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Canadian Paediatric Surveillance Program
A Developmental Check-up
Jeffrey Scott MD FRCPC
Published in Paediatr Child Health 2004;9(1):13-14
Just as children are born, grow, and develop, so too do programs. In 1996 as a medical officer of health, I attended the first steering committee meeting in Ottawa to witness the birth of the Canadian Paediatric Surveillance Program (CPSP), a new overseas cousin to the now ten-year-old British program. Little did I, and others at the meeting, realize how much time and attention this new baby would require.
CPSP, like any developing infant, required nurturing. As it grew, the number of surveillance activities increased. It started slowly with the reporting of three paediatric infectious diseases with important public health implications: acute flaccid paralysis as part of polio surveillance, congenital rubella syndrome and neonatal group B streptococcal infection. As the CPSP gained experience, it extended its reach to undertake surveillance of up to ten conditions simultaneously. It has now been involved with a total of 24 important paediatric conditions covering areas such as infectious diseases, injuries, genetic disorders, metabolic conditions and neurological problems (Table 1). At first, the CPSP had to actively seek out conditions for surveillance, but as its reputation grew, an increasing number of investigators come forward with proposed studies. At the last steering committee meeting, a list of 30 proposed CPSP studies was presented to the group.
Table 1. Timeline (by end date) of Canadian Paediatric Surveillance Program studies |
Studies |
Start date |
End date |
Total confirmed cases to December 2003 |
Group B streptococcal infection |
January 1996 |
December 1996 |
178 |
Neural tube defects |
January 1997 |
December 1998 |
107 |
Creutzfeldt-Jakob disease |
January 1997 |
June 1999 |
1 |
Hemorrhagic disease of the newborn |
January 1997 |
December 2000 |
5 |
Subacute sclerosing panencephalitis |
January 1997 |
December 2000 |
3 |
Cerebral edema in diabetic ketoacidosis |
July 1999 |
June 2001 |
23 |
Progressive intellectual and neurological deterioration |
July 1999 |
June 2001 |
59 |
Anaphylaxis |
January 2000 |
June 2001 |
732 |
Hemolytic uremic syndrome |
April 2000 |
March 2002 |
140 |
Smith-Lemli-Opitz syndrome |
January 2000 |
December 2002 |
35 |
Hepatitis C virus infection |
February 2001 |
January 2003 |
58 |
Neonatal liver failure/perinatal hemochromatosis |
February 2001 |
January 2003 |
10 |
Necrotizing fasciitis |
September 2001 |
August 2003 |
37 |
Neonatal herpes simplex virus infection |
October 2000 |
September 2003 |
58 |
Neonatal hyperbilirubinemia – severe |
July 2002 |
June 2004 |
48 |
Vitamin D deficiency rickets |
July 2002 |
June 2004 |
20 |
CHARGE association/syndrome |
September 2001 |
August 2004 |
78 |
Acute flaccid paralysis |
January 1996 |
December 2004 |
354 |
Congenital rubella syndrome |
January 1996 |
December 2004 |
9 |
Prader-Willi syndrome |
January 2003 |
December 2004 |
9 |
Osteogenesis imperecta |
January 2004 |
December 2004 |
- |
Early-onset eating disorders |
March 2003 |
February 2005 |
23 |
Lap-belt syndrome |
September 2003 |
August 2005 |
1 |
Adverse drug reactions – serious and life-threatening |
January 2004 |
December 2005 |
- |
As the program approached seven years of age, Health Canada and the Canadian Paediatric Society decided that a developmental checkup was needed to see if the CPSP was maturing according to expectations. Assessing the CPSP’s adaptability to respond effectively to the changing Canadian health-care delivery environment was also deemed essential.
