@article{Karan_2023b,

title = {The effect of durative computer usage on intraocular pressure},

author = {Siddharth Karan and Sheetal Baldava and Rahel Afzal and Farheen Fatima and Saira Begum},

url = {https://www.ijlbpr.com/uploadfiles/29vol12issue4pp162-165.20231019052727.pdf},

issn = {2250-3137},

year  = {2023},

date = {2023-10-31},

urldate = {2023-10-31},

journal = {International Journal of Life Sciences, Biotechnology and Pharma Research},

volume = {12},

issue = {4},

pages = {162-165},

abstract = {Aim: To investigate the changes in the Intraocular pressure (IOP) in adults on prolonged computer usage. Methods:31 adult subjects working with computers for prolonged hours had their Intraocular pressure checked with Schiotz tonometer. Measurements were taken initially on every individual before computer usage and then following 3 hours of computer usage. Results: There was significant rise in the Intraocular pressure (Mean Increase of Intraocular pressure is 1.23mm of Hg) in most of the myopic subjects after 3 hours of continuous usage of computer. Conclusions: Prolonged computer usage could induce transient Intraocular pressure elevation. Mostly Intraocular pressure elevation is seen in myopic subjects whereas emmetropic subjects showed little or no elevation.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Karan_2023,

title = {Recurrent episcleritis-a rare presentation of mixed connective tissue disease},

author = {Siddharth Karan and Arshia Mohammed and Sana Fatima},

url = {https://www.worldwidejournals.com/international-journal-of-scientific-research-(IJSR)/fileview/recurrent-episcleritis--a-rare-presentation-of-mixed-connective-tissue-disease_April_2023_0614198974_5613429.pdf},

doi = {10.36106/ijsr},

issn = {2277-8179},

year  = {2023},

date = {2023-04-30},

urldate = {2023-04-30},

journal = {International Journal of Scientific Research},

volume = {12},

issue = {4},

pages = {51-52},

abstract = {Episcleritis refers to inflammation of the loose connective tissue between the sclera and the conjunctiva. The majority of episcleritis cases are idiopathic, but 26% to 36% of patients have an associated systemic disorder that is responsible for the pathological process and development of episcleritis. It is also well established that the incidence and prevalence of episcleritis are higher in populations with systemic collagen-vascular

disease and autoimmune diseases. However recurrent episcleritis in Mixed Connective Tissue Disease has not been reported before in literature. Here we are reporting a case of recurrent bilateral nodular episcleritis as a rare presentation of MCTD.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{B_2017c,

title = {Clinical profile of patients presenting with rhegmatogenous retinal detachment},

author = {Vijaya Lakhsmi B. and Irfan Faraz and Lokabhi Reddy J. M.},

url = {https://www.medpulse.in/Ophthlmology/Article/Volume3Issue3/Ophthalmology_3_3_11.pdf},

doi = {10.26611/10093311},

issn = {2250-7575},

year  = {2017},

date = {2017-09-26},

urldate = {2017-09-26},

journal = {MedPulse International Journal of Ophthalmology},

volume = {3},

issue = {3},

pages = {87-91},

abstract = {Background: The aim of the study was to evaluate the epidemiological characteristics, risk factors, characteristic of retinal detachment in patients presenting with rhegmatogenous retinal detachment. This study was conducted among patients presenting at Sarojini Devi Eye Hospital. Material and Methods: The study duration spanned over a period from august 2008 to September 2010. Patients presenting to the ophthalmology OPD and diagnosed with rhegmatogenous retinal detachment were included in the study Cases with recurrent retinal detachment, tractional retinal detachment, Combined retinal detachments, exudative retinal detachment. Secondary detachments after vitrectomy, strabismus or ocular surgeries were excluded from the study. Results: Fifty patients who were diagnosed with a rhegmatogenous retinal detachment were included in the study. Majority of the patients belonged to the age group of 40 to 60 (18, 36%) years with a mean age of 40 years. 29 patients(58%) were males. In 21 patients (42%) left eye was involved and in right eye was involved. In two patients both eyes were involved. 15 (30%) patients presented to the clinic within 2 weeks and 66 % of the patients presented within 5 weeks.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{B_2017b,

