ABSTRACT
Objective: To present a case of ocular toxoplasmosis. Materials and methods: A sixteen-year-old female patient presented to our clinic with complaints regarding decreased vision in her right eye (BCVA 0.5), starting five days before the exam. Her anamnestic data revealed a previous history of ocular toxoplasmosis in her left eye. OCT scans of the inner retina identified a huge cystic space, located posterior to the inner line, off the outer plexiform layer, with a small amount of hyperreflective foci. Other features of OCT included membranous-like structures on inner borders and elongation and splitting of the inner segment/outer segment junction. In later stages, beginning signs of retinitis and scaring could be observed. Results: The patient was treated with sulfamethoxazole/trimethoprim and prednisolone. After two weeks, total regression occurred and visual acuity and OCT remained stable for 6 months (BCVA 1.0). Discussion: Ocular toxoplasmosis can cause significant vision loss due to retinitis and scarring. Following treatment with sulfamethoxazole/trimethoprim and prednisolone, the patient's condition improved significantly and her visual acuity remained stable. Conclusion: On clinical examination and using OCT, rare morphological cystoid spaces (CS) can be identified as huge outer retina cysts (HORC), which are pathognomonic for posterior uveitis. Abbreviations: HORC = huge outer retinal cyst, OCT = optical coherence tomography, BCVA = best corrected visual acuity, CS = cyst space, OPL = outer plexiform layer, HRF = hyper reflective foci, RPE = retinal pigment epithelium, IS = inner segment, OS = outer segment, ERM = epiretinal membrane, PORT = punctate outer retinal toxoplasmosis, ELM = external limiting membrane.
Subject(s)
Tomography, Optical Coherence , Toxoplasmosis, Ocular , Visual Acuity , Humans , Female , Toxoplasmosis, Ocular/diagnosis , Toxoplasmosis, Ocular/drug therapy , Toxoplasmosis, Ocular/parasitology , Tomography, Optical Coherence/methods , Adolescent , Trimethoprim, Sulfamethoxazole Drug Combination/therapeutic use , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/parasitology , Eye Infections, Parasitic/drug therapy , Fluorescein Angiography/methods , Prednisolone/therapeutic use , Retina/parasitology , Retina/pathology , Glucocorticoids/therapeutic use , Fundus Oculi , Toxoplasma/isolation & purificationABSTRACT
This case highlights the atypical presentation of Foster-Kennedy syndrome (FKS) associated with Neurocysticercosis (NCC), a prevalent cause of space-occupying lesions in areas endemic to the parasite. We report a newly diagnosed case of NCC in a 13-year-old boy who presented with a one-day history of abnormal movements of the left side of the body and no ocular complaints. Fundus examination of the patient revealed temporal disc pallor and a cup disc ratio (CDR) of 0.6 in the right eye suggesting unilateral optic disc atrophy and a hyperaemic disc with CDR 0.3 and blood vessel tortuosity in the left eye suggesting contralateral impending disc edema, mimicking the classic triad of FKS. He was diagnosed with NCC based on clinical features and radiological findings and was started on Carbamazepine (400 mg), Prednisolone (60 mg), Albendazole (400 mg), Acetazolamide (750 mg), and Vitamin B12 complex. Abbreviations: BCVA = Best Corrected Visual Acuity, CDR = Cup-Disc Ratio, CT = Computed Tomography, FKS = Foster Kennedy Syndrome, IDSA = Infectious Diseases Society of America, ICP = Intracranial Pressure, IOP = Intraocular Pressure, MRI = Magnetic Resonance Imaging, NCC = Neurocysticercosis, OOC = Orbital/Ocular Cysticercosis, OD = Right Eye, OS = Left Eye, OU = Both Eyes, RNFL = Retinal Nerve Fibre Layer, WNL = Within Normal Limits.
