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1.
Iran J Public Health ; 49(7): 1202-1210, 2020 Jul.
Article in English | MEDLINE | ID: mdl-33083286

ABSTRACT

BACKGROUND: We aimed to use the scientometric approach to evaluate immunological studies on the subject of sulfur mustard over the past 20 years. METHODS: In this scientometric study, the Web of Science Core Collection was searched on the studies about sulfur mustard. The published papers related to the field of immunology were retrieved from these papers. HistCite software and VOSviewer were the applied software packages for bibliometric analysis, information visualization, and creating bibliometric networks. RESULTS: Over the past 20 years, 741 researchers from 22 countries have published 201 scientific papers in 95 journals. Iran and the United States with 93 and 68 published articles ranked at the top. The Journal of International Immunopharmacology, with 33 published papers, 439 Total Global Citation Score (TGCS), and 105 Total Local Citation Score (TLCS) was the most productive and most influential in this regard. The paper entitled "Biomonitoring of exposure to chemical warfare agents: A review" and another paper entitled "Sardasht-Iran Cohort Study of Chemical Warfare Victims: Design and Methods" were the most influential papers in this topic with 200 TGCS and 27 TLCS, respectively. The most productive and the most influential centers were "Immunoregulation Research Center of Shahed University" and "The Janbazan Medical and Engineering Research Center (JMERC)," respectively. CONCLUSION: The result of our report as the unique scientometric evaluation of the research on sulfur mustard and Immunology can be used as a roadmap for authors, researchers, and policymakers to define the best ways to allocate their financial and executive resources.

2.
Ophthalmic Plast Reconstr Surg ; 33(3S Suppl 1): S47-S49, 2017.
Article in English | MEDLINE | ID: mdl-26020714

ABSTRACT

Schwartz-Jampel syndrome is an autosomal recessive disease that comprises facial and musculoskeletal deformity. Hereby, the authors report 2 cases of Schwartz-Jampel syndrome and surgical method of their management. The first case was a boy who was result of twin delivery whose sibling was completely normal. The second case was a girl who was the first child of her family. Both were born to a consanguineous marriage. Both had developed characteristic facial expressions of Schwartz-Jampel syndrome between 18 and 24 months of age. They had Botulinum toxin A injection (twice in the first and ones in the second case) with no improvement. Both were referred because of being functionally blind due to inability to open the eyelids around age 3.5 years. Orbicularis oculi myectomy, partial corrugator muscle excision, levator tucking, and lateral tarsal strip procedure was performed on both cases. No complication and no recurrence of eyelid contraction were observed after 4 years and 6 months follow up in the first and second case, respectively.


Subject(s)
Blepharoplasty/methods , Blepharospasm/drug therapy , Botulinum Toxins, Type A/administration & dosage , Eyelids/surgery , Osteochondrodysplasias/complications , Adult , Blepharospasm/etiology , Facial Muscles , Female , Humans , Infant , Injections, Intramuscular , Male , Neuromuscular Agents/administration & dosage , Young Adult
3.
Ophthalmic Epidemiol ; 24(1): 3-10, 2017 02.
Article in English | MEDLINE | ID: mdl-28001456

ABSTRACT

PURPOSE: To determine the measurement properties of the Persian language version of the Graves orbitopathy quality of life questionnaire (GO-QOL). METHODS: Following a systematic translation and cultural adaptation process, 141 consecutive unselected thyroid eye disease (TED) patients answered the Persian GO-QOL and underwent complete ophthalmic examination. The questionnaire was again completed by 60 patients on the second visit, 2-4 weeks later. Construct validity (cross-cultural validity, structural validity and hypotheses testing), reliability (internal consistency and test-retest reliability), and floor and ceiling effects of the Persian version of the GO-QOL were evaluated. Furthermore, Rasch analysis was used to assess its psychometric properties. RESULTS: Cross-cultural validity was established by back-translation techniques, committee review and pretesting techniques. Bi-dimensionality of the questionnaire was confirmed by factor analysis. Construct validity was also supported through confirmation of 6 out of 8 predefined hypotheses. Cronbach's α and intraclass correlation coefficient (ICC) were 0.650 and 0.859 for visual functioning and 0.875 and 0.896 for appearance subscale, respectively. Mean quality of life (QOL) scores for visual functioning and appearance were 78.18 (standard deviation, SD, 21.57) and 56.25 (SD 26.87), respectively. Person reliabilities from the Rasch rating scale model for both visual functioning and appearance revealed an acceptable internal consistency for the Persian GO-QOL. CONCLUSION: The Persian GO-QOL questionnaire is a valid and reliable tool with good psychometric properties in evaluation of Persian-speaking patients with TED. Applying Rasch analysis to future versions of the GO-QOL is recommended in order to perform tests for linearity between the estimated item measures in different versions.


