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. 2003 Jan;8(1):13–15. doi: 10.1093/pch/8.1.13

Vaccine schedules

PMCID: PMC2791069  PMID: 20011549

The Infectious Diseases and Immunization Committee of the Canadian Paediatric Society has intermittently reviewed the recommendations for the routine immunization of children made by the National Advisory Committee on Immunization. The purpose of the present note is to update physicians and other health care providers on the changes related to childhood immunization. Included is a composite schedule for routine immunization of healthy children and adolescents (Table 1).

TABLE 1.

Routine vaccine schedule for healthy children and adolescents*

Age dTap/IPV Hib MMR HBV Vaccines dT±ap VZV PCV-7 conjugate MenC-congugate
2 months X X X X (at 2 or 3 months)§ X (at 2 or 3 months)§
4 months X X X X (at 4 or 5 months)§ X (at 4 or 5 months)§
6 months X X X X (at 6 or 7 months)§ X (at 6 or 7 months)§
12 months X X X (12–15 months)
18 months X X and X or
4–6 years X or X X 3 doses
Teenage years 2 months apart dT±ap at 14–16 years
Adult years at any age dT every 10 years
*

No change in schedule for premature infants. Start first dose at chronological age of two months for routine vaccines;

Infants of Hepatitis B vaccine (HBV)-negative mothers: HBV should be given at two, four and six months of age, can also be given at any age after infancy. Infants of HBV-positive mothers or suspected maternal infection: HBV should be given at birth with an injection of Hepatitis B immune globulin followed by 2nd and 3rd dose of HBV vaccine at one and six months of age;

These vaccines may not be publicly funded in all provinces for this indication;

§

Option of administering meningococcal C (MenC) conjugate and/or pneumococcal conjugate vaccine (PCV)-7 at three, five, seven months (rather than two, four, six months) if parents wish to avoid three to four shots per visit;

HBV is also available for a two-dose schedule in 11 to 15 year olds. ap Acellular pertussis; d Diptheria; IPV Inactivated polio vaccine; Hib Haemophilus influenza type b; MMR Measles mumps rubella; T Tetanus toxoid; VZV Varicella zoster vaccine. ± Plus or minus

Recommendations are also included for immunization under special circumstances:

  • Children one to six years of age who were not previously immunized in infancy (Table 2).

  • For children seven years of age and older who were not previously immunized in infancy (Table 3).

  • Vaccines against encapsulated bacteria, for healthy children not previously immunized in the first three to six months of life (Table 4).

  • For children who have a clinical condition, which increases their susceptibility to severe disease due to encapsulated bacterial organisms, consult Table 5 for vaccines required according to their presenting age.

TABLE 2.

Immunization schedule for children one to six years not previously immunized in infancy (and still nonimmune)

Timing dTap/IPV Hib MMR HBV Vaccines dT±ap VZV PCV-7 conjugate MenC-congugate
1st visit X * X X X X X
2 months later X * X (or per routine) X X (if 12–23 months) (or anytime after, to avoid more than 2 shots per visit)
2 months later X * X *
6–12 months later X * *
Age 4–6 years X * or *
Teenage years X 3 doses dT±ap at 14–16 years
Adult years dT every 10 years
*

See Table 4 for details and the correct number of doses;

These vaccines may not be publicly funded in all provinces for this indication. ap Acellular pertussis; d Diptheria; IPV Inactivated polio vaccine; HBV Hepatitis B vaccine; Hib Haemophilus influenza type b; MenC Meningococcal C; MMR Measles mumps rubella; PCV Pneumococcal conjugate vaccine; T Tetanus toxoid; VZV Varicella zoster vaccine. ± Plus or minus

TABLE 3.

Immunization schedule for children seven years of age and older not previously immunized in infancy (and still nonimmune)

Timing dT±ap IPV Hib MMR Vaccines HBV VZV* PCV-7 conjugate* MenC-congugate*
1st visit X X X X X
2 months later X X X X (if ≥ 13 years old)
6–12 months later X X
Teenage years dT±ap at 14–16 years* X 3 doses
Adult years dT every 10 years
*

These vaccines may not be publicly funded in all provinces for this indication;

Not indicated in this age group;

Hepatitis B vaccine (HBV) is also available for a two-dose schedule in 11- to 15-year-olds. ap Acellular pertussis; d Diptheria; IPV Inactivated polio vaccine; Hib Haemophilus influenza type b; MenC Meningococcal C; MMR Measles mumps rubella; PCV Pneumococcal conjugate vaccine; T Tetanus toxoid; VZV Varicella zoster vaccine. See Table 4 for more details

TABLE 4.

