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73rd AIOC 2015, New Delhi This paper was judged the BEST PAPER of COMMUNITY/ SOCIAL OPHTHALMLOGY-I Session. Study of Enucleated Eyeballs Rejected Due to Sepsis and Malignancy, for Culture and Histopathology. Dr. Sameer G Datar, Dr. Mayur Moreker C orneal diseases are a significant cause of visual impairment and blindness in the developing world. The Andhra Pradesh Eye disease study (APEDS) reported the prevalence of corneal blindness at 0.13% (95% CI: 0.06-0.24), constituting 9% of all blindness.1 Approximately 18.7 million people are blind in India.2 Every year another 20,000 join the list.3 The National Programme for Control of Blindness (NPCB) estimates, there are currently 120,000 corneal blind persons in the country. According to this estimate there is addition of 25,000-30,000 corneal blindness cases every year in the country.4 The burden of corneal disease in our country is reflected by the fact that 90% of the global cases of ocular trauma and corneal ulceration leading to corneal blindness occur in developing countries.5 Corneal transplantation remains a major treatment option for restoring sight among those suffering from corneal blindness. The current cornea procurement rate in India is 22,000 per year. It is estimated that a significant proportion of donor corneas are unsuitable for corneal transplantation.6 Enucleated eyeballs in the eye bank are used for corneal transplantation for corneal diseases. These enucleations were done on the deceased when the relatives consent for eye donation. As this comes under human organ transplant act, there are stringent criteria for their use.7,8 The deceased has to be free of any infection (threatening its spread to the recipient) or malignancy. It is therefore followed that eyeballs from deceased due to terminally malignant, and metastatic disease, cannot be used as there are chances of its spread to the recipient, similar to those of infection. There is no strong evidence to estimate such a risk though. Malignancies are known to spread through blood and lymphatics and metastasize to distant organs. In the eye, barring cornea, lens and vitreous all other tissues are vascular, choroid being characteristically the most vascular of all. Therefore metastasis of malignancies can occur in the eye. Of all the choroidal tumours, metastatic or “secondaries” is very common. The choroid is the most common site for uveal metastases, and the tumors occur most often in the posterior pole of the eye with an average of two tumors per eye.9 Cornea being avascular, has the least chance of showing Other Best Free Papers any metastatic lesion, therefore, though cornea from malignant donors can be used for transplant purposes, it has to be documented by some concrete evidence. This study is therefore designed to utilize the donated tissue for research purpose and actually process it for histopathology to rule in or rule out any evidence of malignancy in various tissues of the eye, cornea being the main concern. Deaths due to septicaemia occur in hospital or home. There are no criteria to define septicaemia, other than blood culture positivity. On most of the occasions when the death is declared and “septicaemia” is mentioned as the cause of death, there are not enough reports available to support the diagnosis of septicaemia. It is more difficult in home deaths to attain the detailed history and reports of the deceased. Commonly available report, and which is one of the criteria to establish a diagnosis of septicaemia is Total Leucocyte Count (TLC). This study was also designed to look into these donated tissues (from deaths due to septicaemia) for evidence or trace of any infection in the ocular tissues. Spread of infection throughout the blood stream is pathologically evident in septicaemia. Spread to ocular tissue is therefore expected. Positive culture report showing growth of any organism in any of the ocular tissue was the basis of this study design. This was to be correlated with the available reports if any (blood culture, TLC etc). Here we study 98 enucleated eyes (from eye donations), 66 septicaemic (11 had to be refused for technical purposes, therefore study eyes were 55) and 32 malignant, to estimate whether there is any trace