BACKGROUND Ocular damage in leprosy is due either to nerve damage or infiltration by mycobacteria. There is currently little information about the magnitude and nature of incident ocular pathology in cured leprosy patients. This information would increase our understanding of the pathophysiology of ocular involvement in leprosy and help in developing programmes to address the eyecare needs of leprosy patients who have been released from treatment. The cumulative incidence of leprosy related ocular pathology and cataract was measured during an 11 year follow up period in cured leprosy patients released from treatment in Korea.
METHODS In 1988 standardised eye examinations were performed on 501 patients in eight resettlement villages in central South Korea. In May 1999 standardised eye examinations were repeated in this population.
RESULTS Among the patients in whom there was no sight threatening leprosy related ocular disease (lagophthalmos, posterior synechia, or keratitis) in 1988, 14.7% developed one or more of these conditions. Overall, among those with no vision reducing cataract in 1988, 26.4% had developed a vision reducing lens opacity in at least one eye. Among patients examined in both 1988 and 1999, 14.3% developed visual impairment and 5.7% developed blindness.
CONCLUSION This study demonstrates that leprosy related ocular pathology progresses in some patients even after they are cured mycobiologically. The progressive leprosy related lesions are the result of chronic nerve damage; ocular lesions due to infiltration by Mycobacterium lepraedid not develop. Based on the factors found to be associated with development of the most visually significant findings (posterior synechia, keratitis, and cataract) certain patients should be targeted at discharge for active follow up eye care. We suggest that patients with lagophthalmos (even in gentle closure), trichiasis, small pupils, and posterior synechiae should be screened regularly for the development of lagophthalmos in forced closure, keratitis, and cataract.
- eye complications
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There are approximately 1.5 million leprosy patients taking multidrug therapy (MDT), the World Health Organisation's recommended treatment regimen for leprosy. Another 10 million have completed and been released from treatment. It is estimated that 1.5–2% of the total are blind from leprosy related causes and another 2% are blind from non-leprosy causes, chiefly age related cataract.1The most common leprosy related causes of blindness are corneal disease secondary to lagophthalmos and “chronic iritis,” which is an incompletely understood condition unique to leprosy that results in extreme miosis, posterior synechiae, iris atrophy, and, often, complicated cataract. In addition, older leprosy patients develop age related cataract with at least the same frequency as the non-leprosy population, although they rarely have access to the same eyecare services.
Although patients who have completed treatment are considered cured (because most of them are microbiologically negative) they still have many disabilities which were present before treatment began. In addition, they may have progressive disability because pre-existing nerve damage is not reversed by treatment. Thus, it is possible that after leprosy cure, new ocular pathology may develop. There is currently little information about the magnitude and nature of new pathology in cured leprosy patients. This is important from two different perspectives. One is to increase our understanding of the pathophysiology of ocular involvement in leprosy; the other is to provide information that would be useful in developing programmes to address the eyecare needs of leprosy patients who have been released from treatment. In most settings, once patients are released from treatment they are generally lost to follow up with the medical system and have little or no access to care.
We studied the incidence of leprosy related ocular pathology and cataract during an 11 year follow up period in patients living in leprosy resettlement villages who had been released from treatment.
STUDY SITE AND POPULATION
The study was undertaken in central South Korea. Leprosy is no longer a public health problem in South Korea; only 39 new cases of leprosy (0.1 per 100 000 population) were registered in 1998 and there are approximately 18 800 patients who have been treated and released. Treated and released patients are divided between domiciliary (53%), resettlement village (36%), and leprosaria (11%). The healthcare infrastructure in South Korea is well developed and includes all medical specialties. All leprosy patients (cured or on MDT) are included in the government provided free healthcare programme. Numerous non-governmental hospitals also provide health care free of charge. Eye care for leprosy patients has been available through the Catholic Skin Clinic and Hospital, Taegu (full time ophthalmologist since 1989), Yosu Aeyeong Hospital, Yosu (visiting ophthalmologists), and the Korean Leprosy Institute, Anyang (visiting ophthalmologists).
This study was carried out through the Catholic Skin Clinic and Hospital (CSCH), which is responsible for eight leprosy resettlement villages in the Taegu area.
During the months of October and November 1988 standardised eye examinations were performed on 501 (83%) of the 605 patients in the eight villages under the care of the CSCH. All villagers were encouraged to come for examination in a central meeting point in the village. At least two trips were made to each village and attempts were made to find villagers who did not come and to see them in their homes if possible. Ophthalmological studies with these patients have been described previously.2-5 In 1989, following the baseline assessment and initiation of a health worker training programme, the CSCH chose to recruit a full time ophthalmologist. Since then the CSCH has provided cataract, lagophthalmos and, to a lesser extent, trichiasis surgery to leprosy patients from throughout South Korea. These patients were traced in 1995 to determine mortality associated with blindness.5 In May 1999 standardised eye examinations were repeated in this population.
