Barbados Study1994
Barbados Study1994
Barbados Study1994
Objective: To describe the design of the Barbados Eye were tested at the study site, 95% completed Humphrey
Study and report on the prevalence of open angle glau- automated perimetry and 97% had photographic or clini-
coma (OAG) in a predominantly black study popula- cal disc gradings; 93% of those referred completed the
tion. ophthalmologic examination. In this adult population,
the prevalence of OAG by self-reported race was 7.0%
Design: Population-based prevalence study. (302/4314) in black, 3.3% (6/184) in mixed-race, and 0.8%
(1/133) in white or other participants. In black and mixed-
Setting and Participants: Residents of Barbados, West race participants, the prevalence reached 12% at age 60
Indies, identified from a simple random sample of Bar- years and older and was higher in men (8.3%) than in
badian-born citizens 40 through 84 years old. women (5.7%), with an age-adjusted male-female ratio
of 1.4. In addition, over 3% of the participants were clas-
Data Collection: Participants had a comprehensive study sified as having suspect OAG.
visit that included automated perimetry, applanation to-
nometry, and fundus photography; persons with spe- Conclusions: To our knowledge, the Barbados Eye Study
cific examination findings, as well as a 10% sample of par- is the largest glaucoma study ever conducted in a black
ticipants, were referred for an ophthalmologic examination population and identified more people with OAG than
and additional tests. did any previous population study. The prevalence of OAG
was high, especially at older ages and in men. Among par-
Outcome: A diagnosis of OAG required both visual field ticipants 50 years old or older, one in 11 had OAG, and
and optic disc criteria for glaucoma damage after exclud- prevalence increased to one in six at age 70 years or older.
ing other causes. The results highlight the public health importance of OAG
in the Afro-Caribbean region and have implications for
Results: The 4709 participants (83.5% of those eli- other populations.
gible) had demographic characteristics that were similar
to the census population. Of the 4631 participants who (Arch Ophthalmol. 1994;112:821-829)
OPEN
ANGLE glaucoma miologic data on OAG, age-related cata¬
(OAG) is major
a cause ract, age-related macular degeneration, and
of visual impairment diabetic retinopathy in a predominantly
and blindness.1"3 A black population. To our knowledge, it was
higher frequency of the first comprehensive study of preva¬
OAG visual loss exists in black than in lence and risk factors for all the major eye
white populations, but the reasons for these diseases based on a simple random sample
From the School of Medicine,
differences are not well understood. I4° De¬ of a country's population; a major goal was
the State University of New
York-Stony Brook (Drs Leske spite its importance and public health rel¬
and Hyman), the Ministry of evance, limited information is available on
Health, Bridgetown, Barbados, the prevalence of OAG or other eye dis¬
West Indies (Dr Connell), and eases in black people and even less is
The Wilmer Ophthalmological See Methods next
Institute, The Johns
known about possible risk factors. on page
Hopkins
University School of Medicine, The Barbados Eye Study (BES) was
Baltimore, Md (Dr Schachat). designed to address the need for epide-
major disability (n=147; 9%). participant was also referred for these additional
The names selected were placed in random or¬ evaluations, regardless of examination findings. The
der into a computerized recruitment system, and in¬ same ophthalmologist examined all referred partici¬
dividuals were contacted in that order to ascertain pants at the polyclinic. The examination provided
their willingness to participate in the BES. The com¬ data on the pathologic findings in the eye, the causes
puterized system was used to generate recruitment of visual acuity or field loss, and clinical diagnoses.
letters and lists of persons who needed to be called It included, for every participant, a slit-lamp exami¬
or visited at home or who required transportation, to nation of the anterior segment, an evaluation of lens
assist in the scheduling of appointments, and to opacities, and a fundus examination with an indirect
monitor participation statistics. Recruitment letters lens (Volk 78, Volk Optical, Mentor, Ohio) during
were signed by the chief medical officer of the Min¬ the slit-lamp examinations. Three-mirror gonios-
istry of Health; nonrespondents received additional copy and other evaluations were also included to es¬
mailings, telephone calls, or home recruitment vis¬ tablish the clinical diagnosis. Participants with sys¬
its. Home examinations were offered to persons who temic and/or ocular abnormalities or glycosylated
were unable to visit the study site. hemoglobin levels greater than 8% were referred
Participants attended the Sir Winston Scott elsewhere for medical evaluation and treatment.
