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            | OJHAS Vol. 10, Issue 2: 
            (Apr-Jun 2011) |  
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            | Blood Transfusions: 
            Are They Life Saving or Transfusing 
            Infections? |  
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                | Amrutha Kumari B, Associate Professor, Deepa S, Assistant Professor,
 Venkatesha D, Prof & Head,
 Department of Microbiology, MMC&RI, Mysore
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                | Dr. Amrutha Kumari B,
          
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            |  |  | Address for Correspondence | Associate Professor,
 Department of Microbiology,
 MMC&RI, Irwin Road,
 Mysore, India.
 E-mail: 
            
                amrutakb@yahoo.co.in
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            | Amrutha Kumari B, Deepa S,
 Venkatesha D. Blood Transfusions: 
            Are They Life Saving or Transfusing 
            Infections? Online J Health Allied Scs. 
            2011;10(2):7 |  
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            | Submitted: Jun 21, 
            2011; Accepted: Jul 16, 2011; Published: Jul 30, 2011 |  
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            | Abstract: |  
            | Introduction: 
There is a risk of 1 - 2 per 1000 recipients receiving contaminated 
blood with viral, bacterial and parasitic agents.TTI’S are the most 
commonly encountered complications in transfusion medicine. The objective 
of the study was to determine the seroprevalence of TTI’s among blood donors, 
who represent healthy population at large. Materials & methods: 
A total of 33,658 blood units were received from voluntary and replacement 
donors over a period of 5 years. Surface antigen of HBV and antibodies 
to HIV and HCV were determined using ELISA. Syphilis was detected using 
TPHA test. Results: 947 (2.81%) 
blood units tested positive for HBV, HCV, HIV and / or syphilis. Overall 
prevalence was HBV – 1.77%, HCV – 0.13%, HIV – 0.63% and Syphilis 
– 0.28%. Nine (0.03%) donors had coinfections. Conclusion: The 
screening of blood donors is the corner stone in assuring the safety 
of blood transfusion.Key Words: 
 Transfusion Transmitted Infections; HBV; HCV; HIV; Syphilis
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            |  |  Transfusion of blood 
and blood components as a specialised modality of patient management 
saves millions of lives worldwide.1 
Getting safe blood is becoming increasingly difficult because of blood 
borne infections like Hepatitis B virus (HBV), Hepatitis C virus (HCV), 
Human immunodeficiency virus (HIV) & Treponema palladium. 
There is a risk of 1–2 per 1000 recipients receiving contaminated 
blood with viral, bacterial or parasitic agents.2 According 
to WHO estimate the lack of effective screening of blood donors’ results 
in up to 16 million new infections with HBV, 5 million new infections 
with HCV, 1, 60,000 new cases of HIV infections every year.3 HIV, HBV & HCV are 
known to cause coinfections due to common route of transmission .The 
viruses are partners in crime augmenting the pathogenesis & there 
by increasing the morbidity & mortality. Evaluation of data for 
the prevalence of transfusion transmitted infections (TTI’s) 
permits an assessment of acquisition of these infections in the blood 
donor population & consequently the safety of the collected blood 
donations. It also gives an idea of epidemiology of these infections 
in the community.4 A total of 33,658 units 
of blood were collected from both voluntary and replacement donors over 
a period of 5 years (Jan 2006 – Dec 2010) at blood bank attached to 
Mysore Medical College & Research Institute, Mysore, Karnataka, 
India. Samples were screened for HBV, HCV, HIV & Syphilis. HBV screening was done 
using ERBALISA kit to detect HBsAg using polyclonal antibodies against 
surface antigen of Hepatitis B virus.  ERBALISA kit was used to detect 
HCV antibodies using a mixture of synthetic peptides & recombinant 
proteins of HCV that is CORE NS3, NS4 
& NS5. ERBALISA kit HIV 1 / HIV 2 a solid phase immunoassay 
utilising a mixture of synthetic peptides for detection of HIV1 & 
HIV2 antibodies was used to detect HIV. Validity of ELISA tests was 
assessed by means of acceptance criteria laid down by the manufacturer. 
