·Clinical Research· ·Current Issue· ·Achieve· ·Search Articles· ·Online Submission· ·About IJO· PMC
Risk
factors of rhegmatogenous retinal detachment associated with choroidal
detachment in Chinese patients
Yong-Hao Gu, Gen-Jie Ke, Lin Wang, Qi-Hong
Gu, En-Liang Zhou, Hong-Biao Pan, Shi-Ying Wang
Department of Ophthalmology, Anhui
Provincial Hospital affiliated to Anhui Medical University, Hefei 230001, Anhui
Province, China
Correspondence
to: Yong-Hao Gu.
Department of Ophthalmology, Anhui Provincial Hospital affiliated to Anhui
Medical University, 7# Road Lujiang, Hefei 230001, Anhui Province, China.
aerolplane@hotmail.com
Received:
2015-08-25
Accepted: 2016-01-06
Abstract
AIM:
To comprehensively analyze
the risk factors of rhegmatogenous retinal detachment (RRD) associated with
choroidal detachment (CD).
METHODS: A
total of 265 eyes of 265 consecutive cases of RRD were retrospectively
analyzed. All patients had
systemic and ophthalmologic examination. CD was diagnosed by indirect
ophthalmoscopy, B-scan ultrasonography, and ultrasound biomicroscope (UBM). Each parameter was
compared between patients of RRD
and rhegmatogenous retinal detachment associated with choroidal detachment
(RRDCD). Logistic regression analysis was used to determine the independent
risk factors of CD.
RESULTS: There were 52 eyes (19.62%) with CD.
Pseudophakia was more commonly seen in RRDCD (21.15% vs 6.10%, P=0.002).
Intraocular pressure (IOP) was lower (8.60±3.62 vs 12.96±3.55, P<0.001), best-corrected visual acuity was worse [3.00 (2.00 to 3.00) vs 1.92
(1.22 to 3.00), P=0.001], and refractive error was more myopic [-4 (-9 to -2) vs -2 (-6 to 0), P=0.007] in RRDCD. Eyes with RRDCD had
larger extent of retinal detachment (P=0.007).
In RRDCD, 34.62% of eyes presented with multiple holes (P=0.044) and 25.00% with macular holes (P=0.012), compared with 20.66% and 14.08% in RRD. High myopia (P=0.039), low IOP (P=0.017), and larger extent of retinal detachment (P<0.001) were significant and
independent risk factors for developing CD.
CONCLUSION: For CD in RRD, related
factors include BCVA, IOP, lens status, refractive error, extent of retinal
detachment, number of holes, and macular hole. Larger extent of retinal
detachment, high myopia, and low IOP are significant and independent risk
factors.
KEYWORDS:
choroidal detachment;
retinal detachment; risk factor
Citation: Gu YH, Ke GJ, Wang L, Gu QH, Zhou EL, Pan HB, Wang
SY. Risk factors of rhegmatogenous retinal detachment associated with choroidal
detachment in Chinese patients. Int J
Ophthalmol 2016;9(7):989-993
INTRODUCTION
The prevalence
of choroidal detachment (CD) in rhegmatogenous retinal detachment (RRD) is
2%-4.5% in western countries[1-3]. Most of these eyes
have low intraocular pressure (IOP), uveal inflammation, and increased breakdown
of the blood-retinal barrier, and
always present with rapid progression, poor prognosis, and difficult
treatment[4]. It is independently
associated with retinal detachment repair failure[5].
Referring to the collection of fluid in the potential space of suprachoroid,
the pathogenic mechanism of CD has not yet been clearly delineated[6]. Previous reported risk factors
include high myopia, aphakia or psedophakia, old age, and presence of macular
hole[1-3,7], but most of these
studies have lacked detailed statistical comparison. The aim of this study was
to comprehensively analyze the risk factors of combined choroidal and retinal
detachment patients in order to improve the understanding and treatment of these
conditions.
