A survey of infectious diseases and vaccination uptake in long-term hematopoietic stem cell transplant survivors in Australia.


Journal

Transplant infectious disease : an official journal of the Transplantation Society
ISSN: 1399-3062
Titre abrégé: Transpl Infect Dis
Pays: Denmark
ID NLM: 100883688

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 09 10 2018
revised: 17 11 2018
accepted: 09 12 2018
pubmed: 27 12 2018
medline: 3 5 2019
entrez: 27 12 2018
Statut: ppublish

Résumé

This cross-sectional survey aimed to establish the prevalence of infectious diseases and vaccination uptake in long-term allogeneic hematopoietic stem cell transplants (HSCT) survivors in New South Wales, in order to reduce long-term post-HSCT morbidity and mortality and enhance long-term care. Hematopoietic stem cell transplants survivors aged over 18 years and transplanted between 2000-2012 in New South Wales (NSW) were eligible to participate. Survivors self-completed the Sydney Post BMT Study survey, FACT-BMT (V4), Chronic Graft versus Host Disease (cGVHD) Activity Assessment Self Report, Lee Chronic GvHD Symptom Scale, DASS21, Post Traumatic Growth Inventory, and the Fear of Recurrence Scale. Of the 583 HSCT survivors contacted, 441 (78%) completed the survey. Respondents included 250 (57%) males and median age was 54 years (range 19-79 years). The median age at the time of transplant was 49 years (Range: 17-71), the median time since HSCT was 5 years (Range: 1-14) and 69% had cGVHD. Collectively, 41.7% of survivors reported a vaccine preventable disease (VPD) with the most common being influenza-like-illness (38.4%), varicella zoster/shingles (27.9%), pap smear abnormalities (9.8%), pneumococcal disease (5.1%), and varicella zoster (chicken pox) (4.6%). Only 31.8% had received the full post-HSCT vaccination schedule, and the majority (69.8%) of these had received the vaccines via their General Practitioner. cGVHD was not found to be a significant factor on multivariate analysis for those who were vaccinated. There was a trend toward lower vaccination rates in patients in a lower income strata. Vaccinating post-HSCT survivors to prevent infections and their consequences have an established role in post-HSCT care. Improving rates of post-HSCT vaccination should be a major priority for BMT units.

Sections du résumé

BACKGROUND BACKGROUND
This cross-sectional survey aimed to establish the prevalence of infectious diseases and vaccination uptake in long-term allogeneic hematopoietic stem cell transplants (HSCT) survivors in New South Wales, in order to reduce long-term post-HSCT morbidity and mortality and enhance long-term care.
PATIENTS AND METHODS METHODS
Hematopoietic stem cell transplants survivors aged over 18 years and transplanted between 2000-2012 in New South Wales (NSW) were eligible to participate. Survivors self-completed the Sydney Post BMT Study survey, FACT-BMT (V4), Chronic Graft versus Host Disease (cGVHD) Activity Assessment Self Report, Lee Chronic GvHD Symptom Scale, DASS21, Post Traumatic Growth Inventory, and the Fear of Recurrence Scale.
RESULTS RESULTS
Of the 583 HSCT survivors contacted, 441 (78%) completed the survey. Respondents included 250 (57%) males and median age was 54 years (range 19-79 years). The median age at the time of transplant was 49 years (Range: 17-71), the median time since HSCT was 5 years (Range: 1-14) and 69% had cGVHD. Collectively, 41.7% of survivors reported a vaccine preventable disease (VPD) with the most common being influenza-like-illness (38.4%), varicella zoster/shingles (27.9%), pap smear abnormalities (9.8%), pneumococcal disease (5.1%), and varicella zoster (chicken pox) (4.6%). Only 31.8% had received the full post-HSCT vaccination schedule, and the majority (69.8%) of these had received the vaccines via their General Practitioner. cGVHD was not found to be a significant factor on multivariate analysis for those who were vaccinated. There was a trend toward lower vaccination rates in patients in a lower income strata.
CONCLUSIONS CONCLUSIONS
Vaccinating post-HSCT survivors to prevent infections and their consequences have an established role in post-HSCT care. Improving rates of post-HSCT vaccination should be a major priority for BMT units.

Identifiants

pubmed: 30585673
doi: 10.1111/tid.13043
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13043

Subventions

Organisme : New South Wales Agency for Clinical Innovation Blood and Marrow Transplant Network
Organisme : Northern Blood Research Centre

Informations de copyright

© 2018 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Auteurs

Gemma Dyer (G)

Blood and Marrow Transplant Network, New South Wales Agency for Clinical Innovation, Sydney, New South Wales, Australia.
Faculty of Medicine, Northern Clinical School, University of Sydney, Sydney, New South Wales, Australia.

Nicole Gilroy (N)

Blood and Marrow Transplant Network, New South Wales Agency for Clinical Innovation, Sydney, New South Wales, Australia.

Lisa Brice (L)

Department of Haematology, Royal North Shore Hospital, Sydney, New South Wales, Australia.

Masura Kabir (M)

Westmead Breast Cancer Institute, Sydney, New South Wales, Australia.

David Gottlieb (D)

Faculty of Medicine and Health, University of Sydney, Sydney, New South Wales, Australia.
Department of Haematology, Westmead Hospital, Sydney, New South Wales, Australia.

Gillian Huang (G)

Department of Haematology, Westmead Hospital, Sydney, New South Wales, Australia.

Megan Hogg (M)

Department of Haematology, Westmead Hospital, Sydney, New South Wales, Australia.

Louisa Brown (L)

Department of Haematology, Calvary Mater Newcastle, Newcastle, New South Wales, Australia.

Matt Greenwood (M)

Faculty of Medicine, Northern Clinical School, University of Sydney, Sydney, New South Wales, Australia.
Department of Haematology, Royal North Shore Hospital, Sydney, New South Wales, Australia.
Northern Blood Research Centre, Kolling Institute, University of Sydney, New South Wales, Australia.

Stephen R Larsen (SR)

Institute of Haematology, Royal Prince Alfred Hospital, Sydney, New South Wales, Australia.

John Moore (J)

Department of Haematology, St Vincents Hospital, Sydney, New South Wales, Australia.

Mark Hertzberg (M)

Department of Haematology, Prince of Wales Hospital, Sydney, New South Wales, Australia.

Jeff Tan (J)

Department of Haematology, St Vincents Hospital, Sydney, New South Wales, Australia.

Christopher Ward (C)

Faculty of Medicine, Northern Clinical School, University of Sydney, Sydney, New South Wales, Australia.
Department of Haematology, Royal North Shore Hospital, Sydney, New South Wales, Australia.
Northern Blood Research Centre, Kolling Institute, University of Sydney, New South Wales, Australia.

Ian Kerridge (I)

Faculty of Medicine, Northern Clinical School, University of Sydney, Sydney, New South Wales, Australia.
Department of Haematology, Royal North Shore Hospital, Sydney, New South Wales, Australia.
Northern Blood Research Centre, Kolling Institute, University of Sydney, New South Wales, Australia.

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