A rapid TPHA test for the diagnosis of syphilis to detect IgG & 
IgM antibodies to Treponema palladium 
was used. Seropositive blood units were discarded. Infected donors were 
referred for specialist care.5 
          A total of 33,658 blood 
samples were included in the study during the period Jan 2006 – Dec 
2010. 947 (2.81%) blood units showed seropositivity for TTI’s.  
| Table: Seroprevalence 
of various Transfusion Transmitted Infections |  | Year | Total donors | HBV | HCV | HIV | Syphilis |  | 2006 | 08487 | 111(1.31%) | 0 | 047(0.55%) | 08(0.09%) |  | 2007 | 06569 | 091(1.38%) | 02(0.03%) | 049(0.74%) | 25(0.38%) |  | 2008 | 06404 | 166(2.59%) | 14(0.22%) | 044(0.69%) | 30(0.47%) |  | 2009 | 06257 | 087(1.39%) | 10(0.16%) | 040(0.64%) | 11(0.18%) |  | 2010 | 05941 | 127(2.14%) | 19(0.32%) | 032(0.54%) | 20(0.34%) |  | Total | 33,658 | 596(1.77%) | 45(0.13%) | 212(0.63%) | 94(0.28%) |  Nine donors had coinfections 
of which six were coinfected with HIV & HBV, two of them were infected 
with HIV & HCV & one donor with HBV & HCV. In recent years there 
has been a special interest in donor selection strategies in blood banks 
in order to provide safer blood supply. There is no screening method 
to reduce the risk of TTI’s to zero. It appears that it is essential 
to adopt strict criteria in the selection of donors and to avoid unnecessary 
transfusions.4 Serosurveys are one of the primary methods 
to determine the prevalence of TTI’s. In our retrospective study, 
we have evaluated the seroprevalence of HBsAg, anti-HCV, anti-HIV and 
syphilitic antibodies among blood donors who are considered to be of 
low risk behaviour group as there is no data available from this region. Over a period of five 
years the prevalence of HBsAg was 1.77% (range 1.31% - 2.59%). A study 
in Orrisa has reported 1.13% and another study in Delhi has reported 
2.23% of HBV infection in blood donors respectively.6,7 A 
low prevalence of HBV of 0.62% was reported in a study at costal Karnataka.8 
In our study a significant rise in HBV prevalence has been noted in 
the year 2010 i.e. 2.59%.  HCV seropositivity 
in our study was 0.13% (0.03% - 0.32%). In India the prevalence of HCV 
in blood donors has been reported to be 0.12% to 2.5%. A study in Delhi 
has reported HCV in blood donors as 0.66% to 2.5% and in Western India 
0.28% respectively.7,9 There is significant increase in HCV 
seropositivity rate in the present study from 0.03% to 0.32% over a 
period of 5years. A study in Eastern India also has reported an increase 
in HCV seropositivity among blood donors.10 High prevalence 
of 6% HCV infection was reported by another study in Hyderabad, South 
India.11 HIV antibodies were detected 
in 0.63% (0.53% - 0.74%) in our study. Other authors have reported HIV 
seropositivity of 0.4% and 0.55% among blood donors.12,13 
Syphilitic antibodies were detected in 0.28% (0.09% - 0.49%) in our 
study. Similar prevalence has been reported by other authors.13,10 Data on the prevalence of >2 
TTIs is limited.14 In 
our study 9 donors (0.03%) had co-infections of which six donors had 
HIV & HBV (2.83% of HIV positive donors), 2 donors (0.91% of HIV 
positive donors) had HCV co-infection. One donor was positive for both 
HBV and HCV. Studies 
on the prevalence of hepatitis viruses in patients with HIV have reported 
HIV and HBV/HCV co-infection rate as 12%–15%. However in India studies, 
this varies with the geographical region ranging from 9%–30% for HBV 
& 2%–8% for HCV. A study in North India has reported 
coinfections in blood donors as 0.05% of which 5 donors had HIV & 
HBV, 2 donors had HIV & HCV and another 2 donors had HBV & HCV 
coinfections.14 The absence of HBsAg 
in blood donors may not be sufficient to ensure the lack of circulating 
HBV and hence there are chances of missing occult HBV infection.8 
A study in central India has shown a positivity of 2.2% for HBV DNA 
in donors who tested negative for HBsAg by ELISA.15 Majority 
of the problems are due to prevalence of asymptomatic carriers in the 
society, as well as, blood donations during the window period of infections. 
Most government hospital blood banks in India use ELISA test kits, which 
cannot detect HIV before 22 days, HBV before 59 days and HCV before 
82 days of infection.16 Considering the vast population of 
the country, even low prevalence amounts to the large number of infected 
people.16 With this prevalence of TTI’s, pit falls in detection 
methods and the morbidity and mortality associated with TTI’s, we 
have to urgently consider the need to modulate and adopt newer sensitive 
technologies. Stringent measures need to be taken for blood donor screening, 
by using more sensitive methods to detect infections early, like Nucleic 
acid amplification technology (NAT) assays.17 Considering the various 
risks in transfusions, we have to adopt judicious blood transfusions 
and sensitive technologies for screening of blood donors in order to 
safeguard recipients of blood and its components. We thank Dr. Manjunath, 
blood bank officer for his cooperation in providing us the materials 
for the study. 
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