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Artykuły w czasopismach na temat „Triamcinolones”

Autor: Grafiati

Data publikacji: 3 czerwca 2025

Data aktualizacji: 31 lipca 2025

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1

Ferdian, Erwin, Soenarjo Soenarjo, and Uripno Budiono. "Perbandingan Penggunaan Triamcinolone Acetonide dan Lidocaine Pada Pipa Endotrakea Terhadap Angka Kejadian Nyeri Tenggorok Pasca Intubasi Pada Anestesi Umum." JAI (Jurnal Anestesiologi Indonesia) 6, no. 3 (2014): 182–92. http://dx.doi.org/10.14710/jai.v6i3.9128.

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Latar Belakang : Salah satu komplikasi pemasangan pipa endotrakea adalah nyeri tenggorok paska operasi akibat kerusakan mukosa trakhea. Triamcinolone acetonide gel mengandung kortikosteroid disamping dapat sebagai agen lubrikasi juga mempunyai efek anti inflamasi. Tujuan : Membandingkan efek lubrikasi pipa endotrakea dengan triamcinolone acetonide gel dan lidocaine jelly terhadap angka kejadian nyeri tenggorok paska intubasi. Metode : 58 pasien yang menjalani operasi elektif dengan anestesi umum di RSUP Dr.Kariadi Semarang dan memenuhi kriteria inklusi dibagi secara acak menjadi 2 kelompok. In

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Wibowo, Adi, Soenarjo Soenarjo, and Hari Hendriarto Satoto. "Perbandingan Penggunaan Triamcinolone Acetonide Dan Gel Larut Air Pada Pipa Endotrakea Terhadap Angka Kejadian Nyeri Tenggorok." JAI (Jurnal Anestesiologi Indonesia) 6, no. 3 (2014): 170–81. http://dx.doi.org/10.14710/jai.v6i3.9122.

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Latar Belakang : Salah satu komplikasi pemasangan pipa endotrakea adalah nyeri tenggorok paska operasi akibat kerusakan mukosa trakea. Pemberian lubrikasi pada pipa endotrakea diharapkan mampu mengurangi angka kejadian nyeri tenggorok. Triamcinolon acetonide gel mengandung kortikosteroid disamping dapat sebagai agen lubrikasi juga mempunyai efek anti inflamasi.Tujuan : Membandingkan efek lubrikasi pipa endotrakea dengan triamcinolone acetonide gel dan gel larut air terhadap angka kejadian nyeri tenggorok paska intubasi.Metode : 50 pasien yang menjalani operasi elektif dengan anestesi umum di R

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Karadzic, Jelena, Igor Kovacevic, Jelena Ljikar, Zorka Grgic, and Gordana Devecerski. "Pharmacological intravitreal treatment for macular edema in branch retinal vein occlusion: Three-month results." Medical review 68, no. 9-10 (2015): 295–300. http://dx.doi.org/10.2298/mpns1510295k.

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Introduction. Macular edema is the main cause of visual loss in patients with branch retinal vein occlusion. Macular edema is initially reversible, but over time, permanent loss of vision occurs from structural damage to the macula. For this reason, there is a need for more rapid and effective treatments than laser photocoagulation which has been established as a gold standard. There are several pharmacologic agents which have changed the management of macular edema. Material and Methods. Twenty eyes of 20 consecutive patients of the Department of Eye Diseases, Clinical Center of Vojvodina, in

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4

&NA;. "Triamcinolone see Desoximethasone/triamcinolone." Reactions Weekly &NA;, no. 293 (1990): 12. http://dx.doi.org/10.2165/00128415-199002930-00050.

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Sun, Wenyangming, Li Qian, Meng He, Dashou Wang, and Xiaohua Zou. "Effects and Mechanism of Epidural Administration of Triamcinolone Acetonide on Nerve Root Inflammation and Epidural Space Adhesion in Rabbits." Journal of Biomedical Nanotechnology 19, no. 5 (2023): 881–86. http://dx.doi.org/10.1166/jbn.2023.3583.

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This study aimed to investigate the effect and mechanism of triamcinolone acetonide on nerve root inflammation and epidural adhesion in rabbits. The experiment involved 30 male New Zealand white rabbits, which were divided into three groups: Model, Dexamethasone, and Triamcinolone. After establishing the rabbit model of nerve root inflammation and epidural adhesion, dexamethasone and triamcinolone acetonide were injected through the epidural catheter. The results showed that triamcinolone acetonide significantly reduced nerve root inflammation, epidural adhesion, and nerve root pain. It also d

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6

Leow, Mabel Qi He, Aik Siew Robyn Hay, Shu Li Ng, et al. "A randomized controlled trial comparing ketorolac and triamcinolone injections in adults with trigger digits." Journal of Hand Surgery (European Volume) 43, no. 9 (2018): 936–41. http://dx.doi.org/10.1177/1753193418756808.