SUBJECTS AND METHODS
We conducted a retrospective review of 265 consecutive cases (265 eyes) of
primary RRD at Anhui Provincial Hospital in Hefei, China between October 2012
and June 2014. The study was performed in accordance with the tenets of the
Declaration of Helsinki and was approved by the Institutional Review Board of
Anhui Provincial Hospital affiliated to Anhui Medical University. The informed
consent was obtained orally from all patients. Patients were excluded from the
study if they had traction-RRD, as seen in diabetes, history of ocular trauma
or vitreoretinal surgery, or congenital ocular syndromes with the potential to
induce vitreoretinal abnormalities. Cases whose causative breaks were detected
intraoperatively were included in the study. CD was diagnosed with indirect
ophthalmoscopy, B-scan ultrasonography (CineScan, Quantel Medical, France), and ultrasound biomicroscope (UBM) (SW3200L, Suoer, China) by
two experienced technicians independently.
General information collected included age at presentation, sex, medical
and ocular history, duration of the presenting syndrome, and medical history of
systemic disease (diabetes mellitus and hypertension). Onset of illness was defined as the time between a
sudden blurring of vision or/and partial loss of vision field and apply to the
physician. All patients underwent a full ophthalmic evaluation, including
best-corrected visual acuity (BCVA), slit-lamp examination, binocular indirect
ophthalmoscopy, applanation tonometry, ultrasonography, and UBM. Lens status,
refractive error, axial length, involvement of macular hole, extent of retinal
detachment, and number of causative retinal breaks were recorded for analysis.
Axial length was measured with A-scan ultrasonagraphy (Tomey, AL-100, Japan).
Two experienced technicians would modify the data for those with retinal
detachment involving posterior pole by differentiating the signal of detached
retina and sclera. Because optometry
is difficult in patients with retinal detachment, refractive error in these
cases was obtained with patients wearing glasses or by accessing their
optometry records before the onset of RRD. For patients without optometry
results, if previous visual acuity of both eyes was same, refractive error was
evaluated by retinoscopy
optometry in the other eye. Refractive
error of all 24 patients of pseudophakic was evaluated by their wearing glasses
or optometry records prior to cataract surgery. Snellen visual acuities were converted to the logarithm of the minimum
angle of resolution (logMAR) for statistical analysis. Counting figures, hand
movement, and light perception were recorded as logMAR 2, 3, and 4,
respectively.
Statistical Analysis Statistical analyses were done with SPSS
19.0 software (SPSS Inc, Chicago, Illinois, USA). Quantitative data were
checked for normality of distribution by Kolmogorov-Smirnov analysis. The
results showed all factors except for IOP did not follow the normal
distribution; hence we expressed them in terms of median (quartile1-quartile3) and used the Mann-Whitney U test
to assess intergroup differences. IOP was expressed as mean±standard deviation and analyzed by independent-sample t-test. Qualitative values were compared by the Fisher
exact test or χ2 test. Finally, stepwise
logistic regression was used to determine the independent clinical risk factors
of CD. Factors that were significant at the level of P<0.4 in the univariate analysis were
included in the logistic regression. Significance
was defined as P<0.05 for all analyses.
RESULTS
This study included 265 eyes (cases) with RRD. Of these, 52 eyes (19.62%
of cases) involved CD. For analysis, we included 213 eyes in a group comprised
of rhegmatogenous retinal
detachment without choroidal
detachment (Group RRD) and 52 eyes in a separate group involving rhegmatogenous retinal detachment with choroidal detachment (Group RRDCD).
Table 1 compares demographic and medical parameters between the two
groups. There were no significant differences between the two groups in sex
ratio, age, onset of illness, or medical history of hypertension and diabetes.
Clinical factors |
Group
RRD (n=213) |
Group
RRDCD (n=52) |
P |
Sex ratio (M/F) |
102/111 |
31/21 |
0.164 |
Age [a (Q1-Q3) ] |
56
(42-62) |
56.5
(44-64) |
0.326 |
Onset of illness [d (Q1-Q3) ] |
15
(7-30) |
15
(7-30) |
0.986 |
Medical history of hypertension (n) |
21 |
5 |
0.958 |
Medical history of diabetes (n) |
8 |
3 |
0.456 |
BCVA [logMAR (Q1-Q3)] |
1.92
(1.22-3.00) |
3.00
(2.00-3.00) |
0.001 |
IOP (mm Hg) ( |
12.96±3.55 |
8.60±3.62 |
<0.001 |
aRefractive
error (diopter) [median (Q1-Q3) ] |
-2
(-6 to 0) |
-4
(-9 to -2) |
0.007 |
Lens status (n) |
|
|
0.002 |
Phakic
|
200 |
41 |
|
Pseudophakia |
13 |
11 |
|
Axial length (mm) [Median (Q1-Q3) ] |
24.11
(22.88-26.30) |
24.70
(23.39-27.59) |
0.128 |
Extent of retinal detachment (n) |
|
|
<0.001 |
1
quadrant |
36 |
1 |
|
2
quadrants |
103 |
4 |
|
3
quadrants |
45 |
6 |
|
4
quadrants |
29 |
41 |
|
No. of retinal holes (n) |
|
|
0.044 |
1-2 |
169 |
34 |
|
≥3 |
44 |
18 |
|
Macular hole (n) |
30 |
13 |
0.012 |
IOP was expressed as mean±standard
deviation and other quantitative
results were expressed as Median (quartile1-quartile3) [median (Q1-Q3)]. Axial length was measured with A-scan ultrasonagraphy. aRefractive
error data was obtained from 179 cases of RRD and 43 cases of RRDCD.