title = {Tackling refractive surprise post cataract surgery\textendasha surgeon’s nightmare},

author = {Vijaya Lakhsmi B. and Irfan Faraz},

url = {https://www.medpulse.in/Ophthlmology/Article/Volume3Issue3/Ophthalmology_3_3_9.pdf},

doi = {10.26611/1009339},

issn = {2250-7575},

year  = {2017},

date = {2017-09-21},

urldate = {2017-09-21},

journal = {MedPulse International Journal of Ophthalmology},

volume = {3},

issue = {3},

pages = {79-83},

abstract = {Cataract surgery is the most common surgery performed by ophthalmologists. The goal of surgery has shifted from restoring vision to providing a spectacle free vision. Refractive surprise post cataract surgery is one of the most frustrating event. In this article, we describe the measures to deal with refractive surprise post cataract surgery. The choice of treatment varies from non invasive modalities like spectacles to invasive procedures like IOL exchange, Laser vision correction etc.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Faraz_2017c,

title = {Spectrum of diseases in ocular tuberculosis},

author = {Irfan Faraz and Vijaya Lakhsmi B. and Mutyala Gopal Kishan},

url = {https://www.medpulse.in/Ophthlmology/Article/Volume3Issue3/Ophthalmology_3_3_8.pdf},

doi = {10.26611/1009338},

issn = {2250-7575},

year  = {2017},

date = {2017-09-20},

urldate = {2017-09-20},

journal = {MedPulse International Journal of Ophthalmology},

volume = {3},

issue = {3},

pages = {75-78},

abstract = {Aim: To study the spectrum of diseases in ocular tuberculosis and their management and to determine the complications, prognostic factors and visual outcome in this disease. Material and Methods: In this retrospective study we present 10 patients presenting to ophthalmology department. Comprehensive evaluation was done in all patients.OCT and FFA was done in selected patients and routine systemic investigations were done in all patients. Observation and Results: Two patients had granulomatous anterior uveitis out of which 2 had cystoid macular edema, 2 had intermediate uveitis, 3 had retinal vasculitis All patients were started on topical steroids and cycloplegics. Oral steroids were given in patients with intermediate uveitis and retinal vasculitis after induction phase of ATT regimen. All patients were started on Anti-tuberculous treatment regime in collaboration with the pulmonologist. },

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{B_2017,

title = {Management of microbial keratitis},

author = {Vijaya Lakhsmi B. and Irfan Faraz},

url = {https://www.medpulse.in/Ophthlmology/Article/Volume3Issue3/Ophthalmology_3_3_6.pdf

},

doi = {10.26611/1009336},

issn = {2250-7575},

year  = {2017},

date = {2017-09-16},

urldate = {2017-09-16},

journal = {MedPulse International Journal of Ophthalmology},

volume = {3},

issue = {3},

pages = {66-70},

abstract = {Microbial keratitis is the one of the common causes of corneal blindness. It is defined as an epithelial defect with infiltrate. It can be caused by bacteria, virus, fungus, acanthamoeba. Detecting the exact causative organism to ensure prompt treatment is important. In this article we describe the evaluation, management (medical and surgical) of the microbial keratitis. We focus predominantly on bacterial and fungal ulcers in this article},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Faraz_2017b,

title = {Ocular manifestations in systemic lupus erythematosus},

author = {Irfan Faraz and Vijaya Lakhsmi B. and Mutyala Gopal Kishan},

url = {https://www.medpulse.in/Ophthlmology/Article/Volume3Issue3/Ophthalmology_3_3_4.pdf},

