Comparison of the rates of joint arthroplasty in patients with severe factor VIII and IX deficiency: an index of different clinical severity of the 2 coagulation disorders

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RESEARCH PRODUCT

Comparison of the rates of joint arthroplasty in patients with severe factor VIII and IX deficiency: an index of different clinical severity of the 2 coagulation disorders

Tagariello G Iorio A Santagostino E Morfini M Bisson R Innocenti M Mancuso Me Mazzucconi Mg Pasta Gl Radossi P Rodorigo G Santoro C Sartori R Scaraggi A Solimeno Lp Mannucci Pm Ciavarella N Valdrè L Targhetta R Biasioli C Vincenzi D Molinari C Boeri E Mariani G Lapecorella M Coppola A Schiavulli M Rocino A Mancuso G Siragusa S Malato A Tagliaferri A Rivolta F Oliovecchio E Marcucci M Dragani A Mancino A D'incà M De Rossi G Luciani M Landolfi R Piseddu G Schinco Pc Rossetti G Barillari G Feola G Gandini G Giuffrida A Castaman G.Giovanni Di Minno

subject

Adult medicine.medical_specialty Adolescent medicine.medical_treatment Immunology Population macromolecular substances Gene mutation Hemophilia A Hemophilia B Severity of Illness Index Biochemistry Arthroplasty Settore MED/15 - Malattie Del Sangue Cohort Studies Young Adult Risk Factors hemic and lymphatic diseases Internal medicine Severity of illness medicine Coagulopathy Humans Child education Retrospective Studies education.field_of_study Hematology hamophilia arthroplasty business.industry Retrospective cohort study Cell Biology Hematology Odds ratio Blood Coagulation Disorders Middle Aged medicine.disease Arthroplasty Surgery Italy Joint Diseases business Algorithms

description

AbstractData from the Italian Hemophilia Centres were collected to perform a retrospective survey of joint arthroplasty in patients with severe hemophilia. Twenty-nine of 49 hemophilia centers reported that 328 of the 347 operations were carried out in 253 patients with severe hemophilia A (HA) and 19 in 15 patients with severe hemophilia B (HB). When results were normalized to the whole Italian hemophilia population (1770 severe HA and 319 severe HB), patients with HA had a 3-fold higher risk of undergoing joint arthroplasty (odds ratio [OR], 3.38; 95% confidence interval [CI], 1.97-5.77; P < .001). These results were confirmed after adjustment for age, HIV, hepatitis C virus (HCV), and inhibitor in a Cox regression model (HR, 2.65; 95% CI, 1.62-4.33; P < .001). The survival analysis of time to joint arthroplasty in the subset of patients with severe HA was not affected by the severity of factor VIII (FVIII) gene mutations. A systematic review of literature articles reporting joint arthroplasties in HA and HB showed that the proportion of HA patients who had undergone arthroplasties was higher than that of HB patients, in agreement with the findings in our Italian cohort. These data suggest that the 2 inherited coagulation disorders have a different severity of clinical phenotype.

year	journal	country	edition	language
2009-01-01

http://hdl.handle.net/10447/55586