Corrigendum to “Rowe P et al. safety and efficacy in parous women of a 52-mg levonorgestrel-medicated intrauterine device: a 7-year randomized comparative study with the TCu380A” [Contraception 2016;93:498–506]

AbstractThis was a double-blind randomized study to compare the safety and efficacy of timethoprim-polymyxin B (TP) and trimethoprim-sulfacetamide-polymyxin B (TSP) drops in the treatment of otorrhea. The 68 cases treated suffered from external otitis, recurrent otitis, recurrent otitis media with tympanic membrance perforation, or infected mastoid cavities and post-operative tympanoplasties. The TP ototopical solution was successful in 60·6 per cent of cases compared to 88·6 per cent of cases with TSP. These rates were statistically different using the Chi Square with Yates' correction method.There were no sings of ototoxicity, fungal infection overgrowth or local sensitivity to either of the solutions.The study has shown that both drugs are equally safe and that TSP is significantly more effective in the treatment of otorrhea.

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A COMPARATIVE STUDY OF THE SAFETY AND EFFICACY OF INTRA VAGINAL MISOPROSTOL TABLET VERSUS INTRA CERVICAL DINOPROSTONE GEL FOR CERVICAL RIPENING AND INDUCTION OF LABOUR

Journal of Evolution of Medical and Dental Sciences ◽

10.14260/jemds/2015/253 ◽

2015 ◽

Vol 04 (11) ◽

pp. 1769-1775

Author(s):

Madhavi K N ◽

◽

Polaiah K P ◽

Thokala Sivaiah

Keyword(s):

Comparative Study ◽

Induction Of Labour ◽

Cervical Ripening ◽

Safety And Efficacy ◽

Vaginal Misoprostol

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One-Year Visual and Refractive Outcomes following LASIK for Myopia and Myopic Astigmatism with MEL 90 versus Schwind Amaris 750S Excimer Laser: A Comparative Study

Journal of Ophthalmology ◽

10.1155/2021/9929181 ◽

2021 ◽

Vol 2021 ◽

pp. 1-10

Author(s):

Sheetal Brar ◽

Dishitha P. Rathod ◽

C. R. Roopashree ◽

Sri Ganesh

Keyword(s):

Comparative Study ◽

Clinical Outcomes ◽

Excimer Laser ◽

Infectious Keratitis ◽

Safety And Efficacy ◽

Refractive Outcomes ◽

The Mean ◽

One Year ◽

Myopic Astigmatism

Purpose. To compare clinical outcomes following LASIK for myopia performed with MEL 90 vs. Schwind Amaris 750S excimer laser. Methods. Data were collected retrospectively for patients who underwent Femto-LASIK, using the MEL 90 and Schwind Amaris 750S excimer laser for correction of myopia and myopic astigmatism within the range of −1.00 to −10.00 D SE from January 2013 till June 2018. Outcomes were analysed at 12 months for safety, efficacy, enhancement rate, and long-term complications. Results. A total of 328 eyes of 328 patients were analysed. One hundred and sixty-three eyes were treated with Schwind Amaris and the remaining 165 eyes with the MEL 90 laser. Twelve months postoperatively, the mean UDVA, CDVA, residual SE, and cylinder in the Amaris group were −0.10 ± 0.09 logMAR, −0.14 ± 0.06 logMAR, −0.21 ± 0.22 D, −0.13 ± 0.18 D versus −0.05 ± 0.07 logMAR, −0.09 ± 0.08 logMAR, −0.23 ± 0.23 D, and −0.14 ± 0.21 D for the MEL 90 group ( p values >0.05). For the Amaris group, safety and efficacy indices were 1.12 and 1.02, whereas for the MEL 90 group, these indices were 1.08 and 1.00, respectively. No eye in either group had any postop flap-related complications, infectious keratitis, diffuse lamellar keratitis, or keratectasia. Two eyes in the Amaris and 4 eyes in MEL 90 group required enhancement for the progression of myopia. Conclusion. At 12 months, both Schwind Amaris 750S and MEL 90 lasers demonstrated comparable clinical outcomes for myopic LASIK in a single surgeon setting.

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Comparative study of safety and efficacy of electrocautery blade with cold scalpel blade for skin opening during fixation of fracture of forearm bone with plate and screws

International Journal of Health & Allied Sciences ◽

10.4103/2278-344x.105065 ◽

2012 ◽

Vol 1 (3) ◽

pp. 153 ◽

Cited By ~ 1

Author(s):

KT Madhukar ◽

MT Ganesh

Keyword(s):

Comparative Study ◽

Safety And Efficacy ◽

Scalpel Blade ◽

Forearm Bone

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Novel Method and Device for Delivery and Retention of Intrauterine Devices in the Immediate Postpartum Period: Pilot Baboon Feasibility Study

2020 Design of Medical Devices Conference ◽

10.1115/dmd2020-9049 ◽

2020 ◽

Author(s):

Etse-Oghena Campbell ◽

Christopher G. Rylander ◽

Lauren Thaxton ◽

Marian Yvette Williams-Brown

Keyword(s):

Pregnant Woman ◽

Feasibility Study ◽

Postpartum Period ◽

Post Partum ◽

Intrauterine Device ◽

Intrauterine Devices ◽

Expulsion Rate ◽

Safety And Efficacy ◽

Novel Method ◽

Post Partum Period

Abstract The immediate post-partum period offers a convenient time to have an intrauterine device placed because of the co-location of a non-pregnant woman and her clinician; however, this practice is associated with increased expulsion rates of up to 30%, compared with a 3% expulsion rate for interval insertions. This paper presents a device and method to improve intrauterine device delivery and retention in the immediate postpartum period. This initial feasibility study illustrates that it is possible to temporarily tether a commercially available intrauterine device within the uterus of an immediately postpartum baboon. The results indicate this device and method are technically feasible, but further studies will be needed to evaluate safety and efficacy in reducing expulsion rates.

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