Subject(s)
Graves Ophthalmopathy/psychology , Quality of Life , Adult , Aged , Aged, 80 and over , Disability Evaluation , Factor Analysis, Statistical , Female , Graves Ophthalmopathy/diagnosis , Humans , Male , Middle Aged , Psychometrics/methods , Reproducibility of Results , Severity of Illness Index , Surveys and Questionnaires
4.
Ophthalmic Plast Reconstr Surg ; 33(5): 350-354, 2017.
Article in English | MEDLINE | ID: mdl-27636242

ABSTRACT

PURPOSE: To report 10-year results of a 1-stage, obstruction-based, endoscopic approach in children with congenital nasolacrimal duct obstruction (CNLDO) with and without prior failed probing/intubation. METHODS: In a retrospective study, children with primary CNLDO of >6 months old previously failed probing/intubation, acute dacryocystitis or dacryocele at any age, and at least 6 months follow up. Diagnosis was based on history of tearing and dye disappearance test. Excluded were patients with complete puncto-canalicular obstruction and craniofacial anomaly. Type of CNLDO was confirmed using endonasal endoscopic guided probing. An endoscopic probing was performed for membranous, intubation for incomplete complex, and dacryocystorhinostomy for complete complex CNLDO. They were followed at 1 week, 1, 3, and 6 months, and then after. Success was defined as no or occasional tearing related to noxious stimulus at least 6 months after the procedure. RESULTS: There were 226 eyes (200 patients). Mean age was 26.72 months. Previous failed probing/intubation was in 34.1%. Inferior turbinate impaction in 73.5% and septal deviation in 2.7% were noted. Membranous CNLDO was found in 38.9%, incomplete complex in 57.9%, and complete complex in 3.1%. Mean time of tube removal was 11.9 weeks and last follow-up time was 24.3 months. There was no significant effect of any variables on the final success rates (probing: 96.5%, intubation: 95.4%, dacryocystorhinostomy: 100%). CONCLUSIONS: One-stage, obstruction-based endoscopic approach to CNLDO resulted in a high success rate for different types of CNLDO (membranous, incomplete complex, and complete complex). No variable significantly affected the success rates.


Subject(s)
Dacryocystorhinostomy/methods , Endoscopy/methods , Lacrimal Apparatus/surgery , Lacrimal Duct Obstruction/congenital , Child, Preschool , Female , Follow-Up Studies , Humans , Infant , Infant, Newborn , Lacrimal Apparatus/diagnostic imaging , Lacrimal Duct Obstruction/diagnosis , Male , Retrospective Studies , Time Factors , Treatment Outcome
5.
Am J Ophthalmol ; 165: 33-8, 2016 05.
Article in English | MEDLINE | ID: mdl-26930225

ABSTRACT

PURPOSE: To compare the results of tear film and lacrimal drainage system tests between anophthalmic socket and normal eye and assess discharge characteristics and frequency of prosthesis removal (questionnaire), eyelid function, and meibomian glad dysfunction (MGD). DESIGN: Prospective masked case control. METHODS: Subjects (≥6 years and ≥6 months of wearing prosthesis) with unilateral acquired anophthalmic socket discharge were included. Excluded was ocular adnexal abnormality of any reason and incomplete tests. The subjective questionnaire was completed. Blinking rate, lagophthalmos, eyelid laxity, MGD, Schirmer test, tear meniscus height, and dye disappearance test were assessed by a masked examiner. Another masked examiner performed an irrigation test 1 week later and interpreted the scintigraphy images at the end of the study. RESULTS: Included were 50 subjects (mean age: 31.3 years, mean prosthesis wear: 96.1 months). Discharge was frequent or very frequent in 85%, mucoid or mucopurulent in 90%, and moderate to severe in 86% of the subjects. MGD in 58%, lagophthalmos in 80%, and eyelid laxity in 46% were observed. Anophthalmic socket sides showed a significantly lower tear production and higher tear drainage obstruction. Subjects with frequent prosthesis removal had a significantly (P = .02) greater lagophthalmos and blinking rate (P = .04). The blinking rate was also significantly greater in subjects with higher frequency of discharge (P = .04). CONCLUSION: Tear film impairment (aqueous and lipid) and lacrimal drainage obstruction should be considered in subjects with anophthalmic socket discharge. A significantly higher blinking rate and lagophthalmos were found in subjects with higher frequency of prosthesis removal.