Eyes in Group RRDCD had larger extent of retinal detachment than eyes in
Group RRD (P<0.001), and 78.85%
eyes in Group RRDCD had nearly total retinal detachment (>3 quadrants)
compared with 13.62% eyes in Group RRD.
In Group RRDCD, 34.62% of eyes presented with more than three holes and 25.00%
with macular holes. In Group RRD, 20.66% of eyes presented with more than three
holes and 14.08% with macular holes. There were significant differences between
the two groups (P=0.044, P=0.012, respectively).
Ten related factors were included in stepwise logistic regression
analysis. The results showed that high myopia, low IOP, and larger extent of
retinal detachment were significant factors for developing CD (Table 2).
Table 2 Relative risks
for choroidal detachment
n (%)
Risk factors |
Without
choroidal detachment (n=213) |
With
choroidal detachment (n=52) |
Odds
ratio (95%CI) |
P |
Gender (male) |
102
(47.8) |
31
(59.61) |
0.961
(0.477-1.937) |
0.912 |
Old age |
80
(37.56) |
23
(44.23) |
1.740
(0.817-3.705) |
0.151 |
Severe impaired VA |
149
(69.95) |
47
(90.38) |
0.837
(0.355-1.974) |
0.685 |
Pseudophakia |
13
(6.10) |
11
(21.15) |
1.680
(0.573-4.929) |
0.345 |
Low IOP |
24
(11.27) |
34
(65.38) |
2.442
(1.173-5.083) |
0.017 |
aHigh myopia |
53
(29.61) |
19
(44.18) |
3.619
(1.069-12.259) |
0.039 |
Long AL |
57
(26.76) |
18
(34.62) |
0.508
(0.150-1.721) |
0.277 |
Extent of retinal detachment (1/2/3/4 quadrants) |
36/103/45/29 |
1/4/6/41 |
0.107
(0.030-0.383) |
0.001 |
0.070
(0.028-0.176) |
<0.001 |
|||
0.141
(0.055-0.358) |
<0.001 |
|||
Multiple holes |
44
(20.66) |
18
(34.62) |
1.028
(0.454-2.327) |
0.948 |
Macular hole (+) |
30
(14.08) |
13
(25.00) |
0.476
(0.179-1.265) |
0.137 |
Old age: ≥60; Severely impaired
VA: VA<0.05 (logMAR>1.30); Low IOP: IOP<10 mm Hg; High myopia:
refractive error ≥-6.0 D; Long AL: axial length ≥26.0 mm; Multiple holes:
Causative holes ≥3. aRefractive error data of high myopia was
obtained from 179 cases of RRD and 43 cases of RRDCD.
DISCUSSION
In this study, we performed an analysis of the risk factors for RRDCD. A retrospective review of 265
consecutive cases of RRD was performed and 52 cases with CD were found. The
incidence of CD in RRD in our report is 19.62%, which is higher than previous
reports in Western countries[1-3].
The higher rates of CD in our study might be attributable to the higher
prevalence of high myopia in Chinese and the use of UBM. As our results have
shown, severe myopia was one of the main risk factors for RRDCD. Chinese people
have the higher prevalence of myopia than non-Chinese people, especially for
high myopia[8-10]. In the present study,
44.18% of the eyes with CD were high myopia, compared with 25% and 22.7% in Gottlieb’s[2] and Seelenfreund et al’s[1]
reports, respectively. A study[11] on RRDCD
in Chinese patients had also shown that 51.52% eyes of RRDCD had
high myopia, which was similar to our results.
