|Year : 2017 | Volume
| Issue : 11 | Page : 1138-1142
Comparison of seropositivity of human immunodeficiency virus, hepatitis B virus, hepatitis C virus, and syphilis among Hospital Cornea Retrieval Programme-Donors versus voluntary cornea donors at a large eye bank in Eastern India
Soham Basak, Samar K Basak, Bani Biswas
Department of Cornea and Eye Bank Services, Disha Eye Hospitals, Kolkata, West Bengal, India
|Date of Submission||20-Jun-2017|
|Date of Acceptance||19-Aug-2017|
|Date of Web Publication||13-Nov-2017|
Disha Eye Hospitals, Barrackpore, Kolkata - 700 120, West Bengal
Source of Support: None, Conflict of Interest: None
Purpose: To compare the serology profile of donors from Hospital Cornea Retrieval Programme-donors (HCRP-D) and voluntary cornea donors (VC-D) from a large eye bank in Eastern India. Methods: This is a retrospective analysis of donor details from January 2011 to December 2016. Donor demographics, cause of death, and serology reports were compiled. Postmortem blood was tested for human immunodeficiency virus 1 and 2 (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV), and syphilis using government-approved kits as per the National Programme for Control of Blindness Standards of Eye Banking. Donors for whom serology was not possible were excluded. Results: A total of 4300 of 4353 donors were included of which 74.3% were hospital donors and 25.7% were voluntary donors. A total of 93 (2.2%) donors with 94 seropositive reports were noted: 79 (84.9%) from HCRP-D and 14 (15.1%) from VC-D which was statistically significantly higher (P = 0.02). Among seropositive reports, HIV, HBV, HCV, and syphilis accounted for 12 (12.8%), 38 (40.4%), 36 (38.3%), and eight (8.5%), respectively. There was no correlation between the cause of death and seropositivity. A statistically significant decreasing trend in seroprevalence among hospital donors was observed over the years (5.3% in 2011 to 1.4% in 2016; P = 0.004). Two (0.47%) of 421 hospital donors with prior negative serology were found to be seropositive. Conclusion: Seropositive rates are significantly higher among hospital donors in spite of medical prescreening compared to nonscreened voluntary donors. Serology should be repeated even when prior reports are available.
Keywords: Eye banking, Hospital Cornea Retrieval Programme-Donor, serology, voluntary donor
|How to cite this article:|
Basak S, Basak SK, Biswas B. Comparison of seropositivity of human immunodeficiency virus, hepatitis B virus, hepatitis C virus, and syphilis among Hospital Cornea Retrieval Programme-Donors versus voluntary cornea donors at a large eye bank in Eastern India. Indian J Ophthalmol 2017;65:1138-42
|How to cite this URL:|
Basak S, Basak SK, Biswas B. Comparison of seropositivity of human immunodeficiency virus, hepatitis B virus, hepatitis C virus, and syphilis among Hospital Cornea Retrieval Programme-Donors versus voluntary cornea donors at a large eye bank in Eastern India. Indian J Ophthalmol [serial online] 2017 [cited 2020 Apr 7];65:1138-42. Available from: http://www.ijo.in/text.asp?2017/65/11/1138/218057
Donor serology is one of the most important preoperative investigations for any organ or tissue transplantation. In corneal transplantation, the donor is screened for various blood-borne infections before the tissue is released for surgery. The mandatory serology tests are mentioned in the National Program for Control of Blindness (NPCB) Standards of Eye Banking in India. The following serology tests should be done using enzyme-linked immunosorbent assay (ELISA) or government-approved rapid kits – human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV), and syphilis. Testing for human T-lymphotropic virus (HTLV I and II) is not mandatory, but tissues from donors with positive reports are not used for surgery. The Eye Bank Association of America (EBAA) tests for HIV 1 and 2, HBV, and HCV for all donors. In addition, tissues from donors who are positive for HTLV I, II, and syphilis are not used for surgery.