Visual acuity was measured with an illuminated tumbling E chart by a trained examiner. Clinical examinations in 1988 were performed by two examiners (SL and Dr Lee Ho-Sung) in a semidarkened room, using a torch to examine the ocular adnexae and a portable slit lamp for the cornea (with fluorescein instillation). Corneal sensation was determined by the reaction to a cotton wisp introduced from below. A Perkins applanation tonometer was used in alternate patients to measure intraocular pressure, both in the upright and then the supine positions. Dilatation and fundus examination were performed if necessary and to assess cause of low vision. Examinations in 1999 were performed in the same rooms by two examiners (SL and NT) using the same equipment and in the same fashion except that all patients had upright IOP measurement; no supine IOP measures were taken.
The following were recorded: visual acuity, blink pattern (observed while the patient was unaware of being examined and graded abnormal when there was more than 15 seconds between blinks or if the blink was incomplete); lagophthalmos (in both gentle and forced closure); pupil size, shape, and reaction to light; presence of corneal opacity and keratitis; conjunctival injection; trichiasis; anterior chamber clarity; presence of posterior synechia; lens clarity; and upright and supine (1988 only) intraocular pressure. If there was any question about synechia or lens clarity, mydriatic drops were instilled and the patient was re-examined. Cataract was defined as the presence of lens opacity judged to be consistent with a corrected visual acuity of 6/18 or worse. Aphakia or pseudophakia was also included as evidence of incident cataract. In both 1988 and 1999, a sample of 10% of patients were examined by both examiners to ensure agreement.
Clinic records were reviewed, and demographics (age, sex, disease duration) and non-ocular clinical data (relapse in intervening periods, disease type, PGL-1 antibody levels) was abstracted.
Incidence of ocular pathology was calculated from those patients who did not have the specific finding in 1988. We considered primary leprosy related ocular findings to include lagophthalmos (either on gentle or forced closure), posterior synechia, or keratitis. We used proportional hazards regression (forward stepwise) to analyse occurrence of specific findings according to demographic and clinical characteristics associated (p<0.05) with pathology by univariate analysis. Relative risks (95% CI) were generated. Our findings are reported by patient rather than by eye. We excluded patients who had died, moved away, or refused examination from our analyses.
Among the 501 patients examined in 1988, 270 (53.9%) were followed up in 1999. Of the patients lost to follow up, there were 84 (16.8%) deaths; 40 (7%) patients moved away, and 107 (21.4%) patients refused examination or were absent from the village at the time of examination. Participation varied widely by village, participation was lowest in the largest village, and was not significantly different in 1999 compared with 1988. Demographic information on the study population is given in Table 1. As described in a previous publication, patients who were blind in 1988 had a 4.8–fold excess risk of death compared with their non-blind same age peers.5 Inclusion of deaths between 1995 and 1998 did not change this association. Consequently, blindness was less common among patients examined in 1999 than in 1988. The patients who accepted examination in 1999 and those who refused in 1999 were not different with respect to vision, lagophthalmos, trichiasis, posterior synechia, and cataract in 1988.
INCIDENCE OF LEPROSY RELATED PATHOLOGICAL LESIONS
A large proportion of these cured patients already had potentially blinding ocular pathology in 1988 (Table 2). Cumulative incidence of leprosy related ocular pathology ranged as high as 20.1% (reduced corneal sensation). All posterior synechia cases were among multibacillary patients; excluding paucibacillary patients from our analysis reveals a cumulative incidence for posterior synechia of 9.3% (95% CI: 4.8–13.8%). Univariate analysis demonstrated that the development of posterior synechia (in the 11 year period) was associated with age, duration of disease, and small pupil size (usually accompanied by poor pupil reaction); regression analysis revealed that only size of pupil (<2 mm) was independently predictive of incident synechia (Table 3).
The only factor associated with incident lagophthalmos on forced closure was lagophthalmos on gentle closure. Among the 19 cases of lagophthalmos on gentle closure in 1988, three (15.8%) progressed to lagophthalmos on forced closure. No factors were associated with the development of lagophthalmos on gentle closure. Univariate analysis revealed that incident keratitis was associated with the presence of lagophthalmos (even on gentle closure), inadequate blink, type of disease, reduced corneal sensation, and trichiasis. Proportional hazards modelling showed that only lagophthalmos (gentle closure) and trichiasis were independently associated with keratitis (Table 3). In none of the trichiasis cases was there any entropion.
As pre-existing leprosy related ocular pathology was associated with the development of additional ocular disease, we divided patients into two groups: patients in whom there was primary leprosy related ocular disease (defined as lagophthalmos, keratitis, or posterior synechia) in 1988 (n=114) and patients in whom none of these conditions was found (n=156). Among the patients in whom there was no primary leprosy related ocular disease, 23 (14.7%) developed one or more of these conditions (Table 4). Incident pathology was more common in multibacillary patients (16.7%) than paucibacillary patients (6.9%) and more common in women (17.4%) than men (10.9%), although these differences were not statistically significant (p>0.05).
