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1.
Professional Medical Journal-Quarterly [The]. 2014; 21 (4): 810-815
in English | IMEMR | ID: emr-149896

ABSTRACT

To evaluate the effect of Intravitreal Bevacuzimab on Best Corrected Visual Acuity in patients with clinically significant diabetic macular edema. A prospective uncontrolled interventional case series in which 42 eyes of 31 consecutive diabetic patients with clinically significant macular edema and no significant comorbid ocular association presenting in the outpatients department of Holy Family Hospital and EYE SURGERY clinic, Rawalpindi Pakistan and opting for the treatment from 1st September 2013 to 31st January 2014 were given an intravitreal injection of Bevacizumab. BCVA was documented prior to and four weeks after the injection. Main outcome measure was changes in BCVA. Out of the 31 patients included in the study 14[45.16%] were male and 17 [54.83%] female. Average age was 56.1 +/- 7.6. All 31 patients [42 eyes] came for follow up and their BCVA recorded. 41 [97.61%] eyes showed an improvement of one or more line on Snellen's chart at 4 weeks. 14 [33.33%] eyes showed an improvement of one line, 19 [45.23%] eyes an improvement of two lines, 6 [14.28%] eyes three lines and just 2 [4.76%] eyes had an improvement of four lines on Snellen's chart at 4 weeks. Only 1[2.38%] eye remained same with no worsening. On log MAR conversion scale for Snellen's letters the BCVA improved from 0.76 +/- 0.27 to 0.47 +/- 0.27 [p< 0.001]. No significant complications were observed in any of the eyes. The use of intravitreal Bevacizumab [1.25mg/0.05ml] is a safe and effective moe of treatment for clinically significant diabetic macular edema


Subject(s)
Humans , Male , Female , Diabetes Mellitus , Antibodies, Monoclonal, Humanized , Intravitreal Injections , Visual Acuity , Prospective Studies
2.
Professional Medical Journal-Quarterly [The]. 2013; 20 (4): 617-622
in English | IMEMR | ID: emr-138460

ABSTRACT

Goldenhar syndrome is a congenital disorder with diverse clinical presentation. This case series describes various clinical manifestations of Goldenhar Syndrome. 11 patients at least two of the described features of Goldenhar syndrome were randomly included in the study to form a case series. Clinical data of all these subjects was documented, described in percentages and analyzed. Out of the 11 patients studied, 6 were females and 5 males. Mean age was 7.3 years [ranging from 1 year to 23 years]. 7 [63.6%] patients had a limbal dermoid, 6 [54.5%] patient had mandibular hypoplasia, whereas only 3 [27.3%] presented with hemifacial microsomia. Spinal defects and polydactyly were present in [36.4%] patients each. There was one patient [9%] who had both microphthalmia and lid coloboma in addition to limbal dermoid. Similarly, renal defect [atrophic kidney], cleft upper lip and palate and CNS defect [7th nerve palsy] were present in one patient [9%] each. None of our patients had either cardiac or GIT defect. In our study we were able to document the variable manifestations of Goldenhar syndrome with their frequencies. This knowledge base will help us in planning treatment and assistance strategies or these patients


Subject(s)
Humans , Female , Male , Congenital, Hereditary, and Neonatal Diseases and Abnormalities , Facial Asymmetry , Random Allocation , Polydactyly , Dermoid Cyst
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