In spite of being an avascular tissue, there are various reports of transmission of diseases after cornea transplantation. There are two cases of HBV transmission, eight reports of rabies transmission, three cases of Creutzfeldt–Jakob disease, and a few cases of seroconversion for herpes simplex and cytomegalovirus. However, there are no reports of transmission of HIV, HCV, or syphilis via ocular tissue transplantation so far. There are reports of nine patients who received corneal tissue from HIV-positive donors, but none of them seroconverted. Krajden et al. and Tugwell et al. both reported cases where HCV-positive multiorgan donors led to the transmission of HCV in other solid organ recipients, but the cornea recipients were unaffected., However, Hung Ming Lee et al. showed that HCV virus is present in corneas of HCV-seropositive individuals. A few reports of postkeratoplasty tuberculosis infection could be attributed to transmission from donors. Although HTLV I- and II-positive donors are excluded by the NPCB and EBAA, respectively, there are no reports of transmission. Hence, among the four diseases being tested in India, there is documented evidence only for HBV transmission after cornea transplantation from seropositive donors.
Tissue collection through Hospital Cornea Retrieval Programme (HCRP) is growing in India. It accounts for about 25%–30% of cornea donation in the country and up to 70%–75% in some large eye banks. The HCRP has the advantage of readily available medical records so that potential donors can be prescreened more accurately. However, all investigations are not always performed in a timely manner in busy hospitals, and admitted patients are more likely to be seropositive than voluntary donors from house calls. In the latter group, serology reports are seldom available, but these are most commonly deaths due to natural causes or chronic diseases.
The aim of this study was to look at the serology profiles of the cornea donors and compare the seroprevalence among hospital donors and voluntary donors at a large eye bank in Eastern India.
| Methods|| |
This was a retrospective, observational study done at a large eye bank in Eastern India. Donor details were obtained from the eye bank records; donor demographics, cause of death, and serology reports were compiled. Only donors in whom serology was done were included. The study period was from January 2011 to December 2016. Donors were divided into two groups, HCRP-donors (HCRP-D) and voluntary cornea donors-(VC-D), based on the mode of retrieval.
The HCRP-donors were from three government-run hospitals, one secondary level and two tertiary level. All donors in this group were prescreened using the available medical records and found to be seronegative. Donors without available serology reports had no clinical evidence for these diseases.
Serology was performed with postmortem blood in all cases. Five milliliters of blood was drawn from the jugular or subclavian vein in an aseptic manner. The blood sample was immediately transferred in vacutainer and then sent to the eye bank along with the corneal tissue. All samples were analyzed within 18 h of collection. Serum was separated by centrifuging at 3500 revolutions per minute for 5 min. The following government-approved kits were used for all tests:
- HIV TRI-DOT (Diagnostic Enterprises, Himachal Pradesh, India) antibody test for gp41 and gp120 of HIV-1 and gp36 of HIV-2
- HEPACARD (Diagnostic Enterprises, Himachal Pradesh, India) HBsAg detection test
- HCV TRI-DOT (Diagnostic Enterprises, Himachal Pradesh, India) antibody test for core, NS3, NS4, and NS5 proteins of HCV
- Rapid Plasma Reagin (RPR) test (Beacon Diagnostics, Maharashtra, India) for antibody against Treponema pallidum.
The processing was done as per manufacturer's instructions in an aseptic environment by a trained technician. Tissues from seropositive donors were discarded. The seropositive samples were double checked by ELISA. In case of donors who received transfusion prior to death, hemodilution calculation was performed as per the NPCB eye banking standard guidelines.
Statistical analysis was done using Microsoft Excel (Microsoft Office Professional Plus 2013, Washington, USA). Percentage, mean, and standard deviation were calculated for each group. Fisher's exact test was used to compare between groups.
| Results|| |
There were a total of 4353 donors in the 6-year study period, of which 4300 donors with serology reports were included. Serology was not done in 53 donors for reasons such as obvious medical contraindication for transplantation, hemodilution, inadequate blood sample, or coagulated sample. These were excluded from the study and the tissues were not used for surgery. Seven donor samples required hemodilution calculation, of which five were discarded.
