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Presenter: William, Mulley, Clayton, Australia
Authors: Mulley W., Visvanathan K., Polkinghorne K., Stuart R., Lewicki M., Kanellis J.
COMPLICATIONS - INFECTIONS
W.R. Mulley1, K. Visvanathan1, K.R. Polkinghorne1, R.L. Stuart1, M.C. Lewicki1, J. Kanellis2
1Department Of Nephrology, Monash Medical Centre, Clayton/AUSTRALIA, 2Nephrology, Monash Medical Centre, Clayton/VIC/AUSTRALIA
Body: Introduction: The current H1N1 influenza worldwide pandemic has resulted in significant mortality and morbidity. The 2009 influenza vaccine available in Australia did not cover this variant. In late 2009 a “Swine Flu” vaccine was generated and recommended by local and international organisations for renal transplant recipients (RTRs). We aimed to measure variations in serological responses to the vaccine in a renal transplant population. Methods: We offered the H1N1 vaccine to our RTR cohort. Patients were vaccinated as outpatients between 10/2009-12/2009. Others patients chose to receive the vaccine from their family doctor. The vaccine was presented in a 5 or 10 dose, multi-dose vial. Demographic and clinical parameters were recorded for patients vaccinated at our clinics. Blood was collected for: anti-H1N1 antibody titres at vaccination and 1mth later; vitamin D levels; and white cell counts. Results: Of our 526 RTRs, 323 (61%) received the H1N1 vaccine (Panvax 15mcg/dose (CSL)) during the study period (see table). 193/226 that we vaccinated had the initial blood test with 162/193 having the second. Median time since transplantation was 55mths (range 1.6-330mths). There were no major side-effects noted and no incidents reported relating to the use of multi-dose vials. Interestingly 153 pts (79%) had low vitamin D levels with 31 (16%) being critically low. Serological responses are currently being assessed. Conclusions: The majority of our RTRs were willing to receive the H1N1 vaccine based on recommendations of transplant authorities despite uncertainty surrounding the likelihood of a protective sero-response. The vaccine was safely administered by appropriately trained nursing staff. Efficacy of this vaccine will soon be established and will guide further vaccination recommendations to patients.
Vaccination details of renal transplant recipient cohort (n=526) | |||||||
Vaccinated at transplant centre | Vaccinated at family doctor | Declined vaccination | Medically unsuitable | Unknown / Not reviewed during vaccin’n period | |||
226 (43.0%) | 97 (18.5%) | 75 (14.3%) | 10 (1.9%) | 118 (22.5%) | |||
Demographics of vaccinated study cohort with initial blood tests performed (n=193) | |||||||
Age: median (range) | Sex | Transplant number | Medications | ||||
50 (22-79) yrs | M 118 (61%) F 75 (39%) | #1 – 172 (89.1%) #2 – 16 (8.3%) #3 – 5 (2.6%) | Ritux n=19; Basilix n=94; Tac n=102; CyA n=70; Myco n=138; Aza n=36; SRL n=8; ERL n=6 |
Disclosure: All authors have declared no conflicts of interest.
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