The role of coagulation abnormalities in the development of Perthes' disease

Citation
Wdc. Kealey et al., The role of coagulation abnormalities in the development of Perthes' disease, J BONE-BR V, 82B(5), 2000, pp. 744-746
Citations number
19
Categorie Soggetti
Ortopedics, Rehabilitation & Sport Medicine","da verificare
Journal title
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME
ISSN journal
0301620X → ACNP
Volume
82B
Issue
5
Year of publication
2000
Pages
744 - 746
Database
ISI
SICI code
0301-620X(200007)82B:5<744:TROCAI>2.0.ZU;2-M
Abstract
Recent reports have suggested an association between Perthes' disease and a n underlying thrombophilic or hypofibrinolytic tendency. In Northern Irelan d there is a high incidence of Perthes' disease (11.7 per 100 000 or 1 in 6 07 children) in a stable paediatric population. We reviewed 139 children with Perthes' disease and compared them with a con trol group of 220 aged- and gender-matched healthy primary schoolchildren w ith similar racial and ethnic backgrounds. There were no significant deficiencies of antithrombotic factors protein C, protein S, antithrombin III or resistance to activated protein C, A total of 53 (38.1%) of the children with Perthes' disease had a prolonged activat ed partial thromboplastin time (> 38) compared with 13 (5.9%) of the contro l group (p < 0.001). Our findings have shown that using standard assays, th rombophilia secondary to antithrombotic factor deficiency or resistance to activated protein does not appear to be an aetiological factor for Perthes' disease. The cause of the prolonged activated partial thromboplastin time, usually associated with a clotting factor deficiency, is under further inv estigation.