of either infection or malignancy in any part of the eyeball. Procedure Enucleation for eye donation call is done under aseptic precautions. It is done at the bedside wherever death has occurred, either hospital or home. With all aseptic measures, the eyes are painted with betadine and draped with a sterile whole towel. All autoclaved sterile instruments are used for the procedure. Eye speculum is used to open the lids, and peritomy is performed. The four rectii muscles are identified and cut with scissors. Then with the enucleation scissors the optic nerve is cut and the whole eyeball is taken out of the socket. It is then washed with gentamicin and placed in a glass bottle on a specialized stand, nicely packed from all sides with cotton, avoiding any injury to the cornea. The bottle is then carried in a cold chain to the eye bank and placed in the refrigerator at 4º Celsius. MaterialS and MethodS Enucleated eye balls which were rejected (for corneal transplantation) due to septicemia or malignancy, irrespective of age and gender were included 73rd AIOC 2015, New Delhi in this study. These eye balls were examined during period September 2011 to October 2013. Enucleation was done on the deceased after consent from relatives of donor for eye donation. The tissue was sent to the laboratory in formalin for histopathological examination and in normal saline for microbiological examination (culture and examination). The Eye balls of donors who had known history of any type of malignancy were examined for histopathology examination to look for inflammatory deposits / malignancy / metastatic cells in eye,. Each part of eye such as cornea, conjunctiva, sclera, choroid, vitreous and lens was separately examined. The eye balls of donors whose death was due to septicemia and multi organ failure were cultured for aerobic and anaerobic growth to look for traces of infection in any tissue. Each part of eye such as cornea, conjunctiva, sclera, choroid, vitreous and lens was separately cultured and examined. Results Total 282 donors donated their eyes to our eye bank during the period September 2011 to October 2013. Out of that, 105 donor’s eyes (210 eye balls) were rejected for corneal transplantation due to the donor having history of malignancy or septicemia. 98 eye balls were considered for present study; where as 7 donor’s eyeballs were not considered due to unavailability of past records (history). Out of these 98 eye balls, 66 (67%) eyes were from donors whose death due to septicemia and 32 (33%) were from donors whose death due to any malignancy. (Figure 1) 32 eye balls of donors whose death was due to any malignancy were examined for histopathology. 22 (68.8%) were male and 10 (31.3%) were female donor with known history of Malignancy. Average age at death of donor was 71.0 ± 11.65 yrs, age ranges from 43 to 88 yrs. (Table 1). All 32 eye balls (100 %) did not showed any type of inflammatory and or neoplasmic pathology. Also we had not observed any involvement by malignant lymphoma and metastatic deposits of carcinoma in the 32 (100 %) eye balls (Table 2). 66 eye balls of donors were those whose death was due to septicemia, but only 55 were examined for microbiology examination as 11 had to be refused for technical purposes. Out of these 66 donors, 37 (56.1%) were male and 29 (43.9%) were female. Average age at death of donor was 73.24 ± 19.41 Other Best Free Papers Table 1: Donors history (Death was due to Malignancy) No. of patients % GenderMale 22 68.8 Female 1031.3 Death at Hospital 16 1650 50 Home Cause of death t cell lymphoma 1 3.1 ca lung 2 6.3 12.5 ca breast 4 ca prostate 3 9.4 ca colon 2 6.3 ca hepato cellular 3 9.4 ca larynx 1 3.1 ca ovary 1 3.1 ca tong 2 6.3 ca oesophagus 4 12.5 ca uterus 1 3.1 3.1 ca renal 1 Leukemia 26.3 Ca head and neck 1 Ca thyroid 2 3.1 Ca gastric 1 6.3 6.3 Table 2: Eye ball status of 32 eyes of donors with known history of malignancy No. of patients % No e/o inflammatory pathology and no neoplastic pathology 2 6.3 No e/o involvement by malignant lymphoma and metastatic deposits of carcinoma 30 93.8 Table 3: Donors history (death due to Septicemia and other infections) Gender Male No. of patients % 3756.1 Female 2943.9 Death at Hospital 45 Home 2131.8 Cause of death Sepsis 56 84.8 other infection 10 15.2 68.2 73rd AIOC 2015, New Delhi yrs, age ranges from 02 to 98 yrs. (Table 3). 