Skip to Content
MDPIMDPI

Advanced

JCMJournal of Clinical Medicine
PDF
  • Article
  • Open Access

28 October 2025

10 Pages

Long-Term Outcome of Endothelial Keratoplasty Among Glaucoma Patients and the Risk of Prostaglandin Analogue (Latanoprost) Use on Graft Rejection

,
and
1
Department of Ophthalmology, College of Medicine, King Saud University, Riyadh 12372, Saudi Arabia
2
King Saud University Medical City, King Saud University, Riyadh 12372, Saudi Arabia
3
Refractive Surgery and Myopia Research Group, Research Excellence Center in Ophthalmology and Visual Sciences, Department of Ophthalmology, College of Medicine, King Saud University, Riyadh 12372, Saudi Arabia
*
Author to whom correspondence should be addressed.
J. Clin. Med.2025, 14(21), 7650;https://doi.org/10.3390/jcm14217650
This article belongs to the Section Ophthalmology
Version Notes
Order Reprints

Abstract

Background/Objectives: To evaluate the long-term outcomes of Descemet stripping automated endothelial keratoplasty (DSAEK) in patients with glaucoma and to investigate if the usage of the prostaglandin analog latanoprost increases the risk of graft rejection. Methods: This study retrospectively reviewed 65 eyes of 61 patients with glaucoma who underwent DSAEK at King Abdulaziz University Hospital between 2009 and 2024. The risk factors for graft rejection were identified using Kaplan–Meier survival analysis and univariate and multivariate Cox regression models. Results: The graft survival rates among patients with glaucoma at 1, 3, and 5 years were 72.4%, 23.1%, and 11.5%, respectively. Latanoprost use was significantly associated with graft failure (71.4% vs. 28.6%, p = 0.024). The graft failure was mostly secondary failure (80%, p = 0.015) and was often linked to endothelial rejection episodes (62.5%). Other antiglaucoma medications were not associated with graft failure. Conclusions: Glaucoma decreases graft longevity after DSAEK. Latanoprost use may further increase the risk of graft rejection by enhancing inflammatory or immune responses. Prospective studies are warranted to confirm these findings.

1. Introduction

Endothelial keratoplasty (EK), a widely used effective procedure for managing corneal endothelial failure, is associated with similar visual outcomes and limited complications when compared with penetrating keratoplasty (PKP), especially in patients with no coexisting ocular comorbidities [1,2,3,4,5].
To control intraocular pressure (IOP) in glaucomatous eyes, EK is preferred over PKP [6,7]. Previous studies have demonstrated that glaucomatous eyes are susceptible to graft failure, post-operative complications, and graft dislocation, especially in patients who have undergone glaucoma filtration surgeries showing up to a 50% decrease in graft survival and a two to threefold higher rate of endothelial cell loss compared with non-glaucomatous eyes [8,9,10,11,12,13,14,15,16,17,18].
The risks of glaucoma and glaucoma surgeries have been well documented. However, limited studies have investigated whether antiglaucoma eyedrops, especially prostaglandin analog-based eyedrops, adversely affect graft survival by increasing post-operative inflammation or immune system activation. This study aimed to evaluate EK outcomes among patients with glaucoma, the risk factors for graft rejection, and the effect of topical antiglaucoma drop usage on graft rejection.

2. Methods

2.1. Study Design and Patients

This retrospective study was conducted at King Abdulaziz University Hospital in Riyadh, Saudi Arabia. The medical records of all patients who underwent Descemet stripping automated EK (DSAEK) between January 2009 and December 2024 were reviewed. All cases with a confirmed diagnosis of glaucoma either pre-existing before DSAEK or newly developed postoperatively and with a minimum postoperative follow-up of three months were included. Eyes with only transient postoperative intraocular pressure (IOP) elevation, without a formal glaucoma diagnosis or the need for medical or surgical glaucoma management, were excluded. Because all available eligible cases during the study period were analyzed, no formal sample-size calculation was performed. This study was approved by the Institutional Review Board of King Saud University Medical City (IRB approval number: E-24-9453; dated 26 January 2025) and performed according to the principles of the Declaration of Helsinki.

