Feeding Management and Palate Repair Timing in Infants with Cleft Palate with and without Pierre Robin Sequence: A Multisite Study.

IF 1.1 4区 医学 Q2 Dentistry Cleft Palate-Craniofacial Journal Pub Date : 2024-03-15 DOI:10.1177/10556656241239766
Jessica L Williams, Kari M Lien, Richard Kirschner, Gregory Allen, Kathy Chapman
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引用次数: 0

Abstract

Objectives: Compare the feeding management practices in infants with cleft palate with and without Pierre Robin sequence (PRS) and determine if specific feeding difficulties or interventions predict delayed palate repair.

Design: Retrospective cross-sectional study.

Setting: Seventeen cleft palate teams contributed data.

Patients: 414 infants were included in this study: 268 infants with cleft palate only and 146 infants with cleft palate and PRS.

Procedures: Data were collected via parent interview and electronic health records.

Main outcome measures: Outcomes for the primary objective included categorical data for: history of poor growth, feeding therapy, milk fortification, use of enteral feeding, and feeding difficulties. The outcome for the secondary objective was age in months at primary palate repair.

Results: Infants with PRS had a significantly higher prevalence of feeding difficulties (81% versus 61%) and poor growth (29% versus 15%) compared to infants with cleft palate only. Infants with PRS received all feeding interventions-including feeding therapy, milk fortification, and enteral feeding-at a significantly higher frequency. Infants with PRS underwent primary palate repair at a mean age of 13.55 months (SD = 3.29) which was significantly (P < .00001) later than infants with cleft palate only who underwent palate repair at a mean age of 12.05 months (SD = 2.36). Predictors of delayed palate repair included diagnosis of PRS as well as Hispanic ethnicity and a history of poor growth.

Conclusions: These findings can be used to establish clinical directives focused on providing early, multimodal feeding interventions to promote optimal growth and timely palate repair for infants with PRS.

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有皮埃尔-罗宾序列和无皮埃尔-罗宾序列腭裂婴儿的喂养管理和腭修复时机:多站点研究。
目的:比较有皮埃尔-罗宾序列(PRS)和无皮埃尔-罗宾序列(PRS)腭裂婴儿的喂养管理方法,并确定特定喂养困难或干预措施是否可预测腭裂修复延迟:比较有皮埃尔-罗宾序列(PRS)和无皮埃尔-罗宾序列(PRS)腭裂婴儿的喂养管理方法,确定特定喂养困难或干预措施是否可预测腭裂修复延迟:设计:回顾性横断面研究:17个腭裂小组提供数据:本研究共纳入 414 名婴儿:268 名仅患有腭裂的婴儿和 146 名患有腭裂和 PRS 的婴儿:主要结果指标:主要结果指标:主要结果指标包括以下方面的分类数据:生长不良史、喂养治疗、母乳强化、使用肠内喂养和喂养困难。次要指标的结果是腭裂初次修复时的月龄:结果:与仅患有腭裂的婴儿相比,患有 PRS 的婴儿出现喂养困难(81% 对 61%)和发育不良(29% 对 15%)的比例明显更高。患有 PRS 的婴儿接受所有喂养干预措施(包括喂养治疗、牛奶强化和肠内喂养)的频率明显更高。患有 PRS 的婴儿在平均 13.55 个月(SD = 3.29)时接受腭裂初次修复,这明显高于其他婴儿(P,结论:PRS 患儿在平均 13.55 个月(SD = 3.29)时接受腭裂初次修复:这些发现可用于制定临床指南,重点是提供早期、多模式喂养干预措施,以促进患有 PRS 的婴儿获得最佳生长和及时的腭裂修复。
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来源期刊
Cleft Palate-Craniofacial Journal
Cleft Palate-Craniofacial Journal DENTISTRY, ORAL SURGERY & MEDICINE-SURGERY
CiteScore
2.20
自引率
36.40%
发文量
0
审稿时长
4-8 weeks
期刊介绍: The Cleft Palate-Craniofacial Journal (CPCJ) is the premiere peer-reviewed, interdisciplinary, international journal dedicated to current research on etiology, prevention, diagnosis, and treatment in all areas pertaining to craniofacial anomalies. CPCJ reports on basic science and clinical research aimed at better elucidating the pathogenesis, pathology, and optimal methods of treatment of cleft and craniofacial anomalies. The journal strives to foster communication and cooperation among professionals from all specialties.
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