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评估一项关于改进婴幼儿带套囊气管导管尺寸选择的新建议。

Evaluation of a new recommendation for improved cuffed tracheal tube size selection in infants and small children.

作者信息

Salgo B, Schmitz A, Henze G, Stutz K, Dullenkopf A, Neff S, Gerber A C, Weiss M

机构信息

Department of Anaesthesia, University Children's Hospital, Zurich, Switzerland.

出版信息

Acta Anaesthesiol Scand. 2006 May;50(5):557-61. doi: 10.1111/j.1399-6576.2006.01003.x.

Abstract

BACKGROUND

The purpose of this study was to evaluate a new recommendation for tracheal tube size selection using second-generation Microcuff paediatric endotracheal tubes (PETs) with optimized outer diameter (OD) of the distal tube.

METHODS

With Ethics Committee approval, patients aged from birth to 5 years, requiring general anaesthesia with orotracheal intubation, were included. Tracheal tube sizes were selected as follows: internal diameter (ID) 3.0 mm, birth (if > or =3 kg) to <6 months; ID 3.5 mm, 6 to <18 months; ID 4.0 mm, 18 months to <3 years; ID 4.5 mm, 3 to <5 years. Tracheal tubes with the cuff not inflated were classified as too large if no air leak was obtained at an airway pressure of < or =20 cmH2O. Post-intubation stridor requiring therapy was noted.

RESULTS

Three hundred and fifty children were studied. Nine tracheal tubes (2.6%) were too large and had to be exchanged: in patients requiring tracheal tubes of ID 3.0 mm and 3.5 mm, three and four tracheal tubes, respectively, and, in patients requiring tracheal tubes of ID 4.0 mm and 4.5 mm, one tracheal tube in each group. In three patients (0.9%), post-intubation stridor occurred which required therapy.

CONCLUSION

The new recommendation presented for the use of second-generation Microcuff PETs with improved OD to ID ratio allows the selection of cuffed tracheal tubes with larger IDs than previously recommended for small children without increased need for tracheal tube exchange or increased incidence of post-intubation stridor in these age groups.

摘要

背景

本研究的目的是评估一项关于气管导管尺寸选择的新建议,该建议使用具有优化远端导管外径(OD)的第二代微套囊儿科气管内导管(PET)。

方法

经伦理委员会批准,纳入年龄从出生至5岁、需要经口气管插管全身麻醉的患者。气管导管尺寸选择如下:内径(ID)3.0 mm,出生时(如果≥3 kg)至<6个月;ID 3.5 mm,6至<18个月;ID 4.0 mm,18个月至<3岁;ID 4.5 mm,3至<5岁。如果在气道压力≤20 cmH₂O时未出现漏气,则将套囊未充气的气管导管归类为过大。记录需要治疗的插管后喘鸣情况。

结果

对350名儿童进行了研究。9根气管导管(2.6%)过大,必须更换:在需要ID 3.0 mm和3.5 mm气管导管的患者中,分别有3根和4根气管导管过大,在需要ID 4.0 mm和4.5 mm气管导管的患者中,每组各有1根气管导管过大。3名患者(0.9%)出现了需要治疗的插管后喘鸣。

结论

所提出的关于使用外径与内径比得到改善的第二代微套囊PET的新建议,允许选择比以前为幼儿推荐的内径更大的带套囊气管导管,而无需增加气管导管更换的需求,也不会增加这些年龄组插管后喘鸣的发生率。

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