Effect of topical diclofenac on postoperative photorefractive keratectomy pain: a randomized, controlled trial

Background A major disadvantage of photorefractive keratectomy is postoperative pain and discomfort. This study aims to evaluate whether topical diclofenac 0.1% therapy adds any extra benefit to systemic diclofenac in controlling pain after photorefractive keratectomy. Design Prospective randomized,...

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Veröffentlicht in:Clinical & experimental ophthalmology 2014-12, Vol.42 (9), p.810-814
Hauptverfasser: Eslampoor, Alireza, Ehsaei, Asieh, Abrishami, Mojtaba
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Sprache:eng
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Zusammenfassung:Background A major disadvantage of photorefractive keratectomy is postoperative pain and discomfort. This study aims to evaluate whether topical diclofenac 0.1% therapy adds any extra benefit to systemic diclofenac in controlling pain after photorefractive keratectomy. Design Prospective randomized, double‐masked clinical trial applied in the Khatam‐al‐Anbia Eye Hospital, Mashhad University of Medical Sciences, Mashhad, Iran. Participants Sixty‐eight individuals (age range, 18–35 years) having bilateral photorefractive keratectomy for myopic correction with or without astigmatism. Methods All patients received 100 mg of extended‐release oral diclofenac two times (12‐h interval) before photorefractive keratectomy surgery. Postoperatively, patients were randomized into the case and control groups. Case group was administered the diclofenac 0.1% drop, one drop 2 h preoperatively and four times daily postoperatively for 3 days, whereas the control group was given artificial tears instead. Main Outcome Measures Pain level, photophobia and functional activity were evaluated by the patient after operation. Results Two days after surgery, no statistically significant difference in pain level was noted between both groups. In addition, photophobia and functional activity was not different between the case and control groups. Eyelid oedema and conjunctival injection levels were significantly higher in the control group (P 
ISSN:1442-6404
1442-9071
DOI:10.1111/ceo.12343