2.2. Patient Selection and Surgical Approach

All patients with corneal edema who underwent DSAEK and had a history of glaucoma or who developed glaucoma after surgery were eligible for inclusion. The indications included Fuchs’ endothelial dystrophy, pseudophakic bullous keratopathy, aphakic bullous keratopathy, decompensated cornea after silicone oil surgery, decompensated cornea after glaucoma surgery, corneal decompensation after herpetic infection, decompensated penetrating keratoplasty, failed Descemet membrane EK, and cases with no specific known cause. All procedures were performed by board-certified corneal consultants or fellows under supervision. The grafts were inserted using the Busin glide or lens glide technique, depending on the preference of the surgeon. Only the most recent surgery data were included in the analysis for patients who underwent multiple DSAEK procedures on the same eye. This study also included the data of patients who underwent combined procedures (e.g., triple procedures) on the same eyes. Donor tissues were mainly obtained from accredited North American eye banks. After surgery, the patients were typically admitted for two days. The patients were discharged once the graft was confirmed to be attached, the anterior chamber was stable, and no immediate complications were observed. Follow-up visits were arranged based on the judgment of the surgeon. The follow-up was scheduled at 1 week, 1 month, and subsequently once every three months for the first year. Post-operative treatment included topical antibiotics (third-generation or fourth-generation fluoroquinolones), lubricants, and corticosteroids, with the frequency adjusted by the surgeon, all patients received the same corticosteroid regimen, irrespective of their antiglaucoma medications. Patients with a history of herpetic eye disease received systemic antiviral prophylaxis. Steroid-tapering schedules varied depending on the surgeons. Graft rejection cases were managed with intensive topical steroids along with topical cyclosporine in some cases.

2.3. Variables

Data were collected using structured data collection sheets. The variables included demographics, systemic or eye comorbidities (such as retinal diseases, cataract surgery, and previous infection), presence or absence of glaucoma preoperatively, medical or surgical management of glaucoma, lens status and clarity, and pre-operative IOP. The following surgical data were collected: the diagnosis, donor and host graft sizes, and post-operative complications. All complications from the day of surgery until the last follow-up (for successful grafts) or the date of diagnosis of failure (for failed grafts) were documented. Graft rejection was defined as the occurrence of new keratic precipitates, anterior chamber inflammation, or worsening of graft edema in a previously clear graft. This study also recorded whether the graft was detached (partially or completely), whether rebubbling was performed, and any episodes of microbial keratitis (diagnosed clinically and confirmed, when possible, by culture, polymerase chain reaction, or confocal microscopy). Post-operative glaucoma was counted only if it required medical or surgical treatment, and short-term IOP spikes were not included. A persistent epithelial defect was defined as epithelial breakdown lasting >14 days.

2.4. Outcome Measures

The primary outcomes of this study were graft survival among patients with glaucoma and the glaucoma-related risk factors for graft failure.

2.5. Statistical Analysis

Data were collected, stored, and managed in a spreadsheet using Microsoft Excel 2010. Figure preparation and data analyses were performed using SPSS® version 21.0 (IBM Corp, Armonk, NY, USA). Categorical variables are represented as frequencies and percentages and compared using the chi-square test. Fisher’s test was used when the data comprised fewer than five cells. The normality of continuous variables was determined using the Shapiro–Wilk test and Q-Q plots. The non-normally distributed data are reported as median (interquartile range [IQR]) and compared using the Mann–Whitney test. The risk factors for graft failure were determined using univariate and multivariate Cox regression analyses. Additionally, Kaplan–Meier survival curves were plotted to visualize and estimate the cumulative survival probabilities. Differences were considered significant at p < 0.05.

