Mucociliary transport using 99mTc-albumin colloid: A reliable screening test for primary ciliary dyskinesia

Thorax

Volumn 60, Issue 5, 2005, Pages 414-417

  De Boeck, K ^a,b   Proesmans, M ^b   Mortelmans, L ^b   Van Billoen, B ^b   Willems, T ^b   Jorissen, M ^b  

^a UNIVERSITY HOSPITALS LEUVEN   (Belgium)

^b UNIVERSITY OF LEUVEN   (Belgium)

Author keywords

[No Author keywords available]

Indexed keywords

ALBUMIN TC 99M COLLOID; NITRIC OXIDE; DIAGNOSTIC AGENT; MACROSALB TC 99M; RADIOPHARMACEUTICAL AGENT;

ADOLESCENT; ARTICLE; CHILD; CILIARY DYSKINESIA; COMPARATIVE STUDY; FEMALE; HUMAN; HUMAN TISSUE; INFANT; MAJOR CLINICAL STUDY; MALE; MUCOCILIARY TRANSPORT; NASAL BIOPSY; PRIORITY JOURNAL; RECURRENT INFECTION; RELIABILITY; RESPIRATORY TRACT INFECTION; SCREENING TEST; SENSITIVITY AND SPECIFICITY; TRANSMISSION ELECTRON MICROSCOPY; BIOPSY; MUCOCILIARY CLEARANCE; NONPARAMETRIC TEST; NOSE; PATHOLOGY; PHYSIOLOGY; PRESCHOOL CHILD; SCINTISCANNING;

ADOLESCENT; BIOPSY; CHILD; CHILD, PRESCHOOL; CILIARY MOTILITY DISORDERS; HUMANS; INFANT; MUCOCILIARY CLEARANCE; NOSE; RADIOPHARMACEUTICALS; SENSITIVITY AND SPECIFICITY; STATISTICS, NONPARAMETRIC; TECHNETIUM TC 99M AGGREGATED ALBUMIN;

EID: 18844374861     PISSN: 00406376     EISSN: None     Source Type: Journal    
DOI: 10.1136/thx.2004.027680     Document Type: Article

References (23)

1. www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=242650 (accessed 15 November 2004).
2. Bush A, Cole P, Hariri M, et al. Primary ciliary dyskinesia: diagnosis and standards of care. Eur Respir J 1998;12:982-8.
3. Turner JA, Corkey CW, Lee JY, et al. Clinical expression of immotile cilia syndrome. Pediatrics 1981;67:805-10.
4. Hellinckx J, Demedts M, De Boeck K. Primary ciliary dyskinesia: evolution of pulmonary function. Eur J Pediatr 1998;157:422-6.
5. Rossman CM, Lee RM, Forrest JB, et al. Nasal cilia in normal man, primary ciliary dyskinesia and other respiratory diseases: analysis of motility and ultrastructure. Eur J Respir Dis Suppl 1983;127:64-70.
6. Jorissen M, Willems T, De Boeck K. Diagnostic evaluation of mucociliary transport: from symptoms to coordinated ciliary activity after ciliogenesis in culture. Review. Am J Rhinol 2000;14:345-52.
7. Jorissen M, Willems T, Van der Schueren B. Ciliary function analysis for the diagnosis of primary ciliary disease: advantages of ciliogenesis in culture. Acta Otolaryngol 2000;120:291-5.
8. Eliasson R, Mossberg B, Camner P, et al. The immotile-cilia syndrome. A congenital ciliary abnormality as an etiologic factor in chronic airway infections and male sterility. N Engl J Med 1977;297:1-6.
9. Stanley P, MacWilliam L, Greenstone M, et al. Efficacy of saccharin test for screening to detect abnormal mucociliary clearance. Br J Dis Chest 1984;78:62-5.
10. Greenstone M, Cole PJ. Ciliary function in health and disease. Br J Dis Chest 1985;79:9-26.
11. Wodehouse T, Kharnitov SA, Mackay IS, et al. Nasal nitric oxide measurements for the screening of primary ciliary dyskinesia. Eur Respir J 2003;21:43-7.
12. Prior MJ, Schofeld K, Boivin CM, et al. Assessment of mucociliary transport in patients with chronic mucoid rhinitis. Clin Otolaryngol 1999;24:242-6.
13. Jorissen M, Willems T, Van der Schueren B, et al. Ultrastructural expression of primary ciliary dyskinesia after ciliogenesis in culture. Acta Otorhinolaryngol Belg 2000;54:343-56.
14. Jorissen M, Willems T, Van der Schueren B, et al. Secondary ciliary dyskinesia is absent after ciliogenesis in culture. Acta Otorhinolaryngol Belg 2000;54:333-42.
15. Corbeel L, Cornillie F, Lauweryns JM, et al. Ultrastructural abnormalities of bronchial cilia in children with recurrent airway infection and bronchiectasis. Arch Dis Child 1981;56:929-33.
16. Escribano A, Armengot M, Marco V, et al. An isotopic study of nasal mucociliary transport in newborn investigation. Pediatr Pulmonol 1993;16:167-9.
17. Englender MD, Chamovitz, Harell M. Nasal transit time in normal subjects and pathologic condition. Otolaryngol Head Neck Surg 1990;103:909-12.
18. Burgersdijk FJ, De Groot JC, Graamans K, et al. Testing ciliary activity in patients with chronic and recurrent infections of the upper airways: experiences in 68 cases. Laryngoscope 1986;96:1029-33.
19. Santamaria F, de Santi MM, Grillo G, et al. Ciliary motility at light microscopy: a screening technique for ciliary defect. Acta Paediatr 1999;88:853-7.
20. Karadag B, James AJ, Gultekin E, et al. Nasal and lower airway level of nitric oxide in children with primary ciliary dyskinesia. Eur Respir J 199, 13:1402-5.
21. Narang I, Ersu R, Wilson NM, et al. Nitric oxide in chronic airway inflammation in children: diagnostic use and pathophysiological significance. Thorax 2002;57:586-9.
22. Horvath I, Loukides S, Wodehouse T, et al. Comparison of exhaled and nasal nitric oxide and exhaled carbon monoxide levels in bronchiectatic patients with and without primary ciliary dyskinesia. Thorax 2003;58:68-72.
23. Coren ME, Meeks M, Morrison I, et al. Primary ciliary dyskinesia: age at diagnosis and symptom history. Acta Paediatr 2002;91:667-9.