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We assessed the efficacy of ketorolac trometamol injections compared with triamcinolone acetonide injections in trigger digits. Patients with trigger digits were randomized to receive either ketorolac or triamcinolone. They were followed up at 3, 6, 12 and 24 weeks, and monitored for resolution of triggering, pain and total active motion. One hundred and twenty-one patients with single trigger digits were recruited (59 ketorolac, 62 triamcinolone). At 6 weeks, 54% of patients in the triamcinolone group had complete resolution of trigger, whereas no patients in the ketorolac group had resolutio

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7

Erna, Riani. "COMPARISON OF MUTANT P53 PROTEIN EXPRESSION IN PTERYGIUM GROUP WITH AND WITHOUT TRIAMCINOLONE ACETONITED INJECTION." Jurnal Ilmu Kesehatan Masyarakat 9, no. 3 (2018): 171–78. http://dx.doi.org/10.26553/jikm.2018.9.3.171-178.

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Background: Mutant p53 protein is produced by mutant p53 gene, this protein takes part in tissue hyperplasia process in pterygium. Triamcinolone acetonide in often use to reduce reccurency. Besides decreasing the inflamation triamcinolone acetonide is assumed to be able to repair the function of p53 gene. Thus, it reactivates cell apoptosis system and prevent the tissue hyperplasia process in pterygium.To compare Mutant p53 Protein Expression in Pterygium Group With and Without Triamcinolone Acetonide InjectionMethods: This research is a randomized clinical trial study consists of 31 subject w

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8

Erna, Riani. "COMPARISON OF MUTANT P53 PROTEIN EXPRESSION IN PTERYGIUM GROUP WITH AND WITHOUT TRIAMCINOLONE ACETONITED INJECTION." Jurnal Ilmu Kesehatan Masyarakat 9, no. 3 (2018): 171–78. http://dx.doi.org/10.26553/jikm.v9i3.309.

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Background: Mutant p53 protein is produced by mutant p53 gene, this protein takes part in tissue hyperplasia process in pterygium. Triamcinolone acetonide in often use to reduce reccurency. Besides decreasing the inflamation triamcinolone acetonide is assumed to be able to repair the function of p53 gene. Thus, it reactivates cell apoptosis system and prevent the tissue hyperplasia process in pterygium.To compare Mutant p53 Protein Expression in Pterygium Group With and Without Triamcinolone Acetonide InjectionMethods: This research is a randomized clinical trial study consists of 31 subject w

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9

Van de Kerkhof, P. C., A. Chang, H. B. Van der Walle, I. Van Vlijmen-Willems, J. B. Boezeman, and R. Huigen-Tijdink. "Weekly treatment of psoriasis with a hydrocolloid dressing in combination with triamcinolone acetonide. A controlled comparative study." Acta Dermato-Venereologica 74, no. 2 (1994): 143–46. http://dx.doi.org/10.2340/0001555574147148.

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In a within subject comparison, the efficacy and the tolerability of topical treatment with triamcinolone acetonide under a hydrocolloid dressing were compared with triamcinolone acetonide monotherapy, monotherapy with hydrocolloid dressing and triamcinolone acetonide under plastic occlusion. The clinical efficacy of hydrocolloid dressing as a monotherapy and the pronounced clinical efficacy of this occlusive in combination with triamcinolone acetonide were confirmed. Comparing the hydrocolloid dressing (Duoderm E) and the plastic semi-occlusive (Opsite IV 3000), we concluded that the tolerabi

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10

Gaddey, Pridhvi Krishna, and Raja Sundararajan. "Liquid Chromatographic-Electrospray Ionization-Mass Spectrometry Method for the Simultaneous Determination of Gramicidin, Neomycin & Triamcinolone Acetonide and Characterization of Novel Forced Degradation Products." Asian Journal of Chemistry 35, no. 2 (2023): 379–88. http://dx.doi.org/10.14233/ajchem.2023.26922.

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The dosage form iotrim (gramicidin, neomycin and triamcinolone) is a combination of two antibiotics (gramicidin and neomycin) and a steroid (triamcinolone). The antibiotics work by killing the bacteria that cause infections. The steroid blocks the action of chemical messengers (prostaglandins) that make the affected area red, swollen and itchy. Consequently, there was still a need to develop a simple, less time consuming and economical method for the simultaneous determination of gramicidin, neomycin and triamcinolone acetonide. The current work is an effort to develop a fast and reproducible

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11

Tang, Bin, Xiaoxuan Wang, Yi Luo, Zhi Li, and Yannan He. "Efficacy and Safety of Intravitreal Injection of Triamcinolone Acetonide and Conbercept for Intraocular Lens after Cataract Surgery." Evidence-Based Complementary and Alternative Medicine 2022 (May 25, 2022): 1–6. http://dx.doi.org/10.1155/2022/5606343.

