Routine Testing Covers a Limited Number of Agents:
Parasites and Other Known Pathogens
Although as many as 25 known pathogens may be present in blood [35],
only HIV, HCV, HBV, and a few others are required to be screened after
collection. Detection tests are not yet developed or implemented for all
recognized pathogens, including parasites.
Risks from parasites With the increase in global travel and migration over the last 20 years,
blood-borne parasitic diseases such as malaria and Chagas' diseases
have become more common in blood transfusions throughout Europe. Parasite
screening tests are not routinely used, and donor interviews remain
the primary defense against such infections.
Malaria Globally, malaria is estimated to infect 300 - 500 million people every
year in tropical regions [36]. Though
primarily spread by mosquito bite, the disease can be transmitted through
blood transfusion, which accounted for 91 cases in the US between 1963
and 1999 [37]. Currently, donors who
have visited areas in which malaria is endemic may be deferred from
donating blood for six months.
| Anopheles mosquito vector |
Ring stage Plasmodium
trophozoites in RBC |
Global distribution
of malarial risk |
Photos and map data courtesy of the CDC (William Brogdon/Dr.
Mae Melvin).
Chagas' DiseaseTrypanosoma cruzi, the causative agent of Chagas' disease,
is endemic in much of South America. Although the disease can be transmitted
through blood transfusion and has been documented in the US and Canada,
routine screening of blood for T. cruzi is not performed.
Studies in the US (Los Angeles, California) have indicated that in some
regions as many as 1 in 7500 blood donors show evidence of infection
[38].
| Reduviid bug vector |
T. cruzi trypomastigote
in
Giemsa-stained thin smear |
Global distribution
of Chagas' disease |
Photo courtesy of World Health Organization / TDR /
Stammers.
Leishmaniasis Leishmaniasis, caused by the Leishmania sp., is a serious illness
endemic to subtropical regions. Recent studies of Leishmania/HIV co-infection
have revealed that the true prevalence of Leishmania in Spain and Southern
Europe may be under-reported and the parasite can pose a serious health
risk to immunocompromised patients [39].
Sandfly vector
(Phlebotomous dubosci) |
Leishmania promastigote
in
fixed Giemsa-stained thin smear |
Global distribution
of Leishmaniasis |
Photos are courtesy of World Health Organization / TDR
/ Stammers, and map data is from WHO/CDC, 1987.
Additional viral risk Although most of the routine screening tests in common use are directed
against viral pathogens, the blood supply remains vulnerable to many
known viral diseases.
- Cytomegalovirus (CMV) is such a common infection
that it is not routinely screened due to its high prevalence (from 40
- 100% in Western adult populations [40]).
However, CMV can pose a serious threat to immunocompromised individuals,
who receive CMV-seronegative units from a limited supply. Although leukoreduction
has been proposed as an alternative to the use of CMV-seronegative units,
some studies have indicated that leuko-filtration is not completely
effective at preventing transmission of CMV [41].
- Parvovirus B19 is another virus which is widespread
(up to 70 - 90% estimated seroprevalence in adults [42]),
and is not included in the panel of blood bank screening tests. Though
many transfusion recipients may already be immune to this agent, B19
infection can be hazardous for certain populations such as those who
are immunocompromised, sickle cell/thalassemia patients, and pregnant
women.
Benefits of the INTERCEPT Blood System The broad-spectrum pathogen inactivation of the INTERCEPT Blood System allows
a single new safety measure to simultaneously address multiple infectious risks
of transfusion.
Read our Technical Data Sheets for a list of CE Mark approved product claims.
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