3. Results

3.1. Demographic and Clinical Characteristics

This study examined the data of 65 eyes from 61 patients with glaucoma who underwent EK. The median age of the patients was 68 years (IQR: 60–76). Most patients were males (n = 32; 52.5%) and Saudi nationals (90.2%) (Table 1).
Table 1. Demographic characteristics of patients.
Pre-existing and post-operative glaucoma were noted in 53 (81.5%) and 12 eyes (18.5%), respectively. Medical therapy was required for 48 eyes (73.8%). The most common medical therapies were brimonidine (Alphagan) (45.8%) and dorzolamide and timolol combination (Cosopt) (47.9%). Latanoprost (Xalatan) was used to treat 14 eyes (29.2%). Several patients were on combination therapy, with 22 patients (45.8%) using two medications and 8 patients (16.7%) using ≥3 medications. Surgical intervention was performed on 44 eyes (67.7%), which was mainly trabeculectomy with mitomycin C (45.5%) or Ahmed valve implantation (25%). The proportion of patients who underwent both medical and surgical treatments in the pre-operative glaucoma group was significantly higher than that in the pre-existing glaucoma group (54.7% vs. 8.3%, p = 0.004) (Table 2).
Table 2. Glaucoma treatment strategies.

3.2. Graft Survival Rates

Kaplan–Meier analysis revealed that the graft survival rates were 72.4% ± 6.1%, 23.1% ± 6.8%, and 11.5% ± 7.1% at 1, 3, and 5 years, respectively (Figure 1).
Figure 1. Kaplan–Meier survival curve for graft survival in 65 glaucoma cases.

3.3. Antiglaucoma Drop Use and the Risk of Graft Failure

The graft failure rate in the latanoprost group was significantly higher than that in the other treatment group (71.4% vs. 28.6%, p = 0.024). Most of these failures were classified as secondary graft failures (80%, p = 0.015). Among the graft failure cases, the incidence rate of endothelial rejection episodes was 62.5%. Other antiglaucoma medications, including brimonidine, timolol, and dorzolamide–timolol combination, were not significantly associated with graft failure (Table 3 and Table 4).
Table 3. Univariate analysis of glaucoma risk factors associated with graft failure.
Table 4. Cases treated with latanoprost (Xalatan).
Next, the outcomes of eyes treated with latanoprost were compared with those of eyes treated with other regimens. Patients in the latanoprost-treated group were slightly older than those in the other treatment group (median age: 69 vs. 68 years, p = 0.633). At the time of surgery, all patients in the latanoprost group were pseudophakic. The incidence rate of secondary graft failure in the latanoprost group was significantly higher than that in the other treatment group (57.1% vs. 26.5%, p = 0.043). Other clinical features, including post-operative complications, presence of diabetes, surgical technique, and graft size, were not significantly different between the groups (Table 5).
Table 5. Subgroup analysis of patients who used latanoprost (Xalatan).