There were 2470 (57.4%) male and 1830 (42.6%) female donors. The mean age was 68.9 ± 13.4 years (range: 7.5–103 years), with maximum donors in the 60–80 years' age group (55.8%). There were 3196 (74.3%) HCRP-Ds and 1104 (25.7%) VC-Ds. Prior negative serology reports were available from 421 (13.2%) of the HCRP donors. [Table 1] summarizes the demographic breakdown of the donors.
|Table 1: Demographic and age distribution of the donors in Hospital Cornea Retrieval Programme and voluntary groups|
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A total of 93 (2.2%) donors with 94 seropositive reports were noted: one HCRP donor was positive for both HIV and HBV. There were 79 (2.47% seroprevalence) seropositive donors among HCRP-Ds compared to 14 (1.27% seroprevalence) among the VC-Ds which was statistically significantly higher (Fisher's exact test, P = 0.02). Of the four diseases tested, HIV accounted for 12 (12.8%), HBV for 38 (40.4%), HCV for 36 (38.3%), and syphilis for 8 (8.5%) positive serology reports. Seroprevalence among the study population was found to be 0.28% for HIV, 0.88% for HBV, 0.84% for HCV, and 0.19% for syphilis [Figure 1].
|Figure 1: Year-wise distribution of seroprevalence of each disease among cornea donors. (HIV: Human immunodeficiency virus, HBV: Hepatitis B virus, HCV: Hepatitis C virus)|
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A total of 421 (13.2%) donors in the HCRP-D group had previous negative serology reports from the hospital medical records. Of them, two (0.47%) were found to be seropositive (1 HBV and 1 HCV).
There was a statistically significant reduction in the annual percentage of seropositive donors from 4.5% in 2011 to 1.4% in 2016 (P< 0.001). This is due to both a decrease in the number of seropositive cases and an increase in the total number of donors each year [Table 2].
|Table 2: Year-wise breakdown of seropositive reports among Hospital Cornea Retrieval Programme-donors and voluntary donors|
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Seropositivity was found to be relatively higher among donors aged <40 years (4.4%) compared to other age groups (range: 1.9%–2.5%), but it was not statistically significant (P = 0.08–0.22) [Table 3]. There was no correlation between the cause of death and the serology status of the donors. We observed that the nine (9.7%) seropositive donors who died of gastrointestinal or hepatobiliary causes were all positive for either HBV or HCV [Figure 2]. This was higher than the incidence of death due to similar causes in the total donor population (9.7% vs. 5.7% overall) but it was not statistically significant (P = 0.11).
|Table 3: Distribution of seroprevalence among different donor age groups|
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|Figure 2: Cause of death of the seropositive donors. (HIV – human immunodeficiency virus; HBV: Hepatitis B virus, HCV: Hepatitis C virus, CVS: Cardiovascular system, RS: Respiratory system, CVA: Cerebrovascular accident, GI/Hep: Gastrointestinal/hepatobiliary, Misc: miscellaneous)|
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| Discussion|| |
Cornea collection, especially through HCRP, has been increasing in India over the last decade., There are two previous reports of seroprevalence among cornea donors from India, but both were from voluntary donors only. In this study, we have separately compared the seroprevalence among voluntary and hospital donors. In spite of the available medical records in hospital cases, these are more at risk of being seropositive, and lack of serology being performed routinely in all cases is of further concern.
The National AIDS Control Organization reports adult HIV prevalence to be 0.27% in India, and 0.22% in West Bengal, which is similar to 0.28% observed in this study. The estimated prevalence of HBV carrier state among adults is between 3.0% and 3.7%, and we found a 0.88% positivity for HBsAg., The estimated prevalence of HCV in India is 1% and the finding in this study was 0.84%.
Compared to the two previous reports from India, the observed seropositivity in this study is less than that of Mahalakshmi et al.'s report (2.2% vs. 5.6%, respectively) and similar to Bhatt's report of 2.3%. In this study, we confirmed the seropositive results with ELISA. Mahalakshmi et al. used Western blot for HIV and immunocomb for HBV and HCV confirmation, whereas Bhatt et al. used ELISA to confirm the seropositive samples., Danneffel and Sugar compared the seroprevalence of HIV among hospital donors and medical examiner cases in the US and did not find any difference between the two groups.
[Table 4] and [Table 5] summarize the comparison of the seropositivity rates from this study with other Indian and international eye bank reports, blood donor, and national population data. It is to be noted that in Western eye banks, serology is determined by antigen-antibody rapid tests, ELISA, and nucleic acid tests.
|Table 4: Comparison of percentage seroprevalence among donors of this study versus other Indian and international eye bank data, blood donor data, and national population seroprevalence|
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|Table 5: Relative distribution of donor seropositivity for human immunodeficiency virus, hepatitis B virus, hepatitis C virus, and syphilis in this study versus other Indian and international eye bank data and blood donor data|
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Chaurasia et al. published a report of seroprevalence among blood donors at AIIMS. Total seroprevalence of 2.51% was noted –0.27% HIV, 1.38% HBV, 0.54% HCV, and 0.32% syphilis.
