Journal of Clinical Ophthalmology

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Research Article - Journal of Clinical Ophthalmology (2022) Volume 6, Issue 5

Outcomes of Medical and Surgical Management in Aqueous Misdirection Syndrome

Reham Al Qahtani1*, Adi Mohammed Al Owaifeer2, Sami Al Shahwan1, Khawlah Al Zebn1, Raghad Al Mansour3

1Department of Ophthalmology, Imam Mohammed bin Saud University, Riyadh, Saudi Arabia

2Department of Surgery, King Faisal University, Al-Ahsa, Saudi Arabia

3Department of Medicine, Imam Mohammed bin Saud University, Riyadh, Saudi Arabia

Corresponding Author:
Reham Al Qahtani
Department of Ophthalmology
Imam Mohammed bin Saud University
Riyadh
Saudi Arabia
E-mail: Reham.d.q@hotmail.com

Received: 27-Jul-2022, Manuscript No. AACOVS-22-70444; Editor assigned: 29-Jul-2022, AACOVS-22-70444 (PQ); Reviewed: 12-Aug-2022, QC No. AACOVS-22-70444; Revised: 26-Sep-2022, Manuscript No. AACOVS-22-70444 (R); Published: 03-Oct-2022, DOI: 10.35841/aacovs.6.5.566-573

Citation:Al Qahtani R, Al Owaifeer AM, Al Shahwan S, et al. Outcomes of medical and surgical management in aqueous misdirection syndrome. J Clin Ophthalmol. 2022;6(5):1-8.

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Abstract

Aim: To report the outcomes of medical and surgical management in patients diagnosed with Aqueous Misdirection Syndrome (AMS).

Methods: A retrospective chart review of all cases diagnosed with AMS at a single tertiary care eye center during the period from 2014 to 2021. Outcome measures were anatomical success deepening of the Anterior Chamber (AC), functional success improvement in visual acuity and treatment success control of Intraocular Pressure (IOP).

Results: A total of 26 eyes with AMS from 24 patients were included. The patients were followed for a mean duration of 24 ± 18 months. Although some patients initially responded to medical and laser therapy, all but one (3.8%) eventually required surgery during the first three months after presentation. The mean duration from presentation until surgery was 45.9 ± 45.8 days (range: 2-119). The majority of cases (69.2%) were managed by pars plana vitrectomy. At the last follow-up visit, anatomical success was achieved in twenty (76%) eyes, 15 (57%) eyes had a final visual acuity that was either similar to or better than baseline and successful control of IOP was achieved in 17 (65%) eyes. Univariate analysis revealed that a history of trabeculectomy as a cause of AMS was a risk factor for treatment failure (OR, 7.8; 95% CI, 1.16-52.35; P, 0.02).

Conclusion: Our findings indicate that medical and laser management of AMS provide temporary control and almost all patients eventually require surgery within the first three months. A history of trabeculectomy was found to be a risk factor for treatment failure.

Abstract

Aim: To report the outcomes of medical and surgical management in patients diagnosed with Aqueous Misdirection Syndrome (AMS).

Methods: A retrospective chart review of all cases diagnosed with AMS at a single tertiary care eye center during the period from 2014 to 2021. Outcome measures were anatomical success deepening of the Anterior Chamber (AC), functional success improvement in visual acuity and treatment success control of Intraocular Pressure (IOP).

Results: A total of 26 eyes with AMS from 24 patients were included. The patients were followed for a mean duration of 24 ± 18 months. Although some patients initially responded to medical and laser therapy, all but one (3.8%) eventually required surgery during the first three months after presentation. The mean duration from presentation until surgery was 45.9 ± 45.8 days (range: 2-119). The majority of cases (69.2%) were managed by pars plana vitrectomy. At the last follow-up visit, anatomical success was achieved in twenty (76%) eyes, 15 (57%) eyes had a final visual acuity that was either similar to or better than baseline and successful control of IOP was achieved in 17 (65%) eyes. Univariate analysis revealed that a history of trabeculectomy as a cause of AMS was a risk factor for treatment failure (OR, 7.8; 95% CI, 1.16-52.35; P, 0.02).

