全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Physiotherapy Treatment in Patients with Hemophilia and Chronic Ankle Arthropathy: A Systematic Review

DOI: 10.1155/2013/305249

Full-Text   Cite this paper   Add to My Lib

Abstract:

Haemophilic arthropathy of the ankle causes pain and deterioration in gait, causing disability. Although some physiotherapy modalities are effective in the management of acute bleeding, the results are unknown in chronic arthropathy. Our objective was to determine the most effective physiotherapy procedures for treating the haemophilic arthropathy of the ankle and to assess the methodological quality of the studies. A systematic review was carried out in the Cochrane Database, PubMed, MEDLINE, ISI Web of Knowledge, PEDro, TESEO, and specialized journals (Haemophilia and Haematologica). It included articles with at least one group undergoing any kind of physiotherapy treatment and with pretest and posttest evaluation, published before April 2013. An analysis of variables was performed and assessed the methodological quality of studies. Five studies met the criteria for inclusion. Hydrotherapy treatments, strength training and balance strength, balance training, and sports therapy, have improved range of movement, pain, balance, and subjective physical performance. The proposed methodological analysis was not possible due to the low quality of the studies. Although the results are positive, they lack rigorous evidence on the effects of treatments. Studies are needed to establish the efficacy of the various forms of physiotherapy in the haemophilic arthropathy of the ankle. 1. Introduction Hemophilia is a blood-clotting disorder caused by a deficiency in factor VIII (FVIII) or factor IX (FIX), which manifests itself through bleeding in the muscles and joints [1]. There are three categories, depending on the percentage of the blood-clotting factor: severe hemophilia (<1% FVIII/IX), characterised by spontaneous bleeding; moderate hemophilia (1–5% FVIII/FIX), with bleeding from slight injuries; and mild hemophilia (>5–40% FVIII/FIX) with bleeding during surgical procedures or from severe injuries [2, 3]. Eighty percent of the episodes in hemophiliac patients involve bleeding in the joints, or haemarthrosis [4, 5], with the ankle being the third most frequently affected joint [6]. The symptoms of intra-articular ankle bleeding are severe pain, limited range of motion, inflammation, and synovial involvement. Without proper treatment, capsular and tendon contractures can develop in the joints [7]. Although experiments on animals cannot be directly related to the humans, Hooiveld et al. [8] observed in a canine model that weight-bearing joints, as opposed to non-weight-bearing joints with haemarthrosis, suffered progressive and degenerative damage after a