doi = {10.26611/1009334},

issn = {2250-7575},

year  = {2017},

date = {2017-09-14},

urldate = {2017-09-14},

journal = {MedPulse International Journal of Ophthalmology},

volume = {3},

issue = {3},

pages = {58-61},

abstract = {Aim: To report the significance of ocular manifestations in Systemic lupus erythematosus Materials and methods: Seven diagnosed cases of Systemic lupus erythematosus, which included both newly diagnosed cases and cases already on treatment, were referred from the treating physician for ophthalmological evaluation. Comprehensive ophthalmic examination was done using BCVA, intraocular pressure measurement, Slit lamp examination of the anterior segment, fundus examination using Slit lamp biomicroscopy and indirect ophthalmoscopy, and Schirmers testing was done. In selected patients, certain special investigations like visual fields 24-2, 10-2 testing, SD-OCT was done. However ERG, could not be done due to lack of resource availability. Patients with history of Diabetes mellitus, Hypertension and other ophthalmic diseases like age related cataract were excluded. Results: Out of the seven cases of SLE examined, xerosis was the most commonly encountered manifestation, seen among 6 patients. Episcleritis was seen in one patient, Anterior

uveitis seen in 2 patients, SLE associated retinopathy was seen in 3 patients. Treatment induced side effects like

glaucoma was seen in 1 patient, posterior subcapsular opacities in 2 patients and Bull’s eye maculopathy suggestive of HCQ toxicity seen in 1 patient. While dryness, episcleritis and retinopathy were managed conservatively, Anterior uveitis was managed with topical steroids. Patients with HCQ associated toxicity were advised to stop the HCQ therapy or to go for an alternative regimen, those with posterior subcapsular opacities were advised cataract surgery, while glaucomatous patients were started on anti glaucoma therapy. Conclusion: Early diagnosis, prompt referral, coordinated treatment and long term follow-up through multi disciplinary approach involving Ophthalmologists, Rheumatologists and Dermatologist play a key role in reducing ocular and systemic morbidity associated with Systemic lupus erythematosus. },

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Faraz_2017,

title = {Combined pars plana vitrectomy and iris claw lens in management of dislocated cataract or IOL},

author = {Irfan Faraz and Vijaya Lakhsmi B. and Mutyala Gopal Kishan},

url = {https://www.medpulse.in/Ophthlmology/Article/Volume3Issue3/Ophthalmology_3_3_2.pdf},

doi = {10.26611/1009332},

issn = {2250-7575},

year  = {2017},

date = {2017-09-11},

urldate = {2017-09-11},

journal = {MedPulse International Journal of Ophthalmology},

volume = {3},

issue = {3},

pages = {51-53},

abstract = {Aim: To report management of posteriorly dislocated cataractous lens/IOL with Combined Pars Plana Vitrectomy and Iris claw lens implantation. Method: This is a retrospective study of 6 cases of dislocated IOL(4) and cataractous lens(2) at a tertiary eye Hospital in Telangana between October 2016 and February 2017 .Two case each of nucleus drop and IOL drop occurred in our hospital. Rest were referred from outside. These six patients were subsequently taken up for secondary procedure after reduction of corneal edema and inflammation. Three port PPV was done in all cases with nucleus/IOL retrieval, Iris claw lens was implanted and surgical peripheral iridectomy. Section was sutured where necessary. All patients were followed up for minimum of 3 months post operatively. Results: All patients had uneventful post op recovery with BCVA of 6/12 - 6/9 at 3months postoperative followup. Long term results are yet to be evaluated. Observation: Iris claw lens along with PPV offers a safe, easy and affordable alternative as a secondary IOL in cases with posteriorly dislocated lens with no or inadequate capsular support. },

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Qudsiya_2017,

title = {Study of intraocular pressure among individuals working on computer screens for long hours},

author = {Sanam Maria Qudsiya and Farisa Khatoon and Aftab Abdul Khader and Mohammed Asghar Ali and Mohammed Abdul Hannan Hazari and Fareen Sultana and Ayesha Farheen},

url = {https://amphysiol.com/index.php/amp/article/view/v1i1.263328},

doi = {10.23921/amp.2017v1i1.263328},

issn = {2456-8422},

year  = {2017},

date = {2017-04-11},

urldate = {2017-04-11},

journal = {Annals of Medical Physiology},

volume = {1},

issue = {1},

pages = {22-25},

publisher = {Quench Academy of Medical Education and Research (QAMER) Publishing House},