Conclusion: Our findings indicate that medical and laser management of AMS provide temporary control and almost all patients eventually require surgery within the first three months. A history of trabeculectomy was found to be a risk factor for treatment failure.

Keywords

Anterior chamber, Aqueous misdirection syndrome, Intraocular pressure, Hyperosmotic therapy, Trabeculectomy

Introduction

Aqueous Misdirection Syndrome (AMS) or malignant glaucoma is a relatively uncommon cause of secondary angle closure glaucoma that can threaten vision if not treated early [1]. It occurs due to anterior rotation of the ciliary body resulting in a misdirected pathway of aqueous humour posteriorly and blockage of the movement into the Anterior Chamber (AC) at the level of the equator of the lens, vitreous face and ciliary processes.

Clinically, it presents as axial shallowing of the AC despite a patent Peripheral Iridotomy (PI) with elevated or normal Intraocular Pressure (IOP). It is considered a diagnosis of exclusion, after ruling out mimickers i.e. pupillary block, serous and hemorrhagic choroidal detachment [2]. AMS may occur following any type of intraocular surgery, but it is most commonly associated with glaucoma surgery [3,4].

The initial management is medical by topical drops (e.g. cycloplegics, sympathomimetics, beta-blockers), in addition to systemic hyperosmotic therapy. The aim of treatment is to shrink the vitreous, displace the lens iris diaphragm and decrease aqueous production. In addition to medical treatment, Nd-Yag laser hyaloidotomy and capsulotomy are laser interventions that are used to treat AMS.

Surgical management is indicated in the event of a failure in the aforementioned treatment modalities and the aim of surgery is to increase the aqueous flow into the AC by either disrupting the vitreous face via trans-corneal needling or removing the vitreous by anterior or Pars Plana Vitrectomy (PPV) [5-9]

The majority of AMS reports in the literature focus on a single treatment modality (e.g. PPV) [10-13]; thus, there is a limited amount of data on the combined outcomes of AMS treatment following different types of interventions. Therefore, the aim of our current study is to report the treatment outcomes of a serial cohort of AMS patients managed at a tertiary care eye hospital.

Materials and Methods

Study design and sample size

We performed a retrospective chart review of all patients diagnosed with AMS (ICD code: H40.839) from 2014 to 2021 at a single tertiary eye care center. The diagnostic criteria of AMS were elevated IOP associated with a uniform (central and peripheral) shallowing of the AC in the presence of a patent PI and the absence of any posterior segment pathology (e.g. choroidal effusion, suprachoroidal hemorrhage, posterior segment tumor).

Demographics and clinical information

At presentation, the following demographic and clinical details were obtained from the electronic medical records: age, sex, systemic disease, laterality of the affected eye, best corrected visual acuity, IOP, refraction, axial length, lens status, cup to disc ratio, number of glaucoma medications used, history of any ocular disease and past surgical history. We also documented whether the patient was diagnosed before presentation at our institute and if so, the period from diagnosis until presentation at our hospital.

In each subsequent follow-up visit, we documented the following: Best corrected visual acuity, IOP, number of glaucoma medications used, AC depth, complications, recurrence and the need for additional laser and/or surgical intervention.

Outcome measure

The three outcome measures in our study were: Anatomical success, functional outcome and treatment success. Anatomical success was defined as further deepening of the AC compared to presentation. The functional outcome was assessed by comparing baseline best corrected visual acuity and acuity at the final follow-up visit. Finally, treatment success was defined as success in achieving an IOP level between 5 and 21 mmHg either with or without glaucoma medications and without loss of light perception.

Data analysis

Statistical analysis was performed using R (RStudio version 1.1.463 Mac, RStudio Inc., Boston, MA). Quantitative variables were reported in mean ± Standard Deviation (SD) and evaluated using the Student’s t-test, while categorical variables were reported in percentages and numbers. Kaplan- Meier survival analysis was used to estimate the success rate in cases that underwent PPV. P-values < 0.05 were considered as statistically significant.