References

[1]  P. Molho, N. Rolland, T. Lebrun et al., “Epidemiological survey of the orthopaedic status of severe haemophilia A and B patients in France,” Haemophilia, vol. 6, no. 1, pp. 23–32, 2000.
[2]  R. R. Montgomery and J. P. Scott, “Hemostasis: diseases of the Xuid phase,” in Hematology of Infancy and Childhood, D. G. Nathan and F. A. Oski, Eds., pp. 1605–1620, Saunders, Philadelphia, Pa, USA, 1992.
[3]  K. S. Upchurch and D. B. Brettler, “Hemophilic arthropathy,” in Kelley's Textbook of Rheumatology, S. Ruddy, E. D. Harris, and C. B. Sledge, Eds., pp. 1567–1574, Saunders, Philadelphia, Pa, USA, 2001.
[4]  R. B. Duthie, J. Matthews, and C. Rizza, The Management of Musculoskeletal Problems in the Haemophilias, Blackwell Scientific Publications, Oxford, UK, 1972.
[5]  E. C. Rodriguez-Merchan, “Effects of hemophilia on articulations of children and adults,” Clinical Orthopaedics and Related Research, vol. 328, pp. 7–13, 1996.
[6]  J. Hoskinson and R. B. Duthie, “Management of musculoskeletal problems in the hemophilias,” Orthopedic Clinics of North America, vol. 9, no. 2, pp. 455–480, 1978.
[7]  W. J. Ribbans and J. L. Rees, “Management of equinus contractures of the ankle in haemophilia,” Haemophilia, vol. 5, supplement 1, pp. 46–52, 1999.
[8]  M. J. J. Hooiveld, G. Roosendaal, K. M. G. Jacobs et al., “Initiation of degenerative joint damage by experimental bleeding combined with loading of the joint: a possible mechanism of hemophilic arthropathy,” Arthritis and Rheumatism, vol. 50, no. 6, pp. 2024–2031, 2004.
[9]  N. Hakobyan, T. Kazarian, A. A. Jabbar, K. J. Jabbar, and L. A. Valentino, “Pathobiology of hemophilic synovitis I: overexpression of mdm2 oncogene,” Blood, vol. 104, no. 7, pp. 2060–2064, 2004.
[10]  E. Gurcay, E. Eksioglu, U. Ezer, B. Cakir, and A. Cakci, “A prospective series of musculoskeletal system rehabilitation of arthropathic joints in young male hemophilic patients,” Rheumatology International, vol. 28, no. 6, pp. 541–545, 2008.
[11]  T. Hilberg, M. Hersbsleb, C. Puta, H. H. W. Gabriel, and W. Schramm, “Physical training increases isometric muscular strength and proprioceptive performance in haemophilic subjects,” Haemophilia, vol. 9, no. 1, pp. 86–93, 2003.
[12]  M. K. Garcia, A. Capusso, D. Montans, E. Massad, and L. R. Battistella, “Variations of the articular mobility of elbows, knees and ankles in patients with severe haemophilia submitted to free active movimentation in a pool with warm water,” Haemophilia, vol. 15, no. 1, pp. 386–389, 2009.
[13]  K. Hill, M. Fearn, S. Williams et al., “Effectiveness of a balance training home exercise programme for adults with haemophilia: a pilot study,” Haemophilia, vol. 16, no. 1, pp. 162–169, 2010.
[14]  D. Czepa, S. von Mackensen, and T. Hilberg, “Haemophilia & Exercise Project (HEP): the impact of 1-year sports therapy programme on physical performance in adult haemophilia patients,” Haemophilia, vol. 19, pp. 194–199, 2013.
[15]  E. C. Rodriguez-Merchan, “The haemophilic ankle,” Haemophilia, vol. 12, no. 4, pp. 337–344, 2006.
[16]  D. Stephensen, R. Tait, N. Brodie et al., “Changing patterns of bleeding in patients with severe haemophilia A,” Haemophilia, vol. 15, no. 6, pp. 1210–1214, 2009.
[17]  M. Funk, H. Schmidt, C. Escuriola-Ettingshausen et al., “Radiological and orthopedic score in pediatric hemophilic patients with early and late prophylaxis,” Annals of Hematology, vol. 77, no. 4, pp. 171–174, 1998.
[18]  M. S. Pearce, M. A. Smith, and G. F. Savidge, “Supramalleolar trial osteotomy for haemophilic arthropathy of the ankle,” Journal of Bone and Joint Surgery Series B, vol. 76, no. 6, pp. 947–950, 1994.
[19]  F. R. van Genderen, K. Fischer, L. Heijnen et al., “Pain and functional limitations in patients with severe haemophilia,” Haemophilia, vol. 12, no. 2, pp. 147–153, 2006.
[20]  K. Fischer, J. G. Van Der Bom, P. Molho et al., “Prophylactic versus on-demand treatment strategies for severe haemophilia: a comparison of costs and long-term outcome,” Haemophilia, vol. 8, no. 6, pp. 745–752, 2002.
[21]  S. Royal, W. Schramm, E. Berntorp et al., “Quality-of-life differences between prophylactic and on-demand factor replacement therapy in European haemophilia patients,” Haemophilia, vol. 8, no. 1, pp. 44–50, 2002.
[22]  R. Tiktinsky, B. Falk, M. Heim, and U. Martinovitz, “The effect of resistance training on the frequency of bleeding in haemophilia patients: a pilot study,” Haemophilia, vol. 8, no. 1, pp. 22–27, 2002.
[23]  L. M. Aledort, R. H. Haschmeyer, and H. Pettersson, “A longitudinal study of orthopaedic outcomes for severe factor-VIII-deficient haemophiliacs,” Journal of Internal Medicine, vol. 236, no. 4, pp. 391–399, 1994.