An internal CPSP evaluation team was created to supervise the evaluation, and a public health epidemiologist was contracted to assist in the process. An external international advisory group was formed with expertise in paediatrics, surveillance, public health and policy development to provide input into the objectives and methodology of the evaluation. A review of the literature indicated that only one other national paediatric surveillance unit, the Australian Paediatric Surveillance Unit, had undergone a formal evaluation, based primarily on the criteria used by the Centres for Disease Control and Prevention for evaluation of a surveillance program.(1,2 ) This, together with other literature on the evaluation of public health programs, served as references to develop and implement an evaluation process.(3) Evaluation objectives were created with the emphasis placed on ensuing feedback from program participants who were frontline paediatricians, researchers, and public health policy makers. Survey questions were sent to over 2469 participants. The survey included specific questions, but also allowed respondents the opportunity to provide suggestions on how the program could be improved. In addition, a review of the health conditions that had undergone surveillance was performed to see how accurately the program was able to detect the true number of events.
The expert advisory group met with the evaluation team for a full day to receive and review the results of the evaluation. The advisory group then caucused separately to review their analysis and provide both immediate verbal and later written comment on the CPSP.
While the results of the evaluation, the recommendations from the expert group and the proposed changes to the CPSP will be provided to readers in the months ahead through posters, articles and published manuscripts, some key points are worth noting.
It is clear that the CPSP has developed into an effective infrastructure for national collaborative surveillance and research into paediatric conditions. These conditions, although occurring at a low frequency, may have a high impact on society in terms of morbidity, mortality or cost. It is an excellent value for money and it is unique in Canada as an ongoing collaborative tool for surveillance and research that provides supporting evidence for policy development. The reach of the program extends beyond Canada as the program continues to provide surveillance results and to collaborate on common surveillance activities with the 13 other members of INoPSU (International Network of Paediatric Surveillance Units).(4) Most importantly the CPSP, through its surveillance activities, provides evidence that can be used to guide actions to improve children’s health, such as improved clinical recognition and management or beneficial changes in policy development. Several examples include the work on vitamin D deficiency rickets, hemorrhagic disease of the newborn due to problems with vitamin K administration, and injuries due to baby walkers. The potential to contribute to many other important public health issues has already been documented by the older British Paediatric Surveillance Unit (5).
One conclusion from the evaluation is that should the CPSP cease to exist, Canada would likely need to invest more time, effort and dollars in creating issue-specific surveillance tools. These tools would be necessary to respond when concerns arise about new or existing low-frequency but high-impact conditions.
What of CPSP’s future? Well, the expert advisory group recognized that while continuing to perform ongoing surveillance activities among paediatricians across Canada, the program must start to reach out to other health care professionals, particularly those among the First Nations who are involved in child care delivery. The group recommended that the potential for a quick response to urgent paediatric public health issues, as exemplified by the snapshot survey of baby walker injuries, be explored. A key recommendation was that the CPSP needs to ensure that the important paediatric and public health evidence found during its work is targeted to clinicians, administrators and policy makers in a manner that promotes effective use in policy development.
As my mother used to say, the future is what you make of it. The CPSP has had a great childhood and has developed the attributes that will enable it to contribute even more to children in Canada and the world. Now it will be up to all those participating in the CPSP to respond to the results and recommendations of the evaluation to ensure that it achieves its potential.
References
- Gazarian M, Williams K, Elliott E, et al. Evaluation of a national surveillance unit. Arch Dis Child 1999;80:21-7
- US Department of Health & Human Services, Centre for Disease Control and Prevention. Updated guidelines for evaluating public health surveillance systems. MMWR, 2001;50:1-35
- A Program Evaluation Tool Kit. Ottawa: Management Services Branch, Ottawa-Carleton Health Department, 1997
- Elliott EJ, Nicoll A, Lynn R, Marchessault V, Hirasing R, Ridley G. Rare disease surveillance: An international perspective. Paediatr Child Health 2001;6:251-60
- Nichol A, Lynn R, Rahi J, Verity C, Haines L, Public health outputs from the British Paediatric Surveillance Unit and similar clinician based systems. J R Soc Med 2000;93:580-5
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