abstract = {In today’s world computers are ubiquitous and found in different forms which can effect intraocular pressure (IOP). Present study was undertaken to find out effect of day-to-day exposure to computer screen on IOP in normal individuals. 70 individuals (who met the screening conditions and devoid of obvious ocular pathology and systemic diseases) had their IOP’s checked before and 4 hour after computer session on same day, all working in general day shift, involving reading English printed material. The results showed significant (p<0.005) increase with IOP values before exposure being 17.89±3.25 and 16.99±2.84 and after exposure being 19.67±3.4 and 18.70±2.4 in left and right eye respectively. Increase in IOP was noted in 70% and 67% individuals in left and right eye. Differences in IOP of right and left eye may be due to dominance of eye or direction of script from left to right.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Karan_2016b,

title = {Clinicopathological study of eyelid tumors in Hyderabad-a review of 57 cases},

author = {Siddharth Karan and Manisha Nathani and M. Tanveer Ali Khan and Sucheta Ireni and Aftab Abdul Khader},

url = {https://jmas.in/fulltext/154-1457890492.pdf?1693286501},

doi = {10.5455/jmas.221842},

issn = {2231-1696},

year  = {2016},

date = {2016-07-31},

urldate = {2016-07-31},

journal = {Journal of Medical and Allied Sciences},

volume = {6},

issue = {2},

pages = {72-76},

abstract = {An eyelid tumor leads to functional and aesthetic problems. The preva-lence and distribution of eye lid tumors have considerable variation. The aim of this study was to categorize the prevalence and distribution of various eyelid tumors among population of Hyderabad over 3 years duration. This was a prospective study of 57 cases who reported to our tertiary hospital in Hyderabad from January 2013 to December 2015. The cases were analyzed for their sex distribution, tumor type, age distribution, incidence of malignant and benign tumors, tumor location, and complications at the time of presentation. The mean age of presentation of malignant tumors and benign tumors was 56 and 39 years respectively. The median age of presentation was 64 years for basal cell carcinoma, 50 years for sebaceous gland carcinoma (SGC) and 62 years for squamous cell carcinoma (SCC). The median age of presentation of various benign lesions were as follows: 33 years for dermoid cyst, 40 years for epidermal cyst, 36 years for capillary hemangioma, 54 years for squamous papilloma, 56 years for granulomatous lesion, 41 years for nevus, 19 years for keratoacanthoma, 58 years for sebaceous keratosis, 40 years for histiocytoma, 33 years for neurofibroma, 43 years for pleomorphic adenoma. The most common location of the tumor was upper lid (55.55%) for all the malignancies. Sebaceous gland carcinoma was the most common malignancy (55.5%) followed by basal cell carcinoma (33.3%) and squamous cell carcinoma (11.1%). Dermoid cyst was the most common type of benign lesion (37.5%). Surgical methods used were wedge excision with primary closure, wide excision, skin grafting and tarso-conjunctival flap. To conclude, sebaceous gland carcinoma was the most common malignancy and dermoid cyst was the most common tumor of benign origin. Hence it is our suggestion to have high degree of suspicion for these tumors for early diagnosis and intervention.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Karan_2016,

title = {A non randomised prospective study of thyroid orbitopathy in tertiary care centre},

author = {Siddharth Karan and Manisha Nathani and M. Tanveer Ali Khan and Aftab Abdul Khader and Sucheta Ireni and Abdul Basith Syed},

url = {https://www.jebmh.com/articles/a-nonrandomised-prospective-study-of-thyroid-orbitopathy-in-a-tertiary-care-centre.pdf.pdf},

doi = {10.18410/jebmh/2016/425},

issn = {2349-2562},

year  = {2016},

date = {2016-05-12},

urldate = {2016-05-12},

journal = {Journal of Evidence Based Medicine and Healthcare},

volume = {3},

issue = {38},

pages = {1910-1914},

abstract = {Graves’ disease is an autoimmune condition where TSH receptors are targeted by the auto-antibodies. Although most patients have clinical or laboratory evidence, the disease process can occur even in the absence of detectable thyroid abnormality. Although most cases of TAO can be managed medically without any visual loss, it may result in exposure keratitis and compressive optic neuropathy. There was female preponderance noted. Maximum number of patients were in the 25-50 years of age group. More than 65% of the patients were hyperthyroid followed by euthyroid in 25% and then hypothyroid in less than ten percent. In both the sexes, the hyperthyroid status was the most common followed by euthyroid and hypothyroid. No male was reported to be hypothyroid. The most common presentation was found to be bilateral than unilateral. Inferior rectus

