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2.
Br J Haematol ; 195(2): 174-185, 2021 10.
Article in English | MEDLINE | ID: mdl-33955555

ABSTRACT

The introduction of clotting factor concentrates has substantially improved the lives of people with clotting factor deficiencies. Unfortunately, the transmission of blood-borne viral infections through these plasma-derived products led to a huge epidemic of human immunodeficiency virus and viral hepatitis in people with haemophilia (PWH). In a significant proportion of PWH exposed to these viruses, the ensuing decades-long chronic infection resulted in excess morbidity and mortality. Fortunately, developments in the safety of blood products, as well as vaccination and highly effective antiviral treatments have improved the prospects of PWH. The present article reviews the background of the viral hepatitis epidemic in PWH, the natural history of hepatitis B and C infections and their long-term management.


Subject(s)
Blood-Borne Infections/prevention & control , HIV Infections/prevention & control , Hemophilia A/therapy , Hepatitis, Viral, Human/prevention & control , Adolescent , Adult , Aged , Aged, 80 and over , Antiviral Agents/therapeutic use , Blood Coagulation Factors/therapeutic use , Blood-Borne Infections/etiology , Blood-Borne Infections/transmission , Carcinoma, Hepatocellular/complications , Carcinoma, Hepatocellular/epidemiology , Disease Management , HIV/isolation & purification , HIV Infections/drug therapy , HIV Infections/epidemiology , HIV Infections/transmission , Hemophilia A/complications , Hemophilia A/epidemiology , Hepatitis, Viral, Human/complications , Hepatitis, Viral, Human/drug therapy , Hepatitis, Viral, Human/transmission , Humans , Liver Neoplasms/pathology , Liver Transplantation/adverse effects , Middle Aged , Morbidity/trends , Mortality/trends , Persistent Infection , Vaccination/methods , Young Adult
3.
Am J Trop Med Hyg ; 104(4): 1577-1581, 2021 02 22.
Article in English | MEDLINE | ID: mdl-33617474

ABSTRACT

There is a high prevalence of blood-borne infections in West Africa. This study sought to determine the seroprevalence of blood-borne infections, including hepatitis B virus (HBV), hepatitis C virus (HCV), HIV, and syphilis, in blood donors in Burkina Faso. Blood donors were recruited from 2009 to 2013 in four major cities in Burkina Faso of urban area (Ouagadougou) and rural area (Bobo Dioulasso, Fada N'Gourma, and Ouahigouya). Serology tests including hepatitis B surface antigen, anti-HCV, anti-HIV, and rapid plasma reagin test were used for screening and were confirmed with ELISA. Disease prevalence was calculated among first-time donors. Incidence and residual risk were calculated from repeat donors. There were 166,681 donors; 43,084 had ≥ 2 donations. The overall seroprevalence of HBV, HCV, HIV, and syphilis were 13.4%, 6.9%, 2.1%, and 2.4%, respectively. The incidence rates (IRs) of HBV, HCV, HIV, and syphilis infection were 2,433, 3,056, 1,121, and 1,287 per 100,000 person-years. There was lower seroprevalence of HBV and HCV in urban area than in rural area (12.9% versus 14.0%, P < 0.001; and 5.9% versus 8.0%, P < 0.001), and no difference in HIV (2.1% versus 2.1%, P = 0.25). The IRs of new HBV, HCV, HIV, and syphilis were 2.43, 3.06, 1.12, and 1.29 per 100,000 person-years, respectively. The residual risk was one per 268 donations for HBV, one per 181 donations for HCV, and one per 1,480 donations for HIV, respectively. In conclusion, this comprehensive study from four blood donation sites in Burkina Faso showed high HBV and HCV seroprevalence and incidence with high residual risk from blood donation.


Subject(s)
Blood Donors , Blood Transfusion/statistics & numerical data , Blood-Borne Infections/epidemiology , Blood-Borne Infections/immunology , Adolescent , Adult , Blood Donors/statistics & numerical data , Blood-Borne Infections/transmission , Blood-Borne Infections/virology , Burkina Faso/epidemiology , Female , HIV Infections/epidemiology , HIV Infections/immunology , Hepatitis B/epidemiology , Hepatitis B/immunology , Hepatitis C/epidemiology , Hepatitis C/immunology , Humans , Incidence , Male , Seroepidemiologic Studies , Young Adult
5.
Transfusion ; 60(9): 1987-1997, 2020 09.
Article in English | MEDLINE | ID: mdl-32743798