Subject(s)
Neurocysticercosis , Humans , Male , Neurocysticercosis/diagnosis , Neurocysticercosis/complications , Neurocysticercosis/drug therapy , Adolescent , Magnetic Resonance Imaging , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/parasitology , Visual Acuity , Tomography, X-Ray Computed , Papilledema/diagnosis , Papilledema/etiology , Papilledema/drug therapy , Papilledema/parasitology , Optic Atrophy/diagnosis , Optic Atrophy/etiologyABSTRACT
BACKGROUND: Prior case reports and animal studies have reported on potential ophthalmologic complications of babesiosis, but this issue has not previously been addressed in a cohort of patients with babesiosis. This cross-sectional descriptive pilot study evaluated the retinas of patients with acute babesiosis to determine if retinal abnormalities are a feature of the disease. METHODS: We screened all patients admitted to Yale New Haven Hospital with laboratory confirmed babesiosis during the summer of 2023 and obtained informed consent. Patients were interviewed and underwent pupil dilation and a retinal examination using an indirect ophthalmoscope. Demographic and clinical information were obtained by questionnaire and through chart review. RESULTS: Ten patients underwent retinal eye exams with results that were generally unremarkable. No study patients showed any signs of retinal inflammation, infection, retinal bleeding, retinal tears, or abnormal vessel formation that could be attributed to infection. CONCLUSION: This small study did not find evidence of retinopathy in patients with babesiosis. Further studies with larger populations, repeated exams, and long term follow up will further elucidate the potential small vessel complications of human babesiosis.
Subject(s)
Babesiosis , Eye Infections, Parasitic , Retinal Diseases , Humans , Pilot Projects , Babesiosis/complications , Babesiosis/diagnosis , Cross-Sectional Studies , Male , Female , Middle Aged , Adult , Retinal Diseases/parasitology , Retinal Diseases/diagnosis , Retinal Diseases/etiology , Eye Infections, Parasitic/parasitology , Eye Infections, Parasitic/diagnosis , Aged , Retina/parasitology , Retina/pathologyABSTRACT
Rhabdomyoma of the orbit is a rare tumor with very few cases reported in the literature. We herein describe a 5-year-old boy who presented to us with a deviation of his left eye. Magnetic Resonance Imaging (MRI) showed a well-defined homogeneous intraconal mass in the superomedial aspect compressing the optic nerve. An excision biopsy was performed and the diagnosis of rhabdomyoma was confirmed on histopathology and immunohistochemistry with a coincidental finding of Trichinella spiralis larvae within the excised specimen. We report this phenomenon in two rare diseases with a predilection for striated muscle occurring simultaneously in a single patient.
Subject(s)
Magnetic Resonance Imaging , Orbital Neoplasms , Rhabdomyoma , Trichinellosis , Humans , Male , Rhabdomyoma/surgery , Rhabdomyoma/diagnosis , Rhabdomyoma/diagnostic imaging , Trichinellosis/diagnosis , Child, Preschool , Orbital Neoplasms/diagnostic imaging , Orbital Neoplasms/pathology , Orbital Neoplasms/surgery , Orbital Neoplasms/diagnosis , Animals , Trichinella spiralis/isolation & purification , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/surgery , Eye Infections, Parasitic/parasitologyABSTRACT
PURPOSE: To assess outcomes of keratoplasty performed in patients diagnosed with keratitis caused by Pythium insidiosum (PI). DESIGN: Retrospective review. METHODS: Preoperative, intra operative and post operative data of patients diagnosed with PI keratitis and who underwent keratoplasty for their condition from January 2020 to December 2021 were collected from the central patient database of a tertiary eye care hospital in India. The data were analyzed for anatomic success, elimination of infection, graft survival, incidence of repeat keratoplasty, final visual acuity and varied complications. RESULTS: In total, 16 eyes underwent penetrating keratoplasty for PI keratitis during the study period. Mean time to keratoplasty from onset of symptoms was 31.3 days and mean graft size was 10.4 mm. Nine out of the 16 cases had recurrence of infection following surgery, seven of which required a repeat keratoplasty for elimination of infection. Mean graft size for repeat keratoplasty performed in recurrent cases was 11.7 mm. Globe was successfully salvaged in 14 out of 16 patients (87.5 %). Three grafts remained clear at 6-month follow up while 11 grafts failed. Mean improvement in uncorrected visual acuity from 2.32 to 2.04 logMAR was observed at last follow up. Endo-exudates, graft infiltration, graft dehiscence, secondary glaucoma and retinal detachment were the various complications noted after keratoplasty. CONCLUSION: PI keratitis is a tenacious and potentially blinding condition. Keratoplasty remains the choice of treatment in this condition, however recurrence of disease and graft failure are common. Large sized grafts, meticulous per-operative removal of infection, adjuvant cryotherapy, and intraoperative and post operative use of antibiotics can help in improving outcome of keratoplasty in these patients.