Results

Baseline characteristics are outlined in Table 1. Twenty-six eyes of 24 patients were included. The mean age of patients was 57.8 ± 22.9 (range from 4-87 years old) and 15 (62%) were female. Five patients (20%) were diagnosed with AMS prior to presentation at our institute with a mean duration of 28.2 ± 20.4 (range 7-80) days from diagnosis until presentation. Eighteen (69%) patients were previously diagnosed with glaucoma and the most common type was primary angle-closure glaucoma (72%). At presentation, the mean IOP was 27.2 ± 10.3 mmHg (range: 9-45) and the mean number of glaucoma medications used was 2.4 ± 1.8 (range: 0-4).

Eyes 26  
Patients 24  
Age
Mean (SD) 57.8 (22.9)  
Range Apr-87  
  n %
Sex
Male 9 37.5
Female 15 62.5
Eye  
Right 13 50.0
Left 13 50.0
Systemic diseases
DLD 6 25.0
IDA 1 4.2
Hypothyroidism 1 4.2
DVT 1 4.2
Bronchial asthma 3 12.5
DM 2 8.3
HTN 5 20.8
Renal Cancer 1 4.2
BPH 1 4.2
IHD 1 4.2
CKD 2 8.3
Diagnosed with AMD prior to presentation?
Yes 5 19.2
No 21 80.8
If Yes, duration (in days) since diagnosis
Mean (SD) 28.2 (20.4)  
Range 7-60  
Time from precipitating surgery until AMD diagnosis
Mean (SD) 26.1 ( 29.1)  
Range 1-90  
Cause of AMD
Phacoemulsification 6 23.1
Trabeculectomy 8 30.8
ECCE 6 23.1
AGV 4 15.4
PKP + AGV 1 3.8
DSAEK 1 3.8
Diagnosed with glaucoma prior to AMD
Yes 18 69.2
No 8 30.8
    0.0
If Yes, glaucoma diagnosis?
PACG 13 72.2
JOAG 2 11.1
PXG 1 5.6
NVG 1 5.6
Phacomorphic 1 5.6
Prior ocular surgery?
Phacoemulsification 10 38.5
ECCE 3  11.5
Combined ECCE + Trab 1 3.8
PKP 1 3.8
PPV 1 3.8
Tube 4 15.4
Trab 5 19.2
Number of glaucoma medications at presentation
Mean (SD) 2.4 (1.8)  
Range 0-4  
BCVA at presentation
20/80 or better 3 11.5
20/100 to 20/400 11 42.3
CF or worse 12 46.2
Refraction
Mild hyperopia ( 0 to +2 D ) 3 11.5
Moderate hyperopia ( +2 to +6 D ) 0  0.0
High hyperopia ( more than +6 D ) 2 7.7
Myopia 5 19.2
n/a 16 61.5
IOP at presentation
Mean (SD) 27.2 (10.3)  
Range 9-45  
Anterior chamber
Shallow peripherally, deep centrally 4 15.4
Shallow all over 11 42.3
Flat (Iridocorneal touch) 11 42.3
Peripheral iridotomy
Present 17 65.4
Absent 9 34.6
Lens status
Phakic 9 34.6
Pseudophakic 16 61.5
Aphakic 1 3.8
CDR
0.1 1 3.8
0.4 2 7.7 
0.5 2 7.7
0.6 2 7.7
0.7 4 15.4
0.8 4 15.4
0.9 6 23.1
total cup 2 7.7
no view 3 11.5
Axial length (in mm)
15 mm 1 3.8
20 mm 1 3.8
21 mm 1 3.8
22 mm 2 7.7
23 mm 2 7.7
n/a 19 73.1

Table 1: Baseline Characteristics.

The majority (76%) of patients were initially managed with medical treatment, whereas the remaining (24%) underwent laser treatment. Almost all (96.2%) patients eventually required surgery to control AMS. The mean duration from presentation until the first surgery was 45.9 ± 45.8 days (range: 2-119).