UBM can detect
the detachment of the ciliary body and anterior choroid, which is difficult for
indirect
ophthalmoscopy and B-type ultrasound[12]. In our
study, some patients presented with characteristics of CD, such as hypotony,
deeper anterior chamber, or iritis, but no CD was detected on fundus
examination and B-type ultrasound. UBM examination found signs of detachment of
ciliary body or anterior choroid in some of these patients. Li et al[11]
showed that UBM was able to detect those RRDCD cases that had been previously
missed on three-mirror funduscope or B-type ultrasound; they also demonstrated
that UBM examination can reduce the false negative rate of RRDCD.
In our study, we
did not find a relationship between CD and systemic factors including sex, age,
onset of illness, or medical history of hypertension and diabetes. Some reports[1,4,13] have concluded that the
majority of RRDCD patients were older, and age is a factor associating with
RRDCD. But these studies lacked detailed statistical comparisons. A total of
44.23% cases of RRDCD in our study were older than 60, which agreed with these
reports. However, statistical analysis failed to detect a significant relation
with CD.
Previous reports[1-5,11,13] have shown that ocular
predisposing factors include hypotony, aphakia/pseudophakia, high myopia, and macular hole. According
to our study, the BCVA, IOP, lens status, refractive error, extent of retinal detachment,
number of holes, and presence of macular hole were related to RRDCD. Low IOP,
high myopia, and larger extent of retinal detachment were significant and
independent risk factors for RRDCD.
We found that
patients with RRDCD tend to have worse visual acuity, which has not been
described by other reports. It might be caused by larger extent of retinal
detachment involving macular, macular hole, and amblyopia induced by
uncorrected high myopia. Moreover, it also may be due to inherent derangement and
retinal pigment epithelial (RPE)
cells abnormality from choroidal and retina detachment.
In the present study, no cases of aphakia were involved. Our results
showed pseudophakia was related to RRDCD. Cataract surgery could disturb the
vitreous and cause its traction and liquefaction, which might induce macular
hole, multiple retinal tear, or larger extent of retinal detachment[14], especially when the rupture of
posterior capsule occurred[15]. In our
cases with pseudophakia, we could not find detailed medical records describing
posterior capsule during their previous cataract surgery. Further investigation
is needed to understand this relationship.
RRDCD cases
tended to have multiple retinal breaks. A previous study[11]
also described that 33% of patients with RRDCD have multiple holes and that
there was significant difference compared with RRD patients. Our data was
similar to it, which suggests that surgeons should carefully search for
additional holes when operating on RRDCD patients.
Kang et al[16]
reported macular hole as a risk factor of RRDCD. These authors concluded that
in cases of RRD with macular holes and posterior vitreous detachment, the
liquefied vitreous passes through macular hole without inhibition and is
absorbed by RPE cells, which results in hypotony and
CD[13,16]. Our results are in agreement
with that study. Moreover, 11 out of 13 cases of macular hole with RRDCD in our
study had high myopia and with posterior staphyloma, which implies that more
accurate, myopic macular hole, may be a risk factor of RRDCD. However, this is
just speculative as the number of cases was relatively small, which yielded low
reliability for statistical analysis.
Hypotony was one
of the essential characteristics and independent risk factors of RRDCD in our
report. Although hypotony may be a consequence of RRDCD rather than a risk
factor, most authors agree that ciliary edema and detachment caused by inflammatory
response reduces aqueous secretion, induces hypotony, and the hypotony could
favor further exudation of fluid out of vessels into the tissue space and
aggravate CD in turn[1-2,13,16]. So
hypotony takes part in the pathogenesis of RRDCD to some extent and might be
set as a risk factor.
High myopia is
defined as having a refractive error of at least -6.0 D or an axial length more
than 26.0 mm in the study[17-18]. Our
results showed that it is the independent risk factors of RRDCD. Vitreous
liquefaction is more prone to take place in eyes with high myopia[19], which predisposing to retinal tear
or macular hole formation[20].