Polyclinic, Ministry of Health, for an extensive stan¬
dardized examination that included automated re¬ PERIMETRY SCREENING PROTOCOL
fraction (Humphrey automated refractor, Humphrey
Instruments Ine, San Leandro, Calif); best corrected Evaluation of the sensitivity and specificity of vari¬
visual acuity (Ferris Bailey charts, following a modi¬ ous visual field tests during the pilot study and the
fied Early Treatment Diabetic Retinopathy Study pretesting phase of the BES led to the following
protocol)8; automated perimetry (Humphrey field screening sequence.12 All participants had a supra-
analyzer, Humphrey Instruments); two blood pres¬ threshold screening test using the full field 120 pro¬
sure measurements (Hawksley random zero sphyg- gram of the Humphrey field analyzer, three-zone
momanometer); height, weight, and circumferences strategy, in the central 30° only (4 minutes per eye);
puter next to the perimeter, the C24-2 data were im¬ All visual fields were analyzed using computer-
mediately analyzed by the hemimeridional compari¬ based criteria to assess abnormalities. In addition, all
son method,13 using the ICEPACK program.14 If the visual field tests were reviewed and classified by one
analysis showed low sum or defects in the compari¬ ophthalmologist, who evaluated the possible artifacts
sons of field sectors 5 vs 6 and 7 vs 8 (sensitivity, 91%; and provided a clinical interpretation of the results
specificity, 64%), these individuals were referred for (normal, suspect glaucoma, definite glaucoma, cata¬
an ophthalmologic examination and a threshold C30-2 ract, other diagnosis, uncertain diagnosis, unreliable
test, which was also analyzed by the hemimeridional or missing/incomplete fields). Optic disc abnormali¬
method.13 To evaluate possible false-negatives, every ties were independently assessed by graders at the
10th person was referred to complete the full perim- fundus photography reading center and also were as¬
etry protocol. sessed by ophthalmologic examination. The ophthal¬
mologic evaluation of possible causes for visual field
OPTIC DISC EVALUATION and/or optic disc damage was sought through exami¬
nation of the participants by the BES ophthalmolo¬
Two independent graders at the reading center clas¬ gist; for those not completing this examination, the
sified the photographs, and discrepancies were re¬ ophthalmologist conducted a confirmatory review of
solved by consensus or adjudication by a third the available records.
grader. In addition to the photographic quality, rel¬ All data from the data collection center and the
evant disc features graded were horizontal and verti¬ fundus photography reading center were sent to the
cal cup-disc ratio using a template,15 narrowest re¬ coordinating center for processing, analyses, and in¬
maining neuroretinal rim, hemorrhages, and dependent glaucoma classification. Because partici¬
unsupported vessels. The ophthalmologic examina¬ pants were a cross section of the population and a
tion form included the same optic disc items as the wide spectrum of OAG stages would be included, it
reading center forms, thus allowing comparisons of was expected to have incomplete visual field or pho¬
clinical and photographic data. A quality assurance tographic data (eg, because of advanced visual loss or
system evaluated the intergrader and intragrader re- media opacities) in older participants with OAG and
producibility, as well as the reproducibility of the in those with advanced OAG. The exclusion of these
consensus photographic gradings of different grader persons would result in a biased underestimate of the
pairs. The system involved 120 sets of quality con¬ true OAG prevalence; on the other hand, the inclu¬
trol photographs that were graded first at baseline sion of persons with missing data could also lead to
and then on an ongoing basis, the masked insertion misclassification. To address this issue and define
of a quality control set after every sixth set of study minimum standards for data completeness, each of
photographs, and the assignment of these quality the BES criteria had two subcategories to specify the
control sets to different grader pairs. The reproduc¬ type of data on which the glaucoma classification was
ibility of the consensus gradings was monitored by based. For simplicity, these subcategories were desig¬
repeated evaluations of the quality control photo¬ nated with double plus signs (+ + ) to mean most
graphs by two different grading teams consisting of complete data and with a single plus sign ( + ) to
different grader pairs (eg, the consensus of graders A mean less complete data but sufficient for glaucoma
and was compared with the consensus of graders classification; they are defined in Table 1.
