中华口腔医学研究杂志(电子版)
中華口腔醫學研究雜誌(電子版)
중화구강의학연구잡지(전자판)
CHINESE JOURNAL OF STOMATOLOGICAL RESEARCH(ELECTRONIC VERSION)
2015年
2期
166-170
,共5页
皮罗氏序列征%小颌畸形%气道梗阻
皮囉氏序列徵%小頜畸形%氣道梗阻
피라씨서렬정%소합기형%기도경조
Pierre Robin sequence%Micrognathia%Airway obstruction
皮罗氏序列征(PRS)是以小颌畸形、舌后坠和气道梗阻为主要特征的疾病,约58%~90%的患儿伴有特征性的U形不完全性腭裂,目前病因不明。 PRS并不构成一个独立的综合征,而是单独发生或者是其他综合征的不同程度的表现和反映。小颌畸形、舌后坠导致的气道梗阻使患儿呼吸和进食困难,进而出现低氧血症、胃食道反流、重度营养不良,严重的会导致患儿体重逐渐下降、消瘦甚至死亡。PRS的评估和治疗需要多学科合作。在采取治疗措施前首先要评估患儿气道梗阻的类型和部位、喂养困难产生的原因等。治疗方案的制定主要围绕着解决患儿气道梗阻和喂养困难两个方面来进行。约70%的患者通过采取俯卧位即可解决气道梗阻的问题。同样,采取正确的喂养姿势也可以解决大部分的喂养问题。如果采用改变体位的方法不能够解决气道梗阻和喂养的问题,则需要分别放置鼻咽通气管和鼻胃管来改善呼吸和进食。经过非手术的气道管理不能缓解气道堵塞,则需要手术治疗。目前,手术治疗的方法主要有唇舌黏连、下颌骨牵引成骨、气管切开等。在手术治疗前多导睡眠检测和支气管纤维镜的检查必不可少,前者为患儿的睡眠呼吸状况提供客观的指标,后者可以明确患儿气道梗阻的位置,排除舌根水平以下的气道梗阻。
皮囉氏序列徵(PRS)是以小頜畸形、舌後墜和氣道梗阻為主要特徵的疾病,約58%~90%的患兒伴有特徵性的U形不完全性腭裂,目前病因不明。 PRS併不構成一箇獨立的綜閤徵,而是單獨髮生或者是其他綜閤徵的不同程度的錶現和反映。小頜畸形、舌後墜導緻的氣道梗阻使患兒呼吸和進食睏難,進而齣現低氧血癥、胃食道反流、重度營養不良,嚴重的會導緻患兒體重逐漸下降、消瘦甚至死亡。PRS的評估和治療需要多學科閤作。在採取治療措施前首先要評估患兒氣道梗阻的類型和部位、餵養睏難產生的原因等。治療方案的製定主要圍繞著解決患兒氣道梗阻和餵養睏難兩箇方麵來進行。約70%的患者通過採取俯臥位即可解決氣道梗阻的問題。同樣,採取正確的餵養姿勢也可以解決大部分的餵養問題。如果採用改變體位的方法不能夠解決氣道梗阻和餵養的問題,則需要分彆放置鼻嚥通氣管和鼻胃管來改善呼吸和進食。經過非手術的氣道管理不能緩解氣道堵塞,則需要手術治療。目前,手術治療的方法主要有脣舌黏連、下頜骨牽引成骨、氣管切開等。在手術治療前多導睡眠檢測和支氣管纖維鏡的檢查必不可少,前者為患兒的睡眠呼吸狀況提供客觀的指標,後者可以明確患兒氣道梗阻的位置,排除舌根水平以下的氣道梗阻。
피라씨서렬정(PRS)시이소합기형、설후추화기도경조위주요특정적질병,약58%~90%적환인반유특정성적U형불완전성악렬,목전병인불명。 PRS병불구성일개독립적종합정,이시단독발생혹자시기타종합정적불동정도적표현화반영。소합기형、설후추도치적기도경조사환인호흡화진식곤난,진이출현저양혈증、위식도반류、중도영양불량,엄중적회도치환인체중축점하강、소수심지사망。PRS적평고화치료수요다학과합작。재채취치료조시전수선요평고환인기도경조적류형화부위、위양곤난산생적원인등。치료방안적제정주요위요착해결환인기도경조화위양곤난량개방면래진행。약70%적환자통과채취부와위즉가해결기도경조적문제。동양,채취정학적위양자세야가이해결대부분적위양문제。여과채용개변체위적방법불능구해결기도경조화위양적문제,칙수요분별방치비인통기관화비위관래개선호흡화진식。경과비수술적기도관리불능완해기도도새,칙수요수술치료。목전,수술치료적방법주요유진설점련、하합골견인성골、기관절개등。재수술치료전다도수면검측화지기관섬유경적검사필불가소,전자위환인적수면호흡상황제공객관적지표,후자가이명학환인기도경조적위치,배제설근수평이하적기도경조。
Pierre Robin sequence ( PRS ) is classically described as a triad of micrognathia , glossoptosis, and airway obstruction. About 58%~90% infants of Pierre Robin sequence are associated with a wide U-shaped cleft palate. The pathogenesis of PRS is not clear. PRS is not a syndrome in itself, but rather a sequence of disorders which are related to several other craniofacial anomalies and may appear in conjunction with a syndromic diagnosis . The micrognathia leads to glossoptosis , which in turn results in airway obstruction and inability to feed, and then results in hyoxemia, gastroesophageal reflux and severe malnutrition. In the most severe case it may lead to weight loss and death. Infants with PRS should be evaluated by a multidisciplinary team to assess the anatomic findings , delineate the source of airway obstruction, and address airway and feeding issues. Treatment decisions should focus on the airway obstruction and feeding issues . Positioning will resolve the airway obstruction in 70% of cases . In the correct position, most children will also be able to feed normally. If the infant continues to show evidence of desaturation, then placement of a nasopharyngeal tube is indicated. A proportion of PRS infants do not respond to conservative measures and will require operative treatment . Tongue-lip adhesion and distraction osteogenesis of the mandible and tracheostomy are usually be used . Prior to considering any surgical procedure, the clinician should first rule out any sources of obstruction below the base of the tongue. A polysomnography also be necessary to monitor the sleep apnea.