ABSTRACT

Risk assessments of transfusion-transmitted emerging infectious diseases (EIDs) are complicated by the fact that blood donors' demographics and behaviors can be different from the general population. Therefore, when assessing potential blood donor exposure to EIDs, the use of general population characteristics, such as U.S. travel statistics, may invoke uncertainties that result in inaccurate estimates of blood donor exposure. This may, in turn, lead to the creation of donor deferral policies that do not match actual risk. STUDY DESIGN AND METHODS: This article reports on the development of a system to rapidly assess EID risks for a nationally representative portion of the U.S. blood donor population. To assess the effectiveness of this system, a test survey was developed and deployed to a statistically representative sample frame of blood donors from five blood collecting organizations. Donors were directed to an online survey to ascertain their recent travel and potential exposure to Middle East respiratory syndrome coronavirus (MERS-CoV). RESULTS: A total of 7128 responses were received from 54 256 invitations. The age-adjusted estimated total number of blood donors potentially exposed to MERS-CoV was approximately 15 640 blood donors compared to a lower U.S. general population-based estimate of 9610 blood donors. CONCLUSION: The structured donor demographic sample-based data provided an assessment of blood donors' potential exposure to an emerging pathogen that was 63% larger than the U.S. population-based estimate. This illustrates the need for tailored blood donor-based EID risk assessments that provide more specific demographic risk intelligence and can inform appropriate regulatory decision making.


Subject(s)
Blood Donors , Blood Transfusion , Blood-Borne Infections/epidemiology , Communicable Diseases, Emerging/epidemiology , Communicable Diseases, Imported/epidemiology , Coronavirus Infections/epidemiology , Environmental Exposure , Risk Assessment/methods , Surveys and Questionnaires , Travel-Related Illness , Adolescent , Adult , Aged , Aged, 80 and over , Blood Banks , Blood Donors/statistics & numerical data , Blood-Borne Infections/blood , Blood-Borne Infections/prevention & control , Blood-Borne Infections/transmission , Communicable Diseases, Emerging/blood , Communicable Diseases, Emerging/prevention & control , Communicable Diseases, Emerging/transmission , Communicable Diseases, Imported/blood , Communicable Diseases, Imported/prevention & control , Communicable Diseases, Imported/transmission , Coronavirus Infections/blood , Coronavirus Infections/prevention & control , Coronavirus Infections/transmission , Decision Making , Female , Humans , Male , Middle Aged , Middle East , Middle East Respiratory Syndrome Coronavirus , Sample Size , Sampling Studies , Transfusion Reaction/prevention & control , United States/epidemiology , Young Adult
7.
Transfus Med ; 30(5): 377-383, 2020 Oct.
Article in English | MEDLINE | ID: mdl-31916330

ABSTRACT

OBJECTIVES: To report the clinical and virologic epidemiology of a recent epidemic of hepatitis C in thalassaemia patients in Sri Lanka. BACKGROUND: Transfusion-dependent thalassaemia patients remain at risk for hepatitis C virus (HCV). Here, we report a cluster of recent HCV infections in Sri Lankan thalassaemia patients and examine the phylogenetic relationship of viral sequences. METHODS: We conducted two prospective cross-sectional surveys of 513 patients in four Sri Lankan thalassaemia centres in 2014/2015 and re-surveyed one centre in 2016. We screened for anti-HCV antibodies using the CTK Biotech enzyme-linked immunosorbent assay (ELISA) kits and confirmed active infection by reverse transcription-polymerase chain reaction (RT-PCR) for HCV-RNA. HCV genomes were sequenced by unbiased target enrichment. RESULTS: Anti-HCV antibodies were found in 116/513 (22.6%) of patients initially tested. Active hepatitis C infection was found in 26 patients with no cases of active hepatitis B infection. Of 26 patients with HCV, two were infected with genotype 1(a), and the rest had 3(a). In a single centre (Ragama), 122 patients (120 new cases and two previously tested, but negative) were retested for anti-HCV antibodies. 32/122 (26.2%) patients were seropositive. Twenty-three (23/122; 18.8%) of these new cases were confirmed by HCV PCR (all genotype 3[a]). CONCLUSION: There is a significant cluster of recent HCV cases in multiply transfused thalassaemia patients in several centres in Sri Lanka. Most of the viruses shared a close phylogenetic relationship. The results are consistent with recent continuing transfusion-transmitted HCV infection. Routine surveillance for HCV of chronically transfused patients is required irrespective of screening of blood products.


Subject(s)
Blood Transfusion , Blood-Borne Infections , Genome, Viral , Hepacivirus , Hepatitis C , Phylogeny , RNA, Viral , Thalassemia , Adolescent , Adult , Blood-Borne Infections/blood , Blood-Borne Infections/epidemiology , Blood-Borne Infections/genetics , Blood-Borne Infections/transmission , Child , Cross-Sectional Studies , Female , Hepacivirus/metabolism , Hepatitis C/blood , Hepatitis C/epidemiology , Hepatitis C/genetics , Hepatitis C/transmission , Hepatitis C Antibodies/blood , Humans , Male , Prospective Studies , RNA, Viral/blood , RNA, Viral/genetics , Sri Lanka/epidemiology , Thalassemia/blood , Thalassemia/epidemiology , Thalassemia/therapy
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