11 had to be refused for technical purposes, therefore study eyes were 55. In that, 30 (54.5 %) eye balls showed no growth in aerobic culture and 25 (45.5 %) had shown growth in aerobic culture (Table 4). Table 4: Eye ball status of (55) eyes of donors whose death due to septicemia No. of patients % No growth in aerobic culture 30 54.5 Growth in culture 25 45.5 Out of total 55 eye examined, only 26 had Total Leukocyte count (TLC) reports available. From those 26 available reports 13 (50.0%) had micro organism growth in one of the tissues barring conjunctiva and cornea and 13 (50.0 %) had no micro organism growth in any of the ocular tissue. From the 13 eyes with growth in one of the tissues 11 (84.6%) had raised TLC’s, which is supposed to be a marker for septicaemia, whereas 2 (15.4%) had normal TLC levels (can be due to general debility also). We observed significant difference (p=0.039) in micro organism growth between donors with high TLC levels and donors with normal TLC levels. This may suggest that donor with high TLC (n=17) levels maximum, i.e. 64.7 % have micro organism growth in ocular tissues, whereas among those 9 who had normal TLC, 77 .7 % had no growth in any of the ocular tissues (p=0.039) (Table 5). Table 5: TLC interpretation of 26 eyes TLC Normal TLC Count interpretation 4000-11000 % Eyeball status High TLC >11000 No growth Growth (n=13) (n= 13) 7 2 53.8% 15.4% Count % Eyeball status TotalCount 13 6 11 46.2% 84.6% 13 p =0.039 Table 6: Micro organism growth in various orbital tissues. (N=55) Eye Tissue Micro Organism Growth Present Micro Organism Growth Absent No of Eye % No of Eye % Choroid16 29.1 39 70.9 Cornea18 32.7 37 67.3 Lens13 23.6 42 76.4 Vitreous12 21.8 43 78.2 Sclera18 32.7 37 67.3 Conjunctiva18 32.7 37 67.3 Other Best Free Papers Discussion There was no attempt in the past to correlate the corneal contamination with the systemic infection directly, in case of tissues collected from septicaemic donors. Clark and associates10 questioned the relationship of bacteremia and corneal contamination. They cultured the aqueous humor in 50 patients who died with infectious or chronic debilitating disease. The aqueous humor was found to remain consistently sterile despite a 45% incidence of postmortem bacteremia. They concluded that the lack of aqueous contamination negated a direct or causal relationship between bacteremia and corneal contamination. Several studies have cited positive conjunctival cultures in cadavers to range from 12% to 100%, depending on the method used for donor preparation.11 These results most likely represent surface contamination only and do not appear to be a frequent cause of postoperative endophthalmitis. Rollins and Stocker12 showed that while 61% of their donor eyes were associated with positive conjunctival cultures, there were no cases of post operative infection. A similar study by Pardos and Gallagher13 of 4,167 donor eyes yielded a 12.4% incidence of positive cultures, and only two occurrences of post keratoplasty endophthalmitis in 1,880 transplants. In both cases of infection, donor corneal cultures were negative. Chittum et. al.11 have found a correlation that patients with documented or suspected sepsis at the time of death have a significantly higher incidence of corneal contamination than control donors. Spelsberg H et. al.14, in their data revealed no contraindication against the use of corneal grafts derived from septic donors, provided, critical graft assessment in organ culture is done. No patient who had received a graft from a septic donor had experienced endophthalmitis. The question if endophthalmitis can be transmitted via donor corneas in properly performed organ culture has not yet been answered, and that study seems to be the first to report on the clinical course of transplanted corneas from septic donors stored in long-term organ culture medium. Long term organ culture at 30–37°C not only allows the growth of pathogens but also a maximal antibiotic effect. Use of organ culture for every corneal tissue can be economically burdening, and not using a tissue from a septicaemic donor for fear of transmitting the infection, will be like wasting a few good tissues. Therefore