Subject(s)
Keratoplasty, Penetrating , Pythiosis , Tertiary Care Centers , Visual Acuity , Humans , India/epidemiology , Retrospective Studies , Male , Female , Adult , Keratoplasty, Penetrating/methods , Middle Aged , Pythiosis/diagnosis , Pythiosis/surgery , Keratitis/diagnosis , Keratitis/surgery , Keratitis/microbiology , Keratitis/epidemiology , Graft Survival , Follow-Up Studies , Pythium/isolation & purification , Young Adult , Cornea/surgery , Cornea/pathology , Cornea/parasitology , Cornea/microbiology , Treatment Outcome , Aged , Eye Infections, Parasitic/surgery , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/parasitology , Eye Infections, Parasitic/epidemiology , AdolescentABSTRACT
BACKGROUND: Echinococcosis, commonly known as hydatid disease, is a zoonotic infection resulting from the tapeworm Echinococcus granulosus. The occurrence of hydatid cysts in the orbital region is uncommon, representing less than 1% of all reported hydatid cases. This report details a unique case of an intramuscular hydatid cyst in the orbital region that led to compressive optic neuropathy. CASE PRESENTATION: A 22-year-old male from Kabul, Afghanistan presented with a five-month history of progressive proptosis in his left eye, associated with a gradual decrease in vision over the past three weeks. The left eye exhibited upward globe dystopia, ocular motility limitation, mild conjunctival injection, and chemosis. Diagnosis was achieved through imaging and histopathological examination. Treatment involves surgical removal of the cyst and prolonged albendazole therapy. The postoperative course showed significant improvement in the patient's condition and restoration of his vision. CONCLUSIONS: Despite its rarity, this case underscores the importance of awareness and knowledge of hydatid disease among physicians, especially those working in endemic areas. It emphasizes the importance of including hydatid disease in the differential diagnosis of orbital masses, particularly in endemic regions.
Subject(s)
Echinococcosis , Eye Infections, Parasitic , Optic Nerve Diseases , Orbital Diseases , Humans , Male , Echinococcosis/diagnosis , Echinococcosis/complications , Young Adult , Optic Nerve Diseases/diagnosis , Optic Nerve Diseases/parasitology , Optic Nerve Diseases/surgery , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/parasitology , Eye Infections, Parasitic/surgery , Orbital Diseases/parasitology , Orbital Diseases/diagnosis , Magnetic Resonance Imaging , Albendazole/therapeutic use , Tomography, X-Ray ComputedABSTRACT
Due to their relatively high prevalence and commensalism, the pathogenicity of Demodex mites has been debated. Recent data, however, show Demodex to be associated with skin and ocular surface diseases such as rosacea, blepharitis, and keratitis. Here the authors report the first known case, to the best of the their knowledge, of Demodex infestation mimicking preseptal cellulitis in an adult human. A 29-year-old male bilaterally blind from advanced retinopathy of prematurity presented with a 2-month history of right-greater-than-left upper eyelid and periocular/cheek swelling, redness, and ocular discharge that did not resolve with oral antibiotics or oral steroids. Based on MRI findings, biopsies of the right lacrimal gland, right orbital fat, and right upper eyelid preseptal skin were obtained which revealed marked intrafollicular Demodex mite density and budding yeasts in the upper eyelid skin. This case serves to alert clinicians to this entity that may not otherwise be usually considered in ophthalmic clinical practice.