C and D, and the consensus of graders A and C with All participants were independently classified at
that of graders and D). Possible drift in gradings the coordinating center according to these study cri¬
over time was monitored by comparing the results of teria. Prevalence is reported both as observed per¬
various grading cycles of the quality control photo¬ centage prevalence, a minimum estimate based on
graphs. the number of cases identified in participants with
complete study visits, and as adjusted percentage
CRITERIA FOR GLAUCOMA CLASSIFICATION prevalence. For the latter, results were age-sex ad¬
justed to account both for refusals and incomplete
The BES classification of definite OAG required the study visits and for nonresponse to referrals to the
presence of both visual field and optic disc criteria in ophthalmologic examination. The adjustment as¬
at least one eye after ophthalmologic exclusion of sumed the same rate of disease in those completing
narrow angles, other types of glaucoma, and other and not completing the data collection protocol
possible causes. If these criteria were only partially within each age-sex stratum. Age-adjusted rates were
met, individuals were classified as having suspect calculated by the direct adjustment method, using a
OAG. The intraocular pressure (lOP) was not con- combined standard population.16
phrey visual field tests for most of the cases (groups 1,3, sons who were classified as having definite OAG, sus¬
5, and 6; Table 4). The rest were unable to complete two pect OAG, or other glaucoma are presented in Table 6.
tests, mainly because of severe visual impairment. Disc The OAG prevalence by self-reported race was 7.0% (302/
damage was documented by photographic and/or clini¬ 4314) in black, 3.3% (6/184) in mixed-race, and 0.8%
cal assessment in most cases (over four fifths) as well (1/133) in white participants (Table 6). All six partici¬
(groups 1, 2, and 5; Table 4). All but 12 cases were ex¬ pants in the mixed-race group were male.
amined by the BES ophthalmologist (groups 1 through
4; Table 4). AGE-SEX SPECIFIC PREVALENCE
Persons with OAG and suspect OAG were signifi¬
cantly older, and there was a higher percentage of male The results that follow are based on the 4498 black and
and black participants than in the nonglaucoma popu¬ mixed-race participants only. The observed overall preva¬
lation (Table 5). The median age of the participants with lence of OAG in this group was 6.8% (95% CI, 6.1 to 7.6)
OAG was 72 years for both men and women. Overall, the and varied significantly by age and sex. It increased steeply
median age of the participants with suspect OAG was 63 with age, reaching 14.8% at ages 70 through 79 years and
years; it was 62 years for men and 65 years for women. 23.2% at older ages (Table 7). In every age group, preva¬
Of the participants with OAG, 49% had received previ¬ lence was higher in men than in women, with an age-
ous diagnoses of OAG and were receiving treatment. There adjusted prevalence ratio of 1.4.
were no differences in the age and sex distribution of par¬ An additional 168 persons (3.7%) (95% CI, 3.2 to
ticipants with newly diagnosed and previously diag¬ 4.3) were classified as having suspect OAG (Table 7). As
nosed OAG. About 11% of those with suspect OAG re¬ in OAG, the prevalence of suspect OAG was higher in
ported treatment for glaucoma but did not meet the study men than in women; however, it remained relatively stable
criteria for OAG. The average IOP was elevated in the with age (6% to 7% in men and 2% to 4% in women). If
OAG and the suspect OAG groups. High cup-disc ratios these suspect OAG cases are added to the definite OAG
were present in participants with OAG and suspect OAG cases, the combined prevalence is 10.6% (95% CI, 9.7 to
as well (Table 5). 11.5), with 13.3% of the men and 8.5% of the women
The sex distribution and self-reported race of per- affected (Table 7).