was the commonest muscle involved followed by medial rectus, superior rectus-LPS complex and lateral rectus in descending order. Incidence and various modes of presentation of ‘Thyroid Orbitopathy’ of our study at our tertiary centre in Hyderabad are correlating with national and international studies. },

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Nathani_2015,

title = {Laurence-Moon-Bardet-Biedl syndrome-a case report},

author = {Manisha Nathani and Siddharth Karan and S. S. Asadullah Hussain Saberi and Syed Abdul Basith},

url = {https://ijmrr.medresearch.in/index.php/ijmrr/article/view/319/623},

doi = {10.17511/ijmrr.2015.i7.140},

issn = {2320-8686},

year  = {2015},

date = {2015-07-29},

urldate = {2015-07-29},

journal = {International Journal of Medical Research and Review          },

volume = {3},

issue = {7},

pages = {773-776},

abstract = {Laurence Moon Bardet Biedle syndrome is a rare, autosomal recessive genetic disorder. It has got wide spectrum of clinical features. Spastic paraplegia is predominant feature in Laurence Moon syndrome and polydactyly and obesity are predominant features in Bardet Biedle syndrome. Pigmentary retinal degeneration, mental retardation and hypogonadism are common to both. We report a case of 7 year old female who presented to us with complaints of night blindness. She showed all ocular features, most of the general features  of Laurence Moon Bardet Biedl syndrome and a typical family history. },

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Kishan_2015d,

title = {Homonymous heminopia: recovery of visual fields in acute stroke},

author = {Mutyala Gopal Kishan and Sheetal Baldava and Syed Abdul Basith},

url = {https://www.jebmh.com/articles/homonymous-hemianopia-recovery-of-visualfields-in-acute-stroke.pdf.pdf},

issn = {2349-2562},

year  = {2015},

date = {2015-05-04},

urldate = {2015-05-04},

journal = {Journal of Evidence Based Medicine and Healthcare},

volume = {2},

issue = {18},

pages = {2786-2791},

abstract = {Homonymous hemianopia the most common cause is stroke. The field defect of vascular origin the prognosis for spontaneous recovery is poor. The objective of this case was to describe the characteristics of spontaneous recovery of homonymous hemianopia. In this case left homonymous hemianopia. We have confirmed by formal visual field testing and CT scan was done which revealed right parietal infarct. Follow up of this case was done after 1 month visual field were analyzed spontaneous recovery was seen.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Baldava_2015b,

title = {Ocular colobamata in a family},

author = {Sheetal Baldava and Mutyala Gopal Kishan},

url = {https://www.jebmh.com/articles/ocular-colobamata-in-a-family.pdf.pdf},

issn = {2349-2562},

year  = {2015},

date = {2015-04-27},

urldate = {2015-04-27},

journal = {Journal of Evidence Based Medicine and Healthcare},

volume = {2},

issue = {17},

pages = {2634-2638},

abstract = {AIM: To identify the proportion of cases affected in a family with ocular colobamata. MATERIAL: Ocular colobomata present in a family METHOD: Visual acuity, Slit lamp examination, Ophthalmoscopy, Fundus Photography, B-Scan, Family members were examined. RESULTS: Family showed poor visual acuity, Iris and Choridal Coloboma without optic disc involvement and normal corneal diameter. CONCLUSION: Ocular coloboma occurring in patients of my study is family and genetically determined.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Kishan_2015,

title = {X linked juvenile retinoschisis},

author = {Mutyala Gopal Kishan and Sheetal Baldava and S. S. Asadullah Hussain Saberi},