Subject(s)
Cellulitis , Eye Infections, Parasitic , Mite Infestations , Humans , Male , Adult , Mite Infestations/diagnosis , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/parasitology , Diagnosis, Differential , Cellulitis/diagnosis , Cellulitis/microbiology , Animals , Mites , Eyelid Diseases/diagnosis , Eyelid Diseases/parasitology , Eyelid Diseases/drug therapy , Eyelids/parasitology , Eyelids/pathology , Magnetic Resonance Imaging , Biopsy , Orbital Cellulitis/diagnosis , Orbital Cellulitis/microbiologyABSTRACT
Myiasis is a neglected tropical disease caused by the larvae of dipterous flies. Cutaneous infestation is the predominant type documented in sub-Saharan Africa, and ocular involvement is uncommon. We report the rare occurrence of a case of eyelid ophthalmomyiasis caused by Cordylobia anthropophaga in a Nigerian female to raise awareness among practitioners in both tropical and nonendemic areas.
Subject(s)
Diptera , Myiasis , Humans , Myiasis/diagnosis , Myiasis/parasitology , Female , Animals , Abscess/diagnosis , Abscess/parasitology , Larva , Nigeria , Diagnosis, Differential , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/parasitology , Adult , Eyelid Diseases/diagnosis , Eyelid Diseases/parasitology , CalliphoridaeABSTRACT
A 33-year-old male presented with unilateral painless vision loss with a history of sub-tenon steroid for the same. The fundus showed an elevated focus of retinochoroiditis with vitritis. On investigating for the cause, polymerase chain reaction test on the anterior chamber tap was found to be positive for Toxoplasma. Such confusing and atypical cases usually produce a clinical dilemma and should be managed in a stepwise manner. Ancillary investigations usually provide a clue to the clinician and should be performed without any hesitation.
Subject(s)
Toxoplasma , Toxoplasmosis, Ocular , Humans , Male , Adult , Toxoplasmosis, Ocular/diagnosis , Toxoplasmosis, Ocular/drug therapy , Toxoplasma/isolation & purification , Toxoplasma/genetics , Polymerase Chain Reaction , Chorioretinitis/diagnosis , Chorioretinitis/parasitology , Fundus Oculi , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/parasitology , DNA, Protozoan/analysis , Diagnosis, Differential , Fluorescein Angiography/methodsABSTRACT
PURPOSE: This study sought to compare the long-term outcomes of surgeries for retinal detachment (RD) secondary to viral or parasitic infectious retinitis. METHODS: A total of 47 eyes that received pars plana vitrectomy with or without scleral buckling due to RD secondary to polymerase chain reaction-proven viral (cytomegalovirus, varicella zoster virus, and herpes zoster virus) or parasitic (toxoplasma and toxocara) retinitis from October 1, 2006, to June 30, 2023, in a single medical center were retrospectively enrolled. RESULTS: Mean follow-up period was 59.03 ± 55.24 months in viral retinitis and 34.80 ± 33.78 months in parasitic retinitis after primary reattachment surgery. During follow-up, nine eyes (24.3%) with viral retinitis and five eyes (50.0%) with parasitic retinitis developed retinal redetachment. Visual acuity success at final follow-up was achieved in 19 eyes (51.4%) with viral retinitis and six eyes (60.0%) with parasitic retinitis (p = 0.64). The incidence of retinal redetachment during the 1st postoperative year was significantly higher in parasitic retinitis compared with viral retinitis (crude incidence, 0.21 vs. 0.85; p = 0.02). Hazard ratio analysis adjusted for age and sex showed 4.58-fold (95% confidence interval, 1.22-17.27; p = 0.03) increased risk of retinal redetachment in parasitic retinitis compared with viral retinitis during the 1st postoperative year. Tamponade with silicone oil and preoperative diagnostic vitrectomy were associated with significantly decreased risk of retinal redetachment in patients with parasitic retinitis. CONCLUSIONS: Compared with RD secondary to viral retinitis, RD secondary to parasitic retinitis showed higher incidence of retinal redetachment during the 1st postoperative year. Tamponade with silicone oil and preoperative diagnostic vitrectomy were associated with significantly decreased risk of retinal redetachment in patients with parasitic retinitis.