Immunization schedule for vaccines against encapsulated bacteria for healthy children not previously immunized in the first three to six months of life

Timing Hib vaccine (age at first visit) PCV-7 conjugate* vaccine (age at first visit) MenC-congugate* vaccine (age at first visit)
7–11 months 12–17 months 18 months to 5 years 7–11 months 12–23 months 24 months to 5 years 4–11 months ≥12 months
At 1st visit X X X X X X X X
2 months later X X X X
4 months later X (past 12 months)
At 18 months X
*

These vaccines may not be publicly funded in all provinces for this indication. Hib Haemophilus influenza type b; MenC Meningococcal C; PCV Pneumococcal conjugate vaccine

TABLE 5.

Recommendations for vaccines against encapsulated bacteria for children considered to be at high risk for these diseases

Presenting age Hib PCV-7 conjugate* Vaccine PPV-23* MenC-congugate* MenACYW-P*
<3 months X 4 routine doses X 4 routine doses X 1 dose at 2 years X 3 routine doses X 1 dose at 2 years
3–11 months X 3–4 routine doses X 3 routine doses X 1 dose at 2 years X 2 routine doses X 1 dose at 2 years
12–17 months X 2 routine doses X 2 routine doses X 1 dose at 2 years X 1 routine dose X 1 dose at 2 years
18–23 months X 1 routine dose X 2 routine doses X 1 dose at 2 years X 1 routine dose X 1 dose at 2 years
2–4 years X 1 dose X 2 doses X 1 dose >2 months later X 1 routine dose X 1 dose >2 weeks later
5–9 years X 1 dose X 2 doses X 1 dose >2 months later X 1 routine dose X 1 dose >2 weeks later
10–19 years X 1 dose X 1 X 1 routine dose X 1 dose >2 weeks later
≥20 years X 1 dose X 1 X 1 routine dose X 1 dose >2 weeks later
*

These vaccines may not be publicly-funded in all provinces for this indication;

The conjugate vaccine dose(s) is/are to be sequentially followed by the polysaccharide vaccine dose(s);

In some circumstances a second pneumococcal polysaccharide vaccine (PPV)-23 dose may be given five years after the first. ACYW-P ACYW-polysaccharide; Hib Haemophilus influenza type b; MenACYW-P Meningococcal ACWP-polysaccharide; MenC Meningococcal C; PCV Pneumococcal conjugate vaccine

Since the committee’s last review, published in January/February 1999:

  • all provinces have introduced routine immunization programs against hepatitis B;

  • an adolescent/adult acellular pertussis (ap) vaccine has been licensed and recommended for use for adolescents; and

  • the 7-valent conjugated pneumococcal vaccine as well as a conjugated meningococcal type C vaccine have been licensed and recommended for inclusion in the routine infant immunization schedule.

Canada does not have a harmonized routine infant immunization schedule. The schedules detailed in the present note have attempted to account for the various provincial recommendations. As well, some routine vaccines for special circumstances are publicly funded in some jurisdictions but not in others. Readers are encouraged to check with their local health departments concerning provincial variations in both the scheduling and funding of these vaccines.

Footnotes

CANADIAN PAEDIATRIC SOCIETY, INFECTIOUS DISEASES AND IMMUNIZATION COMMITTEE

Members: Drs Upton Allen, The Hospital for Sick Children, Toronto, Ontario; H Dele Davies, Alberta Children's Hospital, Calgary, Alberta; Joanne Embree, The University of Manitoba, Winnipeg, Manitoba, (chair); Joanne Langley, IWK Health Centre, Halifax, Nova Scotia; Mireille Lemay, Sainte-Justine Hospital, Montreal, Quebec; Gary Pekeles, The Montreal Children's Hospital, Montreal, Quebec (director responsible)

Consultants: Drs Noni MacDonald, Dalhousie University, Halifax, Nova Scotia ; Victor Marchessault, Cumberland, Ontario

Liaisons: Drs Scott Halperin, IWK Health Centre, Halifax, Nova Scotia (IMPACT); Susan King, The Hospital for Sick Children, Toronto, Ontario (Canadian Paediatric AIDS Research Group); Monique Landry, Direction de la santé publique de Laval, Laval, Québec (Public Health); Larry Pickering, Centre for Pediatric Research, Norfolk, Virginia (American Academy of Pediatrics)

Principal authors: Drs Joanne Embree, The University of Manitoba, Winnipeg, Manitoba; Ben Tan, Royal University Hospital, University of Saskatchewan, Saskatoon, Saskatchewan

The recommendations in this note do not indicate an exclusive course of treatment or procedure to be followed. Variations, taking into account individual circumstances, may be appropriate. This article also appears in Can J Infect Dis 2002;13(6):358–360.


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