Group No. (%) 95% CI No. (%) 95% CI No. (%) 95% CI
OAG
40-49 11(1.9) 0.9-3.3 7(1.0) 0.4-2.0 18(1.4) 0.8-2.2
50-59 21 (4.6) 2.9-7.0 24(3.7) 2.4-5.4 45 (4.1) 3.0-5.4
60-69 40 (9.4) 6.8-12.6 31 (4.9) 3.4-6.9 71 (6.7) 5.3-8.4
70-79 64(17.5) 13.8-21.8 58(12.7) 9.8-16.1 122(14.8) 12.5-17.4
80-86 25 (24.8) 16.7-34.3 27(22.0) 15.0-30.3 52 (23.2) 17.9-29.3
Total 161 (8.3) 7.1-9.7 147 (5.7) 4.9-6.7 308 (6.8) 6.1-7.6
Suspect OAG
40-49 13(2.2) 1.2-3.8 14 (2.0) 1.1-3.3 27 (2.2) 1.4-3.1
50-59 26 (5.8) 3.8-8.3 14(2.1) 1.2-3.6 40 (3.7) 2.7-5.0
60-69 26(6.1) 4.0-8.8 22 (3.5) 2.2-5.2 48 (4.7) 3.5-6.2
70-79 24 (6.6) 4.3-9.6 19(4.2) 2.9-6.4 43 (5.5) 4.0-7.2
80-86 7(6.9) 2.8-13.8 3 (2.4) 0.5-7.0 10(4.0) 1.8-7.5
Total 96 (5.0) 4.1-6.0 72 (2.8) 2.2-3.5 168 (3.7) 3.2-4.3
OAG and Suspect OAG
Total 257(13.3) 11.8-14.9 219 (8.5) 7.5-9.7 476 (10.6) 9.7-11.5
the diseases of interest, and quality control of all data was sider that both visual field and optic disc criteria were
carefully monitored. The fundus photographs were read required for the definition of OAG in the BES. Field loss
by masked graders, and the reproducibility of clinical and and optic disc damage were documented by automated
photographic protocols was evaluated throughout the perimetry, fundus photography, and a standardized oph¬
study. Perimetric reliability was consistent with other re¬ thalmologic examination for most participants with OAG
ports,17 and the sensitivity of the screening protocol was (Table 4). The main reasons for having less complete data
high.12 Despite the difficulties of performing automated were the presence of advanced visual loss and the inabil¬
perimetry, fundus photography, and other tests in a gen¬ ity to complete perimetry or fundus photography.
eral population, a high degree of data completeness was The number of BES participants who reported be¬
achieved (Table 3). ing white or of mixed black and white ancestry was too
As reviewed in detail elsewhere,L·19 most OAG popu¬ small to draw conclusions from, but the results were con¬
lation studies have been limited to white adults, in whom sistent with an increased prevalence of OAG in the black
prevalence has been 1% or less. Therefore, the number participants, as evidenced by the comparisons with the
of prevalent cases identified by these studies has been in¬ nonglaucoma group (Table 5). A gradient in prevalence
sufficient for extensive evaluations. To our knowledge, by racial group is also suggested (Table 6).
the BES included the largest number of OAG cases ever Half of the OAG cases identified in the BES were
cup-disc ratios of 0.8 were also found in this group (Table study used the full field 120 program for screening
5), a result that is consistent with the BES criteria for OAG. and had different perimetry criteria for ophthalmo¬
Of the participants with suspect OAG, who may repre¬ logic referral. The diagnosis of OAG was based on
sent participants with early OAG, 11% were receiving treat¬ Goldmann perimetry, rather than on automated Hum¬
ment for glaucoma, and they had higher average IOPs phrey perimetry. Despite these differences, however, it
and cup-disc ratios than did the nonglaucoma group seems reasonable to conclude that a higher prevalence
Analyses
that were limited to black and times higher than that observed in the Baltimore Eye
mixed-race BES participants show the Survey white participants and 1.5 times higher than
high prevalence of OAG with increas¬ that observed in the Baltimore Eye Survey black par¬
ing age (Table 7). In the 40- through 49- ticipants. Discrepancies between the prevalences from
year age group, the observed prevalence the BES and from studies in the United States and Eu¬
was similar to that observed in much older white popu¬ rope are even larger when BES participants with sus¬
lations.20 24 Large increases are seen in successive age pect OAG are included in these comparisons. These
groups; over half the participants were over the age of 70 differences raise the question of possible genetic fac¬
years, in whom the prevalence reaches about 15%. An tors and require further study.
