Abstract
Objective: To characterize the
ocular and peri-ocular findings in patients with chronic renal failure
undergoing haemodialysis at Prince
Ali Bin
Al- Hussein
Military Hospital.
Methods: This is a
descriptive study. Data were collected from patients with chronic renal failure
undergoing haemodialysis from June 2012 till January 2013. The medical files
were reviewed to report medical, surgical and ophthalmic history of all
candidate patients. All patients underwent full ophthalmic examination on day
one of recruitment.
Results: Forty-four
patients (87 eyes) were reported. Mean age was 56.9 years (56.9 ±12.5). Male to
female ratio was 2:1. Aetiologies of chronic renal failure were: Hypertension (n=17,
39%), glomerulonephritis (n=13, 30%), and diabetes mellitus (n=10, 23%). Some
other aetiologies were also found like: Small kidney (n=4, 9%), renal stones (n=2,
5%), polycystic kidney (n=2, 5%), familial (n=2, 5%) and analgesic nephropathy (n=1,
2%). Ocular findings were seen in 75 eyes (86%), including lid edema (n=66, 76%)),
conjunctival congestion (n=54, 62%), cataract (n=47, 54%), and dry eye (n=44, 51%).
Conclusion: Ocular and
peri-ocular findings were frequent in chronic renal failure patients who were
undergoing hemodialysis, which urges regular ophthalmic examination to detect
and treat sight threatening complications early.
Key words: Ophthalmic
findings, Chronic renal failure, Hemodialysis.
JRMS September
2013; 20(3): 62-67 /DOI: 10.12816/0001043
Introduction
Chronic renal failure (CRF) is considered as one of the important health
problems that affect the population. Its effect on health can be attributed to
renal failure itself or the primary pathology that caused it, haemodialysis,
even renal transplantation, or all of them together. It is estimated that around
10-16% of adult population in USA,
Europe, Asia, and Australia
are suffering from chronic renal failure.(1) In addition to
health problems caused by CRF, management of the disease has financial impact
on government treasury. Previous reports found diabetic nephropathy to be the
most common cause of CRF, followed by hypertensive nephropathy and
glomerulonephropathies.(2) The association between renal diseases
and visual impairment was first described by Bright in 1836. Twenty-three years
later, Liebreich described fundus
changes in uremic patients and called it Bright's disease.(3)
Many studies described the high prevalence of ocular findings in patients
with CRF especially in the fundus, which was blamed to be the main culprit
responsible of deterioration of vision in CRF patients. A study conducted in USA by Grunwald
et al. (4) revealed that the prevalence of ocular
fundus pathology among CRF patients to be 45%. The above mentioned entity
should be differentiated from oculorenal syndromes, which is a group of
inherited and non-inherited malformations and systemic diseases that has
combined ocular and renal manifestations.(5) According to
Jordanian Ministry of Health (MOH) statistics; 2557 Jordanian patients were
reported to have CRF and scheduled for haemodialysis among all health sectors
in 2011, in MOH affiliated hospitals there are 914 patients using 202
haemodialysis units and those patients underwent 123071 haemodialysis session
(average 2.6 per week for each patient) in the year 2011, in Al- Karak
Governorate, there are 69 patients with CRF using 14 haemodialysis units,(6)
according to administrative data half
of those units are located in Prince Ali Military hospital and are used by 51
patients (average 2.1 per week for each patient).
Reviewing the literature, we found no report addressing the ophthalmic
findings of CRF in Jordan.
Methods
This is a descriptive study where data were collected from patients with
chronic renal failure undergoing haemodialysis from June 2012 till January
2013. Files were reviewed to report medical, surgical and ophthalmic history of
all candidate patients. All patients underwent full ophthalmic examination on
day one of recruitment. Patients with known malignancy or oculorenal syndromes
were excluded. Detailed history was obtained from each patient including age, gender,
past medical and surgical history, previous ocular diseases, cause of CRF,
duration and frequency of haemodialysis. Detailed ophthalmologic examination
included best corrected visual acuity, Schirmer’s test, eyelids, anterior
segment using slit lamp biomicroscopy, intra ocular pressure measurement using
Goldmann applanation tonometry, and dilated posterior segment assessment using
78 D non-contact lens. The
approval of the local ethical committee was obtained as well as the patients’
consent.
Data were reported and statistically analysed.
Results
Forty-four patients (87 eyes) were included in this study, 29 of
patients were males with a male to female ratio of 2:1 and the age of the
patients ranged between 23 and 87 years ( mean 56.9 ±12.5 years). Patients were
undergoing haemodialysis for a period ranging from two months to 22 years (mean
4.3 ±3.4 years). The primary pathologies responsible for CRF are summarized in Table
I. The majority of patients had single underlying cause responsible for CRF and
seven had two combined causes.
