Immunization for Child Hematopoietic Stem Cell Transplant (HSCT) Recipients

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Immunization for Child Recipients January 4, 201 Immunization for Child Hematopoietic Stem Cell Transplant () Recipients Revision Date: January 4, 201 Note: This guide is meant to supplement existing recommendations for routine immunization as outlined in the current Alberta Immunization Policy. Consult with an attending transplant physician before providing live vaccines. See Principles of Immunization in Hematopoietic Stem Cell Transplant Recipients and Solid Organ Transplant Recipients. Routine Immunizations Influenza (Inactivated) Pneu-C 13 1,2,3 Live influenza vaccine is contraindicated for patients less than post- and until deemed immunocompetent by the transplant physician. 2 3 DTaP-IPV-Hib MenC-ACYW TAT serology. If low, give a booster dose Hepatitis B Serology for anti-hbs HPV Hepatitis A Pneumo-P MMR At least 3 1st dose 1 Varicella At least 3 1st dose 1 IgG for measles and rubella See detailed recommendations on following pages. 200 201 Government of Alberta Page 1 of

Immunization for Child Recipients January 4, 201 INFLUENZA (Inactivated) Influenza (Inactivated) (a) Live influenza vaccine is contraindicated for patients less than post- and until deemed immunocompetent by the transplant physician. 2 3 INFLUENZA Annual seasonal administration starting before. Inactivated influenza vaccine must be administered at least two weeks prior to transplant conditioning or mobilization chemotherapy. 3 (a) Inactivated Influenza vaccine may be administered as early as four post-transplant in outbreak situations 3 with approval of transplant physician. 4 If administered less than six post-transplant (i.e., 4 ), a 2 nd dose may be administered four weeks later if there is ongoing circulation of virus in the community. 2 Children younger than nine years of age receiving influenza vaccine for the first time post-transplantation require two doses administered at least four weeks apart. 3,5 Live influenza vaccine may be administered to children post- provided that active chronic GVHD is not present, all immunosuppressive drugs have been discontinued for at least three and the child is deemed to be immunocompetent by the transplant physician. Children on maintenance chemotherapy or immunomodulator therapy should not receive live vaccines. 4 Annual influenza vaccine is strongly recommended for close contacts of pre- and post-transplant recipients (e.g., family members, household contacts, etc.). Either inactivated or live influenza vaccines may be administered to close contacts. Note: Individuals who have received FluMist should avoid close association with individuals with severe immunocompromising conditions (e.g., bone marrow transplants recipients requiring protective isolation) for at least two weeks following immunization., Immunity screening immunization is not recommended. PNEUMOCOCCAL 2 3 Pneu-C 13 1,2,3 Pneumo-P PNEUMOCOCCAL The minimum interval between Pneu-C13 doses is four weeks 1 and the minimum interval between the Pneu-C13 and the Pneumo-P is six. 1 The minimum interval between Pneumo-P doses is six. 4 Pneu-C13 may be offered at 3 post transplant at request of transplant physician. 1,4 Pneumo-P may be offered at post transplant respecting the interval between Pneu-C 13 and Pneumo-P. 1,4 Children must be of age or older to receive Pneumo-P. 1 Immunity screening immunization is not recommended at this time. 200 201 Government of Alberta Page 2 of

Immunization for Child Recipients January 4, 201 DTaP-IPV-HIB DTaP-IPV-Hib (a) 2 3 TAT serology. If low, give a booster dose (b) DTaP-IPV-HIB (a) Children younger than seven years of age should receive a 3 rd dose 4 weeks following the 2 nd dose and a 4 th dose at. The minimum interval between each of the first three doses is four weeks and between the 3 rd and 4 th dose is six 1 May offer at post transplant in the event of an outbreak at request of transplant physician. 1,4 Screen for tetanus antitoxin (TAT) immunization at three years post-transplant. If the patient is on intravenous immune globulin (IVIG), serology should be delayed until three the completion of IVIG therapy. (b) If TAT results indicate not immune for tetanus, administer a booster dose of DTaP-IPV/Hib. Immunity screening for diphtheria, pertussis, polio and Hib is not recommended. Ordering serology and booster (if needed) is the responsibility of the transplant physician (allograft recipients) or the primary physician (autograft recipients). Notes: Only inactivated polio vaccine is used in North America. Off-license use of DTaP-IPV/Hib see Biological Products. The immunization recommendations for the general population should be followed long term (i.e., the TAT assessment and recommendations at three years). MENINGOCOCCAL MenC-ACYW 2 3 MENINGOCOCCAL Children younger than two years of age should receive Menveo (not Menactra or Nimenrix ) vaccine. May offer at post transplant at request of transplant physician. 1,4 Immunity screening immunization is not recommended. Immunity screening immunization is not recommended. 200 201 Government of Alberta Page 3 of

