Orthopaedic management of haemophilia arthropathy of the ankle

被引:50
作者
Pasta, G. [1 ,2 ]
Forsyth, A. [3 ]
Merchan, C. R. [4 ,5 ]
Mortazavi, S. M. J. [6 ]
Silva, M. [7 ]
Mulder, K. [8 ]
Mancuso, E. [9 ]
Perfetto, O. [10 ]
Heim, M. [11 ]
Caviglia, H. [12 ]
Solimeno, L.
机构
[1] Maggiore Hosp Fdn, IRCCS, Traumatol Dept, I-20122 Milan, Italy
[2] Maggiore Hosp Fdn, IRCCS, Angelo Bianchi Bonomi Hemophilia Ctr, I-20122 Milan, Italy
[3] Hosp Univ Penn, Haemophilia & Thrombosis Program, Philadelphia, PA 19104 USA
[4] La Paz Univ Hosp, Dept Orthopaed, Madrid, Spain
[5] La Paz Univ Hosp, Haemophilia Unit, Madrid, Spain
[6] Med Sci Univ Tehran, Dept Orthoped Surg, Imam Univ Hosp, Tehran, Iran
[7] Univ Calif Los Angeles, David Geffen Sch Med, Orthopaed Hosp,Hemophilia Treatment Ctr, Dept Orthopaed, Los Angeles, CA 90095 USA
[8] Childrens Hosp, Dept Physiotherapy, Winnipeg, MB R3A 1S1, Canada
[9] Maggiore Hosp Fdn, IRCCS, Angelo Bianchi Hemophilia Ctr, Dept Internal Med & Med Specialties, Milan, Italy
[10] CTO Hosp, Haemophilia Arthopathy Treatment Ctr, Milan, Italy
[11] Tel Hashomer Hosp, Dept Orthopaed Rehabil, Israel Natl Haemophilia Ctr, Tel Aviv, Israel
[12] Acute Hosp Juan Fernandez, Buenos Aires, DF, Argentina
关键词
ankle; haemophilia; haemophilic arthropathy;
D O I
10.1111/j.1365-2516.2008.01720.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Joint bleeding, or haemarthrosis, is the most common type of bleeding episode experienced by individuals with haemophilia A and B. This leads to changes within the joints, including synovial proliferation, which results in further bleeding and chronic synovitis. Blood in the joint can also directly damage the cartilage, and with repeated bleeding, there is progressive destruction of both cartilage and bone. The end result is known as haemophilic arthropathy. The joints most commonly affected are the knees, elbows and ankles, although any synovial joint may be involved. In the ankle, both the tibiotalar and subtalar joints may be affected and joint bleeding and arthropathy can lead to a number of deformities. Haemophilic arthropathy can be prevented through regular factor replacement prophylaxis and implementing physiotherapy. However, when necessary, there are multiple surgical and non-surgical options available. In early ankle arthropathy with absent or minimal joint changes, both radioisotopic and chemical synoviorthesis can be used to reduce the hypertrophied synovium. These procedures can decrease the frequency of bleeding episodes, minimizing the risk of articular cartilage damage. Achilles tendon lengthening can be performed, in isolation or in combination with other surgical measures, to correct Achilles tendon contractures. Both arthroscopic and open synovectomies are available as a means to remove the friable villous layer of the synovium and are often indicated when bleeding episodes cannot be properly controlled by factor replacement therapy or synoviorthesis. In the later stages of ankle arthropathy, other surgical options may be considered. Debridement may be indicated when there are loose pieces of cartilage or anterior osteophytes, and can help to improve the joint function, even in the presence of articular cartilage damage. Supramalleolar tibial osteotomy may be indicated in patients with a valgus deformity of the hindfoot without degenerative radiographic findings. Joint fusion, or arthrodesis, is the treatment of choice in the advanced stages of ankle arthropathy although total ankle replacement is currently available. Early ankle replacement components were associated with a poor outcome, but as implant designs have improved, there have been successful outcomes achieved. As the ankle is a commonly affected joint in many individuals with haemophilia, it is important to add to the knowledge base to validate indications and timing of surgical and non-surgical interventions in ankle arthropathy.
引用
收藏
页码:170 / 176
页数:7
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