Subject(s)
Eye Infections, Parasitic , Eye Infections, Viral , Retinal Detachment , Retinitis , Visual Acuity , Vitrectomy , Humans , Retinal Detachment/surgery , Retinal Detachment/etiology , Retinal Detachment/diagnosis , Female , Male , Retrospective Studies , Vitrectomy/methods , Adult , Follow-Up Studies , Middle Aged , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/parasitology , Eye Infections, Parasitic/surgery , Eye Infections, Parasitic/complications , Eye Infections, Viral/diagnosis , Eye Infections, Viral/virology , Eye Infections, Viral/complications , Retinitis/diagnosis , Retinitis/parasitology , Retinitis/surgery , Retinitis/virology , Scleral Buckling/methods , Young Adult , Adolescent , Incidence , Aged , Treatment Outcome , Time Factors , ChildABSTRACT
INTRODUCTION: Ocular toxocariasis is a rare disease, predominantly affecting children and young adolescents, and usually presenting as unilateral posterior uveitis. We report the case of a child with toxocariasis associated with serous retinal detachment. OBSERVATION: A 8-year-old child with no previous history of toxocariasis was referred for a 1-year decline in visual acuity, unimproved by optical correction, with vitreous condensation on examination, without central or peripheral granulomas, and serous retinal detachment on OCT. The diagnosis was made after extensive questioning, with evidence of contact with dogs and positive serology. Medical treatment combining corticosteroid therapy and antiparasitic therapy was initiated, and the clinical picture improved. DISCUSSION: Ocular toxocariasis is a rare infection, unilateral in 90% of cases. Its clinical manifestation in children is pars planitis, posterior uveitis with a posterior pole chorioretinal focus associated with vitreoretinal traction and/or peripheral granuloma. In our case, the patient presented with vitreous condensation only, with OCT serous retinal detachment and no peripheral or central granulomas. Positive plasma serology or ocular samples confirmed the diagnosis. CONCLUSION: Ocular toxocariasis should not be ruled out in the absence of a typical clinical picture, and seropositivity enables confirmation of the diagnosis when clinical suspicion arises.
Subject(s)
Eye Infections, Parasitic , Retinal Detachment , Toxocariasis , Humans , Toxocariasis/diagnosis , Toxocariasis/drug therapy , Toxocariasis/complications , Child , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/parasitology , Eye Infections, Parasitic/drug therapy , Retinal Detachment/diagnosis , Retinal Detachment/parasitology , Male , Dogs , AnimalsABSTRACT
Extralymphatic filariasis caused by filaria of zoonotic origins has been frequently reported in Thailand over recent years. Here, we report the first case of ocular filariasis in a 7.5-year-old Thai boy who initially presented with progressive conjunctival redness and blurred vision in his right eye. A small, slender, coiled worm was found and surgically removed from the right anterior chamber. Histopathological examination illustrated predominant eosinophilic inflammation surrounding the parasite, which showed smooth and thin cuticle, prominent lateral chords, flat and broad muscle cells, one intestine, and two reproductive tubes with unsegmented ova, typically characteristic of a female adult Brugia filarial nematode. The parasite was also molecularly identified as B. pahangi, based on mitochondrial cytochrome c oxidase subunit I sequence analysis. The patient was then empirically prescribed albendazole, systemic prednisolone, and topical methylprednisolone. Unfortunately, his vision did not recover after 2 months due to severe maculopathy, most likely resulting from parasitic infestation and subsequent vitreous inflammation. To the best of our knowledge, this is the first case of ocular infestation by B. pahangi with visual complications that occurred outside a filariasis-endemic area of Thailand. Furthermore, this report provides clinical data on preceding cases of B. pahangi filariasis formally reported in southeast Asian countries, including Thailand and Malaysia, which facilitate a better understanding of the epidemiology of this sporadic zoonotic infection for effective disease elimination.
Subject(s)
Brugia pahangi , Filariasis , Humans , Male , Thailand , Filariasis/complications , Filariasis/parasitology , Animals , Child , Albendazole/therapeutic use , Eye Infections, Parasitic/parasitology , Macula Lutea/pathology , Macula Lutea/parasitologyABSTRACT
This case report describes the pathogenesis of ocular pentastomiasis in human hosts.