4. Discussion

Recently, EK has become the standard surgical approach for managing endothelial dysfunction. Compared with PK, EK offers several significant advantages, including rapid visual recovery, decreased incidence of post-operative astigmatism, and low overall complication rates [1,19]. Furthermore, previous studies have reported that graft survival rates with EK are up to 79% at 10 years, highlighting the long-term effects of the procedure under optimal conditions [4].
However, glaucoma decreases graft longevity. Patients with glaucoma are reported to be associated with decreased survival rates and increased graft failure rates [3,4,20,21,22,23,24]. This is consistent with the findings of this study, which reported that the graft survival rates were 72.4% ± 6.1, 23.1% ± 6.8, and 11.5% ± 7.1 at 1, 3, and 5 years, respectively, among patients with glaucoma. Several factors contribute to the poor outcomes in patients with glaucoma. Structural and physiological alterations in aqueous humor dynamics, especially glaucoma surgery, may adversely affect graft adhesion, healing, and long-term survival [15,20,25]. These procedures impose additional surgical stress, compromising endothelial health and accelerate endothelial cell loss [8,22,26]. Takemori et al. reported that trabeculectomy was significantly associated with increased endothelial cell loss and graft failure [8]. Moreover, eyes that have undergone trabeculectomy may experience earlier graft failure (25). Kang et al. and Decroos et al. revealed an increased risk of failure in eyes with aqueous shunt devices [10,16]. Nahum et al. reported that the presence of an aqueous shunt increases the risk of repeat surgery [18]. These findings indicate the challenges associated with managing corneal transplantation in eyes with glaucoma.
In addition to the surgical factors, the medical management of glaucoma after endothelial keratoplasty also plays a crucial role. Previous studies have shown that the need for escalation of antiglaucoma therapy following DSAEK ranges from 4% to 47.4% of eyes, reflecting the difficulty in achieving stable intraocular pressure control in these patients [27,28,29]. Such postoperative IOP fluctuations and the requirement for intensified pharmacological treatment may further compromise endothelial cell viability and graft survival.
Latanoprost is a well-established and effective treatment for reducing IOP, offering long-lasting control with minimal systemic effects compared with timolol [30,31,32]. However, its influence on corneal graft health remains uncertain.This study examined the role of the use of topical antiglaucoma medications (latanoprost), an underrecognized but clinically significant variable, in graft rejection after DSAEK. Latanoprost use was significantly associated with graft rejection. Among the eyes treated with latanoprost, the graft success and failure rates were 28.6% and 71.4%, respectively. Additionally, 80% of graft failure cases were classified as secondary graft failures. The incidence of endothelial rejection among graft failure cases was 62.5%. These findings may be explained by the underlying immune mechanisms of post-keratoplasty inflammation. Maharana et al. highlighted that corneal graft rejection results from activation of antigen-presenting cells and T-cell-mediated cytokine cascades once the cornea’s immune privilege is disrupted. Prostaglandin analogues such as latanoprost may further amplify this immune activation by increasing vascular permeability and facilitating leukocyte recruitment, thereby predisposing the graft to inflammatory rejection [33]. In line with this mechanism, previous case reports and observational studies, which reported that prostaglandin analogs, though effective in reducing IOP, compromise corneal graft survival by exacerbating low-grade inflammation. Nouri-Mahdavi et al. described two cases of immunologic graft rejection after the initiation of topical latanoprost [34]. Warwar RE et al. [35] revealed that latanoprost triggers intraocular inflammation as evidenced by the episodes of anterior uveitis and cystoid macular edema. Dvivedi et al. reported a case of severe bilateral herpetic endotheliitis after latanoprost use [36]. Moreover, studies have demonstrated that prostaglandin analogues can disrupt the blood aqueous barrier, leading to increased protein leakage and intraocular inflammation. Miyake et al. reported that latanoprost accelerates disruption of the blood aqueous barrier and increases the incidence of cystoid macular edema in early postoperative pseudophakic eyes [37], while Arcieri et al. confirmed similar findings in pseudophakic and aphakic patients during a 6-month randomized trial [38]. These findings further support the hypothesis that prostaglandin-induced barrier breakdown may facilitate inflammatory mediator entry into the anterior chamber, predisposing the graft to immune rejection.
The proinflammatory effect may be specific to prostaglandin analogs. Other commonly used antiglaucoma agents examined in this study, such as timolol, brimonidine, and dorzolamide–timolol combination, were not significantly associated with graft failure. Thus, glaucoma can compromise long-term graft survival after DSAEK, with latanoprost use being associated with increased risk of graft failure. As this was a retrospective analysis, causality cannot be established. However, the observed patterns of secondary failures and endothelial rejection episodes raise important clinical considerations. The identification of these risks allows ophthalmologists to tailor post-operative glaucoma management strategies, potentially improving the graft outcomes in this vulnerable population.
Additionally, when comparing patients who used latanoprost with those who received other glaucoma treatments, no significant differences in demographic characteristics, including gender distribution, were observed. This indicates that gender was not a contributing factor to the differences in graft survival between the two groups.
This study had some limitations. The results of this study cannot be generalized as this was a retrospective, single-center study with a relatively small cohort, especially in the latanoprost subgroup. Additionally, the details of antiglaucoma medications, such as duration of use and patient compliance, were not consistently available, which may affect the outcomes. Furthermore, the lack of serial endothelial cell count data limited the analysis of endothelial health and the mechanisms of graft failure. Finally, although this study demonstrated that latanoprost use was significantly associated with graft failure, the causality could not be confirmed. Large prospective multicenter studies with standardized reporting are needed to confirm these findings and to better understand the inflammatory pathways linked to prostaglandin use. Future work should also compare different antiglaucoma regimens to identify safer alternatives for post-keratoplasty patients. Establishing clear clinical guidelines for managing glaucoma after endothelial keratoplasty may ultimately help improve long-term graft survival and patient outcomes.