[24]  B. M. Buzzard, “Physiotherapy for the prevention of articular contraction in haemophilia,” Haemophilia, vol. 5, supplement 1, pp. 10–15, 1999.
[25]  J. A. Aznar, M. Magallón, F. Querol, E. Gorina, and J. M. Tusell, “The orthopaedic status of severe haemophiliacs in Spain,” Haemophilia, vol. 6, no. 3, pp. 170–176, 2000.
[26]  C. M. Bleakley, S. O'Connor, M. A. Tully, L. G. Rocke, D. C. MacAuley, and S. M. McDonough, “The PRICE study (Protection Rest Ice Compression Elevation): design of a randomised controlled trial comparing standard versus cryokinetic ice applications in the management of acute ankle sprain [ISRCTN13903946],” BMC Musculoskeletal Disorders, vol. 8, article 125, 2007.
[27]  C. Hermans, P. De Moerloose, K. Fischer et al., “Management of acute haemarthrosis in haemophilia A without inhibitors: literature review, European survey and recommendations,” Haemophilia, vol. 17, no. 3, pp. 383–392, 2011.
[28]  K. Mulder, Exercise for People with Hemophilia, World Federation of Hemophilia, Montreal, Canada, 2006.
[29]  J. G. Gamble, J. Bellah, L. A. Rinsky, and B. Glader, “Arthropathy of the ankle in hemophilia,” Journal of Bone and Joint Surgery Series A, vol. 73, no. 7, pp. 1008–1015, 1991.
[30]  K. Dickersin, R. Scherer, and C. Lefebvre, “Identifying relevant studies for systematic reviews,” British Medical Journal, vol. 309, pp. 1286–1291, 1994.
[31]  M. W. Lipsey, “Identifying interesting variables and analysis opportunities,” in The Handbook of Research Synthesis and Meta-Analysis, H. M. Cooper, L. V. Hedges, and J. C. Valentine, Eds., pp. 147–158, Sage, New York, NY, USA, 2009.
[32]  M. Van Tulder, A. Furlan, C. Bombardier, and L. Bouter, “Updated method guidelines for systematic reviews in the Cochrane Collaboration Back Review Group,” Spine, vol. 28, no. 12, pp. 1290–1299, 2003.
[33]  C. G. Maher, C. Sherrington, R. D. Herbert, A. M. Moseley, and M. Elkins, “Reliability of the PEDro scale for rating quality of randomized controlled trials,” Physical Therapy, vol. 83, no. 8, pp. 713–721, 2003.
[34]  R. Rosenthal, Meta-Analytic Procedures for Social Research, Sage, Beverly Hills, Calif, USA, 1984.
[35]  B. Koch, S. Cohen, N. C. Luban, and G. Eng, “Hemophiliac knee: rehabilitation techniques,” Archives of Physical Medicine and Rehabilitation, vol. 63, no. 8, pp. 379–382, 1982.
[36]  J. R. Pelletier, T. W. Findley, and S. A. Gemma, “Isometric exercise for an individual with hemophilic arthropathy,” Physical Therapy, vol. 67, no. 9, pp. 1359–1364, 1987.
[37]  A.-M. Nazzaro, S. Owens, W. K. Hoots, and K. L. Larson, “Knowledge, attitudes, and behaviors of youths in the US hemophilia population: results of a national survey,” American Journal of Public Health, vol. 96, no. 9, pp. 1618–1622, 2006.
[38]  T. Hilberg, M. Herbsleb, H. H. W. Gabriel, D. Jeschke, and W. Schramm, “Proprioception and isometric muscular strength in haemophilic subjects,” Haemophilia, vol. 7, no. 6, pp. 582–588, 2001.
[39]  S. Harris and L. N. Boggio, “Exercise may decrease further destruction in the adult haemophilic joint,” Haemophilia, vol. 12, pp. 237–240, 2006.
[40]  R. Mulvany, A. R. Zucker-Levin, M. Jeng et al., “Effects of a 6-Week, individualized, supervised exercise program for people with bleeding disorders and hemophilic arthritis,” Physical Therapy, vol. 90, no. 4, pp. 509–526, 2010.
[41]  M. Luterek, M. Baranowski, W. Zakiewicz, A. Biel, and P. Pedzisz, “PNF-based rehabilitation in patients with severe haemophilic arthropathy—case study,” Ortopedia Traumatologia Rehabilitacja, vol. 11, no. 3, pp. 280–289, 2009.
[42]  L. Heijnen and P. de Kleijn, “Physiotherapy for the treatment of articular contractures in haemophilia,” Haemophilia, vol. 5, supplement 1, pp. 16–19, 1999.
[43]  D. J. Filho, L. R. Battistella, and C. Louren?o, “Computerized pedobarography in the characterization of ankle-foot instabilities of haemophilic patients,” Haemophilia, vol. 12, no. 2, pp. 140–146, 2006.
[44]  A. Lambing, B. Kohn-Converse, S. Hanagavadi, and V. Varma, “Use of acupuncture in the management of chronic haemophilia pain,” Haemophilia, vol. 18, pp. 613–617, 2012.
[45]  I. A. d'Young, “Domiciliary application of CryoCuff in severe haemophilia: qualitative questionnaire and clinical audit,” Haemophilia, vol. 14, no. 4, pp. 823–827, 2008.
[46]  S. Von Mackensen, B. Eifrig, D. Z?ch, J. Kalnins, A. Wieloch, and W. Zeller, “The impact of a specific aqua-training for adult haemophilic patients—results of the WATERCISE study (WAT-QoL),” Haemophilia, vol. 18, pp. 714–721, 2012.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133