- © 2007 Canadian Medical Association
In this issue, Ward and colleagues1 report the findings of their study of the incidence of vitamin D–deficiency rickets in Canada. Through the Canadian Paediatric Surveillance Program, they identified 104 confirmed cases of vitamin D–deficiency rickets among children up to 7 years of age, with an estimated annual incidence rate of 2.9 per 100 000 children. These children presented with important clinical manifestations of rickets, such as skeletal deformities, hypocalcemic seizures, delayed developmental milestones and fractures.
As Ward and colleagues note, vitamin D–deficiency rickets is not a new phenomenon, and it is preventable by the simple administration of oral vitamin D supplements. Their article raises many questions: Why is rickets still present in a country where food is abundant? Is a subset of the population at increased risk? How could prevention strategies be improved? Is it important to conduct surveillance of rickets? If so, should surveillance be conducted through the Canadian Paediatric Surveillance Program?
According to the United Nations' Convention on the Rights of the Child,2 children and youth have “the right to the enjoyment of the highest attainable standard of health and to facilities for the treatment of illness and rehabilitation of health.” Health care providers have a duty not only to promote and to safeguard the health of their patients, but also to participate in ethical health research, including epidemiological research that will advance knowledge and guide treatment.
If a disease or condition is uncommon and data are sparse or nonexistent, investigators need a national system to identify cases in order to answer their research questions. The Canadian Paediatric Surveillance Program is a well- established active surveillance system, made strong by the participation of more than 2300 pediatricians and pediatric subspecialists who provide timely national non-nominal data (Figure 1). This system has definite advantages over more traditional passive reporting systems. However, collection of data is only the initial step. The World Health Organization (WHO) defines surveillance as “the ongoing systematic collection, analysis and interpretation of data and dissemination of information to those who need to know in order that action be taken.”3 In other words, information collected through surveillance should not sit on a shelf, but rather it should lead to changes in clinical practice and public health interventions that prevent diseases. In accordance with guidelines from WHO and the US Centers for Disease Control and Prevention for establishing a surveillance system,4 the Canadian Paediatric Surveillance Program follows the “3 Ds” of surveillance: detection, deduction and dissemination.
The Canadian Paediatric Surveillance Program Steering Committee (a governing body composed of multidisciplinary experts from public health, medical and legal fields) favours studies that have strong scientific and public health importance and those for which surveillance is the most appropriate way of collecting data. The program uses a 2-tiered reporting process to identify and investigate cases: an initial check-off form and a detailed follow-up questionnaire. The high mean monthly response rate (82%) and completion rate of the follow-up questionnaire (93%) reflect that the participants value the program and are committed to ongoing pediatric epidemiological research.
Thus far, 34 studies have been conducted through the Canadian Paediatric Surveillance Program on a range of infectious and vaccine-preventable diseases, genetic and metabolic conditions, childhood injuries and mental health disorders.5 The public health impact of studies supported by the program is described in Table 1. For example, one study reported that, in 60% of cases of group A streptococcus-related necrotizing fasciitis, the patient had a documented history of varicella in the preceding month. This result supports the recommendations by the National Advisory Committee on Immunization for universal childhood immunization against varicella;6 and the surveillance program would be useful for monitoring the impact of this public health decision in a follow-up study. In addition, a study of lap-belt syndrome confirmed that inappropriately restrained children injured in motor vehicle accidents have a high rate of permanent spinal cord lesions (25%).7 This study has increased awareness and contributed to the Ontario Ministry of Transportation's decision to mandate the use of booster seats. Advocacy efforts will continue until all provinces and territories adopt both the use of proper child restraints in motor vehicles and booster-seat legislation.
As one of the founding members of the International Network of Paediatric Surveillance Units, which has 15 members (Box 1), the Canadian Paediatric Surveillance Program offers the opportunity for international collaboration.8 Studies conducted in more than one country allow for international comparison of diseases and conditions (e.g., hemorrhagic disease of the newborn,9,10 congenital rubella syndrome,11 severe neonatal hyperbilirubinemia12) and other areas of public health (e.g., hemolytic uremic syndrome13). Countries such as Australia, Cyprus and Greece have initiated studies on vitamin D–deficiency rickets. Since these countries enjoy a much sunnier environment than Canada, comparison of the results from these studies with the Canadian data presented by Ward and colleagues will be most interesting.
The study by Ward and colleagues confirms the validity of the recommendations made by the Canadian Paediatric Society for vitamin D supplementation.14 It also demonstrates the need for heightened efforts by health care providers to ensure adequate vitamin D intake for pregnant and lactating women and breast-fed infants. Epidemiological data also show the need for educational materials aimed at the general public and for a review of prevention strategies that target high-risk groups.
The Canadian Paediatric Surveillance Program is a versatile tool able to acquire timely epidemiological data and to stimulate simultaneous collaborative research on diseases and conditions that are associated with high disability, morbidity, mortality and economic cost to society. However, because the program is based on the voluntary participation of pediatricians and does not include family physicians, the resulting incidence and prevalence rates are probably conservative. Future challenges include maintaining high interest and participation and continuing dissemination (in collaboration with the Canadian Paediatric Society) of results with important medical and public health implications for use in policy development.
As illustrated by Ward and colleagues, children and youth have the right to benefit from nationally funded epidemiological research that can identify risk factors, monitor public health interventions, inform the development of new prevention strategies and guide pediatric clinical practices. National surveillance is an essential tool contributing to the improvement of the health and well-being of children and youth.
@ See related article page 161
Key points
• Children and youth have the right to benefit from ethical health research
• National case identification is necessary to answer research questions about high-impact, low-frequency diseases
• Surveillance provides valuable, timely epidemiological information for action
• Governments have a duty to provide ongoing core funding to national surveillance pediatric research
Footnotes
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Competing interests: None declared.