Regarding surgical interventions, three (12%) patients underwent AC reformation combined with a surgical PI, all of which failed and eventually required PPV. One (4%) patient underwent AC reformation combined with phacoemulsification and the IOP was controlled in this patient without any further intervention. Four (16%) patients were managed by Cyclophotocoagulation (CPC) that was opted due to poor visual potential. Out of these, the IOP remained controlled in one patient, two patients progressed to no light perception and one patient required an additional session of CPC. Finally, glaucoma drainage device surgery and goniosynechiolysis were performed in one (4%) patient each; both of these patients did not require further intervention.

Eighteen (69%) patients eventually required PPV to control IOP. PPV was combined with phacoemulsification in 3 (12%) patients and glaucoma drainage device surgery in 2 (8%) patients. A Kaplan-Meier curve was plotted to assess the survival probability of patients who underwent PPV (Figure 1). The overall success rate of achieving IOP between 5-21 mmHg at five years was 60%. The mean duration of follow-up was 24.5 ± 18.2 months (range: 8-62). At the last follow-up visit, the mean IOP was 17.2 ± 9.5 mmHg (compared to 27.2 ± 10.3 at baseline, P<0.001) and the mean number of glaucoma medications used was 1.8 ± 1.5 (compared to 3.1 ± 1.4 at baseline, P=0.005).

ophthalmology-survival

Figure 1: Survival analysis of cases that underwent Pars Plana Vitrectomy (PPV) for the management of Aqueous Misdirection Syndrome (AMS).

Table 2 outlines the results of the outcome measures of our study (anatomical success, functional outcome and treatment success). Furthermore, a univariate analysis was performed to identify the risk factors for treatment failure (Table 3). The only factor that was significantly associated with failure was a history of trabeculectomy as the cause of AMS (OR: 7.8, 95% CI: 1.16-52.35, P-value: 0.02).

 Final outcomes of the study n %
Anatomical success*
Yes 20 76.9
No 5 19.2
NA 1 3.8
Functional outcome#
Vision improved 4 15.4
Vision worsened 11 42.3
Same 11 42.3
Treatment success$
Yes 15 57.7
No 11 42.3

Table 2: Final outcomes of the study measures (anatomical success, functional outcome and treatment success).

Variable Treatment Failure Univariate Analysis 
n % OR 95% CI P
Cause of AMD          
Trabeculectomy     7.8 (1.16-52.35) 0.020
Yes 6 54.5      
No 5 45.5      
Phaco     NA NA NA
Yes 0 0.0      
No 11 100.0      
ECCE     1.5 (0.24-9.38) 0.660
Yes 3 27.3      
No 8 72.7      
AGV     0.89 (0.12-6.48) 0.91 
Yes 2 18.2      
No 9 81.8      
Lens status
Phakic 5 45.5 0.44 (0.08-2.27)  0.32
Pseudophakic 6 54.5      
Systemic disease
DM     NA NA NA
Yes 2 18.2    
No 9 81.8      
HTN     2.44 (0.33-17.91) 0.370
Yes 3 27.3      
No 8 72.7      
DLD     1.5 (0.24-9.38) 0.660
Yes 1 9.1      
No 10 90.9      
BA     0.65 (0.05-8.23)  0.740
Yes 1 9.1    
No 10 90.9      

Table 3: Analysis of risk factors for failure of treatment.

Discussion

In our current study, we sought to retrospectively review all cases diagnosed with AMS from presentation until the last follow-up documenting all interventions undergone during management, both medical and surgical. We believe that this would provide more insight into the effectiveness of different treatment modalities and the outcomes of AMS management in general.

AMS can be precipitated by many factors including miotics, YAG laser treatment, diode laser CPC, trauma, intraocular surgeries especially glaucoma surgery. In our study, the most common cause of AMS was trabeculectomy (30.8%) as in previous studies. Other less common causes were cataract surgery, glaucoma drainage device surgery and keratoplasty.