5. Conclusions

DSAEK offers a reliable and less invasive option for visual rehabilitation in patients with glaucoma. However, the presence of glaucoma remains a major factor limiting long-term graft survival. In our cohort, graft failure was often secondary and frequently linked to endothelial rejection, particularly among patients using prostaglandin analogues. These findings highlight the need for cautious use of prostaglandins and close postoperative monitoring to maintain graft clarity.

Author Contributions

Conceptualization, M.S.A.; Data curation, M.M.A. and M.Z.A.; Formal analysis, M.Z.A.; Methodology, M.S.A., M.M.A. and M.Z.A.; Supervision, M.S.A. and M.M.A.; Writing—original draft, M.Z.A.; Writing—review & editing, M.S.A., M.M.A. and M.Z.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki and approved by the Institutional Review Board of King Saud University Medical City (IRB approval number: E-24-9453; dated 26 January 2025).

Data Availability Statement

The datasets generated during and/or analyzed during the current study are not publicly available due to legal issues and the policy of our institution.

Acknowledgments

Ongoing Research Funding Program (ORF-Ctr-2025-11), King Saud University, Riyadh, Saudi Arabia.

Conflicts of Interest

All authors declare no conflicts of interest.

References

  1. Price, D.A.; Kelley, M.; Price, F.W., Jr.; Price, M.O. Five-Year Graft Survival of Descemet Membrane Endothelial Keratoplasty (EK) versus Descemet Stripping EK and the Effect of Donor Sex Matching. Ophthalmology 2018, 125, 1508–1514. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  2. Terry, M.A.; Aldave, A.J.; Szczotka-Flynn, L.B.; Liang, W.; Ayala, A.R.; Maguire, M.G.; Croasdale, C.; Daoud, Y.J.; Dunn, S.P.; Hoover, C.K.; et al. Donor, Recipient, and Operative Factors Associated with Graft Success in the Cornea Preservation Time Study. Ophthalmology 2018, 125, 1700–1709. [Google Scholar] [CrossRef] [Scilit] [PubMed] [PubMed Central]
  3. Wakimasu, K.; Kitazawa, K.; Kayukawa, K.; Yokota, I.; Inatomi, T.; Hieda, O.; Sotozono, C.; Kinoshita, S. Five-year follow-up outcomes after Descemet’s stripping automated endothelial keratoplasty: A retrospective study. BMJ Open Ophthalmol. 2020, 5, e000354. [Google Scholar] [CrossRef] [Scilit] [PubMed] [PubMed Central]
  4. Fu, L.; Hollick, E.J. Long-term Outcomes of Descemet Stripping Endothelial Keratoplasty: Ten-Year Graft Survival and Endothelial Cell Loss. Am. J. Ophthalmol. 2022, 234, 215–222. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  5. Wilhelm, T.I.; Gauché, L.; Böhringer, D.; Maier, P.; Heinzelmann, S.; Glegola, M.; Kammrath Betancor, P.; Reinhard, T. Ten-year outcomes after DMEK, DSAEK, and PK: Insights on graft survival, endothelial cell density loss, rejection and visual acuity. Sci. Rep. 2025, 15, 1249. [Google Scholar] [CrossRef] [Scilit] [PubMed] [PubMed Central]