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Objective. To investigate the effect of intravitreal injection of triamcinolone acetonide and conbercept on the efficacy and safety of diabetic macular edema (DME) after cataract intraocular lens (IOL) surgery. Methods. A total of 350 patients with cataract complicated with diabetic macular edema in our hospital from January 2017 to July 2021 were randomly divided into conbercept group and triamcinolone acetonide group. Patients in the conbercept group were given intravitreal injection of conbercept during IOL surgery, and patients in the triamcinolone acetonide group were given injection of t

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12

Li, Chengyan, Guihong Zhao, Lianwei Lu, and Xiuping Du. "Effect of triamcinolone acetonide-loaded nanoparticles on diabetic retinopathy in rats." Materials Express 10, no. 9 (2020): 1511–17. http://dx.doi.org/10.1166/mex.2020.1784.

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Triamcinolone acetonide acetate (TAA)-loaded nanostructured lipid carriers (NLC) were prepared to investigate their transdermal absorption in vitro and establish a diabetic retinopathy (DR) rat model. To evaluate the effect of triamcinolone acetonide-loaded nanoparticle capsules on improving the structure of the retina and pancreas, we measured blood glucose levels and investigated the pathological changes in the retina and pancreas. The effect of triamcinolone acetonide-loaded nanoparticle capsules on the morphology of the retina and pancreas of the rats with DR was determined and compared am

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13

&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1380 (2011): 40–41. http://dx.doi.org/10.2165/00128415-201113800-00147.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1384 (2012): 55–56. http://dx.doi.org/10.2165/00128415-201213840-00218.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1384 (2012): 56. http://dx.doi.org/10.2165/00128415-201213840-00223.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1384 (2012): 56. http://dx.doi.org/10.2165/00128415-201213840-00227.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1385 (2012): 43. http://dx.doi.org/10.2165/00128415-201213850-00157.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1392 (2012): 45. http://dx.doi.org/10.2165/00128415-201213920-00152.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1396 (2012): 39. http://dx.doi.org/10.2165/00128415-201213960-00136.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 715 (1998): 12. http://dx.doi.org/10.2165/00128415-199807150-00035.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 725 (1998): 12. http://dx.doi.org/10.2165/00128415-199807250-00036.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1160 (2007): 30. http://dx.doi.org/10.2165/00128415-200711600-00087.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1163 (2007): 24–25. http://dx.doi.org/10.2165/00128415-200711630-00077.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1164 (2007): 24. http://dx.doi.org/10.2165/00128415-200711640-00069.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1166 (2007): 22. http://dx.doi.org/10.2165/00128415-200711660-00067.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1168 (2007): 26. http://dx.doi.org/10.2165/00128415-200711680-00076.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1173 (2007): 26. http://dx.doi.org/10.2165/00128415-200711730-00081.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1175 (2007): 24–25. http://dx.doi.org/10.2165/00128415-200711750-00084.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1175 (2007): 24. http://dx.doi.org/10.2165/00128415-200711750-00085.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1175 (2007): 25. http://dx.doi.org/10.2165/00128415-200711750-00089.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1176 (2007): 30–31. http://dx.doi.org/10.2165/00128415-200711760-00095.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1177 (2007): 29. http://dx.doi.org/10.2165/00128415-200711770-00089.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1178 (2007): 34. http://dx.doi.org/10.2165/00128415-200711780-00100.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1179 (2007): 34. http://dx.doi.org/10.2165/00128415-200711790-00105.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1181 (2007): 36. http://dx.doi.org/10.2165/00128415-200711810-00109.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1185 (2008): 30. http://dx.doi.org/10.2165/00128415-200811850-00092.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1190 (2008): 25. http://dx.doi.org/10.2165/00128415-200811900-00079.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1192 (2008): 31. http://dx.doi.org/10.2165/00128415-200811920-00083.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1193 (2008): 29. http://dx.doi.org/10.2165/00128415-200811930-00091.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1120 (2006): 18. http://dx.doi.org/10.2165/00128415-200611200-00067.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1123 (2006): 21–22. http://dx.doi.org/10.2165/00128415-200611230-00063.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1125 (2006): 14–15. http://dx.doi.org/10.2165/00128415-200611250-00041.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1135 (2007): 33. http://dx.doi.org/10.2165/00128415-200711350-00125.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1135 (2007): 33–34. http://dx.doi.org/10.2165/00128415-200711350-00128.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1136 (2007): 25. http://dx.doi.org/10.2165/00128415-200711360-00081.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1136 (2007): 26. http://dx.doi.org/10.2165/00128415-200711360-00085.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1146-1147 (2007): 26. http://dx.doi.org/10.2165/00128415-200711460-00083.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1148 (2007): 33. http://dx.doi.org/10.2165/00128415-200711480-00104.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1149 (2007): 25. http://dx.doi.org/10.2165/00128415-200711490-00079.

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&NA;. "Triamcinolone." Reactions Weekly &NA;, no. 1152 (2007): 26. http://dx.doi.org/10.2165/00128415-200711520-00081.

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