Immunization for Child Recipients January 4, 201 Hepatitis B (HBVD) 2 3 Hepatitis B Serology for anti- HBs (a) HEPATITIS B Administer higher dose levels of vaccine 1 : ENGERI -B: Double the μg dose for the age, i.e., 1 ml (20 µg). RECOMBIVA HB : o Children 0 10 years of age inclusive: 0.5 ml (5µg) o Children 11 19 years of age inclusive: 1.0 ml (10µg) Minimal spacing between doses: Four weeks between dose 1 and dose 2; at least two between dose 2 and 3 and four between dose 1 and dose 3. 1 May offer at post transplant at request of transplant physician. 1,4 (a) If patient is on IVIG, serology should be delayed until three the completion of IVIG therapy. *If antibody levels are suboptimal, a repeat HBV series is indicated. 1 Ordering serology and recommending the 2nd series is the responsibility of the transplant physician (allograft recipients) or the primary physician (autograft recipients). HPV HPV 2 3 HUMAN PAPILLOMAVIRUS Girls and Boys 9 to 1 years of age The minimum interval between dose 1 and dose 2 is four weeks and between dose 2 and dose 3 is twelve weeks. 1 Immunity screening immunization is not recommended. Hepatitis A Hepatitis A 2 3 HEPATITIS A Only for those considered high risk (i.e., chronic liver disease; liver transplantation and liver chronic GVHD following ) The minimum interval between 1 st dose and 2 nd dose is six. May be offered at post transplant in a post-exposure situation or travel indication with approval of transplant physician. 1,4 Hepatitis A vaccine is not provided for travellers: refer to local travel clinics. Immunity screening HAV immunization is not routinely recommended. 1 200 201 Government of Alberta Page 4 of

Immunization for Child Recipients January 4, 201 MEASLES, MUMPS, RUBELLA 2 MMR (a) (a) At least 3 1st dose 1 3 IgG for measles and rubella MEASLES, MUMPS, RUBELLA (a) If active chronic GVHD, live vaccines are contraindicated. A live vaccine may be administered all immunosuppressive drugs have been discontinued for at least three and the child is deemed immunocompetent by the transplant physician. 1,5 Children on maintenance chemotherapy or immunomodulator therapy should not receive live vaccines. 4 IVIG: Interval between IVIG and a live vaccine is dependent upon the dose of IVIG used and ranges between eight and eleven. 1,3 Refer to the Canadian Immunization Guide www.phacaspc.gc.ca/publicat/cig-gci/p01-10-eng.php Measles and rubella IgG level at 3 (in case of delayed immunization with live vaccines, IgG level should be determined at least one month the 2 nd MMR dose). If two doses of MMR vaccine, measles IgG is negative or indeterminate consider non-immune to measles no further doses of vaccine should be administered. If patient is exposed to measles in the future, prophylactic IG within six days of exposure should be provided. Ordering serology and booster dose (if needed) is the responsibility of the transplant physician (allograft recipients) or the primary physician (autograft recipients). Varicella 2 Varicella (a) (a) At least 3 1st dose 1 VARICELLA (Chickenpox) (a) If active chronic GVHD, live vaccines are contraindicated. A live vaccine may be administered only all immunosuppressive drugs have been discontinued for at least three and the child is deemed immunocompetent by the transplant physician. 1, Children on maintenance chemotherapy or immunomodulator therapy should not receive live vaccines. 4 Even if the patient has previously developed shingles or chickenpox (pre or post transplant), varicella vaccine should be administered. 2,4 3 All individuals with should be considered susceptible in case of exposure to VZV and should be offered VZIG. 1 Intravenous IG: Interval between IVIG and a live vaccine is dependent upon the dose of IVIG used and ranges between eight and eleven. Refer to the Canadian Immunization Guide www.phacaspc.gc.ca/publicat/cig-gci/p01-10-eng.php Antiviral medications should be discontinued at least hours before receipt of varicellacontaining vaccines 1 and should not be restarted. Immunity screening immunization is not recommended. 200 201 Government of Alberta Page 5 of