  6. Wandling, G.R., Jr.; Rauen, M.P.; Goins, K.M.; Kitzmann, A.S.; Sutphin, J.E.; Kwon, Y.H.; Alward, W.L.; Wagoner, M.D. Glaucoma therapy escalation in eyes with pseudophakic corneal edema after penetrating keratoplasty and Descemet’s stripping automated endothelial keratoplasty. Int. Ophthalmol. 2012, 32, 9–14. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  7. Aldarrab, A.; Alsakran, W.; Al-Swailem, S.A.; Al-Shahwan, S.A. Comparison of Glaucoma Therapy Escalation After Penetrating Keratoplasty to Descemet Stripping Automated Endothelial Keratoplasty for the Treatment of Pseudophakic Bullous Keratopathy: A Cohort Study. Middle East Afr. J. Ophthalmol. 2023, 29, 72–79. [Google Scholar] [CrossRef] [Scilit] [PubMed] [PubMed Central]
  8. Takemori, H.; Higashide, T.; Kobayashi, A.; Yokogawa, H.; Sugiyama, K. Glaucoma-Related Risk Factors for Endothelial Cell Loss and Graft Failure After Descemet’s Stripping Automated Endothelial Keratoplasty. J. Glaucoma 2023, 32, e95–e102. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  9. Pedersen, I.B.; Ivarsen, A.; Hjortdal, J. Graft rejection and failure following endothelial keratoplasty (DSAEK) and penetrating keratoplasty for secondary endothelial failure. Acta Ophthalmol. 2015, 93, 172–177. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  10. Decroos, F.C.; Delmonte, D.W.; Chow, J.H.; Stinnett, S.S.; Kim, T.; Carlson, A.N.; Afshari, N.A. Increased Rates of Descemet’s Stripping Automated Endothelial Keratoplasty (DSAEK) Graft Failure and Dislocation in Glaucomatous Eyes with Aqueous Shunts. J. Ophthalmic Vis. Res. 2012, 7, 203–213. [Google Scholar] [PubMed] [PubMed Central]
  11. Aiello, F.; Matarazzo, F.; Phylactou, M.; Muthusamy, K.; Maurino, V. Endothelial Keratoplasty Following Glaucoma Filtration Surgery: A UK Tertiary Eye Care Referral Centre Experience. J. Clin. Med. 2024, 13, 6097. [Google Scholar] [CrossRef] [Scilit] [PubMed] [PubMed Central]
  12. Ward, M.S.; Goins, K.M.; Greiner, M.A.; Kitzmann, A.S.; Sutphin, J.E.; Alward, W.L.; Greenlee, E.C.; Kwon, Y.H.; Zimmerman, M.B.; Wagoner, M.D. Graft survival versus glaucoma treatment after penetrating or Descemet stripping automated endothelial keratoplasty. Cornea 2014, 33, 785–789. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  13. Quek, D.T.; Wong, T.; Tan, D.; Mehta, J.S. Corneal graft survival and intraocular pressure control after descemet stripping automated endothelial keratoplasty in eyes with pre-existing glaucoma. Am. J. Ophthalmol. 2011, 152, 48–54.e2. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  14. Müller, L.; Kaufmann, C.; Bachmann, L.M.; Tarantino-Scherrer, J.N.; Thiel, M.A.; Bochmann, F. Changes in intraocular pressure after descemet stripping automated endothelial keratoplasty: A retrospective analysis. Cornea 2015, 34, 271–274. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  15. Alshaker, S.; Mimouni, M.; Batawi, H.; Cohen, E.; Trinh, T.; Santaella, G.; Chan, C.C.; Slomovic, A.R.; Rootman, D.S.; Sorkin, N. Four-Year Survival Comparison of Endothelial Keratoplasty Techniques in Patients With Previous Glaucoma Surgery. Cornea 2021, 40, 1282–1289. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  16. Kang, J.J.; Ritterband, D.C.; Lai, K.; Liebmann, J.M.; Seedor, J.A. Descemet Stripping Endothelial Keratoplasty in Eyes With Previous Glaucoma Surgery. Cornea 2016, 35, 1520–1525. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  17. Chiam, P.J.; Cheeseman, R.; Ho, V.W.; Romano, V.; Choudhary, A.; Batterbury, M.; Kaye, S.B.; Willoughby, C.E. Outcome of Descemet stripping automated endothelial keratoplasty in eyes with an Ahmed glaucoma valve. Graefes Arch. Clin. Exp. Ophthalmol. 