Department of Pediatrics, Division of Neonatology, Istanbul Medeniyet University Goztepe Training and Research Hospital, Istanbul, Turkey.
J Perinat Neonatal Nurs. 2022;36(3):305-311. doi: 10.1097/JPN.0000000000000675.
Screening examinations for retinopathy of prematurity (ROP) are critical to reduce ROP-related vision loss; however, the procedure is painful and uncomfortable, and topical anesthetics do not completely suppress the pain responses. The number of safe and effective pharmacological options to reduce pain during eye examinations for ROP screening in preterm infants is limited. This study compared the efficacy of oral ibuprofen and oral paracetamol in reducing pain during screening for ROP in preterm infants. This prospective observational study was conducted at a tertiary-care neonatal intensive care unit. Forty-four preterm infants with gestational age of 32 weeks and less undergoing ROP screening were included. Each enrolled infant received either oral ibuprofen 10 mg/kg (n = 22) or oral paracetamol 10 mg/kg (n = 22) 1 hour before eye examination. The primary outcome measure was pain assessed by the Neonatal Pain, Agitation, and Sedation Scale (N-PASS). Secondary outcome measures were tachycardia, bradycardia, desaturations, and crying time. The groups were similar for gestational age, birth weight, and postnatal age at examination (P > .05). The mean N-PASS scores were not significantly different between the oral ibuprofen and oral paracetamol groups (8.64 ± 1.57 vs 8.50 ± 1.71, respectively, P = .605). Moreover, no significant intergroup differences were observed in the crying time and the incidence of tachycardia/bradycardia and desaturation (P > .05). Ibuprofen or paracetamol administered orally before ROP screening in preterm infants had similar analgesic effects and did not significantly alleviate pain during eye examination.
早产儿视网膜病变(ROP)筛查对减少与 ROP 相关的视力丧失至关重要;然而,该程序会引起疼痛和不适,并且局部麻醉并不能完全抑制疼痛反应。在早产儿 ROP 筛查的眼部检查中,减轻疼痛的安全有效的药物选择数量有限。本研究比较了口服布洛芬和口服扑热息痛在减轻早产儿 ROP 筛查时疼痛的效果。这项前瞻性观察性研究在一家三级保健新生儿重症监护病房进行。共纳入 44 名胎龄为 32 周及以下的早产儿进行 ROP 筛查。每例入组婴儿在眼部检查前 1 小时分别接受口服布洛芬 10mg/kg(n = 22)或口服扑热息痛 10mg/kg(n = 22)。主要结局测量指标是通过新生儿疼痛、躁动和镇静评分(N-PASS)评估的疼痛。次要结局测量指标是心动过速、心动过缓、饱和度降低和哭泣时间。两组的胎龄、出生体重和检查时的出生后年龄相似(P >.05)。口服布洛芬和口服扑热息痛组的平均 N-PASS 评分无显著差异(分别为 8.64 ± 1.57 与 8.50 ± 1.71,P =.605)。此外,两组在哭泣时间和心动过速/心动过缓和饱和度降低的发生率方面无显著差异(P >.05)。在早产儿 ROP 筛查前口服布洛芬或扑热息痛具有相似的镇痛效果,并且在眼部检查期间并未显著减轻疼痛。