In our study, the initial treatment of AMS was medical in 76.9% of patients. Although some initially responded, almost all patients (96%) eventually required surgery. This finding isin concordance with previously reported papers in the literature [14-16]. This supports the evidence that medical management in AMS is a temporizing measure. Cycloplegics act by tightening the lens zonules to pull the lens posteriorly and reverse shallowing of the AC and subsequently improve the flow of aqueous humour; however, it is evident that the cycloplegics effect does not lead to reversal of the underlying pathology. The IOP lowering effect of glaucoma drops could also explain the short-term control of AMS in our study by medical treatment.

Laser therapy is another treatment approach in AMS management. An anterior hyaloidotomy disrupts the posterior capsule and anterior vitreous face to allow free flow of aqueous between the AC and vitreous. However, in our study it was only effective in one (3.8%) patient. Contrary to our findings, Greenfield et al. reported a series of 10 eyes with AMS, out of which four (40%) responded after laser treatment with deepening of the anterior chamber and normalization of IOP [17]. A possible reason for a better response to laser in their study compared to ours is that half of their patients were openangle glaucoma. In contrast, the majority (72.2%) of our patients were angle closure.

Four patients (16%) in our study were initially treated with AC reformation. Three of these were combined with a surgical PI and one was combined with phacoemulsification. In the 3 cases that were combined with a surgical PI, IOP was not controlled postoperatively and the patients eventually required a PPV, whereas in the case that had AC reformation combined with phacoemulsification, the IOP was controlled without further intervention. Our findings imply that AC reformation alone is not a sufficient intervention to control AMS; however, this does not eliminate the utility of AC reformation. A previous report by Thompson [18] showed that patients undergoing AC reformation at presentation, followed by surgery, had a higher chance of achieving IOP control; this could be explained by the effect of immediate AC reformation on reducing the chances of synechiae formation.

Although CPC can be an inciting factor to AMS, some reports have suggested CPC as a treatment option. Thomas reported 5 hyperopic eyes with AMS that were successfully managed with CPC achieving AC deepening and control of IOP over a follow-up period ranging from 1 to 8 years after a single CPC session in 4 cases and two sessions, one year apart, in one patient [19]. The postulated benefit of CPC in AMS is that it may aid in reversing the rotation of the ciliary body and lead to a disruption of the anterior vitreous phase either via laser energy or the inflammation associated with the procedure [20,21]. In our study, CPC was opted as an intervention in four patients (16%). Among these, two patients ended up with no light perception so no further intervention was performed, one required another session of CPC that was enough to provide adequate IOP control and the last patient was controlled after the first CPC treatment and did not need any further intervention.

PPV is considered the treatment of last resort in refractory cases of AMS. The success rate of PPV in our study was 80 %, 80% and 60% at 1,3 and 5 years respectively. The high success of PPV in AMS reflects its utility in counteracting the underlying mechanism by removing the vitreous, which is congested by the shunted aqueous and subsequently contributing to the posterior displacement of the iris lens diaphragm, which in turn leads to deepening of the AC. Our success rate echoes evidence from previous studies that prove the efficacy of PPV in providing adequate IOP control in patients with AMS.

A history of trabeculectomy as the precipitating factor of AMS was significantly associated with treatment failure in our study (OR: 7.8, 95% CI: 1.16-52.35, P-value: 0.02). This observation was also noticed in the study reported by Thompson, in which trabeculectomy was a significant factor associated with a delay in AMS recovery. It is possible that, of a fistulous tract diverting aqueous into the subconjunctival space posttrabeculectomy impedes AC reformation and control of AMS.

Our study is subject to limitations inherent to retrospective studies. Furthermore, due to failure in documentation, our results lack several objective parameters (e.g. refraction and axial length) that could have added more value to our findings.

Conclusion

In conclusion, medical and laser treatment were only helpful in providing short-term control of AMS and almost all patients eventually required surgical intervention. AC reformation with a surgical PI may temporarily reconstruct the anterior chamber; however, it does not reverse AMS. Although some cases showed good response following either phacoemulsification or CPC, most patients eventually required a PPV. Finally, trabeculectomy was a predictor of treatment failure in our study.

References

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