2017, 255, 987–993. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  18. Nahum, Y.; Mimouni, M.; Busin, M. Risk Factors Predicting the Need for Graft Exchange After Descemet Stripping Automated Endothelial Keratoplasty. Cornea 2015, 34, 876–879. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  19. Fuest, M.; Ang, M.; Htoon, H.M.; Tan, D.; Mehta, J.S. Long-term Visual Outcomes Comparing Descemet Stripping Automated Endothelial Keratoplasty and Penetrating Keratoplasty. Am. J. Ophthalmol. 2017, 182, 62–71. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  20. Anshu, A.; Price, M.O.; Price, F.W. Descemet’s stripping endothelial keratoplasty: Long-term graft survival and risk factors for failure in eyes with pre-existing glaucoma. Ophthalmology 2012, 119, 1982–1987. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  21. Nguyen, P.; Khashabi, S.; Chopra, V.; Francis, B.; Heur, M.; Song, J.C.; Yiu, S.C. Descemet stripping with automated endothelial keratoplasty: A comparative study of outcome in patients with pre-existing glaucoma. Saudi J. Ophthalmol. 2013, 27, 73–78. [Google Scholar] [CrossRef] [Scilit] [PubMed] [PubMed Central]
  22. Schoenberg, E.D.; Levin, K.H.; Savetsky, M.J.; Mcintire, L.U.; Ayyala, R.S. Surgical Outcomes of DSAEK in Patients with Prior Ahmed Glaucoma Drainage Device Placement. Eur. J. Ophthalmol. 2013, 23, 807–813. [Google Scholar] [CrossRef] [Scilit]
  23. Aldave, A.J.; Chen, J.L.; Zaman, A.S.; Deng, S.X.; Yu, F. Outcomes After DSEK in 101 Eyes With Previous Trabeculectomy and Tube Shunt Implantation. Cornea 2014, 33, 223–229. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  24. Iverson, S.M.; Spierer, O.; Papachristou, G.C.; Feuer, W.J.; Shi, W.; Greenfield, D.S.; O’Brien, T.P. Comparison of primary graft survival following penetrating keratoplasty and Descemet’s stripping endothelial keratoplasty in eyes with prior trabeculectomy. Br. J. Ophthalmol. 2015, 99, 1477–1482. [Google Scholar] [CrossRef] [Scilit]
  25. Maurino, V.; Aiello, F. Glaucoma risks in advanced corneal surgery. Prog. Brain Res. 2015, 221, 271–295. [Google Scholar] [CrossRef] [Scilit]
  26. Kim, P.; Amiran, M.D.; Lichtinger, A.; Yeung, S.N.; Slomovic, A.R.; Rootman, D.S. Outcomes of Descemet stripping automated endothelial keratoplasty in patients with previous glaucoma drainage device insertion. Cornea 2012, 31, 172–175. [Google Scholar] [CrossRef] [Scilit]
  27. Wiaux, C.; Baghdasaryan, E.; Lee, O.L.; Bourges, J.L.; Deng, S.X.; Yu, F.; Aldave, A.J. Outcomes after Descemet stripping endothelial keratoplasty in glaucoma patients with previous trabeculectomy and tube shunt implantation. Cornea 2011, 30, 1304–1311. [Google Scholar] [CrossRef] [Scilit]
  28. Kaleem, M.; Ridha, F.; Shwani, Z.; Swenor, B.; Goshe, J.; Singh, A. Rates of Intraocular Pressure Elevation and Use of Topical Antihypertensive Medication After Descemet Stripping Automated Endothelial Keratoplasty. Cornea 2017, 36, 669–674. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  29. Jafari, K.; Ashena, Z.; Niestrata, M. A Review of Outcomes of Descemet Membrane Endothelial Keratoplasty and Descemet Stripping Automated Endothelial Keratoplasty Interventions in Patients with Pre-Existing Glaucoma. J. Clin. Med. 2025, 14, 3534. [Google Scholar] [CrossRef] [Scilit]