url = {https://www.jebmh.com/articles/x-linked-juvenile-retinoschisis.pdf.pdf},

issn = {2349-2562},

year  = {2015},

date = {2015-04-20},

urldate = {2015-04-20},

journal = {Journal of Evidence Based Medicine and Healthcare},

volume = {2},

issue = {16},

pages = {2460-2464},

abstract = {X linked juvenile retinoschisis is a rare genetic disorder affecting males. It is recessively inherited due to mutation in XLRS1 gene, localized to Xp22 region.(1) The characteristic funduscopic findings, are a silver-grey retinal reflex, fovealretinoschisis, and peripheral retinoschisis. Electroretinograms (ERGs) typically record reduced b-wave amplitude with relative preservation of the a-wave amplitude. Visual acuity (VA) usually deteriorates slowly until the patient is about 20 years of age, stabilises, and sometimes deteriorates further because of macular degeneration.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Kishan_2015c,

title = {Sclerosing keratitis in reactivated systemic tuberculosis},

author = {Mutyala Gopal Kishan and Sheetal Baldava and Syed Musaab Mohiuddin},

url = {https://www.jebmh.com/articles/sclerosing-keratitis-in-reactivated-systemic-tuberculosis.pdf.pdf},

issn = { 2349-256},

year  = {2015},

date = {2015-04-20},

urldate = {2015-04-20},

journal = {Journal of Evidence Based Medicine and Healthcare},

volume = {2},

issue = {16},

pages = {2438-2441},

abstract = {Interstitial Keratitis is non-ulcerating inflammation of the corneal stroma without the involvement of either epithelium or endothelium.(1) Keratitis in scleritis is either infiltrative or destructive. Infiltrative lesions present as localised or diffuse stromal keratitis, sclerosing keratitis or as deep keratitis. Sclerosing keratitis is known to be associated with rheumatoid arthritis,(2) onchocerciasis, tuberculosis(3) and other infective or auto immune diseases. We are reporting a case of sclerosing keratitis in a patient with reactivated tuberculosis. A 40 year old female patient presented with unilateral sclerosing keratitis and mild anterior uveitis with recent loss of weight

and easy fatigability. She revealed a history of pulmonary tuberculosis in the past, for which she received Anti Tubercular Therapy for 6 months and was then declared cured at the time. A thorough workup for systemic risk factors was performed to evaluate etiological factors responsible for the keratitis and uveitis with special emphasis on tuberculosis. Though the blood work and radiology reports did not allow a definitive diagnosis of tuberculosis, in view of her past history, a therapeutic trial was initiated by restarting ATT. This resulted in improvement in her general condition. Though the corneal opacities didn’t resolve, there was an arrest in their

progression. Over the next 8 months, the corneal lesions remained stable. An ocular event was the only obvious sign in this patient to indicate reactivation of systemic tuberculosis and it helped initiate treatment emphasizing the role of an ophthalmologist in early detection and prompt institution of treatment in systemic diseases.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Kishan_2015e,

title = {Case of bilaterial anterior segment tuberculosis},

author = {Mutyala Gopal Kishan and Sheetal Baldava and Syed Khaleeluddin Aijaz},

url = {https://www.jebmh.com/articles/case-of-bilateral-anterior-segment-tuberculosis.pdf.pdf},

issn = {2349-2562},

year  = {2015},

date = {2015-04-20},

urldate = {2015-04-20},

journal = {Journal of Evidence Based Medicine and Healthcare},

volume = {2},

issue = {16},

pages = {2449-2452},

abstract = {Tuberculosis is an important cause of uveitis in our country. India has been declared the country with the highest tuberculosis burden with 25 % of the cases.(1) This is especially true in Andhra Pradesh and Telangana which have a high percentage of affected patients. However, tuberculous uveitis is usually a unilateral presentation. We report a case of bilateral uveitis of tuberculous origin in a 55 year old woman. She presented with different tuberculous manifestations in the two eyes. While the RE showed non granulomatous uveitis with sclerosing keratitis, the LE showed granulomatous uveitis with mutton fat keratic precipitates. Systemic

examination revealed an enlarged lymph node which was positive for tuberculosis on biopsy. She was hence diagnosed as extra pulmonary tuberculosis and was treated with ATT regimen. In this patient, uveitis was the initial manifestation and resulted in a systemic diagnosis. },