Immunization for Child Recipients January 4, 201 Non-routine Immunizations Hepatitis A 2 3 Rabies Typhoid pre-exposure: 3 doses post-exposure: 5 doses TYVI (inactivated) Travel Vaccines Hepatitis A Hepatitis A 2 3 HEPATITIS A Only for those considered high risk (i.e., chronic liver disease; liver transplantation and liver chronic GVHD following ) The minimum interval between 1 st dose and 2 nd dose is six. May be offered at post transplant in a post-exposure situation or travel indication with approval of transplant physician. 1,4 Hepatitis A vaccine is not provided for travellers: refer to local travel clinics. Immunity screening HAV immunization is not routinely recommended. 1 Rabies Rabies (a) (b) pre-exposure: 2 3 3 doses (c) post-exposure: 5 doses RABIES (a) Pre-exposure: Should be delayed 1 and administered only to those considered highrisk (e.g., workers caring for animals including veterinarians, veterinary health technicians, veterinary assistants; SPCA workers and volunteers; animal research workers; animal control workers; wildlife workers and spelunkers (cavers) in Alberta). (b) Pre-exposure series must be administered intramuscularly: 1.0 ml (days 0,, 21 or 2). 1 Immunity screening is recommended days the third dose of vaccine and then every two years if risk continues. 1 Provide booster if indicated. (c) Post-exposure: Rabies post-exposure prophylaxis (rabies immune globulin/rig and rabies vaccine) may be administered at any time following transplant if indicated (i.e., if bitten by potentially rabid animal). Post-exposure vaccine schedule: RIG day 0 and vaccine - days 0, 3,,, 2 administered IM. 1 Immunity screening is recommended days the last dose of vaccine. 1 200 201 Government of Alberta Page of

Immunization for Child Recipients January 4, 201 May be offered at post transplant for pre-expsoure with approval of transplant physician and as needed in post-exposure situation. 1,4 Ordering serology and booster dose (if needed) is the responsibility of the transplant physician (allograft recipients) or the primary physician (autograft recipients). Typhoid Typhoid month s 2 3 TYVI (inactivated) TYPHOID Only for those considered high-risk (i.e., household or intimate contacts of typhoid carriers; laboratory workers who regularly manipulate the salmonella typhi organism). May be offered at post transplant in the event of an exposure or travel indication with approval of transplant physician. 1,4 Children must be of age or older to receive Typhoid vaccine. 1 Booster every three years if risk continues.1 1 Immunity screening immunization is not recommended. Travel Vaccines Travel Vaccines Travel vaccines are not publicly funded in Alberta. Clients requesting travel vaccines should be referred to one of Alberta Health Services Travel Clinics (in Edmonton or Calgary). For more detailed information and clinic locations, please go to: www.albertahealthservices.ca/services.asp?pid=service&rid=5. Travel vaccines, if needed, should be administered at two years post-transplant or later, as long as the client has been off of immunosuppressive drugs for at least three. This is an absolute requirement for live vaccines. Non-live vaccines may be administered at ; however immunogenicity is limited, so waiting until or later is preferred. Live vaccines (e.g., yellow fever) are contraindicated in the first two years posttransplant. After that, live vaccines may be administered if the client does not have a relapse or chronic GVHD and if the client is off all immunosuppressive drugs. 200 201 Government of Alberta Page of

Immunization for Child Recipients January 4, 201 References 1 National Advisory Committee on Immunization. (Evergreen). Canadian Immunization Guide (Evergreen ed.). Ottawa, On: Public Health Agency of Canada www.canada.ca/en/public-health/services/canadian-immunization-guide.html 2 Ljungman, P., Cordonnier, C., Einsele, H., Englund, J., Macbado, C.M., Storek, J., Small, T. (2009) Vaccination of HCT recipients. In Guidelines for preventing infectious complications among hematopoietic cell transplantation recipients: a global perspective. Biology of Blood and Marrow Transplant, 15, 13 3. 3 Rubin, L. G., et all. (20, February). 2013 IDSA clinical practice guidelines for vaccination of the immunocompromised host. Clinical Infectious Diseases, 5(3), 309-31 4 Expert opinion of Alberta physicians. (April 20 and October 201). 5 National Advisory Committee on Immunization. Statement on seasonal influenza vaccine for 201-201. Hilgendorf, I., et all. (2011, February 1).Vaccination of allogeneic haematopoietic stem cell transplant recipients: Report from the International Consensus Conference on Clinical Practice in chronic GVHD. Vaccine (2011). Doi: 10.101/Journal of Vaccine Verolet, C., Posfay-Barbe, K (2015, April). Live Virus Vaccines in Transplantation: Friend or Foe? Current Infectious Disease Report, (1:) Alberta Advisory Committee on Immunization. (2011, May 31). Record of decisions (unpublished). 200 201 Government of Alberta Page of