Considerable drop of vision (6/18 or less) was seen in 37 eyes (43%) and
severe loss of vision (best corrected visual acuity in the best eye is less
than 6/60 according to WHO classification of blindness) was seen in four
patients (legally blind). Causes of decreased visual acuity among the 37 eyes
are summarized in Table II.
Seventy- five eyes (86%) showed at least one eye pathology as shown in Table
III. None of the eyes had elevated intraocular pressure.
Tables IV and V represent the presence of ocular pathology in relation
to the duration and the frequency of dialysis, respectively.
Discussion
Chronic renal failure is a slowly progressive deterioration of renal
function that usually occurs as a result of another systemic problem and result
in serious systemic problems.
This study showed that males
were more frequently affected than females with a ratio of 2:1 and this ratio
is similar to that found in the literature. This can be explained by the rapid
deterioration of renal function in some forms of glomerulonephritis and polycystic
kidney disease in males.(7)
Taking into consideration the prevalence of diabetes mellitus and hypertension
in older age group and as these are the most important underlying causes of CRF
(8) it was not surprising that the mean age of patients was 56.9 years. Most of CRF in our study was caused by hypertension, glomerulonephritis and diabetes mellitus with hypertension being the most common predisposing factor, those results are similar to those found in many studies all over the world,(9) however the second common cause was glomerulonephritis rather than diabetes mellitus, this support the idea that there is a geographical variation in the prevalence and aetiology of CRF that could be attributed to race and ethnicity, genetic predisposition, difference in prevalence of diabetes, obesity, and smoking.(10) Another explanation could be the longer life expectancy of diabetic patients in developed countries.
Table I: Aetiologies of CRF
Percentage
|
Number of patients
|
Aetiology of CRF
|
39
|
17
|
Hypertension
|
30
|
13
|
Glomerulonephritis
|
23
|
10
|
Diabetes Mellitus
|
9
|
4
|
Small kidney
|
5
|
2
|
Renal stones
|
5
|
2
|
Polycystic Kidney
|
5
|
2
|
Familial
|
2
|
1
|
Analgesic nephropathy
|
15.6
|
7
|
More than one cause
|
Table II: Aetiologies of
reduced vision among eyes with vision drop
%
|
Number of eyes with reduced vision
n= 37
|
Cause
|
19
|
7
|
Band keratopathy
|
43
|
16
|
Lens opacity
|
27
|
10
|
Diabetic retinopathy
|
11
|
4
|
Hypertensive retinopathy
|
17
|
6
|
Maculopathy
|
Table III: Ocular findings among
patients with CRF
%
|
Number of eyes
n=87
|
Ocular finding
|
76
|
66
|
Lid edema
|
2
|
2
|
Blepharitis
|
51
|
44
|
Dryness
|
62
|
54
|
Conjuctival congestion
|
28
|
24
|
Pinguecula
|
9
|
8
|
Conjuctival calcification
|
14
|
12
|
Band keratopathy
|
7
|
6
|
Corneal calcification
|
2
|
2
|
Keratic precipitates
|
1
|
1
|
Posterior synechiae
|
54
|
47
|
Cataractous changes
|
13
|
11
|
Pseudophakia
|
2
|
2
|
Posterior capsular opacification
|
11
|
10
|
Hypertensive retinopathy
|
13
|
11
|
Diabetic retinopathy
|
7
|
6
|
Maculopathy
|
2
|
2
|
Myopic chorio-retinal degeneration
|
Table IV: Presence of ocular
pathology in relation to duration of dialysis
n & % of eyes with posterior segment pathology
|
n & % of eyes with anterior segment pathology
|
n & % of eyes with reduced vision
|
n & % eyes
|
Duration (months)
|
10(20)
|
42(82)
|
17(33)
|
51(58.6)
|
0-36
|
3(25)
|
10(84)
|
5(42)
|
12(13.8)
|
37-72
|
4(33)
|
11(92)
|
7(58)
|
12(13.8)
|
73-108
|
7(58)
|
11(92)
|
8(75)
|
12(13.8)
|
>108
|
Table V: Presence of ocular pathology
in relation to frequency of dialysis
n & % of eyes with posterior segment pathology
|
n & % of eyes with anterior segment pathology
|
n & % of eyes with reduced vision
|
n & % of eyes
|
Frequency of dialysis per week
|
10(26)
|
34(87)
|
16(43)
|
39 (45)
|
2
|
14(29)
|
40(83)
|
21(44)
|
48 (55)
|
3
|
In this series, 37 eyes (43%)
showed reduced vision, which is higher than that of a report in Nepal,(11)
23.4% of chronic renal disease patients not undergoing haemodialysis, which
may explain the difference. The commonest pathology reducing vision in this
series was cataract, followed by diabetic retinopathy, band keratopathy and
hypertensive retinopathy respectively. The
explanation why diabetes was responsible for drop of vision more than
hypertension despite hypertension prevalence among patients is that most of the
diabetic retinopathies found in our patients were in advanced stages unlike
hypertensive retinopathies which were present mostly in early stages.