Subject(s)
Eye Infections, Parasitic , Animals , Female , Humans , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/parasitology , PentastomidaABSTRACT
PURPOSE: Demodex blepharitis, often overlooked in ocular surface disease, involves Demodex mites, prevalent ectoparasites on human skin. Current treatments may not effectively eliminate these mites, prompting a need for targeted therapies. Lotilaner, an antiparasitic agent, shows promise. This systematic review and meta-analysis assesses 0.25% lotilaner ophthalmic solution's efficacy in reducing Demodex mite populations and its impact on ocular surface inflammation in Demodex blepharitis patients. METHODS: A comprehensive literature search was performed in the PubMed and Cochrane Library databases from inception until February 2024 to identify relevant trials investigating the use of lotilaner in patients with Demodex blepharitis. The included studies were assessed for quality, and a meta-analysis was conducted to determine the overall treatment effects of lotilaner. Odds ratios (OR) and 95% confidence intervals (CIs) were calculated for binary variables. All statistical analyses were performed using the R Statistical Software. RESULTS: Five studies met the inclusion criteria and were included in this systematic review and meta-analysis. Lotilaner demonstrated significant efficacy in Collarette Cure [OR = 6.64; 95 % CI 3.78 to 11.04; p < 0.00001, I2 = 62 %] %], clinically meaningful collarette reduction [OR = 6.21; 95 % CI 3.67 to 10.49; p < 0.00001, I2 = 90 %], and achieving at least 1-grade collarette improvement [OR = 5.12; 95 % CI (2.96 to 8.88); p < 0.00001, I2 = 90 %] compared to the placebo group. The treatment also resulted in mite eradication [OR = 6.18; 95 % CI 4.67 to 6.18; p < 0.00001, I2 = 34 %], reduction in mite density [OR = 9.37; 95 % CI 5.36 to 16.36; p < 0.00001, I2 = 84 %], and erythema cure [OR = 2.29; 95 % CI 2.24 to 3.39; p < 0.00001, I2 = 5 %] and composite cure [OR = 7.05; 95 % CI 3.66 13. 61; p < 0.00001, I2 = 11 %]. The study suggests that lotilaner is a promising therapeutic option for collarette and associated symptoms, but the high heterogeneity in some outcomes and limited long-term data warrant further research to confirm its effectiveness and safety. CONCLUSION: This systematic review and meta-analysis provides robust evidence supporting the efficacy of 0.25% lotilaner ophthalmic solution in treating Demodex blepharitis. Approval of this targeted therapy represents a significant milestone in ophthalmology and offers a promising treatment option for patients with Demodex blepharitis. Eye care professionals should consider the potential benefits of lotilaner in managing and alleviating the symptoms associated with Demodex infestations on the eyelids. Further research and long-term follow-up studies are warranted to assess the safety and effectiveness of lotilaner in treating Demodex blepharitis.
Subject(s)
Blepharitis , Eye Infections, Parasitic , Mite Infestations , Mites , Ophthalmic Solutions , Randomized Controlled Trials as Topic , Blepharitis/drug therapy , Blepharitis/parasitology , Mite Infestations/drug therapy , Mite Infestations/parasitology , Humans , Animals , Eye Infections, Parasitic/drug therapy , Eye Infections, Parasitic/parasitology , Eye Infections, Parasitic/diagnosis , Treatment Outcome , Antiparasitic Agents/therapeutic useABSTRACT
PURPOSE: To study the demographic, clinical, and microbiological profile of Demodex-related blepharokeratoconjunctivitis (BKC) at a tertiary eye care hospital. METHODS: This retrospective observational study was conducted from January 2016 to September 2022. It included 83 patients with microbiologically proven Demodex BKC who presented to the cornea department of our tertiary care eye center. The clinical, microbiological, and demographic data of the 83 cases were analyzed. RESULTS: Of the 83 cases, 57 (68.67%) were younger than 40 years, and 25 (30.12%) were below 20. Most patients presented with a good visual acuity of 20/40 or better (93 eyes; 84.55%). The disease was unilateral in 55 patients and bilateral in 28. Cylindrical dandruff was the predominant presentation noted in 61 eyes (54.95%), followed by corneal scarring in 47 eyes (42.34%) and corneal vascularization in 40 eyes (36.04%). On light microscopy, 87.95% of the positive samples were identified as Demodex folliculorum , 7.23% as Demodex brevis , and 6.02% remained unidentified. Tea tree oil and lid scrubs eradicated the disease in most patients clinically (75/83, 90.36%). CONCLUSION: The spectrum of BKC includes both lid signs and corneal involvement. It can be a cause of recurrent BKC and detection of the mite by microscopic evaluation of the lashes can confirm the diagnosis. In most cases, the tea tree oil can effectively manage this condition. However, low doses of topical steroids are needed to control the inflammation in patients with corneal involvement.