it is the need of time we come to some conclusive method whereby we can decide whether the tissue from a septic donor is viable for surgical transplantation or not. Here we studied 55 eyes from septic deaths for microbiology examination where 45.5 % eyes showed growth in aerobic culture. We went on to look for 73rd AIOC 2015, New Delhi total leucocyte count, which is one of the markers for septicemia and which can be easily available with the relatives or hospital reports and found that only 26 patients had Total Leukocyte count (TLC) reports available. From those 26 available reports 50.0% had micro organism growth in one of the tissues barring conjunctiva and cornea. Exclusion of cornea and conjunctiva was a criteria as it can be due to contamination. Of those 13 eyes with growth in one of the tissues, 11 (84.6%) had raised TLC’s, whereas 2 (15.4%) had normal TLC levels (can be due to general debility also). This significant difference (p=0.039) in micro organism growth between donors with high TLC levels and donors with normal TLC levels suggests that donor with high TLC levels may show micro organism growth in ocular tissues, and those with normal TLC level can have sepsis free ocular tissues, thereby making TLC a criterion for judging the suitability of the septicaemic tissue for surgical use, (p=0.039) The incidence of ocular metastases in corneal donors with active malignancy is very low. Donor-recipient tumor transmission through corneal transplantation is highly improbable when the eyes are free of cancer.15 Where all the 32 eye balls of donors whose death was due to any malignancy were examined for histopathology, all 32 eye balls (100%) did not show any type of inflammatory and or neoplasmic pathology. Also we had not observed any involvement by malignant lymphoma and metastatic deposits of carcinoma in the 32 (100 %) eye balls, thereby making them viable for use in patient care. Limitations A bigger sample size needs to be studied, for stronger evidence, and cases with detailed reports of malignancy and sepsis e.g. type and grade of malignancy, type and source of infection will help in establishing a stronger association. Other septicaemia markers and detailed reports of cause of death and pre mortal conditions, though difficult to obtain in such situations would help in a better way to make a conclusion. References 1. Dandona L, Dandona R, Srinivas M, Giridhar P, Vilas K, Prasad MN, et. al. Blindness in Indian state of Andhra Pradesh. Invest Ophthalmol Vis Sci 2001;42:908-16. 2. National Programme for Control of Blindness. Available from: http://pbhealth. gov.in/pdf/Blindness.pdf. 3. Dandona L, Dandona R, John RK. Estimation of blindness in India from 2000 through 2020: Implications for the blindness control policy. Natl Med J India. 2001;14:327–34. Other Best Free Papers 4. Saini JS, Reddy MK, Jain AK, Ravinder MS, Jhaveria S, Raghuram L. Perspectives in eye banking. Indian J Ophthalmol. 1996;44:47–55. 5. Whitcher JP, Srinivasan M, Upadhyay MP. Corneal blindness: A global perspective. Bull World Health Organ 2001;79:214-21. 6. Dandona R, Dandona L, Naduvilath TJ, McCarty CA, Rao GN. Awareness of eye donation in an urban population in India. Aust N Z J Ophthalmol. 1999;27:166–9. 7. Lee P et. al. worldwide legal requirements for obtaining corneas. Cornea11(2):102-107, 1992. 8. Bredehorn T et. al. Requirements for the Acceptance of Tissue Donors for Corneal Donation. Transplantation Proceedings. 2002;34:2340. 9. Shields CL et. al. Survey of 520 eyes with uveal metastases. Ophthalmology. 1997;104:1265-76. 10. Clark WM, Heaton KT, Snider GR, et. al: Donor eye contamination. Am J Ophthalmol 1982;94:395-7. 11. Chittum ME et. al. Contamination of Corneal Tissue from Infected DonorsArch Ophthalmol 1985;103:802-4. 12. Rollins HJ, Stocker FW: Bacterial flora and preoperative treatment of donor corneas. Am J Ophthalmol. 1965;59:247-9. 13. Pardos GJ, Gallagher MA: Microbial contamination of donor eyes. Arch Ophthalmol 1982;100:1611-3. 14. Spelsberg H et. al. Organ-cultured corneal grafts from septic donors: a retrospective study. Eye 2002;16:622–7. Doi: 10.1038/ sj.eye.6700145. 15. López-Navidad A1, Soler N, Caballero F, Lerma E, Gris O. Corneal transplantations from donors with cancer. Transplantation. 2007;83:1345-50.