Subject(s)
Eyelid Diseases/physiopathology , Lacrimal Apparatus/physiopathology , Lacrimal Duct Obstruction/physiopathology , Meibomian Glands/physiopathology , Orbital Diseases/physiopathology , Orbital Implants , Tears/physiology , Adolescent , Adult , Aged , Blinking , Case-Control Studies , Child , Double-Blind Method , Eye, Artificial , Eyelid Diseases/diagnosis , Female , Humans , Lacrimal Duct Obstruction/diagnosis , Male , Middle Aged , Orbital Diseases/surgery , Prospective Studies , Prosthesis Fitting , Surveys and Questionnaires
8.
J Cataract Refract Surg ; 38(1): 92-6, 2012 Jan.
Article in English | MEDLINE | ID: mdl-21983301

ABSTRACT

PURPOSE: To determine the in vitro susceptibility of post-cataract surgery endophthalmitis bacterial isolates to different concentrations of povidone-iodine at different exposure times. SETTING: Poostchi Ophthalmology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. DESIGN: Experimental study. METHODS: Ocular-fluid samples obtained from patients diagnosed with postoperative endophthalmitis were submitted to a microbiology laboratory for culture. One milliliter of microbial isolate suspension with a McFarland standard turbidity of 0.5 was mixed with 1 mL of 1%, 2%, 5%, and 10% povidone-iodine solutions. After 1 minute, 5 minutes, and 15 minutes of exposure at 37°C, each solution was transferred to appropriate culture media and incubated at 37°C for 24 hours. RESULTS: Organisms were isolated in 30 (68%) of the 44 patients evaluated. Coagulase-negative Staphylococcus was identified in 14 cases (47%), Streptococcus species in 8 cases (27%), Staphylococcus aureus in 5 cases (17%), Bacillus cereus in 2 cases (6%), and Pseudomonas aeruginosa in 1 case (3%). Higher povidone-iodine concentrations and longer exposure times were more effective than lower povidone-iodine concentrations or shorter exposure in preventing growth of bacterial isolates. The most effective regimens were 5% povidone-iodine for 15 minutes and 10% povidone-iodine for at least 5 minutes. With a high bacterial load, 13% of bacterial isolates remain viable after exposure to 10% povidone-iodine, even with a long exposure time. CONCLUSION: Results indicate that using 5% povidone-iodine for 15 minutes or 10% povidone-iodine for 5 minutes can prevent the growth of most post-cataract surgery endophthalmitis bacterial isolates.


Subject(s)
Anti-Infective Agents, Local/administration & dosage , Bacteria/drug effects , Endophthalmitis/microbiology , Eye Infections, Bacterial/microbiology , Postoperative Complications , Povidone-Iodine/administration & dosage , Aqueous Humor/microbiology , Bacteria/isolation & purification , Bacteriological Techniques , Colony Count, Microbial , Endophthalmitis/prevention & control , Eye Infections, Bacterial/prevention & control , Humans , Microbial Sensitivity Tests , Microbial Viability , Phacoemulsification , Time Factors , Vitreous Body/microbiology
9.
Cornea ; 29(10): 1091-5, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20628301

ABSTRACT

PURPOSE: To assess the degrees of agreement in measuring corneal thickness in normal eyes between 2 noncontact systems based on the dual Scheimpflug system (Galilei; Ziemer) and rotating Scheimpflug imaging (HR Pentacam; Oculus) and also between each of these methods and the gold-standard method of ultrasound pachymetry. METHODS: In a prospective study, measurement agreement was assessed in 47 eyes of 47 healthy subjects. All eyes were examined with each of the 3 devices. Measurements made with the Galilei and HR Pentacam were compared with those made with ultrasound. The central corneal thickness (CCT) and thinnest pachymetry of the Galilei and HR Pentacam were also compared. RESULTS: The mean values of CCT obtained from Galilei, HR Pentacam, and ultrasound were 560.57 ± 29.10, 542.31 ± 30.50, and 548.61 ± 29.92 µm, respectively. The 95% limits of agreement of each of these devices with ultrasound were -11.03 and +34.94 µm for the Galilei and -33.67 and +20.74 µm for the Pentacam. The 95% limits of agreement of Galilei with Pentacam in measurement of central and thinnest corneal thickness were -3.39 and +33.11 and -10.40 and +27.29 µm, respectively. Although CCT measurements made with the HR Pentacam were thinner (P < 0.001), and those obtained with Galilei were thicker (P < 0.001) than those made with ultrasound, there were significant correlation between Galilei and ultrasound (r = 0.92; P < 0.0001) and between HR Pentacam and ultrasound (r = 0.89; P < 0.0001). The central and thinnest corneal thickness measurements made with the HR Pentacam were thinner (P < 0.0001) than those made with Galilei, but there was a significant correlation between Galilei and HR Pentacam in measuring CCT (r = 0.96; P < 0.0001) and thinnest corneal thickness (r = 0.95; P < 0.0001). Bland-Altman plots showed good agreement between these methods. CONCLUSIONS: Although differences between the devices were statistically significant, there was good correlation and agreement between Galilei and Pentacam in measuring central and thinnest corneal thickness. The corneal thickness measurements made with the HR Pentacam and Galilei also showed good correlation and agreement with those made with ultrasound.


Subject(s)
Cornea/anatomy & histology , Diagnostic Techniques, Ophthalmological/instrumentation , Adult , Anthropometry , Cornea/diagnostic imaging , Female , Humans , Male , Prospective Studies , Reference Values , Reproducibility of Results , Ultrasonography , Young Adult
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