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Kishan_2015b,

title = {Profile of viral conjuctivitis},

author = {Mutyala Gopal Kishan and Sheetal Baldava and Jitha Vinay Reddy},

doi = {https://www.jebmh.com/articles/profile-of-viral-conjuctivitis.pdf.pdf},

issn = {2349-2562},

year  = {2015},

date = {2015-04-13},

urldate = {2015-04-13},

journal = {Journal of Evidence Based Medicine and Healthcare},

volume = {2},

issue = {15},

pages = {2296-2302},

abstract = {INTRODUCTION: Viral conjunctivitis is most commonly seen in the outpatient department. A variety of viruses which are responsible for conjunctival infection, of which Adenovirus is the most common. It is highly contagious during the first 2 weeks of infection. It can cause corneal involvement within 4-5 days after the onset of symptoms. Corneal lesions range from SPK (Superficial Punctate Keratitis) to epithelial defects. These corneal lesions may cause intense photophobia and impairment of vision. AIM: To find out the commonest etiological agent, to study the clinical features and complications related to it. METHODOLOGY: This study

was carried out prospectively. 100 patients who came to outpatient department between October 2013 to October 2014 were enrolled in the study. All the age groups and both the genders were included. Patients underwent slit lamp examination and were diagnosed clinically. 25 cases were submitted for Gram staining and Polymerase Chain Reaction (PCR) study to know the type of virus and serotype. RESULT: 100 patients were diagnosed with viral conjunctivitis and were kept on follow up. 21percent of patients developed SPK. Adenovirus 8 was found to be more common than other viruses. CONCLUSION: The present study showed Adeno virus to be the most common etiological agent causing viral conjunctivitis and complications like subepithelial opacities and diminished vision.},

keywords = {},

pubstate = {published},

tppubtype = {article}

}

@article{Baldava_2015,

title = {Pterygium excision in comparison of bare sclera technique and conjuctival autograft},

author = {Sheetal Baldava and Mutyala Gopal Kishan and Syeda Fatima Shabreen},

url = {https://www.jebmh.com/articles/pterygium-excision-in-comparison-of-bare-sclera-technique-and-conjuctival-autograft.pdf.pdf},

issn = {2349-2562},

year  = {2015},

date = {2015-04-13},

urldate = {2015-04-13},

journal = {Journal of Evidence Based Medicine and Healthcare},

volume = {2},

issue = {15},

pages = {2256-2262},

abstract = {INTRODUCTION: Pterygium is a degenerative condition of the subconjuctival tissue which proliferates as vascularized granulation tissue to invade the cornea, destroying the superficial layers of the stroma and bowmans membrane. Surgical removal remains the main stay of treatment. OBJECTIVE: To compare the recurrence rate of bare sclera technique and conjuctival autografting in primary pterygium excision. METHODOLOGY: This study was carried out as a prospective comparative study. This study was conducted during June 2013 to June 2014. 50 patients of primary pterygium were admitted. 25 patients were treated with bare sclera technique and 25 patients were treated with conjunctival auto graft. Post-operative follow up was

done for 6 months to find out the recurrence of pterygium and any other complications. RESULT: 25 patients received Bare Sclera Technique (n=25) and 25 patients received Conjunctival Auto Graft (CAG) (n=25). There was recurrence in 16 cases (40%) in group A with bare sclera technique and 2 cases (8%) had recurrence in GROUP B with conjunctival autograft. There was statistically significant difference in the recurrence rate in the 2 groups. Of other post-operative complications in bare sclera technique 5 cases (20%) had corneal opacity, 3 cases (12%) had scleral thinning, 5 cases (20%) had pyogenic granuloma. There was no significant post-operative complication with conjuctival auto graft. CONCLUSION: simple excision of pterygium followed by conjuctival autograft has the lowest recurrence rate and minimum incidence of complications compared to bare sclera technique. },

keywords = {},

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