There was an unusual spike of six syphilis cases in 2011. This was probably due to faulty kits, and after the eye bank switched to a different manufacturer, the numbers declined. Interestingly, three of the four women with HIV-positive reports were < 40 years of age, possibly belonging to high-risk groups.
There was a significant reduction in the number of seropositive cases in the HCRP group over the years (5.3% in 2011–1.4% in 2016; P = 0.004) whereas the voluntary figure has not changed much (range: 1–4/year). This is probably due to serology being carried out routinely for more patients in the HCRP-designated hospitals.
We also found two seropositive samples among donors with previous negative serology reports. This could be false positive due to postmortem changes in blood as reported by Wilkemeyer et al. or it could also be that the initial report was false negative.
| Conclusion|| |
Serology tests are a must before tissues are released for surgical use. We found seroprevalence to be significantly higher among HCRP-Ds than VC-Ds. Hence, careful prescreening by the eye donation counselors is also important. And even if prior negative serology reports are available, the tests should be repeated at the eye bank.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Standards of Eye Banking in India. National Programme for Control of Blindness. Available from: http://www.npcb.nic.in/
. [Last accessed on 2017 Jun 05].
2016 Eye Banking Statistical Report. Eye Bank Association of America. Available from: http://www.restoresight.org
. [Last accessed on 2017 Jun 05].
Dubord PJ, Evans GD, Macsai MS, Mannis MJ, Glasser DB, Strong DM, et al.
Eye banking and corneal transplantation communicable adverse incidents: Current status and project NOTIFY. Cornea 2013;32:1155-66.
Krajden M, Bishai F, Quan C, Mahony J, Brunton J, Rootman D, et al.
Multi-organ donor transmission of hepatitis C virus to five solid organ transplant recipients and lack of transmission to corneal transplant recipients. Clin Diagn Virol 1995;3:113-21.
Tugwell BD, Patel PR, Williams IT, Hedberg K, Chai F, Nainan OV, et al.
Transmission of hepatitis C virus to several organ and tissue recipients from an antibody-negative donor. Ann Intern Med 2005;143:648-54.
Lee HM, Naor J, Alhindi R, Chinfook T, Krajden M, Mazzulli T, et al.
Detection of hepatitis C virus in the corneas of seropositive donors. Cornea 2001;20:37-40.
Basak SK. HCRP: A Novel Concept of Indian Eye Banking. Poster Presentation AAO-2012, San Francisco, USA; 2012.
Oliva MS, Schottman T, Gulati M. Turning the tide of corneal blindness. Indian J Ophthalmol 2012;60:423-7. [Full text]
Puri P. Tackling the hepatitis B disease burden in India. J Clin Exp Hepatol 2014;4:312-9.
Mahalakshmi B, Madhavan HN, Pushpalatha R, Margarita S. Seroprevalence of human immunodeficiency virus, hepatitis B virus and hepatitis C virus among eye donors. Indian J Ophthalmol 2004;52:61-2.
] [Full text]
Bhatt SK, Kohli MS, Aggarwal SV, Shah AM, Dani JS. Seroprevalence of HIV, HBV and HCV in the donor eyes in the western regional institute of ophthalmology. Natl J Med Res 2012;2:306-8.
Danneffel MB, Sugar A. Incidence of HIV antibody-positive eye/cornea donors in hospital versus medical examiner cases. Cornea 1990;9:271-2.
Armstrong SA, Gangam N, Chipman ML, Rootman DS. The prevalence of positive hepatitis B, hepatitis C, and HIV serology in cornea donors prescreened by medical and social history in Ontario, Canada. Cornea 1997;16:512-6.
Chaurasia R, Zaman S, Das B, Chatterjee K. Screening donated blood for transfusion transmitted infections by serology along with NAT and response rate to notification of reactive results: An Indian experience. J Blood Transfus 2014;2014:412105.
Wilkemeyer I, Pruss A, Kalus U, Schroeter J. Comparative infectious serology testing of pre- and post-mortem blood samples from cornea donors. Cell Tissue Bank 2012;13:447-52.
[Figure 1], [Figure 2]
[Table 1], [Table 2], [Table 3], [Table 4], [Table 5]