Furthermore, eyes with high myopia had much thinner choroid[21],
so the drop of IOP in RRDCD may aggravate transudation of fluid and CD in these
eyes[2]. These pathologic changes might
associate with the longer axial length and staphyloma. However, as we showed
although refractive
error was much more myopic in Group RRDCD than in Group RRD, while cases with
high myopia (≥-6.0 D) in Group RRDCD were
significantly more than that in Group RRD, there is no difference in axial length between two groups.
There are three possibilities to explain this. First, there is measurement bias
by A-type ultrasound, especially in patients with RRDCD; second, sample size is
relatively small. There are 18 cases of RRD with axial length longer than 26.0
mm, which might yield experimental error; finally, high myopes tended to have
cataract of higher nuclear density, which might influence the refractive power[22]. So it might be not axial length,
but refractive factors such as lens or cornea affecting the refractive error.
In our study, cataract type and keratometric values of cases had not been
measured and recorded. Thus, further investigation should be taken to elucidate
this.
A significantly
greater extent of retinal detachment was found in RRDCD patients, a finding
that has not been described by any other study as a risk factor. Gottlieb[2] and Seelenfreund et al[1]
described totally detached retinas in 31/35 (88.57%) and 41/50 (82%)
RRDCD eyes, which agrees with our present data. Larger extent of retinal detachment
might be more commonly associated with macular detachment. This might partly
explain the worse visual acuity in RRDCD patients. Larger extent of RD and
multiple holes would expose more retinal pigment epithelium cells to vitreous
or subretinal fluid, which could lead to more severe ocular inflammation and
more outflow of fluid through the RPE[23-24], which
play a role in pathogenesis of hypotony and CD[13].
Clinical treatment of RRDCD remains challenging. The retinal reattachment
ratio after the surgery is still lower than that of uncomplicated RRD patients[4]. Our results may be helpful in
understanding pathogenesis and treatment of this disease.
There are
several other limitations in our study. First, the documented extent of retinal
detachment might be masked by CD. A more accurate description could be made
after the alleviation of CD. Second, the sample size is limited. Larger samples
would provide more accurate analysis and multicenter clinical studies are
needed to confirm the findings.
Third, this study was undertaken in a Chinese population. Hence there is a
population bias and the results and conclusions may not be applicable to the
rest of the world population.
ACKNOWLEDGEMENTS
Conflicts of
Interest: Gu YH, None; Ke
GJ, None; Wang L, None; Gu QH, None; Zhou EL, None; Pan
HB, None; Wang SY, None
REFERENCES
1 Seelenfreund MH, Kraushar MF,
Schepens CL, Freilich DB. Choroidal detachment associated with primary retinal
detachment. Arch Ophthalmol 1974;
91(4): 254-258. [CrossRef]
2 Gottlieb F. Combined choroidal and retinal
detachment. Arch Ophthalmol 1972;
88(5): 481-486. [CrossRef]
3 Azad R, Tewari HK, Khosla PK. Choroidal detachment
in association with retinal detachment. Indian
J Ophthalmol 1984;32(3):143-147. [PubMed]
4 Sharma T, Gopal L, Badrinath SS. Primary
vitrectomy for rhegmatogenous retinal detachment associated with choroidal
detachment. Ophthalmology
1998;105(12):2282-2285. [CrossRef]
5 De Smedt S, Sullivan P. Massive choroidal
detachment masking overlying primary rhegmatogenous retinal detachment: a case
series. Bull Soc Belge Ophtalmol
2001;(282):51-55. [PubMed]
6 Adelman RA, Parnes AJ, Michalewska Z, Ducournau D;
European Vitreo-Retinal Society (EVRS) Retinal Detachment Study Group. Clinical
variables associated with failure of retinal detachment repair: the European
