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Immunisation practices of paediatric oncology and shared care oncology consultants: a United Kingdom survey
Jessica Bate1, Soonie R Patel, Julia Chisholm
1Division of Child Health, St. George's University of London, London, UK. jbate@sgul.ac.uk
Insights
Most UK pediatric cancer centers follow re-immunization guidelines after chemotherapy and stem cell transplants. However, pneumococcal conjugate vaccine recommendations were lower than expected, indicating a need for updated guidelines.
Area of Science:
- Pediatric Oncology
- Immunology
- Public Health
Background:
- Royal College of Paediatrics and Child Health (RCPCH) introduced re-immunisation guidelines in 2002.
- Guidelines cover children post-chemotherapy and post-haematopoietic stem cell transplant (HSCT).
Purpose of the Study:
- To assess adherence to RCPCH re-immunisation guidelines among UK pediatric centers.
- To evaluate current practices in principal treatment centres (PTC) and shared care (SC) consultants.
Main Methods:
- An anonymised online survey was distributed to UK PTC and SC consultants in October 2008.
- The survey targeted consultants within the Children's Cancer and Leukaemia Group (CCLG) network.
Main Results:
- High stated compliance (94.3%) with RCPCH guidelines for re-immunisation timing post-chemotherapy.
- Near-universal adherence (93-100%) to recommended re-immunisation timing post-HSCT.
- Lower-than-expected recommendations for Pneumococcal Conjugate Vaccine (PCV) post-chemotherapy (58.3%) and HSCT (51.7%).
- Variations observed in varicella (VZV) post-exposure prophylaxis recommendations between PTC and SC consultants.
Conclusions:
- High reported adherence to RCPCH re-immunisation guidelines.
- Lower PCV recommendations may stem from a lack of specific guidelines post-chemotherapy.
- Discrepancies in VZV prophylaxis necessitate further investigation.
Background:
In March 2002, the Royal College of Paediatrics and Child Health (RCPCH) introduced guidelines for re-immunisation of children after completion of standard-dose chemotherapy and after haematopoietic stem cell transplant (HSCT).
Aims:
To ascertain whether these guidelines form standard unit policy by undertaking a survey of UK paediatric principal treatment centre (PTC) consultants and shared care (SC) consultants.
Procedures:
In October 2008, a link to an on-line anonymised survey was sent by e-mail to all UK PTC consultants in Children's Cancer and Leukaemia Group (CCLG) centres and to SC consultants linked to eight of these centres.
Results:
Responses were received from 55 PTC consultants (representing all 21 CCLG centres) and 54 SC consultants. In accordance with the RCPCH guidelines, most PTC and SC consultants recommend initiating re-immunisation at 6 months after completion of standard-dose chemotherapy (99/105, 94.3%). Re-immunisation at the recommended time after HSCT for each transplant type was reported by 93-100% of respondents. Pneumococcal conjugate vaccine (PCV) was recommended after chemotherapy by 58.3% (35/60) of respondents and by 51.7% (30/58) after HSCT. There were distinct differences between PTC and SC consultants in their choice of varicella (VZV) post-exposure prophylaxis.
Conclusions:
There is a high level of stated compliance with RCPCH guidelines. Recommendations for PCV after chemotherapy and HSCT were lower than expected. This may reflect the absence of specific guidelines after chemotherapy but not in HSCT patients where guidelines do exist. Variation in VZV post-exposure prophylaxis suggests further studies are required.
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