé à fumer après l'accouchement. La cohabitation avec un fumeur, ne pas avoir allaité et avoir cessé d'allaiter étaient associés de façon indépendante à un risque accru de rechute. Conclusion : Cette étude souligne la nécessité d'adapter les interventions d'abandon et de prévention du tabagisme aux groupes de femmes exposées à des risques élevés.


Subject(s)
Postpartum Period/psychology , Pregnancy/psychology , Smoking Cessation/statistics & numerical data , Smoking/epidemiology , Adolescent , Adult , Canada/epidemiology , Cross-Sectional Studies , Female , Humans , Recurrence , Young Adult
4.
Can J Public Health ; 105(1): e40-6, 2014 Jan 15.
Article in English | MEDLINE | ID: mdl-24735696

ABSTRACT

OBJECTIVE: Although the benefit of folic acid (FA) to prevent neural tube defects (NTD) is well established, not all women take supplements in the periconceptional period. This study used data from the Public Health Agency of Canada's Maternity Experiences Survey to evaluate determinants of awareness of FA among recently pregnant women in Canada, and the extent to which that translated into actual supplement usage. METHODS: Telephone interviews took place between October 23, 2006 and January 31, 2007 with women who were 5 to 14 months postpartum to survey their experiences during pregnancy, birth and the postpartum period. These analyses were conducted on women who responded to questions relating to FA supplementation. The 6,421 respondents were weighted to represent 76,508 women using weights which corresponded to the sampling strata, the mother's first language and Aboriginal status. RESULTS: Overall, 77.6% of surveyed women knew that taking FA periconceptionally could help protect against NTD. Women who were younger, single or separated reported less awareness and use of FA, while higher maternal age, level of education and income were positively associated with both knowledge and use. Despite longstanding national guidelines for supplementation, there were regional variations in knowledge and use of FA. CONCLUSION: The data indicate clear socio-demographic differences among Canadian women with respect to their knowledge and use of FA. Although most women understood the benefits of FA supplementation, a little over a third of them did not take FA supplements prior to becoming pregnant, and less than half supplemented according to national guidelines. Identification of those subpopulations whose use of supplements is suboptimal may allow for targeted educational or other interventions to further encourage FA use.


Subject(s)
Dietary Supplements/statistics & numerical data , Folic Acid/therapeutic use , Health Knowledge, Attitudes, Practice , Neural Tube Defects/prevention & control , Adolescent , Adult , Canada , Female , Health Care Surveys , Humans , Middle Aged , Pregnancy , Socioeconomic Factors , Young Adult
6.
Can J Cardiol ; 29(11): 1470-6, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23773895

ABSTRACT

BACKGROUND: Patients with heart failure are a growing population within cardiac rehabilitation. The purpose of this study was to compare, through a single-centre, parallel-group, randomized controlled trial, the effects of Nordic walking and standard cardiac rehabilitation care on functional capacity and other outcomes in patients with moderate to severe heart failure. METHODS: Between 2008 and 2009, 54 patients (aged 62.4 ± 11.4 years) with heart failure (mean ejection fraction = 26.9% ± 5.0%) were randomly assigned to standard cardiac rehabilitation care (n = 27) or Nordic walking (n = 27); both groups performed 200 to 400 minutes of exercise per week for 12 weeks. The primary outcome, measured after 12 weeks, was functional capacity assessed by a 6-minute walk test (6MWT). RESULTS: Compared with standard care, Nordic walking led to higher functional capacity (Δ 125.6 ± 59.4 m vs Δ 57.0 ± 71.3 m travelled during 6MWT; P = 0.001), greater self-reported physical activity (Δ 158.5 ± 118.5 minutes vs Δ 155.5 ± 125.6 minutes; P = 0.049), increased right grip strength (Δ 2.3 ± 3.5 kg vs Δ 0.3 ± 3.1 kg; P = 0.026), and fewer depressive symptoms (Hospital Anxiety and Depression Scale score = Δ -1.7 ± 2.4 vs Δ -0.8 ± 3.1; P = 0.014). No significant differences were found for peak aerobic capacity, left-hand grip strength, body weight, waist circumference, or symptoms of anxiety. CONCLUSIONS: Nordic walking was superior to standard cardiac rehabilitation care in improving functional capacity and other important outcomes in patients with heart failure. This exercise modality is a promising alternative for this population.


Subject(s)
Heart Failure/rehabilitation , Walking , Depression/therapy , Exercise Test , Exercise Tolerance , Female , Hand Strength , Humans , Male , Middle Aged , Severity of Illness Index
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