vitreo-retinal society retinal detachment study report number 4. Ophthalmology 2014;121(9):1715-1719 [CrossRef] [PubMed]
7 Rahman N, Harris GS. Choroidal detachment
associated with retinal detachment as a presenting finding. Can J Ophthalmol 1992;27(5):245-248. [PubMed]
8 Pan CW, Klein BE, Cotch MF, Shrager S, Klein R,
Folsom A, Kronmal R, Shea SJ, Burke GL, Saw SM, Wong TY. Racial variations in
the prevalence of refractive errors in the United States: the multi-ethnic
study of atherosclerosis. Am J Ophthalmol
2013;155(6):1129-1138. [CrossRef]
[PubMed] [PMC free article]
9 Pan CW, Zheng YF, Anuar AR, Chew M, Gazzard G,
Aung T, Cheng CY, Wong TY, Saw SM. Prevalence of refractive errors in a
multiethnic Asian population: the Singapore epidemiology of eye disease study. Invest Ophthalmol Vis Sci 2013;54(4):2590-2598. [CrossRef] [PubMed]
10 Sng CC, Lin XY, Gazzard G, Chang B, Dirani M,
Chia A, Selvaraj P, Ian K, Drobe B, Wong TY, Saw SM. Peripheral refraction and
refractive error in Singapore Chinese children. Invest Ophthalmol Vis Sci 2011;52(2):1181-1190. [CrossRef] [PubMed]
11 Li Z, Li Y, Huang X, Cai XY, Chen X, Li S, Huang
Y, Lu L. Quantitative analysis of rhegmatogenous retinal detachment associated
with choroidal detachment in Chinese using UBM. Retina (Philadelphia, Pa) 2012;32(10): 2020-2025. [CrossRef] [PubMed]
12 Jiang Y, He M, Huang W, Huang Q, Zhang J, Foster
PJ. Qualitative assessment of ultrasound biomicroscopic images using standard
photographs: the liwan eye study. Invest
Ophthalmol Vis Sci 2010;51(4):2035-2042. [CrossRef] [PubMed] [PMC free article]
13 Jarrett WH 2nd. Rhematogenous retinal detachment
complicated by severe intraocular inflammation, hypotony, and choroidal
detachment. Trans Am Ophthalmol Soc
1981;79:664-683. [PMC free article]
[PubMed]
14 Kuhn F, Aylward B. Rhegmatogenous retinal
detachment: a reappraisal of its pathophysiology and treatment. Ophthalmic Res 2014;51(1):15-31. [CrossRef] [PubMed]
15 Ti SE, Yang YN, Lang SS, Chee SP. A 5-year audit
of cataract surgery outcomes after posterior capsule rupture and risk factors
affecting visual acuity. Am J Ophthalmol
2014;157(1):180-185.el
16 Kang JH, Park KA, Shin WJ, Kang SW. Macular hole
as a risk factor of choroidal detachment in rhegmatogenous retinal detachment. Korean J Ophthalmol 2008;22(2):100-103.
[CrossRef] [PubMed] [PMC free article]
17 Grossniklaus HE, Green WR. Pathologic findings in
pathologic myopia. Retina (Philadelphia,
Pa) 1992;12(2):127-133. [CrossRef]
18 Curtin BJ. Physiologic vs pathologic myopia:
genetics vs environment. Ophthalmology
1979;86(5):681- 691. [CrossRef]
19 Morita H, Funata M, Tokoro T. A clinical study of
the development of posterior vitreous detachment in high myopia. Retina (Philadelphia, Pa)
1995;15(2):117-124. [CrossRef]
20 Mitry D, Fleck BW, Wright AF, Campbell H,
Charteris DG. Pathogenesis of rhegmatogenous retinal detachment: predisposing
anatomy and cell biology. Retina
(Philadelphia, Pa) 2010;30(10):1561-1572. [CrossRef] [PubMed]
21 Ikuno Y, Fujimoto S, Jo Y, Asai T, Nishida K.
Choroidal thinning in high myopia measured by optical coherence tomography. Clin Ophthalmol 2013;7:889-893. [CrossRef] [PubMed] [PMC free article]
22 Praveen MR, Vasavada AR, Jani UD, Trivedi RH,
Choudhary PK. Prevalence of cataract type in relation to axial length in
subjects with high myopia and emmetropia in an Indian population. Am J Ophthalmol 2008;145(1):176-181. [CrossRef] [PubMed] [PMC free article]
23 Kaufman PL, Podos SM. Subretinal fluid
butyrylcholinesterase. 1. Source of the enzyme and factors affecting its
concentration in subretinal fluid from primary rhegmatogenous retinal
detachments. Am J Ophthalmol
1973;75(4): 627-636. [PMC free article]
[PubMed]
24 Dai Y,
Wu Z, Sheng H, Zhang Z, Yu M, Zhang Q. Identification of inflammatory mediators
in patients with rhegmatogenous retinal detachment associated with choroidal detachment. Mol
Vis 2015;21:417-427.
[Top]