The Early Operative Burden for Children Born with Cleft lip and Palate.

IF 1.2 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
Cleft Palate-Craniofacial Journal Pub Date : 2024-05-01 Epub Date: 2022-12-04 DOI:10.1177/10556656221143301
Teagan Fink, Nicky Kilpatrick, David Chong, Tony Penington
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引用次数: 0

Abstract

Objectives: to audit the surgical management of infants born with non-syndromic cleft lip and palate (CLP) at an Australian cleft unit in a large tertiary paediatric hospital.

Design: Retrospective cohort study.

Setting: A tertiary Cleft centre.

Patients: 193 infants born with non-syndromic CLP were referred to the centre and underwent primary repair of their CLP between 2009 and 2020.Main Outcome Measures: (1) The timing and surgical repairs performed; (2) the frequency of postoperative complications; (3) the frequency of secondary Cleft surgery; and (4) the total Cleft-related operations performed for infants born with CLP.

Results: Four different surgical repair techniques were performed by six surgeons, and postoperative complications were uncommon (n = 14). Rates of oronasal fistula surgery (10.5% at five years of age; 14.3% at eight years of age) and velopharyngeal insufficiency surgery (8.7% at five years of age; 14.3% at eight years of age) were not significantly different across the surgical repair groups (p-value >0.05) and were comparable to international Cleft centres. Children underwent an average of four operative procedures in this audit period, including primary Cleft repair, ear, nose and throat surgery, and dental care. Surgery for managing Eustachian tube dysfunction was the most common surgical intervention following primary Cleft repair.

Conclusions: Children born with non-syndromic CLP have a high early operative burden, with outcomes similar across the spectrum of techniques and surgeons.

唇腭裂患儿的早期手术负担。
目的:审核澳大利亚一家大型三级儿科医院唇腭裂科对先天性非综合征唇腭裂(CLP)婴儿的手术治疗情况:设计:回顾性队列研究:患者:193 名非先天性唇腭裂婴儿193名出生时患有非综合征CLP的婴儿被转诊至该中心,并在2009年至2020年间接受了CLP初级修复手术:(1)进行修复的时间和手术方式;(2)术后并发症的发生频率;(3)二次裂隙手术的发生频率;以及(4)为先天性CLP婴儿进行的与裂隙相关的手术总数:六名外科医生采用了四种不同的手术修复技术,术后并发症并不常见(14 例)。各手术修复组的口鼻瘘手术率(5岁时为10.5%;8岁时为14.3%)和口咽发育不全手术率(5岁时为8.7%;8岁时为14.3%)无明显差异(P值>0.05),与国际裂隙中心的手术率相当。在审计期间,儿童平均接受了四次手术,包括初级裂隙修复、耳鼻喉手术和牙科护理。治疗咽鼓管功能障碍的手术是初级裂隙修复术后最常见的手术干预:结论:非综合征先天性耳聋患儿的早期手术负担很重,但不同技术和外科医生的手术效果相似。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
2.70
自引率
36.40%
发文量
215
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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