Subject(s)
Blepharitis , Eye Infections, Parasitic , Keratoconjunctivitis , Mite Infestations , Mites , Humans , Retrospective Studies , Male , Female , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/parasitology , Adult , Mite Infestations/diagnosis , Mite Infestations/parasitology , Blepharitis/parasitology , Blepharitis/diagnosis , Blepharitis/microbiology , Middle Aged , Animals , Keratoconjunctivitis/diagnosis , Keratoconjunctivitis/microbiology , Keratoconjunctivitis/parasitology , Young Adult , Adolescent , Aged , Child , Visual AcuityABSTRACT
PURPOSE: Several treatments have been in use for Demodex blepharitis, before the discovery of lotilaner, like tea tree oil and antibiotics; however, they either have irritable effects or systemic adverse effects, respectively. Lotilaner, a novel ectoparasiticide, has been proposed as a treatment for patients grappling with Demodex blepharitis. This review aims to assess the safety and efficacy of lotilaner in the treatment of Demodex blepharitis. DESIGN: Systematic review and meta-analysis. METHODS: An extensive search was conducted on PubMed, Cochrane Library, Scopus, and Google Scholar to find relevant literature till July 31, 2023 following the PRISMA guidelines. A total of 143 articles were retrieved by database searching, out of which 6 studies met the inclusion criteria and were included in the review. Four randomized controlled trials were included in the meta-analysis of mite eradication incidence. The review is registered with PROSPERO: CRD42023459997. RESULTS: Lotilaner is effective in eradicating Demodex mites in individuals suffering from Demodex blepharitis according to RR for the intervention versus the control group of 3.55 (95% confidence interval [CI]: 2.87-4.40, P < .00001, I2 = 0%). The meta-analysis of clinically meaningful collarette score revealed the summary RR for the intervention versus the control group was 3.15 (95% CI: 2.56-3.89, P < 0.00001, I2 = 27%). In conclusion, the results of the included studies were comparable and consistent. CONCLUSIONS: Our results indicated that lotilaner is an effective, well-tolerated, and promising drug in treating patients with Demodex blepharitis. Lotilaner administration and cost-effectiveness should now be contemplated for the study population as these constituents have a vital impact on its treatment success.
Subject(s)
Blepharitis , Eye Infections, Parasitic , Mite Infestations , Mites , Ophthalmic Solutions , Blepharitis/drug therapy , Blepharitis/parasitology , Blepharitis/diagnosis , Humans , Mite Infestations/drug therapy , Mite Infestations/parasitology , Eye Infections, Parasitic/drug therapy , Eye Infections, Parasitic/parasitology , Eye Infections, Parasitic/diagnosis , Animals , Treatment Outcome , Observational Studies as TopicABSTRACT
PURPOSE: To study the role of Toxoplasma IgG avidity in evaluating the stage of systemic infection during manifestation as toxoplasma retinochoroiditis and its clinical implications in eastern India. METHODS: Retrospective chart review of Toxoplasma retinochoroiditis cases with Toxoplasma serology for IgG, IgM, and IgG avidity. RESULTS: Included in this study were 17 eyes of 17 patients who had active retinitis located in the macula (14), mid-periphery (2), or periphery (1). They were either primary lesions (12) or reactivations (5). All the cases had Toxoplasma IgG positive; one case had IgM positivity, while all the cases had high IgG avidity values. IgG avidity had a positive correlation with the duration of symptoms. CONCLUSION: We observed high IgG avidity values in active retinochoroiditis in both primary ocular Toxoplasmosis and reactivation subgroups. These results indicate a late ocular manifestation after initial systemic infection with a possible incubation period ranging from 5 weeks to 5 months.