  30. Alm, A.; Stjernschantz, J. Effects on intraocular pressure and side effects of 0.005% latanoprost applied once daily, evening or morning. A comparison with timolol. Ophthalmology 1995, 102, 1743–1752. [Google Scholar] [CrossRef] [Scilit]
  31. Camras, C.B. Comparison of latanoprost and timolol in patients with ocular hypertension and glaucoma: A six-month masked, multicenter trial in the United States. The United States Latanoprost Study Group. Ophthalmology 1996, 103, 138–147. [Google Scholar] [CrossRef] [Scilit]
  32. Watson, P.; Stjernschantz, J. A six-month, randomized, double-masked study comparing latanoprost with timolol in open-angle glaucoma and ocular hypertension. The Latanoprost Study Group. Ophthalmology 1996, 103, 126–137. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  33. Maharana, P.K.; Mandal, S.; Kaweri, L.; Sahay, P.; Lata, S.; Asif, M.I.; Nagpal, R.; Sharma, N. Immunopathogenesis of corneal graft rejection. Indian J. Ophthalmol. 2023, 71, 1733–1738. [Google Scholar] [CrossRef] [Scilit]
  34. Nouri-Mahdavi, K.; Javadi, M.A.; Jafarinasab, M.R. Immunologic corneal graft rejection after administration of topical latanoprost: A report of two patients. J. Ophthalmic Vis. Res. 2011, 6, 127–130. [Google Scholar]
  35. Warwar, R.E.; Bullock, J.D.; Ballal, D. Cystoid macular edema and anterior uveitis associated with latanoprost use. Experience and incidence in a retrospective review of 94 patients. Ophthalmology 1998, 105, 263–268. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  36. Dvivedi, A.; Murthy, S.I.; Garudadri, C.; Sheba, E.; Sharma, S. Bilateral Severe Herpes Simplex Endotheliitis with a Possible Association with Latanoprost. Ocul. Immunol. Inflamm. 2023, 31, 1073–1075. [Google Scholar] [CrossRef] [Scilit] [PubMed]
  37. Miyake, K.; Ota, I.; Maekubo, K.; Ichihashi, S.; Miyake, S. Latanoprost accelerates disruption of the blood-aqueous barrier and the incidence of angiographic cystoid macular edema in early postoperative pseudophakias. Arch. Ophthalmol. 1999, 117, 34–40. [Google Scholar] [CrossRef] [Scilit]
  38. Arcieri, E.S.; Santana, A.; Rocha, F.N.; Guapo, G.L.; Costa, V.P. Blood-aqueous barrier changes after the use of prostaglandin analogues in patients with pseudophakia and aphakia: A 6-month randomized trial. Arch. Ophthalmol. 2005, 123, 186–192. [Google Scholar] [CrossRef] [Scilit]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Article Metrics

Citations

Article Access Statistics

Journal Statistics
Multiple requests from the same IP address are counted as one view.
A Comparison of Health-Related Quality of Life in Patients with Periprosthetic Joint Infection, Patients with Fracture-Related Infections and the General Population—A Multicenter Analysis of 384 Patients from the Section “Musculoskeletal Infections” of the German Society for Orthopaedics and Traumatology
Previous
Comparison of Laparoscopic and Laparotomic Total Hysterectomy in Terms of Patient Satisfaction and Cosmetic Outcomes
Next