CUMULATIVE INCIDENCE OF CATARACT
Cataract was the most common ocular condition in these patients. Overall, among those with no vision reducing cataract in 1988, 26.4% of patients had developed a vision reducing lens opacity (n=58) or had evidence of cataract extraction (n=3). Univariate analysis revealed that age, duration of disease, pupil reaction, pupil size, and posterior synechia were associated with incident cataract (Table 3). Age and pupil size were independently associated with the development of cataract. Among the cataract cases 29.3% had pre-existing posterior synechia; including individuals who developed posterior synechia in the intervening 11 years, this increased to 34.5%.
CHANGES IN VISION
Among patients examined in both 1988 and 1999, 35 patients (14.3% of those who had vision ⩾6/18 in 1988) developed visual impairment (6/18–6/60) and 15 patients (5.7% of patients who had vision ⩾6/60 in 1988) developed blindness (Table 5) Consideration of the worse eye (thus, including unilateral vision loss) revealed that 21.2% of patients developed vision loss in one or both eyes and 11.6% of patients developed blindness in one or both eyes. Most of the blindness and visual impairment was due to cataract (Table 6).
This study demonstrates that leprosy related ocular pathology progresses in some patients after they are cured mycobacteriologically. Although follow up examinations were not possible on all patients, those who accepted follow up were not different (demographically or in terms of pre-existing pathology) from those who were not examined.
PATHOPHYSIOLOGY OF OCULAR COMPLICATIONS
Among the incident lesions, an abnormal blink pattern, lagophthalmos, and reduced corneal sensation are due directly to nerve damage; these may all contribute to the development of keratitis. Pupil abnormalities and synechiae are part of the so called “chronic iritis” of leprosy which has been suggested to be due, at least in part, to sympathetic nerve damage. Thus, all of the progressive leprosy related lesions, except trichiasis, are the result of chronic nerve damage. Ocular lesions due to infiltration byMycobacterium leprae (for example, iris pearls, limbal nodules) did not develop in this population. The low incidence of lagophthalmos and our sample size provided inadequate numbers for determining factors associated with incidence.
The finding of 9.6% incident trichiasis cases was unexpected. Trichiasis in leprosy may be due to loss of support of lash follicles secondary to infiltration by M leprae.6 However, a recent report demonstrates that eyelash ptosis, associated with laxity in the pretarsal tissues, may be the underlying cause of the trichiasis in many leprosy patients.7 Trichiasis due to infiltration of the lash follicle by M leprae would seem unlikely to progress in patients who have been bacteriologically negative for many years. On the other hand, eyelash ptosis might progress in patients with orbicularis weakness, leading to trichiasis.
From the perspective of the leprosy control programme, these data has several implications. Of the 270 patients examined in both time periods 94 (34.8%) had at least one leprosy related ocular lesion (lagophthalmos, keratitis, or posterior synechia) at baseline. Among those who did not have ocular lesions at baseline 15% developed one or more of these lesions over the 11 years of study (annual increase of 1.3%).
The relatively low cumulative incidence of visual impairment (14.3%) or blindness (5.7%) may not be representative of the true incidence of visual impairment or blindness since blind patients have a significantly higher risk of death compared with their non-blind same age peers.5 Blindness and visual impairment occurred despite the presence of a well established high quality eye care infrastructure and the high cumulative incidence of vision loss and blindness in the worse eye is indicative of a failure in this population to use the services.
Based on the factors found to be associated with development of the most visually significant findings (posterior synechia, keratitis, and cataract) it would be advisable to target certain patients at discharge for active follow up eye care. We suggest that patients with lagophthalmos (even in gentle closure), trichiasis, small (<2 mm) pupils, and posterior synechiae should be screened regularly for the development of lagophthalmos in forced closure, development of keratitis, and significant cataract. In our population, this would include 131 patients (48.5% of total patients) needing active follow up.
Over the 11 year period, cataract was responsible for blindness in 86.7% of patients (three had surgery but remained blind) and visual impairment in 80% of patients (three had surgery but were visually impaired). The exact contribution of leprosy to cataract development is not clear but it is estimated that the presence of leprosy triples the risk of cataract.8 The large number of patients who develop cataract emphasises the need to collaborate with blindness prevention programmes in order to provide necessary services to this population. If we assume that the cataract and lagophthalmos surgery performed in this population either cured or prevented visual disability and blindness, then it is clear that the number of patients who will have progressive visual loss is even higher than what we have demonstrated. Although leprosy programmes may be able to provide some lagophthalmos surgery services, only collaboration with ophthalmological services will meet the needs of the cataract blind.
Although the populations studied vary in a number of ways (for example, race, access to and uptake of ophthalmological services), our findings are in general agreement with a study in Holland9 which reported that lagophthalmos, corneal disease, and cataract comprise the important lesions which may progress in cured leprosy patients.
The patients in our study had all been treated with MDT, but most had also received dapsone in the era before MDT. This reflects the situation for most of the world's cured leprosy patients and our findings should be applicable to these patients. There will, however, be a growing number of cured patients in the future who will have been treated only with MDT from first diagnosis. It is not known yet whether MDT only patients will progress in the same way as those patients who had dapsone before MDT.
This study was supported in part by LEPRA (British Leprosy Relief Association) to whom we are grateful for support. We have had invaluable support from Mrs Pak Ok-Hyeon and the staff at the Catholic Skin Clinic and Hospital.