Arman Vahabi, Erdem Er, Abdussamet Kuyucu, Elcil Kaya Biçer, Semih Aydoğdu
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引用次数: 0
Abstract
Background
Various functional and radiological systems have been developed to evaluate joint health and the severity of arthropathy in hemophilic patients. Clinical relevance of these radiological systems has received minimal attention.
Methods
Through a retrospective chart review, 84 patients with end-stage hemophilic arthropathy of the knee were included. Pettersson and Arnold–Hilgartner scores were assessed by two observers. Correlation between radiological stage and range of motion (ROM), KSS function subscores, KSS pain subscores, total KSS, and surgical time were analyzed.
Results
Interobserver correlation was found to be very strong for Pettersson score, with a value of 0.84 (95% CI: 0.75–0.89) and moderate for the Arnold–Hilgartner with kappa value of 0.4 (95% CI: 0.17–0.62). Correlation between Pettersson score and clinical variables revealed a very weak inverse correlation with ROM (r = −0.12, 95% CI: −0.33 to 0.10), KSS pain (r = −0.09, 95% CI: −0.31 to 0.12), and KSS function (r = −0.16, 95% CI: −0.36 to 0.06), and weak inverse correlation with KSS (r = −0.24, 95% CI: −0.44 to 0.2). Regarding the correlation between Arnold–Hilgartner score, a weak inverse correlation was observed with ROM (r = −0.21, 95% CI: −0.41 to 0.00), and very weak inverse correlations with KSS pain (r = −0.06, 95% CI: −0.16 to 0.27), KSS function (r = −0.00, 95% CI: −0.22 to 0.21), and KSS (r = −0.04, 95% CI: −0.25 to 0.18).
Conclusion
Radiologic staging systems demonstrate weak correlation with clinically meaningful variables in patients with end-stage hemophilic arthropathy of knee, an important consideration in the management of hemophilic arthropathy.
期刊介绍:
Haemophilia is an international journal dedicated to the exchange of information regarding the comprehensive care of haemophilia. The Journal contains review articles, original scientific papers and case reports related to haemophilia care, with frequent supplements. Subjects covered include:
clotting factor deficiencies, both inherited and acquired: haemophilia A, B, von Willebrand''s disease, deficiencies of factor V, VII, X and XI
replacement therapy for clotting factor deficiencies
component therapy in the developing world
transfusion transmitted disease
haemophilia care and paediatrics, orthopaedics, gynaecology and obstetrics
nursing
laboratory diagnosis
carrier detection
psycho-social concerns
economic issues
audit
inherited platelet disorders.