ABSTRACT
Objective: Retinopathy of Prematurity (ROP) stands as a critical challenge faced by neonatal intensive care units (NICUs). The ROP examination usually begins when the patients are in the NICU, then are followed up in policlinics. Thus, side effects of examination procedure may occur in the home, frightening members of the family. So, our objective to investigate the impact of neonatal pain on systemic and procedural side effects of ROP examinations and mydriatic drops to improve screening safety.
Materials And Methods: The study planned as a prospective descriptive investigation, was conducted with 70 preterm infants admitted to the NICU between August and November 2012. Patients monitored during examination and 48 hours after than for vital signs and recording any side effects. Neonatal İnfant Pain Scale was performed all patients. For statistical analysis SPSS 15 was used.
Results: Adverse effects were absent in 41.4% of the infants. Flushing was noted in 22.9%, gastric residuals in 10%, vomiting in 8.6%, and a combination of flushing with apnea and gastric residuals in 2.9% of the infants. The pain group was associated with temporary increases in heart rate and body temperature, which were primarily noticeable in the first hour after the examination. There was no relationship between pain and blood pressure, oxygen saturation level, or respiratory rate.
Conclusions: A comprehensive understanding of the adverse effects associated with mydriatic drops and the examination procedure is essential. During ROP screening, infants should be carefully monitored in standardized clinical settings, with appropriate pain management strategies in place, and caregivers should receive thorough discharge education.
Keywords: Infant, Premature; Mydriatics; Pain; Retinopathy of Prematurity; Vital SignsObjective: Retinopathy of Prematurity (ROP) presents a significant challenge for neonatal intensive care units (NICUs). Therefore, the study aims to investigate the impact of neonatal pain on the systemic and procedural side effects of ROP examinations and mydriatic drops, with the aim of enhancing screening safety.
Materials And Methods: This study, designed as a prospective descriptive investigation, included 70 preterm infants admitted to the NICU between August and November 2012. Patients were monitored during the examination and for 48 hours afterwards, focusing on vital signs and any side effects. The Neonatal Infant Pain Scale was applied to all patients. Statistical analysis was conducted using SPSS version 15.
Results: Adverse effects were absent in 41.4% of the infants. Flushing was observed in 22.9%, gastric residuals were noted in 10%, vomiting occurred in 8.6%, and a combination of flushing, apnea, and gastric residuals was seen in 2.9% of the infants. The pain group exhibited temporary increases in heart rate and body temperature, most notably within the first hour after the examination. There were no significant relationships between pain and blood pressure, oxygen saturation levels, or respiratory rates (p>0.05).
Conclusions: A comprehensive understanding of the adverse effects associated with mydriatic drops and the examination procedure is essential. During ROP screenings, infants should be closely monitored in standardized clinical settings, appropriate pain management strategies should be implemented, and caregivers must receive thorough education upon discharge.
Mydriatic drops neonatal intensive care units neonatal pain preterm infants retinopathy of prematurity
This study was designed in accordance with the Helsinki Principles and received ethical approval from the Ethics Committee of Umraniye Training and Research Hospital. (Date: 16.08.2012, decision no:2012-4). The permissions of the parents of the babies included in the study were obtained via written consent.
There is no conflict of interest.
We would like to express our sincere gratitude to the Neonatology Division of the Department of Pediatrics at Ümraniye Training and Research Hospital for their support during this study. We also thank the parents of all participating infants for their trust and cooperation. Special thanks to the ophthalmologist and healthcare staff who contributed to the examinations and data collection.
Amaç: Prematüre retinopatisi (ROP), yenidoğan yoğun bakım üniteleri (YYBÜ) için önemli bir klinik sorundur. Bu çalışmada, ROP taramaları sırasında uygulanan midriyatik damlaların ve yenidoğanda oluşan ağrının, sistemik ve işlemle ilişkili bulgular üzerindeki etkileri değerlendirilmiş; böylece tarama güvenliğinin artırılması hedeflenmiştir.
Materyal ve Metot: Prospektif tanımlayıcı nitelikteki bu çalışmaya, Ağustos–Kasım 2012 tarihleri arasında YYBÜ’ye yatırılan 70 prematüre bebek dahil edildi. Tüm hastalar, ROP muayenesi sırasında ve sonrasındaki 48 saat boyunca, yaşamsal bulgular ve gelişebilecek yan etkiler açısından takip edildi. Ağrı değerlendirmesi için tüm bebeklere Yenidoğan Bebek Ağrı Ölçeği (NIPS) uygulandı. İstatistiksel analizler SPSS 15.0 programı ile gerçekleştirildi.
Bulgular: Bebeklerin %41,4’ünde herhangi bir yan etki gözlenmedi. %22,9’unda ciltte kızarıklık, %10’unda mide içeriği artışı, %8,6’sında kusma ve %2,9’unda ciltte kızarıklık, apne ve mide içeriği artışının birlikte görüldüğü belirlendi. Ağrı hisseden grupta, özellikle muayeneden sonraki ilk saatte kalp hızı ve vücut sıcaklığında geçici artış izlendi. Ağrı ile kan basıncı, oksijen satürasyonu ve solunum hızı arasında anlamlı bir ilişki saptanmadı (p>0,05).
Sonuç: ROP taramaları sırasında uygulanan midriyatik damlalar ve muayene işlemiyle ilişkili olumsuz etkilerin iyi anlaşılması büyük önem taşımaktadır. Bu süreçte bebeklerin standart klinik koşullarda yakından izlenmesi, etkili ağrı yönetimi sağlanması ve taburculuk öncesinde bakım veren kişilere yeterli eğitim verilmesi gereklidir.
Midriyatik damlalar prematüre bebekler prematüre retinopatisi yenidoğan ağrısı yenidoğan yoğun bakım üniteleri
Birincil Dil | İngilizce |
---|---|
Konular | Çocuk Sağlığı ve Hastalıkları (Diğer) |
Bölüm | Araştırma Makalesi |
Yazarlar | |
Erken Görünüm Tarihi | 24 Haziran 2025 |
Yayımlanma Tarihi | 30 Haziran 2025 |
Gönderilme Tarihi | 7 Şubat 2025 |
Kabul Tarihi | 12 Nisan 2025 |
Yayımlandığı Sayı | Yıl 2025 Cilt: 10 Sayı: 2 |
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