Infections after hematopoietic stem cell transplantation: Difference between revisions
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| [[Cytomegalovirus]] |
| [[Cytomegalovirus]] |
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| Pre-transplant screening of donor and recipient serostatus. |
| Pre-transplant screening of donor and recipient IgG serostatus. |
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| All R+ or D+ recipients should have either prophylaxis or close monitoring with preemptive treatment until at least day 100. Monitoring should start on day 10 and continue weekly until at least day 100. |
| All R+ or D+ recipients should have either prophylaxis or close monitoring with preemptive treatment until at least day 100. Monitoring should start on day 10 and continue weekly until at least day 100. |
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| [[Epstein-Barr virus]], especially PTLD |
| [[Epstein-Barr virus]], especially PTLD |
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| Pre-transplant screening of donor and recipient serostatus, especially in children. |
| Pre-transplant screening of donor and recipient IgG serostatus, especially in children. |
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| Monitor high-risk recipients (T-cell depletion, ant-T-cell antibodies, umbilical cord transplants, and haplo-identical transplants), with reduction in immunosuppression if rising viral load. |
| Monitor high-risk recipients (T-cell depletion, ant-T-cell antibodies, umbilical cord transplants, and haplo-identical transplants), with reduction in immunosuppression if rising viral load. |
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| [[Herpes simplex virus]] |
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| Pre-transplant screening of donor and recipient IgG serostatus. Counselling of seronegative recipients on protective behaviours. |
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| [[Acyclovir]] for all seropositive recipients of alloHSCT from conditioning until engraftment (about 30 days). Not necessary if receiving prophylaxis for CMV. |
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| [[Varicella zoster virus]] |
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| Pre-transplant screening of donor and recipient IgG serostatus. Close contacts should have up-to-date vaccinations before visiting. |
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| [[Acyclovir]] or [[valacyclovir]] for all seropositive recipients of alloHSCT from conditioning until 1 year and during chronic GVHD. Post-exposure prophylaxis with VariZIG for seronegative recipients. |
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| [[Influenza]] |
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| Annual immunization of recipient and close contacts. |
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| Consider prophylaxis of recipient and possibly also close contacts during outbreaks. |
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| [[Adenovirus]] |
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| Weekly screening PCR for the first 6 months and during severe immunosuppression. |
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| [[Hepatitis B virus]] |
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| Pre-transplant screening of donor and recipient serostatus. Immunization of seronegative recipients. |
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| Monitoring ALT during prolonged corticosteroid use with HBV DNA viral load if ALT is elevated, and pre-emptive antiviral therapy if the viral load is positive. Consider prophylaxis for anti-HBc-positive recipients from conditioning to 6 months after transplant. Monitor anti-HBs titres every 3 months, with viral load if it is decreasing. Re-immunize if titres become negative. Treatment of choice is [[lamivudine]] 100 mg/day. |
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| [[Hepatitis C virus]] |
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| Pre-transplant screening of donor and recipient serostatus with viral load if positive or if at elevated risk despite negative serology. |
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| For those with HCV, consider liver biopsy if iron overloaded, alcohol abuse, HCV for longer than 10 years, or clinical evidence of chronic liver disease. Consider treatment after 2 years post-transplant if without GVHD and no immunosuppressing medications for at least 6 months. |
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Revision as of 02:15, 20 May 2020
Timeline of Infections
Time | Risk factors | Bacteria | Viruses | Fungi | Parasites |
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Pre-engraftment day 0 to 30 |