We reported a high incidence of
ocular pathology among CRF patients on dialysis (86% of eyes). All patients
with duration of dialysis more than 6 years had ocular pathology, and as the
duration of haemodialysis increased the number of patients with ocular
pathology or reduced vision increased, suggesting a linear relationship. This conforms
to the results of Kian-Ersi et al.(12) No relation was
found between the frequency of dialysis sessions and the incidence of ocular
pathology and reduced vision. Lid edema was the most common pathology in this
series (76%). Oedema occurs as a result
of limitation in the kidneys' ability to excrete sodium into the urine, which
will increase the hydrostatic pressure in the capillaries forcing the fluids to
accumulate in the interstitial space. The 2nd common ocular pathology
was conjunctival congestion (62%). Causes of conjunctival congestion are
associated hyperparathyroidism and elevated serum calcium concentration which
deposits in conjunctiva causing severe irritation and redness.(5,13) Dryness was present in this series
(51%). Some studies discussed this issue.(11,13) Some
explanations have been put forward. First, deposition of calcium in conjunctiva
and cornea was widely suggested as aetiology due to its high association with
eye dryness.(14) In this series all patients with
conjunctival and corneal calcifications and band keratopathy had dryness, and
it tended to be more severe than dryness in eyes without calcifications. Dursun
et al.(15) found a considerable decrease in goblet
cell density in the conjunctiva of CRF patients. Goblet cells are the primary
source for synthesis of mucin layer of the tear film. William et al.(16)
suggested that dryness is more prevalent in cataract patients, which
may be a third explanation for the high incidence of dryness as the incidence
of cataract was high as well (43%). Pinguecula was seen in 28% of patients. This
pathology is close to that found in other studies,(11) although
it was present in a significant percentage, many studies showed no harmful
complication of this lesion on regular follow up apart from recurrent
inflammations.(2,17) Conjunctival and corneal calcifications
were present in a significant percentage of patients (9% and 7% respectively)
and those calcifications mostly present within the palpebral aperture most
probably due to loss of corneal and conjunctival CO2 in these
areas that results in an increase in the pH which leads to precipitation and
deposition of calcium in the exposed conjunctival and cornea from the elevated serum
calcium. Corneal calcification usually occurs in the periphery of the cornea
but with time it extends to the centre interrupting the visual access, and
called namely band keratopathy.(5) This ocular pathology
was responsible for 19% of reduction of vision.
Cataract was the most common
cause of reduced vision (43%) as 54% of the eyes had catarctous
changes and 13% were pseudophakic. This pathology is higher than in the general
population. David et al (18) found
that prevalence of cataract and pseudophakia / aphakia among adults above the
age of 40 years in the United
States to be 17.2% and 5.1%, respectively.
This supports the assumption that CRF increases the risk of developing cataract.
This may be explained by severe uremia(19) in addition to
increased levels of oxidized glutathione in CRF patients which exposes the lens
to oxidative stress.(20) The higher incidence of diabetes may
be another explanation. Posterior segment pathologies were the most serious
because of their sight- threatening capability and the high possibility of
irreversible damage to the visual system. Twenty-four eyes (28%) had at least
one pathology in the fundus. The most common posterior segment abnormality was
diabetic retinopathy (13%), eight eyes of which (67%) were in the form of
proliferative diabetic retinopathy, while two eyes (17%) were moderate non-
proliferative diabetic retinopathy, and the remaining two eyes (17%) were mild
non-proliferative diabetic retinopathy. Five eyes did not show diabetic
retinopathy; this means that 12 eyes out of 17 eyes (70%) of diabetic patients
with CRF had diabetic retinopathy, a high percentage in comparison to previous
reports in the literature.(21) This may be explained by the
poor control of blood sugar in Jordanian diabetics which was described in
previous studies.(22) Hypertensive retinopathy was found in
11% of eyes and 4% had reduced vision related to diabetic retinopathy, while
the remaining had changes of early grades that did not interfere with vision.
Maculopathy was found in 7% of eyes. The strong relationship between
nephropathy and development of proliferative diabetic retinopathy and
maculapathy was shown before.(23-26) This report
demonstrated that ocular pathologies were frequent in patients with CRF on
dialysis, some of which are serious and pose a threat to vision. Despite these
facts, 55% of patients did not have full and detailed ocular examination. This implies
lack of knowledge among patients of CRF. Therefore an effort should be adopted
to increase the awareness of patients. And a protocol should be put forward by
ophthalmologists and nephrologists suggesting routine ocular examination of CRF
patients on haemodialysis. Potential limitations of this report include lack of
fundus photography, as well as inaccurate or completely lacking medical
records.
Conclusion
Ocular and peri-ocular pathologies are frequent in chronic renal failure
patients who undergo hemodialysis. This urges the need for regular ophthalmic
examination to detect and treat sight threatening complications as soon as
these are detected.
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