Subject(s)
Antibodies, Protozoan , Chorioretinitis , Immunoglobulin G , Toxoplasma , Toxoplasmosis, Ocular , Humans , Toxoplasmosis, Ocular/immunology , Toxoplasmosis, Ocular/diagnosis , Toxoplasmosis, Ocular/parasitology , Retrospective Studies , Immunoglobulin G/blood , Immunoglobulin G/immunology , Female , Male , Toxoplasma/immunology , Chorioretinitis/parasitology , Chorioretinitis/immunology , Chorioretinitis/diagnosis , Adult , Antibodies, Protozoan/blood , Antibodies, Protozoan/immunology , Young Adult , Adolescent , Child , Eye Infections, Parasitic/parasitology , Eye Infections, Parasitic/diagnosis , Eye Infections, Parasitic/immunology , Immunoglobulin M/blood , Immunoglobulin M/immunology , Middle Aged , Antibody Affinity , Follow-Up StudiesABSTRACT
PURPOSE: The aim of this study was to report clinical observations suggesting the efficacy of topical 1% 5-fluorouracil (5-FU) in treating Demodex -associated blepharitis. METHODS: An observational retrospective review of 13 eyes from 13 individuals with conjunctival neoplastic lesions and concomitant Demodex lash infestation that received topical 1% 5-FU eye drops. Patients underwent slit-lamp examination at each follow-up visit. Clinical photographs of the lash line were obtained after treatment initiation. In a subset of patients, lashes were epilated bilaterally and microscopically analyzed for presence of Demodex mites before and after treatment initiation. RESULTS: The mean age of the population was 68 ± 14 years (range: 30-84 years) and 92% were male. In all 13 patients, a marked reduction in cylindrical dandruff was noted in the treated eye by slit-lamp examination after 2 cycles of 5-FU. There was complete resolution of cylindrical dandruff in 10 of 13 treated eyes compared with 0 resolution of cylindrical dandruff in untreated eyes ( P = 0.0001). In the 6 patients who received epilation, the lashes from the treated eye showed no Demodex , whereas lashes from the fellow untreated eye revealed persistent Demodex . CONCLUSIONS: Topical 1% 5-FU shows efficacy in treating Demodex -associated blepharitis. Further studies are indicated to reproduce our findings and evaluate the potential use of 5-FU as a treatment ingredient.
Subject(s)
Blepharitis , Eye Infections, Parasitic , Fluorouracil , Mite Infestations , Mites , Ophthalmic Solutions , Blepharitis/parasitology , Blepharitis/drug therapy , Blepharitis/diagnosis , Fluorouracil/therapeutic use , Fluorouracil/administration & dosage , Humans , Retrospective Studies , Mite Infestations/drug therapy , Mite Infestations/parasitology , Mite Infestations/diagnosis , Male , Aged , Middle Aged , Eye Infections, Parasitic/drug therapy , Eye Infections, Parasitic/parasitology , Eye Infections, Parasitic/diagnosis , Female , Aged, 80 and over , Adult , Animals , Eyelashes/parasitology , Antimetabolites/therapeutic use , Antimetabolites/administration & dosage , Administration, TopicalABSTRACT
INTRODUCTION: Orbital infections and infestations present with varying clinical presentations and incidences ranging from benign ocular condition to disseminated systemic disease. The diagnosis is often difficult initially, due to similar ocular presentations. MATERIALS AND METHODS: This review was compiled using articles available on PubMed using key words like orbital infections, orbital cellulitis, orbital infestations, orbital tuberculosis, orbital fungal infections. Clinical experience in presentation and management at our centre was also included. RESULTS: The varied presentations, management, complications and follow-ups have been summarised in this review. CONCLUSION: As the management is cause-specific, thus lies the importance of early accurate diagnosis, both clinical and radiological. This article aims to review existing literature on orbital infections and infestations for aiding in early accurate diagnosis and management.