Nuesslein T G, Hufnagel C, Stephan V, Rieger C H
Universitäts-Kinderklinik Bochum.
Klin Padiatr. 2004 Jul-Aug;216(4):238-43. doi: 10.1055/s-2004-44897.
The diagnosis of primary ciliary dyskinesia (PCD) is unlikely, if ciliary beat frequency (CBF) is normal. The aim of this study was to test the diagnostic value of an additional bronchial biopsy in cases where nasal CBF are abnormal.
PATIENTS, METHODS: In a paediatric bronchitis population nasal brush biopsies and bronchial forceps biopsies were taken. In both samples we measured CBF and compared results to nasal CBF of infants and children without respiratory disease.
Patients with bronchitis (n = 31; 0.3 to 14.6 years; 10 girls) had a normal CBF in their nasal biopsies in 68 %, and in bronchial biopsies in 48 %, compared to the reference group (n = 72; 0.5 to 17.5 years; 23 girls). One patient had an abnormal nasal, but a normal bronchial ciliary activity. When cilia were beating at both sites (n = 14), nasal CBF agreed well with bronchial CBF (mean difference -0.78 Hz, 95 % confidence interval -1.81 Hz to 0.25 Hz).
By adding the investigation of bronchial mucosa to the measurement of nasal CBF the diagnostic yield to exclude PCD was only improved from 68 % to 71 %. Consequently, if nasal ciliary activity is abnormal in infants and children with bronchitis, we do not recommend additional bronchoscopy to obtain another biopsy.
如果纤毛摆动频率(CBF)正常,则原发性纤毛运动障碍(PCD)的诊断不太可能成立。本研究的目的是测试在鼻CBF异常的病例中进行额外支气管活检的诊断价值。
在一组小儿支气管炎患者中,采集了鼻刷活检和支气管钳活检样本。在这两种样本中,我们测量了CBF,并将结果与无呼吸系统疾病的婴儿和儿童的鼻CBF进行比较。
与参照组(n = 72;0.5至17.5岁;23名女孩)相比,支气管炎患者(n = 31;0.3至14.6岁;10名女孩)的鼻活检样本中68%的CBF正常,支气管活检样本中48%的CBF正常。1例患者鼻纤毛活动异常,但支气管纤毛活动正常。当两个部位的纤毛都在摆动时(n = 14),鼻CBF与支气管CBF高度一致(平均差异-0.78 Hz,95%置信区间-1.81 Hz至0.25 Hz)。
在测量鼻CBF的基础上增加支气管黏膜检查,排除PCD的诊断率仅从68%提高到71%。因此,如果支气管炎婴幼儿和儿童的鼻纤毛活动异常,我们不建议通过额外的支气管镜检查获取另一活检样本。