2020
DOI: 10.3892/etm.2020.9337
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Current practices in haemophilic patients undergoing orthopedic surgery ‑ a systematic review

Abstract: Haemophilia is an inherited disease that requires a different approach in order to evaluate, monitor and treat patients. Despite the great advances in therapeutic agents that have emerged, reports on the impact of monitoring outcomes on treatment decisions are rarely presented. Haemophilia A and haemophilia B are inherited bleeding disorders caused by deficiencies in blood clotting factor proteins. A systematic review was performed to identify literature reports on the current practices in haemophilic patients… Show more

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Cited by 12 publications
(8 citation statements)
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References 30 publications
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“…The limitation of the approach is that it offers a limited view to the quadrilateral plate, lack of direct visualization of the acetabular surface and control in severely displaced posterior column fractures. In addition, a high rate of postoperative infection and iatrogenic injury to the ilio-femoral vessels and femoral nerve is common (6)(7)(8)(9).…”
Section: Introductionmentioning
confidence: 99%
“…The limitation of the approach is that it offers a limited view to the quadrilateral plate, lack of direct visualization of the acetabular surface and control in severely displaced posterior column fractures. In addition, a high rate of postoperative infection and iatrogenic injury to the ilio-femoral vessels and femoral nerve is common (6)(7)(8)(9).…”
Section: Introductionmentioning
confidence: 99%
“…Many of these goals focus on maintaining a proper level of platelets and blood clotting factors throughout the procedure. Badulescu et al 2 specifically focused on management of patients with hemophilia A and B undergoing total arthroplasty and state that recombinant coagulation factor VIII and/or an antifibrinolytic should be used during surgery. To maximize use of intraoperative hemolytic management, patients undergoing ORIF who need additional joint surgery could be candidates to address all operative treatments under 1 anesthetic.…”
Section: Discussionmentioning
confidence: 99%
“…HHC is characterized by increased concentration of homocysteine (HC) in plasma, and is associated with both venous and arterial thrombosis [23][24][25][26]. It is generally accepted that HHC dis-rupts normal endothelial functions, which are the relaxation of blood vessels and the state of anticoagulation of the blood, thus disturbing coagulation-fibrinolysis balance [27,28]. Hyperhomocysteinemia is caused by an inherited or acquired deficiency of the enzymes involved in its metabolism (methylenetetrahydrofolate reductase or cystathionine beta synthetase) or a deficiency of vitamins belonging to the group of B vitamins.…”
Section: Laboratory Assessment Of Dvtmentioning
confidence: 99%