Infections after hematopoietic stem cell transplantation: Difference between revisions

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(: finished viral infections)
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| [[Cytomegalovirus]]
| [[Cytomegalovirus]]
| Pre-transplant screening of donor and recipient serostatus.
| 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.
| 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
| [[Epstein-Barr virus]], especially PTLD
| Pre-transplant screening of donor and recipient serostatus, especially in children.
| 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.
| 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.
|}
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Revision as of 02:15, 20 May 2020

Timeline of Infections

Time Risk factors Bacteria Viruses Fungi Parasites
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