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[皮埃尔·罗宾序列征:腭裂手术后的术后并发症。一项涵盖25年的回顾性研究]

[Pierre Robin sequence: postoperative complications following cleft palate surgery. A retrospective study covering 25 years].

作者信息

Thieme V, Selzer G, Günther L, Rustemeyer J, Bremerich A

机构信息

Klinik für Mund-, Kiefer- und Gesichtschirurgie, Plastische Operationen und Spezielle Schmerztherapie, Klinikum Bremen-Mitte.

出版信息

Mund Kiefer Gesichtschir. 2005 Sep;9(5):306-11. doi: 10.1007/s10006-005-0637-1.

DOI:10.1007/s10006-005-0637-1
PMID:16136349
Abstract

BACKGROUND

In a 25-year retrospective review of 1976-2000, the postoperative course after cleft palate surgery and pharyngeal flap surgery in 87 children with Pierre Robin sequence was studied.

PATIENTS AND METHODS

The study comprised 114 interventions with 87 primary palatoplasties; 17 patients required palatal fistulae repair and 10 children were treated with secondary pharyngoplasty procedures. All children were divided into three postnatal risk groups according to the severity of their symptoms at birth and in the course of the early months of life.

RESULTS

A direct correlation was seen between the incidence of early postnatal difficulties and the postoperative obstructive complications after cleft palate surgery and pharyngeal flap surgery. Thus, children experiencing obstructive problems at birth (high postnatal risk group) displayed more severe complications at the time after cleft palate repair. In children undergoing pharyngeal flap surgery not only early postoperative obstruction but also late obstructive sleep apnea can occur.

摘要

背景

在一项对1976年至2000年的25年回顾性研究中,对87例患有皮埃尔·罗宾序列征的儿童进行腭裂手术和咽瓣手术的术后过程进行了研究。

患者与方法

该研究包括114次干预,其中87次为初次腭裂修复术;17例患者需要修复腭裂瘘管,10例儿童接受了二次咽成形术。根据出生时和生命最初几个月症状的严重程度,将所有儿童分为三个出生后风险组。

结果

出生后早期困难的发生率与腭裂手术和咽瓣手术后的术后阻塞性并发症之间存在直接相关性。因此,出生时出现阻塞性问题的儿童(高出生后风险组)在腭裂修复术后出现更严重的并发症。在接受咽瓣手术的儿童中,不仅术后早期会出现阻塞,而且后期还可能出现阻塞性睡眠呼吸暂停。

相似文献

1
[Pierre Robin sequence: postoperative complications following cleft palate surgery. A retrospective study covering 25 years].[皮埃尔·罗宾序列征:腭裂手术后的术后并发症。一项涵盖25年的回顾性研究]
Mund Kiefer Gesichtschir. 2005 Sep;9(5):306-11. doi: 10.1007/s10006-005-0637-1.
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Cleft Palate Craniofac J. 2016 Mar;53(2):203-9. doi: 10.1597/14-250. Epub 2015 Jun 23.
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本文引用的文献

1
Acute airway obstruction in an infant with Pierre Robin syndrome after palatoplasty.Pierre Robin综合征患儿腭裂修复术后的急性气道梗阻
Acta Anaesthesiol Scand. 2004 Jul;48(6):787-9. doi: 10.1111/j.0001-5172.2004.00407.x.
2
Pierre Robin sequence in Denmark: a retrospective population-based epidemiological study.丹麦的皮埃尔·罗宾序列征:一项基于人群的回顾性流行病学研究。
Cleft Palate Craniofac J. 2004 Jan;41(1):47-52. doi: 10.1597/02-055.
3
Airway obstruction following palatoplasty: analysis of 247 consecutive operations.腭裂修复术后气道梗阻:247例连续手术分析
Cleft Palate Craniofac J. 2002 Mar;39(2):145-8. doi: 10.1597/1545-1569_2002_039_0145_aofpao_2.0.co_2.
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Identification of children at high anaesthetic risk at the time of primary palatoplasty.在初次腭裂修复术时识别高麻醉风险儿童。
Scand J Plast Reconstr Surg Hand Surg. 2001 Jun;35(2):177-82. doi: 10.1080/028443101300165318.
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Pierre Robin syndrome: mandibular growth during the first year of life.皮埃尔·罗宾综合征:出生后第一年的下颌骨生长情况。
Ann Plast Surg. 1999 Feb;42(2):154-7.
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Airway management in children with craniofacial anomalies.患有颅面畸形儿童的气道管理
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Observation of early postoperative hypoxaemia in children undergoing elective plastic surgery.择期整形手术患儿术后早期低氧血症的观察
Paediatr Anaesth. 1996;6(1):21-8. doi: 10.1111/j.1460-9592.1996.tb00347.x.
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Hypoxia: another issue to consider when timing cleft repair.
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Perioperative complications of superior pharyngeal flap surgery in children.
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