Neutropenia, mucositis, and central lines | GPCs and GNBs | BK virus, HSV, and resp/enteric viruses | Candida and Aspergillus | Strongyloides |
Early post-engraftment to day 100 |
Immunosuppressing meds, acute GVHD, central lines | GPCs, encapsulated bacteria, Listeria, Salmonella, Nocardia | HSV, CMV, HHV-6, adenovirus, resp/enteric viruses | Aspergillus, other molds, PJP | Strongyloides, Toxoplasma |
Mid post-engraftment to 1 year |
Immunosuppressing meds, chronic GVHD | Encapsulated bacteria, Listeria, Salmonella, Nocardia | VZV, EBV (and PTLD), CMV, respiratory/enteric viruses | Aspergillus, other molds, PJP | |
Late post-engraftment after 1 year |
Immunosuppresing meds, chronic GVHD | Encapsulated bacteria, Listeria, Salmonella, Nocardia | VZV, CMV, respiratory/enteric viruses |
Prevention
Infection | Preventing exposure | Preventing disease |
---|---|---|
Bacterial infections | ||
Early disease (0-100 days after HCT) | Use levofloxacin or other respiratory fluoroquinolone in adult patients with anticipated neutropenia of 7 or more days until recovery of neutropenia. GM-CSF or G-CSF may decrease risk of infection, but unclear if it decreases mortality. | |
Late disease (100 days after HCT) | Antibiotic prophylaxis is indicated for alloHSCT recipients with chronic GVHD to prevent invasive pneumococcal disease until cGVHD resolves. | |
CLABSI | Implement a CLABSI bundle to ensure maximum sterility on insertion. | If infection rate is still >1 per 1000 catheter days, can consider prophylactic minocycline plus rifampin. |
Streptococcus pneumoniae | Routine precautions. | Immunization for all HCT recipients. Antibiotic prophylaxis for chronic GVHD and for low IgG levels, regardless of vaccination status, usually with penicillin. |
Viridans group streptococci | Pre-conditioning dental consults. | |
Haemophilus influenzae type b | Ensuring up-to-date immunizations of close contacts. | Immunization of all HCT recipients. Post-exposure prophylaxis if exposed. |
Bordatella pertussis | Ensuring up-to-date immunizations of close contacts. | Immunization of all HCT recipients. Post-exposure prophylaxis if exposed. |
Viral infections | ||
Cytomegalovirus | Pre-transplant screening of donor and recipient IgG serostatus. | All R+ or D+ recipients should have either prophylaxis or close monitoring with preemptive treatment until at least day 100. Monitoring should start on day 10 and continue weekly until at least day 100. |
Epstein-Barr virus, especially PTLD | Pre-transplant screening of donor and recipient IgG serostatus, especially in children. | Monitor high-risk recipients (T-cell depletion, ant-T-cell antibodies, umbilical cord transplants, and haplo-identical transplants), with reduction in immunosuppression if rising viral load. |
Herpes simplex virus | Pre-transplant screening of donor and recipient IgG serostatus. Counselling of seronegative recipients on protective behaviours. | Acyclovir for all seropositive recipients of alloHSCT from conditioning until engraftment (about 30 days). Not necessary if receiving prophylaxis for CMV. |
Varicella zoster virus | Pre-transplant screening of donor and recipient IgG serostatus. Close contacts should have up-to-date vaccinations before visiting. | Acyclovir or valacyclovir for all seropositive recipients of alloHSCT from conditioning until 1 year and during chronic GVHD. Post-exposure prophylaxis with VariZIG for seronegative recipients. |
Influenza | Annual immunization of recipient and close contacts. | Consider prophylaxis of recipient and possibly also close contacts during outbreaks. |
Adenovirus | Weekly screening PCR for the first 6 months and during severe immunosuppression. | |
Hepatitis B virus | Pre-transplant screening of donor and recipient serostatus. Immunization of seronegative recipients. | Monitoring ALT during prolonged corticosteroid use with HBV DNA viral load if ALT is elevated, and pre-emptive antiviral therapy if the viral load is positive. Consider prophylaxis for anti-HBc-positive recipients from conditioning to 6 months after transplant. Monitor anti-HBs titres every 3 months, with viral load if it is decreasing. Re-immunize if titres become negative. Treatment of choice is lamivudine 100 mg/day. |
Hepatitis C virus | Pre-transplant screening of donor and recipient serostatus with viral load if positive or if at elevated risk despite negative serology. | For those with HCV, consider liver biopsy if iron overloaded, alcohol abuse, HCV for longer than 10 years, or clinical evidence of chronic liver disease. Consider treatment after 2 years post-transplant if without GVHD and no immunosuppressing medications for at least 6 months. |
Further Reading
- Life-threatening Infection in Transplant Recipients. Crit Care Clin. 2013 Oct;29(4):953-73. doi: 10.1016/j.ccc.2013.06.012