even higher prevalence of 23% was seen in the oldest age The distribution patterns of OAG in the BES
group. Other studies in the Caribbean region with simi¬ showed a preponderance of OAG in men (Tables 5
larly high participation rates have also found a higher through 7). Some studies1·21·27 have reported higher
prevalence of OAG than that in white populations. In Ja¬ rates of glaucoma blindness and a higher prevalence of
maica, West Indies, a study25 with 85% participation re¬ OAG in men than in women (eg, the Framingham Eye
ported a prevalence of 1.4% (9/678), which was three times Study had a twofold higher prevalence in men than in
higher than that in a comparable study in Wales.20 A study women).21 This finding has not been consistently re¬
in St Lucia, West Indies, reported an 8.8% prevalence of ported by other studies in white populations, but re¬
OAG at ages 30 years and older among 1679 black resi¬ sults are based on few cases of OAG. Data from the
dents screened.26 previous smaller studies in blacks found similar sex-
Although the results of the BES and the St Lucia study specific prevalences of OAG. However, the sex-specific
are consistent with a high prevalence of OAG in both is¬ data from St Lucia are difficult to interpret because of
lands, the studies differ in methods and definitions. The the underrepresentation of the male population, ie,
St Lucia protocol did not include fundus photographs. only 32% of their participants were male vs 44% in the
Visual field screening with the full field 120 test was pro¬ population.26 As the authors suggest, the unwilling¬
vided to every third person and to those meeting criteria ness of men to participate led both to an underenu-
based on IOP and clinical assessment of the cup-disc ra¬ meration of men (36%) in the household survey used
tio; 364 persons (70% of those referred) had a C30-2 test. as a sampling frame and to their low participation in
The 8.8% prevalence was based on 147 cases with posi¬ examinations. The Baltimore study did not report sex-
tive hemimeridional analyses after ophthalmologic re¬ specific participation for blacks, but the age- and race-
view of the 410 eyes with reliable C30-2 tests. Preva¬ adjusted prevalence of OAG was similar in both sexes
lence was 16% when based on a secondary definition. The (2.70% for men and 2.35% for women).23
apparently higher age-specific prevalence in the St Lucia Possible biases that would result in differential re¬
study than in the BES could be explained by the differ¬ cruitment of men with OAG into the BES were ex¬
ences in OAG protocols and diagnostic criteria, eg, the plored. The sex-specific participation in the BES
requirement for optic disc plus visual field criteria in the tended to be somewhat higher in women than in men
BES. For example, age-specific prevalences are similar in and would not explain the differences in prevalence.
both studies when the BES definite and suspect cases of There was no evidence of a higher participation of
OAG are combined. There also may be some differences men than women because of their previous diagnosis
between populations. of OAG, because the percentage of cases with a known
The Baltimore Eye Survey23 identified 100 cases of history of glaucoma was similar in both sexes. Simi-
prevalence of blindness in East Baltimore. N Engl J Med. 1991;125:1442-1447. 28. Shiose Y, Kitazawa Y, Tsukahara S, et al. Epidemiology of glaucoma in Japan:
6. Leske MC, Connell AMS. Design of a pilot study of glaucoma in Barbados. a nationwide glaucoma survey. Jpn J Ophthalmol. 1991;35:133-155.
J Natl Med Assoc. 1988;80:727-730. 29. Salmon JF, Mermoud A, Ivey A, Swanevelder SA, Hoffman J. The prevalence
7. Leske MC, Connell AMS, Kehoe R. A pilot project of glaucoma in Barbados. Br of primary angle closure glaucoma and open angle glaucoma in Mamre, West-
J Ophthalmol. 1989;73:365-369. ern Cape, South Africa. Arch Ophthalmol. 1993;111:1263-1268.
8. Ferris FL, Kassoff A, Bresnick GH, Bailey I. New visual acuity charts for clinical 30. Leske MC, Podgor M, Ederer F. An evaluation of glaucoma screening methods.
research. Am J Ophthalmol. 1982;94:91-96. Invest Ophthalmol Vis Sci. 1982;22(suppl):128.
9. Chylack LT Jr, Leske MC, McCarthy D, Khu P, Kashiwagi T, Sperduto R. Lens 31. Sommer A, Tielsch JM, Katz J, et al. Relationship between intraocular pressure
Opacities Classification System II (LOCS II). Arch Ophthalmol. 1989;107:991-997. and primary open angle glaucoma among white and black Americans: the Bal-
10. The Early Treatment Diabetic Retinopathy Study Group. Early Treatment Dia- timore Eye Survey. Arch Ophthalmol. 1991;109:1090-1095.